Little Doctor LD12 Instrukcja obsługi

Marka: Little Doctor

Model: LD12

Kategoria: Jednostki ciśnienia krwi

Typ: Instrukcja obsługi

Wrist Digital Blood Pressure Monitor

Instruction Manual

Ciśnieniomierz elektroniczny

automatyczny LD

do pomiaru ciśnienia tętniczego krwi i pulsu

Instrukcja Obsługi

LD12

ENGPOL

ENG

TABLE OF CONTENTS

PARTS AND COMPONENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3

GENERAL INFORMATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

RECOMMENDATIONS ON CORRECT MEASUREMENTS . . . . . . . . . . . . . . . . . 5

BATTERY INSTALLATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

SETTING OF DATE AND TIME . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

CORRECT POSITION DURING MEASUREMENT . . . . . . . . . . . . . . . . . . . . . . . . . 8

CUFF PREPARATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

MEASUREMENT PROCEDURE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

MEMORY FUNCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11

INFORMATION ABOUT ERRORS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12

CARE, STORAGE, REPAIR AND DISPOSAL . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12

TROUBLESHOOTING TIPS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13

WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14

TECHNICAL SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14

CERTIFICATION AND STATE REGISTRATION. . . . . . . . . . . . . . . . . . . . . . . . . . .16

INFORMATION IN POLISH . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17

ENG

PARTS AND COMPONENTS

1. Electronic Unit.

2. LCD.

3. (Power ON/OFF)

4. «М1» и «М2» (memory).

5. Arm cuﬀ CUFF-LDA.

6. Cover of the battery compartment.

7. Case.

8. Power elements.

9. Instruction Manual.

10. Warranty card.

ENG

GENERAL INFORMATION

This Instruction Manual is designed to assist the user with safe and eﬀ ective operation

of the automatic digital Device for measurement of blood pressure and heartbeat rate

LD, (modiﬁ cation LD12) (hereinafter – the “Device”). Use this Device according to the

rules described in this Manual. Operate the Device only as intended. Do not use the

Device for any other purposes. Read and understand the whole Instruction Manual, in

particular “Recommendations on Correct Measurement”.

INDICATIONS FOR USE

Use this Device to measure your systolic and diastolic blood pressure and

heartbeat rate in patients aged from 15. This Device is recommended for use by

persons with unstable blood pressure or known arterial hypertension at home

as an addition to medical surveillance. The cuﬀ is designed for the wrist with the

circumference approximately from 12,5 to 20,5 cm.

OPERATION PRINCIPLE

This Device uses the oscillometric method of blood pressure with Fuzzy Algorithm

and pulse rate measurement. Wrap the cuﬀ with an electronic unit around your

wrist. Press the button on the live monitor to automatically start inﬂ ating the

cuﬀ and then while gradually deﬂ ating the cuﬀ take its measurements. The sensi-

tive element of the Device feels the weak pressure oscillations in the cuﬀ generated

by widening and contraction of the brachial artery in response to every heartbeat.

Pumping in is ceased when cuﬀ is adequately pumped in to determine diastolic and

systolic pressure (the amplitude of the pressure waves is measured, converted into

millimeters Hg and shown on the display as ﬁ gures) after which air is released from

cuﬀ . The Device has Arrhythmia Indicator and 2 memories, by 90 cells, for storage of

measurement results with Average value of the last three measurements function.

Remember that the Device will not maintain the mentioned accuracy of a measure-

ment if it is used or stored at a temperature or humidity other than those speciﬁ ed

in Technical Speciﬁ cations of this Manual. We are warning about possibility of mis-

takes in blood pressure measurement with this Device in persons with pronounced

cardiac arrhythmia. Consult the doctor concerning blood pressure measurement

of your child.

APPLIED NEW LD TECHNOLOGIES

Fuzzy Algorithm – algorithm for processing the measurement values

with regard to peculiarities of the man’s heartbeat, thus, ensuring

high measurement accuracy

ENG

Scale WHO – classification of measurement results according to

recommendation of World Health Organization (WHO).

