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WO1985003211A1 - Measurement of physiological parameter - Google Patents

Measurement of physiological parameter Download PDF

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Publication number
WO1985003211A1
WO1985003211A1 PCT/GB1985/000030 GB8500030W WO8503211A1 WO 1985003211 A1 WO1985003211 A1 WO 1985003211A1 GB 8500030 W GB8500030 W GB 8500030W WO 8503211 A1 WO8503211 A1 WO 8503211A1
Authority
WO
WIPO (PCT)
Prior art keywords
blood pressure
sensing
transducer
arterial pulse
heart beat
Prior art date
Application number
PCT/GB1985/000030
Other languages
French (fr)
Inventor
Peter Hawkins
Original Assignee
Johnson Matthey Public Limited Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Johnson Matthey Public Limited Company filed Critical Johnson Matthey Public Limited Company
Publication of WO1985003211A1 publication Critical patent/WO1985003211A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/021Measuring pressure in heart or blood vessels
    • A61B5/02108Measuring pressure in heart or blood vessels from analysis of pulse wave characteristics
    • A61B5/02125Measuring pressure in heart or blood vessels from analysis of pulse wave characteristics of pulse wave propagation time
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/021Measuring pressure in heart or blood vessels
    • A61B5/022Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/024Detecting, measuring or recording pulse rate or heart rate
    • A61B5/0245Detecting, measuring or recording pulse rate or heart rate by using sensing means generating electric signals, i.e. ECG signals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/026Measuring blood flow
    • A61B5/0285Measuring or recording phase velocity of blood waves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/24Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/316Modalities, i.e. specific diagnostic methods
    • A61B5/318Heart-related electrical modalities, e.g. electrocardiography [ECG]
    • A61B5/346Analysis of electrocardiograms
    • A61B5/349Detecting specific parameters of the electrocardiograph cycle
    • A61B5/352Detecting R peaks, e.g. for synchronising diagnostic apparatus; Estimating R-R interval

