WO2020013002A1 - Biometric data measurement device, biometric data processing method and program for biometric data processing - Google Patents

Biometric data measurement device, biometric data processing method and program for biometric data processing Download PDF

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Publication number
WO2020013002A1
WO2020013002A1 PCT/JP2019/026065 JP2019026065W WO2020013002A1 WO 2020013002 A1 WO2020013002 A1 WO 2020013002A1 JP 2019026065 W JP2019026065 W JP 2019026065W WO 2020013002 A1 WO2020013002 A1 WO 2020013002A1
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WIPO (PCT)
Prior art keywords
data
subject
unit
measurement
biometric data
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PCT/JP2019/026065
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French (fr)
Japanese (ja)
Inventor
出野 徹
貴広 濱口
湯本 将彦
山内 隆伸
和 松岡
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オムロンヘルスケア株式会社
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Publication of WO2020013002A1 publication Critical patent/WO2020013002A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/021Measuring pressure in heart or blood vessels
    • A61B5/022Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/24Detecting, 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]

Definitions

  • the present invention relates to a biological data measurement device, a biological data processing method, and a program for processing biological data.
  • Measurements capable of measuring biological data such as electrocardiogram and blood pressure have become widespread.
  • the subject can wear the measuring device and measure biological data on a daily basis.
  • biometric data is expected to be used in various fields such as disease diagnosis.
  • the biological data measured in a state where the subject wears the measuring device improperly has low reliability. Therefore, it is preferable that the biometric data be measured in a state where the subject wears the measuring device in an appropriate state.
  • Patent Document 1 discloses a technique for detecting whether or not a cuff is worn on a subject based on the amount of extension of the cuff in the circumferential direction.
  • Patent Literature 1 it is not possible to determine whether the subject is properly or inappropriately wearing the measuring device. Therefore, it is difficult to evaluate the reliability of biometric data using the technique disclosed in Patent Document 1.
  • An object of the present invention is to pay attention to the above circumstances, and to provide a technique for evaluating the reliability of biometric data.
  • a first aspect of the present disclosure is directed to a first measurement unit that measures first biological data of a subject, and a second biological data of the subject within a predetermined period including a measurement date and time of the first biological data.
  • a second measurement unit that measures data, and a first determination unit that determines whether the wearing state of the second measurement unit by the subject is appropriate or inappropriate based on the first biological data
  • a biometric data measurement device comprising: a second determination unit configured to determine whether the reliability of the second biometric data is high or low in accordance with a determination result indicating whether the mounting state is appropriate or inappropriate.
  • biometric data that not only changes according to the mounting state of the measurement unit included in the biometric data measurement device by the subject, but also reacts sensitively to abnormal body changes.
  • biometric data that not only vary according to the state of attachment of the measurement unit included in the biometric data measurement device by the subject, but also do not react so much in the resting state if the abnormality that occurs on the body is mild.
  • the former biometric data is susceptible to abnormalities in the subject's body. For this reason, the former biometric data is not suitable for evaluating whether the mounting state of the measurement unit for measuring the former biometric data included in the biometric data measurement device by the subject is appropriate or inappropriate.
  • the latter biometric data is not frequently affected by abnormalities in the subject's body. Therefore, the latter biometric data is suitable for evaluating whether the mounting state of the measurement unit for measuring the latter biometric data included in the biometric data measurement device by the subject is appropriate or inappropriate.
  • the biological data measuring device includes two measuring units that measure different biological data
  • the mounting state of one measuring unit by the subject is appropriate
  • the mounting state of the other measuring unit by the subject is also appropriate.
  • the biometric data measurement device uses the latter biometric data as first biometric data and the former biometric data as second biometric data. Accordingly, the biological data measurement device cannot directly determine whether the measurement unit that measures the second biological data by the subject is appropriate or inappropriate based on the second biological data.
  • the biometric data measurement device may indirectly evaluate the second biometric data based on the first biometric data. Can be evaluated for the reliability of the biological data.
  • the information processing apparatus further includes an acquisition unit configured to acquire predetermined reference data to be compared with the first biometric data, wherein the first determination unit includes The first biometric data is compared with the reference data, and it is determined whether the wearing state is appropriate or inappropriate based on a comparison result between the first biometric data and the reference data.
  • the biological data measurement device can accurately determine whether the subject is properly or inappropriately wearing the first measurement unit by using the reference data. Can be determined with high accuracy as to whether it is appropriate or inappropriate.
  • the first measurement unit measures data related to the subject's electrocardiogram as the first biological data
  • the second measurement unit Data relating to the blood pressure of the subject is measured as the second biological data. Since the electrocardiographic data is not frequently affected by abnormalities of the subject's body, the electrocardiographic data is suitable for evaluating whether the subject is properly or inappropriately wearing the first measurement unit. Since the blood pressure data is easily affected by abnormalities of the subject's body, it is not suitable for the subject to evaluate whether the second measurement unit is properly or inappropriately mounted.
  • the biological data measurement device can determine whether the second measurement section is properly or inappropriately worn by the subject based on the blood pressure data, even if the subject cannot directly determine whether the second measurement unit is properly mounted.
  • the biological data measurement device can indirectly evaluate the reliability of blood pressure data based on electrocardiographic data.
  • a signal output unit that outputs a signal instructing execution of support for improving the above.
  • the biological data measurement device can measure highly reliable second biological data by supporting the improvement of the state of attachment of the second measurement unit to the subject.
  • the data output that outputs the second biometric data associated with data indicating whether the reliability of the second biometric data is high or low. It further includes a unit.
  • the biometric data measurement device can assist a doctor in making a diagnosis by providing the doctor with the second biometric data associated with the reliability data. By confirming the reliability of the second biometric data, the doctor can easily determine whether or not to use the second biometric data for the examination of the subject.
  • a sixth aspect of the present disclosure is directed to a first measurement unit that measures first biological data of a subject in a first measurement unit included in the biological data measurement device, and a first measurement process that is included in the biological data measurement device.
  • the second measurement unit based on the second measurement process of measuring the second biometric data of the subject within a predetermined period including the measurement date and time of the first biometric data, based on the first biometric data, A first determination step of determining whether the mounting state of the second measurement unit by the subject is appropriate or inappropriate; and a determination result indicating whether the mounting state is appropriate or inappropriate.
  • a second determining step of determining whether the reliability of the second biometric data is high or low.
  • the biological data processing method can obtain the same effects as those of the first aspect.
  • a seventh aspect of the present disclosure is a program for biometric data processing that causes a computer to execute the processing of each unit included in the biometric data measurement device according to any one of the first to fifth aspects. According to the seventh aspect, the program for biometric data processing can obtain the same effect as the above-described first aspect.
  • a technology for evaluating the reliability of biological data can be provided.
  • FIG. 1 is a diagram schematically showing an application example of the measuring device according to the present embodiment.
  • FIG. 2 is a diagram illustrating an example of the overall configuration of the biometric data management system according to the present embodiment.
  • FIG. 3 is a block diagram illustrating a hardware configuration of the measuring device according to the present embodiment.
  • FIG. 4 is a block diagram illustrating a software configuration of the measuring device according to the present embodiment.
  • FIG. 5 is a flowchart illustrating the reliability determination operation in the measuring device according to the present embodiment.
  • the present embodiment will be described with reference to the drawings.
  • the present embodiment described below is merely an example in every respect.
  • the same or similar elements as those already described are denoted by the same or similar reference numerals, and duplicate description will be basically omitted.
  • FIG. 1 is a diagram schematically illustrating an application example of the measuring device A1.
  • the measuring device A1 includes an electrocardiographic measuring unit A11 and a blood pressure measuring unit A12.
  • the electrocardiogram measurement unit A11 measures the electrocardiogram of a subject wearing the measurement device A1.
  • the blood pressure measurement unit A12 measures the blood pressure of the subject wearing the measurement device A1.
  • the blood pressure measurement unit A12 measures the blood pressure of the subject within a predetermined period including the date and time of measuring the electrocardiogram.
  • the measuring device A1 acquires reference data from an EHR (Electronic Health Records) server A3 via the mobile terminal A2.
  • the reference data is data used to determine whether the subject's wearing state of the electrocardiographic measurement unit A11 is appropriate or inappropriate.
  • the measurement device A1 determines whether the subject's wearing state of the electrocardiogram measurement unit A11 is appropriate or inappropriate based on the electrocardiogram data and the reference data.
  • the measurement device A1 determines whether the subject's wearing state of the blood pressure measuring unit A12 is appropriate or inappropriate depending on whether the subject's wearing state of the electrocardiographic measurement unit A11 is appropriate or inappropriate.
  • the measurement device A1 determines whether the reliability of the blood pressure data is high or low according to a first determination result indicating whether the mounting state of the blood pressure measurement unit A12 by the subject is appropriate or inappropriate.
  • the measurement device A1 associates the reliability data with the blood pressure data according to a second determination result indicating whether the reliability of the blood pressure data is high or low.
  • the reliability data indicates whether the reliability of the blood pressure data is high or low.
  • the measurement device A1 transmits the blood pressure data associated with the reliability data to the PHR (Personal Health Records) server A4 via the mobile terminal A2.
  • the PHR server A4 is a server that manages each person's blood pressure data measured by the measurement device A1 in association with reliability data.
  • the measurement device A1 can evaluate the reliability of the biological data.
  • FIG. 2 is a diagram illustrating an overall configuration of the biometric data management system 100.
  • the biometric data management system 100 is a system for managing biometric data of each person.
  • the biological data management system 100 includes a measurement device 1, a mobile terminal 2, a PHR server 3, and an EHR server 4.
  • the mobile terminal 2, the PHR server 3, and the EHR server 4 can communicate with each other via a network.
  • the network is the Internet.
  • the measuring device 1 is a device that measures a physical quantity of a living body of a subject to which the measuring device 1 is worn.
  • the measurement device 1 measures at least two different physical quantities.
  • the measuring device 1 measures an electrocardiogram and a blood pressure.
  • the measurement device 1 measures biological data indicating a physical quantity of a living body of a subject.
  • An example of the biometric data is data indicating an electrocardiogram.
  • Data indicating an electrocardiogram is also referred to as electrocardiogram data.
  • the “electrocardiogram data” may be simply referred to as “electrocardiogram” and may be appropriately read.
  • the electrocardiogram data is waveform data indicating the fluctuation of the electrocardiogram during the measurement period.
  • the electrocardiogram data may be data indicating a feature value of the electrocardiogram during the measurement period.
  • the feature value is a peak value, but is not limited thereto.
  • the electrocardiogram may be a P wave, an R wave, or an S wave, and is not limited.
  • Another example of the biometric data includes data indicating blood pressure.
  • Data indicating blood pressure is also referred to as blood pressure data.
  • the “blood pressure data” may be simply referred to as “blood pressure” and may be appropriately replaced.
  • the blood pressure data is data indicating a value of systolic blood pressure SBP (Systolic Blood Pressure) and a value of diastolic blood pressure DBP (Diastatic Blood Pressure) at the time of blood pressure measurement.
  • the blood pressure data may be waveform data indicating fluctuations in SBP and DBP during the measurement period.
  • the measurement device 1 is also called a biological data measurement device.
  • the portable terminal 2 is a device that acquires electrocardiographic data and blood pressure data from the measuring device 1 and provides the electrocardiographic data and blood pressure data to the PHR server 3.
  • the mobile terminal 2 is a smartphone or a tablet, but is not limited thereto.
  • the mobile terminal 2 is an example of a biometric data providing device.
  • the PHR server 3 is a server that manages the biometric data of each person measured by the measuring device 1.
  • the PHR server 3 collects biometric data of each person from the mobile terminal 2. Instead, the PHR server 3 may directly collect the biometric data of each person from the measurement device 1.
  • the doctor can utilize the biometric data managed by the PHR server 3 for each patient's examination.
  • the EHR server 4 is a server that manages data on medical examinations performed by doctors.
  • the EHR server 4 manages data related to each patient's examination in cooperation with an electronic medical record input by a doctor using a PC (Personal Computer).
  • Data related to the consultation is also referred to as consultation data.
  • the examination data includes reference data indicating the physical quantity of the living body of each person.
  • the reference data is data used for determining whether the mounting state of the measuring unit included in the measuring device 1 by the subject is appropriate or inappropriate, as described later.
  • the reference data is data indicating a physical quantity of a living body measured in a state where the subject appropriately wears the measurement unit included in the measurement device 1.
  • the examination data includes first predetermined reference data relating to the electrocardiogram of each person.
  • the first reference data is data used for determining whether the subject is properly or inappropriately wearing a measurement unit for measuring an electrocardiogram included in the measurement device 1.
  • the first reference data may include a plurality of reference data measured at different time zones.
  • the first reference data includes reference data based on the measurement at the morning time and reference data based on the measurement at the afternoon time. One reason is that the tendency of electrocardiographic data differs depending on the time of day.
  • the first reference data may include a plurality of reference data measured in different states of the subject.
  • the first reference data includes reference data based on the measurement of the subject in a nervous state and reference data based on the measurement of the subject in a resting state.
  • the first reference data may include a plurality of reference data obtained by combining the time zone and the state of the subject.
  • the consultation data includes second predetermined reference data relating to the blood pressure of each individual.
  • the second reference data is data used to determine whether the subject is properly or inappropriately wearing the measurement unit that measures the blood pressure included in the measurement device 1.
  • the second reference data may include a plurality of reference data measured at different time zones.
  • the second reference data includes reference data based on the measurement at the morning time and reference data based on the measurement at the afternoon time.
  • the second reference data may include a plurality of reference data measured in different states of the subject.
  • the second reference data includes reference data based on the measurement of the subject in a nervous state and reference data based on the measurement of the subject in a resting state.
  • the second reference data may include a plurality of reference data obtained by combining the time zone and the state of the subject. Since the second reference data includes a plurality of reference data, the accuracy of the determination whether the measurement unit included in the measurement device 1 that measures the blood pressure included in the measurement device 1 is properly or inappropriately mounted is increased.
  • FIG. 3 is a block diagram illustrating a hardware configuration of the measurement device 1.
  • the measurement device 1 includes a processor 101, a ROM (Read Only Memory) 102, a RAM (Random Access Memory) 103, a storage device 104, a communication interface 105, an input unit 106, a display unit 107, a voice output unit 108, and an electrocardiogram measurement unit 109. And a blood pressure measurement unit 110.
  • Each element is electrically connected to each other.
  • the communication interface is described as “communication I / F”.
  • the processor 101 controls each element of the measuring device 1.
  • the processor 101 is a CPU (Central Processing Unit), but is not limited thereto.
  • the processor 101 loads a program for executing the measuring device 1 stored in the storage device 104 on the RAM 103. Then, the processor 101 can execute various operations by interpreting and executing the program developed in the RAM 103.
  • the storage device 104 is a so-called auxiliary storage device.
  • the storage device 104 is a semiconductor memory such as a built-in or external flash memory, but is not limited thereto.
  • the storage device 104 stores a program executed by the processor 101.
  • the program may be stored in the storage device 104 in advance.
  • the program may be downloaded to the measurement device 1 via a network.
  • the program may be stored on a non-transitory computer-readable medium and distributed.
  • the storage device 104 stores a plurality of electrocardiogram data having different measurement dates and times (measurement timing) measured by an electrocardiogram measurement unit 109 described later.