Indication of arrhythmia – special symbol «



» on Device display

informs about availability of irregular pulse; in this case

RECOMMENDATIONS ON CORRECT MEASUREMENTS

For correct measurement you should know that THE BLOOD PRESSURE IS

SUBJECT TO SHARP VARIATIONS EVEN WITHIN THE SHORT TIME INTERVALS. The

blood pressure depends on many factors. It is usually lower in summer and higher in

winter. The blood pressure varies together with the atmospheric pressure, depends

on physical loads, emotional excitement, stresses and dietary regime. Drugs, drink-

ing alcohol and smoking produce signiﬁ cant eﬀ ect. Even the very procedure of

blood pressure measurement in a polyclinic sends the blood pressure high in many

people, thus, the blood pressure measured at home often diﬀ ers from the values

received in a polyclinic. As the blood pressure tends to rise at low temperatures,

make measurements at an indoor temperature (approximately 20° C). If this Device

stayed under a low temperature, keep it for at least 1 hour at an indoor tempera-

ture before use, otherwise the measurement result may be incorrect. During a day

the diﬀ erence in readings for healthy people may be 30-50 mmHg of systolic pres-

sure and to 10 mmHg of diastolic pressure. The dependence of the blood pressure

on various factors is individual for each person. Accordingly, it is recommended

to keep a special book with blood pressure records. ONLY A CERTIFIED DOCTOR

USING YOUR RECORDS IS CAPABLE TO ANALYZE THE TENDENCY OF YOUR BLOOD

PRESSURE VARIATIONS.

High

Norm

Low

FIG.1

ENG

At cardiovascular and some other diseases requiring blood pressure moni-

toring make measurements in the hours fixed by your attending doctor.

REMEMBER THAT THE DIAGNOSTIC AND ANY TREATMENT OF HYPERTENSION

MAY BE CONDUCTED ONLY BY A CERTIFIED DOCTOR ON THE BASIS OF BLOOD

PRESSURE VALUES OBTAINED BY THIS DOCTOR. TAKING OF DRUGS AND THEIR

DOSES SHOULD BE PRESCRIBED ONLY BY YOUR ATTENDING DOCTOR.

At such disorders as deep vascular

sclerosis, weak pulse wave and also in

patients with the prominent distortions of

cardiac rhythm it may be diﬃ cult to measure

the blood pressure accurately.

IN SUCH CASES CONSULT A CERTIFIED

DOCTOR ABOUT APPLICATION OF THE

ELECTRONIC DEVICE.

4. KEEP QUIET DURING A MEASUREMENT

TO OBTAIN THE ACCURATE VALUES

OF YOUR BLOOD PRESSURE WITH THE

ELECTRONIC DEVICE. MEASURE YOUR

BLOOD PRESSURE IN THE CALM AND

COMFORTABLE CONDITIONS AT THE INDOOR TEMPERATURE. NO EATING

AN HOUR BEFORE MEASUREMENT; NO SMOKING, TAKING TONIC AGENTS,

ALCOHOL 1.52 HOURS BEFORE MEASUREMENT.

5. The accuracy of blood pressure measurement depends on whether the cuﬀ

matches the size of your arm. THE CUFF SHOULD NOT BE TOO SMALL OR TOO

LARGE.

Wait 3 minutes between measurements for the blood to restore its circulation.

However, the persons with prominent atherosclerosis due to considerable loss

of vascular elasticity may need to increase the wait time between measurements

(10-15 minutes). This also refers to the patients suﬀ ering for long from diabetes

For more accurate determination of blood pressure it is recommended to make a

series of 3 consecutive measurements and to use the average value

7. The rate of wrist blood pressure may be diﬀ erent from that of the arm. If to

regard a healthy person, this variation may be speciﬁ ed within the range of +/-10

mm Hg for both the systolic and diastolic pressure. The persons to have such health

problems, as hypertension, diabetes, liver function abnormality, peripheral blood

ﬂ ow etc. must be very careful. In this case, wrist and arm measurements may sub-

stantially vary.

