Rossmax AC1000f Manuale utente

Marca: Rossmax

Modello: AC1000f

Categoria: Unità di pressione sanguigna

Tipo: Manuale utente

Model: AC1000f

www.rossmax.com

Blood Pressure Monitor

Table of Contents:

Introduction .......................................................................................................................................... 3

Cautionary Notes ............................................................................................................................3-5

Notes on Safety ................................................................................................................................5, 6

Name/Function of Each Part ..................................................................................................7, 8

PARR (Pulse Arrhythmia) Technology ...................................................................................... 9

Atrial Fibrillation Detection (AF, AFib) .............................................................................9-10

Premature Contraction Detection (PC) ......................................................................10-11

Tachycardia Detection (TACH) ................................................................................................ 11

Bradycardia Detection (BRAD) ................................................................................................ 11

Pulse Arrhythmia Detection (ARR) ......................................................................................... 12

Real Fuzzy Measuring Technology ....................................................................................... 13

Preliminary Remarks ...................................................................................................................... 13

Display Explanations ..................................................................................................................... 14

Error Codes for your reference ................................................................................................. 15

Cu Wrap Detection ...................................................................................................................... 15

Movement Detection ................................................................................................................... 15

How to Use the POWER Source ......................................................................................16-19

Applying the Cu ..................................................................................................................... 20-22

Measurement Procedures ...................................................................................................23-25

Setting Deation Rate ................................................................................................................... 26

Recalling Values from Memory ............................................................................................... 26

Clearing Values from Memory ................................................................................................. 27

How to clean the unit after use .............................................................................................. 27

Troubleshooting .............................................................................................................................. 27

Specications ..................................................................................................................................... 28

EMC guidance and manufacturer’s declaration ............................................................29

Blood Pressure Log ...................................................................................................................30-31

Introduction

Blood pressure measurements determined with AC1000f are equivalent to

those obtained by a trained observer using cu/stethoscope auscultation

method, within the limits prescribed by the American National Standard, Elec-

tronic or Automated Sphygmomanometers. This unit is to be used by adult

consumers in home, physicians’ oces, hospitals, clinics and other medical fa-

cilities. The patient is an intended operator. Do not use this device on infants

or neonates. AC1000f is protected against manufacturing defects by an estab-

lished International Warranty Program. For warranty information, you can con-

tact the manufacturer, Rossmax International Ltd.

Attention: Consult the accompanying documents. Please read this

manual carefully before use. For specic information on your own blood

pressure, contact your physician. Please be sure to keep this manual.

Cautionary Notes

1. The unit contains high-precision assemblies. Therefore, avoid extreme tem-

peratures, humidity, and direct sunlight. Avoid dropping or strongly shock-

ing the main unit, and protect it from dust.

2. Clean the blood pressure monitor body and the cu carefully with a slightly

damp, soft cloth. Do not press. Do not wash the cu or use chemical cleaner

on it. Never use thinner, alcohol or petrol (gasoline) as cleaner.

3. Leaky batteries can damage the unit. Remove the batteries when the unit is

not used for a long time.

4. The unit should not be operated by children so to avoid hazardous situa-

tions.

5. If the unit is stored near freezing, allow it to acclimate at room temperature

before use.

6. This unit is not eld serviceable. You should not use any tool to open the

device nor should you attempt to adjust anything inside the device. If you

have any problems, please contact the store or the doctor from whom you

purchased this unit or please contact Rossmax International Ltd.

7. As a common issue for all blood pressure monitors using the oscillometric

measurement function, the device may have diculty in determining the

proper blood pressure for users diagnosed with diabetes, poor circulation of

blood, kidney problems, or for users suered from stroke, or for unconscious

users.

8. This unit is able to detect common arrhythmia (atrial or ventricular premature

beats or atrial brillation). The ARR, AF(AFib) and PC icons are displayed after

the measurement if Atrial Fibrillation and Premature Contraction was detect-

ed during the measurement. If ARR, AF(AFib) or PC icons are displayed, you

are advised to wait for a while and take another measurement. It is strongly

recommended that you consult your physician if the ARR, AF(AFib) or PC

icons appears often.