  • the storage device 104 stores a plurality of blood pressure data having different measurement dates and times measured by the blood pressure measurement unit 110 described later.
  • the communication interface 105 is an interface for communicatively connecting the measuring device 1 to another device.
  • the communication interface 105 includes a short-range wireless communication module.
  • the short-range wireless communication method is, for example, a communication method based on Bluetooth (registered trademark), but is not limited thereto.
  • the communication interface 105 communicates directly with the mobile terminal 2 using a short-range wireless communication method.
  • the communication interface 105 may include modules for various wireless communication schemes for mobile communication (3G, 4G, etc.), WLAN (Wireless Local Area Network), and the like. In this case, the communication interface 105 can communicate with the PHR server 3 and the EHR server 4 without passing through the mobile terminal 2.
  • the input unit 106 is a device that receives an instruction based on an input by the subject.
  • the input unit 106 includes a touch panel and operation keys, but is not limited thereto.
  • the input unit 106 outputs a signal to the processor 101 according to an instruction given by the subject.
  • the input unit 106 is not limited to a device that receives an instruction based on an input based on an operation of the target person, and may be a device that receives an instruction based on a voice of the target person.
  • the display unit 107 is a device that displays information.
  • the display unit 107 is a liquid crystal display, but is not limited to this.
  • the audio output unit 108 is a device that outputs audio.
  • the audio output unit 108 is a speaker, but is not limited to this.
  • the electrocardiogram measurement unit 109 is a device that measures the electrocardiogram of a subject to which the measurement device 1 is worn.
  • the electrocardiograph 109 includes two electrodes.
  • the electrocardiogram measurement unit 109 measures the electrocardiogram of the subject based on a potential difference generated between the two electrodes according to the contact of the subject with the two electrodes.
  • the electrocardiogram measurement unit 109 measures the electrocardiogram of the subject while the subject is in contact with the two electrodes.
  • the electrocardiogram measurement unit 109 stores the electrocardiogram data in the storage device 104 every time the electrocardiogram is measured.
  • the electrocardiogram data includes data indicating the measurement date and time of the electrocardiogram.
  • the measurement date and time of the electrocardiogram is detected by a clock function mounted on the measurement device 1.
  • the electrocardiogram measurement unit 109 is an example of a first measurement unit.
  • the blood pressure measurement unit 110 is a device that measures the blood pressure of the subject wearing the measurement device 1.
  • the blood pressure of the subject is measured within a predetermined period including the date and time of measuring the electrocardiogram.
  • the blood pressure measurement unit 110 includes a cuff, a pump, and a pressure sensor.
  • the cuff is formed in a band shape that can be worn around the measurement site of the subject whose blood pressure is to be measured.
  • the cuff has a bladder.
  • the pump supplies air to the interior of the bladder to inflate the bladder.
  • the pressure sensor measures the pressure in the bladder.
  • Blood pressure measurement section 110 measures blood pressure based on data measured by the pressure sensor.
  • the blood pressure measurement unit 110 is an example of a second measurement unit.
  • the blood pressure measurement unit 110 stores the blood pressure data in the storage device 104 every time the blood pressure is measured.
  • the blood pressure measurement unit 110 acquires the SBP value and the DBP value at the time of blood pressure measurement. Instead of this, the blood pressure measurement unit 110 may continuously measure the blood pressure of the subject at every beat, without depending on the blood pressure measurement instruction.
  • the blood pressure measurement unit 110 acquires the SBP value and the DBP value during the blood pressure measurement period.
  • the blood pressure measurement unit 110 stores the blood pressure data in the storage device 104.
  • the blood pressure data includes data indicating the date and time of measuring the blood pressure.
  • the measurement date and time of the blood pressure is detected by a clock function mounted on the measuring device 1.
  • the blood pressure measurement section 110 may measure the blood pressure by a method other than the method of measuring the blood pressure based on the pressure described above.
  • the blood pressure measurement unit 110 may use an optical system, a radio wave system, or an ultrasonic system that applies light, radio waves, or ultrasonic waves to a blood vessel of a subject and measures blood pressure based on the reflected waves.
  • the measurement device 1 may include a plurality of processors.
  • FIG. 4 is a block diagram illustrating a software configuration of the measurement apparatus 1.
  • the processor 101 implements a first acquisition unit 1011, a second acquisition unit 1012, a third acquisition unit 1013, a first determination unit 1014, a second determination unit 1015, a data output unit 1016, and a signal output unit 1017. I do.
  • the first acquisition unit 1011 will be described.
  • the first obtaining unit 1011 obtains first biometric data of the subject as exemplified below.
  • the electrocardiogram data will be described as an example of the first biological data.
  • the first obtaining unit 1011 obtains electrocardiographic data one by one from a plurality of electrocardiographic data of the subject stored in the storage device 104.
  • the first acquisition unit 1011 outputs electrocardiogram data to the second acquisition unit 1012 and the first determination unit 1014.
  • the second acquisition unit 1012 will be described.
  • the second acquisition unit 1012 acquires the second biometric data of the subject measured within a predetermined period including the measurement date and time of the first biometric data, as exemplified below.
  • the blood pressure data will be described as an example of the second biological data.
  • the second acquisition unit 1012 receives electrocardiogram data from the first acquisition unit 1011.
  • the second obtaining unit 1012 obtains data indicating the measurement date and time of the electrocardiogram from the electrocardiogram data.
  • the second acquisition unit 1012 acquires from the storage device 104 the blood pressure data of the subject measured within a predetermined period including the date and time of measuring the electrocardiogram.
  • Second acquisition unit 1012 outputs the blood pressure data to second determination unit 1015 and data output unit 1016.
  • the third acquisition unit 1013 will be described.
  • the third obtaining unit 1013 obtains predetermined first reference data to be compared with electrocardiographic data, as exemplified below.
  • the third acquisition unit 1013 outputs a request for the first reference data of the subject to the EHR server 4 via the communication interface 105.
  • the third acquisition unit 1013 can output a request to the EHR server 4 at an arbitrary timing.
  • the request includes identification information identifying the subject.
  • the third acquisition unit 1013 receives the first reference data from the EHR server 4 via the communication interface 105 as a response to the request.
  • Third acquisition unit 1013 outputs the first reference data to first determination unit 1014.
  • the first determining unit 1014 will be described.
  • the first determination unit 1014 indirectly determines, based on electrocardiographic data, whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate, as exemplified below.
  • the first determination unit 1014 compares the electrocardiogram data with the first reference data, and indirectly performs the operation of the blood pressure measurement unit 110 based on a comparison result between the electrocardiogram data and the first reference data. Judge whether the mounting state is appropriate or inappropriate.
  • the first determination unit 1014 receives electrocardiogram data from the first acquisition unit 1011.
  • First determination unit 1014 receives the first reference data from third acquisition unit 1013.
  • the first determination unit 1014 compares the electrocardiographic data with the first reference data. For example, the first determination unit 1014 compares the waveform data of the electrocardiographic data with the waveform data of the first reference data.
  • the first determination unit 1014 uses reference data that is close to the measurement date and time of the electrocardiogram among a plurality of reference data included in the first reference data.
  • the first determination unit 1014 may use the plurality of reference data.
  • the first determination unit 1014 determines whether the subject's wearing state of the electrocardiogram measurement unit 109 is appropriate or inappropriate based on the comparison result between the electrocardiogram data and the first reference data. For example, when the degree of deviation of the electrocardiographic data from the first reference data is less than the threshold, the first determination unit 1014 determines that the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate.
  • the first determination unit 1014 determines that the subject's wearing state of the electrocardiographic measurement unit 109 is inappropriate.
  • the first determination unit 1014 determines whether the subject's wearing state of the blood pressure measuring unit 110 is appropriate or inappropriate according to whether the subject's wearing state of the electrocardiographic measuring unit 109 is appropriate or inappropriate. I do.
  • the first determination unit 1014 determines that the mounting state of the blood pressure measurement unit 110 by the subject is appropriate according to the determination result indicating that the mounting state of the electrocardiographic measurement unit 109 by the subject is appropriate.
  • the first determination unit 1014 determines that the mounting state of the blood pressure measurement unit 110 by the subject is inappropriate according to the determination result indicating that the mounting state of the electrocardiographic measurement unit 109 by the subject is inappropriate. Is determined.
  • the first determination unit 1014 makes this determination for the following reason.
  • the electrocardiogram measurement unit 109 and the blood pressure measurement unit 110 are composed of different elements, but are both included in the measurement device 1. Therefore, if the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate, there is a high possibility that the subject's wearing state of the blood pressure measurement unit 110 is appropriate. On the other hand, if the subject's wearing state of the electrocardiographic measurement unit 109 is inappropriate, there is a high possibility that the subject's wearing state of the blood pressure measurement unit 110 is inappropriate.
  • the first determination unit 1014 may perform the following when comparing the electrocardiographic data with any of a plurality of reference data included in the first reference data. For example, when the degree of divergence of the electrocardiographic data with respect to at least one reference data is less than the threshold, the first determining unit 1014 may determine that the subject's wearing state of the electrocardiographic measuring unit 109 is appropriate. . The first determination unit 1014 determines that the mounting state of the blood pressure measurement unit 110 by the subject is appropriate according to the determination result indicating that the mounting state of the electrocardiographic measurement unit 109 by the subject is appropriate.
  • the first determination unit 1014 determines that the subject's wearing state of the electrocardiographic measurement unit 109 is not correct. It may be determined that it is appropriate.
  • the first determination unit 1014 determines that the mounting state of the blood pressure measurement unit 110 by the subject is inappropriate according to the determination result indicating that the mounting state of the electrocardiographic measurement unit 109 by the subject is inappropriate. I do. Note that the comparison between the electrocardiographic data and the first reference data may be performed using various methods, and is not limited.
  • the first determination unit 1014 indirectly determines whether the subject is properly or inappropriately wearing the blood pressure measurement unit 110 based on the electrocardiogram data itself.
  • the first determination unit 1014 receives electrocardiogram data from the first acquisition unit 1011.
  • the first determination unit 1014 determines whether the subject's wearing state of the electrocardiogram measurement unit 109 is appropriate or inappropriate based on the degree of physical quantity fluctuation in the electrocardiogram data itself.
  • Various determinations may be made by the subject based on the electrocardiogram data itself to determine whether the electrocardiogram measurement unit 109 is properly or inappropriately mounted, and is not limited.
  • the first determination unit 1014 determines whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate, depending on whether the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate or inappropriate.
  • the first determination unit 1014 generates a first determination result.
  • the first determination result indicates whether the mounting state of the blood pressure measurement unit 110 by the subject is appropriate or inappropriate.
  • First determination unit 1014 outputs the first determination result to second determination unit 1015.
  • the second determination unit 1015 determines whether the reliability of the blood pressure data is high or low according to the first determination result, as exemplified below. First, the second determination unit 1015 receives the blood pressure data from the second acquisition unit 1012. The second determination unit 1015 receives the first determination result from the first determination unit 1014. Next, the second determination unit 1015 analyzes the content of the first determination result. The second determination unit 1015 determines that the reliability of the blood pressure data is high in response to the acquisition of the first determination result indicating that the subject's wearing state of the blood pressure measurement unit 110 is appropriate. One reason is that the accuracy of blood pressure measurement by the blood pressure measurement unit 110 is high if the subject's wearing state of the blood pressure measurement unit 110 is appropriate.
  • the second determination unit 1015 determines that the reliability of the blood pressure data is low in response to the acquisition of the first determination result indicating that the mounting state of the blood pressure measurement unit 110 by the subject is inappropriate.
  • One reason is that the accuracy of blood pressure measurement by the blood pressure measurement unit 110 is low if the subject's wearing state of the blood pressure measurement unit 110 is inappropriate.
  • the second determination unit 1015 generates a second determination result.
  • the second determination result indicates whether the reliability of the blood pressure data is high or low.
  • Second determination unit 1015 outputs the second determination result to data output unit 1016 and signal output unit 1017.
  • the data output unit 1016 will be described.
  • the data output unit 1016 outputs blood pressure data associated with data indicating whether the reliability of the blood pressure data is high or low, as exemplified below.
  • the data output unit 1016 receives the blood pressure data from the second acquisition unit 1012.
  • Data output unit 1016 receives the second determination result from second determination unit 1015.
  • the data output unit 1016 analyzes the contents of the second determination result.
  • the data output unit 1016 generates data indicating whether the reliability of the blood pressure data is high or low in accordance with the second determination result. Data indicating whether the reliability of the blood pressure data is high or low is also referred to as reliability data.
  • the data output unit 1016 associates the reliability data with the blood pressure data.
  • the data output unit 1016 associates the reliability data with the blood pressure data by adding (labeling) the reliability data to the blood pressure data.
  • the data output unit 1016 outputs the blood pressure data associated with the reliability data to the PHR server 3 via the communication interface 105.
  • the PHR server 3 can manage the blood pressure data in association with the reliability data.
  • the signal output unit 1017 will be described.
  • the signal output unit 1017 outputs a support signal according to a second determination result indicating that the reliability of the blood pressure data is low, as exemplified below.
  • the support signal is a signal that instructs execution of support for improving the wearing state of the blood pressure measurement unit 110 for the subject.
  • the signal output unit 1017 receives the second determination result from the second determination unit 1015.
  • the signal output unit 1017 analyzes the content of the second determination result and determines whether the reliability of the blood pressure data is high or low.
  • the signal output unit 1017 outputs a support signal.
  • the signal output unit 1017 omits the output of the support signal.
  • the signal output unit 1017 outputs a support signal to at least one of the display unit 107 and the audio output unit 108.
  • the display unit 107 displays a screen of a message indicating that the wearing state of the blood pressure measurement unit 110 by the subject is not appropriate based on the support signal.
  • the voice output unit 108 outputs a voice message indicating that the wearing state of the blood pressure measurement unit 110 by the subject is not appropriate based on the support signal.
  • the message may be any content as long as the message indicates that the wearing state of the blood pressure measurement unit 110 by the subject is not appropriate, and is not limited.
  • the subject can appropriately re-attach the blood pressure measurement unit 110 by the message. Thereby, the measuring device 1 can obtain highly reliable blood pressure data.
  • the signal output unit 1017 may output the support signal to elements other than the display unit 107 and the audio output unit 108.
  • the signal output unit 1017 may output a support signal to a support providing device that provides an external stimulus to the subject.
  • the external stimulus is, but not limited to, a vibration.
  • FIG. 5 is a flowchart illustrating a reliability determination operation in the measurement device 1.
  • the processing procedure described below is merely an example, and each processing may be changed as much as possible. In the processing procedure described below, steps can be omitted, replaced, and added as appropriate.
  • the first acquisition unit 1011 acquires the subject's electrocardiogram data (step S101).
  • step S101 the first acquisition unit 1011 acquires the subject's electrocardiogram data from the storage device 104 as illustrated.
  • the first acquisition unit 1011 outputs electrocardiogram data to the second acquisition unit 1012 and the first determination unit 1014.
  • the second acquiring unit 1012 acquires the blood pressure data of the subject measured within a predetermined period including the measurement date and time of the electrocardiographic data of the subject (Step S102). In step S102, the second acquisition unit 1012 acquires the subject's blood pressure data from the storage device 104 with reference to the measurement date and time of the electrocardiographic data, as illustrated. The second acquisition unit 1012 outputs to the data output unit 1016.
