R F Technologies CBTX Proximity Reader User Manual 0510 1086 B Series 7 0 Software Users Guide

R F Technologies Inc Proximity Reader 0510 1086 B Series 7 0 Software Users Guide

User Manual

3125 North 126th Street, Brookfield, WI 53005 USAphone: 800.669.9946 web: www.rft.comSeries 7.0 SoftwareUser GuidePN 0510-1086-B
Series 7.0 SoftwareUser GuideSupports the 9450 Series Systems, Quick Response Systems,9500 Series Wired Systems and 9600 Series Systems PN: 0510-1086-B Release Date: 06/29/10Users must read this Guide before using the Product.
Copyright 2009, 2010 by RF Technologies, Inc.All Rights Reserved. No Part of this work may be reproduced or copied in any form or by any means without written permission from RF Technologies, Inc.
Important WarningsIt is important for your facility to implement and enforce the following WARNINGS in order to keep all equipment functioning properly. Disregarding the information and instructions in this document is considered abnormal use and may result in injury or system failure.WARNINGACCESSORIES (SUPPLIES)—To ensure patient safety and proper operation of equipment, use only parts and accessories manufactured or recommended by RF Technologies, Inc. Parts and accessories not manufactured or recommended by RF Technologies, Inc. may not meet the requirements of the applicable safety and performance standards. Failure to use the components and supplies specified by RF Technologies, Inc. may result in equipment and/or system failure.WARNINGEXPLOSION HAZARD—These devices should not be used in the presence of flammable gas mixtures. It should also not be used in oxygen enriched atmospheres.WARNINGINSTALLATION AND CONFIGURATION—It is the responsibility of the facility to follow the installation instructions carefully, as outlined in the applicable system guides, and to use the components and supplies specified by RF Technologies, Inc. for all installations.Failure to use the components and supplies specified by RF Technologies, Inc. may result in equipment and/or system failure.WARNINGINSTRUCTIONS FOR SET UP AND USE—It is the responsibility of the facility to follow the instructions for set up and use carefully, as outlined in this manual, and to use the components and supplies specified by RF Technologies, Inc. for set up and use. Do not attempt to use extension cords or other equipment not supplied by RF Technologies, Inc. Failure to use the components and supplies specified by RF Technologies, Inc. may result in equipment and/or system failure.WARNINGPATIENT GENERATED ALARMS—Do not rely exclusively on patient generated alarms for patient care and safety. The alarm function of equipment in the possession of patients must be verified periodically and regular patient surveillance is recommended.
WARNINGPATIENT MONITORING—The most reliable method of patient monitoring combines close personal surveillance with correct operation of monitoring equipment. It is the responsibility of the facility to periodically check on patients in possession of RF Technologies, Inc.'s equipment (i.e. Pendants, Pull Cords, Control Units) to mitigate risk of inappropriate use of equipment or strangulation and stumbling hazards from cables and cordsWARNINGPRODUCT WARRANTIES—Failure to follow the Warnings and Cautions in this guide voids any and all Product WarrantiesWARNINGSTATIC DISCHARGE—Do not touch the conductor portion of any conductor or port. Damage to the device may result.WARNINGSTRANGULATIONS AND TRIPPING HAZARD—Due to the possibility of strangulation, all cables and cords should be routed away from the patient’s throat. Cables and cords must be routed in a way to prevent tripping hazards.WARNINGSYSTEM INSPECTION—It is the responsibility of the facility to establish and facilitate a regular inspection schedule for your system. RF Technologies, Inc. recommend quarterly inspections of your system for safety and performance by a qualified RF Technologies, Inc. representative.To arrange for a quarterly inspection by RF Technologies, Inc., call our Technical Support Department at (800)-669-9946 or (262) 790-1771.Failure to provide regular inspection of these products may result in equipment and/or system failure.WARNINGSYSTEM MAINTENANCE AND TESTING—It is the responsibility of the facility to establish and facilitate a regular maintenance schedule for your system, as outlined in the applicable system guides. This includes regular inspection, testing, and cleaning. RF Technologies, Inc. recommend monthly maintenance and testing of your system. It is also recommended that your facility keep records of maintenance and test completions.Failure to provide regular maintenance and testing of these products may result in equipment and/or system failure.
Bio-Incompatibility NoticeDo not use Pendants with people that have sensitivities or allergies to device materials. The device materials include Acrylonitrile butadiene styrene (ABS), Silicon Rubber and NeopreneWARNINGSYSTEM WIRING—All permanent supply connections must be done in accordance with National Electric Code, NFPA 70.WARNINGUSER TRAINING—Only users who have received adequate training on the use of the system, as outlined in this manual, should use the system. It is the responsibility of the facility to ensure all users have been trained. Failure to adequately train employees may cause system failure due to user error. In addition, incorrect use of the equipment may also result in system failure.WARNINGWORN OR DAMAGED PARTS—If the control unit pads or cables are worn or damaged, you must have the product serviced. For more information, see the section entitled “Service and Return.” WARNINGAll RF Technologies transmitters, pendants and banding material “PRODUCT” have been determined to be MR Unsafe as defined by ASTM F 2503-05. Use of “PRODUCT” in a Magnetic Resonance Imaging system will cause injury to patients and staff, MR system malfunction or “PRODUCT” malfunction. Do not bring “PRODUCT” into the MR system area and follow your facilities policies to classify and label “PRODUCT” as MR Unsafe.CAUTIONDISPOSAL—At the end of their service life the products described in this manual, as well as accessories (i.e. lithium batteries, banding material, disposable pads, etc.), must be disposed of in compliance with all applicable federal, state and local guidelines regulating the disposal of products containing potential environmental contaminants. Dispose of the packaging material by observing the applicable waste control regulations.
ComplianceFederal Communication Commission (FCC) Compliance This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation of the device. This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the instruction manual, may cause harmful interference to radio communications. Operation of this equipment in a residential area is likely to cause harmful interference in which case the user will be required to correct the interference at his own expense. Changes or modifications not expressly approved by the party responsible for compliance voids the user’s authority to operate the equipment. FCC and IC Radiation Exposure Statement for Mobile Devices(For the Pull Cord model 0800-0285 and model 0800-0317; Universal Transceiver model 0800-0301, which covers part numbers 0800-0303 and 0800-0304; Extended Range Universal Transceiver model 0800-0388, which covers part numbers 0800-0389 and 0800-0390; Extended Range Router model 0800-0351 and model 0800-0354; Router model 0800-0364; Asset Transceivers model 0800-0286 and model 0800-0302 and Motion Control Unit model 0800-0318)This equipment complies with FCC and IC radiation exposure limits set forth for an uncontrolled environment. This equipment should be installed and operated with minimum distance 20cm between the radiator and your body. This transceiver must not be co-located or operating in conjunction with any other antenna or transceiver.FCC and IC Radiation Exposure Statement for Portable Devices(For the Pendant Transceivers model 0800-0288 and model 0800-0349; Call Pendant model 0800-0375; and Care Manager model 9600-0500)This equipment complies with FCC and IC radiation exposure limits set forth for an uncontrolled environment. This equipment is in direct contact with the body of the user under normal operating conditions. This transceiver must not be co-located or operating in conjunction with any other antenna or transceiver.Industry Canada Compliance Changes or modifications not expressly approved by RF Technologies could void the user’s authority to operate the equipment. The Term “IC” before the radio certification number only signifies that Industry Canada technical specifications were met. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation of the device. This device has been designed to operate with the antennas listed below, and having a maximum gain of 3dBi. Antennas not included in this list or having a gain greater than 3dBi are strictly prohibited for use with this device. The required antenna impedance is 50 ohms. Acceptable antennas are PCB antennas in all cases of the Router which uses a 2.4 GHz 1/2 wave RP-SMA.To reduce potential radio interference to other users, the antenna type and its gain should be so chosen that the equivalent isotropically radiated power (e.i.r.p.) is not more than that permitted for successful communication.
Series 7.0 Software  (0510-1086-B) - User Guide    iContentsPreface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19450 System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1Quick Response (QR) Wired System  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29500 Series Wired Call System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .29600 Series Wireless Call System  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2Intended Audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3Additional Detailed Documentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3Contact Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3Product Warranty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3Chapter 1 Equipment Overview  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5Central Server and Client Computers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5Quick Look Display  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59450 System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6Staff Alert Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6Exit Alarm Controller. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7Card Reader Access Device. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7The Exit Alarm Zone . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7Exit Alarm Receiver . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8Magnetic Reed Switch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8CodeLock Electromagnetic Lock. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8Alarming Band Receivers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9Alarming Band Zone . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9Alarming Band Transmitters  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9Patient and Infant Transmitters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9Smart Sense™ Infant Transmitter and Banding Material . . . . . . . . . . . . . . . . . . . . . 10Mother Transmitter  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11Wander Management Transmitter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12CodeWatch Transmitter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Contentsii    Series 7.0 Software  (0510-1086-B) - User GuideQuick Response System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13Wireless Receiver  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13Repeater. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14Locator  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14Paging Base . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14Back-Up Interface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14Pendant Transmitter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15Wall Mount Transmitter. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15Pull Cord . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15Check-in Pull Cord . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16Smoke Detector  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16PIR Sensor. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16Door/Window Transmitter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17Universal Transmitter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .179600 Series Wireless Call System  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18Gateway. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18Router . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18Quick Look Router. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1932 Channel Controller Router . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19Dome Light  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .20Transceivers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .20Pull Cord  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20Check-in Pull Cord. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21Wall Mount Emergency Call . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21Nurse Call Transceiver. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22Universal Transceiver  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22Universal Nurse Call . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23Door/Window Transceiver. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24Smoke Detector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24PIR Sensor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24Pendant Transceiver. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 259500 Series Wired System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26Central Power Supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2632 Zone Staff Alert Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .26Dome Light  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .27Assistance Call Devices  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .27Nurse Call  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27Pull Cord  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27Fall Management System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28Fall Management System Control Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .29Fall Management System Sensor Pad  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .29
Series 7.0 Software  (0510-1086-B) - User Guide    iiiContentsFall Management System Nurse Call . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29Advanced 3-Way Care Solution  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30Advanced 3-Way Control Unit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .31Advanced 3-Way Care Sensor Pads . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .31Motion Sensor Pad. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31Incontinence Sensor Pad . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31Advanced 4-Way Care Solution  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32Advanced 4-Way Control Unit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .33Advanced 4-Way Care Sensor Pads . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .33Motion Sensor Pad. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33Incontinence Sensor Pad . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34Messaging Services . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35Event Messaging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .35Messaging Delays, Retries and Escalation  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35Walkie-Talkie. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .36Chapter 2 Software Features. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37Start the Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37Sleep Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .37Window Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38Touchscreen Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39Quick Reference Tutorial. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40Map Orientation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41Ruleset for Displaying Patient Name  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42The Main Window  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44Event List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45Census  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46Map  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47Devices Displayed on the Map  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .47
Contentsiv    Series 7.0 Software  (0510-1086-B) - User GuideHelp  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48Silence  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48Alarm Message Box  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49Low Battery Icon  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49Chapter 3 Using the Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51Commonly Used Terms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51Login and Passwords  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .51Device Supervision . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .52Inactivity Check-in . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .52Units  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .52Global Lockdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .53Troubleshooter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .54Admit Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55Name An Auto-Enrolled Transmitter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .55Manual Admit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .56Pre-Enroll . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .59Admit Information Windows. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60Admit Information Tabs  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .60Quick Look Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60Main Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61Medical Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63Contact Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63Insert a Picture . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63Enter Transmitter Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64Scheduling an Event. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65Discharge . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67Adjust. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70Escort . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73Transfer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76Update Record. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
Series 7.0 Software  (0510-1086-B) - User Guide    vContentsAdministrative Functions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80Add/Update An Asset . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .81Asset Main Information Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82Staff Drill. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .83System Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .84Changing Client Properties. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .85Configuration  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .86Reports  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .87Messaging Functions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88Scheduled Messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .88Changing Shift. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .91Start Shift. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .92End Shift . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .93Send Message  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .93Chapter 4 Handling Events . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95Events. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95Event Information Window. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .96Event Information Window Properties  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97Event Types . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97Red Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .98Door Alarm  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98Exit Alarm (Wide Gap) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99Smoke Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99Perimeter Alarm. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100Cut Band Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 101Band Off Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102Mismatch Alarm  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 103Match Alarm  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 103Link Alarm. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 104Check Alarm  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 104No Signal Alarm  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 105Assistance Required Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 106Fall Alarm  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 107Wet Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 108Turn Alarm. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .108Server Missing Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 109
Contentsvi    Series 7.0 Software  (0510-1086-B) - User GuideYellow Alarms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .110No Signal Alarm (9600 Series Pendant) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 110Client Missing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 111Device Fault. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 111Low Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 112Tamper Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 113White Alarms  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .114Auto-Enroll  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 114Admit Completed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 114Pre-Enroll Expired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115Discharge Expired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115Discharge Completed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115Escort to Expire . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .116Escort Expired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 116Escort Completed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 116Transfer to Expire  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 117Transfer Expired  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 117Transfer Completed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 117Begin Adjust  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 118Adjust Expired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 118Adjust Competed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .118Scheduled Event. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 118Blue Alarms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .119Door Alarm  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 119Cut Band Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 120No Signal Alarm  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 121Light Blue Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .121Admit Completed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 121Discharge Expired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 122Discharge Completed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 122Escort to Expire . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .122Escort Expired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 123Escort Completed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 123Transfer to Expire  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 123Transfer Expired  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 124Transfer Completed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 124Adjust Expired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 124Adjust Completed  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 125Scheduled Event. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 125
Series 7.0 Software  (0510-1086-B) - User Guide    viiContentsChapter 5 Using System Reports . . . . . . . . . . . . . . . . . . . . . . . . . . . 127Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 127Reports  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .127Report Buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .129Sort By Headings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 130Additional Joint Commission Report Buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 131System Reports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 132Daily Alarms and Activities (Tracer Level 2). . . . . . . . . . . . . . . . . . . . . . . . .132Alarm Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 132Alarm Activities Report. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 133Alarm Response Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 133Care Time Report (Code Alert only) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 134Activities Report  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 134All Activities Report  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 135All Other Reasons Report  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 135Facility Trends (Tracer Level 3) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .136Joint Commission Alarm Trend Report. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 136Joint Commission Assistance Trend Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 138Response Time Trend Report  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 140Staff Reports (Tracer Level 4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .142Users Report. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 142User Training Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 143Staff Care Time Report (Code Alert only). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 143Staff Drill Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 144Training Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 144Facility Maintenance (Tracer level 5) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .145System Maintenance Report  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 145Low Batteries Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 145Device Fault Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 145Additional Reports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .146Census Report  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 146Auto Enrolled History Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 146Adjusted Bands Report  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 147Transfer Report  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 147Escort Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 148Discharge Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 148Device Hardware Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149Device Tree Report (Code Alert only). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149Transmitter Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 150Links Report. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 150Links Activities Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 150Sensatec Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 151
Contentsviii    Series 7.0 Software  (0510-1086-B) - User GuidePatient Reports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 151Review Info Report  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .151Review Activity Report. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .151Review Response Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .152Review Response Reason  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 153Review Response Reason Detail Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .154Asset Reports. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 154Asset Transmitter Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .154Asset Activities Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .154
Series 7.0 Software (0510-1086-B) - User Guide 1PrefaceOverviewThe Series 7.0 Software supports the 9450 Series, Quick Response (QR), 9500 Series Wired Call and 9600 Series Wireless Call Systems. This guide provides detailed information about the Series 7.0 Software, using the software and using system reports. It also provides an overview of the systems as well as an equipment overview.9450 SystemThe 9450 System monitors doors, elevators, hallways, and stairwells, to assist staff in monitoring patients and assets in a facility. The various transmitters and devices of the system alerts staff if a transmitter’s banding material is tampered with, cut or opened without authorization (referred to as Cut Band for Infant and Emergency Department systems only) or if monitored devices in the system are not functioning properly. The Smart Sense technology combines the Smart Sense Infant Transmitter and Banding Material to give you three additional measurements for tamper detection (referred to as Band Off for Infant and Emergency Department systems only). •Temperature—change in transmitter temperature•Resistance—no motion detected from the banding material (i.e. band stretching with normal infant movement)•Capacitance—change in contact between transmitter and infantAn alarm also sounds if a transmitter is detected in an Exit Alarm Zone. If the system fails to detect a transmitter within its monitored area, a No Signal alarm is issued.Depending on which equipment options your facility has installed, the 9450 System can automatically lock doors and deactivate elevators. In addition, the system sounds an alarm at the Central Server and its network of Client computers when the event occurs. If configured, alarms are also annunciated at remote notification locations (i.e. pagers, walkie-talkie, Quick Look Interface).With the Mother/Infant Matching feature activated, an alarm is generated if there is a mismatch, meaning the Infant and Mother transmitters do not match; a linking error, meaning there is a problem linking the Infant transmitter to a Mother transmitter; or if a discharge is attempted without first matching the Infant transmitter with the Mother transmitter.NOTE: The Mother/Infant Matching feature is included in the software; however, if your facility is not currently configured for Mother transmitters, the Mother/Infant Matching feature IS NOT ACTIVE. For more information, contact RF Technologies Technical Support at (800) 669-9946 or (262) 790-1771.
 Preface2 Series 7.0 Software (0510-1086-B) - User GuideQuick Response (QR) Wired SystemThe QR System immediately notifies staff when a patient requires attention, and provides details that are essential in responding quickly to the needs of a patient.The QR System offers a variety of transmitters, each of which interfaces with the Central Server to ensure that when a patient is in need, staff can be alerted via multiple methods (i.e. pagers, walkie-talkie, Quick Look Interface). A QR transmitter may be worn by a patient; it could be mounted to a wall where it is easy to access; it may be integrated with a wireless smoke detector; it could additionally be used in conjunction with the 9450 System.9500 Series Wired Call SystemThe 9500 Series Wired Call System is the simplest implementation of a nurse call system. The system consist of a 15 AMP Class II Central Power Supply, 32 Channel Staff Alert Panel for audible and visual alarms, a visual 9500 Dome Light positioned outside the resident's room, and Assistance Call devices to initiate an alarm. When an emergency call is initiated from an Assistance Call device, the red Dome Light illuminates and an audible alarm sounds at the Staff Alert Panel. Normal calls are indicated by a white Dome Light.9600 Series Wireless Call SystemThe 9600 Series Wireless Call System immediately notifies staff when a patient requires attention, and provides details that are essential in responding quickly to a patient’s needs.The 9600 Series Wireless Call System offers a variety of transceiver devices, each of which interfaces with the Central Server to ensure that when a patient is in need, staff is alerted. A transceiver is a device that periodically transmits a signal containing data to uniquely identify it from other transceivers. It may be worn by a patient; it could be mounted to a wall where it is easy to access; it may be integrated with a wireless smoke detector; it could also be used in conjunction with other systems such as the 9450 System and Code Alert Wanderer Monitoring System.Transceiver devices send data to the Central Server on a regular basis. When an event occurs that warrants a response, staff is alerted by an audible alarm from the Central Server, a message is displayed on-screen and the designated staff is summoned to respond to the situation. Staff can also be notified of an event via the 9600 Series Care Manager.WARNI NG :  The 9450, QR and 9600 Series Wireless Call Systems are designed and intended to work in conjunction with a facility’s overall security program, including reasonable operating policies and procedures. The systems, by themselves, cannot prevent abductions or elopements.
Series 7.0 Software (0510-1086-B) - User Guide  3Intended AudienceIntended AudienceThe  Series 7.0 Software User Guide is intended for users who use the software. It includes detailed information about the 9450, QR and 9600 Series Wireless Call Systems, the software, and how to use the software. This guide is intended to be used in conjunction with the Series 7.0 Administrator’s Guide (PN 0510-1087) along with other user and installation guides when specified.Additional Detailed DocumentationDocumentation for your system is available in Portable Document Format (PDF) on the System Documentation CD-ROM. Please contact your RF Technologies sales representative for replacement CD-ROMs.Contact InformationFor more information about RF Technologies, Inc. products, go to www.rft.com. For technical support, contact the Technical Support Team at (800) 669-9946 or (262) 790-1771. For questions or comments about the System Documentation, contact the RF Technologies Technical Publications team at techpubs@rft.com.Product WarrantyProduct Warranty information can be found on the System Documentation CD-ROM or with your original system proposal and invoice.
 Preface4 Series 7.0 Software (0510-1086-B) - User GuideThis page intentionally left blank.
Series 7.0 Software (0510-1086-B) - User Guide 5Chapter 1Equipment Overview IntroductionThis chapter provides equipment overviews of the devices supported by the system and device supervision. The supervision feature applies to many devices such as the Alarming Band Transmitters, Pendants, Fall Monitoring and Incontinence devices. A supervised device is the system’s way of ensuring that devices are communicating properly and within range of the receivers. This chapter also provides details of the Central Server and Client computers used to run the software as well as Messaging and Walkie-Talkie information. Central Server and Client ComputersThe Central Server is a Windows based computer that runs the software. It contains the database and provides communication with devices in the system as well as the Client computer(s). Depending on your configuration, the system can include several Client computers. The Client computers allow the user to perform such functions as admitting, discharging, and authorizing transfers and escorts. Each Client computer includes a touchscreen monitor that displays alarms as they occur on a floor plan of the facility.The Central Server can be located in any area such as the nurse’s central station or security office. It must be located near a dedicated analog phone line or broadband connection to allow for remote Technical Support access when requested by the customer. Each Client computer must be located in a secure area that can be accessed by staff to enter and retrieve information.Quick Look DisplayThe Quick Look Display shows information from the system at remote locations such as a secondary nurse’s station. When a Red alarm is issued from the system, it is received through the Quick Look Interface. The type of alarm (Cut Band, Door, Check), location of the alarm and the transmitter ID are displayed on a large, easy-to-read 2 x 20 Character Vacuum Fluorescent Displays (VFDs). As new alarms occur, they appear immediately; the display then begins scrolling through each active alarm. For more information about the Quick Look Display, see the Quick Look Display and Interface Installation Guide (0510-1007).WARNING: When installing the Central Server, proper placement/mounting of the server is important. Adequate precautions must be taken to prevent the server from falling, causing injury to persons. Cables must be routed in a way to prevent tripping hazards.Any rack mounted Central Server must be install in a controlled environment that maintains temperature between 50°F and 95°F and humidity between 20% and 50%.
Chapter 1: Equipment Overview 6 Series 7.0 Software (0510-1086-B) - User Guide9450 SystemThe transmitters and devices in this section are supported by the 9450 System running the Series 7.0 Software application.The 9450 System consist of the following equipment.•Central Server and Client Computer(s)•Quick Look Display(s)•Staff Alert Panel•Exit Alarm Controller•Exit Alarm Receiver•Magnetic Reed Switch•CodeLock Electromagnetic Lock•Alarming Band Receivers•Transmitters•Smart Sense•Alarming Band•Mother•Wander Management•CodeWatchStaff Alert PanelThe Staff Alert Panel receives alarm signals from Exit Alarm Controllers and Alarming Band Receivers and indicates with a tone and a red LED that an alarm has occurred. In the space next to each red LED, you can write a brief description identifying the zone or device that issued the alarm. If your facility requires the Staff Alert Panel to be visible, it must be located on a wall near the Nurses Station; or it can be located elsewhere such as a security office, or a phone operator room. For more information about Staff Alert Panel, see the Staff Alert Panel Installation Guide (PN 0510-1008).
