Microlife WatchBP Office Target Navigation Manual

Ofce blood pressure measurement device with built-in Blood Pressure targets.
Instruction Manual
EN
1
WatchBP Ofce Target is designed with built-in blood pressure targets to provide
recommended guidelines of the European Society of Hypertension (ESH)1, American Heart
Association (AHA)2, American Diabetes Association (ADA)3 and World Health Organization
(WHO)4.
1
O’Brien E, Asmar R, Beilin L, Imai Y, et al. European Society of Hypertension recommendations for conventional, ambulatory and home blood pressure
measurement. European Society of Hypertension Working Group on Blood Pressure Monitoring. J Hypertens 2005;23:697-701.
2
Pickering TG, Hall JE, Appel LJ, et al. Recommendations for Blood Pressure Measurement in Humans and Experimental Animals:
Part 1: Blood Pressure Measurement in Humans: A Statement for Professionals From the Subcommittee of Professional and Public Education of the American
Heart Association Council on High Blood Pressure Research. Hypertension 2005;45;142-161.
3
American Diabetes Association. Standards of Medical Care in Diabetes–2006. Diabetes Care, 2006;29; Supplement 1.
4
World Health Organization, International Society of Hypertension Writing Group. 2003 World Health Organization (WHO) / International Society of
Hypertension (ISH) Statement on Management of Hypertension. J Hypertens 2003,21:1983-1992.
Table of Contents
Product description
Name of parts and display ................................. 3–4
Components and accessories...... ...........................5
Before using WatchBP Ofce Target
Activating the device ............................................. 6
Selecting and tting the correct cuff .................. 6–8
Selection of operation modes
«Single» or «Triple» Mode («Double» Mode as
option) .................................................................10
Press «140/90» or «130/80» ..............................10
Trafc light indications
Green light ........................................................... 11
Red light ............................................................... 11
Viewing and deleting of measurements
Viewing the stored values ................................... 12
Pulse pressure (PP) .............................................. 12
Deleting the stored values ...................................13
Replacing slot-in instruction card ......................... 13
Appendix
Battery and power adaptor ........................... 14–15
Error messages ............................................... 16–18
Safety, care, accuracy test and disposal ......... 19–20
Technical specications ....................................... 21
EN
Product description
Name of parts
Display
Instruction
M Button (Memory)
Start/Stop Button
SYS.
mmHg
DIA.
mmHg
PUL.
/min
3
Main Adaptor
Cuff Socket
Battery Compartment
3
SYS.
mmHg
DIA.
mmHg
PUL.
/min
3
1
Mode Switch
3
Display
Target 1 < 140/90
Difference to Target setting
Heart Beat
Interval Time
Battery Symbol
Memory
Triple Mode
Target 2 < 130/80
Systolic Value
Diastolic Value
Pulse Pressure (PP)
Pulse Rate
4
EN
WatchBP Ofce Target and components
3
SYS.
DIA.
PUL.
mmHg
mmHg
/min
WatchBP Ofce Target Blood Pressure Device X 1
M size (22cm~32cm) X 1 L size (32cm~42cm) X 1
AC Adaptor X 1 Input: 100-240V~50/60Hz 0.7A
Output: +6V 0.6A
Instruction Manual X 1 Quick Start Guide X 1
5
Before using WatchBP Ofce Target
Two ways of activating the Device
1) Pull out the protective strip projecting from the battery compartment.
2) Plug the adapter cable into the main adapter socket in the blood pressure monitor; then Plug the adapter plug into the wall socket.
Selecting the correct cuff
Two different cuff sizes are provided with the WatchBP Ofce Target: Medium and Large. Use the cuff marker to select the cuff size that best matches the circumference of the patient’s upper arm.
M (Medium size)
22 - 32 cm (8.7 - 12.6 inches)
L (Large size)
32-42 cm (12.6 - 16.5 inches)
6
EN
Before using WatchBP Ofce Target (cont.)
Connect the cuff to the device
Connect the cuff to the device by inserting the cuff connector into the cuff connector socket.
7
Fitting the cuff properly
1) Place the cuff over the left (right) upper arm so that the air tube and artery mark arrow point towards the lower arm.
2) Lay the cuff on the arm. Make sure that the lower edge of the cuff lies approximately 2 to 3cm ( ¾ to 1 inch) above the elbow.
2-3 cm
(3/4 to 1 inch)
3) Wrap and tighten the cuff around the arm.
4) Leave a little free space between the arm of the patient and the cuff. It must be possible to t 2 ngers between the arm and the cuff. Clothing must not restrict the arm. Remove all clothing covering or constricting the arm to be measured.
5) It may result in incorrect blood pressure readings if the cuff does not t properly. Use a different size cuff if the range index at the end of the cuff does not fall into the range specied by the range stripes.
6) Apply the same steps to the other arm if a measurement of the other arm is required.
When the cuff is wrapped
*
around the arm, the edge of the cuff should be in the range which is marked “OK”.