FIG.2

ENG

BATTERY INSTALLATION

1) Open the cover of the battery compartment

and install 2 ААА size batteries according to

polarity marked inside the compartment.

Do not use much force to remove the cover

of the battery compartment.

2) Close the cover of the battery compartment

Replace all batteries when the Low Battery Indicator

“

”appears on the screen

or when there is no any indication on the screen. The Low Battery Indicator does

not show the discharge level.

SETTING OF DATE AND TIME

To shift to mode of date and time setting, it is necessary to press

. To shift

to mode of date and time setting, it is necessary to press . Parameter will

blink. Change of selected parameter toward increasing is taking place when

depressing button M2, towards decreasing – when depressing button M1.

To shift to setting of the next parameter, year/month/hours/min, it is necessary

to depress .

If no actions are done in mode of date and time setting for more than 1

minute, the Device is independently changed over to mode of date and time

indication.

If battery cells are replaced, date and time values will be reset. It is permitted

to measure pressure and take pulse readings without setting date and time

values.

To switch oﬀ mode of date and time setting, it is necessary to press and hold

for over 5 seconds or to do

no actions more than 3 minutes.

M1 M2

0/I

FIG.3

ENG

CORRECT POSITION DURING MEASUREMENT

Correct position during measurement

1. Sit on the chair.

2. Raise a hand so that your palm is up and place

your elbow on a table.

3. Put a case or folded towel under your forearm

and make sure that the cuﬀ is at the same level

as your heart.

When no table is available

1. Sit on the chair.

2. Bring the cuﬀ to the level of your heart slightly

pressing your left hand to a breast.

3. While measuring slightly rest your left hand on

the right one.

Measurement the blood pressure lying on the

back

1. Lie on your back.

2. Put a case or folded towel under your forearm

and make sure that the cuﬀ is at the same level

as your heart.

• Make 5-6 deep inhales and exhales before taking a measurement and relax.

• Measured results may slightly vary depending on your posture under

measurement. While measuring do not cross your legs.

• Take measurements on the same wrist and at the same posture.

• If the cuﬀ brought up to the level below/above your heart, measurement

results will be overrated/underrated respectively.

FIG.4

FIG.5

FIG.6

ENG

CUFF PREPARATION

While holding your left hand palm up, move the cuﬀ

to your wrist so that the monitor display faces your

palm. Should you fail to put the cuﬀ on your left-hand

wrist, wrap it around the right one and, thereafter,

the measurement results may slightly vary.

5~10mm

2 Place the cuﬀ on your hand so that its edge is

5-10 mm oﬀ your palm end. Align the monitor

on your wrist.

Fasten the cuﬀ on your wrist so that no free space

is left between the cuﬀ and wrist. The cuﬀ must

comfortably ﬁ t. While wrapping the cuﬀ around your

wrist make sure that no cloth occurs under the cuﬀ .

MEASUREMENT PROCEDURE

1. Make 5-6 deep inhales and exhales before taking a measurement and relax. Do not

move, do not speak and do not toughen your arm. Switch on the Device by press –

date and time will display on the screen.

2. Press .

3. All symbols will appear on the display screen for a short

time (ﬁ g. 7) and the Unit will inﬂ ate automatically the air

into the cuﬀ . At ﬁ rst the inﬂ ation will stop at the level of

190 mmHg. (ﬁ g. 8).

4. After reaching the level of 190 mmHg the cuff will

gradually deﬂ ate. The ﬁ gures on the screen will count back.

The pulse symbol« » will start ﬂ ickering.