Series 7.0 Software (0510-1086-B) - User Guide  79450 SystemExit Alarm ControllerThe Exit Alarm Controller receives data from the Exit Alarm Receivers and issues an alarm if a transmitter is detected in the Exit Alarm Zone, and the door is open. The Exit Alarm Controller contains a keypad, and/or card reader access device, that allows authorized staff to reset the system after an alarm. The Exit Alarm Controller is the device that triggers the alarm process for the Central Server and Staff Alert. For more information about the Exit Alarm Controller, see the Delayed Egress Exit Alarm Controller Installation Guide (PN 0510-1023).Card Reader Access DeviceThe Card Reader Access device can be connected to the Exit Alarm Controllers in order to use access cards for triggering bypass cycles and resetting alarms on the Exit Alarm Controller. The Card Reader Access device can be an HID proximity card reader or a magnetic/bar code card reader (available at RF Technologies). The Card Reader is interfaced through an RS-232 serial communications port between the Card Reader and the Exit Alarm Controller. The Card Reader and the Exit Alarm Controller may share a common power supply feed.The Exit Alarm ZoneAn Exit Alarm Zone is the area within range of a door, elevator, hallway, or stairwell that is being monitored by the system. If a transmitter is detected in an Exit Alarm Zone and the door is open, an alarm sounds at the exit. If the door is equipped with a CodeLock, when a transmitter enters the Exit Alarm Zone and the door is closed, it will lock.The devices that are used in an Exit Alarm Zone are an Exit Alarm Controller, Magnetic Reed Switches, and Exit Alarm Receivers. Optional devices include CodeLock™ electromagnetic locks, passive infrared (PIR) detectors, and an External Reset/Bypass Keypad.Power: The red light indicates that power is available to the system.Signal: The yellow light indicates that a signal has been received from the Exit Alarm Receivers.Status: The green light indicates that the system is in bypass or that the unit is in alarm or disarmed.
Chapter 1: Equipment Overview 8 Series 7.0 Software (0510-1086-B) - User GuideExit Alarm ReceiverExit Alarm Receivers are low frequency (LF) antennas placed on or near a door frame in an Exit Alarm Zone. They receive signals from transmitters within a monitored zone and send the signals to the Exit Alarm Controller, which triggers the alarm process. For more information about Exit Alarm Receivers, see the DuoLink Exit Alarm Receiver Installation Guide (PN 0510-1003).Magnetic Reed SwitchThe Magnetic Reed Switch is used by an Exit Alarm Controller to detect that a monitored door is open. The Magnetic Reed Switch should be mounted at the top of a door near the non-hinged edge. It comes in two pieces: a switch and a magnet. The switch is mounted on the door frame; the magnet is attached directly to the door.When normally closed (NC) reed switches are used on a double door, connect the switches in series. The provided Magnetic Reed Switches are normally closed (indicated with a gold Code Alert logo) when the doors are closed so that opening either door opens the switch on that door. CodeLock Electromagnetic LockThe CodeLock option is an electromagnetic lock attached to an exit and connected to the Exit Alarm Controller. If a transmitter is detected in the Exit Zone, the CodeLock activates to help stop the door from opening for as long as the transmitter is within range of the receivers. Refer to the CodeLock Electromagnetic Door Lock Installation Guide (PN 0510-1002) for information on installation and operation.
Series 7.0 Software (0510-1086-B) - User Guide  99450 SystemAlarming Band ReceiversAlarming Band Receivers are placed strategically throughout the monitoring area to receive signals from the alarming band transmitters worn by patients. When using the alarming band transmitter, the system provides an alert if the banding material that holds the transmitter to the patient is tampered with, cut, or opened without authorization. Multiple receivers are used to ensure reception of the signal if there is an effort made to shield the transmitter during abduction or elopement attempts. For more information, see the Alarming Band Receiver Installation Guide (PN 0510-1001). Alarming Band ZoneAn Alarming Band Zone is the area within range of an Alarming Band Receiver, several of which are mounted below the ceiling tiles of a facility. If a Cut Band or Band Off alarm is triggered in an Alarming Band Zone, an alarm is sounded on all Client computers assigned to monitor the transmitter’s unit, a message is displayed in the Event List, and the location of the Alarming Band Receiver that detected the event is indicated on the map on the Client computer(s). Cut Band and Band Off alarms are also posted on remote notification devices.Alarming Band TransmittersA transmitter is a device that periodically transmits a signal containing data to uniquely identify it from other transmitters. Some transmitters are also capable of transmitting information to identify that the band has been cut. These transmitters are referred to as alarming band transmitters.Patient and Infant TransmittersPatient and Infant transmitters are placed on the ankle or wrist of a patient or affixed to an asset. The transmitter becomes active once the banding material remains connected on both sides with banding material in place for 60 seconds. The 60-second window exists to allow for proper adjustment of the banding material. After one minute, the transmitter ID is displayed in the Event List and information of the patient or asset wearing the transmitter can be associated with the transmitter using the Admit or Auto-Enroll function. Alarming band transmitters can be supervised. If a transmitter is configured for Supervision, and fails to regularly communicate to the system, a No Signal alarm will result in the Event List at the computer. For more information about securing, cleaning, and troubleshooting transmitters, refer to the Patient Transmitter User Guide (PN 0510-1013) or Infant Transmitter User Guide (PN 0510-1006).NOTE: The Mother/Infant function requires applicable Alarming Band Receivers.Patient TransmitterInfant Transmitter
Chapter 1: Equipment Overview 10 Series 7.0 Software (0510-1086-B) - User GuideEach transmitter is stamped with a warranty expiration date. This date indicates the date that RF Technologies’ warranty on that transmitter expires (the last day of the month stamped). If the warranty period has expired, discard the transmitter immediately.Smart Sense™ Infant Transmitter and Banding MaterialThe combination of the Smart Sense Infant Transmitter and Banding Material has the capability to recognize if the transmitter has been removed from an infant. It will also sense if it is tampered with or loose. If a transmitter is configured for Supervision, and fails to regularly communicate to the system, a No Signal alarm will result in the Event List at the computer.The Smart Sense technology uses three measurements to provide tamper detection. Depending on your facility, one, two or all three measures for tamper detection can be configured for activation.•Temperature—change in transmitter temperature•Resistance—no motion detected from the banding material (i.e. band stretching with normal infant movement)•Capacitance—change in contact between transmitter and infantThe cloth-like banding material has the capability to stretch or adjust to accommodate infant weight loss, thus reducing re-banding or adjustments caused by slippage. In addition to Cut band technology, band expansion is also a key feature for tampering and unauthorized removal detection. If an unauthorized attempt is made to pull or stretch the banding material, an alert will sound and a Band Off event will be triggered.Each transmitter is stamped with a warranty expiration date. This date indicates the date that RF Technologies’ warranty on that transmitter expires (the last day of the month stamped). If the warranty period has expired, discard the transmitter immediately.WARNING: Using a transmitter beyond the printed EXP date can result in system failure and/or an elopement.WARNING: Using a transmitter beyond the printed EXP date can result in system failure and/or an abduction.
Series 7.0 Software (0510-1086-B) - User Guide  119450 SystemAsset TrackingAlarming band transmitters can be used for asset management. When an alarming band transmitter is attached to an asset and admitted using the Add Asset admit function, Blue alarms are generated and appear in the Event List when an attempt is made to remove the assets from an Exit Zone or the band is tampered with or cut.Non-Alarming Band TransmittersMother TransmitterA Mother transmitter is placed on the wrist of a new mother and then linked to an Infant transmitter worn by her newborn. When the Infant transmitter is in proximity of the Mother transmitter, the Mother transmitter flashes a green light to indicate that the Infant and Mother transmitters match. If there is a mismatch, meaning the Infant and Mother transmitters do not match, the Mother transmitter flashes the red light three times, and sounds a three beep alarm. A Mismatch Transmitter alarm is also generated in the Event List at the computer. If there is a linking problem, for example, the Infant transmitter may already be linked to another Mother transmitter, a Link Transmitter alarm is generated in the Event List at the computer.In cases where the Mother transmitter is linked but no longer active (e.g. the patient has been discharged but the transmitter was never cleared) the transmitter will beep after 24 hours of inactivity. If the transmitter goes undetected and allowed to beep for 15 minutes, it will clear and discharge itself from the system. Tapping the Mother transmitter will temporarily stop the beeping but the transmitter remains in a linked state until manually cleared, refer to the Mother Baby Match Mother Transmitter User Guide (PN 0510-1020). If not cleared, the transmitter will beep again after another 24 hours of inactivity.Each transmitter is stamped with a warranty expiration date. This date indicates the date that RF Technologies’ warranty on that transmitter expires (the last day of the month stamped). If the warranty period has expired, discard the transmitter immediately.NOTE:  Although the Mother transmitter will link to an Asset transmitter, the software does not support this functionality. If this happens, clear the Mother transmitter and re-link the Infant and Mother transmitters. CAUTION: The Mother transmitter can be worn in the shower; complete submersion should be avoided. Prolonged submersion may result in equipment and/or system failure and voids any or all Product Warranty.WARNING: Using a transmitter beyond the printed EXP date can result in system failure and/or an abduction.
Chapter 1: Equipment Overview 12 Series 7.0 Software (0510-1086-B) - User GuideWander Management TransmitterA Wander Management transmitter is a wireless, mobile transmitter that can be worn around the wrist or ankle. An event is reported in the Event List when a patient is near an open monitored door or attempts to leave an Exit Zone.The Wander Management transmitter sends a signal to be received by Exit Alarm Receivers. Exit Alarm Receivers are low frequency (LF) antennas placed on or near a door frame or in an Exit Alarm Zone. They receive signals from transmitters within a monitored zone and send the signals to the Exit Alarm Controller, which triggers the alarm process. The Exit Alarm Controller receives data from the Exit Alarm Receivers and issues an alarm if a resident wearing a transmitter is detected in the Exit Alarm Zone, and the door is open.CodeWatch TransmitterA CodeWatch transmitter is a wireless, mobile transmitter that can be worn around the wrist or ankle. An event is reported in the Event List when a patient is near an open monitored door or attempts to leave an Exit ZoneThe CodeWatch transmitter sends a signal to be received by Exit Alarm Receivers. Exit Alarm Receivers are low frequency (LF) antennas placed on or near a door frame or in an Exit Alarm Zone. They receive signals from transmitters within a monitored zone and send the signals to the Exit Alarm Controller, which triggers the alarm process. The Exit Alarm Controller receives data from the Exit Alarm Receivers and issues an alarm if a resident wearing a transmitter is detected in the Exit Alarm Zone, and the door is open. WARNING: Using a transmitter beyond the printed EXP date can result in system failure and/or an elopement.WARNING: Using a transmitter beyond the printed EXP date can result in system failure and/or an elopement.
Series 7.0 Software (0510-1086-B) - User Guide  13Quick Response SystemQuick Response System Transmitters and devices listed in this section are supported by the Quick Response System running the Series 7.0 Software application. The Quick Response system includes transmitters that are both carried by the patient and fixed devices. A fixed device is a stationary device that is assigned to a room or a unit. This device is not transported with the patient but stays in the unit or room to which it is assigned.Quick Response devices are entered into the system by placing the device into an alarming state. The system senses the device when the device goes into alarm and adds it to the device list in the Configuration-Device window (refer to the Series 7.0 System Administrator Guide). The user must then update the device information; for example, give the device a name and/or enable features.The Quick Responses System consist of the following equipment.•Central Server•Quick Look Display•Wireless Receiver•Repeater•Locator•Paging Base•Back-up Interface•Pendant Transmitter•Wall Mount Transmitter•Pull Cord•Check-in Pull Cord•Smoke Detector•PIR (Passive Infrared) Sensor•Door/Window Transmitter•Universal TransmitterWireless ReceiverThe Receiver is a device that receives signals from the repeater, locator, or QR transmitters and communicates them to the Central Server. The Receiver can be supervised; if no information is received by the system from the Receiver for a specified number of minutes, a Device Fault alarm is generated in the Event List at the computer monitoring the unit that the Receiver is assigned to.
Chapter 1: Equipment Overview 14 Series 7.0 Software (0510-1086-B) - User GuideRepeaterA Repeater is a device that receives the signals from Quick Response transmitter and communicates them to the Receiver. This enables the system to cover larger facilities. Repeaters are supervised; a routine signal is sent from each Repeater and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer.LocatorLocators receive signals from Quick Response transmitters, add location data, and communicates the signals to the receiver. When an event occurs, the map of your facility will indicate the Locator that received the signal from the alarming device. Locators are supervised; a routine signal is sent from each Locator and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer.Paging BaseThe Paging Base (optional) sends radio frequency signals to the pager receiver(s) when events occur. The pager receiver indicates the name, room number, and event type of the transmitter that issued the alarm.Back-Up InterfaceThe Back-up Interface is an optional device that takes over the responsibility of communicating with the paging base and provides alarm information (transmitter number only) in the event of an inoperable computer.NOTE: Please reference Transmitter Report and Device Report to correlate the transmitter number to the patient or the device. It is recommended to reprint the Transmitter Report after new patients are admitted and discharged.
Series 7.0 Software (0510-1086-B) - User Guide  15Quick Response SystemPendant TransmitterA Pendant transmitter is a wireless, mobile transmitter that can be worn around the neck or wrist, or attached to a belt. The Pendant transmitter is suitable for use in showers or baths. To prevent damage to the Pendant transmitter, avoid prolonged submersion. Since the Pendant transmitter is a mobile device, no installation is required. Simply insert the battery and assign the transmitter to a resident, assuming the transmitter has been configured into the system and the transmitter ID number falls within the configured range. The Pendant transmitter is powered by a replaceable 3-volt battery. Wall Mount TransmitterThe Wall Mount transmitter may be mounted on a wall. When a resident presses a button on the transmitter an Assistance Required alarm event is reported Event List at the computer. If the transmitter is supervised, a routine signal is sent from the transmitter and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer. The Wall Mount transmitter is powered by a replaceable 3-volt battery. Pull CordA Pull Cord is usually mounted on a wall. This device is used to request staff assistance and is commonly used in bedrooms and bathrooms. It is suitable for use in close proximity to showers or baths; however to prevent damage, avoid any submersion.An Assistance Required alarm event is reported in the Event List when a patient pulls a cord. The Pull Cord can be supervised; a routine signal is sent from the transmitter and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer. Pull Cords are powered by a replaceable 3-volt battery.
Chapter 1: Equipment Overview 16 Series 7.0 Software (0510-1086-B) - User GuideCheck-in Pull CordA Check-in Pull Cord enables the staff or patient to push a green button to check-in. Pressing the green button indicates to the system that the patient has checked in or been visited by staff. The type of check-in depends on how your Pull Cord is configured (refer to the Series 7.0 Software Administrator Guide).Types of check-in•Patient Check-in—A patient pushes the button to notify the staff that he/she is awake and does not require assistance. •Staff Check-in—A staff member pushes the check-in button once they have checked on a patient. •Staff Care Complete—A staff member pushes the check-in button in response to an Assistance Required alarm once the patient has been checked on and the alarming device is reset. If Joint Commission is enforced, this will clear the White alarm from the Client computer.Smoke DetectorIf your facility is using wireless smoke detectors in conjunction with your Series 7.0 Software, a Smoke alarm event is reported in the Event List each time a smoke detector is activated. A smoke detector can be supervised; a routine signal is sent from the device and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer. The Smoke Detector is powered by a replaceable 3-volt battery.PIR SensorThe Passive Infrared (PIR) Sensor is a motion detector used to sense motion in a room or hallway. Or, it can be used as an Inactivity-Check-in device to sense when no motion is detected within a set period of time (refer to “Inactivity Check-in” in the Series 7.0 Software User Guide). An Assistance Required alarm event is reported in the Event List each time the detector is activated. A PIR motion detector can be supervised; a routine signal is sent from the device and if the signal is not received by the system, a Device Fault event is generated in the Event List. The PIR Sensor is powered by a replaceable 3-volt battery.
Series 7.0 Software (0510-1086-B) - User Guide  17Quick Response SystemDoor/Window TransmitterA Door/Window transmitter is used to protect a door or window against unauthorized egress. An Exit alarm event is reported in the Event List when a door or window is opened. The alarm automatically clears when the door or window is closed. The Door/Window transmitter comes in two pieces: the transmitter enclosure and a magnet. The transmitter enclosure is mounted on the door/window frame; the magnet is attached directly to the door/window. Separating these devices triggers an alarm. The Door/Window transmitter is powered by a replaceable 3-volt battery.Universal TransmitterA Universal transmitter can be used to integrate your facility’s existing equipment such as backup generators, pull-cord devices, or smoke detectors with the Series 7.0 Software. Universal transmitters come as either NO (normally open) or NC (normally closed) devices. They automatically activate when the input from a monitored device has a contact close or open respectively. When this happens, the Universal Transmitter sends event information to the Central Server.The Universal transmitter can be placed in the enclosure of an existing device or inconspicuously mounted near the device. Be sure that the transmitter is not encased in metal that might block the wireless signal to the Repeater or Receiver. The Universal transmitter is powered by a replaceable 3-volt battery.
Chapter 1: Equipment Overview 18 Series 7.0 Software (0510-1086-B) - User Guide9600 Series Wireless Call SystemThe basic components of the 9600 Wireless Call System consist of the Central Server, the Gateway, the Router and the transceiver devices. Other components may consist of the Quick Look Router, 32 Zone Staff Alert Panel, 32 Channel Controller Router and Dome Lights. The 9600 Series Wireless Call System transceiver devices consist of the following:•Pull Cord•Check-in Pull Cord•Wall Mount•Nurse Call•Universal •Universal Nurse Call•Door/Window •Smoke Detector•PIR Sensor•Pendant GatewayThe Gateway receives signals from a Router or transceiver devices and sends them to the Central Server. The Gateway can be supervised; if no information is received by the system from the Gateway for a specified number of minutes, a Device Fault alarm is generated in the Event List at the computer.RouterRouters receive signals from transceivers and re-transmit them to the Gateway. Two factors that affect the placement of Routers are the availability of a power source and sufficient coverage for the supervision of transceivers. There are two variations of Routers, one with an internal antenna and one with an external antenna for greater range. Routers are supervised; a routine signal is sent from each Router and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer.
Series 7.0 Software (0510-1086-B) - User Guide  199600 Series Wireless Call SystemQuick Look RouterA Quick Look Router is an 9600 Series Router connected to a wireless Quick Look Display or High Visibility Display. When an alarm is sent from the Server to the Router, the wireless display shows the type of alarm, location data and transceiver number. As new alarms occur, they appear immediately; the display then begins scrolling through each active alarm. The Quick Look Router also acts as an integral part of the back-up reflector. Reflector functionally allows the 9600 Series network to take over the responsibility of distributing alarm information to the Quick Look Routers in the event of an inoperable Server.Quick Look Routers are supervised; a routine signal is sent from each Quick Look Router and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer.32 Channel Controller RouterThe 32 Channel Controller Router is a 9600 Series Router connected to a 32 Channel Controller. When an alarm is sent from the Server to the Router, the 32 Channel Controller acts as a relay switch and turns on the Dome Light mounted outside the patient’s room. The Dome Light includes two indicator lights: a white indicator light for low priority alarms and a red indicator light for high priority alarms.32 Channel Controller Routers are supervised; a routine signal is sent from each Quick Look Router and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer.WARNING: Quick Look Routers should not be added to multiple units. Since Routers are used to determine location, inaccurate location data could result.
Chapter 1: Equipment Overview 20 Series 7.0 Software (0510-1086-B) - User GuideDome Light The Dome Light includes two different banks of indicator lights: white normal call indicator light and red emergency call indicator lights.•Emergency Calls—Emergency calls are indicated by steady illumination of the red Dome Light associated with the zone or area from which an emergency call has been placed.•Normal Calls—Normal calls are indicated by steady illumination of the white Dome Light associated with the zone or area from which a normal call has been placed.•Concurrent Emergency and Normal Calls—If an emergency and normal call are placed at the same time, the red light connected to the emergency station from which a call was placed will illuminate at the same time as the white light associated with the normal call.TransceiversA transceiver is a device that periodically transmits a signal containing data to uniquely identify it from other transceivers. Additionally, transceivers can receive data back. The transceiver devices listed in this section are supported by the 9600 Series Wireless Call System running the Series 7.0 Software application. The 9600 Series Wireless Call System includes transceivers that are carried by the patient and fixed devices. A fixed device is a stationary device that is assigned to a room or a unit. Fixed devices are not transported with the patient but stay in the unit to which they are assigned.The transceiver devices are entered into the system by placing the device into an alarming state. The system senses the device when the device goes into alarm and adds it to the device list in the Configuration-Device window (refer to the Series 7.0 System Administrator Guide). The user must then update the device information; for example, give the device a name and/or enable features.Pull CordA Pull Cord is usually mounted on the wall. This device is used to request staff assistance and is commonly used in bedrooms and bathrooms. It is suitable for use in close proximity to showers or baths; however to prevent damage, avoid any submersion.An Assistance Required alarm event is reported in the Event List when a patient pulls a cord. The Pull Cord is supervised; a routine signal is sent from the transceiver and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer. Pull Cords are powered by a replaceable 3-volt battery.
Series 7.0 Software (0510-1086-B) - User Guide  219600 Series Wireless Call SystemTo Call for AssistanceTo call for assistance, pull the cord on the Pull Cord transceiver. The red HELP lever comes down indicating that the transceiver is in an alarm state. To Clear an AlarmTo clear the alarm and reset the Pull Cord, rotate the red HELP lever back to the up position. The Pull Cord is now idle and ready for its next usage.Check-in Pull CordA Check-in Pull Cord enables the staff or patient to push a green button to check-in. Pushing the green button indicates to the system that the patient has checked in or been visited by staff. The type of check-in depends on how your Pull Cord is configured (refer to the Series 7.0 Software Administrator Guide).Check-in types•Patient Check In—A patient pushes the button to notify the staff that he/she is awake and does not require assistance. •Staff Check In—A staff member pushes the check-in button once they have checked on a patient. •Staff Care Complete—A staff member pushes the check-in button in response to an Assistance Required alarm once the patient has been checked on and the alarming device is reset. If Joint Commission is enforced, this will clear the White alarm from the Client computerWall Mount Emergency CallA Wall Mount Emergency Call is mounted on the wall. This device is used to request staff assistance and is commonly used in bedrooms and bathrooms. It is suitable for use in close proximity to showers or baths; however to prevent damage, avoid any submersion.An Assistance Required alarm event is reported in the Event List when a patient pushes the red button. The Emergency Call is supervised; a routine signal is sent from the Emergency Call and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer. The Wall Mount Emergency Call is powered by a replaceable 3V battery.
Chapter 1: Equipment Overview 22 Series 7.0 Software (0510-1086-B) - User GuideTo Call for AssistanceTo call for assistance, push the red button on the Wall Mount Emergency Call transceiver. When pushed, the button remains in indicating the device is in an alarm state. To Clear an AlarmTo clear the alarm and reset the Emergency Call, push the red button again. The button pops out indicating the transceiver has changes states and is now idle and ready for its next usage.Nurse Call TransceiverA Nurse Call transceiver is affixed near the bed of the patient. An Assistance Required alarm event is reported in the Event List when a patient pushes the button on the Nurse Call transceiver. The Nurse Call transceiver is supervised; a routine signal is sent from the transceiver and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer. The Nurse Call transceiver is powered by a replaceable 3V battery.Since the Nurse Call transceiver Cord sets, which plugs into the Nurse Call transceiver, require a normally closed (NC) contact, you must configure the Pull Cord transceiver’s Contact Type as normally closed (refer to the section, “Update 9600 Series Pull Cord” in the Series 7.0 Software Administrator’s Guide).To Call for AssistanceTo call for assistance, firmly press down and release the plunger on the Nurse Call. The plunger stays down indicating that the transceiver is in an alarm state. To Clear an AlarmTo clear an alarm or to reset the Nurse Call transceiver, pull the plunger up. When in the up position, the transceiver is idle and ready for its next usage. Universal TransceiverA Universal transceiver can be used to integrate your facility’s existing equipment such as backup generators, pull-cord devices, or smoke detectors with the software. Universal transceivers can be set as either NO (normally open) or NC (normally closed) devices. They automatically activate when the input from a monitored device has a contact close or open respectively. When this happens, the Universal transceiver sends event information to the Central Server. The Universal transmitter can be placed in the enclosure of an existing device or inconspicuously mounted near the device. Be sure that the transmitter is not encased in metal that might block the wireless signal to the Repeater or Receiver. The Universal transmitter is powered by a replaceable 3-volt battery.
