EP2549926A1 - Interference reduction in monitoring a vital parameter of a patient - Google Patents

Interference reduction in monitoring a vital parameter of a patient

Info

Publication number
EP2549926A1
EP2549926A1 EP11716043A EP11716043A EP2549926A1 EP 2549926 A1 EP2549926 A1 EP 2549926A1 EP 11716043 A EP11716043 A EP 11716043A EP 11716043 A EP11716043 A EP 11716043A EP 2549926 A1 EP2549926 A1 EP 2549926A1
Authority
EP
European Patent Office
Prior art keywords
light
channels
dark
signal
multiplexing
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
EP11716043A
Other languages
German (de)
English (en)
French (fr)
Inventor
Jeroen Veen
Theodorus Petrus Henricus Gerardus Jansen
Steven Antonie Willem Fokkenrood
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Koninklijke Philips NV
Original Assignee
Koninklijke Philips Electronics NV
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 Koninklijke Philips Electronics NV filed Critical Koninklijke Philips Electronics NV
Priority to EP11716043A priority Critical patent/EP2549926A1/en
Publication of EP2549926A1 publication Critical patent/EP2549926A1/en
Ceased legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/1455Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using optical sensors, e.g. spectral photometrical oximeters
    • A61B5/14551Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using optical sensors, e.g. spectral photometrical oximeters for measuring blood gases
    • A61B5/14552Details of sensors specially adapted therefor

