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    • 专利摘要:
    The invention relates to a method for monitoring physiological signals, comprising the steps of: acquiring samples of at least one digitized physiological signal, using equipment (DPR, E1, E2) carried by a user, detecting by the equipment events in the digitized physiological signal and extracting by the equipment the characteristics of the detected events, searching the equipment for an anomaly in the events and characteristics of the events extracted, transmitting over a wireless link in encrypted form , the physiological signal digitized by the equipment to a server via a mobile terminal (MP), when an anomaly is detected, otherwise the digitized physiological signal is erased by the equipment.
    公开号:FR3043902A1
    申请号:FR1502422
    申请日:2015-11-19
    公开日:2017-05-26
    发明作者:David Coulon；Jean Michel Tarlet
    申请人:@health；
    IPC主号:
    专利说明:

    METHOD AND SYSTEM FOR ACQUIRING AND ANALYZING DATA
    Physiological
    The present invention relates to systems for acquiring and monitoring physiological signals such as signals relating to cardiac and pulmonary activity, and body temperature. Typically, monitoring of cardiac activity is done by placing electrodes on the patient's skin, amplifying and recording the electrical signals provided by the electrodes. The recording of these electrical signals makes it possible to constitute an electrocardiogram (ECG) representative of the electrical activity of the patient's heart. Today, ECGs are commonly used to detect a number of pathologies that can affect the heart.
    There are portable devices for chronological monitoring and recording of ECG data. Some of these devices are arranged in a holter-type housing, designed to be worn by the patient, for example attached to his belt, this housing being connected by wires to electrodes disposed on the skin of the patient. These devices thus make it possible to record the cardiac activity during the day without disturbing the usual activities of the patient. The recorded data can then be analyzed offline to establish a medical diagnosis of the patient. These devices therefore have the major disadvantage of not allowing real-time monitoring of the patient's condition. Indeed, many conditions related to a cardiac disorder could be avoided if the cardiac abnormality was detected and treated in time. These devices are also relatively heavy and bulky, and the electrodes can easily be torn off inadvertently, so that they can not be worn especially during sleep periods of the patient.
    There are also devices in the form of a wristwatch, designed to be worn permanently especially during a sports activity. However, these devices are generally limited to the acquisition and display of heart rate, this information is insufficient to detect certain pathologies of the heart.
    It has already been proposed to transmit ECG data or data extracted from ECG data, such as heart rate data, from a small acquisition box to a mobile terminal such as a smartphone. using a wireless link, for example of the Bluetooth type. The telecommunication functions of the mobile terminal can be exploited to transmit these data to a medical monitoring center. However, for reasons of economy of the battery of the acquisition device and the mobile terminal in particular, it is desirable to limit the amount of data thus transmitted. This constraint is also intended to allow many patients to transmit ECG data to the same monitoring center, without the need for excessive transmission and storage of data in the monitoring center. Thus, when ECG data do not detect any pathology, either because they correspond to a normal ECG signal, or because they are too disturbed, it is not necessary to transmit them to the center of the ECG. monitoring. However, it is advisable to avoid the so-called "false-negative" cases where ECG data would be wrongly discarded and therefore not transmitted to the monitoring center, or not recorded locally by the device worn by the patient, in case of temporary impossibility. to transmit the ECG data to the monitoring center. It is also desirable to limit the amount of ECG data transmitted to the monitoring center for analysis by a human operator, in order to limit the amount of ECG data to be analyzed and thus limit the number of human operators required, loaded to manually analyze ECG data.
    It is therefore desirable to allow the acquisition of physiological signals of sufficiently good quality to allow the establishment of a reliable diagnosis of the health status of a patient. It is also desirable that this acquisition of physiological signals can be carried out for long periods of time greater than one day, and preferably over several days, so as to be able to constantly monitor the state of health of a patient. It is also desirable that the device responsible for acquiring the physiological signals can be easily installed on a patient for several days, without disturbing its well-being, especially during sleep periods, and is compatible with all the current activities, and particularly the practice of sports activities.
    It may also be desirable to process physiological signals in real time to detect abnormalities that may reveal a pathology, and to transmit them to a monitoring center only when such an abnormality is likely to be detected. It may also be desirable for this anomaly detection to be performed by avoiding false-negative cases and limiting false-positive cases.
    Embodiments provide a method of monitoring physiological signals, comprising: acquiring samples of at least one digitized physiological signal, using user-worn equipment, detecting by the equipment of events in the digitized physiological signal and extracting from the equipment the characteristics of the detected events, searching the equipment for an anomaly in the events and characteristics of the events extracted, and transmitting over a wireless link in encrypted form the digitized physiological signal by the equipment to a server via a mobile terminal, when a fault is detected or when a reinforced monitoring mode is activated, otherwise the digitized physiological signal is erased by the equipment.
    According to one embodiment, the method comprises steps of: acquiring an impedance variation signal between electrodes in contact with the skin of the user, comparing the impedance variation signal with a threshold value, transmitting a notification to the user via the mobile terminal to inform him that the electrodes are not in contact with his skin, when the impedance variation signal does not exceed the threshold value, and extracting a user breathing rate from the impedance variation signal, when the impedance variation signal exceeds the threshold value.
    In one embodiment, the method includes steps of comparing the respiratory rate with low and high threshold values, and detecting an abnormality if the respiratory rate is not between the low and high threshold values.
    According to one embodiment, the event characteristics detected in the digitized physiological signal comprise parameters extracted from the digitized physiological sign, an anomaly being detected if one of the extracted parameters does not belong to a window centered on an average value of one. corresponding parameter extracted from a digitized reference signal.
    According to one embodiment, the method comprises a step of determining a processing priority level of a detected anomaly, among two levels of priorities, the higher priority level anomalies being presented on an operator terminal before lower priority level anomalies.
    According to one embodiment, the digitized physiological signal comprises an electrocardiogram signal, the detected events are R, P, Q, S and T pulses, and the characteristics extracted from the events are relative to the respective amplitudes of these pulses and / or the duration of the time intervals between these pulses.
    According to one embodiment, the pulses R are detected in the digitized physiological signal by comparing the electrocardiogram signal with a threshold value, and the pulses P, Q, S and T are sought in windows determined from a moment of detection of a pulse R.
    According to one embodiment, the method comprises steps of: determining a heart rate by counting the number of R pulses per unit of time, an anomaly being detected if the measured heart rate has an instability greater than a first value of instability threshold, or if the measured heart rate is not between first and second heart rate threshold values, and / or steps of: determining a duration between the Q and S pulses, and comparing the duration between pulses Q and S at a threshold value of time between pulses Q and S, an anomaly being detected if the duration between pulses Q and S is greater than the threshold value of duration between pulses Q and S , and / or steps of: determining a duration between the P and R pulses, comparing an instability of the duration between the P and R pulses to a second instability threshold value, comparing the duration between the pulses P and R with two values of the threshold of duration between the pulses P and R, and detection of an anomaly if the instability of the duration between the pulses P and R is greater than the second value of instability threshold, or if the duration between pulses P and R is not between the two threshold values of duration between P and R pulses.