  • the first determination unit 1014 determines whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate (step S103). In step S103, the first determination unit 1014 indirectly determines whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate based on the electrocardiographic data, as illustrated. First determination unit 1014 outputs the first determination result to second determination unit 1015.
  • the second determination unit 1015 determines whether the reliability of the blood pressure data is high or low (step S104). In step S104, the second determination unit 1015 determines whether the reliability of the blood pressure data is high or low according to the first determination result, as illustrated. Second determination unit 1015 outputs the second determination result to data output unit 1016 and signal output unit 1017.
  • the data output unit 1016 outputs the blood pressure data associated with the reliability data (Step S105). In step S105, the data output unit 1016 outputs the blood pressure data associated with the reliability data according to the second determination result to the external device via the communication interface 105 as illustrated.
  • the signal output unit 1017 determines whether the reliability of the blood pressure data is high or low (step S106). In step S106, as illustrated, the signal output unit 1017 determines whether the reliability of the blood pressure data is high or low based on the second determination result. If the reliability of the blood pressure data is high (No at Step S106), the processor 101 ends the reliability determination operation. When the reliability of the blood pressure data is low (Step S106, Yes), the signal output unit 1017 outputs a support signal (Step S107). In step S107, the signal output unit 1017 outputs a support signal to at least one of the display unit 107 and the audio output unit 108, as illustrated.
  • the processor 101 can repeatedly execute the above-described reliability determination operation every time the subject's electrocardiogram data is acquired from the storage device 104.
  • the measuring device 1 determines whether the reliability of the second biometric data is high or low according to the first determination result based on the first biometric data. Can be determined. For example, there is biometric data that not only fluctuates according to the mounting state of the measurement unit included in the measurement device 1 by the subject, but also sensitively reacts to an abnormal body. On the other hand, there is biometric data that not only varies according to the mounting state of the measuring unit included in the measuring device 1 by the subject but also does not react so much in the resting state if the abnormality that occurs on the body is mild. The former biometric data is susceptible to abnormalities in the subject's body.
  • the former biometric data is not suitable for evaluating whether the mounting state of the measurement unit for measuring the former biometric data included in the measuring device 1 by the subject is appropriate or inappropriate.
  • the latter biometric data is not frequently affected by abnormalities in the subject's body. Therefore, the latter biometric data is suitable for evaluating whether the mounting state of the measurement unit for measuring the latter biometric data included in the measurement device 1 by the subject is appropriate or inappropriate.
  • the measurement device 1 includes two measurement units that measure different biological data, if the wearing state of one measurement unit by the subject is appropriate, the wearing state of the other measurement unit by the subject is also appropriate. Probability is high.
  • the measurement device 1 uses the latter biometric data as first biometric data, and uses the former biometric data as second biometric data. Thereby, even if measurement device 1 cannot directly determine whether the measurement unit that measures the second biometric data by the subject is appropriate or inappropriate based on the second biometric data, Based on the first biometric data, it is possible to indirectly determine whether the mounting state of the measurement unit that measures the second biometric data by the subject is appropriate or inappropriate.
  • the measurement device 1 indirectly uses the second biometric data based on the first biometric data.
  • the reliability of biometric data can be evaluated.
  • the measurement device 1 can determine whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate based on the comparison result between the first biological data and the reference data. .
  • the measurement apparatus 1 can accurately determine whether the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate or inappropriate by using the reference data, so that the subject's wearing state of the blood pressure measurement unit 110 is appropriate. Whether it is inappropriate or not can be accurately determined.
  • the measurement device 1 can acquire the subject's electrocardiographic data as the first biometric data and acquire the subject's blood pressure data as the second biometric data. Since the electrocardiographic data is not frequently affected by abnormalities of the subject's body, the electrocardiographic data is suitable for evaluating whether the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate or inappropriate. Since the blood pressure data is easily affected by abnormalities in the body of the subject, the blood pressure data is not suitable for evaluating whether the wearing state of the blood pressure measurement unit 110 by the subject is appropriate or inappropriate.
  • the measurement device 1 can measure the blood pressure by the subject based on the electrocardiographic data even if it is not possible to directly determine whether the wearing state of the blood pressure measurement unit 110 by the subject is appropriate or inappropriate based on the blood pressure data. It is possible to indirectly determine whether the mounting state of the unit 110 is appropriate or inappropriate. Even if it is difficult to directly evaluate the reliability of the blood pressure data based on the blood pressure data, the measuring device 1 can indirectly evaluate the reliability of the blood pressure data based on the electrocardiographic data.
  • the measurement device 1 can output the support signal in accordance with the second determination result indicating that the reliability of the second biometric data is low.
  • the measurement device 1 can measure highly reliable second biological data by supporting the improvement of the state of attachment of the blood pressure measurement unit 110 to the subject.
  • the measuring device 1 can output the second biological data associated with the reliability data.
  • the measurement device 1 can assist the doctor in diagnosing by providing the doctor with the second biometric data associated with the reliability data. By confirming the reliability of the second biometric data, the doctor can easily determine whether or not to use the second biometric data for the examination of the subject.
  • the electrocardiogram measurement unit 109 is described as an example of a first measurement unit, and the blood pressure measurement unit 110 is described as an example of a second measurement unit.
  • the blood pressure measurement unit 110 may be an example of a first measurement unit, and the electrocardiogram measurement unit 109 may be an example of a second measurement unit.
  • the first obtaining unit 1011 may obtain blood pressure data as first biological data.
  • the second acquisition unit 1012 may acquire electrocardiogram data as second biological data.
  • the third obtaining unit 1013 may obtain second reference data relating to the blood pressure of the subject, and the first determining unit 1014 may compare the blood pressure data with the second reference data.
  • the first acquisition unit 1011 may acquire data indicating physical quantities of a living body other than electrocardiogram and blood pressure as first living body data.
  • the second acquisition unit 1012 may acquire, as the second biometric data, data indicating a physical quantity of a living body different from the first biometric data.
  • the measuring device 1 measures biological data regarding two different physical quantities, but is not limited thereto.
  • the measurement device 1 may measure biological data regarding three different physical quantities.
  • the measuring device 1 determines whether the subject's wearing state of the measuring device 1 is appropriate or inappropriate based on the first biometric data and the second biometric data, and determines a third one according to the determination result. It may be determined whether the reliability of the biometric data is high or low.
  • the present invention is not limited to the present embodiment as it is, and can be embodied by modifying the constituent elements in the implementation stage without departing from the scope of the invention. Further, various inventions can be formed by appropriately combining a plurality of components disclosed in the present embodiment. For example, some components may be deleted from all the components shown in the present embodiment. Further, components of different embodiments may be appropriately combined.
  • a first measurement unit (109) for measuring first biological data of the subject A second measurement unit (110) that measures the second biometric data of the subject within a predetermined period including the measurement date and time of the first biometric data; A first determination unit (1014) that determines whether a mounting state of the second measurement unit by the subject is appropriate or inappropriate based on the first biometric data; A second determination unit (1015) that determines whether the reliability of the second biometric data is high or low according to a determination result indicating whether the mounting state is appropriate or inappropriate;
  • a biological data measurement device (1) comprising:

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Abstract

A technique for evaluating the reliability of biometric data is provided. This biometric data measurement device is provided with: a first measurement unit which measures first biometric data of a subject; a second measurement unit which measures second biometric data of the subject within a prescribed time period including the measurement date and time of the first biometric data; a first determination unit which, on the basis of the first biometric data, determines whether the wearing state of the subject wearing the second measurement unit is suitable or unsuitable; and a second determination unit which, depending on the determination result indicating whether the wearing state is suitable or unsuitable, determines that the reliability of the second biometric data is high or low.

Description

生体データ測定装置、生体データ処理方法及び生体データ処理のためのプログラムBiometric data measurement device, biometric data processing method, and program for biometric data processing
 この発明は、生体データ測定装置、生体データ処理方法及び生体データ処理のためのプログラムに関する。 The present invention relates to a biological data measurement device, a biological data processing method, and a program for processing biological data.
 心電及び血圧などの生体データを測定可能な測定装置が普及している。対象者は、自ら測定装置を装着し、日常的に生体データを測定することができる。このような生体データは、病気の診断など多方面での活用が期待されている。 測定 Measuring devices capable of measuring biological data such as electrocardiogram and blood pressure have become widespread. The subject can wear the measuring device and measure biological data on a daily basis. Such biometric data is expected to be used in various fields such as disease diagnosis.
日本国特開2015-77229号公報Japanese Patent Application Laid-Open No. 2015-77229
 しかしながら、対象者による測定装置の装着状態が適切ではない状態で測定された生体データは、データ自体の信頼性が低い。そのため、生体データは、対象者による測定装置の装着状態が適切な状態で測定されている方が好ましい。 However, the biological data measured in a state where the subject wears the measuring device improperly has low reliability. Therefore, it is preferable that the biometric data be measured in a state where the subject wears the measuring device in an appropriate state.
 特許文献1は、カフの円周方向における伸び量に基づいてカフが対象者に装着されているか否かを検出する技術を開示している。しかしながら、特許文献1に開示された技術では、対象者による測定装置の装着状態が適切か不適切かを判断することはできない。そのため、特許文献1に開示された技術では、生体データの信頼性を評価することは難しい。 Patent Document 1 discloses a technique for detecting whether or not a cuff is worn on a subject based on the amount of extension of the cuff in the circumferential direction. However, according to the technique disclosed in Patent Literature 1, it is not possible to determine whether the subject is properly or inappropriately wearing the measuring device. Therefore, it is difficult to evaluate the reliability of biometric data using the technique disclosed in Patent Document 1.
 本発明の目的は、上記事情に着目してなされたもので、生体データの信頼性を評価する技術を提供することである。 目的 An object of the present invention is to pay attention to the above circumstances, and to provide a technique for evaluating the reliability of biometric data.
 本開示の第1の態様は、対象者の第1の生体データを測定する第1の測定部と、前記第1の生体データの測定日時を含む所定期間内の前記対象者の第2の生体データを測定する第2の測定部と、前記第1の生体データに基づいて、前記対象者による前記第2の測定部の装着状態が適切か不適切かを判断する第1の判断部と、前記装着状態が適切または不適切の何れかを示す判断結果に応じて、前記第2の生体データの信頼性が高いか低いかを判断する第2の判断部とを備える生体データ測定装置である。 
 例えば、対象者による生体データ測定装置に含まれる測定部の装着状態に応じて変動するだけでなく、身体の異変に敏感に反応する生体データがある。他方、対象者による生体データ測定装置に含まれる測定部の装着状態に応じて変動するだけでなく、身体に発生した異変が軽度であれば安静状態ではそれほど反応しない生体データがある。前者の生体データは、対象者の身体の異変に影響されやすい。そのため、前者の生体データは、対象者による生体データ測定装置に含まれる前者の生体データを測定する測定部の装着状態が適切か不適切かの評価に適していない。後者の生体データは、対象者の身体の異変に頻繁には影響を受けない。そのため、後者の生体データは、対象者による生体データ測定装置に含まれる後者の生体データを測定する測定部の装着状態が適切か不適切かの評価に適している。また、生体データ測定装置が異なる生体データを測定する2つの測定部を含む場合、対象者による一方の測定部の装着状態が適切であれば、対象者による他方の測定部の装着状態も適切である可能性が高い。他方、対象者による一方の測定部の装着状態が不適切であれば、対象者による他方の測定部の装着状態も不適切である可能性が高い。生体データ測定装置は、後者の生体データを第1の生体データ、前者の生体データを第2の生体データとして用いている。これにより、生体データ測定装置は、第2の生体データに基づいて対象者による第2の生体データを測定する測定部の装着状態が適切か不適切かを直接的に判断することができなくても、第1の生体データに基づいて対象者による第2の生体データを測定する測定部の装着状態が適切か不適切かを間接的に判断することができる。その結果、生体データ測定装置は、第2の生体データに基づいて第2の生体データの信頼性を直接的に評価することが難しくても、第1の生体データに基づいて間接的に第2の生体データの信頼性を評価することができる。
A first aspect of the present disclosure is directed to a first measurement unit that measures first biological data of a subject, and a second biological data of the subject within a predetermined period including a measurement date and time of the first biological data. A second measurement unit that measures data, and a first determination unit that determines whether the wearing state of the second measurement unit by the subject is appropriate or inappropriate based on the first biological data, A biometric data measurement device comprising: a second determination unit configured to determine whether the reliability of the second biometric data is high or low in accordance with a determination result indicating whether the mounting state is appropriate or inappropriate. .
For example, there is biometric data that not only changes according to the mounting state of the measurement unit included in the biometric data measurement device by the subject, but also reacts sensitively to abnormal body changes. On the other hand, there are biometric data that not only vary according to the state of attachment of the measurement unit included in the biometric data measurement device by the subject, but also do not react so much in the resting state if the abnormality that occurs on the body is mild. The former biometric data is susceptible to abnormalities in the subject's body. For this reason, the former biometric data is not suitable for evaluating whether the mounting state of the measurement unit for measuring the former biometric data included in the biometric data measurement device by the subject is appropriate or inappropriate. The latter biometric data is not frequently affected by abnormalities in the subject's body. Therefore, the latter biometric data is suitable for evaluating whether the mounting state of the measurement unit for measuring the latter biometric data included in the biometric data measurement device by the subject is appropriate or inappropriate. In addition, when the biological data measuring device includes two measuring units that measure different biological data, if the mounting state of one measuring unit by the subject is appropriate, the mounting state of the other measuring unit by the subject is also appropriate. Probably. On the other hand, if the mounting state of one measurement unit by the subject is inappropriate, it is highly likely that the mounting state of the other measurement unit by the subject is also inappropriate. The biometric data measurement device uses the latter biometric data as first biometric data and the former biometric data as second biometric data. Accordingly, the biological data measurement device cannot directly determine whether the measurement unit that measures the second biological data by the subject is appropriate or inappropriate based on the second biological data. Also, it is possible to indirectly determine whether the mounting state of the measurement unit that measures the second biological data by the subject is appropriate or inappropriate based on the first biological data. As a result, even if it is difficult for the biometric data measurement device to directly evaluate the reliability of the second biometric data based on the second biometric data, the biometric data measurement device may indirectly evaluate the second biometric data based on the first biometric data. Can be evaluated for the reliability of the biological data.
 本開示の第2の態様は、上記第1の態様において、前記第1の生体データと比較する予め定められた参照データを取得する取得部をさらに備え、前記第1の判断部が、前記第1の生体データを前記参照データと比較し、前記第1の生体データと前記参照データとの比較結果に基づいて、前記装着状態が適切か不適切かを判断するようにしたものである。 
 生体データ測定装置は、参照データを用いることで対象者による第1の測定部の装着状態が適切か不適切かを精度良く判断することができるので、対象者による第2の測定部の装着状態が適切か不適切かも精度良く判断することができる。
According to a second aspect of the present disclosure, in the first aspect, the information processing apparatus further includes an acquisition unit configured to acquire predetermined reference data to be compared with the first biometric data, wherein the first determination unit includes The first biometric data is compared with the reference data, and it is determined whether the wearing state is appropriate or inappropriate based on a comparison result between the first biometric data and the reference data.