9. While the given device is able to detect specic pulse arrhythmia, the meas-

urement accuracy of the blood pressure meter may be impaired with the

occurrence of pulse arrhythmia.

10. To stop operation at any time, press the ON/OFF or START/STOP key, and the

air in the cu will be rapidly exhausted.

11. Once the ination reaches 300 mmHg, the unit will start deating rapidly

for safety reasons.

12. Please note that this unit can be a home healthcare product, but it is not

intended to serve as a substitute for the advice of a physician or medical

professional.

13. Do not use this device for diagnosis or treatment of any health problem or

disease. Measurement results are for reference only. Consult a healthcare

professional for interpretation of pressure measurements. Contact your

physician if you have or suspect any medical problem. Do not change your

medications without the advice of your physician or healthcare profes-

sional.

14. Electromagnetic interference: The device contains sensitive electronic com-

ponents. Avoid strong electrical or electromagnetic elds in the direct vicin-

ity of the device (e.g. mobile telephones, microwave ovens). These may lead

to temporary impairment of measurement accuracy.

15. Dispose of device, batteries, components and accessories according to lo-

cal regulations.

16. This monitor may not meet its performance specication if stored or used

outside temperature and humidity ranges specied in Specications.

17. Please note that when inating, the functions of the limb in question may

be impaired.

18. During the blood pressure measurement, blood circulation must not be

stopped for an unnecessarily long time. If the device malfunctions, remove

the cu from the arm.

Notes on Safety

Warning:

• Self diagnosis of measured results or treatment is dangerous. Please fol-

low the instruction of the doctor or healthcare provider.

• If cu ination does not stop, remove the cu or pull out the air tube from the

main unit.

• If battery uid gets into your eye or comes in contact with skin, wash the

eected area with water repeatedly. Immediately consult a doctor for treat-

ment.

• Do not wrap the cu over an arm to which intravenous injection or transfu-

sion is being conducted, or when otherwise contraindicated.

• Do not connect the air tube or the cu to other equipment which is con-

nected to an intra corporeal organ. Air embolisms may result.

• Do not use this unit in the presence of ammable gas or anesthetics or in a

high pressure oxygen room or oxygen tent.

• Do not use the battery pack for devices other than for this unit.

• Do not disassemble the battery.

• Do not touch the AC adaptor with wet hands.

19. Avoid any mechanical restriction, compression or bending of the cu line.

20. Do not allow sustained pressure in the cu or frequent measurements. The

resulting restriction of the blood ow may cause injury.

21. Ensure that the cu is not placed on an arm in which the arteries or veins

are undergoing medical treatment, e.g. intravascular access or therapy, or

an arteriovenous (AV) shunt.

22. Do not apply the cu on the side, where a mastectomy has been performed

in your patient history.

23. Do not place the cu over wounds as this may cause further injury.

24. Only ever use the cus provided with the monitor or original replacement

cus. Otherwise erroneous results will be recorded.

25. Batteries can be fatal if swallowed. You should therefore store the batteries

and products where they are inaccessible to small children. If a battery has

been swallowed, call a doctor immediately.

26. Do not use the tubing and/or AC adaptor for any other purpose than those

specied, as they can cause risk of strangulation.

27. Do not service or maintain device and cu while in use.

• Do not use any cu other than the models exclusive for this unit.

• Do not use this unit on infants.

• Do not use this unit on patients using a pump oxygenator.

• Do not use an AC adaptor or battery pack no specied for this unit.

• Do not use a cellular pone near this unit.

• Do not use this unit in a vehicle.

• Do not install the parts and/or instruments not specied for this unit.

• Do not use a broken power cord or AC adaptor.

• Do not install or store this unit where it may come in contact with water or

liquid medication.

• This is a Class II device with double insulation.

General advice:

• Do not place or put anything on this unit.

• Do not drop this unit.

• Turn o power to the unit and unplug the AC adaptor from the electric outlet

before moving the unit.

• Read the instruction manual of the other devices to be used at the same time

with this unit, to understand and be aware of the interaction between the

devices.

• When using the unit:

- Do not inate the cu without being wrapped over the arm.