Series 7.0 Software (0510-1086-B) - User Guide  239600 Series Wireless Call SystemUniversal Nurse CallA Universal Nurse Call is affixed near the bed of the patient. An Assistance Required alarm event is reported in the Event List when a patient pushes the button on the Universal Nurse Call. The Universal Nurse Call is supervised; a routine signal is sent from the transceiver and if the signal is not received by the system, a Device Fault event is generated in the Event List at the computer. The Universal Nurse Call is powered by a replaceable 3-volt battery.To Call for AssistanceTo call for assistance, firmly press down and release the plunger on the Nurse Call. The plunger stays down indicating that the transceiver is in an alarm state. To Clear an AlarmTo clear an alarm or to reset the Nurse Call transceiver, pull the plunger up. When in the up position, the transceiver is idle and ready for its next usage.
Chapter 1: Equipment Overview 24 Series 7.0 Software (0510-1086-B) - User GuideDoor/Window TransceiverA Door/Window transceiver is used to protect a door or window against unauthorized egress. An Exit alarm event is reported in the Event List when a monitored door or window is opened. The alarm automatically clears when the door or window is closed. The Door/Window transceiver is supervised; if no information is received by the system from the transceiver for a specified number of minutes, a Device Fault alarm is generated in the Event List at the computer.The Door/Window transceiver comes in two pieces: the transceiver enclosure and a magnet. The transceiver enclosure is mounted on the door or window frame; the magnet is attached directly to the door or window. An alarm triggers when the devices are separated. The Door/Window transceiver is powered by a replaceable 3-volt battery.Reset ButtonThere are two types of reset buttons. If your Door/Window transceiver comes with a reset button, the alarm must be reset at the door by pressing the reset button once the door/window is closed. The Door/Window transceiver comes in three pieces: the transceiver enclosure, a magnet and a reset button. Smoke DetectorIf your facility is using wireless Smoke Detectors in conjunction with your Series 7.0 Software, a Smoke alarm event is reported in the Event List each time a Smoke Detector is activated. A Smoke Detector is supervised; a routine signal is sent from the device and if the signal is not received by the system, a Device Faultevent is generated in the Event List at the computer. The Smoke Detector is powered by a replaceable 3-volt battery.PIR SensorThe Passive Infrared (PIR) Sensor is a motion detector used to sense motion in a room or hallway. Or, it can be used as an Inactivity-Check-in device to sense when no motion is detected within a set period of time. An Assistance Requiredalarm event is reported in the Event List each time the detector is activated. A PIR motion detector can be supervised; a routine signal is sent from the device and if the signal is not received by the system, a Device Fault event is generated in the Event List. The PIR Sensor is powered by a replaceable 3-volt battery.
Series 7.0 Software (0510-1086-B) - User Guide  259600 Series Wireless Call SystemPendant TransceiverA Pendant transceiver is a wireless, mobile transceiver that can be worn around the neck or wrist, or attached to a belt. The protective boot protects the Pendant transceiver against dropping and water ingress. However to prevent water damage, avoid prolonged submersion and direct contact with a water stream. The Pendant can be supervised; if no information is received by the system from the Gateway for a specified number of times, a No Signal alarm is generated in the Event List at the computer. Since the Pendant is a mobile device, no installation is required. Simply insert the battery and set up the Pendant transceiver for use. The Pendant is powered by a replaceable 3-volt battery. When the battery is low, the Pendent sends a Low Battery notification.To Call for AssistanceTo call for assistance, firmly press and hold the blue button on the transceiver (for about a second). Release the button, the green light flashes a series of times to indicate the transceiver is in an alarm state. If the transceiver flashes red, the signal is blocked. Move to another area of the room until the signal transmits (flashes green).To Clear an AlarmTo clear an alarm or to reset the Pendant transceiver, rapidly but firmly press and release the blue button on the transceiver six (6) times within three (3) seconds (be sure to see the green light flash for each push). The green light flashes a series of times to indicate the transceiver has changed states and is now idle and ready for its next usage. If the transceiver flashes red, the signal is blocked. Move to another area of the room until the signal transmit (flashes green).WA R N I N G:   You must replace the Pendant battery within seven days after receiving a Low Battery notification.Flashing green light
Chapter 1: Equipment Overview 26 Series 7.0 Software (0510-1086-B) - User Guide9500 Series Wired SystemThe 9500 Series Wired System consist of a 15 amp Class II Central Power Supply, a 9500 Series 32 Zone Staff Alert Panel for audible and visual alarms, a visual 9500 Series Dome Light positioned outside the resident's room, and a 9500 Series Assistance Call device to initiate an alarm. When a call is initiated from an Assistance Call device, the Dome Light illuminates and an audible and visual alarm sounds at the Staff Alert Panel. Refer to the 9500 Series Wired Nurse Call Installation Manual (PN 0510-1061) for detailed information on installing the 9500 Series Wired System.Central Power SupplyThe Central Power Supply is used to connect the 9500 Series Dome Lights to a single power source. The Central Power Supply eliminates the need to run 120VAC to each detection zone.Refer to the Class II Central Power Supply Installation Guide (0510-1036) for detailed information on installing the Central Power Supply.32 Zone Staff Alert PanelThe 32 Zone Staff Alert Panel receives alarm signals from the Assistance Call device and indicates with a tone and a red or white light that an alarm has occurred. In the space next to each light, you can affix a label description identifying the zone or device that issued the alarm.
Series 7.0 Software (0510-1086-B) - User Guide  279500 Series Wired SystemDome Light The Dome Light has two different banks of lights: white normal call indicator lights and red emergency call indicator lights.•Emergency Calls—Emergency calls are indicated by steady illumination of the red Dome Light associated with the zone or area from which an emergency call has been placed.•Normal Calls—Normal calls are indicated by steady illumination of the white Dome Light associated with the zone or area from which a normal call has been placed.•Concurrent Emergency and Normal Calls—If an emergency and normal call are placed at the same time, the red light connected to the emergency station from which a call was placed will illuminate at the same time as the white light associated with the normal call.There is no requirement for replacement of lights. If for any reason the white or red lights are no longer functional it is necessary to replace the entire Dome Light. If the Dome Light does not operate as described, contact qualified service personnel. There are no user serviceable parts on the Dome Lights.Assistance Call DevicesA 9500 Series Assistance Call device is a device used to initiate an alarm. There are two Assistance Call devices used with the 9500 Series Wired call System, Nurse Call and Pull Cord.Nurse Call The Nurse Call device allows residents to easily summon help with the push of a button. The Nurse Call device is generally affixed near the bed of a resident for easy access. Pull CordThe Pull Cord device allows residents to easily summon help with the pull of the cord. When the cord is pulled, a visual display “flag” appears assuring them that help was called. The Pull Cord device is suitable for use in close proximity to showers or baths; however, to prevent damage, avoid any submersion.
Chapter 1: Equipment Overview 28 Series 7.0 Software (0510-1086-B) - User GuideFall Management SystemThe Fall Management System provides restraint-free monitoring of a patient who may try to leave a bed or chair without assistance. The Fall Management System can be configured to interface with the software along with your facility’s nurse call system. An Assistance Required alarm is activated in response to a Fall Management System alert when interfaced with the Series 7.0 Software.The Sensor Pad of the Fall Management System is placed on a patient’s bed or chair and connected to a Control Unit. If a patient removes his or her weight from the Sensor Pad, the Control Unit issues an audible alert. Refer to the applicable Control Unit’s manual for detailed information about using the Fall Management System. WA R N I N G:   The Fall Management System may not be suitable for patients who are “AT HIGH RISK FOR FALL.” Other monitoring measures may also be required. The Fall Management System should not be a substitute for routine visual monitoring protocol by caregiving personnel.WA R N I N G:   Due to the possibility of strangulation, all cables should be routed away from the patient’s throat. When securing the strap, take up any extra slack in the cord that may become tangled with a patient’s bed or chair. Failure to do so may result in patient injury. This device should not be used in the presence of flammable anesthetic mixtures.Control UnitSensor PadSensor Pad
Series 7.0 Software (0510-1086-B) - User Guide  29Fall Management System Nurse CallFall Management System Control UnitThe Fall Management System Control Unit is connected to a Fall Management System Sensor Pad and attached to a patient’s bed or chair, out of reach of the patient. If a patient attempts to get up, the Control Unit sounds an alert. An alert can be annunciated in the form of a buzzer. Staff can also be alerted via your facility’s nurse call system or the 9450 software if available. An Assistance Required alarm is activated in response to a Fall Management System alert when interfaced with the Series 7.0 Software. The Control Unit is powered by a 9-volt alkaline battery or by a plug-in power supply.Fall Management System Sensor PadFall Management System Sensor Pads can be used on most standard beds or chairs in your facility. They are disposable, intended for single-patient use, and warranted for 7, 30, 90, or 180 days (offering for pads are subject to change, contact Customer Care at 1-800-669-9946 for the most current offering). The Sensor Pads have a limited expected useful life. You must record the date the warranty expires in the area provided on the label. You must not use the sensor pad after the in-service warranty has expired.Fall Management System Nurse CallYour facility can use the Fall Management System in conjunction with your Nurse Call System. Simply insert the modular jack into the nurse call jack on the control unit then insert the other end of the cable into the jack on the nurse call system’s bedside wall plate.When the nurse call cable is plugged in, the control unit sounds an audible alert and the nurse call output is active during an alarm. If the volume on the control unit is adjusted to its lowest setting, the alarm will not sound at the control unit but will still register at the nurse call output.The nurse call system varies in functionality. Consult your facility’s nurse call system documentation to ensure proper functionality when connecting the Fall Management System to it. WARNING: If the keys on the Control Unit are worn or damaged, you must stop using the Control Unit and contact RF Technologies.WARNING: Pad may become damaged when used on a dynamic mattress (air, water, etc.). Correct operation should be confirmed at every patient rotation.WARNINGS: The control unit will not alarm unless properly connected to the nurse call system.
Chapter 1: Equipment Overview 30 Series 7.0 Software (0510-1086-B) - User GuideAdvanced 3-Way Care SolutionThe Advanced 3-Way Care Solution has been designed to assist in the areas of Fall Management, Incontinence Detection and Re-position Reminder. The system can be used to address all three areas of care or to assist with a single area. The system functions as a stand-alone system or can be configured to interface with the Series 7.0 Software along with your facility’s nurse call system. When interfaced with the Series 7.0 Software, a Fall, Wet or Turn alarm is activated in response to the applicable event.WA R N I N G:   The Advanced 3-Way Care Solution may not be suitable for patients who are “AT HIGH RISK FOR FALL.” Other monitoring measures may also be required. The Advanced 3-Way Care Solution should not be a substitute for routine visual monitoring protocol by caregiving personnel.WA R N I N G:   Due to the possibility of strangulation, all cables should be routed away from the patient’s throat. When securing the strap, take up any extra slack in the cord that may become tangled with a patient’s bed or chair. Failure to do so may result in patient injury. This device should not be used in the presence of flammable anesthetic mixtures.
Series 7.0 Software (0510-1086-B) - User Guide  31Advanced 3-Way Care SolutionAdvanced 3-Way Control UnitThe Advanced 3-Way Care Control Unit connects to a sensor pad and attaches to a patient’s bed or chair, out of reach of the patient. If using the Control Unit for Fall Management or Re-position Reminder, connect the Motion Sensor Pad. If using the Control Unit for Incontinence Detection, connect the Incontinence Sensor Pad. To simultaneously address all three applications, insert the Dual Function Adapter and plug in the Motion Sensor Pad and the Incontinence Sensor Pad into their respective jacks in the adapter. The Control Unit is powered by a 9-volt alkaline battery or by a plug-in power supply.Advanced 3-Way Care Sensor PadsThe sensor pads of the Advanced 3-Way Care Solution is placed on a patient’s bed or chair and connected to a Advanced 3-Way Care Control Unit. Refer to the applicable Control Unit’s in-service manual for detailed information about using the Control Unit with the sensor pads. Motion Sensor PadThe Motion Sensor Pad is used for Fall Management and Re-Position Reminder monitoring. They are disposable, intended for single-patient use, and warranted for 30 days (offering for pads are subject to change, contact Customer Care at 1-800-669-9946 for the most current offering). When used for Fall Management, if a patient removes his or her weight from the Motion Sensor Pad, the Control Unit flashes the green light and beeps to alert the caregiver. When used for a Re-position Reminder, the Motion Sensor Pad connects to the Control Unit to allow you to select a pre-programmed time interval to remind you to change/vary the position of a patient in their bed. When the selected time interval expires, the Control Unit will alert the caregiver that it is time to reposition the patient.Incontinence Sensor PadThe DriTec Incontinence Sensor Pad comes on a roll and is perforated in one-foot sections to allow you to tear off only what is needed. It is recommended that you use three sheets for a bed and one for a chair. Prior to tearing, fold at the perforation to ensure that the pad tears freely from the roll.The Incontinence Sensor Pad connects to the Control Unit via the Incontinence Sensor Clip. When incontinence is sensed from the Incontinence Sensor Pad, the Control Unit flashes the green light and beeps to alert the caregiver.WA R N I N G:   If the keys on the Control Unit are worn or damaged, you must stop using the Control Unit and contact RF Technologies.WA R N I N G:   Pad may become damaged when used on a dynamic mattress (air, water, etc.). Correct operation should be confirmed at every patient rotation.
Chapter 1: Equipment Overview 32 Series 7.0 Software (0510-1086-B) - User GuideAdvanced 4-Way Care SolutionThe Advanced 4-Way Care Solution has been designed to assist in the areas of Fall Management, Incontinence Detection, Re-position Reminder and Nurse Call (call for assistance). The system can be used to address all four areas of care or to assist with a single problem area. The system functions as a stand-alone system or can be configured to interface with the Series 7.0 Software. When interfaced with the Series 7.0 Software, a Fall, Wet, Turn or Assistance Required alarm is activated in response to the applicable event.WA R N I N G:   The Advanced 4-Way Care Solution may not be suitable for patients who are “AT HIGH RISK FOR FALL.” Other monitoring measures may also be required. The Advanced 4-Way Care Solution should not be a substitute for routine visual monitoring protocol by caregiving personnel.WARNING: Due to the possibility of strangulation, all cables should be routed away from the patient’s throat. When securing the strap, take up any extra slack in the cord that may become tangled with a patient’s bed or chair. Failure to do so may result in patient injury. This device should not be used in the presence of flammable gas mixtures.
Series 7.0 Software (0510-1086-B) - User Guide  33Advanced 4-Way Care SolutionAdvanced 4-Way Control UnitThe Advanced 4-Way Care control unit attaches to a patient’s bed or chair, out of reach of the patient. It connects to a Motion sensor pad, an Incontinence Detection pad and a Nurse Call cord set. If using the control unit for Fall Management or Re-position Reminder, connect the Motion sensor pad. If using the control unit for Incontinence Detection, connect the Dri Tec sensor pad. To allow Nurse Call functionality, connect the Nurse Call cord set.The control unit is powered by a 9-volt lithium battery or by a plug-in power supply. To simultaneously address all four applications, insert the Dual Function Adapter and plug in the Motion sensor pad and the Dri Tec sensor pad into their respective jacks in the adapter. Then insert the Nurse Call modular jack cable into the applicable jack on the control unit and plug the Nurse Call cord set into the modular jack.Advanced 4-Way Care Sensor PadsThe sensor pads for the Advanced 4-Way Care Solution are placed on a patient’s bed or chair and connected to the Advanced 4-Way Care control unit. Refer to the applicable control unit’s in-service manual for detailed information about using the control unit with the sensor pads. Motion Sensor PadThe Motion sensor pad is used for Fall Management and Re-Position Reminder monitoring. They are disposable, intended for single-patient use, and warranted for 30 days (offerings for pads are subject to change, contact Customer Care at 1-800-669-9946 for the most current offerings). When the patient’s weight is removed from the pad, the control unit beeps three times every second to alert caregivers. The status indicator light flashes red in conjunction with the beeps for a visual alert. When used for a Re-position Reminder, the Motion sensor pad connects to the control unit to allow you to select a pre-programmed time interval to remind you to change/vary the position of a patient in their bed. At the end of the monitoring period, the control unit beeps once every second indicating the time interval has expired. A red status indicator light flashes in conjunction with the beeps for a visual alert.The Re-position Reminder light on the control unit also flashes red to indicate the specific bed position that the patient was left in at the beginning of the monitoring period.WARNING: If the keys on the control unit are worn or damaged, you must stop using the control unit and contact RF Technologies.WARNING: Pad may become damaged when used on a dynamic mattress (air, water, etc.). Correct operation should be confirmed at every patient rotation.
Chapter 1: Equipment Overview 34 Series 7.0 Software (0510-1086-B) - User GuideIncontinence Sensor PadThe Dri Tec Incontinence sensor pad comes on a roll and is perforated in one-foot sections to allow you to tear off only what is needed. It is recommended that you use three sheets for a bed and one for a chair. Prior to tearing, fold at the perforation to ensure that the pad tears freely from the roll.The Dri Tec sensor pad connects to the control unit via the Dri Tec Sensor Cord. When an incontinence event is detected, the control unit beeps twice every second to alert caregivers. A red status indicator light flashes in conjunction with the beeps for a visual alert.Advanced 4-Way Care with Nurse CallTo use the Advanced 4-Way Care System with the Nurse Call accessory, connect the Nurse Call modular jack cable to the control unit. Then connect the Nurse Call cord set into the modular jack. Nurse Call monitoring starts when the cord set is connected. When a patient pushes the button on the Nurse Call cord set, an Assistance Required alarm is generated. The control unit beeps once every 3-seconds to alert caregivers and a red status indicator light flashes in conjunction with the beeps for a visual alert.NOTE: The Nurse Call cord set is gravity fed and must always be positioned upright as shown. False nurse calls may occur if not positioned properly.
Series 7.0 Software (0510-1086-B) - User Guide  35Messaging ServicesMessaging ServicesEvent MessagingThe Event Messaging system allows staff members to be notified of system events. When an event occurs, the designated staff is summoned, via pager, email, text message or phone to respond to the situation. Each messaging media can be assigned to a messaging group, which can be configured to receive messages specific to that group (nursing staff, maintenance, etc.). Messages may be sent to single message media or sent to entire groups at once.A Message Unit is the top tier of the Event Messaging system. Each Message Unit can be comprised of a number of Messaging Groups and a configured list of alarms and events that trigger messages. For example, Messaging Unit “A” can be configured to receive messages for Cut Band, No Signal and Client Missing events. Message Unit “B” may be configured to respond to the same events as Messaging Unit “A” with the addition of Door Open and Device Fault events. Depending on the needs of your facility, a Messaging Group can be included in more than one unit. In other words, Messaging Group “2” can be included in Messaging Unit “A” and Messaging Unit “B”. If no alarms are selected for a Messaging Unit, alarms will default to a Messaging Group. Shift selections can also be selected to indicate that, within a specified shift’s time period, all messages will be sent to that shift. Messaging Delays, Retries and EscalationMessaging Delay allows the user to enter the number of seconds between an event and the messaging of designated staff. This delay provides enough time for the system to transmit location information to the Client computer(s). Messaging Delay is set by the installer and should not be changed without consulting a factory-trained administrator.The Messaging Retries features will retry a message after a specified number of minutes for any event to which there is no response. Once a message has been retried the configured amount of times, the message can be escalated to another Messaging Group.Messaging escalation is intended to ensure that staff will respond to an emergency call. If a message is sent to a Messaging Group and the relevant staff does not respond within a specified period, the call will escalate to another Messaging Group. It is recommended that the final group be comprised of all the messaging media in the building. The final group will continue to be messaged until the call is answered. The system does not roll over to the first group again.NOTE: White alarms for messaging do not escalate or retry. A white alarm message is only sent once.
Chapter 1: Equipment Overview 36 Series 7.0 Software (0510-1086-B) - User GuideWalkie-Talkie The Walkie-Talkies alert staff members when specific events occur. Staff members equipped with a walkie-talkie will receive an audible message for triggered events. Triggering events for the walkie-talkie are configured in the Configuration menu. The options are: Assistance Required, No Signal, Cut Band Alarm, and Door Alarm. If your system includes the Advanced 3-Way or 4-Way Care system, additional options include Fall, Wet and Turn.Walkie-Talkie configurations allows you to set the number of seconds between the start of an alarm and when the alarm is repeated. This is referred to as a repeat interval. The repeat interval count down starts as soon as the walkie-talkie alarm sounds. Therefore, depending on the number of seconds selected for a repeat interval, an alarm may repeat only seconds after the first alarm stops.
Series 7.0 Software (0510-1086-B) - User Guide 37Chapter 2Software Features IntroductionThis chapter provides details about starting the software and features of the software. It describes the use of the touchscreen monitor, the window conventions and the Main operating window. From the Main application window you can access menu items necessary to operate your system.Start the SoftwareAfter installation, the software automatically starts when you turn on the computer. A splash screen with the logo and the name of the system is displayed while the program loads. This screen contains the version number of your software.FIGURE 2.1:    Startup Splash Screen for the Code Alert SystemSleep ModeSleep mode refers to a low power mode that turns your computer’s monitor off after a certain period of time. If your monitor is in sleep mode a simple touch of the mouse or keyboard usually wakes the monitor within seconds. Additional, any new alarms detected on a Client computer that would maximize the application will reawaken the monitor.
Chapter 2: Software Features 38 Series 7.0 Software (0510-1086-B) - User GuideWindow ConventionsWhen you perform a function using the software, a window appears. Here, you can enter data or select options. The software is designed for use with a touchscreen monitor. The user buttons are large and easy to use. All daily functions, such as admitting and transferring, can be performed using the touchscreen monitor; configuration operations may require you to use the keyboard and mouse. For more information about configuration options, see the Series 7.0 Software Administrator Guide.FIGURE 2.2:    Sample WindowDrag the title bar to move the window.Type information in the text boxes.Click  Save  to accept changes and close the window or dialog box.Use the arrow to select information from the drop-down Click Cancel to close the window or dialog box.
Series 7.0 Software (0510-1086-B) - User Guide  39Touchscreen MonitorTouchscreen MonitorAn on-screen keyboard is available to fully utilize the monitor. Simply use the keyboard on the screen as you would use a keyboard connected to a computer. To turn On/Off the on-screen keyboard1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Select Administrative Functions.4.    Select Change Client Properties.5.    Select Display6.    Select the Display Virtual Keyboard check box.FIGURE 2.3:    On-Screen KeyboardNOTE: When using the Select Multiple feature, anomalies may occur when using the on-screen keyboard while the desktop keyboard is connected to the computer.
Chapter 2: Software Features 40 Series 7.0 Software (0510-1086-B) - User GuideQuick Reference TutorialA Quick Reference Tutorial is embedded in the software to aid users in responding to alarms. The option to display the tutorial can be turned off by deselecting the Display Tutorial Help check box.To deselect the Display Tutorial Help check box1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Select Administrative Functions.4.    Select Change Client Properties.5.    Select Display6.    Deselect the Display Tutorial Help check boxThe Quick Reference Tutorial opens within the Event Information Window when responding to Red, Blue and White alarms (refer to the section “Event Information Window” on page 96 for information on Red, Blue and White alarms). The tutorial contains a quick reference on how to respond to an alarm and common causes for the alarm.FIGURE 2.4:    Quick Reference Tutorial Window
Series 7.0 Software (0510-1086-B) - User Guide  41Map OrientationMap OrientationMaps can be rotated for visual orientation of the unit. Icons distributed on the map represent the location of each device assigned to the unit. Icons do not move from the their original placement on the map; they rotate with the map. An indication of where you are, based on the placement of the computer at the time of configuration, is also displayed on the map. To rotate the Map displayed on the client computer1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Select Administrative Functions.4.    Select Change Client Properties.5.    Select the Map tab.FIGURE 2.5:    Client Properties - Display6.    On the Map tab, select the unit to which you want to rotate the map.7.    Click the radio button next to the Map Orientation that you wish displayed for that unit.8.    Do one of the following:a.    Click Save to save and return to the main window. b.    Click Cancel to return to the main window without saving.