The biological data measurement device can accurately determine whether the subject is properly or inappropriately wearing the first measurement unit by using the reference data. Can be determined with high accuracy as to whether it is appropriate or inappropriate.
 本開示の第3の態様は、上記第1の態様において、前記第1の測定部が、前記第1の生体データとして前記対象者の心電に関するデータを測定し、前記第2の測定部が、前記第2の生体データとして前記対象者の血圧に関するデータを測定するようにしたものである。 
 心電データは、対象者の身体の異変に頻繁には影響を受けないので、対象者による第1の測定部の装着状態が適切か不適切かの評価に適している。血圧データは、対象者の身体の異変に影響されやすいので、対象者による第2の測定部の装着状態が適切か不適切かの評価に適していない。生体データ測定装置は、血圧データに基づいて対象者による第2の測定部の装着状態が適切か不適切かを直接的に判断することができなくても、心電データに基づいて対象者による第2の測定部の装着状態が適切か不適切かを間接的に判断することができる。生体データ測定装置は、血圧データに基づいて血圧データの信頼性を直接的に評価することが難しくても、心電データに基づいて間接的に血圧データの信頼性を評価することができる。
According to a third aspect of the present disclosure, in the first aspect, the first measurement unit measures data related to the subject's electrocardiogram as the first biological data, and the second measurement unit , Data relating to the blood pressure of the subject is measured as the second biological data.
Since the electrocardiographic data is not frequently affected by abnormalities of the subject's body, the electrocardiographic data is suitable for evaluating whether the subject is properly or inappropriately wearing the first measurement unit. Since the blood pressure data is easily affected by abnormalities of the subject's body, it is not suitable for the subject to evaluate whether the second measurement unit is properly or inappropriately mounted. The biological data measurement device can determine whether the second measurement section is properly or inappropriately worn by the subject based on the blood pressure data, even if the subject cannot directly determine whether the second measurement unit is properly mounted. It is possible to indirectly determine whether the mounting state of the second measuring unit is appropriate or inappropriate. Even if it is difficult to directly evaluate the reliability of blood pressure data based on blood pressure data, the biological data measurement device can indirectly evaluate the reliability of blood pressure data based on electrocardiographic data.
 本開示の第4の態様は、上記第1の態様において、前記第2の生体データの信頼性が低いことを示す判断結果に応じて、前記対象者に対する前記第2の測定部の前記装着状態を改善させる支援の実行を指示する信号を出力する信号出力部をさらに備えるようにしたものである。 
 生体データ測定装置は、対象者に対する第2の測定部の装着状態の改善を支援することで、信頼性の高い第2の生体データを測定することができる。
According to a fourth aspect of the present disclosure, in the first aspect, the mounting state of the second measurement unit with respect to the subject in response to a determination result indicating that the reliability of the second biometric data is low. And a signal output unit that outputs a signal instructing execution of support for improving the above.
The biological data measurement device can measure highly reliable second biological data by supporting the improvement of the state of attachment of the second measurement unit to the subject.
 本開示の第5の態様は、上記第1の態様において、前記第2の生体データの信頼性が高いまたは低いの何れかを示すデータと関連付けられた前記第2の生体データを出力するデータ出力部をさらに備えるようにしたものである。 
 生体データ測定装置は、信頼性データと関連付けられた第2の生体データを医師に提供することで、医師による診断を支援することができる。医師は、第2の生体データの信頼性を確認することで、第2の生体データを対象者の診察に活用するか否かを容易に判断することができる。
According to a fifth aspect of the present disclosure, in the first aspect, the data output that outputs the second biometric data associated with data indicating whether the reliability of the second biometric data is high or low. It further includes a unit.
The biometric data measurement device can assist a doctor in making a diagnosis by providing the doctor with the second biometric data associated with the reliability data. By confirming the reliability of the second biometric data, the doctor can easily determine whether or not to use the second biometric data for the examination of the subject.
 本開示の第6の態様は、生体データ測定装置に含まれる第1の測定部において、対象者の第1の生体データを測定する第1の測定過程と、前記生体データ測定装置に含まれる第2の測定部において、前記第1の生体データの測定日時を含む所定期間内の前記対象者の第2の生体データを測定する第2の測定過程と、前記第1の生体データに基づいて、前記対象者による前記第2の測定部の装着状態が適切か不適切かを判断する第1の判断過程と、前記装着状態が適切または不適切の何れかを示す判断結果に応じて、前記第2の生体データの信頼性が高いか低いかを判断する第2の判断過程とを備える生体データ処理方法である。 
 第6の態様によれば、生体データ処理方法は、上述の第1の態様と同様の効果を得ることができる。
A sixth aspect of the present disclosure is directed to a first measurement unit that measures first biological data of a subject in a first measurement unit included in the biological data measurement device, and a first measurement process that is included in the biological data measurement device. In the second measurement unit, based on the second measurement process of measuring the second biometric data of the subject within a predetermined period including the measurement date and time of the first biometric data, based on the first biometric data, A first determination step of determining whether the mounting state of the second measurement unit by the subject is appropriate or inappropriate; and a determination result indicating whether the mounting state is appropriate or inappropriate. A second determining step of determining whether the reliability of the second biometric data is high or low.
According to the sixth aspect, the biological data processing method can obtain the same effects as those of the first aspect.
 本開示の第7の態様は、第1の態様から第5の態様のうちの何れかの生体データ測定装置が備える各部の処理をコンピュータに実行させる生体データ処理のためのプログラムである。 
 第7の態様によれば、生体データ処理のためのプログラムは、上述の第1の態様と同様の効果を得ることができる。
A seventh aspect of the present disclosure is a program for biometric data processing that causes a computer to execute the processing of each unit included in the biometric data measurement device according to any one of the first to fifth aspects.
According to the seventh aspect, the program for biometric data processing can obtain the same effect as the above-described first aspect.
 本発明によれば、生体データの信頼性を評価する技術を提供することができる。 According to the present invention, a technology for evaluating the reliability of biological data can be provided.
図1は、本実施形態に係る測定装置の適用例を模式的に示す図である。FIG. 1 is a diagram schematically showing an application example of the measuring device according to the present embodiment. 図2は、本実施形態に係る生体データ管理システムの全体構成を例示する図である。FIG. 2 is a diagram illustrating an example of the overall configuration of the biometric data management system according to the present embodiment. 図3は、本実施形態に係る測定装置のハードウェア構成を例示するブロック図である。FIG. 3 is a block diagram illustrating a hardware configuration of the measuring device according to the present embodiment. 図4は、本実施形態に係る測定装置のソフトウェア構成を例示するブロック図である。FIG. 4 is a block diagram illustrating a software configuration of the measuring device according to the present embodiment. 図5は、本実施形態に係る測定装置における信頼性判断動作を例示するフローチャートである。FIG. 5 is a flowchart illustrating the reliability determination operation in the measuring device according to the present embodiment.
 以下、本開示に係る実施の形態(以下、「本実施形態」とも表記する)を、図面に基づいて説明する。ただし、以下で説明する本実施形態は、あらゆる点において例示に過ぎない。なお、以降、説明済みの要素と同一または類似の要素には同一または類似の符号を付し、重複する説明については基本的に省略する。 Hereinafter, an embodiment according to the present disclosure (hereinafter, also referred to as “the present embodiment”) will be described with reference to the drawings. However, the present embodiment described below is merely an example in every respect. Hereinafter, the same or similar elements as those already described are denoted by the same or similar reference numerals, and duplicate description will be basically omitted.
 §1 適用例 
 本実施形態は、生体データの信頼性を評価し、信頼性に関するデータを生体データに関連付ける技術である。 
 図1は、測定装置A1の適用例を模式的に示す図である。 
 測定装置A1は、心電測定部A11及び血圧測定部A12を備える。心電測定部A11は、測定装置A1を装着する対象者の心電を測定する。血圧測定部A12は、測定装置A1を装着する対象者の血圧を測定する。典型例では、血圧測定部A12は、心電の測定日時を含む所定期間内の対象者の血圧を測定する。
§1 Application example
The present embodiment is a technique for evaluating the reliability of biometric data and associating data related to the reliability with the biometric data.
FIG. 1 is a diagram schematically illustrating an application example of the measuring device A1.
The measuring device A1 includes an electrocardiographic measuring unit A11 and a blood pressure measuring unit A12. The electrocardiogram measurement unit A11 measures the electrocardiogram of a subject wearing the measurement device A1. The blood pressure measurement unit A12 measures the blood pressure of the subject wearing the measurement device A1. In a typical example, the blood pressure measurement unit A12 measures the blood pressure of the subject within a predetermined period including the date and time of measuring the electrocardiogram.
 測定装置A1は、携帯端末A2を介して、EHR(Electronic Health Records)サーバA3から参照データを取得する。参照データは、対象者による心電測定部A11の装着状態が適切か不適切かの判断に用いられるデータである。測定装置A1は、心電データ及び参照データに基づいて、対象者による心電測定部A11の装着状態が適切か不適切かを判断する。測定装置A1は、対象者による心電測定部A11の装着状態が適切か不適切かに応じて、対象者による血圧測定部A12の装着状態が適切か不適切かを判断する。測定装置A1は、対象者による血圧測定部A12の装着状態が適切または不適切の何れかを示す第1の判断結果に応じて、血圧データの信頼性が高いか低いかを判断する。測定装置A1は、血圧データの信頼性が高いまたは低いの何れかを示す第2の判断結果に応じて、信頼性データを血圧データに関連付ける。信頼性データは、血圧データの信頼性が高いまたは低いの何れかを示す。測定装置A1は、携帯端末A2を介して、信頼性データと関連付けられた血圧データをPHR(Personal Health Records)サーバA4へ送信する。PHRサーバA4は、測定装置A1で測定された各人の血圧データを信頼性データと関連付けて管理するサーバである。 The measuring device A1 acquires reference data from an EHR (Electronic Health Records) server A3 via the mobile terminal A2. The reference data is data used to determine whether the subject's wearing state of the electrocardiographic measurement unit A11 is appropriate or inappropriate. The measurement device A1 determines whether the subject's wearing state of the electrocardiogram measurement unit A11 is appropriate or inappropriate based on the electrocardiogram data and the reference data. The measurement device A1 determines whether the subject's wearing state of the blood pressure measuring unit A12 is appropriate or inappropriate depending on whether the subject's wearing state of the electrocardiographic measurement unit A11 is appropriate or inappropriate. The measurement device A1 determines whether the reliability of the blood pressure data is high or low according to a first determination result indicating whether the mounting state of the blood pressure measurement unit A12 by the subject is appropriate or inappropriate. The measurement device A1 associates the reliability data with the blood pressure data according to a second determination result indicating whether the reliability of the blood pressure data is high or low. The reliability data indicates whether the reliability of the blood pressure data is high or low. The measurement device A1 transmits the blood pressure data associated with the reliability data to the PHR (Personal Health Records) server A4 via the mobile terminal A2. The PHR server A4 is a server that manages each person's blood pressure data measured by the measurement device A1 in association with reliability data.
 このように、測定装置A1は、生体データの信頼性を評価することができる。 測定 Thus, the measurement device A1 can evaluate the reliability of the biological data.
 §2 構成例 
 <生体データ管理システム> 
 図2は、生体データ管理システム100の全体構成を例示する図である。生体データ管理システム100は、各人の生体データを管理するためのシステムである。 
 生体データ管理システム100は、測定装置1、携帯端末2、PHRサーバ3及びEHRサーバ4を備える。携帯端末2、PHRサーバ3及びEHRサーバ4は、互いにネットワークを介して通信可能である。例えば、ネットワークは、インターネットである。
§2 Configuration example
<Biometric data management system>
FIG. 2 is a diagram illustrating an overall configuration of the biometric data management system 100. The biometric data management system 100 is a system for managing biometric data of each person.
The biological data management system 100 includes a measurement device 1, a mobile terminal 2, a PHR server 3, and an EHR server 4. The mobile terminal 2, the PHR server 3, and the EHR server 4 can communicate with each other via a network. For example, the network is the Internet.
 測定装置1は、測定装置1を装着する対象者の生体の物理量を測定する装置である。測定装置1は、少なくとも2種類の異なる物理量を測定する。例えば、測定装置1は、心電及び血圧を測定する。測定装置1は、対象者の生体の物理量を示す生体データを測定する。生体データの一例は、心電を示すデータである。心電を示すデータは、心電データともいう。なお、「心電データ」は、単に「心電」ということもあるので、適宜読み替えてもよい。例えば、心電データは、測定期間における心電の変動を示す波形データである。これに代えて、心電データは、測定期間における心電の特徴量を示すデータであってもよい。例えば、特徴量は、ピーク値であるが、これに限定されない。心電は、P波であっても、R波であっても、S波であってもよく、限定されない。生体データの別の例は、血圧を示すデータを含む。血圧を示すデータは、血圧データともいう。なお、「血圧データ」は、単に「血圧」ということもあるので、適宜読み替えてもよい。例えば、血圧データは、血圧測定時における収縮期血圧SBP(Systolic Blood Pressure)の値及び拡張期血圧DBP(Diastolic Blood Pressure)の値を示すデータである。これに代えて、血圧データは、測定期間におけるSBP及びDBPの変動を示す波形データであってもよい。測定装置1は、生体データ測定装置ともいう。 The measuring device 1 is a device that measures a physical quantity of a living body of a subject to which the measuring device 1 is worn. The measurement device 1 measures at least two different physical quantities. For example, the measuring device 1 measures an electrocardiogram and a blood pressure. The measurement device 1 measures biological data indicating a physical quantity of a living body of a subject. An example of the biometric data is data indicating an electrocardiogram. Data indicating an electrocardiogram is also referred to as electrocardiogram data. Note that the “electrocardiogram data” may be simply referred to as “electrocardiogram” and may be appropriately read. For example, the electrocardiogram data is waveform data indicating the fluctuation of the electrocardiogram during the measurement period. Instead, the electrocardiogram data may be data indicating a feature value of the electrocardiogram during the measurement period. For example, the feature value is a peak value, but is not limited thereto. The electrocardiogram may be a P wave, an R wave, or an S wave, and is not limited. Another example of the biometric data includes data indicating blood pressure. Data indicating blood pressure is also referred to as blood pressure data. Note that the “blood pressure data” may be simply referred to as “blood pressure” and may be appropriately replaced. For example, the blood pressure data is data indicating a value of systolic blood pressure SBP (Systolic Blood Pressure) and a value of diastolic blood pressure DBP (Diastatic Blood Pressure) at the time of blood pressure measurement. Instead, the blood pressure data may be waveform data indicating fluctuations in SBP and DBP during the measurement period. The measurement device 1 is also called a biological data measurement device.
 携帯端末2は、測定装置1から心電データ及び血圧データを取得し、心電データ及び血圧データをPHRサーバ3へ提供する装置である。例えば、携帯端末2は、スマートフォンまたはタブレットであるが、これらに限定されない。携帯端末2は、生体データ提供装置の一例である。 The portable terminal 2 is a device that acquires electrocardiographic data and blood pressure data from the measuring device 1 and provides the electrocardiographic data and blood pressure data to the PHR server 3. For example, the mobile terminal 2 is a smartphone or a tablet, but is not limited thereto. The mobile terminal 2 is an example of a biometric data providing device.
