Dinamap Pro 100V2 Dokumentacja

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Strona 1 - Series 100-400V2

1DINAMAP® PROSeries 100-400V2MonitorOperation Manual

Strona 2 - PRO 400V2 Monitor

10Product ComplianceThe DINAMAP® PRO Monitor is classified in the following categories for compliance with IEC 601-1:• Class l, internally powered•Tra

Strona 3 - Operation Manual

100•Spray bottlesProcedure1. Prepare the enzymatic detergent according to the manufacturer’s instructions and the 10% bleach solution, in separate spr

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101Appendix Fare damaged, they must be disposed of as advised in Appendix F.Storage and Battery CareIf it becomes necessary to store the Monitor for a

Strona 5 - Contents

102• Repeated failure to fully charge the battery will result in a significant reduction in battery life.• The expected lifetime of the battery largel

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103Appendix FDisposal of Product Waste As you use the PRO Monitor, you will accumulate solid wastes that require proper disposal or recycling. These i

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105Appendix GHost Port Connector (rear panel)WARNING! Auxiliary equipment connected to the DINAMAP® PRO Monitor will result in the formation of an ele

Strona 11 - Artifact

2009802-001 BEuropean RepresentativeGE Medical Systems Information Technologies GmbHPostfach 60 02 65D-79032 Freiburg, GermanyTel. +49 761 45 43 - 0Fa

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11SymbolsThe following symbols are associated with the PRO Monitor. Note: The type of model determines which symbols appear on the Monitor. Attention,

Strona 13 - Getting Started

12Packaging label depicting the transportation and storage atmospheric pressure range of 500 to 1060 hPa.The DINAMAP® PRO Monitor is protected against

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13Getting StartedUnpacking the Monitor and AccessoriesBefore attempting to use the PRO Monitor, take a few minutes to become acquainted with the Monit

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14charging. If the battery is not inserted, the external power indicator LED will flash (short flash approx. every 4 sec). When the Monitor is running

Strona 16 - Rear Panel Connections

15Getting Startedin a medical/hospital grade attachment plug, provided with the following cord tag: “Hospital Grade Plug." Grounding integrity ca

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16Rear Panel Connections1 Battery compartment cover: Retains and protects internal battery.2 Mains input: Used to connect to AC power supply.3 Externa

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17Getting StartedFront Panel Controls and Indicators7 Systolic pressure display: 3-digit red LED indicates measured systolic BP in mmHg.8 Active temp

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1814 External power indicator: Green LED indicates external power status and battery charging status of monitor.15 Temperature probe connector: Temper

Strona 20 - Using the Printer

19Getting StartedSwitching the Monitor On and OffTo switch the DINAMAP PRO Monitor on, press and hold the power ON/OFF switch (16) for at least 10 sec

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2DINAMAP® PRO 400V2 Monitor

Strona 22 - Cautions

20appears dark on a light background, while the text of selected buttons appears light on a dark background.Note: Some menus have six option buttons.

Strona 23 - Using the Monitor

21Getting StartedAny time the paper is loaded, the printer automatically prints a test strip with the DINAMAP® PRO name on it. If no print is visible

Strona 24 - General Warnings

22StorageStore thermal paper in a cool, dry place. The printed strip (thermal paper recording) should not be• exposed to direct sunlight,• exposed to

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23Using the MonitorNoninvasive Blood Pressure DeterminationDescriptionThe BP parameter is included in Models 100V2, 200V2, 300V2, and 400V2. Blood pre

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24allowing SpO2 and predictive temperature determinations to be monitored and recorded (depending on Monitor model). In the Vitals (UK: All Obs) mode,

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25Using the Monitorexamine the cuff site and the limb distal to the cuff regularly for signs of impeded blood flow.• Do not apply external pressure ag

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26produce a peripheral pulse or the patient may have poor peripheral perfusion. Also, if a patient’s beat-to-beat pulse amplitude varies significantly

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27Using the MonitorProcedures1. Connect the end of the air hose which has quick-release clips to the cuff connector (30) on the front of the Monitor.