    According to one embodiment, the method comprises the steps of: detection by the event server in the digitized physiological signal received, and extraction by the server of characteristics of the detected events, search by the server for an anomaly in the events and the characteristics of the extracted events, and transmission by the server of the digitized physiological signal received at an operator terminal when an anomaly is detected by the server.
    According to one embodiment, the method comprises steps of: reconstitution and display of the physiological signal by an operator terminal from the digitized physiological signal received by the server, and transmission to the mobile terminal of a notification sent by the terminal of the operator, relating to the physiological signal displayed on the display screen, and transmission of the notification to the user by means of the mobile terminal.
    According to one embodiment, the notifications transmitted by the operator terminal to the mobile terminal comprise at least one of the following elements: an activation command of the reinforced surveillance mode which is transmitted from the mobile terminal to the equipment, equipment transmitting the digitized physiological signal upon receipt of the activation command and as long as the enhanced surveillance mode is activated, a notification to be transmitted from the mobile terminal to the user to inform the user that he must consult his doctor, a notification to transmit the mobile terminal to the user to inform the user that he must wait for help or go to the hospital urgently, and a notification containing anomaly detection parameters in the events and the extracted event characteristics, which is transmitted from the mobile terminal to the equipment, the equipment using the parameters s anomaly detection received to detect anomalies.
    Embodiments may also relate to a physiological signal monitoring equipment, configured to be worn by the user and to acquire in real time a digitized physiological signal, and transmit the digitized physiological signal to a server via a mobile terminal, this equipment being configured to implement the method as defined above.
    According to one embodiment, the equipment comprises electrodes and / or a sensor integrated into a garment, an analog processing circuit connected to the electrodes and / or to the sensor via conductive links integrated into the garment, a circuit of digital processing connected to the analog processing circuit, a transmission / reception circuit connected to the digital processing circuit, the transmission / reception circuit being configured to communicate with the mobile terminal.
    According to one embodiment, the electrodes are placed in the garment so as to come into contact with the skin of the user on the region of the shoulder blades or ribs at the height of the sternum, the electrodes being formed by printing on the garment, and the conductive links being formed by a conductive wire covered with an insulating layer and inserted into the fabric forming the garment.
    Embodiments may also relate to a physiological signal monitoring system, comprising: a server, a mobile terminal of a user, comprising a communication circuit for establishing a communication with the server, a user-worn equipment and configured to acquire in real time a digitized physiological signal, and transmit the digitized physiological signal to the server via the mobile terminal, the system being configured to implement the method defined above.
    Exemplary embodiments of the invention will be described in the following, without limitation in connection with the accompanying figures in which: Figure 1 schematically shows a system for acquiring and monitoring physiological signals obtained on a patient, according to one embodiment, FIG. 2 diagrammatically represents a device for acquiring and processing physiological signals intended to be worn by a patient, according to one embodiment, FIGS. 3A, 3B, 3C schematically represent a garment in which are integrated elements of the acquisition and processing device, according to various embodiments, FIG. 4 represents steps of procedures implemented in the acquisition and processing device, according to one embodiment, FIGS. 5A, 5B represent a schematic waveform of an ECG signal, illustrating a method of analyzing such a signal, In one embodiment, FIGS. 6 to 10 show the steps of procedures implemented in the acquisition and processing device, according to various embodiments, FIG. 11 represents a schematic waveform of an ECG signal. , illustrating a method for analyzing such a signal, according to another embodiment, FIG. 12 represents an exemplary embodiment of the hardware architecture of the acquisition system.
    FIG. 1 represents a system for acquiring and monitoring physiological signals obtained on a patient, according to one embodiment, for the implementation of a medical surveillance service. The acquisition and monitoring system comprises a device for acquiring physiological signals carried by a patient comprising sensors and / or electrodes E1, E2, a signal processing circuit DPR provided by the sensors and / or the electrodes E1. , E2, a mobile terminal MP such as a smartphone ("smartphone"), and an SRV server. The terminal MP and the circuit DPR communicate with each other via a wireless link WL, for example of the BLE (Bluetooth Low Energy) type. The MP terminal and the SRV server communicate with each other via NT networks, such as the Internet and one or more mobile networks. The sensors and the electrodes E1, E2 can comprise in particular one or more of the following elements: electrodes for collecting a cardiac rhythm and / or an electrocardiogram, and / or a skin conductance (Galvanic Skin Response) and / or a respiratory rhythm, a sensor for measuring the pH of the body, a sensor for measuring the body temperature, a blood pressure sensor, one or more sensors for detecting and / or measuring the concentration of chemical elements such as glucose, tumor markers, pregnancy markers, etc.
    The terminal MP can execute a dedicated application configured to send to the processing circuit DPR a wake-up signal via the link WL, to detect the presence of the processing circuit DPR connected by the link WL and to display on its screen information relating to the presence of the DPR processing circuit connected by the WL link. This dedicated application is also configured to receive the data relating to the signals acquired by the DPR processing circuit and retransmit this data to the server SRV. This dedicated application is also configured to receive commands for example from the SRV server and retransmit them to the processing circuit DPR. The commands intended for the circuit DPR may comprise a command for updating the software installed in the circuit DPR, commands for updating operating parameters of the circuit DPR, or else commands triggering, for example, the memorization and the packet transmission. for example every 12 or 24 hours of acquired signals or characteristics of these signals. This dedicated application is also configured to receive notifications from the SRV server to be presented to the patient on the display screen of the MP terminal. It can thus be provided several notifications. These notifications can trigger from the SRV server the display on the screen of the terminal MP messages informing the patient that he must consult his doctor without or with urgency, or that he must go urgently to the hospital or wait for the emergency arrival. For this purpose, the terminal MP may comprise a geographical location circuit, such as GPS (Global Positioning System), the dedicated application being configured to transmit on request from the SRV server the geographical position provided by the location circuit of the terminal.
    The SRV server is connected to a DB database in which data relating to patients carrying physiological signal acquisition devices and data relating to the physiological signals transmitted by these devices are stored.
    FIG. 2 represents the processing circuit DPR, according to one embodiment. The DPR circuit comprising an analog processing circuit AP connected to the sensors and / or the electrodes E1, E2, an ADC analog / digital conversion circuit, a PRC processor, and a transmission interface circuit TM. The analog circuit AP comprises an analog signal signal processing channel to be processed. Each signal processing channel comprises in particular one or more filters, and a signal amplifier. The ADC circuit receives the signals processed by the AP circuit, scans them and provides the digitized signals to the PRC processor. The digitization of the signals can be performed on 12 or 16 bits with a sampling frequency set between 25 and 800 Hz, depending on the type of signal to be processed. For an ECG signal, the sampling frequency may for example be set at 500 Hz. The PRC processor processes the digitized signals provided by the ADC conversion circuit to develop physiological data to be transmitted by the interface circuit TM. The PRC processor may comprise a microprocessor or a microcontroller, and may be connected to one or more volatile and / or nonvolatile MEM memories, in particular to store the physiological data it has developed from the signals received from the ADC circuit.
    The DPR circuit may also comprise a DENC encryption circuit for encrypting the physiological data produced by the PRC processor, before transmitting them by the transmission interface circuit TM. For this purpose, the encryption circuit DENC can use a symmetric encryption key known only to it and the server SRV, or an asymmetric public encryption key corresponding to a private key known only to the server SRV. According to one embodiment, the DENC circuit implements the Advanced Encryption Standard (AES) algorithm using a 256 or 512-bit encryption key.