Chapter 2: Software Features 42 Series 7.0 Software (0510-1086-B) - User GuideRuleset for Displaying Patient NameThe ruleset for displaying the patient’s name on the Quick Look Display, Pager and in the Alarm Message Box on the central server and client computer(s) is based on the patient information entered during the admit process and whether the HIPAA option is enabled in the software (refer to the Series 7.0 Software Administrator Guide). When HIPAA is enabled, the patient’s name is not shown on the Quick Look Display.The patient’s first name or last name is required when entering patient information during the admit process. Depending on what information is entered, the following ruleset applies.Patient Information What is displayed on the Quick Look DisplayFirst and Last name Last name, First nameLast name only Last name First name only First nameIf HIPAA privacy is enabled Last name-Gender
Series 7.0 Software (0510-1086-B) - User Guide  43The Main WindowThe Main WindowWhen the software is started, the main window appears. It contains all the necessary information to operate your system.FIGURE 2.6:    Main WindowMenu Bar Click to open the Low Batteries Report (only appears when there are low batteries currently in the system).Event List
Chapter 2: Software Features 44 Series 7.0 Software (0510-1086-B) - User GuideFunctionsThe Functions menu provides access to commonly used functions found in the User Functions menu. The User Functions available will depend on your software licenses. To access User Functions menu, click Functions.FIGURE 2.7:    User FunctionsNAME AN AUTO-ENROLLED TRANSMITTER—Click to access the Admit Auto-Enrolled window. This window displays a list of only Auto-Enrolled transmitters. See “Name An Auto-Enrolled Transmitter” on page 55.MANUAL ADMIT—Click to access the Admit Information window. This is where you enter a new patient or asset into the system. This selection is also used to update existing patients or assets. See “Manual Admit” on page 56.PRE-ENROLL—Click to access the Pre-Enroll Information window. Alarming band transmitters that are not banded but are available for use with a proper transmitter number (a Transmitter ID within the range set in Configuration), can be Pre-Enrolled. See “Pre-Enroll” on page 59. DISCHARGE—Click to access the Discharge window. This allows you to take a patient or asset out of the census of monitored transmitters. If the patient is wearing an alarming band transmitter, you then have a limited time to remove the banding material from the transmitter. The discharge time is configured per unit or can be set to discharge the patient or asset immediately. See “Discharge” on page 67.
Series 7.0 Software (0510-1086-B) - User Guide  45Event ListADJUST—Click to access the Adjust Bands window. This allows you to temporarily suspend the alarm function for a patient or asset’s alarming band transmitter so the banding material can be readjusted. If there are no 9450 transmitters configured for the system, this key is disabled. See “Adjust” on page 70.ESCORT—Click to access the Escort window. This is where you select the amount of time required to take a patient /asset out of a protected area and back to the same protected unit. See “Escort” on page 73.TRANSFER—Click to access the Transfer window. This is where you select the amount of time required to move a patient or asset from one protected area to another protected unit.UPDATE RECORD—Click to access the Admit Information-Update Record window. This is where you select a patient to update patient information. See “Update Record” on page 79.ADMINISTRATIVE FUNCTIONS—Use Administrative Functions to Add/Update Assets, enter Staff Drill and System Maintenance information, Change Client Properties, access the Configuration options and access available Reports. See “Administrative Functions” on page 80.MESSAGING FUNCTIONS—This option allows you to schedule system messages, manage messaging shifts, and send messages to staff members. See “Messaging Functions” on page 88.EXIT TO MAIN SCREEN—This option closes the Administrative Function window and returns you to the Main Screen.Event ListClick Event List to display all events that are in the system. Clicking on an event takes you directly to that event’s information window.FIGURE 2.8:    Event List Window•Click Next to scroll down through events in the list. •Click Previous to scroll back up through events in the list.
Chapter 2: Software Features 46 Series 7.0 Software (0510-1086-B) - User GuideCensusClick Census to display a census screen of every Auto-enroll transmitter, patient and asset in the system.FIGURE 2.9:    Census WindowIn the top right corner of the Census screen are buttons to allow you to print or scroll through the census.•Click  Print for a print out of the census screen. A printer must be connected to the computer from which the print command is initiated and set as its default printer.•Click Next to scroll down through the census.•Click Previous to scroll back up through the censusThe information displayed includes:Name—the name of the patient, asset or transmitter enrolled in the system.Room—the room assigned to the patient.Status—the status (mode of operation) that the transmitter is in (monitor, transfer, escort, adjust, or discharge).Last Known Location—the location of the receiver that best picked up the last signal from the transmitter.Destination—the destination of the patient in escort or transfer.Time Remaining—the time remaining to complete the escort or transfer.Transmitter ID—the identification number of the transmitter.Risk—the risk level assigned to the patient.Gender—the gender of the patient.NOTE: The information for State, Last Known Location and Time Remaining only update every 10 minutes.
Series 7.0 Software (0510-1086-B) - User Guide  47MapMapClick  Map to display a floor plan of each unit the Client computer(s) is configured to monitor. Icons distributed on the map represent the location of each device assigned to the unit; the icons flash when an event occurs. •Click Prev to scroll back to the previous map viewed. Only those maps assigned to the units monitored on the Client computer(s) are available.•Click Next to scroll ahead to the next available map. Only those maps assigned to the units monitored on the Client computer(s) are available.Devices Displayed on the MapDevices are displayed on the map or floor plan on the Client computer(s). The display is configured to assist the staff in monitoring devices. The location of a device issuing an alarm is indicated by a flashing icon on the map. FIGURE 2.10:    Main WindowYou are h ereDevice assigned to a room is in alarm (location of client computer) Flashing icon indicates the location of thedevice reporting the event
Chapter 2: Software Features 48 Series 7.0 Software (0510-1086-B) - User GuideIf a transmitter location changes, for example if an alarm is activated while the transmitter is in motion, the receiving device closest to the transmitter triggers the alarm. The icon representing the receiving device flashes on the Client computer map. Below is a table of how devices are displayed on the map in the Main Window.Devices Assigned to a RoomDevices assigned to a room will not show on the map until the room device goes into alarm. The map will display the room to which the alarming device is assigned. By clicking on the alarming device icon, you can bring up details of the device. If more than one device is assigned to a room, details on both devices are displayed. Click OK to dismiss the device detail. The icon will continue to flash until the alarm is cleared.HelpClick Help to access the on-line help window for the Series 7.0 System. Here you can navigating through user help topics.SilenceYou can click Silence to stop the alarm sound. The alarm is silenced for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound. This Silence button is green when the Silence feature is turned ON. To configure the Alarm Silence Time-out, refer to Series 7.0 Software Administrator Manual.Normal Mode  Alarming Device FaultGreen Flashing Red Flashing Yellow
Series 7.0 Software (0510-1086-B) - User Guide  49Alarm Message BoxAlarm Message BoxFrom the Map or Census view, click in the alarm message box to access the Event Information window for that alarm. Alarms are displayed sequentially as they occur and by priority. Alarms are color coded according to the alarm.Red Alarm—high priority alarmsYellow Alarm—medium priority alarmsWhite Alarm—low priority alarmsBlue Alarm—high priority asset alarmsLight Blue Alarm—low priority asset alarms•Click Next to scroll down through alarms in the list. •Click Previous to scroll back up through alarms in the list.      Low Battery IconLocated on the bottom of the Main Window is a Low Battery icon. The Low Battery icon only appears when there are transmitters and/or devices with low batteries currently in the system. When visible, the Low Battery icon appears in yellow.Click on Low Battery to go directly to the Low Batteries Report.
Chapter 2: Software Features 50 Series 7.0 Software (0510-1086-B) - User GuideThis page intentionally left blank.
Series 7.0 Software (0510-1086-B) - User Guide 51Chapter 3Using the Software IntroductionThis chapter provides detailed information about the Series 7.0 Software functions. For information about tasks such as adding devices or adding users to a Client computer, see the Series 7.0 Software Administrator Guide. In addition, for specific information about securing and cleaning alarming band transmitters, see the appropriate Transmitter User Guide. Commonly Used Terms Throughout this guide terms are used to describe functions that may be enabled/disabled in the software or actions necessary for using the software. Following are commonly used terms and their definitions.Login and PasswordsSome functions of your system may be password protected. This simply means that a staff member must enter a login and password or use his or her proximity card or magnetic/barcode card before performing a task. When you select a function that requires a password, the Login and Password dialog box appears.To access a password protected function1.    Enter your login name in the Login box.2.    Enter your password in the Password box.3.    Press Enter or click OK. 4.    If enabled, use your proximity card or magnetic/barcode card approved for use with the software.NOTE: The Login, Password and Swipe Card information is case sensitive. If a “User not Authorized to perform this function” error message occurs, try turning off the Caps Lock on your keyboard.
Chapter 3: Using the Software52 Series 7.0 Software (0510-1086-B) - User GuideDevice SupervisionThe Supervision feature applies to many devices such as the alarming band transmitters, Pendants, Fall Monitoring and Incontinence devices. A supervised device is the system’s way of ensuring that devices are communicating properly and within range of the receivers. When the Supervised transmitter function is enabled, a No Signal alarm will be posted in the Event List if the system does not receive a signal from the device within a specified time interval. The supervision interval is configured in the Configuration-Units menu. The Supervision function defaults ON.Inactivity Check-inAn Inactivity Check-in is when the system generates an event when no check-in is received or activity is detected within the selected period of time. This feature is commonly used with Check-in Pull Cords but can also be used with a PIR Sensor. If the PIR Sensor does not detect motion within the check-in time period, the system generates an Assistance Required alarm.The Inactivity Check-in feature is enabled during the Admit process under the Transmitter tab. Inactivity Check-in devices must first be assigned to a room/and or unit at the Configuration level (refer to the Series 7.0 Software Administrator Guide).UnitsUpon admission, a patient or asset must be assigned to a Unit. A Unit represents a protected area in your facility that is monitored as a unit, such as the Nursery or Intensive Care. All devices in the area are assigned to the unit, and are identified on a map or floor plan specific to the unit.Some units may have more than one patient or asset occupying the same room. It is important when admitting a patient or asset to a double-occupancy room that you specify which bed or side of the room the patient or asset is assigned, for example room 101-A or room 101-B.If an alarm occurs, the relevant alarm information, such as the patient’s or asset’s name, the type of event, and the location of the event, is displayed at any Client computer that has been configured to monitor the unit. Some System Properties, such as the time allowed for the discharge and adjust function, are defined at the unit level.
Series 7.0 Software (0510-1086-B) - User Guide  53Commonly Used TermsGlobal LockdownA Global Lockdown is when all of the doors are automatically locked during a Cut Band or Band Off alarm. If a door is already open at the time a Cut Band or Band Off alarm occurs or if a door is opened at any time while the system is in Global Lockdown:•an alarm sounds at the Exit Alarm Controller•a message is displayed on the Client computer(s) in the unit configured to monitor the door and on all Quick Look Displays for that unit •the location of the Exit Alarm is indicated by a flashing icon on the map on the Client computer(s)If your facility has enabled the Lockdown on Cut Band Alarms or Lockdown on Band Off Alarms feature, a Cut Band Alarm or Band Off triggers a Global Lockdown. You can configure the Global Lockdown feature to lock doors at All exits or By transmitter units. However if a Cut Band or Band Off alarm is triggered during an Escort or a Transfer, the system automatically locks All exits and posts the alarms on all Client computer(s). This is because the transmitter in Escort or Transfer may be outside of its protected unit.NOTE: When a transmitter is configured as a low priority asset transmitter, a Cut Band Alarm will not trigger a Global Lockdown. High Priority configured asset transmitters will trigger a Global Lockdown.
Chapter 3: Using the Software54 Series 7.0 Software (0510-1086-B) - User GuideTroubleshooterA Troubleshooter dialog box appears after three consecutive No Signal alarms are received and the user clicks in the Alarm Message box for that alarm.How to respond to Troubleshooter1.    Click Help to open a Help window.2.    Click Close to close the Troubleshooter and open the Event Information window allowing you to select an Event Cause for the alarm.3.    Click Discharge to open the following information dialog. 4.    Click OK. The Event Information window opens allowing you to select an Event Cause for the alarm.5.    Click Transmitter In Use to open the following information dialog. 6.    Click OK. The Event Information window opens allowing you to select an Event Cause for the alarm.7.    Click Transmitter Not In Use to open the following information dialog. 8.    Click OK. The Event Information window opens allowing you to select an Event Cause for the alarm.
Series 7.0 Software (0510-1086-B) - User Guide  55Admit FunctionsAdmit FunctionsAdmit Functions such as Name An Auto-Enrolled Transmitter and Manual Admit are found in the User Functions menu. To Add/Update An Asset is found in the second tier of the User Functions menu underAdministrative Functions.Name An Auto-Enrolled TransmitterTransmitters that are automatically enrolled in the system can be assigned to a patient using this option. When you click on a window opens with only Auto-Enrolled transmitters.To admit a patient from Name An Auto-Enrolled Transmitter1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Name An Auto-Enrolled Transmitter. The Admit Selection - Auto-Enrolled window appears. Auto-enrolled transmitters that currently exist in the census are listed in the window.FIGURE 3.1:    Admit Selection –Auto Enrolled4.    Use the arrow buttons to find and select the transmitter number to be assigned. 5.    Double click on the Auto-Enrolled transmitter to bring up the Admit Information window and enter admit information; the yellow fields designate required entry 6.    Once admit information has been entered, click Save.If the admit is successful, you will get the following dialog box:7.    Click OK.
Chapter 3: Using the Software56 Series 7.0 Software (0510-1086-B) - User GuideManual Admit Using the Manual Admit function, you can admit a patient and enable the system to associate the transmitter with information of the patient being admitted. To admit a patient from the Manual Admit button1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Manual Admit.4.    The Admit Information window opens for you to enter admit information; the yellow fields designate required entry. FIGURE 3.2:    Admit Information5.    Once admit information has been entered, click Save.If the admit is successful, you will get the following dialog box:6.    Click OK.
Series 7.0 Software (0510-1086-B) - User Guide  57Admit FunctionsTo admit with a Pendant, Fall Monitoring or Incontinence device1.    Alarm then reset the device.2.    Select Login (or Functions if password protection is disabled).3.    Enter your Login and Password or use your identification card. 4.    Click Manual Admit.The Admit Selection window appears.5.    Enter patient information; the yellow fields designate required entry. 6.    Select the Transmitter tab.7.    Select the Transmitter ID number (printed on Pendant) from the pull-down.8.    Click AddThe Admit Information window appears allowing you to select the transmitter type.FIGURE 3.3:    Admit Information to Select Transmitter Type9.    Select the Transmitter Type from the pull-down menu.•Pendant•Fall Monitoring•Incontinence10.   For a QR transmitter the Supervised option is selected by default. If desired, deselect it.NOTE: The Transmitter tab will not appear until a QR Transmitter ID Range is configured into the system (refer to the Series 7.0 Software Administration Guide).
Chapter 3: Using the Software58 Series 7.0 Software (0510-1086-B) - User Guide11.   For an 9600 Series transceiver the Supervised time defaults to the unit’s Transmitter Supervise Time, set during configuration. However, you can select a different time from the drop-down list.12.   Select SAVE.If the admit is successful, you will get the following dialog box:13.   Click OK.For more information on the Transmitter tab, refer to “Enter Transmitter Information” on page 64.To admit with a fixed device 1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Manual Admit. The Admit Information window appears.4.    Enter patient information; the yellow fields designate required entry. 5.    Select the Room that was configured with device from the drop-down menu.6.    Click Save.NOTE: To ensure supervision configuration changes are accepted by the Pendant transceiver, it is important to alarm the Pendant after a change in device configuration.NOTE: Pull Cords and Smoke Detectors are considered fixed devices. They are assigned to a room and/or unit at the Configuration level. Refer to the Series 7.0 Software Administrator Guide.
Series 7.0 Software (0510-1086-B) - User Guide  59Admit FunctionsPre-EnrollAlarming band transmitters that are not banded but are available for use with a proper transmitter number (a Transmitter ID within the range set in Configuration), can be pre-enrolled. To Pre-Enroll a transmitter1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Pre-Enroll.4.    The Pre-Enroll Information window opens for you to enter admit information; the yellow fields designate required entry. FIGURE 3.4:    Pre-Enroll Information5.    Once admit information has been entered, click Save.If the admit is successful, you will get the following dialog box:6.    Click OK. 7.    The Pre-Enroll transmitter appears in the Census with a status of Pre-Enroll. The transmitter must be banded within the time set in Configuration. A white Pre-Enroll Expired alarm message is generated if the time expires before banding. You must Clear the alarm and Pre-Enroll the transmitter again, making sure that it is properly banded within the configured time.
Chapter 3: Using the Software60 Series 7.0 Software (0510-1086-B) - User GuideAdmit Information WindowsFrom the Admit Information window you can enter the general information about the patient being admitted. The yellow fields designate required entry. There are six tabs for entering patient admit information and one for Scheduling Events (see “Scheduling an Event” on page 65). FIGURE 3.5:    Admit Information WindowAdmit Information TabsQuick Look TabThe Quick Look tab allow users to see the what entered patient information will look like on a simulated Quick Look. The fields are subject to the same rules for truncation currently used for the Quick Look Display.FIGURE 3.6:    Quick Look Tab
Series 7.0 Software (0510-1086-B) - User Guide  61Admit Information WindowsMain TabThe Main information tab allows you to enter general information about the patient being admitted; the yellow fields designate required entry. Depending on your configuration, the Birth Date field may be a required entry for the Series 7.0 Software. When updating admit information for patients who were enrolled in the system prior to software version 7.0, you must enter the patient’s birth date even if that information was not previously entered. 1.    Click the Main tab.2.    In the First Name box, type the first name of the patient being admitted (either first or last name is required). 3.    In the Last Name box, type the last name of the patient being admitted (either first or last name is required).4.    Type the patient’s Address, City, State, Zip.5.    In the Phone field, type the phone number of the patient.6.    In the Unit field, select the unit to which the patient is currently assigned, even if the patient will not remain in that unit (required).7.    In the Room field, select the patient’s room number.8.    In the Birth Date field, enter the patient’s birthday (two digit month, two digit day, four digit year).9.    Click Female or Male to indicate the gender of the patient.10.   In the Discharge Planning Date field, enter the planned date of discharge (the appearance of this field depends on your system configuration)11.   In the Training Delivered field, indicate the type of training material used by entering the date training was delivered to the patient or patient’s family.12.   In the Transmitter ID field, type the 3-digit ID number printed on the transmitter to be assigned to the patient.13.   Click Configure to configure the Band Off settings for the transmitter. (See “Configure Band Off” on page 62.)14.   Click the Risk level for abduction or elopement associated with the patient. Choices are Low, Medium or High.NOTE: Information entered can only contain alphabetic and numeric characters, spaces, and the following special characters: ! - _ , . ; [ ]{ }( )
Chapter 3: Using the Software62 Series 7.0 Software (0510-1086-B) - User GuideConfigure Band OffThe default Band Off settings are configured at the Unit Properties level (refer to Configure Units in the Series 7.0 Administrator Manual). However, the default settings for Band Off can be changed for each transmitter being admitted using the Configure option. To configure the Band Off settings1.    Click the Configure button on the Main Tab of the Admit screen. The Configure Transmitter window opens.2.    Click the Band Off Alarm Enabled checkbox to enable/disable the Band Off feature for the transmitter being admitted.3.    To restore the Unit’s current defaults, click the Restore Unit Defaults button.4.    To change a transmitter’s settings for generating a Band Off alarm, select any valid combination of Combined Alarm radio buttons and the Alarm on Any checkboxes. From the Combined Alarm, each parameter must have a value of And, Or, or Off.a.    Click the And radio button next to a parameter to select it as “one” of the required parameters for a Band Off alarm. At least one other parameter must be set to And to generate a Band Off alarm (i.e. Capacitance and Resistance). You can also select And for one parameter and Or for at least two other parameters to generate a Band Off alarm (i.e. Temperature and Capacitance or Resistance).b.    Click the Or radio button next to a parameter to select it as “one” of the required parameters for a Band Off alarm. At least one other parameter must be set to Or to generate a Band Off alarm (i.e.Resistance or Temperature).c.    Click the OFF radio button next to a parameter to select it as a parameter that will not be used for determining a Band Off alarm.5.    Click the Alarm On Any check box next to a parameter to individually choose it to generate a Band Off alarm.6.    The Band Off Delay settings can also be changed for each parameter. Once a Band Off condition is met, the alarm will be delayed for the configured time. If the Band Off condition resolves within the delayed time, the Band Off alarm will not be sent. For Combined Alarms, the parameter with the longest delay takes precedence. NOTE: The Configure button will not be present if Band Off alarms are not enabled for the currently assigned unit.Parameters:•Capacitance—the change in contact between transmitter and infant’s extremity•Resistance—the stretch of the banding material•Temperature—the change in transmitter temperature
Series 7.0 Software (0510-1086-B) - User Guide  63Admit Information WindowsMedical TabThe Medical information tab is only accessible from the Patient Admit Information window. To access the Medical Info tab, the user must be a configured into the system as a Care Provider (refer to the Series 7.0 Software Administrator Guide). The Medical Info tab allows you to enter medical information about the patient being admitted. Fields are provided here for you to enter information necessary per your facility’s policies and procedures. Contact TabThe Contact information tab allows you to enter contact information about the patient or asset being admitted.1.    Click the Contact tab.2.    In the Special Instructions field, type any special instructions associated with the patient or asset.3.    In the Name field, type the name of the primary contact for inquires regarding the patient or asset.4.    In the Phone field, type the phone number of the primary contact.5.    Type the Address, City, State, Zip of the primary contact.If there is more than one contact, you can enter that information in the subsequent contact fields. Insert a PictureThe Picture tab allows you to insert a picture of the patient or asset being admitted. The patient’s picture is displayed on patient generated reports. When available, the patient’s picture also appears in the Event Information window for Cut Band, Door, and No Signal alarms as well as alarms generated from Pendant, Fall Monitoring and Incontinence devices. All of the pictures in the system are stored on the P: drive on the Server. When you need to enter a picture for a patient, go to the P: drive. 1.    To insert a picture, click or press the (...Browse) button.2.    Select a picture from the Browse Picture Files dialog box.NOTE: Information entered can only contain alphabetic and numeric characters, spaces, and the following special characters:! - _ , . ; [ ]{ }( )NOTE: Information entered can only contain alphabetic and numeric characters, spaces, and the following special characters: ! - _ , . ; [ ]{ }( )IMPORTANT: All pictures must be placed in the P: directory. If you are using a digital camera, removable USB drive, or any other removable media, you must first save the picture file to the P: directory before removing the media. It is the responsibility of the customer to have the system work on their domain which governs the security access to their network.