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285. Inspect cuff for damage. Replace cuff when aging, tearing, or weak closure is apparent. Do not inflate cuff when unwrapped.Precaution: Do not use

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29Using the MonitorManual ModeTo start a determination, press the START/STOP BP key (29). A normal, uninterrupted Manual cycle takes about 40 seconds.

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3DINAMAP® PRO MonitorOperation ManualThis manual is for DINAMAP® PRO Monitor Models 100V2, 200V2, 300V2, and 400V2, all with printers. • PRO 100V2: BP

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30When Auto mode is selected, a number at the right of the Auto button indicates the time interval between each reading. To change the time interval,

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31Using the Monitorinitial target pressure selection for neonates is 110 mmHg. Artifact rejection is relaxed in the Stat mode for adult/pediatric pati

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32Temperature is shown on the temperature display in degrees Celsius or Fahrenheit, and the unit of measure is indicated by the °C °F display (13). Th

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33Using the MonitorWhen a monitor mode measurement is in progress, it is terminated when the probe is inserted into the probe holster.Note: These temp

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34readings may occur unless IVAC® probe covers are used. • If a patient’s temperature is below 96.0 °F, the unit will automatically switch from the n

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35Using the Monitor7. Remove the probe. Discard the disposable cover by holding the probe as you would a syringe and pressing the button on the probe

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36Procedures for Monitor Mode Determinations (Axillary Determinations)1. Connect the temperature probe cable to the temperature probe connector. 2. Re

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37Using the Monitor• If the probe tip temperature is 92.0° F or higher (33.3° C) when taken out of the probe holster, the thermometer will not be able

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38Pulse rate derived from SpO2 appears in the Pulse Rate window, and the SpO2 pulse indicator flashes synchronization with the real-time pulse rate me

Strona 42 - Warnings

39Using the MonitorIf the Monitor is unable to detect a pulse for 10 seconds during normal SpO2 monitoring, the values in the LED flash, alternating p

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4other purposes or copying thereof is prohibited without prior written consent by GE Medical Systems Information Technologies, Tampa, Florida.Illustra

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40- there is excessive illumination from light sources such as surgical lamp, a bilirubin lamp, or sunlight- a blood pressure cuff is inflated on the

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41Using the Monitormeasurements. Always remove oximetry devices and attachments from the MRI environment before scanning a patient.• The use of cardio

Strona 46 - OxiMAX™ SpO

42• Use or patient-applied parts are latex-free.Procedures1. Select a sensor that is appropriate for the patient and the clinical situation.Warning: D

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43Using the Monitor• Observe the sensor site to assure adequate distal circulation. Sensor sites should be checked at least every 2 hours and rotated

Strona 48 - General Cautions

44use a disposable adhesive sensor that may tolerate more motion.• Replace the sensor.PROBLEM: The SpO2 value or the pulse rate changes rapidly; the p

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45Using the MonitorSOLUTION:• Check that calculations have been corrected appropriately for the relevant variable. In general, calculated saturation v

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46• If there is excessive light, cover the sensor with opaque material.PROBLEM: A sensor error indicating a bad sensor has occurred.CAUSE:• The sensor

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47Using the Monitorthat are derived from the SpO2 signal. A tone sounds at a rate corresponding to the SpO2 saturation level. The pitch is highest at

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48normal SpO2 reporting of values when several consecutive good pulse determinations are made.General Warnings• Do not use the SpO2 function during ma

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49Using the Monitor• Do not perform any testing or maintenance on a sensor while it is being used to monitor a patient.• Bright light sources (e.g., i

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5Introduction ...7About the DINAMAP® PRO Monitor ...

