Microlife WatchBP Office BASIC+, BP3AJ1-7A Instruction Manual

Page 1
Ofce blood pressure measurement device with Ab detection
Instruction Manual
EN
1
Page 2
1
Page 3
2
Product description
Name of parts ................................................................. 3
Display ............................................................................ 4
Components and accessories ......................................... 5
Before using WatchBP Ofce
Selecting and tting the correct cuff .............................. 6
Activating the Device ..................................................7–8
Connect the cuff to the device ........................................ 9
Fitting the cuff properly .............................................9–10
Three operation modes
«SINGLE» Mode ............................................................ 11
«CYCLING» Mode .......................................................... 12
«AUSCULTATION» Mode ................................................ 12
Viewing the stored values
Viewing the stored values ............................................ 13
Special Functions
Mean arterial pressure ................................................. 13
Atrial brillation detection ...................................... 14-16
Skipping the countdown time ...................................... 17
Taking fewer than three measurements ..................... 17
Appendix
Rechargeable battery and power adaptor ................... 18
Error messages ....................................................... 19–20
Safety, care, accuracy test and disposal ................. 21–22
Technical specications ................................................ 23
Guarantee card ............................................................. 24
Table of Contents
Page 4
3
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
Display
Time/Test
Start/Stop
Auscultation button
MAP
M Button (Memory)
Mode switch Single/Cycling (3, Ab)
DC 7.5V 2.0A
USB Port
Main Adapter
Cuff Socket
Product description
Name of parts
Page 5
4
Display
Single Mode
Cycling MOde
Auscultation Mode
Ination indicator
(for Auscult. Mode)
External Power
PC Link Indicator
Battery Symbol
Interval Time
Month/Date Time
Systolic Value
Diastolic Value
Memory Number of Stored Data Pulse Mean Arterial Pressure
Pulse Rate
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5
Product and components
Blood Pressure Device X 1
AC Adaptor X 1
(Input100 - 240V~ 50/60Hz 0.48A; Output+7.5V 2A)
Cuff for upper arm
M size (22cm~32cm) X 1 L size (32cm~42cm) X 1
Instruction Manual X 1 Quick Start Guide X 1
SYS
mmHg
DIA
mmHg
PUL
/min
Auscult.
O/I Interval
Alarm/Limit
Time/Test
SYS
mmHg
DIA
mmHg
PUL
/min
Auscult.
Alarm/Limit
How to take blood pressure measurement in three different modes
Quick start guide
Flip over the quick start guide to see ‘Product description’.
Printed 2011 June
1
Plug cuff connector in the cuff socket
Switch the mode
«Single» Mode
«Cycling» Mode
«AUSCULTATION» Mode Press Auscult.
button to begin a measurement
Note blood pressure using auscultatory method
Place the stethoscope on the hollow of the elbow, over the brachial artery
Press Start/Stop button to start a measurement
Result will be displayed after the measurement
2
3
Press to start
Single
Cycling
2
SYS
mmHg
DIA
mmHg
PUL
/min
Auscult.
Single Cycling
O/I Interval
Alarm/Limit
Time/Test
M
SYS
mmHg
DIA
mmHg
PUL
/min
Auscult.
O/I Interval
Alarm/Limit
Time/Test
SYS
mmHg
DIA
mmHg
PUL
/min
Auscult.
Alarm/Limit
Auscult.
Press Start/Stop button to start cycling measurements
Ofce blood pressure measurement device with Ab detection
Instruction Manual
EN
1
USB Cable
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
Page 7
6
Before using the device
Selecting the correct cuff
Two different cuff sizes are provided with the device: 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)
Page 8
7
Activating the Device
Open the cover of the battery compartment then plug in
the rechargeable battery socket.
Use the device for the rst time
1) Set the year – When the power is on, the Year number ashes in the display. Press the M Button to select the Year. Press the Time/Test Button to conrm. The Month number ashes after.
ABRIR
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
MAP
Start/Stop
Time/Test
M
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Start/Stop
Time/Test
BASIC
+
2) Set the month – Use the M Button to select the
Month. Press the Time/Test Button to conrm. The Day number ashes after.
