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WO2018211963A1 - Dispositif d'affichage d'informations et programme - Google Patents

Dispositif d'affichage d'informations et programme Download PDF

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Publication number
WO2018211963A1
WO2018211963A1 PCT/JP2018/017365 JP2018017365W WO2018211963A1 WO 2018211963 A1 WO2018211963 A1 WO 2018211963A1 JP 2018017365 W JP2018017365 W JP 2018017365W WO 2018211963 A1 WO2018211963 A1 WO 2018211963A1
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WO
WIPO (PCT)
Prior art keywords
blood pressure
measurement
unit
data
control unit
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2018/017365
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English (en)
Japanese (ja)
Inventor
皓介 井上
就介 江下
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Omron Corp
Omron Healthcare Co Ltd
Original Assignee
Omron Corp
Omron Healthcare Co Ltd
Omron Tateisi Electronics Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Omron Corp, Omron Healthcare Co Ltd, Omron Tateisi Electronics Co filed Critical Omron Corp
Publication of WO2018211963A1 publication Critical patent/WO2018211963A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/021—Measuring pressure in heart or blood vessels
    • A61B5/022—Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers

Definitions

  • the present invention relates to an information display device and a program for displaying information related to a blood pressure value of a measurement subject.
  • Sudden blood pressure fluctuations can cause brain / cardiovascular disease, so it is desirable to improve them. For example, if an apnea condition continues during sleep due to sleep apnea syndrome (SAS), blood pressure surges due to the lungs pressing the heart and applying a sudden compression load when breathing returns from a state where breathing stopped. At that time, plaque in the blood vessel may fly to the brain or heart, resulting in a blood clot or rupture of the blood vessel.
  • SAS sleep apnea syndrome
  • CPAP continuous positive pressure respiratory therapy
  • JP-A-2015-216970 there is a technique described in JP-A-2015-216970.
  • the present invention has been made paying attention to the above circumstances, and an object of the present invention is to provide an information display device and a program capable of notifying data on a measurement result during sleep so that the measurement subject can easily recognize.
  • the information display device includes a measurement data acquisition unit that acquires a measurement result of a blood pressure value while the measurement subject is sleeping, and the measurement subject is awakened.
  • a display control unit that displays information indicating the measurement result acquired by the measurement data acquisition unit on the display unit when determining that the person to be measured has woken up by the wake-up determination unit; It is what has.
  • An information display device is the information display device according to the first aspect, wherein the display control unit displays aggregated data obtained by aggregating measurement data obtained by measuring the blood pressure value on the display unit. It is.
  • the information display device is the information display device according to any one of the first and second aspects, wherein the display control unit determines at least based on measurement data obtained by measuring the blood pressure value.
  • the risk level that causes the onset of cardiovascular disease is displayed on the display unit.
  • the wake-up determination unit determines that the person to be measured has woken up, at least a part of the information display device It further has a vibration part that vibrates the housing that contacts the measurer.
  • the information display device is the information display device according to any one of the first to fourth aspects, wherein the display control unit determines at least based on measurement data obtained by measuring the blood pressure value.
  • the display control unit determines at least based on measurement data obtained by measuring the blood pressure value.
  • the information display device is the information display device according to any one of the first to fifth aspects, further comprising: a blood pressure sensor that measures a blood pressure value of the person to be measured; And a measurement control unit that executes measurement of blood pressure values while the person is sleeping.
  • An information display device is the information display device according to the sixth aspect, wherein the blood pressure sensor is at least one of a PTT method, a tonometry method, an optical method, a radio wave method, or an ultrasonic method.
  • the sensor used for the measurement method is included.
  • an information display device capable of informing the measurement subject so as to easily recognize the data related to the measurement result during sleeping.
  • the second aspect of the present invention it is possible to display aggregated data obtained by aggregating measurement data obtained by measuring a blood pressure value during sleep when waking up is detected, and measurement during sleep when the measurement subject wakes up. The result can be recognized.
  • the third aspect of the present invention it is possible to display on the display unit the risk of causing the onset of a cerebral / cardiovascular disease that is determined based on at least the measurement data of the blood pressure value during sleeping when waking up is detected, The degree of risk determined from the measurement result while sleeping when the person to be measured gets up can be recognized.
  • the housing when the wake-up is detected, can be vibrated together with the display of the measurement result, and it is vibrated to confirm the measurement result while sleeping when the measurement subject wakes up. Can be prompted by.
  • the information indicating the measurement result when the risk of causing the onset of the cerebral / cardiovascular disease determined based on at least the measurement data of the blood pressure value during sleeping is equal to or greater than the predetermined value.
  • the device that can measure the blood pressure value during sleep can be notified so that the measurement subject can easily recognize the data related to the measurement result.
  • the blood pressure sensor for measuring the blood pressure value is not limited to a specific method, and data related to the measurement result during sleeping can be notified to the measurement subject.
  • FIG. 1 is a diagram schematically showing a configuration example of a blood pressure information processing system according to an embodiment of the present invention.
  • FIG. 2 is a block diagram illustrating a configuration example of the wearable device.
  • FIG. 3 is a block diagram illustrating a configuration example of the user terminal.
  • FIG. 4 is a block diagram illustrating a configuration example of the server.
  • FIG. 5 is a block diagram for explaining functions realized by the control unit of the wearable device.