- Do not use a damaged cu.

- Be sure that patients do not touch the buttons of this unit.

• After using the unit:

- Do not disinfect this unit by autoclave or gas sterilization (EtO, glutaralde-

hyde, or high concentration ozone).

• Do not install or store this unit in the following places.

- Under the direct sunlight.

- Dusty or salty environment.

- Places having slope or where combustible gas may be generated.

- Under high temperature and high humidity.

Name/Function of Each Part

Arm Cu

Auto / Manual

Switching Key Deation Rate

setting key

LCD Display

ON/OFF key

START/

STOP key

Charging

LED

Memory/

Marker key

Air Tube and

Connector

Battery Cover

(Located on back of unit)

Battery Pack:

4.8V, 1800mAh

NIMH Battery

Data Link

Socket

Protection Jelly

AC Adaptor

Jack

Monitor Installation - Trolley (Optional)

Placing Protection Jelly

onto the Monitor

Installing Monitor

on the Trolley

PARR (Pulse Arrhythmia) Technology

Pulse Arrhythmia (PARR) technology specically detects the existence of

pulse arrhythmia, including atrial brillation (AF, AFib), Atrial and / or Ventricu-

lar Premature Contractions (PC), Tachycardia (TACH), and Bradycardia (BRAD).

Pulse Arrhythmia may be related to cardiac disorders, needs medical atten-

tion and thus early diagnosis is of paramount importance. The PARR tech-

nology detects arrhythmia during regular blood pressure checks without

any additional user skills, user interaction and measurement prolongation.

Beside the blood pressure diagnosis a specic pulse arrhythmia diagnosis is

provided with PARR.

Note: The PARR detection of AF(AFib), PC, TACH and BRAD is provided with a

clinically proven high detection probability [1]. However, the sensitivity

and specicity is limited, thus most, but not all pulse arrhythmia will

be detected and displayed. In certain patients with uncommon clini-

cal conditions the PARR technology may not be able to detect pulse

arrhythmia. This partly comes from the fact that some arrhythmia can

only be found with an ECG diagnosis, but not with a pulse diagnosis.

Thus PARR is not meant to replace any medical ECG diagnosis by your

doctor. PARR provides an early detection of certain pulse arrhythmia,

which inevitably need to be presented to your doctor in charge.

Remark: [1] Clinical Investigation of PARR - A new Oscillometric Pulse Arrhyth-

mia Type Discriminating Detection Technology

Atrial Fibrillation Detection (AF, AFib)

The upper chambers of the heart (the atria) do not contract, but quiver and

thus blood is driven irregularly and with lower eciency into the ventricles.

Subsequently irregular heartbeats occurs, which mostly are associated with

a fast, yet highly instable heart rate. This condition is associated with a higher

risk for the formation of cardiac blood clots. Amongst others, they may el-

evate the risk of brain strokes. Beside this atrial brillation may contribute to

the severity of a chronic or acute heart failure condition and may be associ-

ated with other heart-related complications. Age dependent, about 10 %- 20

% percent of patients who suer from an ischemic stroke also suer from

atrial brillation.

Premature Contraction Detection (PC)

Extra abnormal heartbeats generated in irregular excitation sites of your

heart, either in the atria (PAC), the ventricle (PVC) or the cardiac conduction

nodes (PNC). These extra beats may disrupt your regular rhythm, they may

come in early or cause a signicant pauses regarding your perceivable pulse.

This is called palpitations, which can be felt in your chest. They may occur

as isolated, single events, as a series of irregular pulses or can be distributed

all over your pulse beats. If they are not related to mental stress, or acute

demanding physical load, they may be a marker for a multitude of cardiac

disorders. Some of these disorders go along with an elevated risk prole for

ischemic events, either in the heart (e,g, coronary heart disease) or outside

the heart, e.g. an elevated risk for a stroke. Some PCs may indicate on val-

vular or myocardial disorders and become very important if a myocarditis

(infection of the heart muscle) is suspected. This unit is able to detect prema-

ture contractions. The ARR and PC icons ( ) are displayed right after the

measurement if premature contractions have been detected.