Strona 55 - Using the Menu System

50pulsation and inaccurate measurement of oxygen saturation.• Excessive pressure from the sensor may cause necrosis of the skin.• For additional warni

Strona 56 - Normal Mode Menu

51Using the Monitor3. Plug the SpO2 sensor into the SpO2 sensor extension cable. Then plug the SpO2 sensor extension cable into the SpO2 sensor connec

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52SOLUTION:Check the patient.• If possible, keep the patient still; check whether the sensor is applied securely and properly, and replace it if neces

Strona 58 - Main Menu

53Using the Monitor• If there is excessive light, cover the sensor with opaque material.• Circulation distal to the sensor site should be checked rout

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54• The sensor or cable may be defective, or the cabling may be improperly connected.SOLUTION:Check the patient.• If possible, keep the patient still;

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55Using the Menu SystemIntroductionThe PRO Monitor is equipped with a liquid crystal display (25) and a rotor (21). Used together, these allow the ope

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56Normal Mode Menu

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57Using the Menu SystemClinician Mode Menu

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58RotorRotating the rotor causes option buttons to be highlighted (light text on a dark background). Turning the rotor produces a click. Turning it cl

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59Using the Menu SystemVitals Button (UK: All Obs)Selection of this button initiates a BP determination while allowing SpO2 and predictive temperature

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6Appendix A...77Technical Specifications...

Strona 66 - More... Menu

60Note: If the SpO2 plethysmograph is displayed on the LCD, the waveform pauses for 2 minutes or until the Clear button is selected. SpO2 values are a

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61Using the Menu Systemoperating mode returns to the default setting of Manual. The default setting of Manual can be overridden to return to the previ

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62Alarms ButtonSelection of this button displays the Alarms menu. This menu is used to adjust the violation limits for BP, Pulse Rate, and SpO2. The v

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63Using the Menu SystemAutoSelection of this button updates the alarm limits relative to the current parameter values. Pressing this button cancels an

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64DisplaySelection of this button allows the operator to view the trend data. Note: If the trend data have been lost (e.g., if the clock settings have

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65Using the Menu SystemMain Selection of this button returns the user to the Main menu.Print ButtonSelection of this button displays the Print menu.Au

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66More... MenuThis menu is used to set the various operating modes of the Monitor.SpO2 Button (Models 300V2 and 400V2)Selection of this button display

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67Using the Menu SystemResponse Mode (Nellcor Only)Response mode allows the user to specify the averaging technique to optimize measurements in the pr

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68Pwr Sav (Sleep Mode)Selection of this button allows the operator to specify the time, in minutes, that elapses before the Monitor goes into “sleep”

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69Using the Menu SystemTimeSelection of this button allows the operator to change the internal time and date of the Monitor. The clock, which is maint

Strona 76 - Main menu

7About the DINAMAP® PRO MonitorDINAMAP® PRO Monitors provide noninvasive determination of systolic blood pressure, diastolic blood pressure, mean arte

Strona 77 - Appendix A

70Main Selection of this button returns the user to the Main menu.TempSelection of this button displays the temperature submenu, which allows the user

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71Using the Menu SystemSpO2 PlethWhen this option is checked and SpO2 data are available, the plethysmograph waveform and the pulse amplitude bar will

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72Clinician MenuPress. Selection of this button displays a panel for setting the default BP target inflation pressure. Adjusting the default target pr

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73Using the Menu SystemOK. Selection of this button returns the user to the Clinician menu.More... Selection of this button displays the More... menu

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74For monitors with Nellcor SpO2 technology, the SpO2 configuration menu includes Response Mode and SatSeconds™. Response Mode can be set to “1” or “

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75Using the Menu SystemSilence. Selection of this button will cause all alarms except the FAILSAFE alarm to be muted. A confirmation menu will appear

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76OK ButtonSelection of this button acknowledges the error. The Monitor clears the identified error and then returns the user to the Main menu.