Chapter 3: Using the Software64 Series 7.0 Software (0510-1086-B) - User GuideTo save a picture to the P: drive on the Server1.    Insert the removable media (USB drive).2.    On the Computer Desktop, double-click My Computer.3.    Double-click the removable media. 4.    Right-click the pictures on the media you want to access and select Copy.5.    Double-click P:.6.    Double-click Pictures.7.    Double-click Patient or Asset.8.    Right-click and select Paste to paste the pictures to the P: drive for access. Enter Transmitter InformationThe Transmitters tab is only accessible from the Patient Admit Information window. The Transmitter tab allows you to enter Pendant, Fall Monitoring and Incontinence transmitter information of the patient being admitted.To enter transmitter information of the patient being admitted:1.    Click the Transmitters tab.2.    Select the patient’s transmitter number in the Transmitter ID: field.3.    Click Add.4.    From the Transmitter Assigned field, select the transmitter type.5.    For a QR transmitter the Supervised option is selected by default. If desired, deselect it.6.    For an 9600 Series transceiver the Supervised time defaults to the unit’s Transmitter Supervise Time, set during configuration. However, you can select a different time from the drop-down list.7.    If you want to enable the Inactivity Check-In feature for the transmitters, select the check box.8.    Enter the Begin and the End times for the Inactivity Check-In.9.    Click Save.NOTE: Information entered can only contain alphabetic and numeric characters, spaces, and the following special characters: ! - _ , . ; [ ]{ }( )
Series 7.0 Software (0510-1086-B) - User Guide  65Admit Information WindowsScheduling an Event The Schedule tab is only accessible for patients already admitted to the system. The Schedule tab allows you to schedule one time only, daily, weekly or monthly activities (events) to alarm on a per patient basis.To schedule an event:1.    Click on the Schedule tab to open the following window.FIGURE 3.7:    Schedule Tab2.    Click Add to open the Scheduling Detail window for adding events.FIGURE 3.8:    Schedule Detail window3.    Select the Schedule Type. Do you want the scheduled event to:•Run only once•Daily•Weekly•Monthly
Chapter 3: Using the Software66 Series 7.0 Software (0510-1086-B) - User Guide4.    If you choose to run the scheduled event daily, you must select the day(s) you wish to run the event. Choose the day(s) from the Starting On Day field.5.    From the Starting Date and Time field, select a date and time to start the scheduled event. The current date is displayed in the Start Date field. To change the date, click on Change Date and choose a date from the popup calendar.6.    Choose a Start Time. The current time is displayed, click Increase or Decrease to select the desired start time.7.    If you choose to run the scheduled event more than once daily, you must select a run Interval and Run only between times. The Interval is how often you want the scheduled event to run. Increments are 1 minute (0:01) to 11 hours and 59 minutes (11:59). Click Increase or Decrease to select interval.8.    The Run only between range can be set for any minute of the day. Click Increase or Decrease to select the starting Run only between time AND click Increase or Decrease to select the ending Run only between time.NOTES:•The scheduled event Start Time must fall within the starting Run only between time and the ending Run only between time range. For example, a scheduled event with a start time of 8:00 A.M. must have a Run only between time window that includes 8:00 A.M. A Run only between time of 7:00 A.M to 10:00 A.M. is legitimate; it includes 8:00 A.M. A time of 4:00 A.M. to 7:00 A.M. is not a legitimate Run only between time.•The scheduled event’s Interval time must be less than the time window created by the Run only between times. For example, a scheduled event with an interval of 5 hours must have a Run only between time window of at least 6 hours. 9.    The Audio button toggles On/Off. When Audio is turned On, the scheduled event will alarm at the Client computer(s).10.   Select a reason for the scheduled event from the Select A Reason pull down or enter free text in the Message field.11.   Click Save to save your changes or Cancel if you do not wish save your changes.
Series 7.0 Software (0510-1086-B) - User Guide  67DischargeDischarge When it is time for a patient to leave your facility, he/she must be discharged from the software. If applicable, the alarming band transmitter is removed from the patient within the period of time specified in the software by your facility. Finally, the transmitter must be disinfected in order to be ready to be used again.To discharge a patient or asset1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Discharge. The Discharge window appears. Patients, assets or Auto-Enrolled transmitters that currently exist in the census are listed in the window. FIGURE 3.9:    Discharge WindowNOTE: If a transmitter is in alarm, the event must be cleared before the patient or asset can be discharged.
Chapter 3: Using the Software68 Series 7.0 Software (0510-1086-B) - User Guide4.    Use the arrow buttons to find and select the patient or asset to be discharged. Multiple patients or asset can be selected for discharge. a.    Hold down the Ctrl key on the keyboard or, if the virtual keyboard is activated, click on the Select Multiple button in the Discharge window. The Select Multiple button highlights when activated.b.    Select the patients or assets to be discharged.5.    Click Discharge.a.    If the discharge is for a Wander Management transmitter, Pendant, Fall Monitoring or Incontinence device, the discharge occurs immediately.b.    If the discharge is for an alarming band transmitter, a dialog box appears showing the patient’s or asset’s name and the amount of time you have to remove the banding material from the transmitter. The amount of time you have to remove the banding material can be set in the Configuration, Units menu (refer to the Series 7.0 Software Administrator Guide).Click Confirm to confirm the Discharge.Click Cancel or X to cancel the Discharge request and close the window.c.    If the amount of time for discharge is set to immediate, a dialog box appears asking you if you are sure you want to discharge the patient or asset.6.    Click Yes.7.    Remove the alarming band transmitter from the patient or asset within the time allowed; the patient’s or asset’s name is automatically removed from the census. NOTE: You cannot discharge a patient or asset that is not in the unit being monitored by the Client computer you are currently using.
Series 7.0 Software (0510-1086-B) - User Guide  69DischargeTo cancel a dischargeIf the discharge is for an alarming band transmitter, you can cancel the discharge before the discharge time expires. 1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Discharge.The Discharge window appears (Figure 3.9 on page 67). Patients, assets or auto-enrolled transmitters that currently exist in the census are listed in the window.4.    Use the arrow buttons to find and select the patient or asset whose discharge is to be canceled. Multiple patients or asset can be selected for canceling.5.    Click Cancel.A dialog box appears indicating that the discharge for the selected patient or asset has been canceled.6.    Click OK.Transmitter is no longer communicating with the systemThe following dialog box appears when a transmitter is no longer communicating with the system and a Discharge attempt is made. 1.    Follow the steps outline in the dialog box.2.    Click OK.NOTE: If the unit is configured for immediate discharge, you will be unable to cancel the discharge.
Chapter 3: Using the Software70 Series 7.0 Software (0510-1086-B) - User GuideAdjustThe Adjust feature is only applicable with alarming band transmitters. In the normal course of a patient’s stay in your facility, it may become necessary to adjust the banding material so that the alarming band transmitter fits the patient’s ankle or wrist more comfortably and securely. The Adjust function temporarily suspends the Cut Band feature for a selected transmitter, allowing the banding material to be adjusted without triggering an alarm. The time period allowed for the band adjustment is specified by your facility. To adjust banding material on a Transmitter1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Adjust. The Adjust Bands window appears. Patients or assets with alarming band transmitters that currently exist in the Census are listed in the window.FIGURE 3.10:    Adjust Bands WindowNOTE: If a transmitter is in alarm, the event must be cleared before the Adjust function can be initiated.
Series 7.0 Software (0510-1086-B) - User Guide  71Adjust4.    Use the arrow buttons to find and select the patient or asset whose banding material needs adjustment. Multiple patients or assets can be selected for adjusting. a.    Hold down the Ctrl key on the keyboard or, if the virtual keyboard is activated, click on the Select Multiple button in the Adjust window. The Select Multiple button highlights when activated.b.    Select the patients or assets whose banding material needs adjustment.5.    Click Start Adjust.a.    If the alarming band transmitter is in alarm, a dialog box appears indicating that the transmitter is in alarm and the adjust function could not be performed. You must clear the alarm and re-try the Adjust.b.    If successful, a dialog box appears showing the name of the patient or asset and the amount of time allowed to adjust the banding material.6.    Click Confirm to confirm the Adjust.7.    Adjust the banding material and re-attach the transmitter. The transmitter is active 60 seconds after both sides of the banding material are re-clamped. The patient or asset being monitored by the transmitter is once again supervised by the system. 8.    Click Cancel or X to cancel the Adjust request and close the window.NOTE: If the banding material is not removed within the time allowed, a message appears on the Client computer indicating that the adjust time expired. Do not continue with the adjustment; a new adjust function must be initiated. Adjusting the banding material after the adjustment time has expired will cause a Cut Band alarm.
Chapter 3: Using the Software72 Series 7.0 Software (0510-1086-B) - User GuideTo cancel an adjust1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Adjust. 4.    The Adjust Bands window appears.5.    Select the patient or asset currently being adjusted.6.    Click Cancel. A dialog box appears to confirm that the adjust was canceled.7.    Click OK.
Series 7.0 Software (0510-1086-B) - User Guide  73EscortEscortIt may be necessary to temporarily move patients or assets within your facility from a protected area to an unprotected area, or an area that is not monitored by the software, for example taking a patient to X-Ray. The Escort function allows for movement of patients or assets by authorized staff within a facility while maintaining a record of the patient or asset being escorted and the staff who authorized the action. If an alarm from a Pendant, Fall Monitoring or Incontinence device is generated for the patient while he/she is in Escort, the alarm cancels the Escort function. The alarm must then be cleared before the patient can be placed back into Escort.To perform an escort1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Escort. The Escort window appears. Patients or assets with alarming band transmitters, Wander Management transmitters or Pendant, Fall Monitoring or Incontinence devices that currently exist in the census are listed in the window.FIGURE 3.11:    Escort WindowNOTE: If a patient or asset is in alarm, the event must be cleared before the patient or asset can be placed into Escort.
Chapter 3: Using the Software74 Series 7.0 Software (0510-1086-B) - User Guide4.    Use the arrow buttons to find and select the patient or asset to be escorted. Multiple patients and assets can be selected for escort providing that the Destination and Escort Duration is the same. a.    Hold down the Ctrl key on the keyboard or, if the virtual keyboard is activated, click on the Select Multiple button in the Escort window. The Select Multiple button highlights when activated.b.    Select the patients or assets to be escorted.5.    Use the arrow buttons to find and select the Destination, or the location to which the patient is to be escorted.6.    Select the Escort Duration; the choices are Hours or Days. You can choose to set the Escort Duration from 1 to 23 Hours or 1 to 23 Days.7.    Use the Increase and Decrease arrows to select the amount of time required to escort the patient.8.    Click Start Escort.A dialog box appears showing the name of the patient or asset and the amount of time allowed for the escort.9.    Click Confirm to confirm the Escort. The patient or asset must be returned to the same unit within the selected time allowed, or an alarm is issued. When initiating an Escort for a patient or asset using an alarming band transmitter, you must wait 45 seconds before returning the patient or asset to the unit. Returning a patient or asset to the unit before the 45 seconds time-lapse will result in an incomplete Escort.10.   Click Cancel or X to cancel the Escort request and close the window.To reset escort duration time1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Escort. The Escort window appears (Figure 3.11 on page 73). Patients or assets with alarming band transmitters, Wander Management transmitters or Pendant, Fall Monitoring or Incontinence devices that currently exist in the census are listed in the window.4.    Use the arrow buttons to find and select the patient or asset whose escort duration time is to be reset. Multiple patients or asset can be selected for resetting duration time, providing that the Destination and reset duration time is the same.5.    Use the Hours or Days arrows to select the new time needed to escort the patient or asset.
Series 7.0 Software (0510-1086-B) - User Guide  75Escort6.    Click Reset Duration.A dialog box appears showing the patient’s or asset’s name and the Escort Reset Duration hours or days.7.    Click OK.To cancel an escort1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Escort.The Escort window appears (Figure 3.11 on page 73). Patients or assets with alarming band transmitters, Wander Management transmitters or Pendant, Fall Monitoring or Incontinence devices that currently exist in the census are listed in the window.4.    Use the arrow buttons to find and select the patient or asset whose escort is to be canceled. Multiple patients or assets can be selected for canceling.5.    Click Cancel.A dialog box appears indicating that the escort for the selected patient or asset has been canceled.6.    Click OK.Transmitter is no longer communicating with the systemThe following dialog box appears when a transmitter is no longer communicating with the system and an Escort attempt is made. 1.    Follow the steps outlined in the dialog box.2.    Click OK.
Chapter 3: Using the Software76 Series 7.0 Software (0510-1086-B) - User GuideTransferThe Transfer function is used to move a patient or asset from one protected area to another protected area, for example from Labor and Delivery to Post Partum. Use the following steps to transfer a patient.To perform a transfer1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Transfer. The Transfer window appears. Patients or assets with alarming band transmitters, Wander Management transmitters or Pendant, Fall Monitoring or Incontinence devices that currently exist in the census are listed in the window.FIGURE 3.12:    Transfer Window4.    Use the arrow buttons to find and select the patient or asset to be transferred.5.    Use the arrow buttons to find and select the Destination, or the location to which the patient or asset is to be transferred.6.    Use the Increase or Decrease arrows to select the amount of time required for the transfer. 7.    Click Start Transfer.NOTE: If a transmitter is in alarm, the event must be cleared before the patient or asset can be placed into Transfer.
Series 7.0 Software (0510-1086-B) - User Guide  77Transfer8.    A dialog box appears showing the patient’s or asset’s name, the amount of time allowed to transfer the patient or asset, and the destination.If the Transfer is for a Wander Management transmitter, Pendant, Fall Monitoring or Incontinence device, the transfer occurs immediately.9.    Click Confirm to confirm the Transfer.As soon as the patient's or asset’s transmitter passes through a protected zone that belongs to the selected designation, the system recognizes that the transfer was successful and the Transfer completes.10.   Click Cancel or X to cancel the Transfer request and close the window.To reset a transfer duration time1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Transfer. The Transfer window appears (Figure 3.12 on page 76). Patients or assets that currently exist in the census are listed in the window.4.    Use the arrow buttons to find and select the patient or asset whose transfer duration time is to be reset.5.    Use the Increase or Decrease arrows to select the new time needed to transfer the patient or asset.6.    Click Reset Duration.A dialog box appears showing the patient or asset name and the number of minutes that the transfer is extended.7.    Click OK.NOTE: When a transmitter successfully transfers to a unit with a different setting for Band Slippage, a Begin Adjust alarm may be generated upon completion of the transfer.
Chapter 3: Using the Software78 Series 7.0 Software (0510-1086-B) - User GuideTo cancel a transfer1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Transfer.The Transfer window appears (see Figure 3.12 on page 76). Patients or assets with alarming band transmitters, Wander Management transmitters or Pendant, Fall Monitoring or Incontinence devices that currently exist in the census are listed in the window.4.    Select the patient or asset currently being transferred.5.    Click Cancel. A dialog box appears to confirm that the transfer was canceled. 6.    Click OK.Transmitter is no longer communicating with the systemThe following dialog box appears when a transmitter is no longer communicating with the system and a Transfer attempt is made. 1.    Follow the steps outline in the dialog box.2.    Click OK.
Series 7.0 Software (0510-1086-B) - User Guide  79Update RecordUpdate RecordThe Update Record function is used to update a patient or asset from one protected area to another protected area, for example from Labor and Delivery to Post Partum. Use the following steps to transfer a patient.To update a record1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Update Record. The Admit Selections - Update Records window appears. Patients or that currently exist in the census are listed in the window.FIGURE 3.13:    Upgrade Record4.    Use the arrow buttons to find and select the patient to be updated. 5.    Double click on the patient to bring up the Admit Information window and update admit information; the yellow fields designate required entry. 6.    Once information has been updated, click Save.NOTE: If a transmitter is in alarm, the event must be cleared before the patient or asset can be placed into Transfer.
Chapter 3: Using the Software80 Series 7.0 Software (0510-1086-B) - User GuideAdministrative FunctionsUse Administrative Functions to Add/Update Assets, enter Staff Drill and System Maintenance information, Change Client Properties, access the Configuration options and access available Reports.FIGURE 3.14:    Administrative FunctionsThe Back button closes the Administrative Function window and returns you to the Main Screen. WARNING: When the software application is closed, indicators of alarms and events will not be seen at the computer. Important! Only close the software application if instructed to do so by authorized staff.
Series 7.0 Software (0510-1086-B) - User Guide  81Administrative FunctionsAdd/Update An AssetTransmitters that are automatically enrolled in the system can be assigned to an asset using this option. When you click Add/Update An Asset, a window opens with only auto-enrolled transmitters.FIGURE 3.15:    Admit SelectionTo Add/Update an asset1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Click Administrative Functions.4.    Click Add/Update An Asset.The Admit Selection window appears. Asset transmitters that currently exist in the census are listed in the window.5.    Use the arrow buttons to find and select the transmitter number to be assigned. 6.    Click on the Asset transmitter to bring up the Admit Information window and enter admit information; the yellow fields designate required entry.
Chapter 3: Using the Software82 Series 7.0 Software (0510-1086-B) - User GuideFIGURE 3.16:    Admit Information7.    Once admit information has been entered, click Save.If the admit is successful, you will get the following dialog box:8.    Click OK. Asset Main Information TabThe Asset Main information tab allows you to enter identification information about the asset being admitted. The yellow fields designate required entry.1.    Click Main on the toolbar.2.    In the Model field, type the model or description of the asset being admitted (required). 3.    In the Make field, type the manufacturer’s information of the asset being admitted.4.    In the SN field, type the serial number of the asset being admitted.5.    In the Transmitter ID field, type the 3-digit ID number printed on the alarming band transmitter to be assigned to the asset.6.    In the Unit field, select the unit to which the asset is currently assigned, even if the asset will not remain in that unit (required).7.    Click the Risk level associated with the asset. Choices are Low or High. If your facility has enabled the Lockdown on Cut Band Alarms feature, a Cut Band Alarm will trigger a Global Lockdown when a High Risk level is selected for an asset transmitter.NOTE: Information entered can only contain alphabetic and numeric characters, spaces, and the following special characters: ! - _ , . ; [ ]{ }( )
Series 7.0 Software (0510-1086-B) - User Guide  83Administrative FunctionsStaff DrillWhen a staff drill is requested, the attendant performing the drill enters the information in the Staff Drill window.To access the Staff Drill window1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Press Enter or click OK.4.    Select Administrative Functions.5.    Select Staff Drill.The Staff Drill window opens.FIGURE 3.17:    Staff Drill6.    Enter the Date of the Staff Drill as the two digit month, followed by the two digit day, followed by the four digit year. Enter the Time as the two digit hour followed by the two digit minute.7.    In the Comments field, enter your comments.8.    Do one of the following:a.    Click Save to save and return to the main window. b.    Click Cancel to return to the main window without saving.
Chapter 3: Using the Software84 Series 7.0 Software (0510-1086-B) - User GuideSystem MaintenanceA log of maintenance performed on the system is logged in the System Maintenance window.To access the System Maintenance window1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Press Enter or click OK.4.    Select Administrative Functions.5.    Select System Maintenance.The System Maintenance window opens.FIGURE 3.18:    System Maintenance6.    Enter the Date of the System Maintenance as the two digit month, followed by the two digit day, followed by the four digit year. Enter the Time as the two digit hour followed by the two digit minute.7.    In the Comments field, enter your comments.8.    Do one of the following:a.    Click Save to save and return to the main window. b.    Click Cancel to return to the main window without saving.
Series 7.0 Software (0510-1086-B) - User Guide  85Administrative FunctionsChanging Client Properties When the software is running on the Central Server and each Client computer, and the System settings have been defined, the next step in the installation process is to define the properties or settings of each Client computer.The changes you make in Client Properties affect only the Client computer you are configuring.To access the Client Properties window1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Press Enter or click OK.4.    Select Administrative Functions.5.    Select Change Client Properties.The Client Properties window opens.FIGURE 3.19:    Client PropertiesFor more information about Client Properties, see the Series 7.0 Software Administrator Guide.
Chapter 3: Using the Software86 Series 7.0 Software (0510-1086-B) - User GuideConfigurationThe Configuration options allow you to configure devices in the system. System configurations are done by the System Administrator. To access the Configuration home page1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card.3.    Press Enter or click OK.4.    Select Administrative Functions.5.    Select Configuration, or double-click the desk top icon.The System Management home page opens.6.    Select Configuration.The Configuration page opens with links to the Configuration menus.FIGURE 3.20:    Configuration PageFor more information about Configuration, see the Series 7.0 Software Administrator Guide.
Series 7.0 Software (0510-1086-B) - User Guide  87Administrative FunctionsReportsThe Reports option accesses a list of all available reports. There are several System Reports that enable you to view information about the activities of the system throughout the day, week, or month.To access Reports1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Press Enter or click OK.4.    Select Administrative Functions.5.    Select Reports.The Reports window opensFIGURE 3.21:    ReportsRefer to Chapter 5, Using System Reports for detailed information about viewing, printing, saving and filtering reports.
Chapter 3: Using the Software88 Series 7.0 Software (0510-1086-B) - User GuideMessaging FunctionsThe Messaging Functions allows you to schedule system messages, manage paging shifts and send messages to staff via pager, text, Cisco phone, Care Manager and email.FIGURE 3.22:    Messaging FunctionsScheduled MessagesThe Scheduled Messages feature allows you to schedule system messages to be sent to staff one time only or on a daily, weekly or monthly basis.To access the Scheduled Messages window1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Press Enter or click OK.4.    Select Messaging Functions.
Series 7.0 Software (0510-1086-B) - User Guide  89Messaging Functions5.    Select Scheduled Messages.The Scheduled Messages window opens.FIGURE 3.23:    Scheduled Messages6.    Click Add to open the Scheduled Messages window.FIGURE 3.24:    Scheduled Messages window7.    Select the Schedule Type. Do you want the schedule message to:•Run only once•Daily•Weekly•Monthly8.    If you choose to run the scheduled message daily, you must select the day(s) you wish to run the message. Choose the day(s) from the Starting On Day field.
Chapter 3: Using the Software90 Series 7.0 Software (0510-1086-B) - User Guide9.    From the Starting Date and Time field, select a date and time to start the scheduled message. The current date is displayed in the Start Date field. To change the date, click on Change Date and choose a date from the popup calendar.10.   Choose a Start Time. The current time is displayed, click Increase or Decrease to select the desired start time.11.   If you choose to run the scheduled message more than once daily, you must select a run Interval and Run only between times. The Interval is how often you want the scheduled event to run. Increments are 1 minute (0:01) to 11 hours and 59 minutes (11:59). Click Increase or Decrease to select interval.12.   Click Increase or Decrease to select interval.13.   The Run only between range can be set for any minute of the day. Click Increase or Decrease to select the starting Run only between time AND click Increase or Decrease to select the ending Run only between time.NOTES:•The scheduled message Start Time must fall within the starting Run only between time and the ending Run only between time range. For example, a scheduled message with a start time of 8:00 A.M. must have a Run only between time window that includes 8:00 A.M. A Run only between time of 7:00 A.M to 10:00 A.M. is legitimate; it includes 8:00 A.M. A time of 4:00 A.M. to 7:00 A.M. is not a legitimate Run only between time.•The scheduled message’s Interval time must be less than the time window created by the Run only between times. For example, a scheduled message with an interval of 5 hours must have a Run only between time window of at least 6 hours. 14.   The Audio button toggles On/Off. When Audio is turned On, the scheduled message will alarm at the Client computer(s).15.   Enter the message you wish to send in the free text Message field.16.   From the Send scheduled messages to: pull down, select a message group or recipient to whom the message will be sent.17.   Click Save or Cancel if you do not wish save your changes.
Series 7.0 Software (0510-1086-B) - User Guide  91Messaging FunctionsChanging ShiftIn some cases, it may be necessary to change a message unit’s work shift. Use this feature to select a different messaging unit and work shift. This feature can only be used if you currently use messaging with your system. To change a messaging unit work shift1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Press Enter or click OK.4.    Select Messaging Functions.5.    Select Change Shift.The Change Messaging Unit Work Shift window opens.FIGURE 3.25:    Change Message Unit Work Shift6.    From the Messaging Units drop-down, select the Message Unit you wish to change.7.    From the Work Shift drop-down, select a different work shift. The Change Work Shift button enables.8.    If you wish to Switch back to timed work shift at the end of this shift, click the check box.9.    Click the Change Work Shift button.