Atrial brillation most often initially occurs with temporary periods of arrhyth-

mia and may progress to a permanent state of this disorder in the course of

time. No matter, whether you intent to safeguard yourself from an undetect-

ed AF(AFib) state, or you measure during an ongoing period of active atrial

brillation, or you measure in between periods of AF(AFib), the PARR technol-

ogy can be applied at any of these conditions. This unit is able to detect Atrial

brillation (AF, AFib). The ARR and AF(AFib) icons ( ) are displayed right

after the measurement if Atrial Fibrillation was detected.

Note: It is strongly recommended, that you consult your physician, if either

the AF(AFib) icon occurs newly for several times, or, if your AF(AFib) is

known to your doctor, but the incidence of AF(AFib) readings changes

over time. Your doctor will then be able to provide all required medical

test and possible therapeutic procedures.

Note: The presence of a cardiac pacemaker may impair the AF(AFib) detec-

tion by PARR.

Tachycardia Detection (TACH)

A fast heart rate of higher than 100 beats per minute (bpm) in adults. Unless

being caused by physical or mental stress, a tachycardia may be an indicator

for both cardiac (e.g. Coronary heart disease, valvular disorder), or extra-car-

diac disorders (e.g. hyperthyroidism, fever, hypoxemia), as well as medication

and stimulant substance side eects (e.g. caeine). The unit is able to detect

Tachycardia (TACH). The ARR and TACH icons ( ) are displayed right

after the measurement if tachycardia has been detected.

Note: It is strongly recommended, that you consult your physician, if either

the TACH icon occurs newly for several times, or, if your TACH is known

to your doctor, but the incidence of TACH readings changes over time.

Your doctor will then be able to provide all required medical test and

possible therapeutic procedures.

Note: It is strongly recommended, that you consult your physician, if either

the PC icon occurs newly for several times, or, if your PC is known to

your doctor, but the incidence of PC readings changes over time. Your

doctor will then be able to provide all required medical test and pos-

sible therapeutic procedures.

Bradycardia Detection (BRAD)

A slow heart rate of less than 55 beats per minute (bpm) in adults. Unless not

genetically determined or subsequent to a high cardiac endurance training

adaptation, bradycardia may be related to multitude of cardiac disorders (e.g.

valvular heart disease, heart failure) or extra-cardiac disorders (e.g. hypothy-

roidism, electrolyte imbalance) or medications (e.g. beta-receptor blocker).

This unit is able to detect Bradycardia (BRAD). The ARR and BRAD icons (

) are displayed right after the measurement if bradycardia was de-

tected.

Note: It is strongly recommended, that you consult your physician, if either

the BRAD icon occurs newly for several times, or, if your BRAD is known

to your doctor, but the incidence of BRAD readings changes over time.

Your doctor will then be able to provide all required medical test and

possible therapeutic procedures.

Pulse Arrhythmia Detection (ARR)

Once the occurrence of pulse arrhythmia has been detected in the course of

your blood pressure measurement, the icon ARR is displayed. In the case, that

the found pulse arrhythmia can be specied by the PARR technology, the

ARR icon is accompanied by the specically detected type of arrhythmia, e.g.

PC, AF(AFib), TACH or BRAD. Once the kind of found pulse arrhythmia cannot

be safely determined by PARR, the device is displaying ARR without any ad-

ditional pulse arrhythmia type icon.

Note: It is strongly recommended, that you consult your physician, if either

the ARR icon occurs newly for several times, or, if your ARR is known

to your doctor, but the incidence of ARR readings changes over time.

This is independent whether the ARR icon is specied by another pulse

arrhythmia icon or not. Your doctor will then be able to provide all re-

quired medical test and possible therapeutic procedures.

The PARR technology is able to detect and display combined pulse arrhyth-

mia ndings.