3) Set the day – Press the M Button to select the Day.
Press the Time/Test Button to conrm. The Hour number ashes after.
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
MAP
Start/Stop
Time/Test
M
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Start/Stop
Time/Test
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
MAP
Start/Stop
Time/Test
M
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Start/Stop
Time/Test
BASIC
+
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8
Select the correct cuff
Two different cuff sizes are provided with the device: Medium and Large. Use the cuff marker to select the cuff size that best matches the circumference of the patient’s upper arm.
*
please use only Microlife cuffs!
4) Set the time – Press the M Button to select the time
then press the Time/Test Button to conrm. The set time is displayed on the screen.
5) If you want to change the year, date and time, just press the Time/Test Button then repeat the process as instructed above.
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Start/Stop
Time/Test
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Start/Stop
Time/Test
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Start/Stop
Time/Test
BASIC
+
M (Medium size)
22 - 32 cm (8.7 - 12.6 inches)
L (Large size)
32-42 cm (12.6 - 16.5 inches)
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9
Connect the cuff to the device
Connect the cuff to the device by inserting the cuff connector into the cuff connector socket.
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) Put the cuff around 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)
Before using the device (cont.)
Page 11
10
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”.
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SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
«Single » «Cycling»
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Start/Stop
BASIC
+
Three operation modes: Single, Cycling or Auscultation mode
Select an operation mode
There are three measuring modes can be used. Slide the switch to seletct Single mode (standard single measurement) or Cycling mode (automatic triple measurements).
Press and hold «Auscult.» button to start auscultation measurement.
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
«Single »
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
BASIC
+
«Single» Mode (standard single measurement)
Select «Single» Mode then press «Start/Stop» button to perform single blood pressure measurement. The measurement reading is displayed and saved after the measurement.
*
Press «Start/Stop» Button to terminate the measurement
when inating or deating.
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12
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Start/Stop
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Start/Stop
BASIC
+
60 sec.
1 2
60 sec.
3
60 sec.
«AUSCULTATION» Mode
«AUSCULTATION» Mode is used for blood pressure measurement of patients to conrm if a patient is suitable for the oscillometric method.
Press and hold «Auscult.» button to start pumping. Release the button when it reaches the needed pressure. Press and hold the «Auscult.» button to repump during deaing; press «Start/Stop» button to release pressure during deating. There is no measurement readings displayed in this mode. The user has to use with a stethoscope to determine the blood pressure.
«Cycling»
DIA
mmHg
PUL /min
Auscult.
MAP
Start/Stop
Time/Test
BASIC
+
*
The device will automatically return to ‘Single’ or ‘Cycling’
mode if there is no operation for one minute after the auscultation operation.
«Cycling» Mode (automatic triple measurements)
Select «Cycling» Mode then press «Start/Stop» button to perform automatic triple blood pressure measurement with 60 seconds intervals. The average reading measurement readings is displayed and saved after the measurements.
*
User can set measurement intervals at 15 or 60 seconds in
Cycling Mode. Press «Start/Stop» Button for 3 seconds then press «Auscult.» Button to select 15 or 60. Press «Start/Stop»
Button to conrm the selection.
Page 14
13
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
BASIC
+
Viewing the stored values
The device stores only the blood pressure values of the last measurement procedure in Single mode and Cycling mode. Press the M Button in Single mode or Cycling mode to review the stored readings.
In Cycling mode, the average is displayed rst. Press M Button repeatly to review the indevidual readings of the 3 measurements in Cycling mode.
«Single »
«Cycling»
Viewing the stored values
Special Functions
MAP (Mean Arterial Pressure)
The device measures the true mean arterial pressured (MAP) of the patient. Each measurement includes a single MAP value. The average measurement will display the average MAP value. Press the "MAP" button to view the MAP when the measurements is displayed or when viewing the memory.
*
The Mean Arterial Pressure MAP in this device is
determined from the maximum peak of the oscillometric envelope curve.
