WO2017072626A1 - Système et procédé pour ajuster, notifier ou arrêter automatiquement les compressions thoraciques quand une impulsion spontanée est détectée durant la réanimation cardiopulmonaire automatisée - Google Patents

Système et procédé pour ajuster, notifier ou arrêter automatiquement les compressions thoraciques quand une impulsion spontanée est détectée durant la réanimation cardiopulmonaire automatisée Download PDF

Info

Publication number
WO2017072626A1
WO2017072626A1 PCT/IB2016/056248 IB2016056248W WO2017072626A1 WO 2017072626 A1 WO2017072626 A1 WO 2017072626A1 IB 2016056248 W IB2016056248 W IB 2016056248W WO 2017072626 A1 WO2017072626 A1 WO 2017072626A1
Authority
WO
WIPO (PCT)
Prior art keywords
compression
compressions
pulse
spontaneous
person
Prior art date
Application number
PCT/IB2016/056248
Other languages
English (en)
Inventor
Jens MÜHLSTEFF
Ralph Wilhelm Christianus Gemma Rosa WIJSHOFF
Eefje Janet Hornix
Original Assignee
Koninklijke Philips N.V.
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 N.V. filed Critical Koninklijke Philips N.V.
Publication of WO2017072626A1 publication Critical patent/WO2017072626A1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H31/00Artificial respiration or heart stimulation, e.g. heart massage
    • A61H31/004Heart stimulation
    • A61H31/006Power driven
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/48Other medical applications
    • A61B5/4836Diagnosis combined with treatment in closed-loop systems or methods
    • 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
    • A61B5/0215Measuring pressure in heart or blood vessels by means inserted into the body
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/08Detecting, measuring or recording devices for evaluating the respiratory organs
    • A61B5/0809Detecting, measuring or recording devices for evaluating the respiratory organs by impedance pneumography
    • 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
    • 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]
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/72Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7235Details of waveform analysis
    • A61B5/7253Details of waveform analysis characterised by using transforms
    • A61B5/7257Details of waveform analysis characterised by using transforms using Fourier transforms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/01Constructive details
    • A61H2201/0173Means for preventing injuries
    • A61H2201/0176By stopping operation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/50Control means thereof
    • A61H2201/5007Control means thereof computer controlled
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/50Control means thereof
    • A61H2201/5058Sensors or detectors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/50Control means thereof
    • A61H2201/5058Sensors or detectors
    • A61H2201/5084Acceleration sensors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/50Control means thereof
    • A61H2201/5058Sensors or detectors
    • A61H2201/5092Optical sensor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/50Control means thereof
    • A61H2201/5097Control means thereof wireless
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2230/00Measuring physical parameters of the user
    • A61H2230/04Heartbeat characteristics, e.g. E.G.C., blood pressure modulation
    • A61H2230/045Heartbeat characteristics, e.g. E.G.C., blood pressure modulation used as a control parameter for the apparatus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2230/00Measuring physical parameters of the user
    • A61H2230/04Heartbeat characteristics, e.g. E.G.C., blood pressure modulation
    • A61H2230/06Heartbeat rate
    • A61H2230/065Heartbeat rate used as a control parameter for the apparatus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2230/00Measuring physical parameters of the user
    • A61H2230/20Blood composition characteristics
    • A61H2230/207Blood composition characteristics partial O2-value
    • A61H2230/208Blood composition characteristics partial O2-value used as a control parameter for the apparatus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2230/00Measuring physical parameters of the user
    • A61H2230/30Blood pressure
    • A61H2230/305Blood pressure used as a control parameter for the apparatus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2230/00Measuring physical parameters of the user
    • A61H2230/65Impedance, e.g. skin conductivity; capacitance, e.g. galvanic skin response [GSR]
    • A61H2230/655Impedance, e.g. skin conductivity; capacitance, e.g. galvanic skin response [GSR] used as a control parameter for the apparatus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/38Applying electric currents by contact electrodes alternating or intermittent currents for producing shock effects
    • A61N1/39Heart defibrillators
    • A61N1/3904External heart defibrillators [EHD]
    • A61N1/39044External heart defibrillators [EHD] in combination with cardiopulmonary resuscitation [CPR] therapy