Definitions

  • the invention relates to the field of light attenuation measurements, and especially to a method of and a device for monitoring a vital parameter of a patient by measuring attenuation of light emitted onto tissue of the patient.
  • the measurement of light absorption and/or scattering when propagating through or reflecting from a certain medium forms the basis of a number of optical spectroscopic methods widely applied in various medical domains, such as patient monitoring.
  • One illustrative example is transmissive pulse oximetry.
  • Pulse oximetry is an optical method for non- invasive monitoring of arterial oxygen saturation of a patient and has become one of the most commonly used techniques in clinical practice.
  • the protein haemoglobin (Hb) binds oxygen in the red blood cells for transport through the body, and has the property of changing from dark red to bright red in color when oxygenated.
  • pulse oximeters determine the light absorbance in a peripheral vascular bed to arrive at an indirect estimate of oxygen saturation, i.e. the concentration fraction of oxyhaemoglobin (Hb0 2 ).
  • Pulse oximeters rely on the changes in arterial blood volume caused by cardiac contraction and relaxation to determine the amount of light absorbed by pulsating arterial blood alone, thereby largely factoring out the contributions of tissue and venous blood.
  • TDM time division multiplexing
  • FDM frequency division multiplexing
  • CDM code division multiplexing
  • light attenuation measurements applied in e.g. patient monitoring suffer from electromagnetic interference.
  • interference comprises ambient light at various optical wavelengths and with different modulation frequencies.
  • Common examples include natural daylight, which is typically not modulated, as well as artificial light from incandescent lamps, which is modulated at the double mains frequency (100 Hz or 120 Hz) and 50 Hz or 60 Hz harmonics, and from fluorescent lamps with flicker rates ranging from tens to hundreds of kilohertz depending on the specific electric ballast.
  • spectrometric devices measures are taken to mitigate the effect of external interference on the measurements.
  • the light sources are modulated such that at the photo detector the emitted light can be distinguished from ambient light by filtering or demodulation.
  • conventional methods rely on knowledge of the spectral modulation of the environmental light and assume that the light source modulation frequency or band that is used can remain fixed for the lifetime of the device.
  • the ambient light modulation spectrum is only partly known or not known a priori, such as is the case when the spectrometric device operates in the vicinity of light communication systems, then interference may be present in the modulation spectrum of the detected light at the device operation frequency.
  • new operation schemes of high- intensity discharge (HID) lamps might result in an interference signal with a wide frequency range. If an interferer contaminates the operation frequency band, the signal-to- interference ratio (SIR) may decrease to a large extent, thereby degrading the measurement quality.
  • SIR signal-to- interference ratio
  • a method of monitoring a vital parameter of a patient by emitting light onto tissue of the patient with at least one light source and collecting light which is transmitted through the tissue and/or which is reflected from the tissue comprising the following steps:
  • patient does not only refer to diseased persons but to all human beings and animals, no matter whether healthy or not.
  • light which is transmitted through the tissue or/and which is reflected from the tissue, is collected which is necessary for the attenuation measurement in order to monitor the vital parameter of the patient.
  • this light it cannot totally be avoided to collect at least some ambient light, too. This collected ambient light can cause interferences.
  • a dark detection channel i.e. a detection channel which is at least temporarily not used for spectrometric purposes, to reduce interferences caused by ambient light or other sources influencing the detection signals.
  • this method is used for pulse oximetry.
  • the invention does not only apply to pulse oximetry, but can also be used for other spectroscopic methods for monitoring a vital parameter of a patient where a dark channel can be assigned, and where interference components present in the dark channel output relate in some way to the interference components in the other outputs.
  • the dark channel output can therefore be used as a reference for reduction of interference components in another channel.
  • the signal of the dark detection channel could be directly used as the reference signal.
  • the signal of the dark detection channel is adaptively filtered, and the reference signal is preferably subtracted from the signal of the at least one of the other detection channels.
  • LMS least-mean-squares
  • x(k-N+l) is the reference signal vector, taken from a dark detection channel
  • d(k) x(k) - w (k)x(k) is the difference of the channel/detector signal and the filtered reference.
  • the output of the subtraction is d(k), giving the result of the light extinction measurement for the light source, but from which the interference is removed.
  • the adaptation constant determines the convergence speed of the algorithm as well as the final misadjustment and can be
  • the signals of the detection channels can be processed without any pre- processing. However, according to an embodiment of the invention, the signals of the respective detection channels are low-pass filtered. In this way, reduction out-of-band signals can be achieved.
  • one dark channel is assigned continuously and interference reduction is activated continuously.
  • the interference level is estimated on the basis of the dark detection channel signal and/or the reference signal, and the signal of the dark detection channel is used for generating the reference signal for reducing interference of the at least one of the other detection channels only when the interference level exceeds a predefined threshold.
  • a plurality of light sources is provided for emitting light of different wavelengths.
  • a plurality, preferably all, of the multiplexing channels are consecutively arranged to be the dark channel for which no light is emitted by the at least one light source, respectively, resulting in an alternately changing dark detection channel.
  • one of the light sources can be switched off periodically, thus creating a dark channel periodically.
  • any of the channels can become the dark channel by switching off the respective light source. If the dark channel is rotated among the channels, still spectrometric information for all wavelengths can be obtained while reducing interference.
  • the structure can be expanded to take multiple reference inputs.
  • a device for monitoring a vital parameter of a patient comprising:
  • At least one light source for emitting light onto tissue of the patient
  • At least one light detector for collecting light which is transmitted through the tissue and/or which is reflected from the tissue
  • a multiplexer adapted for multiplexing the emitted light according to a predefined multiplexing scheme having a plurality of multiplexing channels, wherein at least one of the multiplexing channels is a dark multiplexing channel for which no light is emitted by the at least one light source;
  • a plurality of detection channels being connected to the least one light detector and being adapted for detecting the collected light according to the predefined multiplexing scheme, wherein at least one of the detection channels relating to the at least one dark multiplexing channels is a dark detection channel;
  • a reference signal generator adapted for using the signal of the dark detection channel as a reference signal for reducing interference in the signal of at least one of the other detection channels.