  • FIG. 6 is a block diagram for explaining functions realized by the control unit of the server.
  • FIG. 7 is a flowchart for explaining a first operation example of the wearable device.
  • FIG. 8 is a diagram illustrating an example of a display screen displayed by the wearable device.
  • FIG. 9 is a flowchart for explaining an operation example of the server.
  • FIG. 10 is a diagram illustrating an example of a display screen displayed by the user terminal.
  • FIG. 11 is a flowchart for explaining a second operation example of the wear
  • FIG. 1 is a diagram schematically illustrating a configuration example of a blood pressure information processing system according to an embodiment.
  • the blood pressure information processing system 1 includes a wearable device (blood pressure measurement device, information display device) 2, a CPAP device (treatment device) 3, an information processing system (information processing device) 4, and the like.
  • the information processing system 4 is a data processing system including devices that can communicate with the wearable device 2 and the CPAP device 3.
  • the information processing system 4 includes a user terminal 11 and a server 12. Measurement data including blood pressure data continuously measured and measurement data of various elements is acquired, and the acquired measurement data is analyzed.
  • the wearable device 2 and the CPAP device 3 are connected to a user terminal 11, and the user terminal 11 is connected to the server 12 via a network so that they can communicate with each other.
  • the configuration of the blood pressure information processing system 1 and the information processing system 4 is not limited to the configuration shown in FIG.
  • part or all of the functions (processing) realized by the server 12 described later may be performed by the user terminal 11.
  • the information processing apparatus as the information processing system 4 may be realized by the user terminal 11 by omitting the server 12.
  • what is necessary is just to comprise so that the operation
  • the CPAP device 3 may be connected to the wearable device 2 instead of the user terminal 11.
  • the CPAP device 3 may communicate with the user terminal 11 or the server 12 via the wearable device 2.
  • the functions of the information processing system 4 may be configured to be realized by the wearable device 2.
  • the CPAP device 3 is configured to be communicably connected to the wearable device 2, the user terminal 11 and the server 12 can be omitted, and the blood pressure information processing system described in the present embodiment using the wearable device 2 and the CPAP device 3 is the same. Can be configured.
  • the wearable device 2 is a blood pressure measurement device having a function of measuring a blood pressure value of a measurement subject (user).
  • the wearable device 2 has a wristwatch-type configuration that a user can wear, and is a device capable of sleeping while wearing and measuring a blood pressure value while sleeping.
  • the wearable device 2 has a function of measuring not only blood pressure values but also biological data such as activity amount, number of steps and sleep state, environmental data such as temperature and humidity, and the like.
  • Wearable device 2 is also a computer capable of data processing by an application program stored in a memory.
  • CPAP device 3 is a treatment device worn by a user who has symptoms of sleep apnea syndrome (SAS) during sleep for the purpose of treatment.
  • SAS sleep apnea syndrome
  • the CPAP device 3 sends air under pressure from a mask attached to the user's nose to the airway and widens the airway to prevent apnea during sleep.
  • the CPAP device 3 is a treatment device that should be worn during a period in which the wearable device 2 measures a blood pressure value (during monitoring).
  • the CPAP device 3 includes a device main body 3a, a mask 3b, and a tube 3c.
  • the device body 3a and the mask 3b are connected via a tube 3c.
  • the mask 3b is attached to the user's nose.
  • the device main body 3a is installed in a range where the mask 3b connected via the tube 3c can be maintained while being worn on the user's nose at bedtime.
  • the apparatus main body 3a sends the pressurized air into the tube 3c. Air from the device main body 3a is supplied to the mask 3b through the tube 3c.
  • the mask 3b sends the pressure-applied air supplied through the tube 3c from the nose to the user into the airway.
  • the CPAP device 3 has a function of communicating with the user terminal 11 and transmits information indicating an operation state to the user terminal 11.
  • the device main body 3a of the CPAP device 3 detects whether the mask 3b is correctly attached to the user by a signal detected by a sensor or the like provided on the mask 3b.
  • the apparatus main body 3a may detect the mounting state on the user by a magnetic field electrode provided on the mask 3b.
  • the apparatus main body 3a may detect the mounting state of the mask 3b based on signals detected by, for example, an atmospheric pressure sensor and a flow rate sensor.
  • the device main body 3a supplies a signal indicating the wearing state of the mask 3b to the user terminal 11.
  • the wearable device 2 or the server 12 connected via the user terminal 11 and the user terminal 11 can detect whether the CPAP device 3 is correctly attached to the user by a signal from the device main body 3a. Further, the device main body 3a and the wearable device 2 of the CPAP device 3 may acquire information indicating the wearing state of the mask 3b to the user by mutual sensing of the magnetic field electrodes provided on the mask 3b.
  • User terminal 11 is an information communication terminal used by individual users.
  • the user terminal 11 is a portable information communication terminal such as a smartphone, a mobile phone, a tablet PC, or a notebook PC.
  • the user terminal 11 may have at least a communication function with the wearable device 2 and the CPAP device 3.
  • the server 12 has a communication function with the user terminal 11.
  • the server 12 communicates with the user terminal 11 via a network.
  • the server 12 only needs to be able to communicate with the user terminal 11, and the communication method and communication form are not limited to specific ones.
  • the server 12 acquires data from the wearable device 2 and the CPAP device 3 via the user terminal 11.