Definitions

  • the following relates generally to the medical arts, medical emergency response arts, medical monitoring arts, cardiopulmonary resuscitation arts, and related arts.
  • Cardiopulmonary resuscitation is indicated for cardiac arrest and is applied by manual chest compressions and rescue breaths.
  • Current CPR guidelines call for alternating between 30 chest compressions followed by two ventilating breaths for a period of 2 min. After such a 2 min block, the electrocardiography (ECG) signal is analyzed, followed by a pulse check by manual palpation if an organized ECG rhythm has been observed.
  • ECG electrocardiography
  • the goal of CPR is to achieve return of spontaneous circulation (ROSC) in which the beating heart drives life- sustaining blood circulation.
  • ROSC spontaneous circulation
  • the quality of manual CPR chest compressions can be adversely impacted by lack of experience or skill of the emergency responder, or by the increasing exhaustion of the emergency responder if ROSC is not achieved in the first few minutes. These factors can lead to a non-uniform or too slow compression rate, and/or to shallow compressions that may be insufficient to drive life-sustaining blood circulation.
  • An automated CPR device comprises a compression robot strapped to the torso of the person in cardiac arrest.
  • the compression robot includes a piston or other actuator that delivers CPR chest compressions at a precise compression rate and with precise depth.
  • the compression robot does not tire, and can deliver high-quality CPR chest compressions essentially indefinitely.
  • the automated CPR device also frees the emergency responder to perform other tasks.
  • CPR achieves the goal of ROSC
  • the chest compressions should be stopped. Best practice recommendations vary: some recommend stopping chest compressions immediately upon detection of ROSC, while others recommend continuing compressions for up to a few tens of seconds after detection of ROSC to shortly extend the support to the recovering heart. Problems which can arise if CPR chest compressions are continued after ROSC is achieved include compression-induced cardiac re-fibrillation, or physical injury of the reviving person. Thus, it is important to quickly and accurately detect when ROSC is achieved by administered CPR and to stop chest compressions immediately or shortly after ROSC.
  • Detection of ROSC is typically done by manual palpation to detect spontaneous arterial blood pressure pulsations.
  • the carotid artery, the femoral artery or the radial artery in the wrist is usually palpated for this purpose.
  • an automated external defibrillator (AED) is connected to the unconscious person receiving first aid (which is often the case as electric shock using the AED is the appropriate response if it is determined the unconscious person is in ventricular fibrillation) then the AED will acquire ECG information.
  • the ECG is intended to detect a shockable cardiac rhythm.
  • the ECG generally does not provide reliable detection of ROSC, because cardiac electrical activity, even if organized, does not necessarily translate into physical heart contractions effective to deliver life-sustaining circulation.
  • the emergency responder In automated CPR, the emergency responder must therefore synchronize manual palpation pulse checks with pre-programmed periodic interruptions of the chest compressions delivered by the compression robot. Compared with manual CPR, this can actually increase the likelihood of failing to quickly detect ROSC, because the emergency responder may become distracted and fail to perform a pulse check during a pre-programmed compression interruption, leading to longer time intervals between pulse checks. More generally, automated compressions provide greater opportunity for the emergency responder to become distracted and fail to diligently monitor the arrested person for ROSC.
  • a cardiopulmonary resuscitation (CPR) device comprises: a compression robot configured to automatically deliver CPR chest compressions to a person; a physiological sensor configured to measure a physiological signal of the person; and an electronic processor programmed to (i) derive a spontaneous pulse representation from the physiological signal and (ii) control the compression robot based on the spontaneous pulse representation.
  • the electronic processor may be programmed to determine a pulse rate of the spontaneous pulse representation derived from the physiological signal and adjust a compression rate at which the compression robot automatically delivers CPR chest compressions to the person to a new compression rate that differs from the determined pulse rate by at least 10%.
  • the electronic processor may be programmed to control the compression robot to stop the automatic delivery of CPR chest compressions to the person if the spontaneous pulse representation satisfies a return of spontaneous circulation (ROSC) criterion, or to send an audiovisual message to the caregiver that a spontaneous pulse representation satisfying a ROSC criterion has been detected so the caregiver can decide how to proceed next.
  • ROSC return of spontaneous circulation
  • a control device for controlling a compression robot configured to automatically deliver CPR chest compressions to a person.
  • the control device comprises an electronic processor programmed to: determine a pulse rate of the person from a physiological signal measured for the person; and adjust an initial compression rate at which the compression robot automatically delivers CPR chest compressions to the person to a new compression rate that differs from the determined pulse rate by a larger amount than the initial compression rate differs from the determined pulse rate.
  • the initial compression rate differs from the determined pulse rate by less than 10% and the new compression rate differs from the determined pulse rate by at least 10%.
  • the electronic processor may be programmed to determine the pulse rate by operations including: generating a compressions signal component by fitting to the physiological signal a harmonic series whose fundamental frequency is set to the compression rate; generating a compressions- free signal component representing the spontaneous pulse by subtracting the compressions signal component from the physiological signal; and determining the pulse rate as a fundamental frequency of the compressions-free signal component.
  • a control device for controlling a compression robot configured to automatically deliver CPR chest compressions to a person.