Chapter 3: Using the Software92 Series 7.0 Software (0510-1086-B) - User GuideStart ShiftAt the start of the shift, use this feature to check out a Cisco phone. Cisco phones are configured by the System Administrator and can only be used if you currently use Cisco phones with your system. For more information, see the Series 7.0 Software Administrator Guide.To check out a Cisco phone1.    Select Start Shift.2.    Use your proximity card or magnetic/barcode card or enter your Login and Password then press Enter or click OK.3.    The Device Dialog window opens. Cisco phones currently available for checkout are listed in the window.FIGURE 3.26:    Device DialogNOTE: The option to clear alarms at the point of care a feature of the Cisco phone. Below are guide lines when clearing an alarm from the Cisco phone:•If the “Clear” function is password protected, the user must be assigned that function in order to clear an alarm from the Cisco phone. Additionally the phone or care manager must be checked out to the user assigned.•The Cisco phone chimes when a message is cleared. It is important to select the “When the event occurs” field concurrently with the “When the event is cleared” field to avoid getting chimes without getting the original alarm message.
Series 7.0 Software (0510-1086-B) - User Guide  93Messaging Functions4.    Double click anywhere in the row containing the phone you wish to checkout. The user name replaces Available/Select in the Assigned To column. 5.    Click Save to close the window and checkout the phone. Only one phone can be checked out per login. To check out another phone you must click Save and repeat the process.6.    Click Close to close the window without checking out the phone.End ShiftAt the end of the shift, use this feature to return the CISCO phone back into the system. To return a phone, select End Shift. Use your proximity card or magnetic/barcode card or enter your Login and Password then press  OK. All phones checked out to the user are automatically returned to the Device Dialog list, no confirmation of the return is given.Send MessageIn some cases, it may be necessary to send a manual message to a staff member.This feature can only be used if your system is configured for messaging. There are five messaging methods. •Send Pager Message•Send Text Message (see note on page 94 regarding text message)•Send Cisco Message (see notes on page 94 regarding Cisco phone message)•Send Care Manager Message•Send EmailSelect the method that best suit your needs. The example below is for sending a manual Pager Message.To send manual messages1.    Select Login (or Functions if password protection is disabled).2.    Enter your Login and Password or use your identification card. 3.    Press Enter or click OK.4.    Select Messaging Functions.
Chapter 3: Using the Software94 Series 7.0 Software (0510-1086-B) - User Guide5.    Select Send Cisco Messages.Send Manual Cisco Phone Message window opens.FIGURE 3.27:    Send Cisco Phone Message6.    From the Send Cisco Message to: drop-down, select the message group you wish to send a manual page.7.    Type your message in the Enter the message to send: field.8.    Click Send to send your message.9.    Click Cancel if you do not wish to send the message.10.   Follow the same steps to send Pager, Text, Email, or Care Manager messages.NOTE: The text messaging functionality is dependant on the performance constraints of your network. This means that text messages may take a long time to get through or they may appear in a different order then they were sent. Text message notifications should not be used as the primary form of notification.NOTES: •The Cisco phone system will not issue a busy signal when the phone is in use. If there is no answer on the other end, it may mean that the patient is on the phone. •The following alarm events and information cannot be messaged to Cisco phones.a.   Asset Alarmsb.   Scheduled Eventsc.   Any event that initially triggers a White Alarms (i.e. Auto-enroll, Discharge expired)
Series 7.0 Software (0510-1086-B) - User Guide 95Chapter 4Handling EventsIntroductionThis chapter provides information about the Events. It provides a detail description of alarming events, the devices that triggered the events and information about responding to the specific events. Events An event is an action that occurs in the software that requires a response from an authorized user. When an event occurs, a message is displayed in the Event List indicating the relevant device, the patient’s or asset’s name when applicable, and the type of event received. FIGURE 4.1:    Main WindowClick anywhere in the Alarm Message Box to access more information about the event and to select a cause for the event, if applicable, from the Event Information window. These event causes are then logged into the applicable reports. For information about reporting, see Chapter 5, Using System Reports.WARNING: The Series 7.0 Software is designed and intended to work in conjunction with a facility’s overall patient security program, including reasonable operating policies and procedures. The Series 7.0 Software, by itself, cannot prevent abductions or elopements. Alarm Message Box
Chapter 4: Handling Events96 Series 7.0 Software (0510-1086-B) - User GuideEvent Information WindowWhen an event occurs, an Alarm Message Box is displayed in the Event List. Click anywhere in the Alarm Message Box to access the Event Information window. The Event Information window contains detailed information about the event. If a picture is available, certain events will display the picture of the patient or asset associated with the event. Selecting an Event Cause will clear an alarm.FIGURE 4.2:    Event Information WindowNOTE: The Event Cause buttons in the Event Information window are different for each event. See the following sections for detailed information. Event Cause Buttons
Series 7.0 Software (0510-1086-B) - User Guide  97Event TypesEvent Information Window PropertiesThe following table provides brief descriptions of the properties that appear in the Event Information window.Event TypesThere are several different event types that can occur when using the Series 7.0 Software. The following sections provide a brief overview of each event as well as an action to take if this event occurs.Event Information WindowEvent:  the type of event recorded. Time: the time that the event occurred.Name: the transmitter ID number, or the name of the patient or asset to whom the transmitter is assigned.Room: the room number of the patient or asset. Gender: the gender of the patient.Unit: the unit that the patient or asset is assigned to. Risk: the risk level assigned to the patient or asset.Admitted By: the staff member who performed the admission.Transmitter: the identification number of the transmitter that initiated the event. Type: the type of transmitter that sent the signal.Device LocationDevice Name: the name of the device that received the alarm.Device Type: the type of device that received the alarm.Help—displays help information for the Event Information windowReview Print Info—opens an Event Information Report with patient or asset, event and deice location informationClose—closes the Event Information window without clearing the alarm.WARNING: If you do not already have procedures in place, you must establish procedures for your staff to follow to ensure patient safety and to secure the area in the event of an alarm. Existing procedures may require modification to incorporate optional features. Failure to create or modify these procedures may result in patient abduction or elopement.
Chapter 4: Handling Events98 Series 7.0 Software (0510-1086-B) - User GuideRed AlarmsThe following sections provide detailed information about Red Alarms, responding to alarming events, and the the way the event should be cleared. Red Alarms are high priority alarms. They are displayed in the Alarm Message Box and the Event List sequentially as they occur. Red Alarms are displayed first in the Alarm Message Box and Event list.Door AlarmWhen a patient wearing an alarming band transmitter is in an Exit Alarm Zone and the monitored door is open, an alarm sounds at the Exit Alarm Controller, a message is displayed on the Client computer(s) in the unit configured to monitor the transmitter, and the location of the Exit Alarm Zone is indicated by a flashing icon on the map on the Client computer(s). Door Alarms are also displayed on remote notification devices.To respond to a Door Alarm1.    Always follow your facility’s policies and procedure to ensure patient safety and secure the area.2.    Go to the alarming device and use your card reader access card (if applicable) or enter the appropriate 4-digit security code to reset the alarm at the device. For more information about the Security Code, contact your System Administrator. 3.    If the Enforce Joint Commission reporting feature is activated, you must select an Event Cause once the alarming device has been reset. When you reset the alarming device, the Red Alarm changes to a White Alarm in the Alarm Message Box and Event List. If the Enforce Joint Commission reporting feature is not activated, the Alarm Message Box clears once the alarm is cleared at the device.4.    From the Client computer, click anywhere in the Door Alarm Message Box to access the Event Information window.5.    Select one of the following causes for the Door Alarm:•Escort problem—there was an issue while the patient was in escort.•Transfer problem—there was an issue while the patient was in transfer.•Accidentally too close to open door—the patient was near a door when it was opened.•Noise —there were noise issues with the device.•Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Series 7.0 Software (0510-1086-B) - User Guide  99Event TypesExit Alarm (Wide Gap)A Wide Gap Exit Alarm occurs when a door or window monitored by a Door/Window transmitter is opened. A Door/Window transmitter is a device that protects a door or window against unauthorized egress. When a Wide Gap Exit Alarm occurs, a message is displayed on the Client computer(s) in the unit configured to monitor the door or window, and the location of the Exit Alarm is indicated by a flashing icon on the map on the Client computer(s). To respond to a Wide Gap Exit Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Locate the door or window that initiated the alarm. 3.    Close the door or window. The system records the event and clears the alarm when the door or window is closed.Smoke AlarmWhen a smoke detector that is integrated with the system is activated, an alarm sounds, a message is displayed on the Client computer(s) in the unit configured to monitor the device, and the location of the Smoke Alarm is indicated by a flashing icon on the map on the Client computer(s). An event is reported in the Event List each time the smoke detector is activated.To respond to a Smoke Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Locate the alarming device. Smoke Alarms must be reset at the alarming device.The system records the event as a Reset when the smoke detector is reset.NOTE: No local audible alarms are sounded from the Door/Window transmitter when an alarm occurs. NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Chapter 4: Handling Events100 Series 7.0 Software (0510-1086-B) - User GuidePerimeter AlarmA Perimeter Alarm occurs when the doors monitored by the system are in Perimeter mode and a door is opened. Perimeter mode is when a door is in a lockdown state as a result of system configuration or an event. Perimeter mode also occurs when a door is open at the time a Cut Band Alarm occurs.When a Perimeter alarm occurs, an alarm sounds at the Exit Alarm Controller, a message is displayed on the Central Server or Client computer(s) in the unit configured to monitor the door, and the location of the Exit Alarm is indicated by a flashing icon on the map on the Client computer(s).To respond to a Perimeter Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Locate the alarming device. Perimeter Alarms must be reset at the alarming device.3.    Go to the Exit Alarm Controller and use your card reader access card (if applicable) or enter the appropriate 4-digit security code. For more information about the Security Code, contact your System Administrator. The system records the event as a Reset when the appropriate code is entered. 4.    If the Enforce Joint Commission reporting feature is activated, you must select an Event Cause once the alarming device has been reset. When you reset the alarming device, the Red Alarm changes to a White Alarm in the Alarm Message Box and Event List. If the Enforce Joint Commission reporting feature is not activated, the Alarm Message Box clears once the alarm is cleared at the device.5.    From the Central Server or Client computer, click anywhere in the Perimeter Alarm Message Box to access the Event Information window.6.    Select one of the following causes for the Perimeter Alarm:•Escort problem—there was an issue while the patient was in escort.•Transfer problem—there was an issue while the patient was in transfer.•Accidentally close to open door—the patient was near a door when it was opened.•Noise —there were noise issues with the device.•Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.NOTE: You cannot silence or reset the Exit Alarm Controller’s alarms from the Central Server and Client computer(s). You must reset the alarm at the Exit Alarm Controller. NOTE: Any perimeter alarms that occur due to a door open during a Cut Band Alarm require that the Cut Band Alarm be cleared at the computer first, before the doors are reset or cleared.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Series 7.0 Software (0510-1086-B) - User Guide  101Event TypesCut Band AlarmWhen the banding material on a patient’s alarming band transmitter is cut, tampered with or opened without authorization (which includes opening the transmitter when a timed event has expired), an alarm is sounded on the computer configured to monitor the unit, a message is displayed in the Event List, and the location of the Alarming Band Receiver that detected the event is indicated on the map on the computer(s). Cut Band Alarms are also displayed on remote notification devices.If your facility has enabled the Lockdown on Cut Band Alarms feature, a Cut Band Alarm will trigger a Global Lockdown.You can configure the Global Lockdown feature to lock doors at All exits or By transmitter units. However if a Cut Band Alarm is initiated during an Escort or a Transfer, the system automatically locks All exits since the transmitter in Escort or Transfer may be outside of its protected unit and displays the alarm on all Client computers and Quick Look displays.To respond to a Cut Band Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Verify the transmitter is applied correctly and without signs of damage or tampering.3.    From the Client computer, click anywhere in the Cut Band Alarm Message Box to access the Event Information window.4.    Select one of the following event causes: •Clasp open —one of the clasps on the transmitter was open.•Band cut—the banding material on the transmitter was cut.•Band worn—the banding material on the transmitter is worn and must be replaced.•Unauthorized open-—an unauthorized person opened the transmitter clasp.•Adjust—a transmitter was being adjusted without authorization, an adjust was not requested or an adjust occurred after the adjust time expired.•Discharged —the transmitter was being removed in a discharge without authorization, a discharge was not requested or a discharge occurred after the adjust time allowed.•Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.NOTE: Any perimeter alarms that occur due to a door open during a Cut Band Alarm require that the Cut Band Alarm be cleared at the computer first, before the doors are reset or cleared.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Chapter 4: Handling Events102 Series 7.0 Software (0510-1086-B) - User GuideBand Off AlarmWhen the Smart Sense Banding Material on a Smart Sense Infant Transmitter is removed, tampered with or comes off of the infant’s extremity due to newborn weight loss, an alarm is sounded on the computer configured to monitor the unit, a message is displayed in the Event List, and the location of the Alarming Band Receiver that detected the event is indicated on the map on the computer(s). Band Off Alarms are also displayed on remote notification devices. There are three measurements of tamper detection for a Band Off Alarm.•Temperature—detects the change in temperature of the transmitter•Resistance—detects the stretching of the banding material•Capacitance—detects the change in contact between transmitter and infantIf your facility has enabled the Lockdown on Band Off Alarms feature, a Band Off Alarm will trigger a Global Lockdown.You can configure the Global Lockdown feature to lock doors at All exits or By transmitter units. However if a Band Off Alarm is initiated during an Escort or a Transfer, the system automatically locks All exits since the transmitter in Escort or Transfer may be outside of its protected unit and displays the alarm on all Client computers and Quick Look displays.To respond to a Band Off Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Verify the transmitter is applied correctly and without signs of damage or tampering.3.    From the Client computer, click anywhere in the Band Off Alarm Message Box to access the Event Information window.4.    Select one of the following event causes: • Band Off—the banding material is off the infant.•Clasp open —one of the clasps on the transmitter was open.•Band cut—the banding material on the transmitter was cut.•Band worn—the banding material on the transmitter is worn and must be replaced.•Unauthorized open-—an unauthorized person opened the transmitter clasp.•Adjust—a transmitter was being adjusted without authorization, an adjust was not requested or an adjust occurred after the adjust time expired.•Discharged —the transmitter was being removed in a discharge without authorization, a discharge was not requested or a discharge occurred after the adjust time allowed.•Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unitNOTE: Any perimeter alarms that occur due to a door open during a Band Off Alarm require that the Band Off Alarm be cleared at the computer first, before the doors are reset or cleared.
Series 7.0 Software (0510-1086-B) - User Guide  103Event TypesMismatch AlarmA Mismatch alarm occurs if an Infant transmitter is located within proximity of a Mother transmitter that is linked to a different infant transmitter. To respond to a Mismatch Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Click anywhere in the message box to access the Event Properties window.3.    Select one of the following Event reasons: •No problem—no issue was found.•Wrong Infant—the Infant transmitter is brought to the wrong Mother transmitter.•Mothers bonding—while two mothers were socializing, one of the Mother transmitters picked up the other Mother’s Infant transmitter signal.•Infant not present—an Infant transmitter was not present. •Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.Match AlarmYou can configure the system to require a Mother/Infant match before an infant can be discharged. The Match Alarm occurs when an infant is discharged and the alarming band material is cut, before performing the required Mother/Infant match. The Require Mother/Infant match before discharge is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).To respond to a Match Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Click anywhere in the Match Alarm Message Box to access the Event Information window.3.    Click Clear. If necessary, perform the discharge function again by first performing the Mother/Infant match.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound. NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Chapter 4: Handling Events104 Series 7.0 Software (0510-1086-B) - User GuideLink AlarmThis alarm occurs when there is a problem linking the Infant transmitter to a Mother transmitter. For example, the Infant transmitter may already be linked to another Mother transmitter.To respond to a Link Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Click anywhere in the Link Alarm Message Box to access the Event Information window.3.    Click Clear.4.    If necessary, verify the identity of the mother and infant then relink the Mother and Infant transmitters.Check AlarmNo message has been received from the patient’s transmitter or the device in the patient’s room during the Inactivity Check-In period. The Check message will remain until the patient’s transmitter checks in, an Alarm message is received, or the event is manually cleared at the Client computer(s).To respond to a Check Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Locate the device.3.    Verify that no patient emergency exists.4.    From the Client computer, click anywhere in the Inactivity Check-In Alarm Message Box to access the Event Information window.5.    Select Clear to clear the Inactivity Check-In alarm.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Series 7.0 Software (0510-1086-B) - User Guide  105Event TypesNo Signal Alarm A No Signal alarm occurs when the system is unable to locate the transmitter within the required supervision time.To respond to a No Signal Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Verify transmitter is fastened correctly and without signs of damage.For more information, refer to the Patient Transmitter User Guide (PN 0510-1013) or the Infant Transmitter User Guide (PN 0510-1006).3.    From the Client computer, click anywhere in the No Signal Alarm Message Box to access the Event Information window.4.    Select one of the following event causes: •Clasp open —one of the clasps on the transmitter was open.•Band cut—the banding material on the transmitter was cut.•Band worn—the banding material on the transmitter is worn and must be replaced.•Unauthorized open-—an unauthorized person opened the transmitter clasp.•Adjust—a transmitter was being adjusted without authorization.• Discharged —the transmitter was being removed in a discharge without authorization.•Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.5.    Multiple No Signal alarms may be an indication that Receiver coverage may be inadequate. Contact your System Administrator.WARNING: You must test all transmitters prior to use, and periodically thereafter, to verify proper operation. Failure to test the transmitters before use can result in system failure and/or an elopement or abduction. In addition, failure to test transmitters voids the RF Technologies Product Warranty.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Chapter 4: Handling Events106 Series 7.0 Software (0510-1086-B) - User GuideAssistance Required AlarmAn Assistance Required alarm occurs when a QR or 9600 Series device belonging to a patient alarms. The Alarm message will remain until the alarming device is reset. An Assistance Required alarm is also activated in response to a Fall Management System alert.To respond to an Assistance Required Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Locate the alarming device. Assistance Required Alarms must be reset at the alarming device.3.    Reset the alarming device. The system records the event as a Reset when the alarming device is reset.4.    If responding to a Fall Management System alert, the system will automatically reset and begin monitoring once the patient is placed back on the Sensor Pad (refer to the “Advanced 3-Way Care Solution” on page 30 or the “Advanced 4-Way Care Solution” on page 32).5.    If the Enforce Joint Commission reporting feature is activated, you must select an Event Cause once the alarming device has been reset. When you reset the alarming device, the Red Alarm changes to a White Alarm in the Alarm Message Box and Event List. If the Enforce Joint Commission reporting feature is not activated, the Alarm Message Box clears once the alarm is cleared at the device.6.    From the Client computer, click anywhere in the Assistance Required Alarm Message Box to access the Event Information window.7.    Select one of the following event causes: •Fall —the patient had fallen and needed assistance.•Water—the patient required water.•Food—the patient required food.•Talk-—the patient had matters to discuss with the attendant.•Bathroom—the patient required bathroom assistance.•Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Series 7.0 Software (0510-1086-B) - User Guide  107Event TypesFall AlarmThis alarm occurs when a patient removes his/her weight from the sensor pad. The alarm clears when weight is re-applied to the pad. The Alarm Message Box will remain on the Client computer until the alarming device is reset.To respond to an Fall Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Secure the patient from a potential fall situation.3.    The system will automatically reset and begin monitoring once the patient is placed back on the Sensor Pad.4.    If the Enforce Joint Commission reporting feature is activated, you must select an Event Cause once the alarming device has been reset. When you reset the alarming device, the Red Alarm changes to a White Alarm in the Alarm Message Box and Event List. If the Enforce Joint Commission reporting feature is not activated, the Alarm Message Box clears once the alarm is cleared at the device.5.    From the Client computer, click anywhere in the Fall Alarm Message Box to access the Event Information window.6.    Select one of the following event causes: •Confused —the patient attempted to get up without assistance.•Bathroom—the patient required bathroom assistance.•Water—the patient required water.•Food—the patient required food.•Talk-—the patient had matters to discuss with the attendant.•Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Chapter 4: Handling Events108 Series 7.0 Software (0510-1086-B) - User GuideWet AlarmThis alarm occurs when fluids are detected on an incontinence pad. To respond to a Wet Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Proceed to the patient and verify incontinence occurrence. Detach the incontinence pad; the alarm clears when the incontinence pad is detached.3.    If the Enforce Joint Commission reporting feature is activated, you must select an Event Cause once the alarming device has been reset. When you reset the alarming device, the Red Alarm changes to a White Alarm in the Alarm Message Box and Event List. If the Enforce Joint Commission reporting feature is not activated, the Alarm Message Box clears once the alarm is cleared at the device.4.    From the Client computer, click anywhere in the Wet Alarm Message Box to access the Event Information window.5.    Select one of the following event causes: •Urine —the patient has urinated on him/herself.•Sweat—the patient’s sweat has caused the bed to be wet.•Stool—the patient has defecated on him/herself.•Spill—the patient has spilled liquid on the bed.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.Turn AlarmThis alarm occurs when the time on the Control Unit expires. To respond to a Turn Alarm1.    Always follow your facility’s policies and procedures to ensure patient safety and secure the area.2.    Proceed to the patient and re-position the patient (refer to the applicable Control Unit’s in-service manual).NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Series 7.0 Software (0510-1086-B) - User Guide  109Event Types3.    If the Enforce Joint Commission reporting feature is activated, you must select an Event Cause once the alarming device has been reset. When you reset the alarming device, the Red Alarm changes to a White Alarm in the Alarm Message Box and Event List. If the Enforce Joint Commission reporting feature is not activated, the Alarm Message Box clears once the alarm is cleared at the device.4.    From the Client computer, click anywhere in the Turn Alarm Message Box to access the Event Information window.5.    Select one of the following event causes: •Left —the patient needs to be turned to his/her left side.•Right—the patient needs to be turned to his/her right side.•Supine—the patient needs to be turned to the Supine position, on his/her back.•Fowler—the patient needs to be turned to the Fowler position, semi-upright sitting 45-60 degrees.•Semi-Fowlers —the patient needs to be turned to the Semi-Fowler’s position (semi-upright sitting 30-45 degrees).You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unitServer Missing AlarmThis alarm occurs when the Client computer has lost communications with the Central Server. To respond to a Server Missing Alarm1.    Verify with the System Administrator that the Series 7.0 Software is running on the Client computer(s).2.    From the Client computer, click anywhere in the Server Missing Alarm Message Box to access the Event Information window.The Event Information window only provides time of the Server Missing event. This information may be helpful when communicating the event to your System Administrator.3.    Click Close. 4.    Contact your System Administrator or call RF Technologies Technical Support Team at (800) 669-9946 or (262) 790-1771.NOTE: A Server Missing alarm will automatically clear when communications with the Server is restored. It cannot be cleared by the user.