    The PRC processor may be configured by a program stored in memory, to process the digitized signals provided by the ADC circuit, for detecting events, control their encryption by the DENC circuit, transmit them to the MP terminal, and record them on command received the MP terminal.
    Of course, the system may comprise other acquisition channels connected to electrodes or sensors, each acquisition channel comprising an analog circuit comprising one or more filters, one or more signal amplifiers, and possibly an analog / digital converter. digital.
    FIGS. 3A, 3B, 3C show garment 1, such as an undergarment, in which the processing circuit DPR, the electrodes E1, E2, electrical connection links 2, 3 are integrated between the electrodes E1, E2 and the DPR circuit. The electrodes E1, E2 are disposed on the garment 1 at a location where they are assured of remaining in contact with the skin of the patient, for example in the region of the shoulder blades as shown in Figures 3A, 3B, 3C, or in the region anterior of the ribs at the level of the sternum (derivation DI in medical ECG). The circuit DPR can for example be housed with a rechargeable battery for example in a lining or hem of the garment 1 or in a pocket formed on the garment. The connection between the battery and an external charging circuit of the battery can be ensured by an inductive coupling.
    According to one embodiment, the electrodes E1, E2 are dry electrodes. They can be made by a printing technique or application of paint, on the fabric of the garment 1 (or on a coating of PDMS - Poly Di Methyl Siloxane - deposited on the fabric), using an electrically conductive ink, by example based on PEDOT: PSS (poly (3,4-ethylenedioxythiophene: sodium polystyrene sulfonate).) To ensure good electrical contact with the skin, the electrodes can be covered with an ionic gel (ion conductive ion trapped in a polymer matrix) which can also be deposited by a painting or printing application technique The electrodes E1, E2 can also be made of a metallic material such as ΓΙΝΟΧ or gold and fixed by any means on the clothing, their contact with the skin being favored by their positioning (shoulder blades, ribs).
    The electrical connections 2, 3 can be made using a conductive wire (Al, Au, Ag, Cu) covered with an electrically insulating layer, and knitted or woven with the son forming the fabric of the garment 1, or laminated on the garment, or housed in textile pockets formed on the garment. Thus, the wire forming the electrical connections 2, 3 can be isolated by being dipped in a resin such as PET (Poly Ethylene Terephthalate).
    The DPR circuit can be formed on a flexible support and be embedded in a waterproof and flexible material. Thus, the DPR circuit can be formed on a substrate, for example PDMS, PET or polyimide, and encapsulated in one of these materials or in alumina. The components forming the DPR circuit can be thinned and deposited without being encapsulated on the substrate by the "pick and place" method. The different components forming the circuit DPR can comprise the analog circuit AP and the converter ADC, the microcontroller PRC including the function of encryption ENC, the communication module IM (Bluetooth or BLE), a battery or a capacitor of great capacity rigid, conformable or flexible, Bluetooth / BLE antennas and an antenna coil for charging the inductive battery. The encapsulation of the DPR circuit can be performed by an Atomic Layer Deposition (ALD) atomic layer method. The connections between the electrodes E1, E2, the wires 2, 3 and the circuit DPR can be made by reflow soldering or more generally by a wire-bonding and / or with chip flip-chip.
    According to one embodiment, the analog processing circuit AP can be realized, not in the circuit DPR, but associated with one and / or the other of the electrodes E1, E2. The circuit AP can thus be configured to generate an analog signal that can be transmitted without excessive degradation by the wires 2, 3 to the circuit DPR.
    FIG. 4 represents steps S1 to S9 of a signal analysis procedure P1 by the processor PRC, according to one embodiment. The analyzed signals are provided by the ADC conversion circuit. Steps S1 and S2 are first executed. In step S1, the processor PRC receives samples of a time slot of a digitized signal SGL, for example of a duration of between ten seconds and one minute. In step S2, the processor PRC determines whether the acquired signal SGL is representative of physiological signals of a person, or in other words, whether the electrodes E1, E2 are in contact with the skin of the patient, or if the sensors receive many physiological signals. If the acquired signal is not representative of physiological signals of a person, the processor PRC executes step S7, otherwise it executes steps S3 and S4. In step S3, the processor analyzes the received digital signal SGL to search for characteristic elements to be measured. In step S4, if searched characteristic elements are detected in the received SGL signal, the PRC performs steps S5 and S6, otherwise it executes step S8. In step S5, the processor PRC processes the signal SGL and the detected signal characteristic elements to detect anomalies therein. In step S6, if no anomaly is detected, the time slot of the scanned signal SGL thus analyzed is erased and the procedure P1 is again executed from step S1 to acquire and analyze a new time slice of the signal digitized SGL. On the other hand, if an abnormality is detected in step S6, the PRC performs step S9 where it initiates or continues monitoring operations depending on the severity of the abnormality, such as transmission and / or storage. of the received SGL signal for a certain time, and / or the transmission of an AL alarm signal to the SRV server. In step S7, an alarm message is transmitted to the terminal MP to trigger the display on the screen of the terminal of a notification warning the patient that the electrodes and / or sensors are incorrectly positioned. The terminal MP can also retransmit the alarm message to the server SRV. In step S8, the SGL signal received by the PRC processor has a shape too far from an expected form, an alarm signal AL can then be transmitted to the mobile terminal MP and / or the server SRV. Depending on the nature of the signal, it may also be decided to memorize or transmit the SGL signal to the SRV server via the mobile terminal MP. Following the execution of one of the steps S6, S7, S8 and S9, the procedure P1 is executed again from the step S1 to acquire and analyze a new time slot of the digitized signal SGL.
    If the connection with the terminal MP is absent, the processor PRC can memorize the data to be transmitted, that is to say the received SGL signal and / or characteristic elements extracted from the received signal, as well as the alarm messages, until the link is restored.
    The anomaly detection may consist in comparing the SGL digitized signal with a reference digital signal, or comparing characteristics extracted from the SGL signal with those extracted from the reference signal. The reference signal may have been determined from one or more signals acquired on the patient himself, for example in different situations, at a time when he is in good health.
    Figs. 5A, 5B show a typical waveform of a normal ECG signal, including two heart beats, as may be provided by the analog processing circuit AP. This waveform comprises pulses P, Q, R, S, T and U extending from a base voltage I, called "isopotential line", generally detected between the pulse T or U and the pulse P of the next heartbeat. R pulses occur at times t0, t1, ... (Figure 5A), and have the form of a peak to the positive voltages. Since the R pulses have a higher amplitude than any other pulse P, Q, S, T, U, and a relatively short duration, they are generally used to determine the heart rate. The pulses P occur at times tj-tP (j = 0, 1, ...), ie a certain time tP before the pulses R. The pulses P have a rounded shape with a duration DP (FIG. 5B) that is relatively long, greater than the duration of the pulses R, and of relatively low amplitude towards the positive voltages. The Q pulses occur at times tj-tQ (j = 0, 1, ...), which is a time tQ before the R pulses. The Q pulses have the shape of a peak towards the negative voltages, of relatively short duration and low amplitude. The pulse S follows the pulse R at times tj + tS (j = 0, 1, ...), a certain time tS after the pulse R, and has the shape of a peak towards the negative voltages. The Q and S pulses have substantially the same duration and the same amplitude. The pulse T occurs at times tj + tT (j = 0, 1, ...), a certain time tT after the pulse R. The pulse T has a rounded shape towards the positive voltages, a relative amplitude between the pulses P and R, and a duration DT greater than that of the pulse P. The pulse U is a small pulse of rounded shape towards the positive voltages immediately following the pulse T. The pulse U is absent from ECG signals in 25 to 50% of cases.