AS THE BLOOD PRESSURE AND PULSE ARE MEASURED

DURING AIR DEFLATION FROM THE ARM CUFF KEEP

QUIET AND DO NOT MOVE YOUR ARM AND DO NOT

TOUGHEN YOUR ARM MUSCLES

When the measurement is complete the arm cuff

completely deflates and your measurement results

ﬂ ash on the screen and Indicator «М1/М2» will blink,

reminding that to retain results, it is necessary to

choose memory 1 or 2, having depressed M1 or M2,

respectively. If memory is not choosed for more than 3

minutes the Device is independently changed over to

mode of date and time indication.

FIG.8

FIG.9

FIG.7

ENG

If irregular pulse rhythm is detected during

measurement, symbol of arrhythmia “ ”, will appear

upon measurement end. Appearance of arrhythmia

indicator may also be caused by body movement during

measurement. During periodical appearance of this

indication apply to You attending doctor.

Apart from numerical value of pressure, result is also

displayed on scale WHO (fig. 10). Scale WHO – three-

color scale of classiﬁ cation of received value of arterial

pressure, according to recommendation of World Health

Organization. Using the scale on the left display field,

estimate your ﬁ ndings against the following classiﬁ cation:

blood pressure is normal; blood pressure is exceeded or

speciﬁ c degree of arterial hypertension is detected.

6. Press to change to mode of date and time

indication. For taking a new measurement repeat

all steps described in this paragraph.

TO OBTAIN THE ACCURATE RESULT MAKE

INTERVAL BETWEEN MEASUREMENTS TO

RESTORE THE BLOOD CIRCULATION. WAIT FOR

AT LEAST 3 MINUTES BEFORE MAKING A NEW

MEASUREMENT.

Result of each measurement

(pressure, pulse) will kept in the device memory

automatically.

THE DATA WILL BE KEPT IN THE MEMORY EVEN IF THE DEVICE IS STORED WITHOUT

BATTERIES. TO DELETE ALL VALUES STORED IN THE MEMORY YOU SHOULD MAKE

ACTIONS DESCRIBED IN “MEMORY FUNCTION”.

If no actions are done in mode of date and time setting for more than 3 minute, the

Device is independently changed over to mode of date and time indication.

AUTOMATIC REINFLATION

When during the first blood pressure measurement the cuff inflation to a

level of 190 mmHg is not sufficient or you move your arm the Unit stops

measurement and re-inﬂ ates the cuﬀ to the higher level. The Unit has 4 ﬁ xed

levels of the arm cuﬀ inﬂ ation: 190, 230, 270 and 300 mmHg.

The automatic re-inﬂ ation is repeated until the measurement is completed

successfully. This is not a defect.

FORCED DEFLATION FROM A CUFF

For rapid air release from of the arm cuﬀ during arm cuﬀ inﬂ ation or during

a measurement (slow deﬂ ation) press the . Button. The device will quickly

release all air from cuﬀ and will switch oﬀ .

FIG.9

FIG.10

ENG

MEMORY FUNCTION

Result of each measurement (pressure, pulse, time and date of measurement)

may be kept in the device memory. For this purpose, after measurement, within

not more than 3 minutes, memory M1 or M2 shall be selected for memory storage.

IF THE NOTICE ON ERROR APPEARS THE MEASUREMENT

RESULT WILL NOT BE STORED

2. Up to 90 measurement results and mean value of last 3

measurements may be kept in each device memory. When

the number of measurements exceeds 90, the oldest record

is deleted to save the most recent values.

3. Press the M1 (or M2) Button to see the ﬁ gures stored in

the memory.At the ﬁ rst depression of button M1 (or M2),

will appear on the screen, marked by symbol«А» (fig. 11).

At repeated depression of button M1 (or M2) indicator

of selected memory М1 (or М2) and number of memory

cell will appear on the screen,

and in 1 second its content is

displayed (ﬁ g. 12). When content

of memory cell is displayed,

date and time of measurement

are displayed alternately in

the display lower line. Each

depression of button M1 (or

M2) causes shifting to the next

memory cell.