  • the device is adapted for emitting light with at least two different wavelengths, e.g. by comprising two different light sources. Further, it is especially preferred that the device comprise a pulse oximeter.
  • the reference signal generator can be designed in different ways.
  • the reference signal generator comprises an adaptive filter which is adapted for adaptively filtering the signal of the dark channel for generating the reference signal.
  • a subtractor is provided which is adapted for subtracting the reference signal from the at least one of the other detection channels.
  • the device comprises a low-pass filter which is adapted for filtering the signals of the respective detection channels. In this way out-of-band signals can be reduced and, thus, to a certain degree excluded from further processing. It is preferred that the device comprises a plurality of light sources for emitting light of different wavelengths, respectively. Moreover, it is preferred that a common light detector for all detection channels is provided. According to a preferred embodiment of the invention, the adaptive filter is adapted to provide the reference signal based on a least-mean-square algorithm. This has shown to be advantageous to many applications of the invention, since the least-mean square algorithm is especially useful to significantly reduce interferences from the signal coming from a light detector without reducing the information content relevant to the monitoring of a vital parameter of a patient.
  • Fig. 1 shows a typical setup for transmission pulse oximetry
  • Fig. 2 depicts a generalized block diagram of a transmission pulse oximetry method according to an embodiment of the invention
  • Fig. 3 shows a demodulator with a periodic square wave reference signal
  • Fig. 4 shows a block diagram of a four-channel device for monitoring a vital parameter of a patient
  • Fig. 5 shows a comparison of an original signal and a signal from which the interference is removed
  • Fig. 6 shows a further a comparison of an original signal and a signal from which the interference is removed.
  • Figure 1 shows a typical setup for transmission pulse oximetry: A red light source 1 and an infrared (IR) light source 2 are used for irradiating red light of 660 nm and IR light of 940 nm onto tissue of a patient, respectively, i.e. onto a finger 3. The part of the light which is transmitted through the finger 3 is then collected with a common light detector 4.
  • IR infrared
  • FIG. 2 depicts a general block diagram of a transmission pulse oximeter.
  • the system comprises a processing unit 5 that adjusts the parameters of a light modulator 6 which acts a multiplexer and a pulse controller and modulates the light sources 1, 2.
  • a light modulator 6 which acts a multiplexer and a pulse controller and modulates the light sources 1, 2.
  • the configuration of the light modulator 6 depends on the specific multiplexing scheme applied, e.g. in case of TDM the light sources 1, 2 are activated alternatingly, whereas for FDM the light sources 1, 2 radiate light simultaneously but with different modulation frequencies.
  • the reason for applying such a multiplexing scheme is that in this way the single light detector 4 can be used to estimate the attenuation of the light from both light sources 1 , 2.
  • the light detector 4 detects the light that has propagated through the finger 3 and converts it into an electrical signal.
  • This signal is then pre-processed by a signal- conditioning block 8, which comprises analog amplifiers and band-pass filters, which make the signal suitable for conversion to the digital domain by an analog-to-digital converter (ADC) 9.
  • Correlators 10 each comprising a demodulator 1 1 and a demultiplexer 12, are used to simultaneously demodulate and demultiplex the detected light, and the results are presented to the processing unit 5, which determines the parameters of interest by evaluating the transmitted and demodulated signals.
  • Figure 3 shows a demodulator 1 1 with a periodic square wave reference signal.
  • Figure 3 depicts a generic operational scheme; the exact implementation of the functionality can be optimized for the specific modulation scheme being applied. It should be noted that the square wave in Fig. 3 is only illustrative, as any periodic signal can be applied to both modulate the light sources and demodulate the received signal as long as the fundamental frequencies and/or harmonics coincide.
  • Figure 4 shows a block diagram of a four-channel device for monitoring a vital parameter of a patient according to an embodiment of the invention.
  • Fig. 4 shows an example where four detection channels 16, 17, 18, 19 are available, but only three detection channels 16, 17, 18 are in use for spectrometric measurement and the fourth detection channel 19 is used as the reference for interference reduction. During the time-slot assigned to the fourth detection channel 19, no light source is active.
  • the fundamental frequency is shifted by 90° in a shifting device 20.
  • the output of the dark detection channel 19 feeds to adaptive filters 14 to provide a reference signal such that when subtracted from the signal of one of the other detection channels 16, 17, 18, interference for these signals is reduced.
  • the adaptive filter 14 is based on a least-mean-square algorithm, but the method according to the invention is by no means limited to this adaption.
  • a subtracter 15 the reference signal is subtracted from the signal coming from the detection channels 16, 17, 18.
  • the use of a low pass filter 13 is an optional feature. It should be noted that the subtractor 15 can also be fed with the signals directly after the demodulator 11.
  • one dark detection channel is assigned continuously, and the subtractor 15 is activated continuously, or becomes active when a certain interference level is detected in the dark channel output.
  • one of the light sources 1 , 2 is switched off periodically, thus creating a dark channel periodically, and the output is used as an input for the adaptive filter 14 only if significant interference is present in the dark channel.
  • any of the channels can become the dark channel by switching off a respective light source. If the dark channel is switched among the channels, still spectrometric information for all wavelengths can be obtained while interference is reduced.
  • the structure can be expanded to take multiple reference inputs.
  • Figure 5 shows an examplatory measurement result taken from a pulse oximeter front-end.
  • a large 100 Hz interference pulse pattern was deliberately applied to the instrument.
  • Some of the harmonics of the interference coincided with harmonics of the 275 Hz pulse wave used as the demodulation reference, and as a result the channel outputs contain interference originating from 100 Hz harmonics.
  • one of the original channel outputs is depicted as a thin line.
  • One dark channel was assigned and its output was taken as the reference for an LMS algorithm with a 64 tap weight vector, and the result of reduction is shown as a thick line.
  • the algorithm is able to suppress the interference component in the channel by 20 dB, such that it is close to the background noise level. Is should be noted that the signals are DC free because of a high-pass filter applied to the channel output in this case.
  • Figure 6 shows a measurement result under the same conditions as in Fig. 5, but contrary to the case shown in Fig. 5, now the pulse oximeter probe was attached to a human finger.
  • the pulsating wave form caused by the blood volume pulse is clearly present in the output processed according to the inventive method (thick line), whereas in the original output (thin line) the signal is swamped by interference.
  • the interference was no longer present and the inventive device stopped working, then both signals being equal.