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
MAP
Start/Stop
Time/Test
BASIC
+
Page 15
14
Appearance of the atrial brillation indicator for early detection
The device is designed to detect asymptomatic atrial brillation during blood pressure measurements in the «CYCLING» Mode. If two out of three measurements detect atrial brillation, the Ab icon is displayed. This device is able to detect atrial brillation with high
sensitivity of 97% and specicity of 89%.* If the
atrial brillation icon is displayed after the measurement,
it is recommended to visit a doctor.
*
Joseph Wiesel, Lorenzo Fitzig, Yehuda Herschman and Frank
C. Messineo. Detection of Atrial Fibrillation Using a Modied
Microlife Blood Pressure Monitor. American Journal of Hypertension 2009; 22, 8, 848–852. doi:10.1038/ajh.2009.98
*
This device detects atrial brillation, a major cause of stroke.
Not all risk factors for stroke, including atrial utter, may be
detected by this device.
*
This device may not detect atrial brillation in people with
pacemakers or debrillators. People with pacemakers or debrillators should not use this device to detect atrial brillation.
Page 16
15
Special Function (cont.)
About Atrial Fibrillation
Atrial brillation is a common heart rhythm problem. It affects more than 2 million people in North America. It is more common in older age and it is found in 10% of people over 80 years old. It is a common cause of major strokes. About 15% of all strokes are caused by atrial brillation.
The elderly or those with high blood pressure, diabetes or heart disease are more likely to get a stroke if they have atrial brillation.
Atrial brillation is a rhythm problem that can last from a few minutes, to days, weeks or even years. Atrial brillation can cause blood clots in the upper chambers of the heart (the atria). These clots can break off and ow to the brain causing a stroke.
The use of blood thinners, such as warfarin, can lower the risk of stroke in patients with atrial brillation.
A doctor can conrm the presence of Ab by using an ECG. Sometimes Ab is present incidentally. Therefore, a doctor may not see it on regularly scheduled visits.
One method of detecting Ab is by mean of palpations. This method is not very reliable. Failure of detecting Ab may in the end lead to the occurrence of a stroke; whereas early detection may lead to early treatment that can signicantly reduce the chances of a stroke.
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16
Atrial Fibrillation Detector
The device can screen for atrial brillation during blood pressure measurement.
Some people may have atrial brillation occasionally that lasts longer than a day. In this situation the device allows frequent screening on multiple days for optimal diagnosis of atrial brillation.
Sometimes the device might falsely detect atrial brillation which can have two causes:
1) The arm has moved during blood pressure measurement. For this reason it is of essential importance that the arm is kept still during the measurement.
2) Some other arrhythmia (irregular heart beat) than atrial brillation might be present.
For people with pacemakers or debrillators it is not recommended to use the device for detecting Atrial Fibrillation.
Information for the doctor
This device is designed to detect atrial brillation and false negative readings are very rare. Though it is programmed to specically detect atrial brillation, frequent premature beats, marked sinus arrhythmia or other rhythm abnormalities might cause false positive readings. If atrial brillation is detected by the device, we suggest to perform another measurement in the doctor’s ofce. If the atrial brillation icon is not displayed then the previous abnormal readings may have been due to transient atrial brillation. If the atrial brillation icon is displayed then EKG performance is suggested for determining the exact rhythm abnormality.
Page 18
17
Taking fewer than Three measurements
In «CYCLING» Mode , the measurement sequence can be stopped at anytime by pushing the «Start/Stop» button. The device enters stand-by and remaining measurements are cancelled. Data from the measured blood pressure can be viewed by pushing the M Button.
Skipping the countdown time
The 15 seconds countdown before measurement in
«CYCLING» Mode can be skipped by pressing the «Start/ Stop» button. The device will immediately begin the next
measurement.
*
The device goes into stand-by by pressing the «Start/Stop»
button after the measurements completed. The device will automatically switch to stand-by if left unattended for one minutes.
Cancel remaining measurements at anytime during the measurement sequence.
Skip the countdown time and begin measurement.
Stand by mode
Special Function (cont.)
SYS
mmHg
DIA
mmHg
PUL /min
Start/Stop
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Start/Stop
BASIC
+
SYS
mmHg
DIA
mmHg
PUL /min
Start/Stop
BASIC
+
Page 19
18
Rechargeable Battery
The device features a built-in, rechargeable Ni-MH battery pack that delivers up to
400~500 measurement cycles.