  • FIG. 2 is a block diagram showing a configuration example of the wearable device 2 shown in FIG.
  • the wearable device 2 includes a control unit 21, a communication unit 22, a storage unit 23, an operation unit 24, a display unit 25, a vibration unit 26, a biosensor 27, an environment sensor 28, an acceleration sensor 29, and the like.
  • the control unit 21 includes at least one processor 21a and a memory 21b.
  • the control unit 21 implements various types of operation control, data processing, and the like by the processor 21a executing a program using the memory 21b.
  • the processor 21a is, for example, a CPU (Central Processing Unit) or an MPU (Micro Processing Unit) including an arithmetic circuit.
  • CPU Central Processing Unit
  • MPU Micro Processing Unit
  • the memory 21b includes a non-volatile memory that stores a program executed by the processor 21a and a memory such as a RAM that is used as a work memory. Further, the control unit 21 has a clock (not shown) and has a clock function for measuring the current date and time.
  • the processor 21 a can execute control of each unit and data processing by executing a program stored in the memory 21 b or the storage unit 23. That is, the processor 21a performs operation control of each unit in accordance with an operation signal from the operation unit 24, and performs data processing on measurement data measured by the biological sensor 27 and the environment sensor 28. For example, the control unit 21 continuously measures the blood pressure value of the measurement subject in accordance with an instruction from the operation unit 24, and transmits the blood pressure value data (hereinafter referred to as blood pressure data) continuously measured to the user terminal 11 or the server 12. The operation in the mode (monitoring mode) is executed.
  • the communication unit 22 is a communication interface for communicating with the user terminal 11.
  • the communication unit 22 transmits data to the user terminal 11 and receives data from the user terminal 11.
  • Communication by the communication unit 22 may be either wireless communication or wired communication.
  • the communication unit 22 is described assuming that it communicates with the user terminal 11 by short-range wireless communication.
  • the communication unit 22 is not limited to this, and may communicate using a communication cable. Communicating via a network such as a LAN (Local Area Network) may be used.
  • the storage unit 23 is program data for controlling the wearable device 2, setting data for setting various functions of the wearable device 2, measurement data measured by the biosensor 27, the environment sensor 28, the acceleration sensor 29, and the like. Memorize etc.
  • the storage unit 23 may be used as a work memory when the program is executed.
  • the operation unit 24 includes operation devices such as a touch panel and operation buttons (operation keys).
  • the operation unit 24 detects an operation by a user (a person to be measured) and outputs an operation signal indicating the operation content to the control unit 21.
  • the operation unit 24 is not limited to a touch panel or operation buttons.
  • a voice recognition unit that recognizes an operation instruction by a user's voice
  • a biometric authentication unit that authenticates a part of the user's biological body, a user's face or body, and the like. You may provide the image recognition part etc. which recognize a user's facial expression and gesture from the image
  • the display unit 25 includes, for example, a display screen (for example, an LCD (Liquid Crystal Display) or EL (Electroluminescence) display), an indicator, and the like, and display contents are controlled according to a control signal from the control unit 21.
  • a display screen for example, an LCD (Liquid Crystal Display) or EL (Electroluminescence) display
  • indicator for example, an LED (Liquid Crystal Display) or EL (Electroluminescence) display
  • the operation part 24 and the display part 25 are demonstrated as what is comprised with the indicator which has a touch panel.
  • the display unit 25 includes a display device 25a.
  • the display device 25a is a display device capable of display control independently of the display screen of the display unit 25.
  • the display device 25a is configured by, for example, an LED.
  • the display device 25a has, for example, a configuration for lighting a plurality of colors, and has a function of lighting a predetermined lighting portion with a color corresponding to a control signal from the control unit 21.
  • the vibration unit 26 vibrates at least a part of the housing of the wearable device 2.
  • the vibration part 26 is comprised with the weight decentered from the rotation center of the rotating shaft of a motor and the rotating shaft of a motor, for example.
  • the vibration unit 26 generates vibration by rotating the motor in accordance with a control instruction from the control unit 21.
  • the vibration unit 26 can vibrate the housing in various patterns in accordance with instructions from the control unit 21.
  • the biosensor 27 measures the biometric information of the user and outputs biometric data as measurement data of the biometric information.
  • the biometric sensor 27 includes a sensor for detecting signals indicating values of various types of biometric information such as blood pressure in contact with or close to a part of the body of the measurement subject.
  • the biosensor 27 is configured so as to contact or approach a predetermined position of the person to be measured using, for example, a band.
  • the control unit 21 acquires each measurement data output from the biological sensor 27 as biological data associated with the measurement time set based on the time information.
  • the biological sensor 27 includes at least a blood pressure sensor 27a.
  • the blood pressure sensor 27a obtains blood pressure data as biological data by measuring the blood pressure value of the user.
  • a sensor for measuring these biological data is a biological data. It can be provided as a sensor 27.
  • These biological data may be output as measurement data of elements other than blood pressure.
  • the electroencephalogram data can be measured data indicating a human sleep state.
  • the blood pressure sensor 27a is a blood pressure sensor that can measure the value of blood pressure (for example, systolic blood pressure and diastolic blood pressure).
  • the blood pressure sensor 27a will be described as a continuous measurement blood pressure sensor that can continuously measure blood pressure for each beat.
  • the blood pressure sensor 27a may include a continuous measurement type blood pressure sensor, but is not limited thereto.