Definitions

  • This -invention relates to a method and apparatus for the determination of arterial blood pressure.
  • determination of the time interval between a heart beat and the associated arterial pulse is related, inter alia, to arterial blood pressure and hence may be used to provide a continuous, non-invasive method for the determination of arterial blood pressure.
  • the non-invasive method uses a sphygmomanometer which comprises an inflatable rubber cuff connected to a mercury manometer.
  • the cuff is placed around the upper arm and inflated until blood flow in the brachial artery is occluded.
  • a stethoscope is then used, as the pressure in the cuff is gradually reduced, to determine the systolic and diastolic measuring points. The pressure of each of these points is read from the manometer and quoted as the blood pressure.
  • the technique is simple to operate and firmly established in general and clinical medical practice but is not particularly accurate and, since each measuring operation takes some 20-30 seconds to perform, is discontinuous.
  • a method for the measurement of arterial blood pressure comprises sensing a heart beat, sensing an arterial pulse at at least one location and ascertaining the time interval between at least one heart beat and at least one associated arterial pulse.
  • the invention also includes apparatus for the measurement of arterial blood pressure, the apparatus comprising first sensing means for sensing a heart beat, second sensing means for sensing an arterial pulse at at least one location, and means for ascertaining the time interval between at least one heart beat and at least one associated arterial pulse.
  • the present invention therefore, provides a continuous, non—invasive technique and the output of the apparatus according to the invention is representative, inter alia, either of dynamic comparative blood pressure or, with suitable calibration, dynamic absolute blood pressure.
  • the heart beat sensing means may comprise a simple pressure transducer in contact with the chest but it is preferred for reasons of accuracy to utilise electrocardiography.
  • electrocardiography we have found that the R wave of an electrocardiogram, which corresponds to the beginning of ventricular systole, is a convenient reference for measurement of cardioarterial dela .
  • the arterial pulse may be sensed at one or more locations, for example at the carotid or temporal arteries in the head and neck, at the brachial radial or ulnar arteries in the arm and wrist, and/or in the fingertip, groin and leg.
  • Sensors which may be used include temperature sensitive devices, piezo-electric transducers, strain gauges, ultrasonic transducers and plethys ographic transducers.
  • Ultrasonic transducers rely on the Doppler effect to detect movement in the arterial wall and/or the flow of blood corpuscles while plethysmographic transducers measure volume changes which result from arterial pulsatile blood flow.
  • Volume changes may be detected by measurement of impedance changes or temperature changes but we prefer to use - ⁇ - photoplethysmography, which is an optical technique.
  • photoplethysmography light is transmitted into the tissues and the amount of light reflected is inversely proportional to the volume of blood present in the artery, thereby affording a means of detecting changes in volume of the artery with pulse.
  • light in the near infra-red region (wavelength 700- lOOOnm) is used since such light has a relatively high transmittance through tissue but is scattered by blood.
  • ⁇ light emitting diode which emits in the infra-red may be used as the source of light and a light-sensitive photo-transistor may be used to measure reflected light.
  • An infra-red light emitting diode is particularly convenient because the degree of scattering of light of this wavelength is substantially Independent of the degree of oxygenation of the blood.
  • the time interval between heartbeats and associated arterial pulses may be ascertained using either an analogue or a digital approach.
  • the time intervals are electronically processed to give information such as average and instantaneous values of blood pressure and/or to cause operative reactions in other equipment of a diagnostic or therapeutic nature, such as warning devices and the like.
  • Fig. 1 is a block diagram illustrating the equipment and procedures to which subjects were subjected to determine a delay (Td) between heart beats and associated arterial pulses;
  • Fig. 2 is a block diagram showing an electrocardiograph system
  • Fig. 3 is a block diagram showning an arterial pulse transducer system
  • Figs. 4.1 to 4.7 are plots of Td against average blood pressure for each of seven subjects.
  • a subject under test was connected as shown to an electrocardiograph and to an arterial pulse transducer.
  • a standard application of bipolar recording was used in which three identical electrodes are attached one to each arm and one to the left leg of the subject. The two arm electrodes were conncted to the inputs of a differential amplifier, the leg one being connected to common.
  • the differential output was fed to a band pass filter with an approximate 3dB bandwidth of 0.08-80 Hz. This filter was used to remove noise and unrelated spurious signals.
  • the output of the band pass filter was fed to a 50 Hz notch filter. This provided some 20dB's of attenuation at 50 Hz.
  • the output of the notch filter was differentiated for convenience to provide a signal based on the rate of change of the ECG.
  • the ZERO crossings of the derived waveform indicate the peaks of the original ECG waveform.
  • the arterial pulse transducer comprised a Texas Instruments' TIL 139 combined gallium arsenide IR-emitting diode/npn silicon phototransistor mounted together in a moulded ABS plastics housing and held against the finger to detect the arterial pulse therein.
  • the emission from this device typically peaks at wavelength of 940nm. At this wavelength, variations in the optical density of the underlying tissue are primarily determined by the pressure pulse.
  • the output of the phototransistor was amplified and fed to a band pass filter and a notch filter similar to those described with reference to Fig. 2. The notch filter output was then fed via a variable non-inverting amplifier to a differentiating circuit identical to that used for the electrocardiograph signal.
  • ECG electrocardiograph
  • AP arterial pulse
  • the subject under test was connected to the equipment as shown in Fig. 1.
  • the arterial pulse signals were obtained by using the AP transducer to detect the subject's finger pulsations.
  • the experiment was divided into three parts: i. Initially measurements were made of the systolic and diastolic arterial blood .pressure with the subject "at rest", using a sphygmomanometer . ii. A period of exercise was undertaken consisting of a short jogging session around a predetermined route, sufficient to raise the subject's blood pressure to a high value. iii. Periodic measurements of systolic and diastolic blood pressure were then made until the subject's blood pressure had returned to the "at rest" value measured in (i).
  • the ECG and AP results were recorded simultaneously with the blood pressure measurements being taken.
  • the Medelec UV recorder used for the differentiated outputs is an instrument consisting of both an oscilloscope and UV trace recorder. Traces displayed on the oscilloscope screen can also be recorded on UV sensitive paper producing a permanent record of the waveform being displayed.
  • the oscilloscope has four inputs, two of which are connected to ECG and AP differentiator outputs. The other two are calibrated to ground and positioned to be superimposed on the AP and ECG traces to provide a reference. This ground reference is used to determine the zero crossing that defines the peaks of the input waveforms.
  • a set of average Td values and a set of average blood pressure values measured manually by sphygmomanometer were derived.
  • sets of 7 or 8 values were obtained.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Cardiology (AREA)
  • Engineering & Computer Science (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Surgery (AREA)
  • Veterinary Medicine (AREA)
  • Biophysics (AREA)
  • Pathology (AREA)
  • Biomedical Technology (AREA)
  • Public Health (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Physics & Mathematics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Physiology (AREA)
  • Vascular Medicine (AREA)
  • Hematology (AREA)
  • Signal Processing (AREA)
  • Ophthalmology & Optometry (AREA)
  • Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)