    Certain characteristics of an ECG signal can be analyzed to detect pathologies. Thus, it is known to analyze the amplitude and the duration of the pulse P, the duration of the segment PR between the end of the pulse P and the beginning of the pulse Q, the duration of the interval PR between the beginning of the pulse P and the beginning of the pulse Q, the duration of the QRS complex between the beginning of the pulse Q and the end of the pulse S, the shape and the duration of the segment ST between the end of the pulse S and the beginning of the pulse T, the shape of the pulse T, the duration of the segment QT between the beginning of the pulse Q and the end of the pulse T, as well as the shape of the U pulse, if any.
    In the case where the signal is an ECG signal, step S2 in Fig. 4 may include searching for the presence of R pulses in the SGL signal. Step S3 may include searching for the presence of P, Q, S, and T pulses in the SGL signal. Step S5 can be executed if at least one of these pulses is detected in the SGL signal. Step S8 is executed if none of the P, Q, S and T pulses can be detected in the SGL signal. In step S7 executed when the pulses R are not detected, another signal may be analyzed to determine whether the electrodes E1, E2 are in contact with the skin of the patient. The processing performed in step S7 depends on this detection. Thus, if the electrodes E1, E2 are not detected in contact with the skin, the processor PRC sends the terminal MP a notification to be displayed on the screen of the terminal to inform the patient that he must put on the garment 1. If the electrodes are detected in contact with the skin of the patient, the PRC processor sends an alarm signal AL to the server SRV via the terminal MP.
    In the case of an ECG signal, step S2 may consist in comparing the samples of the digitized signal with a threshold voltage value RT (FIG. 5A), for example set at 1 + 0.3 mV, the pulses R being considered detected when the ECG signal voltage exceeds the threshold value RT. If the comparison of the ECG signal makes it possible to extract a heart rate, the processor PRC seeks to detect the other pulses P, Q, S and T in step S3. These pulses can be detected from each pulse R detected at times tj (j = 0, 1, ...). Thus, the top of the pulse P can be detected by searching for a maximum value in the time interval [tj-tP-DP / 2, tj-tP + DP / 2] (j = 0, 1, ...) . The top of the Q pulse can be detected by searching for a minimum value in the time interval [tj-tQ-DQ / 2, tj-tQ + DQ / 2] (j = 0, 1, ...). The top of the S pulse can be detected by looking for a minimum value in the time interval [tj + tS-DS / 2, tj + tS + DS / 2] (j = 0, 1, ...). The top of the pulse T can be detected by searching for a maximum value in the time interval [tj + tT-DT / 2, tj + tT + DT / 2] (j = 0, 1, ...). For a man in good health, the values tP and DP may for example be set respectively at 145 ms and 130 ms, the values tQ and DQ may for example be set respectively at 60 ms and 20 ms, the values tS and DS may be for example fixed respectively at 60 ms and 20 ms, and the values tT and DT may be for example fixed respectively at 300 ms and 200 ms.
    According to one embodiment, the processor PRC verifies in step S5, that the respective amplitudes of the pulses P, Q, S, and T are located in particular ranges. If this is not the case (step S6), it is considered that an anomaly is detected and step S9 is executed. Thus, the processor PRC verifies that the maximum value of the pulse P is in the interval [0, DVP], that the minimum value of the pulse Q is in the interval [-DVQ, 0], that the minimum value of the pulse S is in the range [-DVS, 0], and the maximum value of the pulse T is in the range [mT, mT + DVT]. For a man in good health, the values DVP and DVQ, DVS, DVT and mT are for example set at 1 + 0.25 mV, 1 + 0.3 mV, 1 + 0.5 mV, 1 + 0.25, respectively. mV and 1 + 0.05 mV.
    If in steps S5, S6, the peaks of pulses P, Q and T are not in the windows defined above, the processor PRC sends via the interface TM to the server SRV, the signal SGL and an alarm signal AL1 for triggering a monitoring of the ECG signals (step S9). If the pulses R are not detected (crossing the threshold RT) and if the peaks of the pulses S are not found in the windows defined above, the processor PRC sends via the interface TM to the server SRV, the signal SGL and an alarm signal AL2 of gravity level higher than the alarm signal AL1 (step S9). AL1 and AL2 alarm signals are transmitted to the OT terminal of an operator connected to the SRV server. The alarm signals AL1, AL2 make it possible to define different priority levels for the processing of the associated SGL signals, the SGL signals associated with the alarm signal AL2 being processed in priority by an operator connected to the server SRV. In step S5, the processor PRC can also check the shape and the duration of the segment ST between the end of the pulse S and the beginning of the pulse T. If these elements of the signal SGL are not in conformity, the processor PRC sends via the TM interface to the SRV server, the SGL signal and an alarm signal. For example, the conformity of the segment ST may consist in verifying that at times tj + 100ms Q = 0, 1, ...), the voltage of the signal SGL is greater than 1-0.02 or lies between this value and 1 + 0.02 mV (presence of the ST segment at the voltage I), and that between the instants tj + 200 ms and tj + 400 ms, the signal SGL has one or more values higher than the voltage I (for example 0 mV) revealing the presence of the pulse T. If the ST segment at the voltage I is absent, the PRC processor can send via the interface TM to the server SRV, the signal SGL and the alarm signal AL2. If the pulse T is absent, the processor PRC can send via the interface TM to the server SRV, the signal SGL and the alarm signal AL1.
    If the pulses R are detected, the processor PRC can also calculate and memorize in step S3, the average and the standard deviation of the heart rate during each period of ten seconds to a minute, and send these data by packet to the SRV server for example every 12 or 24 hours.
    FIGS. 6 to 9 show other steps of procedures for analyzing characteristic elements of an ECG signal and for processing anomalies, which can also be executed during step S2 or S5 of the procedure P1.
    FIG. 6 represents steps S11 to S14 that can be executed respectively during the steps S1, S2, S3 and S7 of the procedure P1. In step S11, another signal IS acquired by the circuits AP, ADC, is processed by the processing circuit DPR. The acquisition period of the signal IS may be identical to that of the signal SGL, so that the signals IS and SGL are acquired in an alternative manner. The signal IS may be representative of the respiratory activity of the patient. This signal can be acquired for example by continuously measuring the impedance between the electrodes E1 and E2 (FIG. 3A). For this purpose, a current intensity between 5 and 100 μΑ at a frequency between 1 and 40 kHz can for example be sent between the electrodes E1, E2. The impedance measurement can then be obtained from a voltage measurement between the electrodes. Typically, the impedance that can thus be measured varies between -0.1 and +0.1 Ohm around a central value situated between 0.1 and 1 kOhm. In step S12, the signal IS is analyzed to determine if the electrodes E1, E2 are in contact with the skin and if this signal is representative of a respiratory rhythm. It can be determined that the electrodes E1, E2 are in contact with the skin if the signal IS remains below a first impedance threshold value, for example 2 kOhm. If the electrodes E1, E2 are not detected in contact with the skin of the patient, the processor executes step S14 (or S7) where it transmits to the mobile terminal MP a notification intended to warn the patient that the electrodes are not in contact with the patient. contact with his skin. This notification can also be transmitted to the SRV server. If in step S12, an impedance signal is well detected, it means that the electrodes E1, E2 are in contact with the skin of the patient and that the SGL signal is well measured on the patient. The processor then executes step S13 where it seeks to detect the respiratory rhythm BR. The breathing rate BR can be obtained by comparing the signal IS with a second impedance threshold value, and by counting the number of times per unit of time that the signal IS exceeds the threshold value, for example set at 500 Ohm. At the end of steps S13 and S14, the processor PRC executes step S11 again.