  • the blood pressure sensor 27a a continuous measurement type blood pressure sensor using a PTT method, a tonometry method, an optical method, a radio wave method, an ultrasonic method, or the like can be applied.
  • the PTT method is a method in which a pulse wave propagation time (PTT) is measured and a blood pressure value is estimated from the measured pulse wave propagation time.
  • the tonometry method is a method in which a blood pressure value is measured using information detected by a pressure sensor by bringing a pressure sensor into direct contact with a living body part through which an artery such as the radial artery of the wrist passes.
  • the optical system, radio wave system, and ultrasonic system are systems in which light, radio waves, or ultrasonic waves are applied to blood vessels and blood pressure values are measured from the reflected waves.
  • the continuous measurement type blood pressure sensor can measure the blood pressure waveform of the user, can obtain a blood pressure value based on the measured blood pressure waveform, and calculates a heart rate based on the period of the measured blood pressure waveform.
  • the heart rate data may include, for example, a heart rate, but is not limited thereto.
  • the heart rate is not limited to being measured by a continuous measurement type blood pressure sensor, and may be measured by a heart rate sensor.
  • the environmental sensor 28 includes a sensor that measures environmental information around the user and acquires the measured environmental data.
  • the environmental sensor 28 includes an air temperature sensor 28a.
  • the environmental sensor 28 may include a sensor that measures temperature, humidity, sound, light, and the like in addition to the air temperature.
  • the environmental sensor 28 may include a sensor that measures environmental information (environmental data) that is assumed to be directly or indirectly related to fluctuations in blood pressure values.
  • the control unit 21 acquires measurement data measured by the environment sensor 28 as measurement data (environment data) in association with a measurement time set based on the time information.
  • the acceleration sensor 29 detects the acceleration received by the main body of the wearable device 2. For example, the acceleration sensor obtains 3-axis or 6-axis acceleration data. The acceleration data can be used to estimate the amount of activity (posture and / or movement) of the user wearing the wearable device 2.
  • the change in the posture of the measured person estimated from the acceleration data measured by the acceleration sensor 29 can be data indicating the sleeping state (sleeping depth) of the measured person.
  • the control unit 21 associates the measurement time with the acceleration data measured by the acceleration sensor 29 and outputs it as sleep state measurement data.
  • the change in motion estimated from the acceleration data can be data indicating the amount of activity of the user (for example, the amount of activity due to exercise such as walking or running).
  • the control unit 21 associates the measurement time with the acceleration data measured by the acceleration sensor 29 and outputs the data as activity measurement data.
  • the user's getting up may be detected by the user's movement detected by the acceleration sensor 29.
  • the wake-up may be specified according to the user's operation.
  • the operation unit 24 may instruct the user to go to bed immediately before going to bed, or the operation unit 24 may instruct the user to get up immediately after getting up.
  • FIG. 3 is a block diagram showing a configuration example of the user terminal 11 shown in FIG.
  • the user terminal 11 includes a control unit 31, a storage unit 32, a communication unit 33, a display unit 34, an operation unit 35, a device interface (I / F) 36, and the like.
  • the user terminal 11 is, for example, a mobile communication terminal such as a smartphone or a tablet, and has application software (program) installed so that the processing described later can be executed.
  • the control unit 31 includes at least one processor 31a and a memory 31b.
  • the control unit 31 performs various kinds of operation control, data processing, and the like by the processor 31a executing a program using the memory 31b.
  • the processor 31a is, for example, a CPU or MPU including an arithmetic circuit.
  • the memory 31b includes a non-volatile memory that stores a program executed by the processor 31a and a volatile memory such as a RAM that is used as a work memory. Further, the control unit 31 has a clock (not shown) and has a clock function for measuring the current date and time.
  • the storage unit 32 is a data memory.
  • the storage unit 32 includes, for example, a semiconductor memory (memory card, SSD (Solid State Drive)), a magnetic disk (HD (Hard Disk)), or the like.
  • the storage unit 32 may store a program executed by the processor 31a of the control unit 31.
  • the storage unit 32 may store data supplied from the wearable device 2 and the CPAP device 3. Further, the storage unit 32 may store display data to be displayed on the display unit 34.
  • the communication unit 33 is a communication interface for communicating with the server 12.
  • the communication unit 33 transmits data to the server 12 via the network and receives data from the server 12.
  • Communication by the communication unit 33 may be wireless communication or wired communication.
  • the description will be made on the assumption that the network is the Internet, for example.
  • the present invention is not limited to this, and may be another type of network such as a LAN, or a communication cable such as a USB cable.
  • One-to-one communication may be used.
  • the display unit 34 includes a display screen (for example, an LCD or an EL display).
  • the display unit 34 controls display contents displayed on the display screen under the control of the control unit 31.
  • the operation unit 35 transmits an operation signal corresponding to the operation by the user (measured person) to the control unit 31.
  • the operation unit 35 is, for example, a touch panel provided on the display screen of the display unit 34.
  • the operation unit 35 is not limited to a touch panel, and may be an operation button, a keyboard, a mouse, or the like.
  • the operation unit 35 includes a voice recognition unit that recognizes an operation instruction by the user's voice, a biometric authentication unit that authenticates a part of the user's biological body, an image recognition unit that recognizes the user's facial expression and gesture, and the like. It may be.