 PHRサーバ3は、測定装置1で測定された各人の生体データを管理するサーバである。PHRサーバ3は、携帯端末2から各人の生体データを収集する。これに代えて、PHRサーバ3は、測定装置1から直接、各人の生体データを収集してもよい。医師は、PHRサーバ3で管理されている生体データを各人の診察に活用することができる。 The PHR server 3 is a server that manages the biometric data of each person measured by the measuring device 1. The PHR server 3 collects biometric data of each person from the mobile terminal 2. Instead, the PHR server 3 may directly collect the biometric data of each person from the measurement device 1. The doctor can utilize the biometric data managed by the PHR server 3 for each patient's examination.
 EHRサーバ4は、医師による各人の診察に関するデータを管理するサーバである。EHRサーバ4は、医師がPC(Personal Computer)を用いて入力する電子カルテと連携して、各人の診察に関するデータを管理する。診察に関するデータは、診察データともいう。 The EHR server 4 is a server that manages data on medical examinations performed by doctors. The EHR server 4 manages data related to each patient's examination in cooperation with an electronic medical record input by a doctor using a PC (Personal Computer). Data related to the consultation is also referred to as consultation data.
 診察データは、各人の生体の物理量を示す参照データを含む。参照データは、後述するように、対象者による測定装置1に含まれる測定部の装着状態が適切か不適切かの判断に用いられるデータである。参照データは、対象者が適切に測定装置1に含まれる測定部を装着した状態で測定された生体の物理量を示すデータである。 The examination data includes reference data indicating the physical quantity of the living body of each person. The reference data is data used for determining whether the mounting state of the measuring unit included in the measuring device 1 by the subject is appropriate or inappropriate, as described later. The reference data is data indicating a physical quantity of a living body measured in a state where the subject appropriately wears the measurement unit included in the measurement device 1.
 診察データは、各人の心電に関する予め定められた第1の参照データを含む。第1の参照データは、後述するように、対象者による測定装置1に含まれる心電を測定する測定部の装着状態が適切か不適切かの判断に用いられるデータである。第1の参照データは、異なる時間帯に測定された複数の参照データを含んでいてもよい。例えば、第1の参照データは、午前の時刻における測定に基づく参照データ及び午後の時刻における測定に基づく参照データを含む。一つの理由は、心電データの傾向が時間帯よって異なるからである。これに代えて、第1の参照データは、対象者の異なる状態で測定された複数の参照データを含んでいてもよい。例えば、第1の参照データは、対象者の緊張状態での測定に基づく参照データ及び対象者の安静状態での測定に基づく参照データを含む。一つの理由は、心電データの傾向が対象者の状態によって異なるからである。なお、第1の参照データは、時間帯及び対象者の状態を組み合わせた複数の参照データを含んでいてもよい。第1の参照データが複数の参照データを含むことで、対象者による測定装置1に含まれる心電を測定する測定部の装着状態が適切か不適切かの判断精度は高まる。 The examination data includes first predetermined reference data relating to the electrocardiogram of each person. As will be described later, the first reference data is data used for determining whether the subject is properly or inappropriately wearing a measurement unit for measuring an electrocardiogram included in the measurement device 1. The first reference data may include a plurality of reference data measured at different time zones. For example, the first reference data includes reference data based on the measurement at the morning time and reference data based on the measurement at the afternoon time. One reason is that the tendency of electrocardiographic data differs depending on the time of day. Alternatively, the first reference data may include a plurality of reference data measured in different states of the subject. For example, the first reference data includes reference data based on the measurement of the subject in a nervous state and reference data based on the measurement of the subject in a resting state. One reason is that the tendency of the electrocardiographic data differs depending on the condition of the subject. Note that the first reference data may include a plurality of reference data obtained by combining the time zone and the state of the subject. When the first reference data includes a plurality of reference data, the accuracy of the determination by the subject as to whether the measurement unit included in the measurement device 1 that measures the electrocardiogram is properly or inappropriately mounted is increased.
 診察データは、各人の血圧に関する予め定められた第2の参照データを含む。第2の参照データは、後述するように、対象者による測定装置1に含まれる血圧を測定する測定部の装着状態が適切か不適切かの判断に用いられるデータである。第2の参照データは、異なる時間帯に測定された複数の参照データを含んでいてもよい。例えば、第2の参照データは、午前の時刻における測定に基づく参照データ及び午後の時刻における測定に基づく参照データを含む。一つの理由は、血圧データの傾向が時間帯よって異なるからである。これに代えて、第2の参照データは、対象者の異なる状態で測定された複数の参照データを含んでいてもよい。例えば、第2の参照データは、対象者の緊張状態での測定に基づく参照データ及び対象者の安静状態での測定に基づく参照データを含む。一つの理由は、血圧データの傾向が対象者の状態によって異なるからである。なお、第2の参照データは、時間帯及び対象者の状態を組み合わせた複数の参照データを含んでいてもよい。第2の参照データが複数の参照データを含むことで、対象者による測定装置1に含まれる血圧を測定する測定部の装着状態が適切か不適切かの判断精度は高まる。 The consultation data includes second predetermined reference data relating to the blood pressure of each individual. As will be described later, the second reference data is data used to determine whether the subject is properly or inappropriately wearing the measurement unit that measures the blood pressure included in the measurement device 1. The second reference data may include a plurality of reference data measured at different time zones. For example, the second reference data includes reference data based on the measurement at the morning time and reference data based on the measurement at the afternoon time. One reason is that the tendency of the blood pressure data differs depending on the time of day. Alternatively, the second reference data may include a plurality of reference data measured in different states of the subject. For example, the second reference data includes reference data based on the measurement of the subject in a nervous state and reference data based on the measurement of the subject in a resting state. One reason is that the tendency of the blood pressure data differs depending on the state of the subject. Note that the second reference data may include a plurality of reference data obtained by combining the time zone and the state of the subject. Since the second reference data includes a plurality of reference data, the accuracy of the determination whether the measurement unit included in the measurement device 1 that measures the blood pressure included in the measurement device 1 is properly or inappropriately mounted is increased.
 <測定装置> 
  [ハードウェア構成] 
 図3は、測定装置1のハードウェア構成を例示するブロック図である。 
 測定装置1は、プロセッサ101、ROM(Read Only Memory)102、RAM(Random Access Memory)103、記憶装置104、通信インタフェース105、入力部106、表示部107、音声出力部108、心電測定部109及び血圧測定部110を備える。各要素は、互いに電気的に接続されている。なお、図3では、通信インタフェースを、「通信I/F」と記載している。
<Measuring device>
[Hardware configuration]
FIG. 3 is a block diagram illustrating a hardware configuration of the measurement device 1.
The measurement device 1 includes a processor 101, a ROM (Read Only Memory) 102, a RAM (Random Access Memory) 103, a storage device 104, a communication interface 105, an input unit 106, a display unit 107, a voice output unit 108, and an electrocardiogram measurement unit 109. And a blood pressure measurement unit 110. Each element is electrically connected to each other. In FIG. 3, the communication interface is described as “communication I / F”.
 プロセッサ101は、測定装置1の各要素を制御する。例えば、プロセッサ101は、CPU(Central Processing Unit)であるが、これに限定されない。プロセッサ101は、記憶装置104に格納された測定装置1を実行させるためのプログラムをRAM103に展開する。そして、プロセッサ101がRAM103に展開されたプログラムを解釈及び実行することで、プロセッサ101は、各種動作を実行可能である。 The processor 101 controls each element of the measuring device 1. For example, the processor 101 is a CPU (Central Processing Unit), but is not limited thereto. The processor 101 loads a program for executing the measuring device 1 stored in the storage device 104 on the RAM 103. Then, the processor 101 can execute various operations by interpreting and executing the program developed in the RAM 103.
 記憶装置104は、いわゆる補助記憶装置である。例えば、記憶装置104は、内蔵または外付けのフラッシュメモリなどの半導体メモリであるが、これらに限定されない。記憶装置104は、プロセッサ101で実行されるプログラムを記憶する。なお、プログラムは、予め記憶装置104に記憶されていてもよい。プログラムは、ネットワークを介して測定装置1にダウンロードされてもよい。プログラムは、非一時的なコンピュータ可読媒体に記憶され、流通していてもよい。 
 記憶装置104は、後述する心電測定部109で測定された測定日時(測定タイミング)の異なる複数の心電データを記憶する。記憶装置104は、後述する血圧測定部110で測定された測定日時の異なる複数の血圧データを記憶する。
The storage device 104 is a so-called auxiliary storage device. For example, the storage device 104 is a semiconductor memory such as a built-in or external flash memory, but is not limited thereto. The storage device 104 stores a program executed by the processor 101. Note that the program may be stored in the storage device 104 in advance. The program may be downloaded to the measurement device 1 via a network. The program may be stored on a non-transitory computer-readable medium and distributed.
The storage device 104 stores a plurality of electrocardiogram data having different measurement dates and times (measurement timing) measured by an electrocardiogram measurement unit 109 described later. The storage device 104 stores a plurality of blood pressure data having different measurement dates and times measured by the blood pressure measurement unit 110 described later.
 通信インタフェース105は、測定装置1を他の装置と通信可能に接続するためのインタフェースである。通信インタフェース105は、近距離無線通信方式用のモジュールを含む。近距離無線通信方式は、例えばブルートゥース(登録商標)による通信方式であるが、これに限定されない。通信インタフェース105は、近距離無線通信方式を用いて、携帯端末2と直接的に通信する。なお、通信インタフェース105は、移動通信(3G、4Gなど)及びWLAN(Wireless Local Area Network)などのための各種無線通信方式用のモジュールを含んでいてもよい。この場合、通信インタフェース105は、携帯端末2を介することなく、PHRサーバ3及びEHRサーバ4と通信することができる。 The communication interface 105 is an interface for communicatively connecting the measuring device 1 to another device. The communication interface 105 includes a short-range wireless communication module. The short-range wireless communication method is, for example, a communication method based on Bluetooth (registered trademark), but is not limited thereto. The communication interface 105 communicates directly with the mobile terminal 2 using a short-range wireless communication method. The communication interface 105 may include modules for various wireless communication schemes for mobile communication (3G, 4G, etc.), WLAN (Wireless Local Area Network), and the like. In this case, the communication interface 105 can communicate with the PHR server 3 and the EHR server 4 without passing through the mobile terminal 2.
 入力部106は、対象者の入力による指示を受け付ける装置である。例えば、入力部106は、タッチパネル及び操作キーを含むが、これらに限定されない。入力部106は、対象者の入力による指示に応じた信号をプロセッサ101へ出力する。なお、入力部106は、対象者の操作に基づく入力による指示を受け付ける装置に限定されるものではなく、対象者の音声に基づく入力による指示を受け付ける装置であってもよい。 The input unit 106 is a device that receives an instruction based on an input by the subject. For example, the input unit 106 includes a touch panel and operation keys, but is not limited thereto. The input unit 106 outputs a signal to the processor 101 according to an instruction given by the subject. In addition, the input unit 106 is not limited to a device that receives an instruction based on an input based on an operation of the target person, and may be a device that receives an instruction based on a voice of the target person.
 表示部107は、情報を表示する装置である。例えば、表示部107は、液晶ディスプレイであるが、これに限定されない。 The display unit 107 is a device that displays information. For example, the display unit 107 is a liquid crystal display, but is not limited to this.
 音声出力部108は、音声を出力する装置である。例えば、音声出力部108は、スピーカであるが、これに限定されない。 The audio output unit 108 is a device that outputs audio. For example, the audio output unit 108 is a speaker, but is not limited to this.
 心電測定部109は、測定装置1を装着する対象者の心電を測定する装置である。例えば、心電測定部109は、2つの電極を備える。心電測定部109は、2つの電極における対象者の接触に応じて、2つの電極間に発生する電位差に基づいて対象者の心電を測定する。例えば、心電測定部109は、対象者が2つの電極に接触している期間、対象者の心電を測定する。心電測定部109は、心電を測定する毎に、心電データを記憶装置104に保存する。心電データは、心電の測定日時を示すデータを含む。心電の測定日時は、測定装置1に実装される時計機能によって検出される。心電測定部109は、第1の測定部の一例である。 The electrocardiogram measurement unit 109 is a device that measures the electrocardiogram of a subject to which the measurement device 1 is worn. For example, the electrocardiograph 109 includes two electrodes. The electrocardiogram measurement unit 109 measures the electrocardiogram of the subject based on a potential difference generated between the two electrodes according to the contact of the subject with the two electrodes. For example, the electrocardiogram measurement unit 109 measures the electrocardiogram of the subject while the subject is in contact with the two electrodes. The electrocardiogram measurement unit 109 stores the electrocardiogram data in the storage device 104 every time the electrocardiogram is measured. The electrocardiogram data includes data indicating the measurement date and time of the electrocardiogram. The measurement date and time of the electrocardiogram is detected by a clock function mounted on the measurement device 1. The electrocardiogram measurement unit 109 is an example of a first measurement unit.
 血圧測定部110は、測定装置1を装着する対象者の血圧を測定する装置である。典型例では、心電の測定日時を含む所定期間内の対象者の血圧を測定する。例えば、血圧測定部110は、カフ、ポンプ及び圧力センサを備える。カフは、血圧を測定する対象者の被測定部位に巻き付けて装着可能な帯状で構成されている。カフは、空気袋を備える。ポンプは、空気袋を膨らませるために、空気袋の内部に空気を供給する。圧力センサは、空気袋内の圧力を測定する。血圧測定部110は、圧力センサで測定されるデータに基づいて、血圧を測定する。血圧測定部110は、第2の測定部の一例である。 The blood pressure measurement unit 110 is a device that measures the blood pressure of the subject wearing the measurement device 1. In a typical example, the blood pressure of the subject is measured within a predetermined period including the date and time of measuring the electrocardiogram. For example, the blood pressure measurement unit 110 includes a cuff, a pump, and a pressure sensor. The cuff is formed in a band shape that can be worn around the measurement site of the subject whose blood pressure is to be measured. The cuff has a bladder. The pump supplies air to the interior of the bladder to inflate the bladder. The pressure sensor measures the pressure in the bladder. Blood pressure measurement section 110 measures blood pressure based on data measured by the pressure sensor. The blood pressure measurement unit 110 is an example of a second measurement unit.
 血圧測定部110は、血圧を測定する毎に、血圧データを記憶装置104に保存する。血圧測定部110は、血圧測定時におけるSBPの値及びDBPの値を取得する。これに代えて、血圧測定部110は、血圧測定指示によらず、対象者の血圧を1拍毎に連続的に測定してもよい。血圧測定部110は、血圧測定期間におけるSBPの値及びDBPの値を取得する。 The blood pressure measurement unit 110 stores the blood pressure data in the storage device 104 every time the blood pressure is measured. The blood pressure measurement unit 110 acquires the SBP value and the DBP value at the time of blood pressure measurement. Instead of this, the blood pressure measurement unit 110 may continuously measure the blood pressure of the subject at every beat, without depending on the blood pressure measurement instruction. The blood pressure measurement unit 110 acquires the SBP value and the DBP value during the blood pressure measurement period.
 血圧測定部110は、血圧データを記憶装置104に保存する。血圧データは、血圧の測定日時を示すデータを含む。血圧の測定日時は、測定装置1に実装される時計機能によって検出される。 The blood pressure measurement unit 110 stores the blood pressure data in the storage device 104. The blood pressure data includes data indicating the date and time of measuring the blood pressure. The measurement date and time of the blood pressure is detected by a clock function mounted on the measuring device 1.