  • the control device comprises an electronic processor programmed to determine a spontaneous pulse representation for the person from a physiological signal measured for the person, and control the compression robot to stop the automatic delivery of CPR chest compressions to the person in response to the spontaneous pulse representation satisfying a return of spontaneous circulation (ROSC) criterion, or to send an audiovisual message to the caregiver that a spontaneous pulse representation satisfying a ROSC criterion has been detected so the caregiver can decide how to proceed next in response to the spontaneous pulse representation satisfying a ROSC criterion.
  • ROSC return of spontaneous circulation
  • the electronic processor may be programmed to determine the spontaneous pulse representation by operations including: generating a compressions signal component by fitting to the physiological signal a harmonic series whose fundamental frequency is set to the compression rate; and generating the spontaneous pulse representation by subtracting the compressions signal component from the physiological signal.
  • the ROSC criterion may include a spontaneous pulse representation target criterion threshold (TROSCY e -g > a minimum required pulse amplitude threshold, a minimum required pulse rate threshold, a maximum allowed variation in pulse interval threshold, or a combination thereof.
  • the electronic processor may be programmed to control the compression robot to stop the automatic delivery of CPR chest compressions to the person one of: (1) immediately after the spontaneous pulse representation is determined to satisfy the ROSC criterion; and (2) a predefined time interval after the spontaneous pulse representation is determined to satisfy the ROSC criterion.
  • the electronic processor may be programmed to send an audiovisual message to the caregiver that a spontaneous pulse representation satisfying a ROSC criterion has been detected so the caregiver can decide how to proceed next.
  • ROSC return of spontaneous circulation
  • CPR automated cardiopulmonary resuscitation
  • Another advantage resides in providing effective detection of a spontaneous pulse during CPR chest compressions. Another advantage resides in providing effective detection of a spontaneous pulse during CPR chest compressions even when the pulse is closely synchronized with the compressions.
  • the invention may take form in various components and arrangements of components, and in various steps and arrangements of steps.
  • the drawings are only for purposes of illustrating the preferred embodiments and are not to be construed as limiting the invention.
  • FIGURE 1 diagrammatically illustrates an automated cardiopulmonary resuscitation (CPR) device as disclosed herein.
  • CPR cardiopulmonary resuscitation
  • FIGURE 2 diagrammatically illustrates an embodiment of the compression component separator of the automated CPR device of FIGURE 1.
  • FIGURE 3 diagrammatically illustrates an embodiment of the compression rate setting controller of the automated CPR device of FIGURE 1.
  • an automated cardiopulmonary resuscitation (CPR) device includes a CPR compression robot 10 comprising a motor-driven piston or other compression actuator 12 configured to be secured to the front of a torso of a person in cardiac arrest (not shown) by a harness or housing 14 that wraps around the torso.
  • the harness or housing 14 houses various internal components not visible in FIGURE 1, such as a motor for driving the compression actuator 12 and a microprocessor or microcontroller and ancillary electronics programmed to operate the compression actuator 12 to deliver CPR chest compressions at a programmed compression rate and compression force or depth, optionally with periodic interruptions of the compressions to deliver one or two rescue breaths (i.e. ventilations).
  • the automated CPR device to also include an air compressor and suitable electronics synchronizing with the CPR compression robot 10 to deliver the ventilations (alternatively, an emergency responder can deliver manual breaths during the compression interruptions).
  • the automated CPR device further includes a physiological sensor configured to measure an arterial blood characteristic whose value exhibits variations correlating with arterial blood pressure pulsations caused by a spontaneous pulse and/or by CPR chest compressions.
  • a physiological sensor configured to measure an arterial blood characteristic whose value exhibits variations correlating with arterial blood pressure pulsations caused by a spontaneous pulse and/or by CPR chest compressions.
  • FIGURE 1 Two examples of such a physiological sensor are shown in FIGURE 1 to provide illustrative examples.
  • One suitable physiological sensor is a photoplethysmography (PPG) device 20.
  • the illustrative PPG device 20 is configured as a clip (e.g. spring-biased to close) for connection to a fingertip, earlobe, or other anatomy.
  • the PPG device 20 is configured to measure a transmission PPG signal 22 indicating transmission through the tissue (e.g. fingertip or earlobe portion) probed by the PPG device 20.
  • a PPG device configured to operate in reflection mode, or a non-contact PPG imaging device such as a camera are contemplated.
  • the measured optical transmission varies as a function of arterial blood volume in the probed tissue due to light absorption by arterial blood, so that the PPG signal 22 exhibits temporal variations correlating with arterial blood pressure pulsations.
  • the PPG device 20 may be a dual-wavelength device known as a "pulse oxymeter" that is also configured to measure saturation of peripheral oxygen (Sp0 2 ) based on ratioing of the PPG signals at the two wavelengths.
  • An invasive arterial blood pressure (iABP) device 30 is also illustrated in FIGURE 1 as another example of a physiological sensor configured to measure an arterial blood characteristic whose value exhibits variations correlating with arterial blood pressure pulsations caused by a spontaneous pulse and/or by CPR chest compressions.
  • the iABP device 30 generates an iABP signal 32 that can be quantitatively correlated with arterial blood pressure (both in terms of waveform and amplitude).
  • the illustrative iABP sensor 30 comprises a saline (or other) fluid- filled invasive arterial line 34 terminated at one end by an arterial cannula or catheter configured for insertion into an artery of the person in cardiac arrest.
  • the opposite end of the arterial line 34 is connected with a pressure transducer 36 (preferably with automatic flushing).
  • a pressure bag 38 is installed to maintain a pressurized fluid column in the arterial line 32.
  • the iAPB transducer 36 outputs the iABP signal 32 that can be quantitatively correlated with arterial blood pressure (both in terms of waveform and amplitude).
  • An alternative for the iABP device with a fluid-filled line can be a catheter with a micro-tip (pressure) transducer to obtain a physiological signal of the person which reflects heart beats.