  • the device I / F 36 is a communication interface for communicating with the wearable device 2 and the CPAP device 3.
  • the device I / F 36 receives data from the wearable device 2 and the CPAP device 3 and transmits an operation instruction to the wearable device 2 and the CPAP device 3.
  • the device I / F 36 may include an interface for the wearable device 2 and an interface for the CPAP device 3. Communication by the device I / F 36 may be wireless communication or wired communication.
  • the device I / F 36 will be described on the assumption that the device I / F 36 communicates with the wearable device 2 and the CPAP device 3 by short-range wireless communication (for example, Bluetooth (registered trademark)), but is not limited thereto.
  • Wearable device 2 or CPAP device 3 may include an interface for communication via a communication cable.
  • the device I / F 36 may communicate serially via a communication cable, or may communicate via a network such as a LAN.
  • the CPAP device 3 that can communicate via the device I / F 36 supplies information indicating the wearing state of the mask 3b to the user terminal 11. Further, the CPAP device 3 may supply data indicating the user's breathing state detected by the atmospheric pressure sensor and the flow rate sensor to the user terminal 11.
  • FIG. 4 is a block diagram illustrating a configuration example of the server 12 illustrated in FIG.
  • the server 12 includes a control unit 41, a storage unit 42, and a communication unit 43.
  • the server 12 will be described assuming that a general-purpose computer apparatus is installed with a program (software) so as to perform processing described later.
  • the control unit 41 includes at least one processor 41a and a memory 41b.
  • the control unit 41 performs various types of operation control, data processing, and the like by the processor 41a executing a program using the memory 41b.
  • the processor 41a is, for example, a CPU or MPU including an arithmetic circuit.
  • the memory 41b includes a non-volatile memory that stores a program executed by the processor 41a and a volatile memory such as a RAM used as a work memory. Further, the control unit 41 has a clock (not shown) and has a clock function for measuring the current date and time.
  • the storage unit 42 is a data memory.
  • the storage unit 42 includes, for example, a magnetic disk (HD), a semiconductor memory (memory card, SSD), an optical disk, a magneto-optical disk, and the like.
  • the storage unit 42 stores various measurement data acquired from the user terminal 11.
  • the storage unit 42 may store a program executed by the processor 41a of the control unit 41.
  • the communication unit 43 is a communication interface for communicating with the user terminal 11.
  • the communication unit 43 transmits data to the user terminal 11 via the network and receives data from the user terminal 11.
  • Communication by the communication unit 43 may be wireless communication or wired communication.
  • the communication unit 43 will be described assuming a configuration that communicates with the user terminal 11 via a network.
  • the communication by the communication unit 43 is not limited to a specific communication method.
  • FIG. 5 is a block diagram illustrating functions of the control unit 21 of the wearable device 2.
  • the control unit 21 of the wearable device 2 implements various processing functions by executing programs stored in the memory 21b by the processor 21a.
  • the control unit 21 of the wearable device 2 includes an operation detection unit 51, a display control unit 52, a vibration control unit 53, a risk level display unit 54, a measurement control unit 55, and a wake-up as shown in FIG. It has the determination part 56 grade
  • the operation detection unit 51 has a function of detecting an operation instruction input by the user (measured person) using the operation unit 35 or an operation instruction input by the user through a specific operation.
  • the control unit 21 detects information input using the operation unit 24 as a touch panel. Further, the control unit 21 detects a specific operation by the user based on the acceleration data measured by the acceleration sensor 29, and detects an operation instruction corresponding to the detected specific operation.
  • the display control unit 52 is a function for controlling display contents displayed on the display unit 25.
  • the control unit 21 causes the display control unit 52 to display a display screen described later on the display unit 25.
  • the control unit 21 also controls the on / off of the display device as the display unit 25.
  • the vibration control unit 53 has a function of controlling the vibration generated in the vibration unit 26.
  • the control unit 21 controls the vibration pattern and the strength of vibration that cause the vibration control unit 53 to drive the vibration unit 26 to vibrate the housing of the wearable device 2.
  • the risk level display unit 54 is a function for displaying the risk level using the display 25a in the display unit 25.
  • the control unit 21 displays, as the risk level display unit 54, information (for example, a color corresponding to the risk level) indicating the risk level determined from the blood pressure measurement data continuously measured by the display unit 25a. For example, when the risk level for the blood pressure surge extracted from the measurement data is determined in three stages (super risk, medium risk, low risk), the control unit 21 has “super risk” and “medium risk” as the risk levels. , “Low risk” and “normal” are displayed on the display 25a in “red”, “orange”, “yellow” and “blue”, respectively.
  • the measurement control unit 55 has a function of controlling the continuous measurement of the blood pressure value using the blood pressure sensor 27a and acquiring measurement data obtained by continuously measuring the blood pressure value.
  • the control unit 21 acquires, as the measurement control unit 55, blood pressure data indicating the blood pressure value measured continuously (for example, every beat) by the blood pressure sensor 27a and stores the blood pressure data in the storage unit 23, or the user terminal 11 or the server 12 Or transfer to.
  • the wake-up determination unit 56 has a function of detecting (determining) that the user has woken up. As the wake-up determination unit 56, for example, it is determined (detected) that the measurement subject has woken up by the movement of the measurement subject specified from the acceleration data measured by the acceleration sensor 29. The wake-up determination unit 56 may detect wake-up by an operation by the measurement subject.