 なお、血圧測定部110は、上述の圧力に基づいて血圧を測定する方式以外の方式により、血圧を測定してもよい。例えば、血圧測定部110は、光、電波または超音波を対象者の血管に当て、その反射波に基づいて血圧を測定する光学方式、電波方式または超音波方式を用いてもよい。 The blood pressure measurement section 110 may measure the blood pressure by a method other than the method of measuring the blood pressure based on the pressure described above. For example, the blood pressure measurement unit 110 may use an optical system, a radio wave system, or an ultrasonic system that applies light, radio waves, or ultrasonic waves to a blood vessel of a subject and measures blood pressure based on the reflected waves.
 なお、測定装置1の具体的なハードウェア構成に関して、実施形態に応じて、適宜、構成要素の省略、置換及び追加が可能である。例えば、測定装置1は、複数のプロセッサを含んでもよい。 Regarding the specific hardware configuration of the measuring device 1, it is possible to appropriately omit, replace, and add components according to the embodiment. For example, the measurement device 1 may include a plurality of processors.
  [ソフトウェア構成] 
 図4は、測定装置1のソフトウェア構成を例示するブロック図である。 
 プロセッサ101は、第1の取得部1011、第2の取得部1012、第3の取得部1013、第1の判断部1014、第2の判断部1015、データ出力部1016及び信号出力部1017を実装する。
[Software Configuration]
FIG. 4 is a block diagram illustrating a software configuration of the measurement apparatus 1.
The processor 101 implements a first acquisition unit 1011, a second acquisition unit 1012, a third acquisition unit 1013, a first determination unit 1014, a second determination unit 1015, a data output unit 1016, and a signal output unit 1017. I do.
 第1の取得部1011について説明する。第1の取得部1011は、以下に例示するように、対象者の第1の生体データを取得する。ここでは、心電データを第1の生体データの例として説明する。第1の取得部1011は、記憶装置104に記憶されている対象者の複数の心電データから、心電データを一つずつ取得する。第1の取得部1011は、心電データを第2の取得部1012、第1の判断部1014へ出力する。 <1> The first acquisition unit 1011 will be described. The first obtaining unit 1011 obtains first biometric data of the subject as exemplified below. Here, the electrocardiogram data will be described as an example of the first biological data. The first obtaining unit 1011 obtains electrocardiographic data one by one from a plurality of electrocardiographic data of the subject stored in the storage device 104. The first acquisition unit 1011 outputs electrocardiogram data to the second acquisition unit 1012 and the first determination unit 1014.
 第2の取得部1012について説明する。第2の取得部1012は、以下に例示するように、第1の生体データの測定日時を含む所定期間内に測定された対象者の第2の生体データを取得する。ここでは、血圧データを第2の生体データの例として説明する。まず、第2の取得部1012は、第1の取得部1011から心電データを受ける。次に、第2の取得部1012は、心電データから心電の測定日時を示すデータを取得する。次に、第2の取得部1012は、心電の測定日時を含む所定期間内に測定された対象者の血圧データを記憶装置104から取得する。第2の取得部1012は、血圧データを第2の判断部1015及びデータ出力部1016へ出力する。 <2> The second acquisition unit 1012 will be described. The second acquisition unit 1012 acquires the second biometric data of the subject measured within a predetermined period including the measurement date and time of the first biometric data, as exemplified below. Here, the blood pressure data will be described as an example of the second biological data. First, the second acquisition unit 1012 receives electrocardiogram data from the first acquisition unit 1011. Next, the second obtaining unit 1012 obtains data indicating the measurement date and time of the electrocardiogram from the electrocardiogram data. Next, the second acquisition unit 1012 acquires from the storage device 104 the blood pressure data of the subject measured within a predetermined period including the date and time of measuring the electrocardiogram. Second acquisition unit 1012 outputs the blood pressure data to second determination unit 1015 and data output unit 1016.
 第3の取得部1013について説明する。第3の取得部1013は、以下に例示するように、心電データと比較する予め定められた第1の参照データを取得する。まず、第3の取得部1013は、通信インタフェース105を介して、対象者の第1の参照データの要求をEHRサーバ4へ出力する。第3の取得部1013は、任意のタイミングで要求をEHRサーバ4へ出力することができる。要求は、対象者を特定する識別情報を含む。次に、第3の取得部1013は、通信インタフェース105を介して、要求に対する応答として、第1の参照データをEHRサーバ4から受ける。第3の取得部1013は、第1の参照データを第1の判断部1014へ出力する。 <3> The third acquisition unit 1013 will be described. The third obtaining unit 1013 obtains predetermined first reference data to be compared with electrocardiographic data, as exemplified below. First, the third acquisition unit 1013 outputs a request for the first reference data of the subject to the EHR server 4 via the communication interface 105. The third acquisition unit 1013 can output a request to the EHR server 4 at an arbitrary timing. The request includes identification information identifying the subject. Next, the third acquisition unit 1013 receives the first reference data from the EHR server 4 via the communication interface 105 as a response to the request. Third acquisition unit 1013 outputs the first reference data to first determination unit 1014.
 第1の判断部1014について説明する。第1の判断部1014は、以下に例示するように、心電データに基づいて、間接的に、対象者による血圧測定部110の装着状態が適切か不適切かを判断する。 The first determining unit 1014 will be described. The first determination unit 1014 indirectly determines, based on electrocardiographic data, whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate, as exemplified below.
 一例では、第1の判断部1014は、心電データを第1の参照データと比較し、心電データと第1の参照データとの比較結果に基づいて、間接的に、血圧測定部110の装着状態が適切か不適切かを判断する。この例では、まず、第1の判断部1014は、第1の取得部1011から心電データを受ける。第1の判断部1014は、第3の取得部1013から第1の参照データを受ける。次に、第1の判断部1014は、心電データを第1の参照データと比較する。例えば、第1の判断部1014は、心電データの波形データを第1の参照データの波形データと比較する。第1の判断部1014は、第1の参照データに含まれる複数の参照データのうち、心電の測定日時に近い参照データを用いることが好ましい。第1の参照データが対象者の異なる状態で測定された複数の参照データを含む場合、第1の判断部1014は、複数の参照データを用いてもよい。次に、第1の判断部1014は、心電データと第1の参照データとの比較結果に基づいて、対象者による心電測定部109の装着状態が適切か不適切かを判断する。例えば、第1の参照データに対する心電データの乖離度合が閾値未満である場合、第1の判断部1014は、対象者による心電測定部109の装着状態が適切であると判断する。他方、第1の参照データに対する心電データの乖離度合が閾値以上である場合、第1の判断部1014は、対象者による心電測定部109の装着状態が不適切であると判断する。次に、第1の判断部1014は、対象者による心電測定部109の装着状態が適切か不適切かに応じて、対象者による血圧測定部110の装着状態が適切か不適切かを判断する。第1の判断部1014は、対象者による心電測定部109の装着状態が適切であることを示す判断結果に応じて、対象者による血圧測定部110の装着状態が適切であると判断する。他方、第1の判断部1014は、対象者による心電測定部109の装着状態が不適切であることを示す判断結果に応じて、対象者による血圧測定部110の装着状態が不適切であると判断する。第1の判断部1014がこのように判断するのは、以下の理由による。心電測定部109及び血圧測定部110は、異なる要素で構成されているが共に測定装置1に含まれている。そのため、対象者による心電測定部109の装着状態が適切であれば、対象者による血圧測定部110の装着状態が適切である可能性が高い。他方、対象者による心電測定部109の装着状態が不適切であれば、対象者による血圧測定部110の装着状態が不適切である可能性が高い。 In one example, the first determination unit 1014 compares the electrocardiogram data with the first reference data, and indirectly performs the operation of the blood pressure measurement unit 110 based on a comparison result between the electrocardiogram data and the first reference data. Judge whether the mounting state is appropriate or inappropriate. In this example, first, the first determination unit 1014 receives electrocardiogram data from the first acquisition unit 1011. First determination unit 1014 receives the first reference data from third acquisition unit 1013. Next, the first determination unit 1014 compares the electrocardiographic data with the first reference data. For example, the first determination unit 1014 compares the waveform data of the electrocardiographic data with the waveform data of the first reference data. It is preferable that the first determination unit 1014 uses reference data that is close to the measurement date and time of the electrocardiogram among a plurality of reference data included in the first reference data. When the first reference data includes a plurality of reference data measured in different states of the subject, the first determination unit 1014 may use the plurality of reference data. Next, the first determination unit 1014 determines whether the subject's wearing state of the electrocardiogram measurement unit 109 is appropriate or inappropriate based on the comparison result between the electrocardiogram data and the first reference data. For example, when the degree of deviation of the electrocardiographic data from the first reference data is less than the threshold, the first determination unit 1014 determines that the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate. On the other hand, if the degree of deviation of the electrocardiographic data from the first reference data is equal to or greater than the threshold, the first determination unit 1014 determines that the subject's wearing state of the electrocardiographic measurement unit 109 is inappropriate. Next, the first determination unit 1014 determines whether the subject's wearing state of the blood pressure measuring unit 110 is appropriate or inappropriate according to whether the subject's wearing state of the electrocardiographic measuring unit 109 is appropriate or inappropriate. I do. The first determination unit 1014 determines that the mounting state of the blood pressure measurement unit 110 by the subject is appropriate according to the determination result indicating that the mounting state of the electrocardiographic measurement unit 109 by the subject is appropriate. On the other hand, the first determination unit 1014 determines that the mounting state of the blood pressure measurement unit 110 by the subject is inappropriate according to the determination result indicating that the mounting state of the electrocardiographic measurement unit 109 by the subject is inappropriate. Is determined. The first determination unit 1014 makes this determination for the following reason. The electrocardiogram measurement unit 109 and the blood pressure measurement unit 110 are composed of different elements, but are both included in the measurement device 1. Therefore, if the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate, there is a high possibility that the subject's wearing state of the blood pressure measurement unit 110 is appropriate. On the other hand, if the subject's wearing state of the electrocardiographic measurement unit 109 is inappropriate, there is a high possibility that the subject's wearing state of the blood pressure measurement unit 110 is inappropriate.
 なお、第1の判断部1014は、心電データを第1の参照データに含まれる任意の複数の参照データと比較する場合、以下のようにしてもよい。例えば、少なくとも1つの参照データに対する心電データの乖離度合が閾値未満である場合、第1の判断部1014は、対象者による心電測定部109の装着状態が適切であると判断してもよい。第1の判断部1014は、対象者による心電測定部109の装着状態が適切であることを示す判断結果に応じて、対象者による血圧測定部110の装着状態が適切であると判断する。他方、任意の複数の参照データのうちの全ての参照データに対する心電データの乖離度合が閾値以上である場合、第1の判断部1014は、対象者による心電測定部109の装着状態が不適切であると判断してもよい。第1の判断部1014は、対象者による心電測定部109の装着状態が不適切であることを示す判断結果に応じて、対象者による血圧測定部110の装着状態が不適切であると判断する。なお、心電データと第1の参照データとの比較は種々の手法を用いてよく、限定されない。 Note that the first determination unit 1014 may perform the following when comparing the electrocardiographic data with any of a plurality of reference data included in the first reference data. For example, when the degree of divergence of the electrocardiographic data with respect to at least one reference data is less than the threshold, the first determining unit 1014 may determine that the subject's wearing state of the electrocardiographic measuring unit 109 is appropriate. . The first determination unit 1014 determines that the mounting state of the blood pressure measurement unit 110 by the subject is appropriate according to the determination result indicating that the mounting state of the electrocardiographic measurement unit 109 by the subject is appropriate. On the other hand, when the degree of divergence of the electrocardiographic data with respect to all the reference data of the arbitrary plurality of reference data is equal to or greater than the threshold, the first determination unit 1014 determines that the subject's wearing state of the electrocardiographic measurement unit 109 is not correct. It may be determined that it is appropriate. The first determination unit 1014 determines that the mounting state of the blood pressure measurement unit 110 by the subject is inappropriate according to the determination result indicating that the mounting state of the electrocardiographic measurement unit 109 by the subject is inappropriate. I do. Note that the comparison between the electrocardiographic data and the first reference data may be performed using various methods, and is not limited.
 別の例では、第1の判断部1014は、心電データ自体に基づいて、間接的に、対象者による血圧測定部110の装着状態が適切か不適切かを判断する。この例では、まず、第1の判断部1014は、第1の取得部1011から心電データを受ける。第1の判断部1014は、心電データ自体における物理量の変動度合に基づいて、対象者による心電測定部109の装着状態が適切か不適切かを判断する。なお、心電データ自体に基づく対象者による心電測定部109の装着状態が適切か不適切かの判断は種々の手法を用いてよく、限定されない。第1の判断部1014は、対象者による心電測定部109の装着状態が適切か不適切かに応じて、対象者による血圧測定部110の装着状態が適切か不適切かを判断する。 In another example, the first determination unit 1014 indirectly determines whether the subject is properly or inappropriately wearing the blood pressure measurement unit 110 based on the electrocardiogram data itself. In this example, first, the first determination unit 1014 receives electrocardiogram data from the first acquisition unit 1011. The first determination unit 1014 determines whether the subject's wearing state of the electrocardiogram measurement unit 109 is appropriate or inappropriate based on the degree of physical quantity fluctuation in the electrocardiogram data itself. Various determinations may be made by the subject based on the electrocardiogram data itself to determine whether the electrocardiogram measurement unit 109 is properly or inappropriately mounted, and is not limited. The first determination unit 1014 determines whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate, depending on whether the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate or inappropriate.
 第1の判断部1014は、第1の判断結果を生成する。第1の判断結果は、対象者による血圧測定部110の装着状態が適切または不適切の何れかを示す。第1の判断部1014は、第1の判断結果を第2の判断部1015へ出力する。 The first determination unit 1014 generates a first determination result. The first determination result indicates whether the mounting state of the blood pressure measurement unit 110 by the subject is appropriate or inappropriate. First determination unit 1014 outputs the first determination result to second determination unit 1015.
 第2の判断部1015について説明する。第2の判断部1015は、以下に例示するように、第1の判断結果に応じて、血圧データの信頼性が高いか低いかを判断する。まず、第2の判断部1015は、第2の取得部1012から血圧データを受ける。第2の判断部1015は、第1の判断部1014から第1の判断結果を受ける。次に、第2の判断部1015は、第1の判断結果の内容を解析する。第2の判断部1015は、対象者による血圧測定部110の装着状態が適切であることを示す第1の判断結果の取得に応じて、血圧データの信頼性が高いと判断する。一つの理由は、対象者による血圧測定部110の装着状態が適切であれば、血圧測定部110による血圧の測定精度が高いからである。他方、第2の判断部1015は、対象者による血圧測定部110の装着状態が不適切であることを示す第1の判断結果の取得に応じて、血圧データの信頼性が低いと判断する。一つの理由は、対象者による血圧測定部110の装着状態が不適切であれば、血圧測定部110による血圧の測定精度が低いからである。 The second determination unit 1015 will be described. The second determination unit 1015 determines whether the reliability of the blood pressure data is high or low according to the first determination result, as exemplified below. First, the second determination unit 1015 receives the blood pressure data from the second acquisition unit 1012. The second determination unit 1015 receives the first determination result from the first determination unit 1014. Next, the second determination unit 1015 analyzes the content of the first determination result. The second determination unit 1015 determines that the reliability of the blood pressure data is high in response to the acquisition of the first determination result indicating that the subject's wearing state of the blood pressure measurement unit 110 is appropriate. One reason is that the accuracy of blood pressure measurement by the blood pressure measurement unit 110 is high if the subject's wearing state of the blood pressure measurement unit 110 is appropriate. On the other hand, the second determination unit 1015 determines that the reliability of the blood pressure data is low in response to the acquisition of the first determination result indicating that the mounting state of the blood pressure measurement unit 110 by the subject is inappropriate. One reason is that the accuracy of blood pressure measurement by the blood pressure measurement unit 110 is low if the subject's wearing state of the blood pressure measurement unit 110 is inappropriate.