If no measurement results are

stored in the memory and M1 (or

M2) buttons are pressed for the ﬁ rst time, current date and time will be displayed.

MEMORY CLEARING

To delete all values stored in the memory, press the M1 (or M2) Button and hold it

down for more than 3 seconds. Symbols “Clr” will appear on the screen and all values

will be deleted from the memory.

FIG.11

FIG.12

ENG

INFORMATION ABOUT ERRORS

Indication Likely cause Methods of correction

The arm cuﬀ is applied incorrectly

or the air tube plus is inserted not

tightly enough.

Measurements cannot be made

due to hand movement or talking

during measurements.

At such disorders as deep vascular

sclerosis, weak pulse wave and

also in patients with the prominent

distortions of cardiac rhythm it may

be difficult to measure the blood

pressure accurately.

Be sure that the arm cuff is

applied correctly and the plug is

inserted tightly. Repeat the whole

measurement procedure.

Repeat the measurement following

strictly the recommendations of this

Manual.

In such cases consult a certified

doctor about application of the

electronic Unit.

Batteries are discharged. Replace the batteries for new

ones.

CARE, STORAGE, REPAIR AND DISPOSAL

1. Keep this Device from exposure to higher humidity, direct sunlight, shocks,

vibration. THIS DEVICE IS NOT WATERTIGHT!!

2. Do not keep and use this Device near heating installations and open ﬁ re.

3. Remove the batteries if the Unit will be unused for a long time. Battery

leaking may damage the Unit. KEEP BATTERIES OUT OF REACH OF

CHILDREN!

4. Keep the Unit clean and protect it from dust. Use the dry soft cloth to clean

the Unit.

5. Keep the Unit and its components away from water, solvents, spirit and petrol.

6. Protect the arm cuﬀ from contacting on sharp things; do not stretch or fold

tightly the arm cuﬀ .

7. Do not subject the Unit to strong shocks, such as dropping on the ﬂ oor.

8. This Unit does not contain special controls to adjust the measurement

accuracy. It is prohibited to open individually the electronic block. Repair

the Unit only in authorized organizations.

9. On expiration of the warranted service life apply from time to time to

authorized repair organizations to check the technical condition of the Unit.

ENG

10. Dispose of the Unit and its components according to the application local

regulations. No special requirements to disposal of this Unit are deﬁ ned by

the manufacturer.

11. The arm cuﬀ may withstand multiple sanitary treatments. The internal tissue

surface of the arm cuﬀ (contacting on arm) may be cleaned with cotton ball

soaked in 3%-solution of hydrogen peroxide. At long use the partial color

fading of the tissue coating of the arm cuﬀ is possible. Washing and ironing of

the arm cuﬀ are not allowed

TROUBLESHOOTING TIPS

PROBLEM LIKELY CAUSE

METHOD OF CORRECTION

After pressing the

no indication

on the display.

Discharge of batteries.

Polarity of batteries is not

observed.

Battery terminals are

contaminated.

Replace all batteries for new ones.

Install batteries correctly.

Clean the terminals with dry cloth.

Inﬂ ation is

stopped and

resumed.

Automatic re-inﬂ ation to

obtain correct measurements.

Perhaps you talk or move your

arm during the measurement?

See MEASUREMENT PROCEDURE.

Calm down and repeat the

measurement.

Every time the

blood pressure

is diﬀ erent.

Measurements

are too low/

high.

Check that the arm cuﬀ is level

with your heart?

Check that the arm cuﬀ is

applied correctly?

Perhaps your arm muscles are

tough?

Perhaps you talk or move your

arm during the measurement?

Take the correct position for

measurement.

Take the correct position for

measurement.

Apply the arm cuﬀ correctly.

Keep silence and quiet during

measurement.

Measurements

of the pulse rate

are too low/

high.

Perhaps your arm muscles are

tough?

Perhaps you talk or move your

arm during the measurement?