  • the automated CPR device of FIGURE 1 may include the PPG 20 but omit the iABP 30; or alternatively may include the iABP 30 but omit the PPG 20. In other embodiments both the PPG 20 and iABP 30 are provided. Moreover, these are merely illustrative examples, and replacing the illustrative sensors 20, 30 by a different physiological sensor configured to measure an arterial blood characteristic is further contemplated.
  • the PPG signal 22 or iABP signal 32 will exhibit temporal variations corresponding to CPR compressions performed by the compression robot 10, and will exhibit temporal variations corresponding to a spontaneous pulse generated by the heart once it has resumed beating. If both CPR compressions and a spontaneous pulse are present, then the PPG or iABP signal 22, 32 will exhibit a superposition of pulsations due to both chest compressions and spontaneous heart beats.
  • the automated CPR device of FIGURE 1 further includes a compression component separator 40 which processes the PPG or iABP signal 22, 32 to separate out a compressions signal component 42 and a compressions-free signal component 44, the latter being a representation of the spontaneous pulse (if any).
  • the compression component separator 40 further receives a compressions reference from which compression rate (and optionally also compression phase) information is obtained.
  • compression rate information 50 is communicated from the compression robot 10 to the compression component separator 40.
  • This compression rate information 50 may, for example, be in the form of a digital value indicating the programmed compression rate at which the compression robot 10 is delivering compressions, or may be in the form of a control signal generated by the microprocessor or microcontroller of the compression robot 10 that cycles with the delivered CPR compressions, or so forth.
  • an automated external defibrillator (AED) 52 or more advanced monitor- defibrillator is connected to the torso of the person under cardiac arrest by defibrillator pads 54, and the AED 52 is programmed to measure trans-thoracic impedance ( ⁇ ) between the defibrillator pads 54.
  • a TTI signal 56 is input from the AED 52 to the compression component separator 40.
  • the ⁇ signal 56 exhibits cycling corresponding to the CPR chest compressions delivered by the compression robot 10.
  • This embodiment leverages the AED 52, which is connected to the unconscious person under some emergency response protocols in order to deliver defibrillation shock(s) if it is determined that the person is in ventricular defibrillation, in order to perform the auxiliary function of providing the TTI signal 56 from which CPR compression rate can be determined.
  • Either one or both of the compressions signal component 42 and the compressions-free signal component 44 are optionally displayed on a display device 60, e.g. a medical monitoring device.
  • a trend line 62 of the compressions signal component 42 is displayed in parallel with a trend line 64 of the compressions-free signal component 44.
  • the compressions signal trend line 62 if displayed, can inform emergency responders of the effectiveness of CPR chest compressions delivered by the compressions robot 10.
  • the compressions-free signal trend line 64 if displayed, can inform emergency responders if a pulse is observed which may indicate the CPR has (potentially) achieved ROSC.
  • a compression rate setting controller 70 receives the compressions-free signal component 44, along with a compression rate 72 received from the compression component separator 40.
  • the compression rate 72 is, or is generated from, the compression rate information 50, 56.
  • the compression rate setting controller 70 programs the compression rate of the compression robot 10.
  • the compression component separator 40 identifies the compressions signal component 42 of the PPG or iABP signal 22, 32 as the frequency component of the PPG or iABP signal 22, 32 at the compression rate 72 (i.e. compression frequency) and its harmonics. If a spontaneous pulse is also present, it is separated into the compression-free signal component 44 if the pulse rate is sufficiently different from the compression rate.
  • the compression rate setting controller 70 operates to reduce or eliminate the likelihood that the pulse (if present) has a frequency within 10% of the compression rate 72.
  • the compression rate setting controller 70 performs a compression rate sweep 74 over a sweep range of (for example) 90-110 compressions/minute or 80-100 compressions/minute or 80-120 compressions/minute. Such a sweep may be performed periodically to ensure that if a pulse is present the compression rate is not by chance at the pulse rate.
  • a pulse rate avoidance control 76 operates to adjust the compression rate away from the pulse rate. For example, if the pulse rate is 95 beats/minute and the compression rate is 90 compressions/minute (-5% difference), then the pulse rate avoidance control 76 operates to adjust the compression rate to (for example) 110 compressions per minute (-15% difference).
  • the compression rate setting controller 70 may include a stop compressions function 80 that instructs the compression robot 10 to stop delivering CPR compressions or prompts for user input from the emergency caregiver to determine whether compressions should be continued or not.
  • the compression rate setting controller 70 outputs a compression rate setting control signal 82 to cause the compression robot 70 to perform the desired operation.
  • the compression rate setting control signal 82 may be a numeric value or continuous control signal programming the compression rate of the robot 10, or may be a binary value turning compressions on or off.
  • the stop compressions function 80 may (in addition to or instead of actually causing the robot 10 to switch off compressions) send a ROSC indicator signal 84 to cause the display component 60 to display a ROSC indicator 86.
  • FIGURE 2 an illustrative embodiment of the compression component separator 40 is described.
  • the approach of FIGURE 2 generally follows the compression component separation approach of Wijshoff et al, "Photoplethysmography-Based Algorithm for Detection of Cardiogenic Output During Cardiopulmonary Resuscitation", IEEE Trans. On Biomedical Engineering vol. 62 no. 3 pp. 909-921 (2015).
  • the iABP compression component separator 40 receives as inputs the PPG or iABP signal 22, 32 and the trans-thoracic impedance (TTI) signal 56 from the AED 56.
  • TTI trans-thoracic impedance
  • Digital signal processing (DSP) 90 is performed on the TTI signal 56 to extract the CPR compression rate 72, denoted herein as R[k].
