AU2004242459A1 - Physiological signal acquisition cable - Google Patents

Physiological signal acquisition cable Download PDF

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Publication number
AU2004242459A1
AU2004242459A1 AU2004242459A AU2004242459A AU2004242459A1 AU 2004242459 A1 AU2004242459 A1 AU 2004242459A1 AU 2004242459 A AU2004242459 A AU 2004242459A AU 2004242459 A AU2004242459 A AU 2004242459A AU 2004242459 A1 AU2004242459 A1 AU 2004242459A1
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AU
Australia
Prior art keywords
biological
display
signals
acquisition
data
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Abandoned
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AU2004242459A
Inventor
Vladimir Jankov
Harry Louis Platt
Allan Michael Shell
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Individual
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Individual
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Publication date
Priority claimed from AU40941/00A external-priority patent/AU4094100A/en
Application filed by Individual filed Critical Individual
Priority to AU2004242459A priority Critical patent/AU2004242459A1/en
Publication of AU2004242459A1 publication Critical patent/AU2004242459A1/en
Abandoned legal-status Critical Current

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Description

24/12/2004 1S13 Chr 'sIllou Law 95534755 7/35 o PHYSIOLOGICAL SIGNAL ACQUISITION CABLE o The present invention relates to physiological monitoring of patients and, in particular, to physiological signal acquisition cable which provides real time and/or simultaneous transmission of the acquired signals via a serial RS232 port.
BACKGROUND TO THE INVENTION ci Shifts in patient care, practices are changing the nature of monitoring. Increasingly, hospitals are attempting to lower costs by moving high-acuity patients as quickly as possible from intensive care units (ICU) to intermediate care and general ward areas.
This trend has dramatically reduced the need for the high end stationary, multi-parameter monitoring systems typically employed in the ICU. This has intensified demand for a more flexible, and therefore less expensive, systems that can easily be integrated into lower-acuity areas and contfigured to individual patient needs.
This is particularly the case in heart rate monitoring where the ECG is the well known form of monitoring.
In respect of foetal monitoring, the foetal heart rate (FHR) is the primary indicator of foetal viability. Current methods utilise FHR charts and are based on the detection of the mechanical activity of the heart via active ultrasound devices and interpretation by the clinician or nurse.
Foetal heart electrical activity has been analysed since the beginning of this century.
However, problems associated with the small amplitude of the foeal signals and the influence of noise, have made the foetal ECG (FECG) difficult. FECG acquired from surface electrodes have a very low amplitude and the FECG data is masked by the maternal ECG (MECG). This problem results in the requirement of expensive ultrasound analysis systems for calculating the foetal heart rate.
Therefore it is seen that inexpensive monitoring technologies are needed to enable surveillance of all pregnancies during the second and the last trimester and, in particular, to Z0I"' I) Nu. SM-I 01055837 Rcoivcd L, Ti;. 1mm) 1:22 Datc 200, 12 2.
24,' 1 2/2004 15: 13 24/2/001813Ci~vsIIIio Law 95534755 8/3S 2 o determine the appropriateness of intervention to minimise a potentia] risk to mother and C-I foetus.
Therefore it would be advantageous to provide a physiological signal acquisition apparatus CI which provides real time and/or simultaneous transmission of the acquired signals which is simpler and therefore less expensive than known apparatus.
OBJECT OF THE INVENTION S It is an object of the present invention to provide a physiological signal acquisition apparatus which substantially overcomes or ameliorates the above mentioned disadvantages. At the very least, the object of the invention is to provide an alternative: to known physiological signal acquisition apparatus.