Display Results

- Normal nding

ARR Pulse Arrhythmia without type-specic detection

ARR PC Pulse Arrhythmia-Premature ventricular, atrial or nodal

beat detection

ARR AF(AFib) Pulse Arrhythmia-Atrial brillation detection

ARR TACH Tachycardia detection

ARR BRAD Bradycardia detection

ARR PC BRAD Combined Pulse Arrhythmia: Premature beats &

Bradycardia detection

ARR PC TACH Combined Pulse Arrhythmia: Premature beats &

Tachycardia detection

ARR AF(AFib) TACH Combined Pulse Arrhythmia: Atrial brillation &

Tachycardia detection

ARR AF(AFib) PC Combined Pulse Arrhythmia: Atrial brillation & Premature

beats detection

ARR AF(AFib) PC TACH Combined Pulse Arrhythmia: Detection of Atrial Fibrillation,

Premature Beats and Tachycardia.

Real Fuzzy Measuring Technology

This unit uses the oscillometric method to detect your blood pressure. Be-

fore the cu starts inating, the device will establish a baseline cu pressure

equivalent to the air pressure. This unit will automatically determine the ap-

propriate ination level based on pressure oscillations, followed by cu dea-

tion.

During the deation, the device will detect the amplitude and slope of the

pressure oscillations and thereby determine your actual the systolic blood

pressure, diastolic blood pressure, and pulse rate.

Preliminary Remarks

This Blood Pressure Monitor complies with the European regulations and

bears the CE mark “CE 1639”. The quality of the device has been veried and

conforms to the provisions of the EC council directive 93/42/EEC (Medical

Device Directive), Annex I essential requirements and applied harmonized

standards.

EN 1060-1: 1995/A2: 2009 Non-invasive sphygmomanometers - Part 1 - Gen-

eral requirements

EN 1060-3: 1997/A2: 2009 Non -invasive sphygmomanometers - Part 3 - Sup-

plementary requirements for electro-mechanical blood pressure measuring

systems

EN 1060-4: 2004 Non-invasive sphygmomanometers - Part 4: Test Procedures

to determine the overall system accuracy of automated non-invasive sphyg-

momanometers.

ISO 81060-2: 2013 Non-invasive sphygmomanometers - Part 2: Clinical inves-

tigation of automated measurement type

This blood pressure monitor was designed for long service periods. In order

to ensure continued accuracy, it’s recommended that all digital blood pres-

sure monitors require re-calibration. This monitor (under normal usage with

approx. 3 measurements a day) does not require re-calibration

for 2 years. Once the unit should be re-calibrated the device

will display . The unit should also be re-calibrated if the mon-

itor sustains damage due to blunt force (such as dropping) or

exposure to uids and / or extreme hot or cold temperature /

humidity changes. When appears, simply return your device

to your nearest dealer for re-calibration service.

Display Explanations

21 3 4 5

1. Arrhythmia Detection

(ARR)

2. Premature Contraction

Detection (PC)

3. Atrial Fibrillation Detection

(AF, AFib)

4. Tachycardia Detection

(TACH)

5. Bradycardia Detection

(BRAD)

6. Movement Mark

7. Cu Wrap Detection

8. AC Power Mark

9. Battery Mark

10. Auto Mode

11. Manual Mode

12. Memory Mark

13. Systolic Pressure

14. Diastolic Pressure

15. Pulse Rate

16. Set Deation Mark

17. Deation Rate

Loose Cu Detection

If the cu was applied too loosely, it may cause unreliable measurement re-

sults or measurements can fail to start. The “Cu Wrap Detection” can help to

determine if the cu is wrapped snugly enough. The specied icon appears

once a “loosen cu” has been detected during measurement. Otherwise the

specied icon appears if the cu is wrapped correctly during measurement.

Movement Detection

The “Movement Detection” helps reminding the user to remain still and is indi-

cating any adverse body movement during measurement. The specied icon

appears once a “body movement” has been detected during and after such a

measurement.

Note: It’s highly recommended that you measure again if the icon appears.

Error Codes for your reference

EE / Measurement Error: Make sure the L-plug is securely connected to the

air socket and calmly measure again. Wrap the cu correctly around your arm

and keep arm steady during measurement. If the error keeps occurring, return

the device to your local distributor or service centre.

E1 / Air Circuit Abnormality: Make sure the L-Plug is securely connected to

the air socket on the side of the unit and calmly measure again. If the errors

still occur, return the device to your local distributor or service centre for help.