  • the DSP 90 optionally also extracts a CPR chest compressions phase, and/or optionally also extracts an "envelope", denoted A[k], which indicates when chest compressions are interrupted (typically to perform ventilation and/or a pulse check by manual palpation).
  • DSP digital signal processing
  • the envelope A[k] may be extracted, for example, by applying a peak detector or a low-pass filter and thresholding and digitizing the peak or low-pass filtered signal.
  • the compression rate 72 can be extracted by a technique such as a Fast Fourier Transform (FFT) or other frequency-domain DSP to detect the fundamental frequency component of the ⁇ signal 56.
  • FFT Fast Fourier Transform
  • the envelope A[k] and compression rate 72 can be determined by detecting the individual compressions in the TTI signal.
  • the compression rate R[k] 72 is provided directly as the information 50 provided by the compression robot 10, in which case no DSP component 90 is needed to extract that rate.
  • the PPG or iABP signal 22, 32 is optionally pre-processed to facilitate extraction of the component(s) corresponding to blood circulation pulsations due to chest compressions and/or spontaneous beating of the heart.
  • the PPG or iABP signal 22, 32 is high-pass filtered using a high-pass filter 92 with a cut-off frequency of 0.7 Hz or lower to generate a high pass filtered PPG or iABP signal 232.
  • the cut-off frequency of the high-pass filter 92 is preferably chosen to pass the fundamental frequency component due to CPR chest compressions and (if present) spontaneous pulse while removing lower frequency components that are too low to be due to CPR chest compressions or a life-sustaining pulse.
  • a cut-off frequency of 0.3-0.7 Hz is contemplated.
  • the illustrative embodiment of the compression component separator 40 shown in FIGURE 2 employs an adaptive algorithm that estimates the CPR chest compression component 42 in the high pass filtered signal 232 by making use of the compression rate 72 determined in real-time from the compression information 50, 56 of FIGURE 1.
  • the estimate of the CPR chest compressions signal component 42 is by way of an operation 94 in which a harmonic series whose fundamental frequency is set to the CPR chest compression rate R[k] 72 is fit to the high pass filtered signal 232.
  • the compression-free signal component 44 is obtained, which is a representation of the spontaneous pulse.
  • the compressions signal component 42 i.e. cmp est [k] is modelled in the operation 94 by a harmonic signal model of N H sinusoidal harmonic components:
  • cmp est [k] A[k] Om + b m [k]sin(m(p[k]) (1) m-l
  • N H is the number of harmonic components
  • ⁇ p[/e] is an instantaneous compression phase (in radians): where again R[k] is the CPR chest compression rate 72 (in Hertz, i.e. compressions per second), T s is the sampling interval (in seconds), and ⁇ 0 is an arbitrary constant phase offset (in radians).
  • the coefficients m [/ ] and 0 m [/ ] of the harmonic series of Expression (1) can be estimated using a least mean-square (LMS) algorithm or other optimization algorithm to fit the harmonic model of Expression (1) to the high-pass filtered signal 232.
  • LMS least mean-square
  • the illustrative compression component separator 40 can detect a spontaneous pulse representation sp est [k], i.e. the compressions-free signal component 44, during CPR chest compressions. This is a representation of the spontaneous pulse in that it has the same fundamental frequency. Furthermore, if determined from the iABP, the spontaneous pulse in s Pest[k] has an amplitude that roughly correlates with pulse strength. However, in the case of the PPG signal 22, PPG does not provide quantitative blood pressure information, in that the amplitude of the compressions-free signal component 44 of the PPG signal 22 is not necessarily related to pulse strength.
  • the amplitude of the compressions-free signal component 44 of the iABP signal 32 is a blood pressure and hence is more directly related to pulse strength.
  • iABP is an invasive measurement and may not be readily available in the case of a person in cardiac arrest outside of a hospital or other in-patient medical care facility; whereas it is straightforward to clip the PPG sensor 20 to a fingertip or earlobe.
  • the fundamental frequency component of the compressions-free signal component 44 is extracted, for example by FFT or another frequency-domain DSP, or by time-domain analysis such as detecting the individual pulses or analyzing the autocorrelation.
  • the operation 100 outputs the fundamental frequency 102 and the amplitude 104 of the fundamental frequency component of the compressions-free signal component 44.
  • This fundamental frequency component 102, 104 is assumed to be a representation of the spontaneous pulse; accordingly, in an operation 106 if the operation 100 fails to detect a credible pulse then the process stops. This stoppage 106 may be triggered if the operation 100 fails entirely (e.g.
  • a call to an FFT operations returns an error) or if the amplitude 104 is too small so as to indicate the compressions-free signal component 44 is close to being flat-line, or if the fundamental frequency 102 is not a credible pulse rate (e.g. too low or too high to be physiologically plausible).
  • the fundamental frequency 102 is interpreted as a pulse rate and its amplitude 104 is interpreted as (at least roughly) corresponding to the strength of the pulse.
  • This detected spontaneous pulse representation can then be further processed.
  • the pulse rate 102 is compared with the compression rate 72, and if these two rates are within 10% (inclusive) of each other, then the pulse rate avoidance control 76 is invoked to adjust the compression rate of CPR compressions applied by the compression robot 10 to be more than 10% different from the detected pulse rate 102.
  • Table 1 provides a suitable algorithm for the compression rate adjustment to ensure the compression rate differs from the pulse rate (in beats per minute, i.e. bpm) by at least 20%.
  • the amplitude 104 is taken as a (rough) metric of pulse strength and is compared with a minimum threshold T R0SC for identifying a return of spontaneous circulation. If the amplitude 104 meets this minimum threshold in the operation 112, and if the frequency 102 exceeds a minimum rate threshold, and if the variability in spontaneous pulse interval is below a maximum threshold, then the stop compressions function 80 is executed to instruct the compression robot 10 to stop delivering CPR compressions, and/or the ROSC indicator signal 84 is sent to the display component 60 to inform emergency responders that the automated CPR device of FIGURE 1 has detected potential ROSC based on which the emergency responders can decide whether the robot should stop compressions or still continue delivering compressions.
  • the operation 112 can employ a different ROSC criterion.