  • FIG. 6 is a block diagram illustrating functions of the control unit 41 of the server 12.
  • the control unit 41 of the server 12 implements various processing functions by executing programs stored in the memory 41b by the processor 41a.
  • the control unit 41 of the server 12 includes a measurement data acquisition unit 61, a blood pressure fluctuation detection unit 62, a risk determination unit 63, a totaling processing unit 64, a totaling data output unit 65, and a terminal as shown in FIG.
  • a display control unit 66 and the like are included.
  • the measurement data acquisition unit 61 has a function of acquiring measurement data including blood pressure data measured by the wearable device 2. Further, the measurement data acquisition unit 61 may acquire information measured by the CPAP device 3.
  • the control unit 41 receives the measurement data acquired from the wearable device 2 or the CPAP device 3 via the user terminal 11 by the communication unit 43 as the measurement data acquisition unit 61 and stores the received measurement data in the storage unit 42. For example, the control unit 41 acquires measurement data transferred from the wearable device 2 via the user terminal 11.
  • the blood pressure fluctuation detection unit 62 has a function of detecting blood pressure fluctuations equal to or higher than a reference value for determining a blood pressure surge from the continuously measured blood pressure data.
  • the blood pressure surge is defined by a preset reference value. For example, a blood pressure change of 20 mmHg or more during 30 beats is defined as a surge (blood pressure surge).
  • Control part 41 performs processing which detects blood pressure fluctuation more than the standard value judged as a blood pressure surge from blood pressure data measured continuously over the measurement period as blood pressure fluctuation detection part 62.
  • the risk determination unit 63 has a function of determining the risk of causing the onset of a brain / cardiovascular disease. This degree of risk is determined based on various factors including a blood pressure surge. For example, people who have factors that may cause cerebrovascular and cardiovascular disease other than blood pressure and those who do not have the same risk level even if the number and magnitude of blood pressure surges are the same. It is done. For this reason, the determination of the risk level is made based on a criterion set according to the risk level of each user, taking into account factors other than the user's own blood pressure. However, in the present embodiment, the risk level determination unit 63 will be described with reference to an example in which the risk level for the detected blood pressure surge is determined.
  • a blood pressure change of 20 mmHg or more during 30 beats is defined as a surge (blood pressure surge).
  • blood pressure changes of less than 20 mmHg during 30 beats are normal values
  • blood pressure changes of 20 mmHg to less than 40 mmHg are considered low risk surges during 30 beats
  • blood pressure changes of between 40 mmHg and less than 60 mmHg are moderately dangerous during 30 beats.
  • a surge is defined as a blood pressure change of 60 mmHg or more during 30 beats as a super-danger surge.
  • the control unit 41 determines the risk level as the risk level determination unit 63 based on a preset reference value.
  • the criteria for determining the definition of blood pressure surge and the degree of risk are information that should be appropriately set based on medical viewpoints and operational viewpoints, and are not limited to specific reference values.
  • a description will be given on the assumption that a blood pressure surge at a plurality of stages of risk is detected as a blood pressure fluctuation equal to or greater than a reference value.
  • an adjustment ability for returning an increased blood pressure value to a normal value is detected as a blood pressure fluctuation.
  • the aggregation processing unit 64 is a function that aggregates blood pressure data measured by the wearable device 2 and generates aggregate data. How to collect blood pressure data is set according to the display content to be displayed on the display unit 25 of the wearable device 2. For example, the control unit 41 aggregates the maximum blood pressure, the number of occurrences of blood pressure surge during sleep (during monitoring) (sleep surge), the detected risk level of blood pressure surge, and the like as the aggregation processing unit 64.
  • the aggregate data output unit 65 is a function for outputting aggregate data.
  • the control unit 41 transmits, as the total data output unit 65, the total data obtained by totaling the measurement data by the total processing unit 64 to the wearable device 2 that is the transmission source of the measurement data.
  • the terminal display control unit 66 is a function for controlling display contents displayed on the user terminal 11.
  • the control unit 41 supplies, as the terminal display control unit 66, display data generated from the measurement data accumulated in the storage unit or the like in accordance with the display request from the user terminal 11 and the total data to the user terminal 11 of the user.
  • the user instructs the continuous measurement (monitoring) of the blood pressure value at bedtime by operating the wearable device 2.
  • the wearable device 2 starts continuous measurement of blood pressure values in response to monitoring instructions.
  • the wearable device 2 monitors the user's getting up while sleeping (during monitoring).
  • the wearable device 2 ends the monitoring and displays information indicating the monitoring result on the display unit.
  • the information indicating the monitoring result displayed on the display unit when waking up is information (aggregated data including the degree of risk) generated by the server 12 from the measurement data (sleeping blood pressure data).
  • FIG. 7 is a flowchart for explaining a first operation example of the wearable device 2 according to the present embodiment.
  • the user (measured person) instructs the continuous measurement (monitoring) of the blood pressure value at bedtime by operating the wearable device 2.
  • the control unit 21 of the wearable device 2 receives various operation instructions by the function of the operation detection unit 51.