Landscapes

  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biomedical Technology (AREA)
  • Medical Informatics (AREA)
  • Biophysics (AREA)
  • Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Optics & Photonics (AREA)
  • Molecular Biology (AREA)
  • Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
  • Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
EP11716043A 2010-03-23 2011-03-16 Interference reduction in monitoring a vital parameter of a patient Ceased EP2549926A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP11716043A EP2549926A1 (en) 2010-03-23 2011-03-16 Interference reduction in monitoring a vital parameter of a patient

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP10157293 2010-03-23
EP11716043A EP2549926A1 (en) 2010-03-23 2011-03-16 Interference reduction in monitoring a vital parameter of a patient
PCT/IB2011/051100 WO2011117780A1 (en) 2010-03-23 2011-03-16 Interference reduction in monitoring a vital parameter of a patient

Publications (1)

Publication Number Publication Date
EP2549926A1 true EP2549926A1 (en) 2013-01-30

Family

ID=44262953

Family Applications (1)

Application Number Title Priority Date Filing Date
EP11716043A Ceased EP2549926A1 (en) 2010-03-23 2011-03-16 Interference reduction in monitoring a vital parameter of a patient

Country Status (4)

Country Link
EP (1) EP2549926A1 (ja)
JP (1) JP6184318B2 (ja)
CN (1) CN102811663A (ja)
WO (1) WO2011117780A1 (ja)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103479363B (zh) * 2013-09-30 2015-03-18 深圳市倍轻松科技股份有限公司 血液中血氧饱和度的测量方法及系统
JP6450085B2 (ja) * 2014-04-14 2019-01-09 フェムトディプロイメンツ株式会社 健康状態検査装置
WO2018029127A1 (en) 2016-08-12 2018-02-15 Koninklijke Philips N.V. Sensor device and method, device and method for communication with the sensor device
CN109561860A (zh) * 2016-08-12 2019-04-02 皇家飞利浦有限公司 传感器设备和方法、用于与传感器设备通信的设备和方法
EP3581092A1 (en) * 2018-06-12 2019-12-18 Koninklijke Philips N.V. System and method for determining at least one vital sign of a subject
EP3581091A1 (en) * 2018-06-12 2019-12-18 Koninklijke Philips N.V. System and method for determining at least one vital sign of a subject

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5632272A (en) * 1991-03-07 1997-05-27 Masimo Corporation Signal processing apparatus
US6606511B1 (en) * 1999-01-07 2003-08-12 Masimo Corporation Pulse oximetry pulse indicator