  • the ROSC criterion may be a conjunctive criterion such as the amplitude 104 being greater than a minimum threshold T R0SC and the pulse rate 102 being within a chosen range and the variation in spontaneous pulse interval being below a variability threshold.
  • the ROSC criterion may, in general, be parameterized by the person's age, gender, size or weight, or other factors. Table 1
  • the stoppage may be programmed to occur immediately upon the operation 112 being satisfied so as to indicate potential ROSC, or may be delayed by a delay interval in accordance with governing CPR guidelines. For example, in some embodiments compressions are continued until a complete (2 min) CPR compression phase is finished and the emergency responder can prepare for a manual pulse check.
  • the stop compressions function 80 is executed to instruct the compression robot 10 to stop delivering CPR compressions and the physiological sensor 20, 30 continues to measure the PPG or iABP signal 22, 32 after the compressions have stopped. After the stoppage of compressions there is no any confounding compressions signal component, and so the PPG or iABP signal 22, 32 measured after the compressions have stopped provides a more accurate verification that ROSC has been achieved. On the other hand, if the measured PPG or iABP signal 22, 32 goes to a flat-line condition after the compressions have stopped then this verification fails, i.e.
  • the compression rate setting controller 70 suitably instructs the compression robot 10 to resume delivery of CPR compressions.
  • This monitoring is also contemplated to be extended to cause the compression robot 10 to start compressions whenever the measured PPG or iABP signal 22, 32 goes to a flat-line condition, so as to (for example) provide nearly immediate re-start of CPR in the event of a re-arrest.
  • the stop compressions function 80 is executed to prompt to the emergency responder that a potential ROSC has been detected and that further input is required to determine whether compressions should be stopped.
  • a trans-thoracic impedance ( ⁇ ) sensor is built into the compression robot 10 along with suitable thoracic electrodes to provide the TTI signal 56, in which case the AED 52 and defibrillator pads 54 may be omitted or not used to provide the ⁇ signal 56.
  • the compression component separator 40 may be implemented on a microprocessor or microcontroller of the compression robot 10 or on a microprocessor or microcontroller of the display device 60, or on another electronic processor.
  • the compression rate setting controller 70 may be implemented on a microprocessor or microcontroller of the compression robot 10 or on a microprocessor or microcontroller of the display device 60, or on another electronic processor. If these components 40, 70 are both integrated into the compression robot 10, or are implemented as one or more electronic processors other than the display device 60, then the display device 60 may optionally be omitted. It will also be appreciated that the functionality implemented on one or more electronic processors described herein may be embodied by a non-transitory storage medium storing instructions readable and executable by one or more electronic processors.
  • the non-transitory storage medium may, for example, comprise a magnetic disk drive or other magnetic storage medium, a flash memory or other electronic storage medium, an optical disk or other optical storage medium, or so forth.
  • each of the illustrative physiological sensors 20, 30 is shown as a discrete component, such a physiological sensor configured to measure an arterial blood characteristic may alternatively be integrated with the compression robot 10.
  • a reflection-mode PPG sensor can be built into the inside of the harness or housing 14 that wraps around the torso of the person in cardiac arrest.
  • a wired reflective or transmissive PPG sensor may be integrated with the compression robot, to allow for placement at a body site convenient for pulse detection.
  • a non-contact imaging PPG sensor such as a camera may also be integrated with the compression robot to detect spontaneous pulses.
  • another physiological sensor other than the illustrative sensors 20, 30 to assess spontaneous pulse, such as an accelerometer mounted on the torso of the person in cardiac arrest, or a radar sensor to measure spontaneous pulse through clothing.
  • the physiological sensor 20, 30 is used to automatically measure spontaneous pulse (if any) only during time intervals over which the compressions robot 10 does not deliver CPR chest compressions.
  • the information 50 from the compressions robot 10 indicates time intervals during which compressions are interrupted and the signal 22, 32 from the physiological sensor 20, 30 is used to determine the spontaneous pulse only during those interruptions.
  • the sensor signal 22, 32 is the spontaneous pulse representation (i.e.
  • the compression rate setting controller 70 suitably performs the operation 100 on the sensor signal 22, 32 directly (without the separation processing loop 94, 96 of FIGURE 2, and optionally without the high pass filter 92) to determine the pulse rate 102 and (correlative) amplitude 104, which can then be used to perform the ROSC indicator assessment operation 112 and to invoke the stop compressions function 80 as appropriate.
  • This approach advantageously rapidly detects ROSC and promptly automatically stops CPR chest compressions, albeit with a possible delay of up to one compressions block (e.g. 30 compressions in accord with some CPR guidelines).
  • the signals 22, 32, 50, 56, 42, 44, 72, 82, 84 may be transferred between different components, the signals may be communicated via any suitable communication pathway or media, e.g. via wired links, wireless links, or so forth.
  • the pulse rate avoidance control 76 may invoke various approaches, in addition to or alternative to those already described, to invoke the pulse rate avoidance control 76.
  • the pauses for ventilations can be used to perform a rapid pulse detection and pulse rate determination. If a pulse is detected and the detected pulse rate in such a pause is close to the current compression rate, then the compression rate is adjusted, for example in accord with Table 1, to facilitate monitoring of the spontaneous pulse during subsequent ongoing compressions.
  • the pulse rate avoidance control 76 adjusts the compression rate to facilitate monitoring of the spontaneous pulse during ongoing compressions.
  • CPR is continued.
  • the automated chest compression rate can be slightly adjusted, e.g. using the sweep control 74, to facilitate tracking the spontaneous pulse and its pulse rate, based on the pulse rate measured during the preceding pulse check. In this way, better decisions can be made during compressions.