DISCLOSURE OF THE INVENTION According to one aspect of the present invention there is disclosed a physiological signal acquisition monitoring apparatus having a bio sensor connected by cable means to an electrically isolated bio acquisition unit including a amplifying and control means which is serially connected by cable means to a display device for displaying in real time the resulting graphically representation of the physiological signal.
Preferably, the display device is a notebook PC, a palmtop PC and/or smart panel.
Preferably, the physiological signal acquisition cable monitor is used to acquire and display ECG, FECG, or to monitor blood pressure, asthma control, pacemaker monitoring, monitoring oxygen saturation, diabetes measurements, heart sounds and the like.
Preferably the bio sensor is electrodes or other pickup device.
Preferably the results are recorded by the display device as well as being shown in real time.
COMS~R D No :C!OO53 b z Tai irn H~n 1C:22 Dt (YV MT A)DMC 1224 24/12/2004 18:14 24/2/0041814Chrysi liar Law 85534755 9/38 03 o According to one aspect of the present invention there is disclosed a portable and multipurpose medical device for biological signals acquisition, display and biological data storage, said device comprising: a display and storage device a display and storage device comprising: a first housing; V) a display screen being provided on the first housing for displaying the acquired data; control means disposed within the first housing to control data acquisition options, storage of the acquired data, and other application specific furnctions of the medical device; 0 a biological signals acquisition module comprising: a second housing; a plurality of biological senisors; an analog circuit to amplify and pre-condition biological signals from the plurality of the biological sensors; a digital circuit for digitizing the biological signal and to send the biological data to said first housing; and connector means connecting the first and second housings.
Preferably, the connector means is a cable means serially connecting the first and second housings.
Preferably, the display device is a notebook PC, a pahntop PC and/or Smart panel.
Preferably, the physiological signal acquisition monitoring and display device is used to simultaneously acquire and physiological signals from a plurality of sensors measuring al least one of the group including multilead ECG, FECG, FEFG, FNG, oximetry, blood pressure whether detected by invasive or non-invasive means, respiration, temperature, phonocardiogram, tokolytic, blood glucose, pCO2, p02 and pacemaker pulses, and condition the signals and transmit data representing the signals in real time to an input/output port of the display device.
COMS ID N SSMkIOSC7 P.:0i yI1A0;aTu Nt152 ak33'YV4-22 24/12/2004 10:14 24/2/001614Ctrysi I ou Low 95534755 04 o Preferably, the circuit means includes an isolated section, a non-isolated section with an isolation barrier therebetween, the isolated section being isolated from the input/output port of the display device. The isolated section receives the signals from the sensors and amplifies and preconditions the signals into data specific to the signal type prior to transmitting the data through the isolation barrier.
Preferably, the non-isolated section receives the data transmitted through the isolation barrier and prepares the data for transmission to input/output port of the display device via an input/output interface in the first housing and a cablIe mneans to the input/output port of S the display device which is a second housing of the apparatus.
BRIEF DESCRIPTION OF THE DRAWINGS The present invention will be now be described with reference to the accompanying drawings in which: Fig. I is a perspective view of a preferred embodiment of the the apparatus of the present invention, Fig, 2 is a block diagram of the apparatus of Fig, 1, and Fig. 3 is a block diagram of another preferred embodiment of the apparatus of the present invention.
BEST MODE OF CARRYING OUT TIHE INVENTION One embodiment of a physiological signal acquisition cable monitoring apparatus 10 is illustrated in Figs. I and 2 of the drawings. The apparatus 10 preferably acquires an ECG and therefore includes electrodes or Nio sensor I 1 connected by cable 12 to an acquisition unit 13. The unit 13 includes a bio amplifier 14 and a control unit 1.5. The acquisition unit 13 is serially connected by cable 16 to a laptop display and storage device 17.