Abstract

A method of and apparatus for determination of blood pressure continuously and non-invasively. The method comprises sensing the heart beat, preferably via ECG, sensing the associated arterial pulse and measuring the time interval between them. Photoplethysmography is conveniently used for sensing the arterial pulse.

Description

MEASUREMENT OF PHYSIOLOGICAL PARAMETER This -invention relates to a method and apparatus for the determination of arterial blood pressure. We have found that determination of the time interval between a heart beat and the associated arterial pulse is related, inter alia, to arterial blood pressure and hence may be used to provide a continuous, non-invasive method for the determination of arterial blood pressure.
Of the two common methods for determination of arterial blood pressure, one is non-invasive but discontinuous and the other is continuous but invasive. The non-invasive method uses a sphygmomanometer which comprises an inflatable rubber cuff connected to a mercury manometer. In use, the cuff is placed around the upper arm and inflated until blood flow in the brachial artery is occluded. A stethoscope is then used, as the pressure in the cuff is gradually reduced, to determine the systolic and diastolic measuring points. The pressure of each of these points is read from the manometer and quoted as the blood pressure. The technique is simple to operate and firmly established in general and clinical medical practice but is not particularly accurate and, since each measuring operation takes some 20-30 seconds to perform, is discontinuous.
_ The continuous method involves the surgical insertion of a catheter in the brachial artery. The catheter is connected to a suitable pressure transducer and this provides a direct, accurate and continuous determination of blood pressure. However, since the method is invasive, it is suitable for use only during relatively major surgery. According to the present invention, a method for the measurement of arterial blood pressure comprises sensing a heart beat, sensing an arterial pulse at at least one location and ascertaining the time interval between at least one heart beat and at least one associated arterial pulse.
The invention also includes apparatus for the measurement of arterial blood pressure, the apparatus comprising first sensing means for sensing a heart beat, second sensing means for sensing an arterial pulse at at least one location, and means for ascertaining the time interval between at least one heart beat and at least one associated arterial pulse.
The present invention, therefore, provides a continuous, non—invasive technique and the output of the apparatus according to the invention is representative, inter alia, either of dynamic comparative blood pressure or, with suitable calibration, dynamic absolute blood pressure.
The heart beat sensing means may comprise a simple pressure transducer in contact with the chest but it is preferred for reasons of accuracy to utilise electrocardiography. In particular, we have found that the R wave of an electrocardiogram, which corresponds to the beginning of ventricular systole, is a convenient reference for measurement of cardioarterial dela .
The arterial pulse may be sensed at one or more locations, for example at the carotid or temporal arteries in the head and neck, at the brachial radial or ulnar arteries in the arm and wrist, and/or in the fingertip, groin and leg. Sensors which may be used include temperature sensitive devices, piezo-electric transducers, strain gauges, ultrasonic transducers and plethys ographic transducers. Ultrasonic transducers rely on the Doppler effect to detect movement in the arterial wall and/or the flow of blood corpuscles while plethysmographic transducers measure volume changes which result from arterial pulsatile blood flow. Volume changes may be detected by measurement of impedance changes or temperature changes but we prefer to use - Λ - photoplethysmography, which is an optical technique. In photoplethysmography, light is transmitted into the tissues and the amount of light reflected is inversely proportional to the volume of blood present in the artery, thereby affording a means of detecting changes in volume of the artery with pulse. Conveniently, light in the near infra-red region (wavelength 700- lOOOnm) is used since such light has a relatively high transmittance through tissue but is scattered by blood. Δ light emitting diode which emits in the infra-red may be used as the source of light and a light-sensitive photo-transistor may be used to measure reflected light. An infra-red light emitting diode is particularly convenient because the degree of scattering of light of this wavelength is substantially Independent of the degree of oxygenation of the blood.
The time interval between heartbeats and associated arterial pulses may be ascertained using either an analogue or a digital approach. Preferably the time intervals are electronically processed to give information such as average and instantaneous values of blood pressure and/or to cause operative reactions in other equipment of a diagnostic or therapeutic nature, such as warning devices and the like. The invention will now be described by way of example with reference to the accompanying drawings of which:
Fig. 1 is a block diagram illustrating the equipment and procedures to which subjects were subjected to determine a delay (Td) between heart beats and associated arterial pulses;
Fig. 2 is a block diagram showing an electrocardiograph system; Fig. 3 is a block diagram showning an arterial pulse transducer system;
Figs. 4.1 to 4.7 are plots of Td against average blood pressure for each of seven subjects. Referring first to Fig. 1, a subject under test was connected as shown to an electrocardiograph and to an arterial pulse transducer. In connecting the electrocardiograph, a standard application of bipolar recording was used in which three identical electrodes are attached one to each arm and one to the left leg of the subject. The two arm electrodes were conncted to the inputs of a differential amplifier, the leg one being connected to common.
As shown in Fig. 2, the differential output was fed to a band pass filter with an approximate 3dB bandwidth of 0.08-80 Hz. This filter was used to remove noise and unrelated spurious signals. In order to reduce 50 Hz mains interference, the output of the band pass filter was fed to a 50 Hz notch filter. This provided some 20dB's of attenuation at 50 Hz. The output of the notch filter was differentiated for convenience to provide a signal based on the rate of change of the ECG. The ZERO crossings of the derived waveform indicate the peaks of the original ECG waveform. The arterial pulse transducer comprised a Texas Instruments' TIL 139 combined gallium arsenide IR-emitting diode/npn silicon phototransistor mounted together in a moulded ABS plastics housing and held against the finger to detect the arterial pulse therein. The emission from this device typically peaks at wavelength of 940nm. At this wavelength, variations in the optical density of the underlying tissue are primarily determined by the pressure pulse. As shown in Fig. 3, the output of the phototransistor was amplified and fed to a band pass filter and a notch filter similar to those described with reference to Fig. 2. The notch filter output was then fed via a variable non-inverting amplifier to a differentiating circuit identical to that used for the electrocardiograph signal.
The electrocardiograph (ECG) and arterial pulse (AP) transducer differentiator circuits indicated the rate of change of the respective signals and thus of their peaks. The results were recorded on a Medelec UV recorder to allow manual measurement of the values of the time intervals Td.
In use, the subject under test was connected to the equipment as shown in Fig. 1. The arterial pulse signals were obtained by using the AP transducer to detect the subject's finger pulsations. The experiment was divided into three parts: i. Initially measurements were made of the systolic and diastolic arterial blood .pressure with the subject "at rest", using a sphygmomanometer . ii. A period of exercise was undertaken consisting of a short jogging session around a predetermined route, sufficient to raise the subject's blood pressure to a high value. iii. Periodic measurements of systolic and diastolic blood pressure were then made until the subject's blood pressure had returned to the "at rest" value measured in (i). The ECG and AP results were recorded simultaneously with the blood pressure measurements being taken. The Medelec UV recorder used for the differentiated outputs is an instrument consisting of both an oscilloscope and UV trace recorder. Traces displayed on the oscilloscope screen can also be recorded on UV sensitive paper producing a permanent record of the waveform being displayed. The oscilloscope has four inputs, two of which are connected to ECG and AP differentiator outputs. The other two are calibrated to ground and positioned to be superimposed on the AP and ECG traces to provide a reference. This ground reference is used to determine the zero crossing that defines the peaks of the input waveforms.
A sufficient length of UV trace recording was done to capture six or more cardiac cycles for each sphygmomanometer measurement. On each UV trace, the subject's initials and blood pressure readings were also recorded. For each experiment on a particular subject a set of 7 or 8 UV trace recordings was obtained. The values of Td were measured, using a rule, from the differentiated zero crossing corresponding to the R wave peak of the ECG to the zero crossing corresponding to the first peak of the AP . Together with the blood pressure readings these were entered into a computer program to calculate: i. the individual values of Td in msecs for each cardiac cycle; i_i . the average value of Td in msecs over each sphygmomanometer measurement; and ill. the average manually measured blood pressure in mm Hg.
Thus, for a given subject, a set of average Td values and a set of average blood pressure values measured manually by sphygmomanometer were derived. Typically, sets of 7 or 8 values were obtained.
These values were then plotted on to graphs of average Td vs average measured blood pressure, and were also used as input data to a linear regression program to test the degree of correlation. The graphs are shown in Figs. 6.1 to 6.7, each graph representing results for one subject. In the graphs, the straight line is derived from linear regression and the deviation of the plotted points for Td vs blood pressure gives an indication of the degree of correlation.