    As illustrated in FIG. 3B, a third electrode E0 can be provided as a reference electrode. Trans-thoracic impedance values are measured between each of the electrodes E1, E2 and the reference electrode E0, to determine trans-thoracic impedances between the electrode E1 and the reference electrode on the one hand, and secondly, between the electrode E2 and the reference electrode (DM and DM derivations in medical ECG). The electrode E0 can also be used to measure the signal SGL corresponding to the variations of the voltage between the electrodes E1 and E0 and between the electrodes E2 and E0. Of course, each electrode E1, E2 may be associated with a separate reference electrode, to perform these measurements of impedance and voltage. Thus, as illustrated in FIG. 3C, the electrode E1 is associated with a first reference electrode E3, and the electrode E2 is associated with a second reference electrode E4. Trans-thoracic impedance values are measured between the electrode E1 and the reference electrode E3, and between the electrode E2 and the electrode E4 to determine trans-thoracic impedances between the electrodes E1 and E3 and between the electrodes. electrodes E2 and E4.
    Fig. 7 shows steps S20 to S26 of heart rate analysis, performed when this has been detected in the SGL signal. These steps can be executed in step S5 of the procedure P1. In step S20, the processor PRC detects the instants where the pulses R of the ECG signal occur. In step S21, the processor PRC evaluates the stability of the heart rhythm RR for a certain time, for example between about ten seconds and a minute, by determining whether it remains in an interval for example between -15% and + 15% around an average value. In step S21, if the heart rate is stable, the PRC processor executes step S22, otherwise it executes the step, S26. In step S22, the PRC processor compares the average heart rate R-R with a high threshold value RT2. If the average heart rate R-R derived from the detection of the pulses R is greater than the threshold value RT2, the processor PRC executes the step S26, otherwise it executes the step S23. In step S23, the PRC processor compares the average heart rate R-R with a low threshold value RT1. If the average heart rate RR is less than the threshold value RT1, the processor PRC executes the step S25, otherwise (the heart rate RR is between the threshold values RT1 and RT2) the monitoring of the cardiac rhythm is continued by executing again steps S20 and S21. The threshold values RT1, RT2 depend on the profile of the patient. For a man in good health, the threshold values RT1 and RT2 are, for example, set respectively at 400 ms and 1600 ms for the duration between two consecutive pulses R, namely respectively 50 and 150 beats per minute. In step S25, the processor PRC sends via the interface TM to the server SRV the signal SGL and the alarm signal AL1 making it possible to trigger a monitoring of the ECG signals by a human operator having a terminal connected to the server SRV. In step S26, the processor PRC transmits to the server SRV the signal SGL and the alarm signal AL2.
    Moreover, the reception of the alarm signals AL1, AL2 by the server SRV can trigger the transmission by an operator to the patient, for example to his terminal MP, of a message asking the patient to consult a doctor. The operator receiving the alarm signal AL1, AL2 can trigger an emergency procedure, and the message transmitted to the patient's MP terminal can warn the patient that he must urgently consult a doctor. The alarm signals AL1, AL2 can also trigger the display of messages on the patient's MP terminal, before these signals are transmitted to the SRV server. At the conclusion of steps S25 and S26, the PRC processor again executes the steps of Fig. 7 from step S20 to acquire and re-analyze the R-R heart rate.
    FIG. 8 represents steps S30 to S35 for analyzing the QRS complex of an ECG signal. These steps can be executed in step S5 of procedure P1, if Q and S pulses are respectively detected before and after an R pulse. In step S30, the PRC processor analyzes the QRS complex of the ECG signal, in particular to determine the duration. In step S31, the processor PRC sets this duration to a high threshold value QT2. If the duration of the QRS complex is greater than the threshold value QT2, the PRC performs step S33, otherwise the procedure is executed again from step S30 to acquire and analyze a new occurrence of the QRS complex. In step S33, the PRC processor compares the R-R heart rate with a threshold value RT3. For a man in good health, the threshold values QT2 and RT3 are for example fixed respectively at 120 ms and 500 ms corresponding to a heart rate of 120 beats per minute. If the heart rate R-R is greater than the threshold value RT3, the processor executes step S34, otherwise it executes step S35. In steps S34 and S35, the processor PRC transmits to the server SRV the signal SGL and respectively the alarm signals AL1 and AL2. At the end of steps S34 and S35, the procedure is executed again from step S30.
    FIG. 9 represents steps S40 to S46 for analyzing the duration of the segment PR of an ECG signal. These steps can be executed in step S5 of procedure P1, if P pulses are detected before an R pulse. In step S40, the PRC processor analyzes the PR segment, in particular to determine the duration. In step S41, the stability of the duration of the segment PR is analyzed for a certain time, for example between about ten seconds and one minute, by determining whether this duration remains in an interval, for example between -15% and + 15% around an average value. If the duration of the segment PR is stable, the processor PRC executes the step S42, otherwise it executes the step S46. In step S42, the PRC processor compares the duration of the PR segment to a low threshold value PRT1. If the duration of the segment PR is greater than the threshold value PRT1, the processor executes step S43, else it executes step S44. In step S43, if the duration of the segment PR is greater than a high threshold value PRT2, the processor PRC executes the step S45, otherwise (duration of the segment PR is between the threshold values PRT1 and PRT2) the procedure is executed again from step S40 to acquire and analyze a new occurrence of the PR segment. For a man in good health, the threshold values PRT1 and PRT2 are for example set at 80 ms and 250 ms, respectively. In step S44, the PRC processor compares the R-R heart rate with the threshold value RT2. If the R-R heart rate is greater than the threshold value RT2, the processor executes step S46, otherwise it executes step S45. In steps S45 and S46, the processor PRC transmits to the server SRV the signal SGL and respectively the alarm signal AL1 and the alarm signal AL2. At the end of steps S45 and S46, the procedure is executed again from step S40.