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77Appendix ATechnical SpecificationsBPCuff Pressure Range 0 to 290 mmHg (adult)(Normal operating range) 0 to 140 mmHg (neonate)Default Target: Cuff In

Strona 85 - Appendix B

78TURBOTEMP TemperatureScale °Fahrenheit (F)°Celsius (C)RangePredictive mode Max: 41.1° C; 106.0° FMin: 33.6° C; 96.0° F Monitor mode Max: 41.1° C;

Strona 86 - Hierarchy of Alarms

79Appendix APulse RateWithout Motion 20 to 250 beats/min ±3 digits With Motion normal physiologic range 55 to 125 beats/min ±5 digits Low Perfusion 20

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8been reports of sensors causing patient burns when operating in an MRI environment.• Do not use the Monitor in the presence of flammable anesthetics.

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80Nellcor Patents4,621,643; 4,653,498; 4,700,708; 4,770,179; 4,802,486; 4,869,254; 4,928,692; 4,934,372; 5,078,136; 5,351,685; 5,421,329; 5,485,847; 5

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81Appendix Astandard deviation. Plus or minus one standard deviation encompasses 68% of the population.‡The Masimo SET® SpO2 parameter has been valida

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82Default Settings SpO2 (%) HIGH: 100 SpO2 (%) LOW: 90Sensitivity Mode 2 (for low perfusion-Default)Averaging Time 12 secondsFastSAT Mode 0 (for Off)M

Strona 91 - Appendix C

83Appendix Asupplied from a source conforming to IEC 601-1.AC input is protected by two internal fuses, replaceable by qualified service personnel onl

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84Compatibility Requirements and Tests and CISPR 11 (Group 1, Class A) for radiated and conducted emissions.IPX1The DINAMAP® PRO Monitor is protected

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85Appendix BAlarm CodesAll alarm indications are accompanied by an audible signal unless Alarm Silence is selected.A microprocessor system failure wil

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86Hierarchy of AlarmsAlarms in the DINAMAP® PRO Monitor are in three priority levels. They are:AlarmPriority LevelFailsafe 1Patient and system 2 (High

Strona 95 - Appendix D

87Appendix BProcedural and Error Alarm CodesAlarm CodeLED DisplayLCD DescriptionAudible Tone and VolumeEffect of Alarm Silence SwitchEffect of Clear v

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88Procedural and Error Alarm Codes (cont.)Alarm CodeLED DisplayLCD DescriptionAudible Tone and VolumeEffect of Alarm Silence SwitchEffect of Clear via

Strona 97 - Appendix E

89Appendix BProcedural and Error Alarm CodesAlarm CodeLED DisplayLCD DescriptionAudible Tone and VolumeEffect of Alarm Silence SwitchEffect of Clear v

Strona 98 - Service Manuals

9presence of equipment which does not conform to these specifications.• Place the PRO Monitor on a rigid, secure surface. Monitor must only be used wi

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91Appendix CPrinciples of Noninvasive Blood Pressure DeterminationThe oscillometric method of determining NIBP is accomplished by a sensitive transduc

Strona 101 - Appendix F

92Full NIBP Determination Sequence for AdultAt each step the microprocessor stores cuff pressure, the matched pulse amplitude, and the time between su

Strona 102 - Leak Testing

93Appendix CNIBP - Auto ModeSystolic SearchIf systolic pressure is not found, the NIBP parameter can search at cuff pressures higher than the initial

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94make an accelerated determination of blood pressure if it has been 16 minutes or less since the last determination.

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95Appendix DReorder CodesPROD PRODUCTCODE ECATDINAMAP PRO Monitor Operations Manual-English 2009802-001DINAMAP PRO Monitor Service Manual 2009829-001B

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97Appendix EWarranty, Service, and Spare PartsWarning: There are no user serviceable parts inside the DINAMAP® PRO Monitor. Refer all servicing to qua

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98RepairsIf your product requires warranty, extended warranty, or non-warranty repair service, call GE Medical Systems Information Technologies and a

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99Appendix FMaintenanceCleaning the MonitorThe Monitor and accessories are to be kept clean and used according to the instructions provided here and i

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