Abstract

Robot de compression (10) distribuant automatiquement des compressions thoraciques de réanimation cardiopulmonaire (CPR) à une personne. Un capteur physiologique (20, 30) mesure un signal physiologique (22, 32) de la personne. Un processeur électronique (40, 70) est programmé pour dériver une représentation d'impulsion spontanée à partir du signal physiologique et commander le robot de compression sur la base de la représentation d'impulsion spontanée. Un taux d'impulsion de la représentation d'impulsion spontanée peut être déterminé, et un taux de compression du robot de compression ajusté à un nouveau taux de compression qui diffère du taux d'impulsion déterminé d'au moins 10 %. Le processeur électronique peut être programmé pour commander le robot de compression afin d'arrêter la distribution automatique de compressions thoraciques de CPR à la personne si la représentation d'impulsion spontanée satisfait un retour de critère de circulation spontanée (ROSC), ou indiquer au soignant qu'un ROSC potentiel a été détecté de telle sorte que le soignant peut déterminer s'il faut ou non arrêter ou continuer les compressions thoraciques.
PCT/IB2016/056248 2015-10-27 2016-10-18 Système et procédé pour ajuster, notifier ou arrêter automatiquement les compressions thoraciques quand une impulsion spontanée est détectée durant la réanimation cardiopulmonaire automatisée WO2017072626A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201562246783P 2015-10-27 2015-10-27
US62/246,783 2015-10-27

Publications (1)

Publication Number Publication Date
WO2017072626A1 true WO2017072626A1 (fr) 2017-05-04

Family

ID=57227011

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2016/056248 WO2017072626A1 (fr) 2015-10-27 2016-10-18 Système et procédé pour ajuster, notifier ou arrêter automatiquement les compressions thoraciques quand une impulsion spontanée est détectée durant la réanimation cardiopulmonaire automatisée

Country Status (1)

Country Link
WO (1) WO2017072626A1 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110881965A (zh) * 2018-09-11 2020-03-17 苹果公司 生理传感器的接触检测
WO2021007518A1 (fr) * 2019-07-11 2021-01-14 Zoll Medical Corporation Activation sélective de compressions thoraciques synchronisées avec l'activité myocardique
CN112423658A (zh) * 2018-07-13 2021-02-26 皇家飞利浦有限公司 用于心肺复苏的光体积描记脉搏血氧计
EP4011287A1 (fr) * 2020-12-11 2022-06-15 Koninklijke Philips N.V. Aide à la décision en réanimation cardiopulmonaire

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1079310A2 (fr) * 1999-08-27 2001-02-28 Laerdal Medical AS Système pour réduire les perturbations dans des signaux ECG , notamment les perturbations provoquées par la réanimation cardio-pulmonaire
US20100114220A1 (en) * 2004-10-25 2010-05-06 Norman A. Paradis Non-invasive device for synchronizing chest compression and ventilation parameters to residual myocardial activity during cardiopulmonary resuscitation
US20100204623A1 (en) * 2003-12-02 2010-08-12 Ideker Raymond E Methods, Systems and Computer Program Products to Inhibit Ventricular Fibrillation During Cardiopulmonary Resuscitation
US20120016279A1 (en) * 2010-07-13 2012-01-19 Banville Isabelle L Cpr chest compression machine stopping to detect patient recovery
US20120330199A1 (en) * 2010-07-02 2012-12-27 ResQSystems, Inc. Methods and systems for reperfusion injury protection after cardiac arrest
EP2883493A2 (fr) * 2013-12-16 2015-06-17 Peking Union Medical College Hospital, Chinese Academy of Medical Sciences Dispositifs et systèmes pour une reconnaissance en temps réel du rétablissement de la circulation spontanée (ROSC) dans un procédé de réanimation cardio-pulmonaire (CPR)
WO2015095729A1 (fr) * 2013-12-19 2015-06-25 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Systèmes automatiques de compression thoracique incorporant une rétroaction biologique
WO2015121114A1 (fr) * 2014-02-11 2015-08-20 Koninklijke Philips N.V. Détermination de retour de circulation spontanée pendant une rcp