The battery can be recharged between use with the power adaptor provided. Battery charging indicator is displayed when the rechargeabe battery is being charged. Empty battery indicator is displayed when battery is weak.
Rechargeable battery and power adaptor
DC 7.5V 2.0A
DC 7.5V 2.0A
Using a power adaptor
Please only use the Microlife adaptor supplied with the device to recharge the device.
1) Plug the adapter cable into the Power Plug of the
device.
2) Plug the adaptor plug into the wall socket. When the power adaptor is connected, no battery power is consumed.
*
Battery is weak.
*
Battery is being
charged.
Page 20
19
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
The pulse signals on the cuff are too weak. Re-position the cuff and repeat the measurement.
«Err 2» Error signal During the measurement,
error signals were
detected by the cuff, caused for instance by movement or muscle tension. Repeat the measurement, keeping your arm still.
Error messages
Page 21
20
«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.
«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.
Page 22
21
Protect the device from water and moisture
Protect the device from extreme heat and cold
Protect device from impact and drops
Protect the device from direct sunlight
Avoid proximity to electromagnetic elds, such as those produced by mobile phones
Never open device
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 liable for damage caused by incorrect
application.
Observe the storage and operating conditions described in the “Technical specications” section of this manual.
Ensure that children do not use the device
unsupervised; some parts are small enough to be
swallowed.
Only activate the pump when cuff 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.
Page 23
22
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
Device care
Clean the device with a soft, dry cloth.
Accuracy test
We recommend the device be tested for accuracy every 2 years or after mechanical impact (e.g. being dropped). Please contact Microlife to arrange for an accuracy test.
Do not iron the cuff!
Cleaning the cuff
Take out the bladder. Fold and place the cuff cover inside a washing bag. Wash cuff cover with warm water and a mild detergent in washing machine. Air dry the cuff. DO NOT iron the cuff cover
Disposal
Batteries and electronic instruments must be disposed of in accordance with the locally applicable regulations, and not as domestic
waste.
Page 24
23
Technical specications
Operation temperature:
10 to 40 °C (50 to 104 °F)
Storage temperature/ humidity:
-20 to 55 °C (-4 to 131 °F)
15 - 90 % relative maximum humidity
Weight:
625 g (including rechargeable battery
pack)
Dimensions:
110 x 177 x 175 mm
Measuring method:
Oscillometric, corresponding to
Korotkoff
Measurement range:
30 - 280 mmHg – blood pressure
40 - 200 beats per minute – pulse
Cuff pressure display:
Range: 0 - 299 mmHg
Resolution: 1 mmHg
Static accuracy: pressure within ± 3
mmHg
Pulse accuracy: ±5 % of the readout
value
Voltage source:
Rechargeable battery pack;
4.8V, 2400 mAh
Mains adapter DC 7.5V, 2 A
Reference to Standards:
• 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
Electromagnetic compatibility:
• 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.
Type BF applied part
Microlife reserves the right to alter technical speccations without prior written notice.
Page 25
24
SYS
mmHg
DIA
mmHg
PUL /min
Auscult.
Single Cycling
MAP
Start/Stop
Time/Test
M
(3, Afib)
BASIC
+
This device is covered by a two-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. Batteries and cuff
are not covered by this guarantee.
Product: WatchBP Ofce BASIC+
Product Number: BP3AJ1-7A
Date:
Name:
Address:
Date:
Telephone:
Email:
Guarantee card
Page 26
25
IB WatchBP Ofce BASIC+ BP3AJ1-7A EN 5116
Read the instruction manual carefully before using this device, especially the safety instructions, and keep the instruction manual for future use.
Europe / Middle-East / Africa
Microlife WatchBP 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 U.S.A.,Inc.
1617 Gulf To Bay Blvd Floor 2
Clearwater , Florida , 33755 , United States
Phone: 1- 727-4425353 Fax: 1-727-4425331 Email: msa@microlifeusa.com www.watchbp.com
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