8
EN
SYS.
mmHg
1
3
Selecting the operation mode: Standard or Triple mode
Select an operation mode
There are two measuring modes to be selected,
Standard mode (standard single measurement) or Triple mode (automatic triple measurements).
To select Standard mode, slide the switch on the right side of the device downwards to position «1».
To select Triple mode , slide this switch upwards to position «3».
SYS.
mmHg
DIA.
mmHg
PUL.
/min
3
1
9
Automated triple measurements
In «3» Mode, the WatchBP Ofce Target device automatically takes three consecutive measurements at default 15 second intervals. Because blood pressure constantly uctuates, a result determined in this way is more reliable than one produced by a single measurement.
1 2
15 sec.
15 seconds of interval is adequate according to «Blood
*
Pressure Monitoring, 2001, 6:145-147» for oscillometric instruments).
15 sec.
3
3 measurements are averaged
3
SYS.
DIA.
PUL.
mmHg
mmHg
/min
On the bottom of the right hand section of the display shows a number to indicate which of the consecutive measurement is currently being taken. The readings of these consecutive measurements are averaged to produce the routine visit blood pressure measurement.
Press «140/90» or «130/80» button
Press the button ON/OFF «140/90» or ON/OFF «130/80», to select the preferred target value. The device will then start to inate.
Do not remove the cuff between the measurements. If one of the individual measurements is
questionable, an extra measurement will be taken automatically.
.Press either the ON/OFF «140/90» or ON/OFF «130/80
*
any time if you want to quit the measurement.
10
EN
Trafc Light Indication in the display
Green light
If both the measured systolic and diastolic blood pressure values are below the set target values (140/90 or 130/80), the screen will light in green with two «OK» signs.
Additionally, the lowest column in the screen shows the pulse pressure «PP»
11
Red light
If either the measured systolic or diastolic result is above the set target value (140/90 or 130/80), the screen will light in red with the difference to the desired value shown in display as number, e.g. «+24, +22».
Viewing the stored values
3
SYS.
DIA.
PUL.
mmHg
mmHg
/min
The device stores only the blood pressure values of the last measurement procedure. To view the stored values, press the M-button when the instrument is switched off. The display rst shows «A» and then the values.
5 seconds later, the display will change and show the systolic/diastolic difference with the set target values (140/90 or 130/80), together with the pulse pressure .
PP (Pulse Pressure)
The WatchBP Ofce Target device provides the pulse pressure (PP) of the patient: pulse pressure = systolic
- diastolic pressure. Each measurement includes the calculation of a single PP value. The average measurement will display the average PP value. When viewing in Memory mode, the PP value will be displayed with the systolic/diastolic pressure once every 5 seconds.
12
EN
Clearing all values
SYS.
DIA.
PUL.
mmHg
mmHg
/min
SYS.
DIA.
PUL.
mmHg
mmHg
/min
If you are sure that you want to permanently remove all stored values, hold down the M-button (the instrument must have been switched off beforehand) until «CL» appears and then release the button. To permanently clear the memory, press the M-button while «CL» is ashing. Single values cannot be cleared.
Press and hold
13
Replacing the inserted Instruction Card
You can replace the inserted instruction card by pulling it out to the side and replacing the paper. Extra cards are supplied with the instrument for this purpose.
SYS.
mmHg
DIA.
mmHg
PUL.
3
/min
Battery and power adaptor
Battery Indicator and Battery change Low battery
When the batteries are approximately ¾ empty the battery symbol will ash as soon as the instrument is switched on (partly lled battery displayed). Although the instrument will continue to measure reliably, the batteries need to be replaced soon.
Flat battery – replacement
When the batteries are at, the battery symbol will ash as soon as the instrument is switched on (at battery displayed). You cannot take any further measurements and must replace the batteries.
1) Open the battery compartment at the back of the instrument by pushing inwards at the two arrows and pulling out the battery compartment cover.
2) Replace the batteries – ensure correct polarity as shown by the symbols in the compartment.
Use 4 new, long-life 1.5V, size AA batteries.
*
Do not use batteries beyond their date of expiry.
*
Remove batteries if the instrument is not going to
*
be used for a prolonged period.
14
EN
Using a mains adaptor
Please use only the Microlife adaptor (DC 6V, 600mA) supplied with the WatchBP Ofce Target to operate the device.
1) Plug the adapter cable into the Power Plug of the WatchBP Ofce Target device.
2) Plug the adaptor plug into the wall socket. When the power adaptor is connected, no battery power is consumed.
15
Error messages
If an error occurs during measurement, the measurement is interrupted and an error message «Err» is displayed.
Please contact your local
Microlife service center if the error persists.
If you think the results
are unusual, please read through the information in this instruction manual carefully.
Error Description Potential cause and
remedy
«Err 1» Signal too
weak
«Err 2» Error signal During the
The pulse signals on the cuff are too weak. Re-position the cuff and repeat the measurement.
measurement, error signals were detected by the cuff, caused for instance by movement or muscle tension. Repeat the measurement, keeping your arm still.