 第2の判断部1015は、第2の判断結果を生成する。第2の判断結果は、血圧データの信頼性が高いまたは低いの何れかを示す。第2の判断部1015は、第2の判断結果をデータ出力部1016及び信号出力部1017へ出力する。 The second determination unit 1015 generates a second determination result. The second determination result indicates whether the reliability of the blood pressure data is high or low. Second determination unit 1015 outputs the second determination result to data output unit 1016 and signal output unit 1017.
 データ出力部1016について説明する。データ出力部1016は、以下に例示するように、血圧データの信頼性が高いまたは低いの何れかを示すデータと関連付けられた血圧データを出力する。まず、データ出力部1016は、第2の取得部1012から血圧データを受ける。データ出力部1016は、第2の判断部1015から第2の判断結果を受ける。データ出力部1016は、第2の判断結果の内容を解析する。データ出力部1016は、第2の判断結果に応じて、血圧データの信頼性が高いまたは低いの何れかを示すデータを生成する。血圧データの信頼性が高いまたは低いの何れかを示すデータは、信頼性データともいう。データ出力部1016は、信頼性データを血圧データに関連付ける。例えば、データ出力部1016は、信頼性データを血圧データに付加(ラべリング)することで、信頼性データを血圧データに関連付ける。次に、データ出力部1016は、通信インタフェース105を介して、信頼性データと関連付けられた血圧データをPHRサーバ3へ出力する。これにより、PHRサーバ3は、血圧データを信頼性データと関連付けて管理することができる。 The data output unit 1016 will be described. The data output unit 1016 outputs blood pressure data associated with data indicating whether the reliability of the blood pressure data is high or low, as exemplified below. First, the data output unit 1016 receives the blood pressure data from the second acquisition unit 1012. Data output unit 1016 receives the second determination result from second determination unit 1015. The data output unit 1016 analyzes the contents of the second determination result. The data output unit 1016 generates data indicating whether the reliability of the blood pressure data is high or low in accordance with the second determination result. Data indicating whether the reliability of the blood pressure data is high or low is also referred to as reliability data. The data output unit 1016 associates the reliability data with the blood pressure data. For example, the data output unit 1016 associates the reliability data with the blood pressure data by adding (labeling) the reliability data to the blood pressure data. Next, the data output unit 1016 outputs the blood pressure data associated with the reliability data to the PHR server 3 via the communication interface 105. Thereby, the PHR server 3 can manage the blood pressure data in association with the reliability data.
 信号出力部1017について説明する。信号出力部1017は、以下に例示するように、血圧データの信頼性が低いことを示す第2の判断結果に応じて、支援信号を出力する。支援信号は、対象者に対する血圧測定部110の装着状態を改善させる支援の実行を指示する信号である。まず、信号出力部1017は、第2の判断部1015から第2の判断結果を受ける。次に、信号出力部1017は、第2の判断結果の内容を解析し、血圧データの信頼性が高いまたは低いの何れかを判断する。第2の判断結果が血圧データの信頼性が低いことを示す場合、信号出力部1017は、支援信号を出力する。他方、第2の判断結果が血圧データの信頼性が高いことを示す場合、信号出力部1017は、支援信号の出力を省略する。 The signal output unit 1017 will be described. The signal output unit 1017 outputs a support signal according to a second determination result indicating that the reliability of the blood pressure data is low, as exemplified below. The support signal is a signal that instructs execution of support for improving the wearing state of the blood pressure measurement unit 110 for the subject. First, the signal output unit 1017 receives the second determination result from the second determination unit 1015. Next, the signal output unit 1017 analyzes the content of the second determination result and determines whether the reliability of the blood pressure data is high or low. When the second determination result indicates that the reliability of the blood pressure data is low, the signal output unit 1017 outputs a support signal. On the other hand, when the second determination result indicates that the reliability of the blood pressure data is high, the signal output unit 1017 omits the output of the support signal.
 例えば、信号出力部1017は、表示部107及び音声出力部108の少なくとも何れか一方へ支援信号を出力する。表示部107は、支援信号に基づいて、対象者による血圧測定部110の装着状態が適切ではない旨のメッセージの画面を表示する。音声出力部108は、支援信号に基づいて、対象者による血圧測定部110の装着状態が適切ではない旨のメッセージを音声で出力する。メッセージは、対象者による血圧測定部110の装着状態が適切ではない旨の内容であればよく、限定されない。対象者は、メッセージにより、血圧測定部110を適切に装着し直すことができる。これにより、測定装置1は、信頼性の高い血圧データを取得することができる。なお、信号出力部1017は、支援信号を表示部107及び音声出力部108以外の要素へ出力してもよい。信号出力部1017は、対象者に外部刺激を与える支援提供装置へ支援信号を出力してもよい。例えば、外部刺激は、振動であるが、これに限定されない。 For example, the signal output unit 1017 outputs a support signal to at least one of the display unit 107 and the audio output unit 108. The display unit 107 displays a screen of a message indicating that the wearing state of the blood pressure measurement unit 110 by the subject is not appropriate based on the support signal. The voice output unit 108 outputs a voice message indicating that the wearing state of the blood pressure measurement unit 110 by the subject is not appropriate based on the support signal. The message may be any content as long as the message indicates that the wearing state of the blood pressure measurement unit 110 by the subject is not appropriate, and is not limited. The subject can appropriately re-attach the blood pressure measurement unit 110 by the message. Thereby, the measuring device 1 can obtain highly reliable blood pressure data. Note that the signal output unit 1017 may output the support signal to elements other than the display unit 107 and the audio output unit 108. The signal output unit 1017 may output a support signal to a support providing device that provides an external stimulus to the subject. For example, the external stimulus is, but not limited to, a vibration.
 §3 動作例 
 <測定装置> 
 [信頼性判断動作]  
 図5は、測定装置1における信頼性判断動作を例示するフローチャートである。なお、以下で説明する処理手順は一例に過ぎず、各処理は可能な限り変更されてよい。また、以下で説明する処理手順については、適宜、ステップの省略、置換及び追加が可能である。
§3 Operation example
<Measuring device>
[Reliability judgment operation]
FIG. 5 is a flowchart illustrating a reliability determination operation in the measurement device 1. The processing procedure described below is merely an example, and each processing may be changed as much as possible. In the processing procedure described below, steps can be omitted, replaced, and added as appropriate.
 第1の取得部1011は、対象者の心電データを取得する(ステップS101)。ステップS101では、第1の取得部1011は、例示したように、記憶装置104から対象者の心電データを取得する。第1の取得部1011は、心電データを第2の取得部1012及び第1の判断部1014へ出力する。 The first acquisition unit 1011 acquires the subject's electrocardiogram data (step S101). In step S101, the first acquisition unit 1011 acquires the subject's electrocardiogram data from the storage device 104 as illustrated. The first acquisition unit 1011 outputs electrocardiogram data to the second acquisition unit 1012 and the first determination unit 1014.
 第2の取得部1012は、対象者の心電データの測定日時を含む所定期間内に測定された対象者の血圧データを取得する(ステップS102)。ステップS102では、第2の取得部1012は、例示したように、心電データの測定日時を参照し、記憶装置104から対象者の血圧データを取得する。第2の取得部1012は、データ出力部1016へ出力する。 The second acquiring unit 1012 acquires the blood pressure data of the subject measured within a predetermined period including the measurement date and time of the electrocardiographic data of the subject (Step S102). In step S102, the second acquisition unit 1012 acquires the subject's blood pressure data from the storage device 104 with reference to the measurement date and time of the electrocardiographic data, as illustrated. The second acquisition unit 1012 outputs to the data output unit 1016.
 第1の判断部1014は、対象者による血圧測定部110の装着状態が適切か不適切かを判断する(ステップS103)。ステップS103では、第1の判断部1014は、例示したように、心電データに基づいて、間接的に、対象者による血圧測定部110の装着状態が適切か不適切かを判断する。第1の判断部1014は、第1の判断結果を第2の判断部1015へ出力する。 The first determination unit 1014 determines whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate (step S103). In step S103, the first determination unit 1014 indirectly determines whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate based on the electrocardiographic data, as illustrated. First determination unit 1014 outputs the first determination result to second determination unit 1015.
 第2の判断部1015は、血圧データの信頼性が高いか低いかを判断する(ステップS104)。ステップS104では、第2の判断部1015は、例示したように、第1の判断結果に応じて、血圧データの信頼性が高いか低いかを判断する。第2の判断部1015は、第2の判断結果をデータ出力部1016及び信号出力部1017へ出力する。 The second determination unit 1015 determines whether the reliability of the blood pressure data is high or low (step S104). In step S104, the second determination unit 1015 determines whether the reliability of the blood pressure data is high or low according to the first determination result, as illustrated. Second determination unit 1015 outputs the second determination result to data output unit 1016 and signal output unit 1017.
 データ出力部1016は、信頼性データと関連付けられた血圧データを出力する(ステップS105)。ステップS105では、データ出力部1016は、例示したように、通信インタフェース105を介して、第2の判断結果に応じた信頼性データと関連付けられた血圧データを外部装置へ出力する。 The data output unit 1016 outputs the blood pressure data associated with the reliability data (Step S105). In step S105, the data output unit 1016 outputs the blood pressure data associated with the reliability data according to the second determination result to the external device via the communication interface 105 as illustrated.
 信号出力部1017は、血圧データの信頼性が高いまたは低いの何れかを判断する(ステップS106)。ステップS106では、信号出力部1017は、例示したように、第2の判断結果に基づいて、血圧データの信頼性が高いまたは低いの何れかを判断する。血圧データの信頼性が高い場合(ステップS106、No)、プロセッサ101は、信頼性判断動作を終了する。血圧データの信頼性が低い場合(ステップS106、Yes)、信号出力部1017は、支援信号を出力する(ステップS107)。ステップS107では、信号出力部1017は、例示したように、表示部107及び音声出力部108などの少なくとも何れかへ支援信号を出力する。 The signal output unit 1017 determines whether the reliability of the blood pressure data is high or low (step S106). In step S106, as illustrated, the signal output unit 1017 determines whether the reliability of the blood pressure data is high or low based on the second determination result. If the reliability of the blood pressure data is high (No at Step S106), the processor 101 ends the reliability determination operation. When the reliability of the blood pressure data is low (Step S106, Yes), the signal output unit 1017 outputs a support signal (Step S107). In step S107, the signal output unit 1017 outputs a support signal to at least one of the display unit 107 and the audio output unit 108, as illustrated.
 プロセッサ101は、記憶装置104から対象者の心電データを取得する毎に、上述の信頼性判断動作を繰り返し実行することができる。 The processor 101 can repeatedly execute the above-described reliability determination operation every time the subject's electrocardiogram data is acquired from the storage device 104.
 §4 作用・効果
 以上説明したように、本実施形態では、測定装置1は、第1の生体データに基づく第1の判断結果に応じて、第2の生体データの信頼性が高いか低いかを判断することができる。 
 例えば、対象者による測定装置1に含まれる測定部の装着状態に応じて変動するだけでなく、身体の異変に敏感に反応する生体データがある。他方、対象者による測定装置1に含まれる測定部の装着状態に応じて変動するだけでなく、身体に発生した異変が軽度であれば安静状態ではそれほど反応しない生体データがある。前者の生体データは、対象者の身体の異変に影響されやすい。そのため、前者の生体データは、対象者による測定装置1に含まれる前者の生体データを測定する測定部の装着状態が適切か不適切かの評価に適していない。後者の生体データは、対象者の身体の異変に頻繁には影響を受けない。そのため、後者の生体データは、対象者による測定装置1に含まれる後者の生体データを測定する測定部の装着状態が適切か不適切かの評価に適している。また、測定装置1が異なる生体データを測定する2つの測定部を含む場合、対象者による一方の測定部の装着状態が適切であれば、対象者による他方の測定部の装着状態も適切である可能性が高い。他方、対象者による一方の測定部の装着状態が不適切であれば、対象者による他方の測定部の装着状態も不適切である可能性が高い。測定装置1は、後者の生体データを第1の生体データ、前者の生体データを第2の生体データとして用いている。これにより、測定装置1は、第2の生体データに基づいて対象者による第2の生体データを測定する測定部の装着状態が適切か不適切かを直接的に判断することができなくても、第1の生体データに基づいて対象者による第2の生体データを測定する測定部の装着状態が適切か不適切かを間接的に判断することができる。その結果、測定装置1は、第2の生体データに基づいて第2の生体データの信頼性を直接的に評価することが難しくても、第1の生体データに基づいて間接的に第2の生体データの信頼性を評価することができる。
§4 Function / Effect As described above, in the present embodiment, the measuring device 1 determines whether the reliability of the second biometric data is high or low according to the first determination result based on the first biometric data. Can be determined.
For example, there is biometric data that not only fluctuates according to the mounting state of the measurement unit included in the measurement device 1 by the subject, but also sensitively reacts to an abnormal body. On the other hand, there is biometric data that not only varies according to the mounting state of the measuring unit included in the measuring device 1 by the subject but also does not react so much in the resting state if the abnormality that occurs on the body is mild. The former biometric data is susceptible to abnormalities in the subject's body. For this reason, the former biometric data is not suitable for evaluating whether the mounting state of the measurement unit for measuring the former biometric data included in the measuring device 1 by the subject is appropriate or inappropriate. The latter biometric data is not frequently affected by abnormalities in the subject's body. Therefore, the latter biometric data is suitable for evaluating whether the mounting state of the measurement unit for measuring the latter biometric data included in the measurement device 1 by the subject is appropriate or inappropriate. In addition, when the measurement device 1 includes two measurement units that measure different biological data, if the wearing state of one measurement unit by the subject is appropriate, the wearing state of the other measurement unit by the subject is also appropriate. Probability is high. On the other hand, if the mounting state of one measurement unit by the subject is inappropriate, it is highly likely that the mounting state of the other measurement unit by the subject is also inappropriate. The measurement device 1 uses the latter biometric data as first biometric data, and uses the former biometric data as second biometric data. Thereby, even if measurement device 1 cannot directly determine whether the measurement unit that measures the second biometric data by the subject is appropriate or inappropriate based on the second biometric data, Based on the first biometric data, it is possible to indirectly determine whether the mounting state of the measurement unit that measures the second biometric data by the subject is appropriate or inappropriate. As a result, even if it is difficult for the measurement device 1 to directly evaluate the reliability of the second biometric data based on the second biometric data, the measurement device 1 indirectly uses the second biometric data based on the first biometric data. The reliability of biometric data can be evaluated.