    FIG. 10 represents steps S50 to S54 of analysis of the respiratory rhythm BR extracted from the signal IS acquired in step S2. These steps can be executed by the processor PRC during step S5 of the procedure P1. In step S50, the breathing rate is extracted from the impedance signal provided by the analog circuit AP and the circuit ADC. In step S51, the PRC processor compares the breathing rate BR with a low threshold value BRT1. If the breathing rate BR is lower than the threshold value BRT1, the processor PRC executes the step S52, else it executes the step S53. In step 553, the PRC processor compares the breathing rate BR with a high threshold value BRT2. If the breathing rate BR is greater than the threshold value RT2, the processor PRC executes the step S54, otherwise (the breathing rate is between the threshold values BRT1 and BRT2) it continues the monitoring of the respiratory rhythm by running again steps S50 and S51. The threshold values BRT1, BRT2 depend on the profile of the patient. For a man in good health, the threshold values BRT1 and BRT2 are, for example, set respectively at 10 and 25 beats per minute. In steps S52 and S54, the PRC processor transmits the SGL signal and the AL1 and AL2 alarm signals respectively to the SRV server. At the end of steps S52 and 554, the procedure is executed again from step S50. In steps S52 and S54, the PRC processor may also transmit the value of the respiratory rate BR. Whenever the processor PRC transmits the alarm signal AL1 or AL2, it can also transmit to the server SRV the samples of the signal SGL / IS which led to the transmission of this alarm signal, as well as information on the nature of the anomaly detected.
    Naturally, other methods of analyzing an ECG signal than those described with reference to FIGS. 6 to 10 can be implemented. Thus, it can be expected to compare the SGL signal with a reference signal. The reference signal can be obtained during an initialization phase of the DPR treatment circuit, by triggering the acquisition of an ECG signal on the patient at rest (for example sitting), then triggering the acquisition of a signal ECG on the moving patient. Each ECG signal can be acquired for a few minutes, for example 2 minutes. Each signal thus acquired is then stored as a reference signal by the PRC processor. The reference signal may also be provided by the SRV server to the DPR processing circuit. This reference signal can thus be independent of the patient.
    An example of reference ECG signal REF is shown in FIG. 11. The processing of an SGL signal acquired by the circuit DPR may comprise a comparison processing of the signal SGL with the reference signal REF. For this purpose, the signal REF is processed to extract a certain number of parameters such as: the positions and the amplitudes of the pulses P, Q, R, S and T in the signal REF, the positions of the pulses P and Q being defined with respect to the position of the next R pulse, and the positions of the S and T pulses being defined with respect to the previous R pulse, - the voltage of the isopotential I of the REF signal (sought for example between -y and + y, where y is chosen to be equal to a value between 0.025 and 0.5 mV), the slope of the signal REF between the peaks of the pulses Q and R, the slope of the signal REF between the peaks of the pulses R and S the slope of the signal REF between the vertex and the end S1 of the pulse S, the slope TS1 of the signal REF between the beginning T0 and the peak of the pulse T, the slope TS2 of the signal REF between the vertex and the end T1 of the pulse T, the slope PS1 of the reference signal between the beginning PO and the vertex of the pulse P, the slope PS2 of the signal REF between the peak and the end P1 of the pulse P, the duration between the peaks of the pulses R in the signal REF, the voltages yP, yQ, yS and yT of the vertices of the pulses P, Q, S and T in the signal REF, and - the time between the peaks of the pulses Q and T in the signal REF.
    Average values of these parameters over the acquisition time of the REF reference signal can be calculated.
    The respective average positions of the peaks of the pulses P, Q, S and T of the reference signal REF make it possible to define reference areas of the vertices of the pulses P, Q, S and T of the signal SGL acquired by the circuit DPR. The reference area of the pulse P can be defined between times tj-210ms and tj-80 ms, tj being the instant of the peak of the next pulse R, and between the voltages yP +/- x%. The reference area of the Q pulse can be defined between times tj-70 ms and tj-50 ms and between voltages yQ +/- x%. The reference area of the pulse S following the pulse R at the instant tj can be defined between the instants tj and tj + 80 ms and between the voltages yS +/- x%. The reference zone of the pulse T following the pulse R at the instant tj can be defined between the instants tj + 200 and tj + 400 ms and between the voltages yT +/- x%. The quantity x% can be defined between 5 and 15% by an operator. The slopes PS1, PS2, Q-R, R-S, TS1, TS2 also make it possible to define acceptable reference windows comprised between 5 and 15% of the respective average slopes extracted from the REF reference signal. Other parameters can thus be extracted from the REF reference signal, these parameters being used to define reference windows centered on an average value of one of these parameters. Corresponding parameters are extracted from the acquired signal SGL, and if they are not in the corresponding window, an alarm signal AL1 / AL2 is generated and transmitted to the server SRV.
    The comparison processing of the signal SGL acquired by the circuit DPR with the reference signal REF can consist for the processor PRC in searching for the vertices of the pulses R, for example by a comparison with a threshold voltage (step S3), to determine the value of the voltage of the isopotential I and to determine whether this value is in the range [-y, + y] (y being between 0.025 and 0.5 mV, for example chosen to be equal to 1 mV), search for P, Q, S and T pulse vertices relative to the apex of one (or each) R pulse in the SGL signal and determine slopes PS1, PS2, QR, RS, TS1, TS2 in the SGL signal (Step S5), and finally, to determine if the vertices of the pulses P, Q, S and T of the signal SGL are located in the reference areas defined above from the reference signal REF, and if the slopes are located in the reference windows defined above from REF reference signal (step S6). If the R pulses are not detected in the SGL signal or if the voltage of the isopotential I is not in the range [-y, + y], or if the signal pulse SGL has a anomaly (top of the pulse outside the reference area, or slope (s) outside the reference window (s)), the PRC processor transmits the scanned SGL signal associated with the alarm signal AL2 (step S9). If the P, Q or T pulse of the SGL signal has an anomaly (peak of the pulse outside the reference zone, or slope (s) outside the reference window (s)), the PRC processor transmits the scanned SGL signal associated with AL1 alarm signal (step S9).
    The operators can, by means of the terminal OT, control the update of the different threshold values, the different dimensions and positions of the reference areas, and the widths of the reference windows previously described, implemented by the circuit processor PRC. DPR of a designated patient. Operators can also trigger the update of all or part of the program executed by the PRC processor. Thus, the different threshold and signal values used in the processes described above can be modified on request transmitted by the SRV server to the processing circuit DPR via the mobile terminal MP of the patient. This arrangement makes it possible to adapt the detection of abnormalities to the common physiological conditions of each patient. Likewise, the program executed by the processor PRC can be modified and replaced by a new program on request transmitted by the server SRV to the processing circuit DPR via the mobile terminal MP.
    The server SRV thus receives from several patient processing circuits DPR alarm signals AL1, AL2 each associated with samples of SGL signals, as well as a patient identifier provided by the dedicated application installed in the terminal MP or by the PRC processor. This data is decrypted, if necessary, then stored in the database DB, for example in two tables according to the alarm level AL1, AL2. Operators can view the data stored in the DB database by means of OT terminals connected to the SRV server, in the form of chronograms of the transmitted SGL signals, reconstructed from the samples of the SGL signal transmitted by the PRC processor, knowing the period of samples (each sample or sequence of samples being time stamped). The server SRV can trigger the display by an OT terminal of the SGL signals associated with an alarm signal AL2, in particular when the terminal OT does not already display such a signal. The SGL signals associated with an alarm signal AL2 are displayed first by the OT terminals, the SGL signals associated with an alarm signal AL1 being displayed when all the SGL signals associated with an alarm signal AL2 have been processed.