Chapter 4: Handling Events110 Series 7.0 Software (0510-1086-B) - User GuideYellow AlarmsThe following sections provide detailed information about Yellow Alarms, responding to alarming events, and the way the event should be cleared. Yellow Alarms are medium priority alarms. They are displayed in the Event List sequentially as they occur. Yellow Alarms are displayed below Red Alarms.No Signal Alarm (9600 Series Pendant)A No Signal alarm for the 9600 Series Pendant occurs when the system is unable to locate the pendant within the required supervision time. It is important to note if the person to whom the pendant is assigned has taken the pendant out of the area (i.e. weekend pass, doctor’s appointment). If the pendant is not out of the area, locate the pendant and verify proper operation.Multiple No Signal alarms may also be an indication that Router coverage is inadequate. If problem persist, contact your System Administrator or call RF Technologies Technical Support Team at (800) 669-9946 or (262) 790-1771. To respond to a No Signal Alarm1.    Always follow your facility’s policies/procedures to ensure patient safety.2.    From the Client computer, click anywhere in the No Signal Alarm Message Box to access the Event Information window.3.    Click Clear to clear the alarm. If you attempt to clear the alarm before it has been on the screen for more than 30 seconds, it will keep re-posting and then auto clear at the end of the 30 seconds. NOTE: No Signal alarms will repeat at each supervision check-in time as long as the system is unable to locate the pendant. If the transmitter is lost, stolen or does not exist, remove the pendant from the person to whom it is assigned.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Series 7.0 Software (0510-1086-B) - User Guide  111Event TypesClient MissingThis alarm occurs when the Client computer is not communicating with the system network.To respond to a Client Missing Alarm1.    Verify with the System Administrator that the Series 7.0 Software is running on the Client computer(s).2.    Check the power and network cable connecting the missing Client computer.3.    From the Client computer, click anywhere in the Client Missing Alarm Message Box to access the Event Information window.The Event Information window provides more information about the Client Missing event. This information may be helpful when communicating the event to your System Administrator.  4.    Click Close. 5.    Contact your System Administrator or call RF Technologies Technical Support Team at (800) 669-9946 or (262) 790-1771.Device FaultThis alarm occurs when a problem has been detected with a device. There are several types of Device Fault events that can occur in the system, for example: Device Tamper, RF Interference, Communications Failure, RFT Paging Manager. Other possible causes for Device Fault alarms are that the device has experienced a loss of power, it has an invalid address, or the network connection is broken. Quick Response devices also report low battery conditions. Additionally, if a Serial Receiver has been enrolled in the system, a Device Fault alarm will occur until a QR transmitter is enrolled.NOTE: A Client Missing alarm may not necessarily involve a Client computer. The Client Missing alarm could be generated by a service utilized by the system, for example the SNMP Agent, DB Service or Paging Manager.NOTE: A Device Tamper alarm is generated when the Nurse Call cord set is removed from the CA520 control unit while a patient is being monitored. To avoid this type of alarm, disconnect the Nurse Call cord set while the control unit is in the Silence mode.NOTE: When a RFT Paging Manager Device Fault occurs, pages will not be sent or received. Additionally, any new alarms will be ignored by the paging system until the Device Fault is resolved.
Chapter 4: Handling Events112 Series 7.0 Software (0510-1086-B) - User GuideTo respond to a Device Fault Alarm1.    From the Client computer, click anywhere in the Alarm Message Box to access the Event Information window.2.    The Event Information window provides more information about the Device Fault event. This information may be helpful when communicating the event to your System Administrator.3.    Contact your System Administrator or call RF Technologies Technical Support Team at (800) 669-9946 or (262) 790-1771.Low Battery This alarm appears in bottom toolbar when a transmitter currently enrolled in the system has a low battery. You cannot clear a Low Battery Alarm; the alarm remains for the duration of time that the transmitter is enrolled in the system. It does not disappear until the transmitter is discharged from the system and removed from the facility or assigned a Missing status in the Configurations, Global Settings menu (refer to the Series 7.0 Software Administrator Guide). Once the transmitter is discharged from the system, follow your warranty policy regarding the discard of the transmitter. For more information about transmitters and transmitter care, see the appropriate Transmitter User Guide. NOTES: •The system will not allow you to link a Mother transmitter that has a low battery.•Quick Response devices page low battery conditions as Device Faults.•A Low Battery Alarm is cleared for a QR or 9600 Series device when the battery is replaced.•When the battery on the CA420 or CA520 is low, the red light flashes every 10 seconds, the buzzer chirps and the nurse call triggers momentarily. When CA420 or CA520 is used with a Universal transmitter a low battery will also triggers an Assistance Required alarm at the computer every few seconds. Replace the low battery immediately to avoid this anomaly.
Series 7.0 Software (0510-1086-B) - User Guide  113Event TypesTamper AlarmThe Universal Transceiver’s tamper functionality operated in several modes depending on the device and the type of tamper interference. In either case, when initiated, a Ta mp er   alarm event will be listed on the Event List at the Central Server. The types of tamper events are:•Case Open Tamper— initiated when the case to the Universal transceiver is opened. •Mounting Tape Tamper—initiated when the PCB is separated from the enclosure•Nurse Call Cord Set Tamper—initiated when the Nurse Call Cord set is removed from the Nurse Call transceiver.•Externals Enclosure Tamper —initiated when the external closure of the PIR Sensor is opened.Below is a table showing the type of tamper event associated with a particular device.Nurse Call EAC Door/Window Door Manual Reset Door Check-in PIR Smoke COCase Open Tamper xx x x x xMounting Tape Tamper xx x x xNurse Call Cord Set Tamper xExternal Enclosure Tamper x
Chapter 4: Handling Events114 Series 7.0 Software (0510-1086-B) - User GuideWhite AlarmsThe following sections provide detailed information about White Alarms, responding to alarming events, and the way the events should be cleared. White Alarms are low priority alarms. They are displayed in the Alarm Message Box and the Event List sequentially as they occur. White Alarms are displayed below Yellow Alarms.Auto-Enroll The Auto-Enroll feature automatically enrolls alarming band transmitters into the system without requiring a manual admit. Once the transmitter is auto-enrolled, the system monitors the transmitter for Door, Cut Band, or No Signal alarms.To respond to an Auto-Enroll1.    From the Client computer (s), click anywhere in the Auto-Enroll Alarm Message Box to access the Event Information window.2.    Select one of the followings: •Clear—clears the Auto-Enroll from the Alarm Message Box and the Event List.•Admit—opens the Admit Information window for that transmitter so that you can assign the transmitter to a patient. •Close—closes the Admit Information window without clearing the Auto-Enroll.To permanently silence an Auto-Enroll1.    From the Client computer(s), click anywhere in the Auto-Enroll Alarm Message Box to access the Event Information window.2.    Click the Silence button. When an alarm is permanently silenced, a silence icon appears in the Alarm Message box for that alarm. Admit CompletedThis alarm occurs when the Admit function for a patient is completed. This dialog box only appears if the software has been configured to confirm the Admit.The Confirm Admit is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).
Series 7.0 Software (0510-1086-B) - User Guide  115Event TypesPre-Enroll ExpiredThis alarm occurs when the amount of time allowed for a Pre-Enroll transmitter to be banded has expired and the Pre-Enroll has not completed properly.To respond to a Discharge Expired Alarm1.    If the transmitter has not yet been banded, click anywhere in the Pre-Enroll Expired Alarm Message Box to access the Event Information window. 2.    Select Clear. 3.    Perform the Pre-Enroll function again.Discharge ExpiredThis alarm occurs when the amount of time allowed for an alarming band transmitter to be removed has expired and the discharge has not been completed properly.To respond to a Discharge Expired Alarm1.    If the transmitter has not yet been removed, click anywhere in the Discharge Expired Alarm Message Box to access the Event Information window. 2.    Select one of the following event causes: •Patient Delayed—the patient is delayed and requires more time for the discharge.•Attendant Delayed—the attendant was delayed in discharging the patient.•Test—the system was being tested. •Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. If the patient is not being discharged, the patient’s information is still in the database and the software continues to assist staff in monitoring the patient.3.    Perform the Discharge function again.Discharge CompletedThis alarm occurs when the Discharge for a patient is completed. This dialog box only appears if the software has been configured to confirm the discharge.The Confirm Discharge is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).
Chapter 4: Handling Events116 Series 7.0 Software (0510-1086-B) - User GuideEscort to ExpireThis alarm occurs when the time allowed for a patient to be escorted will expire in the configured time. The alarming band transmitter, in the Escort mode, has not been moved from or has not yet been returned to the protected area.To respond to an Escort to Expire1.    Determine the location of the patient.2.    If the patient is secure and will not be returned to the protected area soon, clear the Escort to Expire alarm and reset the duration time for the Escort. 3.    If the patient has not yet been moved, clear the Escort to Expire alarm and cancel the escort. Escort ExpiredThis alarm occurs when the selected amount of time required for a patient to be escorted has expired and the transmitter, in the Escort mode, has not been moved from or has not yet been returned to the protected area.To respond to an Escort Expired Alarm1.    Determine the location of the patient.2.    From the Client computer, click anywhere in the Escort Expired Alarm Message Box to access the Event Information window.3.    Select one of the following event causes:•Patient Delayed—the patient was delayed and the Escort may need more time.•Failed to start—the Escort was never started.•Escort Completed—the patient was successfully escorted.•Test—the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event.4.    If the patient has not yet been moved, perform the Escort function again.5.    If the patient has been escorted and is being returned to the monitored area: a.    Bring the patient back through the door; a Door Alarm will occur.b.    Follow the procedures for handling a Door Alarm (refer to “Door Alarm” on page 98).c.    Select Escort problem for the cause of the Door Alarm.Escort CompletedThis alarm occurs when the Escort for a patient is completed. This dialog box only appears if the software has been configured to confirm the escort. The Confirm Escort is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).
Series 7.0 Software (0510-1086-B) - User Guide  117Event TypesTransfer to ExpireThis alarm occurs when the time allowed for a patient to be transferred will expire in the configured time (if the allotted time was configured for greater than 15-minutes) and the alarming band transmitter, in the Transfer mode, has not been moved from one protected area to another.To respond to a Transfer to Expire1.    Determine the location of the patient.2.    If the patient is secure and will not be transferred to a protected area soon, clear the Transfer to Expire alarm and reset the duration time for the Transfer. 3.    If the patient has not yet been moved, clear the Transfer to Expire alarm and cancel the Transfer. Transfer ExpiredThis alarm occurs when the selected amount of time required for a patient to be transferred has expired and the alarming band transmitter, in the Transfer mode, has not reached its destination.To respond to a Transfer Expired Alarm1.    Determine the location of the patient.2.    From the Client computer, click anywhere in the Transfer Expired Alarm Message Box to access the Event Information window.3.    Select one of the following event causes: •Patient Delayed—the patient was delayed and needs more time for the transfer.•Failed to Start—the Transfer was never started; or the patient was never transferred.•Transfer Completed—the patient was successfully transferred to the destination.•Test—the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event.4.    If the patient has not yet been transferred, perform the Transfer function again.5.    If the patient has left the initial unit but has not arrived at the transfer unit: a.    Bring the patient through the door of the unit to which they are being transferred; a Door Alarm may occur.b.    Follow the procedures for handling a Door Alarm (refer to “Door Alarm” on page 98).c.    Select Transfer problem for the cause of the Door Alarm.d.    If No Signal alarms occur, contact an Administrative user to manually transfer the transmitter to the new unit.Transfer CompletedThis alarm occurs when a Transfer for a patient is completed. This dialog box only appears if the software has been configured to confirm the transfer.The Confirm Transfer is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).
Chapter 4: Handling Events118 Series 7.0 Software (0510-1086-B) - User GuideBegin AdjustThis alarm occurs after a configured amount of time to remind staff to check the alarming band transmitter for band slippage. The time for the Require band slippage check is configured in the Configuration, Units menu (refer to the Series 7.0 Software Administrator Guide).To respond to an Adjust Alarm 1.    Determine that the patient is secure.2.    Click anywhere in the Begin Adjust Alarm Message Box to access the Event Information window.3.    Click Clear.4.    If necessary, perform the Adjust function.Adjust ExpiredThis alarm occurs when the selected amount of time required for the adjustment of the banding material has expired and the adjustment has not been completed properly.To respond to an Adjust Expired Alarm 1.    Determine that the patient is secure.2.    If the banding material has not yet been adjusted, click anywhere in the Adjust Expired Alarm Message Box to access the Event Information window.3.    Click Clear.4.    Perform the Adjust function again.Adjust CompetedThis alarm occurs when the Adjust function for a patient is completed. This dialog box only appears if the software has been configured to confirm the Adjust.The Confirm Adjust is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).Scheduled EventThis alarm occurs when the scheduled time for an event (activity) is at hand. The event can be scheduled as a one time only event or it can be scheduled to run daily, weekly or monthly.To respond to a Scheduled Event1.    Proceed to the Client computer to view the reason for the scheduled event. 2.    Click anywhere in the Scheduled Event Alarm Message Box to access the Event Information window.3.    Click Clear.4.    If necessary, perform the Scheduled Event.
Series 7.0 Software (0510-1086-B) - User Guide  119Event TypesBlue AlarmsThe following sections provide detailed information about Blue Alarms, responding to alarming events, and the way the events should be cleared. Blue Alarms are high priority asset alarms. They are displayed in the Event List sequentially as they occur. Blue Alarms are displayed below White Alarms.Door AlarmWhen an asset banded with an alarming band transmitter is in an Exit Alarm Zone and the monitored door is open an alarm sounds at the Exit Alarm Controller, a message is displayed on the Client computer(s) in the unit configured to monitor the transmitter, and the location of the Exit Alarm Zone is indicated by a flashing icon on the map on the Client computer(s).To respond to a Blue Door Alarm1.    Go to the alarming device and use your card reader access card (if applicable) or enter the appropriate 4-digit security code to clear the alarm at the device. For more information about the Security Code, contact your System Administrator. 2.    If the Enforce Joint Commission reporting feature is activated, you must select an Event Cause once the alarming device has been reset. When you reset the alarming device, the Blue Alarm changes to a Light Blue Alarm in the Alarm Message Box. If the Enforce Joint Commission reporting feature is not activated, the Alarm Message Box clears once the alarm is cleared at the device.3.    From the Client computer, click anywhere in the Door Alarm Message Box to access the Event Information window.4.    Select one of the following causes for the Door Alarm:•Clear—no reason specified.•Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Chapter 4: Handling Events120 Series 7.0 Software (0510-1086-B) - User GuideCut Band AlarmWhen an asset transmitter is tampered with (cut band, improperly removed), an alarm is sounded on every Client computer configured to monitor the unit, a message is displayed in the Event List, and the location of the Alarming Band Receiver that detected the event is indicated on the map on the Client computer(s). If your facility has enabled the Lockdown on Cut Band Alarms feature and the transmitter is configured as a “High Risk” asset transmitter, a Cut Band Alarm will trigger a Global Lockdown. You can configure the Global Lockdown feature to lock doors at All exits or By transmitter units. However, if a Cut Band Alarm is initiated during an Escort or a Transfer, the systems automatically locks All exits and displays the alarm on all Client computers and Quick Look displays.To respond to a Blue Cut Band Alarm1.    Verify transmitter is applied correctly and without signs of damage or tampering.2.    From the Client computer, click anywhere in the Cut Band Alarm Message Box to access the Event Information window.3.    Select one of the following event causes: •Clear—no reason specified.•Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.NOTE: When an asset transmitter is configured as HIGH priority, a Cut Band Alarm will trigger a Global Lockdown. An asset transmitter configured as LOW priority will not trigger a Global Lockdown during a Cut Band.NOTE: Any perimeter alarms that occur due to a door open during a Cut Band Alarm require that the Cut Band Alarm be cleared at the computer first, before the doors are reset or cleared.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Series 7.0 Software (0510-1086-B) - User Guide  121Event TypesNo Signal Alarm The specified asset transmitter has not sent a signal to the system within the required time.To respond to a Blue No Signal Alarm1.    Verify transmitter is fastened correctly and without signs of damage or tampering.2.    From the Client computer, click anywhere in the No Signal Alarm Message Box to access the Event Information window.3.    Select one of the following event causes: •Test —the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. The event is cleared from the Event List of every Client computer configured to monitor the unit.4.    A No Signal alarm may be an indication that Receiver coverage may be inadequate. Contact your System Administrator.Light Blue AlarmsThe following sections provide detailed information about Light Blue Alarms, responding to alarming events, and the way the event should be cleared. Light Blue Alarms are low priority asset alarms. They are displayed in the Alarm Message Box and the Event List sequentially as they occur. Light Blue Alarms are displayed below Blue Alarms.Admit CompletedThis alarm occurs when the Admit function for an asset is completed. This dialog box only appears if the software has been configured to confirm the Admit. The Confirm Admit is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).WARNING: You must test all transmitters prior to use, and periodically thereafter, to verify proper operation. Failure to test the transmitters before use can result in system failure and/or asset abduction. In addition, failure to test transmitters voids the RF Technologies Product Warranty.NOTE: You can click Silence to stop the alarm sound at the Central Server or Client computer. The alarm is silenced at that computer only, for the configured length of time; however, the event still appears in the Event List. The next event automatically restarts the alarm sound.
Chapter 4: Handling Events122 Series 7.0 Software (0510-1086-B) - User GuideDischarge ExpiredThis alarm occurs when the amount of time allowed for an alarming band transmitter to be removed has expired and the discharge has not completed properly.To respond to a Discharge Expired Alarm1.    If the transmitter has not yet been removed, click anywhere in the Discharge Expired Alarm Message Box to access the Event Information window. 2.    Select one of the following event causes: •Test—the system was being tested. •Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event. If the asset is not being discharged, the asset’s information is still in the database and the software continues to assist staff in monitoring the asset.3.    Perform the Discharge function again.Discharge CompletedThis alarm occurs when the Discharge for an asset is completed. This dialog box only appears if the software has been configured to confirm the discharge. The Confirm Discharge is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).Escort to ExpireThis alarm occurs when the time allowed for an asset to be escorted will expire in 15-minutes (if the allotted time was configured for greater than 15-minutes). This will occur when the alarming band transmitter, in the Escort mode, has not been moved from or has not yet been returned to the protected area.To respond to an Escort to Expire1.    Determine the location of the asset.2.    If the asset is secure and will not be returned to the protected area soon, clear the Escort to Expire alarm and reset the duration of the Escort function. 3.    If the asset has not yet been moved, clear the Escort to Expire alarm and cancel the escort.
Series 7.0 Software (0510-1086-B) - User Guide  123Event TypesEscort ExpiredThis alarm occurs when the selected amount of time required for an asset to be escorted has expired and the transmitter, in the Escort mode, has not been moved from or has not yet been returned to the protected area.To respond to an Escort Expired Alarm1.    Determine the location of the asset.2.    From the Client computer, click anywhere in the Escort Expired Alarm Message Box to access the Event Information window.3.    Select one of the following event causes:•Test—the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event.4.    If the asset has not yet been moved, perform the Escort function again.5.    If the asset has been escorted and is being returned to the monitored area: a.    Bring the patient back through the door; a Door Alarm will occur.b.    Follow the procedures for handling a Door Alarm (refer to “Door Alarm” on page 98).c.    Select Escort problem for the cause. of the Door Alarm.Escort CompletedThis alarm occurs when the Escort for an asset is completed. This dialog box only appears if the software has been configured to confirm the escort. The Confirm Escort is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).Transfer to ExpireThis alarm occurs when the time allowed for an asset to be transferred will expire in 15-minutes (if the allotted time was configured for greater than 15-minutes) and the alarming band transmitter, in the Transfer mode, has not been moved from one protected area to another.To respond to a Transfer to Expire1.    Determine the location of the asset.2.    If the asset is secure and will not be transferred to a protected area soon, clear the Transfer to Expire alarm and reset the duration of the Transfer function. 3.    If the asset has not yet been moved, clear the Transfer to Expire alarm and cancel the Transfer.
Chapter 4: Handling Events124 Series 7.0 Software (0510-1086-B) - User GuideTransfer ExpiredThis alarm occurs when the selected amount of time required for an asset to be transferred has expired and the alarming band transmitter, in the Transfer mode, has not reached its destination.To respond to a Transfer Expired Alarm1.    Determine the location of the asset.2.    From the Client computer, click anywhere in the Transfer Expired Alarm Message Box to access the Event Information window.3.    Select one of the following event causes: •Test—the system was being tested.•Other—opens a Clear Reason window, user must enter the cause in this window.You cannot clear an event until you select the appropriate cause for the event.4.    If the asset has not yet been transferred, perform the Transfer function again.5.    If the asset has left the initial unit but has not arrived at the transfer unit: a.    Bring the asset through the door of the unit to which it is being transferred; a Door Alarm may occur.b.    Follow the procedures for handling a Door Alarm (refer to “Door Alarm” on page 119).c.    Select Transfer problem for the cause of the Door Alarm.d.    If No Signal alarms occur, contact an Administrative user to manually transfer the transmitter to the new unit.Transfer CompletedThis alarm occurs when a Transfer for an asset is completed. This dialog box only appears if the software has been configured to confirm the transfer. The Confirm Transfer is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).Adjust ExpiredThis alarm occurs when the selected amount of time required for the adjustment of the banding material has expired and the adjustment has not been completed properly.To respond to an Adjust Expired Alarm 1.    Determine that the asset is secure.2.    If the banding material has not yet been adjusted, click anywhere in the Adjust Expired Alarm Message Box to access the Event Information window.3.    Click Clear.4.    Perform the Adjust function again.
Series 7.0 Software (0510-1086-B) - User Guide  125Event TypesAdjust CompletedThis alarm occurs when the Adjust function for an asset is completed. This dialog box only appears if the software has been configured to confirm the Adjust. The Confirm Adjust is configured in the Configuration, Global Settings menu (refer to the Series 7.0 Software Administrator Guide).Scheduled EventThis alarm occurs when the scheduled time for an event (activity) is at hand. The event can be scheduled as a one time only event or it can be scheduled to run daily, weekly or monthly.To respond to a Scheduled Event1.    Proceed to the Client computer to view the reason for the scheduled event and, if required, perform the Scheduled Event. 2.    Click anywhere in the Scheduled Event Alarm Message Box to access the Event Information window.3.    Click Clear.
Chapter 4: Handling Events126 Series 7.0 Software (0510-1086-B) - User GuideThis page intentionally left blank.
Series 7.0 Software (0510-1086-B) - User Guide 127Chapter 5Using System ReportsIntroductionThis chapter provides detailed information about viewing and printing System Reports. In addition, it provides detailed information about using and filtering reports. Following is a list of the types of reports that are available in the software.ReportsThere are several Reports that enable you to view information about the activities of the system throughout the day, week, or month. The Reports List is divided in sections. The sections depend on how your system is configured. The following section provides detailed information about viewing, printing, saving, using, and filtering Reports.FIGURE 5.1:    Example of a Reports List Window
Chapter 5: Using System Reports128 Series 7.0 Software (0510-1086-B) - User GuideTo view a report1.    Click Reports on the toolbar.The Report List window appears.2.    In the Report List window, use the up and down arrows to select the report you want to run.3.    Click Report or double click on the selected report in the Report List.The Report window appears with the report you requested. FIGURE 5.2:    Report WindowNOTE: The Reports List configuration will depend on your software application. The available reports will depend on your licenses.
Series 7.0 Software (0510-1086-B) - User Guide  129IntroductionReport ButtonsThe Report buttons allow you to save a report, print a report, page through a report, and adjust the view of the report. You can also select to Filter the report and Close the report window.SaveA report can be saved directly to the Client computer(s). To save a report, click on the save button located in the upper left corner of the toolbar. Type in a File Name and select a File of Type from the drop-down list. It is recommended that you do not select HTML or XLS as the file type due to anomalies that may occur in the saved report. Reports saved in XLS may require additional formatting to view all text and align columns.PrintA report can be printed directly from the generated report’s window. To print a report, click on the print icon located in the upper left corner of the toolbar. The printer must be connected and configured to the Client computer as a default printer.FilterBy clicking the Filter button on the toolbar, you can select the criteria to run a specific report. Using the Filter window, you can select which unit, which patient or asset, and what time frame you want to view (24 hours, 7 days, or 30 days). Once you select your criteria, click OK.FIGURE 5.3:    Report Filter Window
Chapter 5: Using System Reports130 Series 7.0 Software (0510-1086-B) - User GuideCloseUse this button to close the reports window.Arrow ButtonsUse this button to page up to the previous page.Use this button to scroll up to the previous entry on the page.Use this button to scroll down to the next entry on the page.Use this button to page down to the next page.Sort By HeadingsMany of the reports allow you to sort information by column heading. Click on the column heading to sort by that specific heading. Click on the column heading a second time to reverse the sort order. Reports can be saved or printed in the sorted format.