Keep silence and quiet during

measurement.

Repeat the measurement at least

in 5 min.

Impossibility

to make a large

of number of

measurements.

Application of poor batteries.

Use only alkali batteries of well-

known manufacturers.

ENG

Spontaneous

failure of power

supply.

Actuation of automatic

de-energizing system

This is not a defect. The Unit is

disconnected automatically in 3

minutes after the last operation

of the Unit.

If regardless of the above recommendation you are unable to get correct

measurement results, stop the use of this Device and apply to a maintenance

organization (addresses and telephones of authorized organizations may be found

in the warranty card). Do not try to adjust the internal mechanism by yourself.

WARRANTY

1. The following LD product is covered by warranty for the period speciﬁ ed in

the warranty card.

2. The warranty liabilities are contained in the warranty card given at the sale

of this unit to a purchaser.

3. The addresses of organizations for warranty maintenance are given in the

warranty card.

TECHNICAL SPECIFICATIONS

Measurement method

oscillometric with Fuzzy Algorithm

Display

LCD

Pressure indication range in an arm cuﬀ , mmHg

from 0 to 300

Measurement range:

pressure in an arm cuﬀ , mmHg

pulse rate, 1/min

from 40 to 260

from 40 to 160

Range of admissible absolute error at

measurement of air pressure in an arm cuﬀ ,

mmHg ±3

Range of admissible absolute error at

measurement of pulse rate measurement, %

±5

Date and time yes

Memory

2х90 recent measurements + average

value of the last three measurements

Power source, V

Type of power supply

2 АAA size batteries

Max power intake, W

1,5

ENG

Operation conditions:

temperature, °C

relative humidity, % Rh

from 10 to 40

85 and lower

Storage and transportation conditions

temperature, °C

relative humidity, % Rh

from -20 to 50

85 and lower

Cuﬀ :

Type

Size

CUFF-LD12

a preformed type cuﬀ

adult (circumference 12,5 –20,5 cm)

Dimensions:

Size (electronic block), mm

Weight (without package, case, batteries and

adapter), g

66 х 70 х 32

118

Completness

electronic Unit, cuﬀ (connect to

electronic Unit), 2 power elements,

case, instruction manual, warranty card,

package

Service life of the Device (without cuﬀ ), years

Service life of cuﬀ , years

Year of manufacture

year the manufacture is given in the

bottom of the Device body in a serial

number after symbols “AA”

Symbols

Type BF

Important: Read the instructions

Type II

ENG

CERTIFICATION AND STATE REGISTRATION

This Device manufacturing is certified according to international standard ISO

13485:2003.

Devices LD12 comply with the requirements of European Directive MDD 93/42/ЕЕС,

international standards, EN980.



Complaints and requests should be addressed to:

Little Doctor Europe Sp. z o.o.

57G Zawila Street, 30-390, Krakow, Poland

Service phone: +48 12 2684748, 2684749

Manufactured under control:

Little Doctor International (S) Pte. Ltd., 35 Selegie Road # 09-02 Parkline

Shopping Centre, Singapore 188307

Manufacturer:

Little Doctor Electronic (Nantong) Co. Ltd., No.8, Tongxing Road Economic &

Technical Development Area, Nantong 226010, Jiangsu, PEOPLE'S REPUBLIC OF

CHINA

Distributor in Europe:

Little Doctor Europe Sp. z o.o.

57G Zawila Street, 30-390, Kraków, Poland

Sales Oﬃ ce phone: +48 12 2684746, 12 2684747, fax: +48 12 268 47 53

E-mail: biuro@littledoctor.pl

www.LittleDoctor.pl

Authorized Representative in the EU:

Shanghai International Trading Corp.GmbH

Eiﬀ estrasse 80, 20537 Hamburg, Germany.