    The processing of an SGL signal by an operator can consist in visualizing and analyzing the SGL signal in the form of a reconstructed curve from the transmitted signal samples, for detecting anomalies, and in transmitting a notification to the user's MP terminal. corresponding according to the anomalies observed. For this purpose, the data relating to the user stored in the database DB can be retrieved from the user identifier transmitted with the SGL signal data, and displayed on the screen of the terminal OT.
    The notifications that may be transmitted on command from the operator may include a first notification intended to activate a reinforced monitoring mode in which the SGL signal is systematically transmitted by the DPR circuit to the SRV server via the terminal MP, in real time. either in packets, for example 12 or 24 hours of SGL signal recording. A second notification can trigger the display by the terminal MP of a message to the patient, for example to advise him to make an appointment with his doctor. A third notification can trigger the display by the terminal MP of a message to the patient, asking him to make an appointment with his doctor as soon as possible. A fourth notification may trigger the display by the terminal MP of a message to the patient, asking him to go to the emergency room of the nearest hospital or not to move while waiting for help. For this purpose, the data transmitted with the alarm signal AL2 include the geographical position of the terminal MP. Note that the geographical position of the terminal MP can be transmitted only on request received from an OT operator terminal. An operator connected to the SRV server can call helpers near the geographic position of the patient. The SRV server can also transmit a message concerning the anomaly observed to the patient's physician, possibly with the SGL signal portion where the abnormality has been noted.
    Of course, the enhanced monitoring mode may be activated when any of the second to fourth notifications are issued.
    The database DB can thus include a so-called "hot" database and a so-called "cold" database. The hot database stores recent data transmitted during the last weeks (6 to 12 weeks) by the DPR treatment circuits of the patients, and in particular identity data transmitted data relating to the heart rate recorded continuously every day on several weeks, anomalies detected and validated by an operator associated with SGL signals transmitted and a description of the action taken (notification issued) by the operator. The cold database stores for each patient, medical data, and all the signals and alarms associated with the transmitted signals, without limitation of time, as well as, in particular, the version of the software installed in the circuit DPR, and / or the values operating and abnormality detection parameters implemented by the patient's DPR circuit, such as the different threshold values described above and the different definition values of the pulse detection windows P, Q, S and T implemented by the DPR circuit.
    FIG. 12 represents an exemplary embodiment of the hardware architecture of the acquisition system. The acquisition system comprises at least two redundant DC data centers, receiving and storing the physiological signal data and the alarm signals emitted by the patient's mobile terminals MP, at least one monitoring center SC grouping terminal terminals. OT operators with access to data stored in DC data centers. The data is transmitted between the MP terminals, the SC monitoring center and the DC data centers via one or more NT networks including the Internet. The data stored in DC datacenters can be accessed by MT terminals connected to the NT network, physicians of patients or physicians participating in the medical surveillance service.
    OT operator terminals may be interconnected LAN connected to the NT network through one or more routers or modems MR.
    The data centers DC can be connected to the network NT via a load balancing device LB, the processing of a data transmission request transmitted by the MP terminals or data transmission required by the terminals OT, MT, being ensured at every moment by the least busy DC data center. Whenever one of the data centers DC receives data from an MP terminal via the network NT, it transmits them immediately (with a very low latency typically less than 5 ms) to the other center of DC data via a dedicated private PL link. In this way, the data stored by the two data centers are identical.
    Each DC datacenter may include a database system that collects all data received from the MP, OT terminals, and multiple clustered SRV servers and dynamically assigned to the processing of a data request or data storage as a function of the load of each server. The SRV servers in each data center have access to the data center DB database system to store the received data and read the data required by the OT, MT terminals.
    It will be apparent to those skilled in the art that the present invention is capable of various alternative embodiments and various applications. In particular, the invention is limited to the capture and processing of ECG signals, nor to the use of electrodes in contact with the skin of a patient, to acquire physiological signals. Nor is the invention limited to the use of an impedance measurement to determine whether electrodes are in contact with the skin of a patient. Other methods within the reach of those skilled in the art can easily be implemented. Also, means such as glue other than a garment can be used to hold electrodes or sensors at a specific location on the skin of a patient.
    It goes without saying also that the physical structure of the physiological signal acquisition device constitutes a fully-fledged invention that can implement other monitoring methods than those defined in the appended claims.
    It may also be expected that the SRV server will apply further processing to the SGL signals received from the DPRs, such as filtering processes to eliminate more "false-positive" cases, in order to reduce the workload. operator analysis. Indeed, it may be advantageous to have the SRV server, which has more efficient computing means than the PRC processor, run SGL signal analysis tests received from the DPR equipment, to avoid analysis by an operator. the signals reveal no real anomaly, for example by exploiting patient information available in the database DB. Of course, these treatments should not increase the risk of occurrence of "false-negative" cases. In the case where the SRV server detects a case to be processed by an operator in a received SGL signal, the processing applied to the signal received by the server SRV may lead to modifying the alarm signal AL1 / AL2 transmitted by the equipment DPR or to refine it by introducing other levels of priority.
    Moreover, the mobile terminal MP and the processing circuit DPR can be integrated in the same processing unit and transmission / reception of signals. For this purpose, the processing circuit DPR can integrate transmission circuits using the mobile telephone networks.
    权利要求:
    Claims (15)
    [1" id="c-fr-0001]
    A method for monitoring physiological signals, comprising the steps of: acquiring samples of at least one digitized physiological signal (SGL), using equipment (DPR, E1, E2) carried by a user, detecting by the equipment the events in the digitized physiological signal and extracting from the equipment the characteristics of the detected events, searching the equipment for an anomaly in the events and characteristics of the events extracted, and transmitting over a wireless link in form encrypted, the physiological signal digitized by the equipment to a server (SRV) via a mobile terminal (MP), when a fault is detected or when a reinforced monitoring mode is activated, otherwise the digitized physiological signal is erased by the 'equipment.
    [2" id="c-fr-0002]
    2. Method according to claim 1, comprising steps of: acquisition of an impedance variation signal (IS) between electrodes (E1, E2) in contact with the skin of the user, comparison of the signal of variation of impedance to a threshold value, transmission of a notification to the user via the mobile terminal (MP) to inform him that the electrodes are not in contact with his skin, when the signal of variation impedance does not exceed the threshold value, and extracting a user's breathing rate (BR) from the impedance variation signal, when the impedance variation signal exceeds the threshold value.
    [3" id="c-fr-0003]
    3. A method according to claim 2, comprising steps of comparing the respiratory rate with low and high threshold values (BRT1, BRT2), and detecting an abnormality if the respiratory rate is not between the values of low and high threshold.
    [4" id="c-fr-0004]
    4. Method according to one of claims 1 to 3, wherein the characteristics of events detected in the digitized physiological signal (SGL) comprise parameters extracted from the digitized physiological signal, an anomaly being detected if one of the parameters extracted belongs to not to a window centered on an average value of a corresponding parameter extracted from a digitized reference signal (REF).
    [5" id="c-fr-0005]
    5. Method according to one of claims 1 to 4, comprising a step of determining a priority level of treatment of a detected anomaly, among two levels of priorities (AL1, AL2), the anomalies of higher priority level being presented on an operator terminal (OT) before the lower priority level anomalies.