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04166133A (ja) * 1990-10-31 1992-06-12 A & D Co Ltd 光学式血液測定装置
WO1992015955A1 (en) * 1991-03-07 1992-09-17 Vital Signals, Inc. Signal processing apparatus and method
JP3291581B2 (ja) * 1994-02-14 2002-06-10 日本光電工業株式会社 酸素飽和度測定装置および信号処理方法
JP2001008908A (ja) * 1999-06-28 2001-01-16 Omron Corp 電子血圧計
US6397092B1 (en) 1999-12-17 2002-05-28 Datex-Ohmeda, Inc. Oversampling pulse oximeter
WO2002096288A1 (en) * 2001-05-29 2002-12-05 Reproductive Health Technologies, Inc. System for detection and analysis of material uterine, maternal and fetal cardiac and fetal brain activity
JP2002367298A (ja) * 2001-06-05 2002-12-20 Sony Corp ノイズキャンセラー装置及びノイズキャンセル方法
EP1485015A1 (en) * 2002-02-22 2004-12-15 Datex-Ohmeda, Inc. Cepstral domain pulse oximetry
US7343186B2 (en) * 2004-07-07 2008-03-11 Masimo Laboratories, Inc. Multi-wavelength physiological monitor
CN100362963C (zh) * 2004-08-05 2008-01-23 香港理工大学 可进行运动补偿的便携式保健监测装置及其补偿方法
CN1309344C (zh) * 2004-11-08 2007-04-11 中国科学院物理研究所 应用于心磁噪声抑制的自适应数字滤波方法
CN101422362A (zh) * 2008-12-09 2009-05-06 华南理工大学 具有运动伪差消除功能的无线心电监护系统
CN100589759C (zh) * 2008-12-19 2010-02-17 北京航空航天大学 一种血氧饱和度检测方法
CN101627902B (zh) * 2009-07-15 2011-12-28 深圳先进技术研究院 基于环境光的低功耗、高精度光电容积描记信号前端处理模块

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5632272A (en) * 1991-03-07 1997-05-27 Masimo Corporation Signal processing apparatus
US6606511B1 (en) * 1999-01-07 2003-08-12 Masimo Corporation Pulse oximetry pulse indicator

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2011117780A1 *

Also Published As

Publication number Publication date
JP6184318B2 (ja) 2017-08-23
JP2013530728A (ja) 2013-08-01
WO2011117780A1 (en) 2011-09-29
CN102811663A (zh) 2012-12-05

Similar Documents

Publication Publication Date Title
EP2285271B1 (en) Monitoring a vital parameter of a patient with "in-situ" modulation scheme to avoid interference
EP2549926A1 (en) Interference reduction in monitoring a vital parameter of a patient
US8676542B2 (en) Adaptive filtering for more reliably determining physiological parameters
US4846183A (en) Blood parameter monitoring apparatus and methods
US8676286B2 (en) Method and apparatus for reducing coupling between signals in a measurement system
US7400919B2 (en) Oximeter ambient light cancellation
JP3710570B2 (ja) 医療用モニタ方法
US20040054269A1 (en) Pulse oximeter
US7403806B2 (en) System for prefiltering a plethysmographic signal
CN104507381B (zh) 光电体积描记设备和方法
US8295901B2 (en) Spectral analysis for a more reliable determination of physiological parameters
MXPA06010306A (es) Seleccion de ponderaciones de promediacion de conjuntos para un oximetro de pulso basada en metricas de calidad de senal.
JP2002511291A (ja) パルス式計測システムにおける信号復調方法および装置
EP0761159A2 (en) Apparatus for medical monitoring, in particular pulse oximeter
US20100292593A1 (en) Spread-spectrum method for determining physiological parameters
JP7261736B2 (ja) 生理学的情報を感知するためのセンサ装置及び方法、センサ装置との通信のための装置及び方法
WO2018029127A1 (en) Sensor device and method, device and method for communication with the sensor device
JP2551059B2 (ja) 非観血血中色素測定装置

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20121023

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: KONINKLIJKE PHILIPS N.V.

17Q First examination report despatched

Effective date: 20150610

REG Reference to a national code

Ref country code: DE

Ref legal event code: R003

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 20170824