IM ID NO~ t;I-1SSZ Pc .c P Austrclia: T:'c (H-Lm) IC:22' Dht 2/ j)2Y2M 21 24/12/2004 16:15 C1rysllIou Law 95534755 11 38 0 oThe acquisition unit 13 acquires the ECG while simultaneously displaying the ECG waveform on the display of the laptop in real time. The type of display and software of the display determine the level of cardiac information to be analysed, displayed and/or recorded.
The cable 16 includes access for a power supply line 18 to the acquisition unit 13 from the laptop, a serial control data line 19 and a output serial data line 20. The cable is connected to the laptop via a RS232 serial port 21 which allows the various signals to be acquired and displayed in real time.
0The invention, however, is not limited to acquisition of ECG signals only. For example, FECG, EEG, EMG, oximetry, blood pressure whether detected by invasive or non-invasive means, respiration, temperature, phonocardiogram, tokolytic, blood glucose, pCO2, pO2 and pacemaker pulses.
A block diagram of another ECG acquisition module 30 is shown in Fig. 3. The ECG signal is collected via the sensors 31 and amplified by amplifier 32. The amplifier 32 is DC biased by the virtual ground potential produced by a virtual ground generator 33. The amplified analogue signal is fed to the input of analogue to digital converter (ADC) 34.
The ADC 12 has two control inputs (-CS and CLK) and one output Control signals -CS and CLK are supplied by the display device 17 via its serial port 21, the connector and the cable 16 to a serial port interface 35 of the ECG acquisition module The amplified analogue signal is converted into digital ECG data (DO) and sent to the display device 17 via the serial port interface 35 of the ECG acquisition module 30, the cable 16, the connector and internal circuitry of the display and storage device 17.
Digital ECG data being stored in the display device 17 are accessible for displaying, calculations and overwriting. Control and data signals flow is defined by the display device 17.
COMS D Nc: SMI D 57237 Rezcivc, bi IPAjustral;a. Tmc 2 Datc Y M 1 I,2 24 24/IZ/2004 15:15 ChrysI llou Law 9553475 12/38 6 0 o Hardware Implementation ci
(N
SThe ECG amplifier 32 is comprised of a high input impedance front stage voltage follower _(Ul a, Ulb), instrumentation amplifier U2, high pass filter (C3, R4), second amplification stage U1d and a low pass anti-aliasing filter (R7, C4).
Front stage voltage followers use popular LMC6464 operational amplifier from National C Semiconductors with input current less than InA.
Cl o It is believed that the preferred embodiment as described meets AAMI/ANSI ECG 0 recommended safety standards which will include an electrical isolation barrier 36 as seen in Fig. 3.
All digital signals are transferred via digital optical isolators. A high pass filter defines the low end of the frequency band of the acquired ECG signal at 0.05Hz. A low pass filter removes high frequency noise on the input of ADC. Frequency response of the ECG amplifier for the selected filters values is 0.05Hz 100Hz. 1 00Hz high end frequency is defined by the selected sample rate of 200Hz is in a compliance with the AAMI/ANSI ECG recommended frequency response standards.
Instrumentation amplifier INA 126 from Burr-Brown Corporation is configured for a gain of 5. DC offset voltage is calculated as VCC/Gain, where VCC 5V and Gain 5. DC offset voltage Vdc 5/5 ±500mV is well above required by the AAMI/ANSI ECG standard of minimum of ±300mV.
The ECG acquisition module 30 uses single positive voltage derived from the display device 17 serial connector.
In order to amplify bipolar AC ECG signal without distortions, input stage voltage followers and instrumentation amplifier are referenced to AMPREF voltage VCC/2 generated by the virtual ground generator Ulc.
COMS !D l'c S 015S537 R1,-c c1 by IP Austrlia: Hm) 1 :22 Datc (Y M d, 2004 1 21 2 1 24/12/2004 18:15 Chrysl llou Law 95534755 13/3B 7 0 o Second stage of the amplifier is referenced to AMPREF as well in order to bring the .output signal to the halfofADC reference voltage.
U
The gain of second amplifier stage is defined by the values R5 and R6 and set to 151.
CI Overall gain is 755.
The foregoing describes only some embodiments of the present invention, and C- modifications obvious to those skilled in the art can be made thereto without departing c- from the scope of the present invention.
0 0 c-I C S ID S M! C' M37 Rcc b A tra ,*nc 1C:2 Date d) 20OC.'- 1