Claims

1. A method for the determination of arterial blood pressure, comprising sensing a heart beat, sensing an arterial pulse at at least one location and ascertaining the time interval between at least one heart beat and at least one associated arterial pulse.
2. A method according to Claim 1 in which the heart beat is sensed by electrocardiography.
3. A method according to Claim 1 In which the arterial pulse is sensed by a plethysmographic transducer.
4. A method according to Claim 3 in which the plethysmographic transducer comprises a photoplethysmographic transducer.
5. A method according to Claim 4 in which the photoplethysmographic transducer utilises light in the near infra-red region of the spectrum having a wavelength In the range 700 to lOOOn .
6. A method according to any preceding claim, further including processing and/or recording of the results to give average blood pressure, instantaneous blood pressure, and/or to cause operative reactions in other equipment of a diagnostic or therapeutic nature.
7. Apparatus for the measurement of cardioarterial delay comprising first sensing means for sensing a heart beat, second sensing means tor sensing an arterial pulse at at least one location, and means for ascertaining the time interval between at least one heart beat and at least one associated arterial pulse.
8. Apparatus according to Claim 7 in which the first sensing means comprises an electrocardiograph.
9. Apparatus according to Claim 7 in which the second sensing means comprises a plethysmographic transducer.
10. Apparatus according to Claim 9 in which the plethysmographic transducer comprises a photoplethysmographic transducer.
11. Apparatus according to Claim 10 in which the photoplethysmographic transducer utilises light in the near Infra-red region of the spectrum having a wavelength in the range 700 to lOOOnm.
12. Apparatus according to any of Claims 8 to 11 further including means for processing and/or recording of the results to give figures representing average blood pressure, instantaneous blood pressure, and/or to cause operative reactions in other equipment of a diagnostic or therapeutic nature.
PCT/GB1985/000030 1984-01-20 1985-01-21 Measurement of physiological parameter WO1985003211A1 (en)

Applications Claiming Priority (2)

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GB8401500 1984-01-20
GB848401500A GB8401500D0 (en) 1984-01-20 1984-01-20 Measurement of physiological parameter

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Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989008424A1 (en) * 1988-03-09 1989-09-21 Vectron Gesellschaft Für Technologieentwicklung Un Method of continuous measurement of blood pressure in humans
EP0377554A1 (en) * 1989-01-05 1990-07-11 Edmund Schauer Method for measuring blood pressure
WO1991011956A1 (en) * 1990-02-16 1991-08-22 Lindberg Lars Goeran A monitor which analyses puls frequency by photoplethysmographic measurement and a measuring method therefor
EP0443267A1 (en) * 1990-02-23 1991-08-28 Sentinel Monitoring, Inc. Method and apparatus for continuous non-invasive blood pressure monitoring
US5316008A (en) * 1990-04-06 1994-05-31 Casio Computer Co., Ltd. Measurement of electrocardiographic wave and sphygmus
DE19542019C1 (en) * 1995-11-10 1997-03-06 Fraunhofer Ges Forschung Sensor for non=invasive and continuous detection of arterial pulse wave delay esp in human arteria radialis, for blood pressure measurement
EP0821910A2 (en) * 1996-08-01 1998-02-04 Colin Corporation Blood pressure monitor apparatus
WO1998025516A1 (en) * 1996-10-11 1998-06-18 Dxtek, Inc. Non-invasive cuffless determination of blood pressure
EP1057449A2 (en) * 1996-08-28 2000-12-06 Colin Corporation Apparatus for evaluating cardiac function of living subject
GB2356251A (en) * 1999-11-12 2001-05-16 Micro Medical Ltd Determining the stiffness of arteries in a person
AT407949B (en) * 1998-06-09 2001-07-25 Cnsystems Medizintechnik Gmbh Haemodynamic patient monitor
EP1484010A2 (en) * 2003-06-02 2004-12-08 Cyberfirm Inc. Laser blood-flow meter and system for monitoring bio-data
CN100453034C (en) * 2002-05-07 2009-01-21 欧姆龙健康医疗事业株式会社 Device for diagnosing arteriostenosis and device for measuring ankle blood pressure
WO2015162566A1 (en) * 2014-04-24 2015-10-29 Ecole Polytechnique Federale De Lausanne (Epfl) A method and a device for non invasive blood pressure measurement