POL

SPIS TREŚCI

Podstawowe części i komponenty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18

Informacje ogólne . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

Zalecenia dotyczące prawidłowego pomiaru . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20

Zasilanie elektryczne urządzenia . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

Ustawianie daty i godziny . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

Przyjęcie pozycji umożliwiającej pomiar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

Zakładanie mankietu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

Procedura pomiaru . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

Funkcja pamięci. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25

Zawiadomienia o błędach . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25

Konserwacja, przechowywanie, naprawa i utylizacja . . . . . . . . . . . . . . . . . . . . . . . . . . 26

Wykrywanie usterek . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27

Charakterystyki techniczne . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28

Certyﬁ kacja i rejestracja państwowa . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

POL

PODSTAWOWE CZĘŚCI I KOMPONENTY

1. Panel przedni urządzenia.

2. Wyświetlacz LCD.

3. Przycisk (włącz/wyłącz zasilanie)

4. Przycisk «M1» i «M2» (pamięć).

5. Mankiet.

6. Pokrywa komory baterii.

7. Etui.

8. Baterie.

9. Instrukcja obsługi.

10. Karta gwarancyjna.

POL

INFORMACJE OGÓLNE

Niniejsza instrukcja ma służyć użytkownikom pomocą w bezpiecznym i efektywnym

posługiwaniu się automatycznym, elektronicznym urządzeniem do pomiaru ciśnienia

tętniczego krwi i pulsu LD, model LD12 (dalej w tekście: URZĄDZENIE). Urządzenie

powinno być stosowane zgodnie z zasadami przedstawionymi w niniejszej instrukcji,

nie należy wykorzystywać go do celów innych, niż tu opisane. Należy przeczytać

i zrozumieć całą instrukcję obsługi, zwłaszcza rozdział “Zalecenia dotyczące

prawidłowego pomiaru”.

WSKAZANIA DO STOSOWANIA

Urządzenie przeznaczone jest do pomiaru skurczowego i rozkurczowego ciśnienia

tętniczego krwi oraz pulsu u pacjentów w wieku od 15 lat. Ciśnieniomierz zalecany

jest do stosowania u pacjentów z niestabilnym ciśnieniem tętniczym krwi lub

nadciśnieniem tętniczym w warunkach domowych jako uzupełnienie nadzoru

lekarskiego. Mankiet dostosowany jest do nadgarstka o obwodzie 12,5 - 20,5 cm.

ZASADA DZIAŁANIA

Do pomiaru ciśnienia tętniczego krwi i pulsu urządzenie wykorzystuje metodę

oscylometryczną z technologią Fuzzy Algorithm. Mankiet połączony z panelem

przednim urządzenia, owijany wokół nadgarstka. Po naciśnięciu przycisku ,

urządzenie automatycznie zacznie pompować mankiet, a następnie podczas

stopniowego uwalniania powietrza z mankietu zostanie wykonany pomiar. Czujnik

wychwytuje delikatne wahania zmiany ciśnienia w mankiecie, powodowane

rozszerzaniem i kurczeniem się tętnicy ramiennej odpowiednio do bicia serca.

Mierzona amplituda fal ciśnienia przekładana jest na wartość wysokości słupa

rtęci, wyświetlaną na wyświetlaczu LCD. Urządzenie posiada funkcję identyﬁ kacji

arytmii, dwa bloki pamięci po 90 pomiarów i wyliczenie średniej wartości 3

ostatnich pomiarów.

NALEŻY PAMIĘTAĆ, że aby urządzenie wyświetlało poprawne wyniki, musi ono

być przechowywane i wykorzystywane w temperaturach i przy wilgotności, nie

odbiegających od opisanych w dziale ”Charakterystyki techniczne” danej instrukcji.

Uprzedzamy o możliwości przekłamania pomiarów u osób z rozrusznikami serca,

arytmią serca, zwężeniem naczyń, zaburzeniami wątroby i cukrzycą. Przed pomiarem

ciśnienia u dzieci wskazane jest skonsultowanie się z lekarzem

ZASTOSOWANIE NOWYCH TECHNOLOGII

Fuzzy Algorithm – algorytm przetwarzania danych pomiarowych, który

pozwala dokładniej odzwierciedlić specyfikę pracy ludzkiego serca, co

zapewnia wyższą dokładność danych.