16
EN
Error Description Potential cause and
remedy
«Err 3» No pressure
in the cuff
An adequate pressure cannot be generated in the cuff. A leak may have occurred. Replace the batteries if necessary. Repeat the measurement.
«Err 5» Abnormal
result
The measuring signals are inaccurate and no result can therefore be displayed. Read through the checklist for performing reliable measurements and then repeat the measurement.
17
Error Description Potential cause and
remedy
«Err 6 Triple Mode There were too many
errors during the measurement in Triple mode, making it impossible to obtain a nal reliable result. Read through the checklist for performing reliable measurements and then repeat the measurement.
Error Description Potential cause and
remedy
«HI» Pulse or cuff
pressure too high
The pressure in the cuff is too high (over 300 mmHg) OR the pulse is too high (over 200 beats per minute). Relax for 5 minutes and repeat the measurement.
«LO» Pulse too
low
The pulse is too low (less than 40 beats per minute). Repeat the measurement.
18
EN
Safety, care, accuracy test and disposal
Safety and protection
This device may be used only for the purpose described in this booklet. The device comprises of sensitive components and must be treated with caution. The manufacturer cannot be held responsible for damage caused by incorrect application.
Observe the storage and operating conditions described in the “Technical specications” section of this manual.
Protect the device from water and moisture
Ensure that children do not use the device
unsupervised; some parts are small enough to be swallowed.
Only activate the pump when the cuff tube is
installed.
Do not use the device if you think it is damaged or
if anything appears unusual.
Read the further safety instructions in the
individual sections of the instruction manual.
Do not connect the device to a computer
until prompted to do so by the computer software.
19
Protect the device from direct sunlight
Protect the device from extreme heat and cold
Avoid proximity to electromagnetic elds, such as those produced by mobile phones
Never open device
Protect device from impact and drops
Device care
Clean the device with a soft, dry cloth.
SYS.
mmHg
DIA.
mmHg
PUL.
/min
3
1
Cleaning the cuff
DO NOT wash the cuff. DO NOT iron the cuff cover.
Do not wash the cuff!
Do not iron the cuff!
Accuracy test
An accuracy test is recommended every 2 years or after mechanical impact (e.g. being dropped). Please contact Microlife to arrange for an accuracy test.
Disposal
Batteries and electronic instruments must be disposed of in accordance with the locally applicable regulations.
20
EN
Technical specications
Operation temperature/ humidity:
Storage temperature/ humidity:
Weight:
Dimensions:
Measuring method:
Measurement range:
Cuff pressure display:
Voltage source:
21
10 to 40 °C (50 to 104 °F)
-20 to 55 °C (-4 to 131 °F)
15 - 90 % relative maximum humidity
690 g (including batteries)
160 x 125 x 98 mm
Oscillometric, corresponding to
Korotkoff method: phase I systolic, phase V diastolic.
30 - 280 mmHg – blood pressure
40 - 200 beats per minute – pulse
Range: 0 - 299 mmHg
Resolution: 1 mmHg
Static accuracy: pressure within ± 3
mmHg or 2% of reading > 200mmHg
Pulse accuracy: ±5 % of the readout
value
4 X 1.5V Batteries; size AA
Mains adapter DC 6V, 1 A
Reference to Standards:
Electromagnetic compatibility:
Type BF applied
part
Serial number Manufacturer
• Device standard: Device corresponds to the
requirements of the standard for noninvasive blood pressure monitor.
EN 1060-1 EN 1060-3 EN 1060-4 IEC 60601-1 IEC 60601-1-2
• Device fullls the stipulations of the standard IEC 60601-1-2.
The stipulations of the EU Directive 93/42/ EEC for Medical Devices Class IIa have been fullled.
Reference number
Microlife reserves the right to alter technical speccations without prior written notice.
Guarantee card
This device is covered by a two-year
guarantee and accessories are cover by
a one-year guarantee from the date of
purchase. This guarantee is valid only
on presentation of the guarantee card
completed by the owner conrming date of
purchase or purchase receipt.
Product: WatchBP Ofce Target Product Number: BP 3MD1-4 Date:
Name:
Address:
Date:
Telephone:
Email:
Europe / Middle-East / Africa
Microlife AG Espenstrasse 139 9443 Widnau, Switzerland Tel +41 71 727 7000 Fax +41 71 727 7011 Email: watchbp@microlife.ch www.watchbp.com
Asia
Microlife Corporation 9F, 431, RuiGang Road, NeiHu Taipei, 114, Taiwan, R.O.C. Tel +886 2 8797 1288 Fax+886 2 8797 1283 Email: watchbp@microlife.com.tw www.watchbp.com
North / Central / South America
Microlife Medical Home Solutions, Inc. 2801 Youngeld St., Suite 241 Golden, CO 80401, USA Tel +1 303 274 2277 Fax +1 303 274 2244 Email: watchbp@mimhs.com www.watchbp.com
Read the instructions carefully before using this device.
IB WatchBP Ofce Target BP3MD1-4 031010
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