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1079310A2 (fr) * 1999-08-27 2001-02-28 Laerdal Medical AS Système pour réduire les perturbations dans des signaux ECG , notamment les perturbations provoquées par la réanimation cardio-pulmonaire
US20100204623A1 (en) * 2003-12-02 2010-08-12 Ideker Raymond E Methods, Systems and Computer Program Products to Inhibit Ventricular Fibrillation During Cardiopulmonary Resuscitation
US20100114220A1 (en) * 2004-10-25 2010-05-06 Norman A. Paradis Non-invasive device for synchronizing chest compression and ventilation parameters to residual myocardial activity during cardiopulmonary resuscitation
US20120330199A1 (en) * 2010-07-02 2012-12-27 ResQSystems, Inc. Methods and systems for reperfusion injury protection after cardiac arrest
US20120016279A1 (en) * 2010-07-13 2012-01-19 Banville Isabelle L Cpr chest compression machine stopping to detect patient recovery
EP2883493A2 (fr) * 2013-12-16 2015-06-17 Peking Union Medical College Hospital, Chinese Academy of Medical Sciences Dispositifs et systèmes pour une reconnaissance en temps réel du rétablissement de la circulation spontanée (ROSC) dans un procédé de réanimation cardio-pulmonaire (CPR)
WO2015095729A1 (fr) * 2013-12-19 2015-06-25 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Systèmes automatiques de compression thoracique incorporant une rétroaction biologique
WO2015121114A1 (fr) * 2014-02-11 2015-08-20 Koninklijke Philips N.V. Détermination de retour de circulation spontanée pendant une rcp

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
RALPH W. C. G. R. WIJSHOFF ET AL: "Photoplethysmography-Based Algorithm for Detection of Cardiogenic Output During Cardiopulmonary Resuscitation", IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, vol. 62, no. 3, 1 March 2015 (2015-03-01), pages 909 - 921, XP055181684, ISSN: 0018-9294, DOI: 10.1109/TBME.2014.2370649 *
WIJSHOFF ET AL.: "Photoplethysmography-Based Algorithm for Detection of Cardiogenic Output During Cardiopulmonary Resuscitation", IEEE TRANS. ON BIOMEDICAL ENGINEERING, vol. 62, no. 3, 2015, pages 909 - 921, XP055181684, DOI: doi:10.1109/TBME.2014.2370649

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112423658A (zh) * 2018-07-13 2021-02-26 皇家飞利浦有限公司 用于心肺复苏的光体积描记脉搏血氧计
CN110881965A (zh) * 2018-09-11 2020-03-17 苹果公司 生理传感器的接触检测
CN110881965B (zh) * 2018-09-11 2022-10-04 苹果公司 生理传感器的接触检测
US11478193B2 (en) 2018-09-11 2022-10-25 Apple Inc. Contact detection for physiological sensor
US11484267B2 (en) 2018-09-11 2022-11-01 Apple Inc. Contact detection for physiological sensor
WO2021007518A1 (fr) * 2019-07-11 2021-01-14 Zoll Medical Corporation Activation sélective de compressions thoraciques synchronisées avec l'activité myocardique
EP4011287A1 (fr) * 2020-12-11 2022-06-15 Koninklijke Philips N.V. Aide à la décision en réanimation cardiopulmonaire
WO2022122539A1 (fr) * 2020-12-11 2022-06-16 Koninklijke Philips N.V. Aide à la décision en matière de réanimation cardio-pulmonaire

Similar Documents

Publication Publication Date Title
US11660249B2 (en) CPR chest compression machine stopping to detect patient recovery
US11129560B2 (en) Systems and methods for filtering ECG artifacts
EP3313268B1 (fr) Détermination du retour de la circulation spontanée pendant la réanimation cardio-respiratoire
US20220280378A1 (en) Assisting a cpr treatment
US9216001B2 (en) Pulse detection using patient physiological signals
US11179570B2 (en) Pacing device with acoustic sensor
CN107257653B (zh) 用于处理用在对对象的生命体征进行监测中的加速度计信号的处理设备、系统和方法
WO2017072626A1 (fr) Système et procédé pour ajuster, notifier ou arrêter automatiquement les compressions thoraciques quand une impulsion spontanée est détectée durant la réanimation cardiopulmonaire automatisée
EP3104771A1 (fr) Détermination de retour de circulation spontanée pendant une rcp
US11911336B2 (en) Detection of myocardial contractions indicative of perfusion
EP3432981A1 (fr) Procédé et appareil permettant de déterminer l'état hémodynamique
WO2017072055A1 (fr) Système et procédé de surveillance d'impulsion spontanée et de compressions au moyen de la pression artérielle endovasculaire pendant une réanimation cardio-pulmonaire
US11439568B2 (en) Smart prompting to improve responders CPR performance
US20210045967A1 (en) System and method for optimization of cpr chest compressions
CN115702981A (zh) 一种用于心肺复苏的转复识别方法及系统、设备和除颤仪
CN117062651A (zh) 用于起搏装置的控制器
US20240041381A1 (en) Arrhythmia detection in a wearable medical system
EP4251265A2 (fr) Analyse d'électrocardiogramme à segments mixtes en coordination avec une réanimation cardio-respiratoire pour une électrothérapie de défibrillation efficace

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 16790710

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 16790710

Country of ref document: EP

Kind code of ref document: A1