Claims (7)

  1. 3. The physiological signal acquisition monitoring apparatus according to claim 1, wherein the physiological signal acquisition cable monitor is used to acquire and display ECG, FECG, or to monitor blood pressure, asthma control, pacemaker monitoring, monitoring oxygen saturation, diabetes measurements, heart sounds and the like.
  2. 4. The physiological signal acquisition monitoring apparatus according to claim 1, wherein the bio sensor is electrodes or another pickup device.
  3. 5. The physiological signal acquisition monitoring apparatus according to claim 1, wherein the results are recorded by the display device as well as being shown in real time.
  4. 6. A multipurpose medical device for biological signals acquisition, display and biological data storage, said device comprising: a display and storage device a display and storage device comprising: a first housing; a display screen being provided on the first housing for displaying the acquired data; control means disposed within the first housing to control data acquisition options, storage of the acquired data, and other application specific functions of the medical device; a biological signals acquisition module comprising: a second housing; COMS ODNo. SBMV-01D5Z2-37 7n;2;c Aut~~ ~c m) 16.2-^ tatc d)'2001 12214 24/12/2004 10:16 Chrysi Ilou Law 05534755 15/38 o a plurality of biological sensors; an analog circuit to amplify and pre-condition biological signals from the plurality of the C) biological sensors; a digital circuit for digitizing the biological signal and to send the biological data to said first housing; and connector means connecting the first and second housings.
  5. 7. A multipurpose medical device for biological signals acquisition, display and o biological data storage according to claim 6, wherein the connector means is a cable means 0 serially connecting the first and second housings. 1(1 8. A multipurpose medical device for biological signals acquisition, display and biological data storage according to claim 6, wherein the display device is a notebook PC, a palmtop PC and/or smart panel.
  6. 9. A multipurpose medical device for biological signals acquisition, display and biological data storage according to claim 6, wherein the physiological signal acquisition monitoring and display device is used to simultaneously acquire and physiological signals from a plurality of sensors measuring at least one of the group including multilead ECG, FBCG, EGC, EMG, oxitnetry, blood pressure whether detected by invasive or non-invasive means, respiration, temperature, phonocardiogram, tokolytic, blood glucose, pCO2, p02 and pacemaker pulses, and condition the signals and transmit data representing the signals in real time to an input/output port of the display device. A multipurpose medical device for biological signals acquisition, display and biological data storage according to claim 6, wherein the circuit means includes an isolated section, a non-isolated section with an isolation barrier therebetween, the isolated section being isolated from the input/output port of the display device.
  7. 11. A multipurpose medical device for biological signals acquisition, display and biological data storage according to claim 10, wherein the isolated section receives the COMS ID No SDMI-OI0ZrZ'77 foSc L, !7 .raE Tinc im) l alz Y* 2004-112 24 24/12/2004 16:1$ Chrvsililu Law 95534755 1./39 0 o signals from the sensors and amplifies and preconditions the signals into data specific to the signal type prior to transmitting the data through the isolation barrier. 12, A multipurpose medical device for biological signals acquisition, display and biological data storage according to claim 11, wherein the non-isolated section receives the data transmitted through the isolation barrier and prepares the data for transmission to input/output port of the display device via an input/output interface in the first housing and Ca cable means to the input/output port of the display device which is a second housing of C, the apparatus. CO-MS IDN.Lc:SDM 1D837 Rcz,'d P" Australia. ,irnc Date (Y 2004-'2-24
AU2004242459A 1999-05-06 2004-12-24 Physiological signal acquisition cable Abandoned AU2004242459A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2004242459A AU2004242459A1 (en) 1999-05-06 2004-12-24 Physiological signal acquisition cable

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
AUPQ0184 1999-05-06
AUPQ2257 1999-08-16
AU40941/00A AU4094100A (en) 1999-05-06 2000-05-08 Physiological signal acquisition cable
AU2004242459A AU2004242459A1 (en) 1999-05-06 2004-12-24 Physiological signal acquisition cable

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
AU40941/00A Division AU4094100A (en) 1999-05-06 2000-05-08 Physiological signal acquisition cable

Publications (1)

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AU2004242459A1 true AU2004242459A1 (en) 2005-01-20

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Family Applications (1)

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AU2004242459A Abandoned AU2004242459A1 (en) 1999-05-06 2004-12-24 Physiological signal acquisition cable

Country Status (1)

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AU (1) AU2004242459A1 (en)

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MK1 Application lapsed section 142(2)(a) - no request for examination in relevant period