    [6" id="c-fr-0006]
    6. Method according to one of claims 1 to 5, wherein the digitized physiological signal (SGL) comprises an electrocardiogram signal, the detected events are pulses R, P, Q, S and T, and the characteristics extracted from events relate to the respective amplitudes of these pulses and / or the duration of the time intervals between these pulses.
    [7" id="c-fr-0007]
    The method of claim 6, wherein the R pulses are detected in the digitalized physiological signal (SGL) by comparing the electrocardiogram signal with a threshold value, and the P, Q, S and T pulses are searched for in windows determined from a moment of detection of an R pulse.
    [8" id="c-fr-0008]
    8. Method according to one of claims 6 and 7, comprising steps of: determining a heart rate (RR) by counting the number of pulses R per unit of time, an anomaly being detected if the heart rate measured present instability greater than a first instability threshold value, or if the measured heart rate is not between first and second heart rate threshold values (RT1, RT2), and / or steps of: a time between the Q and S pulses, and comparing the duration between the Q and S pulses to a threshold value of duration between the Q and S pulses (QT2), an anomaly being detected if the duration between the Q pulses and S is greater than the threshold value of duration between the pulses Q and S, and / or steps of: determining a duration between the pulses P and R, comparing an instability of the duration between the pulses P and R to a second v instability threshold value, comparison of the duration between the pulses P and R at two threshold values of duration between the pulses P and R (PRT1, PRT2), and detection of an anomaly if the instability of the duration between the pulses P and R are greater than the second instability threshold value, or if the duration between the P and R pulses is not between the two threshold values of duration between the P and R pulses.
    [9" id="c-fr-0009]
    9. Method according to one of claims 1 to 8, comprising steps of: detection by the server (SRV) of events in the received digitized physiological signal (SGL), and extraction by the server characteristics of detected events, search by the server of an anomaly in the events and characteristics of the events extracted, and transmission by the server of the digitized physiological signal received at an operator terminal (OT) when an anomaly is detected by the server.
    [10" id="c-fr-0010]
    10. Method according to one of claims 1 to 9, comprising steps of: reconstitution and display of the physiological signal by an operator terminal (OT) from the digital physiological signal received by the server (SRV), and transmission to the mobile terminal (MP) of a notification issued by the operator terminal, relating to the physiological signal displayed on the display screen, and transmission of the notification to the user by means of the mobile terminal.
    [11" id="c-fr-0011]
    The method of claim 10, wherein the notifications transmitted by the operator terminal (OT) to the mobile terminal (MP) comprise at least one of the following: an activation command of the enhanced surveillance mode which is transmitted from the mobile terminal to the equipment (DPR), the equipment transmitting the digitized physiological signal (SGL) upon receipt of the activation command and as long as the reinforced surveillance mode is activated, a notification to be transmitted from the terminal Mobile (MP) to the user to inform the user that he must consult his doctor, a notification to transmit the mobile terminal (MP) to the user to inform the user that he must wait for help or to surrender in the hospital, and a notification containing anomaly detection parameters in the events and the extracted event characteristics, which is transmitted from the mobile terminal to the equipment, the equipment using the flaw detection parameters received to detect abnormalities.
    [12" id="c-fr-0012]
    Physiological signal monitoring equipment (DPR), configured to be worn by the user and for acquiring a scanned physiological signal (SGL) in real time, and transmitting the digitized physiological signal to a server (SRV) via a mobile terminal , characterized in that it is configured to implement the method according to one of claims 1 to 9.
    [13" id="c-fr-0013]
    Equipment according to claim 12, comprising electrodes (E1, E2) and / or a sensor integrated in a garment (1), an analog processing circuit (AP, APC) connected to the electrodes and / or to the sensor by the intermediate conductive links (2, 3) integrated in the garment, a digital processing circuit (PRC) connected to the analog processing circuit, a transmission / reception circuit (TM) connected to the digital processing circuit, the circuit of transmission / reception being configured to communicate with the mobile terminal (MP).
    [14" id="c-fr-0014]
    Equipment according to claim 13, wherein the electrodes (E1, E2) are placed in the garment (1) so as to come into contact with the skin of the user on the region of the shoulder blades or ribs at the height of the sternum. , the electrodes being formed by printing on the garment, and the conductive links (2, 3) being formed by a conductive wire covered with an insulating layer and inserted into the fabric forming the garment.
    [15" id="c-fr-0015]
    A physiological signal monitoring system, comprising: a server (SRV), a mobile terminal (MP) of a user, comprising a communication circuit for establishing a communication with the server, a device (DPR) carried by the user and configured to acquire in real time a digitized physiological signal (SGL), and transmit the digitized physiological signal to the server via the mobile terminal, characterized in that it is configured to implement the method according to one of claims 1 at 11.
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    EP3376943A1|2018-09-26|
    US11020008B2|2021-06-01|
    RU2018122091A|2019-12-30|
    RU2018122091A3|2020-01-31|
    US20180333058A1|2018-11-22|
    WO2017085403A1|2017-05-26|
    JP2018534118A|2018-11-22|
    FR3043902B1|2018-02-23|
    CA3005277A1|2017-05-26|
    CN108471956A|2018-08-31|
    AU2016355074A1|2018-07-05|
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    法律状态:
    2016-11-24| PLFP| Fee payment|Year of fee payment: 2 |
    2017-05-26| PLSC| Publication of the preliminary search report|Effective date: 20170526 |
    2017-10-20| PLFP| Fee payment|Year of fee payment: 3 |
    2018-10-24| PLFP| Fee payment|Year of fee payment: 4 |
    2020-05-06| PLFP| Fee payment|Year of fee payment: 5 |
    2021-05-07| PLFP| Fee payment|Year of fee payment: 6 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1502422A|FR3043902B1|2015-11-19|2015-11-19|METHOD AND SYSTEM FOR ACQUIRING AND ANALYZING PHYSIOLOGICAL DATA|
    FR1502422|2015-11-19|FR1502422A| FR3043902B1|2015-11-19|2015-11-19|METHOD AND SYSTEM FOR ACQUIRING AND ANALYZING PHYSIOLOGICAL DATA|
    US15/777,429| US11020008B2|2015-11-19|2016-11-16|Method and system for acquiring and analyzing physiological data|
    JP2018545697A| JP2018534118A|2015-11-19|2016-11-16|Method and system for acquisition and analysis of physiological data|
    PCT/FR2016/052973| WO2017085403A1|2015-11-19|2016-11-16|Method and system for acquiring and analyzing physiological data|
    CN201680079433.8A| CN108471956A|2015-11-19|2016-11-16|Method and system for acquiring and analyzing physiological data|
    CA3005277A| CA3005277A1|2015-11-19|2016-11-16|Method and system for acquiring and analyzing physiological data|
    RU2018122091A| RU2756426C2|2015-11-19|2016-11-16|Method and system for obtaining and analyzing physiological data|
    BR112018010013-7A| BR112018010013A2|2015-11-19|2016-11-16|process and system for acquisition and analysis of physiological data|
    EP16815574.5A| EP3376943A1|2015-11-19|2016-11-16|Method and system for acquiring and analyzing physiological data|
    AU2016355074A| AU2016355074A1|2015-11-19|2016-11-16|Method and system for acquiring and analyzing physiological data|
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