  • the control unit 21 When it is detected that monitoring is instructed (S11, YES), the control unit 21 starts the continuous measurement of the blood pressure value for the measurement subject using the blood pressure sensor 27a by the function of the measurement control unit 55 (S12). After starting the continuous measurement of the blood pressure value, the control unit 21 performs the continuous measurement of the blood pressure value using the blood pressure sensor 27a by the function of the measurement control unit 55 (S13). In the continuous measurement of the blood pressure value, the control unit 21 accumulates the measured blood pressure value (blood pressure data) in the storage unit 23. The control unit 21 transfers the blood pressure data accumulated in the storage unit 23 to the server 12 via the user terminal 11 or the user terminal 11 at the end of measurement.
  • control unit 21 may transfer the blood pressure data stored in the storage unit 23 to the server 12 via the user terminal 11 or the user terminal 11 at a predetermined cycle.
  • the control unit 21 may transfer the blood pressure data to the server 12 via the user terminal 11 or the user terminal 11 without saving the blood pressure data in the storage unit 23.
  • the timing for transferring the blood pressure data to the user terminal 11 or the server 12 depends on the storage capacity of the storage unit 23 in the wearable device 2, the timing of the data processing by the server 12 or the user terminal 11 for the blood pressure data, or the communication environment. It is set appropriately.
  • the control unit 21 monitors (detects) the measurement subject's wake-up by the function of the wake-up determination unit 56. For example, the control unit 21 detects that the measurement subject has woken up by the movement of the measurement subject detected by the acceleration sensor 29. Moreover, you may make it the control part 21 detect a wake-up according to operation by a to-be-measured person. If the wake-up of the measurement subject is not detected (S14, NO), the control unit 21 returns to S13 and continuously performs the continuous measurement of the blood pressure value for the measurement subject.
  • the control unit 21 When the measurement subject's wake-up is detected (S14, YES), the control unit 21 indicates that the measurement subject has woken up and blood pressure data associated with identification information for identifying the measurement subject or the wearable device (continuously measured blood pressure).
  • the measurement data including the value is transferred to the server 12 via the user terminal 11 (S15).
  • the server 12 aggregates measurement data including blood pressure data by a process described later (for example, the processes of S31 to S35 in FIG. 9), and transmits the aggregated data as the aggregation result to the wearable device 2.
  • the control unit 21 of the wearable device 2 transmits the measurement data to the server 12 when getting up, and then acquires the aggregate data supplied from the server 12 (S16).
  • the aggregated data acquired from the server 12 includes information indicating the maximum blood pressure value, the number of blood pressure surges, the degree of risk, and the like.
  • the control unit 21 causes the vibration unit 26 to vibrate the casing (main body) by the function of the vibration control unit 53 (S17). Further, the control unit 21 displays the risk level on the display 25a by the function of the risk level display unit 54 (S18). For example, the control unit 21 specifies a risk level for the monitoring result (blood pressure value continuously measured during sleep) based on information included in the aggregated data acquired from the server 12, and uses a color corresponding to the specified risk level. The display 25a is displayed.
  • the wearable device 2 displays the degree of danger to the measurement result while vibrating the casing (main body) when getting up.
  • the person to be measured recognizes that the total data has been obtained by vibration when getting up, and can intuitively visually recognize the degree of risk with respect to the measurement results displayed by color.
  • control unit 21 causes the display unit 25 to display aggregate data for the measurement result in accordance with the operation by the measurement subject. That is, the control unit 21 receives an instruction to display the total data from the measurement subject in a state where the risk level is displayed by vibrating the main body (housing) (S19). When receiving the display instruction of the total data (S19, YES), the control unit 21 displays the total data on the display unit 25 according to the operation by the measurement subject (S20). Moreover, the control part 21 complete
  • FIG. 8 is a diagram illustrating an example of a display screen displayed by the display unit 25 of the wearable device 2 in accordance with the above-described operation.
  • a display screen 80 shown in FIG. 8 is an example of an initial screen that is displayed first when waking up.
  • the display 25a displays a color corresponding to the degree of danger, and no specific information is displayed on the display unit 25.
  • the display screen 80 it is assumed that the main body of the wearable device 2 is vibrated by the vibration unit 26.
  • the initial screen displayed when you wake up may display a message indicating that the measurement has been completed, such as “measurement during sleep (monitoring) completed”, or a wake-up such as “Good morning” will be detected. You may display the message which shows that it was carried out.
  • the display screen 81 is a first example of a measurement result display screen that is displayed in response to an instruction to display aggregated data (measurement results) by the measurement subject.
  • the maximum blood pressure value is displayed as one of the measurement results.
  • An instruction to display the measurement result may be received by input to the touch panel as the operation unit 24 or may be received according to the movement of the measurement subject.
  • the control unit 21 Upon receiving the measurement result display instruction, displays a display screen 81 on the display unit 25.
  • the control unit 21 can detect an operation in which the main body (housing) of the wearable device 2 is shaken in a specific direction by the acceleration sensor 29. In this case, the control unit 21 may accept the movement of the main body in a specific direction as a measurement result display instruction.
  • the display screen 82 is a second example of a measurement result display screen displayed as a next screen on the display screen 81.
  • the display screen 82 shown in FIG. 8 as the next screen of the display screen 81, the number of blood pressure surges (sleep surges) during sleep is displayed as one of the measurement results.
  • the display screen 83 is a third example of a measurement result display screen displayed as the next screen of the display screen 82.
  • information indicating the risk level based on the blood pressure surge detected from the measurement data and a comment corresponding to the risk level are displayed as the next screen of the display screen 82.