Series 7.0 Software (0510-1086-B) - User Guide  131IntroductionAdditional Joint Commission Report ButtonsAdditional Report Buttons are found on selective Joint Commission Reports in the software. Following is an explanation of these buttons.First PageUse this button to view the first page of a multiple page report. Last PageUse this button to view the last page of a multiple page report. Next PageUse this button to view the next page of the report. Previous PageUse this button to view the previous page of the report. Actual SizeUse this button to adjust the view of the report to its actual size.Fit PageUse this button to fit the report to the size of the display screen.Fit WidthUse this button to fit the report to the width of the display screen.Zoom InUse this button to maximize the view of the report by zooming in.Zoom OutUse this button to minimize the view of the report by zooming out.Zoom RatioThe zoom ratio corresponds to the size in which the report is currently being viewed. You can also select to minimize or maximize a view by selecting the percent you which to adjust the view in the Zoom Ratio drop-down list.
Chapter 5: Using System Reports132 Series 7.0 Software (0510-1086-B) - User GuideSystem ReportsThe reports generated by the software have the same basic format. The header portion of the report identifies the name of report. It also includes:. Unit—the units included in the report.Time Range—the range selected for the report. Patient —the patients or assets included in the report.Facility Name—the name of the facility.Facility Address—the address of the facility.The bottom portion of the report varies depending on the report. Following are details on each individual report listed in the Report List.Daily Alarms and Activities (Tracer Level 2)Alarm ReportThe Alarm Report lists all of the Red (high priority) alarms that occurred in the system within a specified period of time. The Alarm Report includes: Name—the name of the patient or asset to whom the transmitter is assigned. Activity—the description of the alarm’s activity. Time—the time of the alarm.Transmitter ID—the identification number of the transmitter.Transmitter Type—the type of transmitterLocation—the device that received the event.Risk—the risk level assigned to the patient or asset.By clicking the Filter button on the bottom of the Alarm report you can also select the criteria to run a specific Alarm Report.
Series 7.0 Software (0510-1086-B) - User Guide  133System ReportsAlarm Activities ReportThe Alarm Activities Report lists all of the alarms that occurred in the system within a specified period of time. The Alarm Activities Report includes:Time—the time the alarm occurred.Name—the name of the patient or asset to whom the transmitter is assigned. Type—the type of event recorded.Activity—the description of the alarm’s activity.Transmitter ID—the identification number of the transmitter.Transmitter Type—the type of transmitter that sent the signal.Location—the device that received the event.User—the staff member who cleared the event (when applicable).Clear—the event reason used to clear the alarm (when applicable).By clicking the Filter button on the bottom of the report, you can also select the criteria to run a specific Alarm Activities Report.Alarm Response ReportThe Alarm Response Report enables you to gauge how your staff responds to system events. The Alarm Response Report includes:Name—the name of the patient or asset to whom the transmitter is assigned. Transmitter ID—the identification number of the transmitter. Location—the device, unit, and/or room that received the alarm.Activity—the description of the event’s activity.Event Time—when the event occurred.Clear Time—when the event was cleared.Response Time—the amount of time it took for the staff to respond to and clear the alarm at the device.Clear Reason—the event reason used to clear the alarm (when applicable).By clicking the Filter button on the bottom of the report, you can also select the criteria to run a specific Alarm Response Report.
Chapter 5: Using System Reports134 Series 7.0 Software (0510-1086-B) - User GuideCare Time Report (Code Alert only)The Care Time Report enables you to gauge how your staff responds to system events. The Care Time Report includes:Name—the name of the patient or asset to whom the transmitter is assigned. Care Time—the difference between the time the device was reset and the alarm was actually cleared at the computer. Reset Time—when the device was reset.Clear Time—when the event was cleared at the computer.Location—the device, unit, and/or room that received the alarm.Activity—the description of the event’s activity.Clear Reason—the event reason used to clear the alarm (when applicable).User—the staff member who responded to the event.By clicking the Filter button on the bottom of the report, you can also select the criteria to run a specific Care Time Report.Activities ReportThe Activities Report lists all of the activities or events that have occurred in the system with respect to each patient or asset. The Activities Report includes:Name—the name of the patient or asset to whom the transmitter is assigned. Activity—the description of the event’s activity.Type—the type of event recorded.Time—the time of the event.Transmitter ID—the identification number of the transmitter.Transmitter Type—the type of transmitter.Location—the device, unit and/or room that received the event.User—the staff member who authorized or cleared the event (when applicable).Risk—the risk level assigned to the patient or asset.By clicking the Filter button on the bottom of the report, you can also select the criteria to run a specific Activities Report.NOTE: This report is sorted alphabetically by patient or asset and then by event time.
Series 7.0 Software (0510-1086-B) - User Guide  135System ReportsAll Activities ReportThe All Activities Report lists all of the activities or events that have occurred in the system. The All Activities Report includes:Time—the time of the event or activity.Name—the device, or the name of the patient or asset to whom the transmitter is assigned. Type—the type of event recorded.Activity—the description of the event’s activity.Transmitter ID—the identification number of the transmitter.Transmitter Type—the type of transmitter that sent the signal.Location—the device that received the event.User—the staff member who authorized the activity (when applicable).Clear—the event reason used to clear the alarm (when applicable).By clicking the Filter button on the bottom of the report you can select the criteria to run a specific All Activities Report.All Other Reasons ReportThe All Other Reasons Report provides a summary of all the “other” reasons used when clearing an alarm. “Other” are the reasons for alarm events that are manually entered by staff members when they clear alarms. These reasons are reflected on the Joint Commission report as well. The All Other Reasons Report includes:Time—the time of the event.Name—the name of the patient or asset to whom the transmitter is assigned or the auto-enrolled transmitter. Type—the type of event recorded.Activity—the description of the event.Transmitter ID—the identification number of the transmitter involved.Transmitter Type—the type of transmitter that sent the signal.Location—the device that received the event.User—the staff member who cleared the event (when applicable).Clear—the manually entered reason (“other” reasons) for the event.By clicking the Filter button on the bottom of the All Other Reasons Report, you can select the criteria to run a specific report.
Chapter 5: Using System Reports136 Series 7.0 Software (0510-1086-B) - User GuideFacility Trends (Tracer Level 3)Joint Commission reports are generated in three tiers, Trend, Trend Reason and Trend Reason Detail reports. Alarms that occur when Enforce Joint Commission is “off” only populates the Trend report. Once Enforce Joint Commission is activated, the Trend Reason and Trend Reason Detail reports will begin to populate. Since alarms may have been generated before Enforce Joint Commission was activated, the numbers between the Trend report and the Trend Reason and Trend Reason Detail reports may not match. Joint Commission Alarm Trend ReportThe Joint Commission Alarm Trend Report lists the different events that have occurred in the system in six-month segments and then provides a bar graph to track the events. By clicking the Print icon, you can print this report. FIGURE 5.4:    Joint Commission Alarm Trend ReportNOTE: If the Event cause is “Other,” go to the All Other Reasons Report and review the memo field for more information. You can also select the “Other” hyper-link from any Joint Commission Details Report.
Series 7.0 Software (0510-1086-B) - User Guide  137System ReportsJoint Commission Alarm Trend Reason ReportClick on the links at the bottom of the Joint Commission Alarm Trend Report to access the Joint Commission Alarm Trend Reason Report. This report provides detailed information about the Event Causes that were selected each time an Event was cleared.FIGURE 5.5:    Joint Commission Alarm Trend Reason ReportJoint Commission Alarm Trend Reasons Detail ReportClicking on the Event Cause link at the bottom of the Joint Commission Alarm Trend Reason Report opens the Reasons Detail Report that lists all events that went into the calculation of the Joint Commission Alarm Trend Report. The Reasons Detail Report includes:Date—the date and time the event occurred.Response Time—the amount of time it took for the staff to respond and clear the event.User—the staff member who responded to the event. Location—the unit or room to which the device is assigned.Transmitter—the identification number of the transmitter.Name—the name of the device or the patient or asset to whom the device is assigned.Event Cause
Chapter 5: Using System Reports138 Series 7.0 Software (0510-1086-B) - User GuideJoint Commission Assistance Trend ReportThe Joint Commission Assistance Trend Report supports events generated by Emergency Assistance, Pull Cord, Pendant, Fall Monitoring, and Incontinence devices. This report lists the different events for these devices that have occurred in the system in six-month segments and then provides a bar graph to track the events. By clicking the Print icon, you can print this report.FIGURE 5.6:    Joint Commission Assistance Trend ReportNOTE: If the Event cause is “Other,” go to the All Other Reasons Report and review the memo field for more information. You can also select the “Other” hyper-link from any Joint Commission Details Report.
Series 7.0 Software (0510-1086-B) - User Guide  139System ReportsJoint Commission Assistance Trend Reason ReportClick on the links at the bottom of the Joint Commission Assistance Trend Report to access the Joint Commission Assistance Trends Reason Report. This report provides detailed information about the Event Causes that were selected each time an Event was cleared.FIGURE 5.7:    Joint Commission Assistance Trend Reason Report Joint Commission Assistance Trend Detail ReportClicking on the Event Cause link at the bottom of the Reason Report opens a Reason Detail Report that lists all events that went into the calculation of the Joint Commission Assistance Trend Report. The Reasons Detail Report includes:Date—the date and time the event occurred.Response Time—the amount of time it took for the staff to respond and clear the event.User—the staff member who responded to the event. Location—the unit or room to which the device is assigned.Transmitter ID—the identification number of the transmitter.Name—the name of the device or the patient or asset to whom the device is assigned.Event Cause
Chapter 5: Using System Reports140 Series 7.0 Software (0510-1086-B) - User GuideResponse Time Trend ReportThe Response Time Trend Report lists the response time for specific events that have occurred in the system in six-month segments and then provides a bar graph to track the response time (in seconds) for those events.FIGURE 5.8:    Response Time Trend ReportNOTE: If the Event cause is “Other,” go to the All Other Reasons Report and review the memo field for more information. You can also select the “Other” hyper-link from any Joint Commission Details Report.
Series 7.0 Software (0510-1086-B) - User Guide  141System ReportsResponse Time Trend Reason ReportClick on the links at the bottom of the Response Time Trend Report to access the Response Time Trend Reason Report. This report provides detailed information about the Event Cause that was selected each time an Event was cleared. FIGURE 5.9:    Response Time Trend Reason ReportResponse Time Trend Reasons Detail ReportClicking on the Event Cause link at the bottom of the Reasons Report opens the Reasons Detail Report that lists all events that went into the calculation of the Response Time Report. The Reasons Detail Report includes:Date—the date and time the event occurred.Response Time—the amount of time it took for the staff to respond and clear the event.User—the staff member who responded to the event. Location—the unit or room to which the device is assigned.Transmitter ID—the identification number of the transmitter.Name—the name of the device or the patient or asset to whom the device is assigned.Event Cause
Chapter 5: Using System Reports142 Series 7.0 Software (0510-1086-B) - User GuideStaff Reports (Tracer Level 4)Users ReportThe User Report lists all of the staff members who are current users of the system. The User Report includes:User—the name of the staff member.Login—the login name of the staff member.Assigned Functions— all functions assigned to the user.Door Card Access— if the user has door card access.By clicking the Filter button on the bottom of the Users Report, you can filter the report by assigned function as well as build a report showing users that have not been active in the system for the last 30 days or maximum of 60 days (the previous month plus the preceding number of days in the current month. FIGURE 5.10:    User Report Filter window
Series 7.0 Software (0510-1086-B) - User Guide  143System ReportsUser Training ReportThe User Training Report tracks the use of the on-line user help feature by staff members with login. The User Training Report includes:Event Time—the time the user help file was opened.User—the staff member who opened the user help file.Topic—the topic or subject matter of the user help file.Staff Care Time Report (Code Alert only)The Staff Care Time Report enables you to gauge how your staff responds to system events. The Staff Care Time Report includes:User—the staff member who responded to the event.Care Time—the difference between the time the event occurred and the time it was cleared at the computer. Care Started—the time the event occurred.Care Completed—when the event was cleared at the computer.Location—the device, unit, and/or room that received the alarm.Activity—the description of the event’s activity.Clear Reason—the event reason used to clear the alarm (when applicable).Name—the name of the patient or asset to whom the transmitter is assigned. By clicking the Filter button on the bottom of the report, you can also select the criteria to run a specific Staff Care Time Report.
Chapter 5: Using System Reports144 Series 7.0 Software (0510-1086-B) - User GuideStaff Drill ReportThe Staff Drill Report lists the drills performed by the staff members. The Staff Drill Report includes:Time—the time of the staff drill.Comments—the comments about the drill function performed.User—the staff member who authorized and performed the drill.Training ReportThe Training Report identifies the training delivered to the patient upon admission. The Training Report includes:Name—the name of the patient. Time—the date the delivery of training was entered into the system.Handout Training—the date any handout was delivered to the patient.Video Training—the date any video was shown to the patient.Verbal—the time any verbal training was delivered to the patient.User—the staff member who entered dates into the system.Location—the unit to which the patient is assigned.By clicking the Filter button on the bottom of the report, you can also select the criteria to run a specific Staff Training Report.
Series 7.0 Software (0510-1086-B) - User Guide  145System ReportsFacility Maintenance (Tracer level 5)System Maintenance ReportThe System Maintenance Report lists the maintenance functions performed on the system. The System Maintenance Report includes:Time—the time the maintenance was performed.Comments—the comments about the maintenance function performed.User—the service personnel who authorized and performed the maintenance.Low Batteries ReportThe Low Batteries Report provides a list of the transmitters and devices that currently have transmitted low battery signals. The Low Batteries Report includes:Name—the name of the device or the patient or asset to whom the transmitter is assigned. Time—the time the low battery was recognized by the system.Transmitter ID—the identification number of the transmitter.Unit—the unit of the device or the patient or asset to whom the transmitter is assigned.Device—the type of device reading the transmitter signal.Room—the room of the device or the patient or asset to whom the transmitter is assigned.Device Fault ReportThe Device Fault Report provides detailed information about issues that occurred with system devices. This Device Fault Report includes:Time—the time the activity was reported.Type—the type of event recorded.Comport—the comport to which the device is assigned.Physical Address—the network address of the device within the comport.Location—the unit and room to which the device is assigned.Last Checkin—the last time the device checked into the system.Activity—the description of the event’s activity,.By clicking the Filter button on the bottom of the Device Fault Report, you can select the criteria to run a specific report.
Chapter 5: Using System Reports146 Series 7.0 Software (0510-1086-B) - User GuideAdditional ReportsCensus ReportThe Census Report lists all of the patients, in the unit you are monitoring, that are currently admitted in the system. This report is sorted alphabetically by unit and then by patient. The Census Report includes:Name—the name of the patient. Gender—the sex of the patient.Unit—the unit to which the patient is assigned.Room—the patient’s room number. Transmitter ID—the identification number of the alarming band or Wander Management transmitter assigned to the patient.Admitted By—the staff member who performed the admission.Risk—the risk level assigned to the patient.Auto Enrolled History ReportThe Auto Enrolled History Report lists the alarming band transmitters that were auto-enrolled. This report is a history report; therefore, not all transmitters listed may be actively monitored by the system at the time of the report. The report includes:Enroll Time—the time when the transmitter was auto enrolled. Location—the alarming band receiver (ABR) that picked up the auto-enroll and the unit the device is assigned to.Type—the type of event recorded.Transmitter ID—the identification number of the transmitter.By clicking the Filter button on the bottom of the Auto-Enrolled History Report, you can also select the criteria to run a specific report.
Series 7.0 Software (0510-1086-B) - User Guide  147System ReportsAdjusted Bands ReportThe Adjusted Bands Report enables you to see which alarming band transmitter bands were adjusted. The Adjust Bands Report includes:Name—the name of the patient or asset to whom the transmitter is assigned.Activity—the description of the band adjustment’s activity.Type—the type of event recorded.Time—the time of the event.Transmitter ID—the identification number of the transmitter.Location—the device that received the event.User—the staff member who authorized the adjustment (when applicable).Risk—the risk level assigned to the patient or asset.By clicking the Filter button on the bottom of the Adjusted Bands Report, you can also select the criteria to run a specific report.Transfer ReportThe Transfer Report lists all of the patients or assets who were transferred from one protected area to another protected area. The Transfers Report includes:Name—the name of the patient or asset.Activity—the description of the transfer’s activity.Type—the type of event recorded.Time—the time of the eventTransmitter ID—the identification number of the transmitter (when applicable).Location—the device that received the event.User—the staff member who authorized the transfer (when applicable).Risk—the risk level assigned to the patient or asset.By clicking the Filter button on the bottom of the Transfer Report, you can select the criteria to run a specific report.
Chapter 5: Using System Reports148 Series 7.0 Software (0510-1086-B) - User GuideEscort ReportThe Escort Report lists all of the patients or assets who were escorted from a protected area and back to the same protected area. The Escort Report includes:Name—the name of the patient or asset to whom the transmitter is assigned. Activity—the description of the escort’s activity.Type—the type of event recorded.Time—the time of the event.Transmitter ID—the identification number of the transmitter.Location—the device that received the event.User—the staff member who authorized the escort (when applicable).Risk—the risk level assigned to the patient or asset.By clicking the Filter button on the bottom of the Escort Report, you can select the criteria to run a specific report. Discharge ReportThe Discharge Report lists all of the patients or assets that were discharged from the system within a specified period of time. The Discharge Report includes:Name—the name of the patient or asset. Activity—the description of the discharge’s activity.Type—the type of event recorded.Time—the time of the event.Transmitter ID—the identification number of the transmitter (when applicable).Location—the device that received the event.User—the staff member who authorized the discharge (when applicable.)Risk—the risk level assigned to the patient or asset.By clicking the Filter button on the bottom of the Discharge Report, you can select the criteria to run a specific report.
Series 7.0 Software (0510-1086-B) - User Guide  149System ReportsDevice Hardware ReportThe Device Hardware Report lists all of the devices in the system. The report includes:Description—the name of the device.Type—the type of device.Comport—the comport to which the device is assigned.Physical Address—the network address of the device within the comport.Location—the unit to which the device belongsH/w Version—the device hardware version.S/w Version—the device software version.Linger—the linger time assigned to the EAC.Device Tree Report (Code Alert only)The Device Tree Report keeps a running history of 9600 Series devices that are enrolled in the system, even if the device becomes disconnected from the system. The report includes:Description—the name of the device.Type—the type of device.Comport—the comport to which the device is associated.Path—the path that the device follows through the network to communicate with the Gateway.Short Address—the address assigned by the Gateway and Routers on the network. Different networks may use the same addresses.MAC—the Media Access Control address of the device.Location—the unit to which the device is assigned during configuration.NOTE: If the device belongs to more than one unit, only the first unit (alphabetically) is displayed.NOTE: Device associations are not cleared from the Device Tree until the device reassociates with the network or the Server is rebooted.
Chapter 5: Using System Reports150 Series 7.0 Software (0510-1086-B) - User GuideTransmitter ReportThe Transmitter Report provides general details about transmitters admitted to the system. The Transmitter Report includes: Transmitter —the identification number of the transmitter.Transmitter Type—the type of transmitter.Name—the name of the patient or asset. Location—the unit to which the device belongs.Links ReportThe Links Report provides general details about mothers and infants admitted to the system and currently linked. The Link Report includes: Link Transmitter ID—the ID number of the mother transmitter. Transmitter ID—the identification number of the infant transmitter linked to the mother transmitter.Name—the name of the infant. Unit Name—the unit to which the infant transmitter is associated.Link Time—the time at which the infant was linked.Links Activities ReportThe Links Activities Report is a history report of all activities related to mother and infant transmitters that were linked in the system. This report includes any activity that triggered an event for the linked transmitters. The Links Activities Report includes: Name—the name of the infant or mother. Transmitter—the identification number of the infant transmitter involved.Activity—the description of the event.Time—the time of the event.Mother Transmitter—the identification number of the mother transmitter involved.Location—the device that received the event.User—the staff member who cleared the event (when applicable).By clicking the Filter button on the bottom of the Link Activities Report, you can select the criteria to run a specific report.
Series 7.0 Software (0510-1086-B) - User Guide  151Patient ReportsSensatec ReportThe Sensatec Report enables you to gauge how your staff responds to Sensatec events. The Sensatec Report includes:Name—the name of the patient to whom the control unit is assigned. User—the staff member who responded to the event.Location—the device, unit, and/or room that received the alarm.Activity—the description of the event’s activity.Event Time—when the event occurred.Clear Time—when the event was cleared.Care Time—the amount of time it took for the staff to respond and clear the white alarm.Clear Reason—the event reason used to clear the alarm (when applicable).By clicking the Filter button on the bottom of the report, you can also select the criteria to run a specific Sensatec Report.Patient ReportsPatient reports are specific to the individual patient. They are accessed from the Main tab of the patient’s Admit Information window. The patient reports are as follows:Review Info ReportThe Review Info Report identifies admit information that was entered for the patient. The Review Info Report includes the patient’s picture, if entered, and demographic information for the patient and the patient’s contacts. It also includes the patient’s allergies, medication information, medical history information and any special instructions that were entered.Review Activity ReportThe patient’s Review Activity Report lists all of the activities or events that have occurred in the system with respect to the patient. The Review Activities Report includes:Time—the time of the event.Activity—the description of the event’s activity.Type—the type of event recorded.Reason—the event reason used to clear the alarm (when applicable).User—the name of the patient to whom the transmitter is assigned. Location—the device, unit and/or room that received the event.Transmitter Type—the type of transmitter.Transmitter ID—the identification number of the transmitter.
Chapter 5: Using System Reports152 Series 7.0 Software (0510-1086-B) - User GuideReview Response ReportThe Review Response Report lists the response time for specific events that have occurred for the patient in six-month segments and then provides a bar graph to track the number of events. The blue mark indicates the events for the patient, the red mark indicate the average events for the facility.FIGURE 5.11:    Review Response Report
Series 7.0 Software (0510-1086-B) - User Guide  153Patient ReportsReview Response ReasonBy clicking on an event link at the bottom of the report, you can access the Response Reason Report. This report provides detailed information about the Event Cause that was selected each time an Event was cleared for the patient and then provides a bar graph to track the response time (in seconds) for those events. The blue mark indicates the response time for the patient, the red mark indicate the average response time for the facility. FIGURE 5.12:    Review Response Reason Reports
Chapter 5: Using System Reports154 Series 7.0 Software (0510-1086-B) - User GuideReview Response Reason Detail ReportClicking on the Event Cause link at the bottom of the Reasons Report opens a Reason Detail Report that lists all events that went into the calculation of the Review Response Report. The Detail Report includes:Date—the date and time the event occurred.Response Time—the amount of time it took for the staff to respond and clear the event.User—the staff member who responded to the event. Transmitter ID—the identification number of the transmitter.Name—the name of the device or the patient to whom the device is assigned.Asset ReportsAsset reports are specific to the individual asset. The Asset Transmitter Report is accessed from the Assetsselection on the Menu bar of the Main window. The Asset Activities Report is accessed from the Main tab of the Asset Admit Information window.Asset Transmitter ReportThe Asset Transmitter Report lists all the assets that are currently admitted in the system. The Asset Transmitter Report includes:Make—the assets manufacturer’s information.Model—the model/description of the asset.SN—the serial number of the asset. Transmitter ID—the identification number of the transmitter assigned to the asset.Location—the unit or room to which the asset is assigned.Asset Activities ReportThe Asset Activity Report lists all of the activities or events that have occurred in the system with respect to the asset. The Asset Activities Report includes:Time—the time of each event.Activity—the description of the event’s activity.Type—the type of event recorded.Transmitter ID—the identification number of the transmitter.Location—the device, unit and/or room that received the event.User—the staff member who authorized or cleared the event (when applicable).Reason—the event reason used to clear the alarm (when applicable).

Navigation menu