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Elektronik, Volume 29, No. 12, June 1980 Munchen (DE) K. SINGER et al.: "Die Messung der Pulswellen-Geschwindigkeit beim Menschen", pages 49-52, see page 49, Abstract; page 10, left-hand column, lines 27-47; figures 1, 2; page 51; figures 3, 4 *
IEEE Transactions on Biomedical Engineering, Volume BME-19, No. 4, July 1972 New York (US) B. TURSKY et al.: "Automated Constant Cuff-Pressure System to Measure Average Systolic and Diastolic Blood Pressure in Man", pages 271-276, see page 271, Abstract pages 272-274, the Paragraphs "Rationale for Median Cuff Pressure" and "Description of the Constant Cuff-Pressure System" *

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989008424A1 (en) * 1988-03-09 1989-09-21 Vectron Gesellschaft Für Technologieentwicklung Un Method of continuous measurement of blood pressure in humans
EP0377554A1 (en) * 1989-01-05 1990-07-11 Edmund Schauer Method for measuring blood pressure
WO1991011956A1 (en) * 1990-02-16 1991-08-22 Lindberg Lars Goeran A monitor which analyses puls frequency by photoplethysmographic measurement and a measuring method therefor
US5396893A (en) * 1990-02-16 1995-03-14 Oberg; Ake P. Method and apparatus for analyzing heart and respiratory frequencies photoplethysmographically
EP0443267A1 (en) * 1990-02-23 1991-08-28 Sentinel Monitoring, Inc. Method and apparatus for continuous non-invasive blood pressure monitoring
US5316008A (en) * 1990-04-06 1994-05-31 Casio Computer Co., Ltd. Measurement of electrocardiographic wave and sphygmus
DE19542019C1 (en) * 1995-11-10 1997-03-06 Fraunhofer Ges Forschung Sensor for non=invasive and continuous detection of arterial pulse wave delay esp in human arteria radialis, for blood pressure measurement
EP0821910A3 (en) * 1996-08-01 1998-12-09 Colin Corporation Blood pressure monitor apparatus
EP0821910A2 (en) * 1996-08-01 1998-02-04 Colin Corporation Blood pressure monitor apparatus
EP1057449A2 (en) * 1996-08-28 2000-12-06 Colin Corporation Apparatus for evaluating cardiac function of living subject
EP1057449A3 (en) * 1996-08-28 2001-07-04 Colin Corporation Apparatus for evaluating cardiac function of living subject
WO1998025516A1 (en) * 1996-10-11 1998-06-18 Dxtek, Inc. Non-invasive cuffless determination of blood pressure
AT407949B (en) * 1998-06-09 2001-07-25 Cnsystems Medizintechnik Gmbh Haemodynamic patient monitor
GB2356251A (en) * 1999-11-12 2001-05-16 Micro Medical Ltd Determining the stiffness of arteries in a person
GB2356251B (en) * 1999-11-12 2003-09-24 Micro Medical Ltd Apparatus for determining the stiffness of arteries in a person
CN100453034C (en) * 2002-05-07 2009-01-21 欧姆龙健康医疗事业株式会社 Device for diagnosing arteriostenosis and device for measuring ankle blood pressure
EP1484010A2 (en) * 2003-06-02 2004-12-08 Cyberfirm Inc. Laser blood-flow meter and system for monitoring bio-data
EP1484010A3 (en) * 2003-06-02 2005-02-09 Cyberfirm Inc. Laser blood-flow meter and system for monitoring bio-data
US7096058B2 (en) 2003-06-02 2006-08-22 Cyberfirm Inc. Laser blood-flow meter and system for monitoring bio-data
WO2015162566A1 (en) * 2014-04-24 2015-10-29 Ecole Polytechnique Federale De Lausanne (Epfl) A method and a device for non invasive blood pressure measurement
US10357164B2 (en) 2014-04-24 2019-07-23 Ecole Polytechnique Federale De Lausanne (Epfl) Method and device for non-invasive blood pressure measurement

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EP0168461A1 (en) 1986-01-22
GB8401500D0 (en) 1984-02-22

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