Skala WHO – klasyfikacja wyników pomiaru odpowiednio do zaleceń

Światowej Organizacji Zdrowia (WHO).

Identyﬁ kacja arytmii – specjalny znak “

” na wyświetlaczu urządzenia,

informujący o wykryciu nieregularnego pulsu.

High

Norm

Low

POL

ZALECENIA DOTYCZĄCE PRAWIDŁOWEGO POMIARU

1. Dla przeprowadzenia prawidłowego pomiaru należy pamiętać, że CIŚNIENIE

TĘTNICZE PODLEGA SILNYM WAHANIOM NAWET W KRÓTKIM PRZEDZIALE

CZASOWYM. Wartość ciśnienia tętniczego krwi zależy od wielu czynników.

Zwykle jest ona niższa w okresie letnim i wyższa w okresie zimowym. Ciśnienie

krwi zależy od ciśnienia atmosferycznego, wysiłku fizycznego, pobudliwości,

stresu, diety. Duży wpływ mają używki; narkotyki, alkohol i palenie tytoniu. U

wielu osób samo przeprowadzenie pomiaru ciśnienia w przychodni wywołuje

podniesienie wskaźników. Z tego powodu wyniki pomiarów ciśnienia tętniczego

przeprowadzonych w warunkach domowych często różnią się od wyników pomiarów,

przeprowadzonych w ośrodkach medycznych. Z uwagi na fakt, że ciśnienie w niskiej

temperaturze podwyższa się, należy je mierzyć w temperaturze pokojowej (około

20° C). W przypadku, gdy urządzenie było przechowywane w niskiej temperaturze,

przed użyciem trzeba je przynajmniej przez godzinę przetrzymać w temperaturze

pokojowej, inaczej wyniki pomiaru mogą być przekłamane. W ciągu doby wahania

ciśnienia u zdrowych ludzi mogą wynieść 30-50mmHg dla ciśnienia skurczowego

(górnego) i do 10 mmHg dla ciśnienia rozkurczowego (dolnego). Wahania ciśnienia u

różnych ludzi mogą mieć różne podstawy, dlatego zaleca się prowadzenie dziennika

pomiarów. TYLKO LEKARZ NA PODSTAWIE DANYCH Z TAKIEGO DZIENNIKA MOŻE

PRZEANALIZOWAĆ TENDENCJE ZMIAN I STWIERDZIĆ EWENTUALNE PRZYCZYNY

ZABURZEŃ CIŚNIENIA TĘTNICZEGO.

2. W chorobach układu krążenia, jak i wielu innych, które wymagają monitorowania

ciśnienia tętniczego, ważne jest dokonywanie pomiarów w porach zaleconych przez

lekarza. PAMIĘTAJ, ŻE DIAGNOSTYKA I JAKIEKOLWIEK LECZENIE NADCIŚNIENIA

TĘTNICZEGO MOGĄ BYĆ PRZEPROWADZANE TYLKO PRZEZ LEKARZA NA

ZASADZIE WSKAŹNIKÓW NADCIŚNIENIA TĘTNICZEGO, UZYSKANYCH

BEZPOŚREDNIO PRZEZ LEKARZA. PRZYJMOWANIE LEKÓW I ZMIANY W ICH

DOZOWANIU NALEŻY UPRZEDNIO SKONSULTOWAĆ Z LEKARZEM.

RYS.13

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Little Doctor LD12 Instrukcja obsługi

Marka: Little Doctor

Model: LD12

Kategoria: Jednostki ciśnienia krwi

Typ: Instrukcja obsługi

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English: Little Doctor LD12 User manual

Little Doctor LD12 Instrukcja obsługi

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