E2 / Pressure Exceeding 300 mmHg: Switch the unit o and measure again

quietly. If the error keeps occurring, return the device to your local distributor

or service centre.

E3 / Data Error: Remove the batteries, wait for 60 seconds, and reload. If the

error keeps occurring, return the device to your local distributor or service cen-

tre.

Er / Exceeding Measurement Range: Measure again quietly. If the error

keeps occurring, return the device to your local distributor or service centre.

How to Use the POWER Source

How to Use the AC Adaptor

1. Connect the AC adaptor with the AC adaptor jack in the back of the unit.

2. Plug the AC adaptor into the socket. Please use the compatible AC adap-

tors. (AC adaptors with required voltage and current indicated near the AC

adaptor jack.)

• When using the battery pack and connect the AC adaptor, the unit also

functions as the charger.

Note: The AC adaptor can use with unit individually. (without battery pack).

AC Adaptor

(Ø3.8 / Ø1.35)

How to Use the POWER Source

Warning:

• Do not use this unit in places where inammable gas, such as highly

inammable anesthetic, may be generated or in a high pressure oxy-

gen room or an oxygen tent. It may cause ignition and explosion.

• Do not touch the AC adaptor with wet hands. You may suer electric

shock.

Caution:

• Be sure to use the AC adaptor appropriate for your country. It may

cause re or you may suer electric shock.

• Do not install or store this unit where it may be sprayed with water or

medication. You may suer electric shock.

General advice:

• Read the instruction manual of the other advices to be used at the

same time with this unit to understand and be aware of the interaction

between the devices.

Installation and Replacement of Battery Pack

Warning:

• If the uid in the battery gets into your eye, wash the eye with suf-

cient water without rubbing the eye, then immediately consult the

doctor for treatment. There is danger in losing your eyesight.

• Do not use the exclusive battery pack other than for this unit.

• Do not throw the battery pack into re, or heat, or disassemble it. It may

cause heat, ignition, short-circuit, or rupture.

Caution:

• Do not short-circuit the polarities of the optional battery pack with a

metal object such as wire.

• If the uid in the battery is stained on your skin or clothes, immediately

wash o the uid with water. Your may suer injury, or the battery may

leak, heat, ignite re, or explode.

1. Remove the screw on the battery cover (Located on back of unit) of this

unit.

2. Installation: Connect the battery pack to the connector in the battery

cover to install it.

Replacement: Disconnect the battery pack from the connector and re-

place with a new one.

3. Install the battery cover and fasten it with screws. At this time, be careful

not to pinch the lead wire.

4. Connect the main unit and the AC adaptor, then charge the battery pack.

The battery pack is not charged when you purchase the monitor. When

you use the battery pack for the rst time, charge it for more than twelve

hours before use.

How to Use the POWER Source

Battery life:

• You can use the unit for approximately six hundred measurements with one

charge.

• Approximate life of battery pack is two years. However the battery pack life

from each charging may be shortened depending on the state of using.

Charging time:

• After connecting the AC adaptor, the battery pack will start charging auto-

matically.

• While the battery is being charged, the and battery marks turn on and

LED shows orange light.

• While the charging is completed, LED shows green light.

Battery low:

• If a mark is displayed, the battery is low (blood pressure cannot be

measured). Please charge the battery.

Automatic Power O:

• If you use the unit with the battery pack only, the unit will turn o automati-

cally in approximately ve minutes even if you forget to turn o the power.

• While the AC adaptor is connected, the Auto Power O function does not

work.

How to Use the POWER Source

Full battery Low battery

Applying the Cu

1. Select cu according to arm size:

Rossmax

Cu size

Arm

circumference

L size 34~46 cm

(13.4”~18.1”)

M size 24~36 cm

(9.4”~14.2”)

S size 16~26 cm

(6.3”~10.2”)

2. Connect the air tube securely.

• Connect the air tube to the main unit by securing the air plug to the base

of the air connector.

• Securely connect the air tube and the cu set by rotating Luer connector.

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Rossmax AC1000f Manuale utente

Marca: Rossmax

Modello: AC1000f

Categoria: Unità di pressione sanguigna

Tipo: Manuale utente

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