 さらに、本実施形態では、測定装置1は、第1の生体データと参照データとの比較結果に基づいて、対象者による血圧測定部110の装着状態が適切か不適切かを判断することができる。 
 測定装置1は、参照データを用いることで対象者による心電測定部109の装着状態が適切か不適切かを精度良く判断することができるので、対象者による血圧測定部110の装着状態が適切か不適切かも精度良く判断することができる。
Further, in the present embodiment, the measurement device 1 can determine whether the subject's wearing state of the blood pressure measurement unit 110 is appropriate or inappropriate based on the comparison result between the first biological data and the reference data. .
The measurement apparatus 1 can accurately determine whether the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate or inappropriate by using the reference data, so that the subject's wearing state of the blood pressure measurement unit 110 is appropriate. Whether it is inappropriate or not can be accurately determined.
 さらに、本実施形態では、測定装置1は、第1の生体データとして対象者の心電データを取得し、第2の生体データとして対象者の血圧データを取得することができる。 
 心電データは、対象者の身体の異変に頻繁には影響を受けないので、対象者による心電測定部109の装着状態が適切か不適切かの評価に適している。血圧データは、対象者の身体の異変に影響されやすいので、対象者による血圧測定部110の装着状態が適切か不適切かの評価に適していない。測定装置1は、血圧データに基づいて対象者による血圧測定部110の装着状態が適切か不適切かを直接的に判断することができなくても、心電データに基づいて対象者による血圧測定部110の装着状態が適切か不適切かを間接的に判断することができる。測定装置1は、血圧データに基づいて血圧データの信頼性を直接的に評価することが難しくても、心電データに基づいて間接的に血圧データの信頼性を評価することができる。
Furthermore, in the present embodiment, the measurement device 1 can acquire the subject's electrocardiographic data as the first biometric data and acquire the subject's blood pressure data as the second biometric data.
Since the electrocardiographic data is not frequently affected by abnormalities of the subject's body, the electrocardiographic data is suitable for evaluating whether the subject's wearing state of the electrocardiographic measurement unit 109 is appropriate or inappropriate. Since the blood pressure data is easily affected by abnormalities in the body of the subject, the blood pressure data is not suitable for evaluating whether the wearing state of the blood pressure measurement unit 110 by the subject is appropriate or inappropriate. The measurement device 1 can measure the blood pressure by the subject based on the electrocardiographic data even if it is not possible to directly determine whether the wearing state of the blood pressure measurement unit 110 by the subject is appropriate or inappropriate based on the blood pressure data. It is possible to indirectly determine whether the mounting state of the unit 110 is appropriate or inappropriate. Even if it is difficult to directly evaluate the reliability of the blood pressure data based on the blood pressure data, the measuring device 1 can indirectly evaluate the reliability of the blood pressure data based on the electrocardiographic data.
 さらに、本実施形態では、測定装置1は、第2の生体データの信頼性が低いことを示す第2の判断結果に応じて、支援信号を出力することができる。 
 測定装置1は、対象者に対する血圧測定部110の装着状態の改善を支援することで、信頼性の高い第2の生体データを測定することができる。
Further, in the present embodiment, the measurement device 1 can output the support signal in accordance with the second determination result indicating that the reliability of the second biometric data is low.
The measurement device 1 can measure highly reliable second biological data by supporting the improvement of the state of attachment of the blood pressure measurement unit 110 to the subject.
 さらに、本実施形態では、測定装置1は、信頼性データと関連付けられた第2の生体データを出力することができる。 
 測定装置1は、信頼性データと関連付けられた第2の生体データを医師に提供することで、医師による診断を支援することができる。医師は、第2の生体データの信頼性を確認することで、第2の生体データを対象者の診察に活用するか否かを容易に判断することができる。
Further, in the present embodiment, the measuring device 1 can output the second biological data associated with the reliability data.
The measurement device 1 can assist the doctor in diagnosing by providing the doctor with the second biometric data associated with the reliability data. By confirming the reliability of the second biometric data, the doctor can easily determine whether or not to use the second biometric data for the examination of the subject.
 §5 変形例 
 (5-1 変形例1) 
 本実施形態では、心電測定部109を第1の測定部の一例とし、血圧測定部110を第2の測定部の一例として説明したが、これに限定されない。血圧測定部110が第1の測定部の一例であり、心電測定部109が第2の測定部の一例であってもよい。この例では、第1の取得部1011は、第1の生体データとして血圧データを取得してもよい。第2の取得部1012は、第2の生体データとして心電データを取得してもよい。第3の取得部1013は対象者の血圧に関する第2の参照データを取得し、第1の判断部1014は、血圧データを第2の参照データと比較してもよい。
§5 Modification
(5-1 Modification 1)
In the present embodiment, the electrocardiogram measurement unit 109 is described as an example of a first measurement unit, and the blood pressure measurement unit 110 is described as an example of a second measurement unit. However, the present invention is not limited to this. The blood pressure measurement unit 110 may be an example of a first measurement unit, and the electrocardiogram measurement unit 109 may be an example of a second measurement unit. In this example, the first obtaining unit 1011 may obtain blood pressure data as first biological data. The second acquisition unit 1012 may acquire electrocardiogram data as second biological data. The third obtaining unit 1013 may obtain second reference data relating to the blood pressure of the subject, and the first determining unit 1014 may compare the blood pressure data with the second reference data.
 第1の取得部1011は、第1の生体データとして心電及び血圧以外の生体の物理量を示すデータを取得してもよい。第2の取得部1012は、第2の生体データとして第1の生体データとは異なる生体の物理量を示すデータを取得してもよい。 The first acquisition unit 1011 may acquire data indicating physical quantities of a living body other than electrocardiogram and blood pressure as first living body data. The second acquisition unit 1012 may acquire, as the second biometric data, data indicating a physical quantity of a living body different from the first biometric data.
 (5-2 変形例2) 
 なお、本実施形態では、測定装置1は、2つの異なる物理量に関する生体データを測定しているが、これに限定されない。測定装置1は、3つの異なる物理量に関する生体データを測定してもよい。この例では、測定装置1は、第1の生体データ及び第2の生体データに基づいて対象者による測定装置1の装着状態が適切か不適切かを判断し、判断結果に応じて第3の生体データの信頼性が高いか低いかを判断してもよい。
(5-2 Modification 2)
In the present embodiment, the measuring device 1 measures biological data regarding two different physical quantities, but is not limited thereto. The measurement device 1 may measure biological data regarding three different physical quantities. In this example, the measuring device 1 determines whether the subject's wearing state of the measuring device 1 is appropriate or inappropriate based on the first biometric data and the second biometric data, and determines a third one according to the determination result. It may be determined whether the reliability of the biometric data is high or low.
 (5-3 変形例3) 
 要するにこの発明は、本実施形態そのままに限定されるものではなく、実施段階ではその要旨を逸脱しない範囲で構成要素を変形して具体化できる。また、本実施形態に開示されている複数の構成要素の適宜な組み合せにより種々の発明を形成できる。例えば、本実施形態に示される全構成要素からいくつかの構成要素を削除してもよい。さらに、異なる実施形態に亘る構成要素を適宜組み合わせてもよい。
(5-3 Modification 3)
In short, the present invention is not limited to the present embodiment as it is, and can be embodied by modifying the constituent elements in the implementation stage without departing from the scope of the invention. Further, various inventions can be formed by appropriately combining a plurality of components disclosed in the present embodiment. For example, some components may be deleted from all the components shown in the present embodiment. Further, components of different embodiments may be appropriately combined.
 §6 付記 
 本実施形態の一部または全部は、特許請求の範囲のほか以下の付記に示すように記載することも可能であるが、これに限定されない。 
 (付記) 
 対象者の第1の生体データを測定する第1の測定部(109)と、
 前記第1の生体データの測定日時を含む所定期間内の前記対象者の第2の生体データを測定する第2の測定部(110)と、
 前記第1の生体データに基づいて、前記対象者による前記第2の測定部の装着状態が適切か不適切か否かを判断する第1の判断部(1014)と、
 前記装着状態が適切または不適切の何れかを示す判断結果に応じて、前記第2の生体データの信頼性が高いか低いかを判断する第2の判断部(1015)と、
 を備える生体データ測定装置(1)。
§6 Additional notes
A part or all of the present embodiment can be described as shown in the following supplementary notes in addition to the scope of the claims, but is not limited thereto.
(Note)
A first measurement unit (109) for measuring first biological data of the subject;
A second measurement unit (110) that measures the second biometric data of the subject within a predetermined period including the measurement date and time of the first biometric data;
A first determination unit (1014) that determines whether a mounting state of the second measurement unit by the subject is appropriate or inappropriate based on the first biometric data;
A second determination unit (1015) that determines whether the reliability of the second biometric data is high or low according to a determination result indicating whether the mounting state is appropriate or inappropriate;
A biological data measurement device (1) comprising:
 1…測定装置
 2…携帯端末
 3…PHRサーバ
 4…EHRサーバ
 100…生体データ管理システム
 101…プロセッサ
 102…ROM
 103…RAM
 104…記憶装置
 105…通信インタフェース
 106…入力部
 107…表示部
 108…音声出力部
 109…心電測定部
 110…血圧測定部
 1011…第1の取得部
 1012…第2の取得部
 1013…第3の取得部
 1014…第1の判断部
 1015…第2の判断部
 1016…データ出力部
 1017…信号出力部
 A1…測定装置
 A2…携帯端末
 A3…EHRサーバ
 A4…PHRサーバ
 A11…心電測定部
 A12…血圧測定部
DESCRIPTION OF SYMBOLS 1 ... Measuring device 2 ... Portable terminal 3 ... PHR server 4 ... EHR server 100 ... Biometric data management system 101 ... Processor 102 ... ROM
103 ... RAM
104 storage device 105 communication interface 106 input unit 107 display unit 108 audio output unit 109 electrocardiogram measurement unit 110 blood pressure measurement unit 1011 first acquisition unit 1012 second acquisition unit 1013 third Acquisition unit 1014 ... first judgment unit 1015 ... second judgment unit 1016 ... data output unit 1017 ... signal output unit A1 ... measurement device A2 ... portable terminal A3 ... EHR server A4 ... PHR server A11 ... electrocardiogram measurement unit A12 … Blood pressure measurement unit

Claims (7)

  1.  対象者の第1の生体データを測定する第1の測定部と、
     前記第1の生体データの測定日時を含む所定期間内の前記対象者の第2の生体データを測定する第2の測定部と、
     前記第1の生体データに基づいて、前記対象者による前記第2の測定部の装着状態が適切か不適切かを判断する第1の判断部と、
     前記装着状態が適切または不適切の何れかを示す判断結果に応じて、前記第2の生体データの信頼性が高いか低いかを判断する第2の判断部と、
     を備える生体データ測定装置。
    A first measurement unit that measures first biological data of the subject;
    A second measurement unit that measures the second biometric data of the subject within a predetermined period including the measurement date and time of the first biometric data;
    A first determination unit configured to determine whether the mounting state of the second measurement unit by the subject is appropriate or inappropriate based on the first biometric data;
    A second determination unit that determines whether the reliability of the second biometric data is high or low, according to a determination result indicating whether the mounting state is appropriate or inappropriate;
    A biological data measurement device comprising:
  2.  前記第1の生体データと比較する予め定められた参照データを取得する取得部をさらに備え、
     前記第1の判断部は、前記第1の生体データを前記参照データと比較し、前記第1の生体データと前記参照データとの比較結果に基づいて、前記装着状態が適切か不適切かを判断する、請求項1に記載の生体データ測定装置。
    An acquisition unit that acquires predetermined reference data to be compared with the first biological data,
    The first determination unit compares the first biometric data with the reference data, and determines whether the wearing state is appropriate or inappropriate based on a comparison result between the first biometric data and the reference data. The biological data measurement device according to claim 1, wherein the determination is performed.
  3.  前記第1の測定部は、前記第1の生体データとして前記対象者の心電に関するデータを測定し、
     前記第2の測定部は、前記第2の生体データとして前記対象者の血圧に関するデータを測定する、
     請求項1に記載の生体データ測定装置。
    The first measurement unit measures data related to the subject's electrocardiogram as the first biological data,
    The second measurement unit measures data on the blood pressure of the subject as the second biological data,
    The biological data measurement device according to claim 1.
  4.  前記第2の生体データの信頼性が低いことを示す判断結果に応じて、前記対象者に対する前記第2の測定部の前記装着状態を改善させる支援の実行を指示する信号を出力する信号出力部をさらに備える、請求項1に記載の生体データ測定装置。 A signal output unit that outputs a signal that instructs the subject to perform support for improving the wearing state of the second measurement unit in accordance with a determination result indicating that the reliability of the second biometric data is low. The biological data measurement device according to claim 1, further comprising:
  5.  前記第2の生体データの信頼性が高いまたは低いの何れかを示すデータと関連付けられた前記第2の生体データを出力するデータ出力部をさらに備える、請求項1に記載の生体データ測定装置。 The biometric data measurement device according to claim 1, further comprising: a data output unit configured to output the second biometric data associated with data indicating whether the reliability of the second biometric data is high or low.
  6.  生体データ測定装置に含まれる第1の測定部において、対象者の第1の生体データを測定する第1の測定過程と、
     前記生体データ測定装置に含まれる第2の測定部において、前記第1の生体データの測定日時を含む所定期間内の前記対象者の第2の生体データを測定する第2の測定過程と、
     前記第1の生体データに基づいて、前記対象者による前記第2の測定部の装着状態が適切か不適切かを判断する第1の判断過程と、
     前記装着状態が適切または不適切の何れかを示す判断結果に応じて、前記第2の生体データの信頼性が高いか低いかを判断する第2の判断過程と、
     を備える生体データ処理方法。
    A first measuring unit included in the biological data measuring device, a first measuring step of measuring the first biological data of the subject;
    A second measurement unit included in the biological data measurement device, a second measurement process of measuring the second biological data of the subject within a predetermined period including the measurement date and time of the first biological data,
    A first determining step of determining whether the mounting state of the second measuring unit by the subject is appropriate or inappropriate based on the first biological data;
    A second determination step of determining whether the reliability of the second biometric data is high or low, according to a determination result indicating whether the wearing state is appropriate or inappropriate;
    A biological data processing method comprising:
  7.  請求項1から5のうちの何れか1項に記載の生体データ測定装置が備える各部の処理をコンピュータに実行させる生体データ処理のためのプログラム。 A program for biometric data processing that causes a computer to execute processing of each unit included in the biometric data measurement device according to any one of claims 1 to 5.
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Citations (3)

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WO2017086071A1 (en) * 2015-11-17 2017-05-26 株式会社村田製作所 Pulse wave propagation time measurement device and biological state estimation device

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008245943A (en) * 2007-03-30 2008-10-16 Citizen Holdings Co Ltd Pulse wave measuring instrument
JP2014012072A (en) * 2012-07-04 2014-01-23 Sony Corp Measurement apparatus, measurement method, program, storage medium, and measurement system
WO2017086071A1 (en) * 2015-11-17 2017-05-26 株式会社村田製作所 Pulse wave propagation time measurement device and biological state estimation device

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