  • control unit 21 switches the display screens 81, 82, and 83 that display the measurement results as the next screen or the previous screen in response to a swipe (touch operation that moves horizontally on the screen) of the touch panel as the operation unit 24.
  • control unit 21 may detect a motion that can be detected by the acceleration sensor 29 as a switching instruction for the display screens 81, 82, and 83.
  • FIG. 9 is a flowchart for explaining an operation example of the server 12.
  • the control unit 21 of the server 12 receives the measurement result (measurement data) of the continuous measurement (monitoring) of the blood pressure value at bedtime transferred from the wearable device 2 via the user terminal 11 by the function of the measurement data acquisition unit 61. ing.
  • the control unit 41 stores the received measurement data in the storage unit 42 in association with the identification information of the person being measured or the identification information of the wearable device 2 (S32). .
  • the control unit 41 detects a blood pressure fluctuation (blood pressure surge) equal to or higher than the reference value from the blood pressure data included in the received measurement data by the function of the blood pressure fluctuation detection unit 62 (S33).
  • a blood pressure fluctuation blood pressure surge
  • the control unit 41 determines the risk level for the detected blood pressure surge by the function of the risk level determination unit 63 (S34). Further, the control unit 41 aggregates various data including the blood pressure surge obtained from the measurement data and the risk of the blood pressure surge by the function of the aggregation processing unit 64, and generates aggregate data (S35).
  • the control unit 41 When generating the aggregated data from the received measurement data, the control unit 41 transmits the generated aggregated data to the wearable device 2 that is the transmission source of the measurement data by the function of the aggregated data output unit 65 (S36). Further, the control unit 41 stores the generated aggregate data in the storage unit 42 in association with the measurement data and the identification information of the measurement subject or the identification information of the wearable device 2.
  • control unit 41 determines whether to display the aggregated data on the user terminal 11 of the measurement subject (S37). For example, the control unit 41 determines whether or not to perform display on the user terminal 11 according to the setting by each user (measured person). When it is determined to be displayed on the user terminal 11 (S37, YES), the control unit 41 uses the function of the terminal display control unit 66 to display detailed data based on the total data and measurement data to be displayed on the user terminal 11. Is generated (S38).
  • the display data of the detailed information displayed on the user terminal 11 includes information for confirming the total data and the measurement data in detail. Further, the display data of the detailed information may include an evaluation comment for evaluating the total data. The evaluation comment may be generated by the control unit 41 based on a comparison result with past measurement data or standard data of the measurement subject. When such detailed information display data is generated, the control unit 41 transmits the generated detailed information display data to the user terminal 11 (S39). Note that the display data of the detailed information to be displayed on the user terminal 11 may be generated after receiving a request from the user terminal 11.
  • FIG. 10 is a diagram illustrating an example of a display screen displayed by the display unit 34 of the user terminal 11.
  • FIG. 10A shows a display screen 101 displayed on the display unit 34 of the user terminal 11 when getting up.
  • the display screen 101 is displayed on the display unit 34 based on receiving display data of detailed information generated based on the measurement data acquired by the server 12 from the wearable device 2 when the user wakes up. That is, when the user wakes up, the control unit 31 of the user terminal 11 receives detailed information display data from the server 12 and displays the display screen 101 on the display unit 34.
  • the display data of the detailed information acquired from the server 12 is held in the storage unit 32, for example.
  • the display screen 101 is a screen that displays that detailed information can be displayed, and the message display part 101a functions as a button that instructs to display the detailed information.
  • the control unit 31 of the user terminal 11 displays the display data of the detailed information acquired from the server 12 on the display unit 34.
  • a display screen 102 in FIG. 10B is an example in which display data of detailed information acquired from the server 12 is displayed.
  • evaluation comments on the measurement data, risk level, maximum blood pressure, number of occurrences of surge during sleep (sleep surge frequency), sleep time, calendar, and the like are displayed as detailed information.
  • the control unit 31 of the user terminal 11 may display the display screen 101 upon receiving a wake-up notification from the wearable device 2. That is, the control unit 31 of the user terminal 11 may display the display screen 101 on the display unit 34 when receiving a notification from the wearable device 2 indicating that waking up has been detected. In this case, when the display part 101a of the message on the display screen 101 is touched, the control unit 31 of the user terminal 11 requests display data of detailed information from the server 12, and the server 12 transmits in response to this request. The display data of the detailed information to be displayed may be displayed on the display unit 34.
  • FIG. 11 is a flowchart for explaining a second operation example by the wearable device 2.
  • the second operation example when the degree of risk determined from the measurement data is equal to or higher than a predetermined value, an alert at the time of waking up (display of vibration and risk level) is performed, and when the degree of risk is lower than the predetermined value, It is an operation example in which an alert is not performed.
  • the processing of S51 to S56 shown in FIG. 11 can be realized by the same operation as the processing of S11 to S16 shown in FIG. Further, the processing of S58 to S62 shown in FIG. 11 can be realized by the same operation as the processing of S17 to S21 shown in FIG. For this reason, in the description of the second operation example, detailed description of the processing of S51-S56 and S58-S62 shown in FIG. 11 is omitted.
  • the control unit 21 of the wearable device 2 has a risk level included in the total data acquired from the server 12 equal to or higher than a predetermined value. It is determined whether there is (S57). When it is determined that the degree of risk is less than the predetermined value (S57, NO), the control unit 21 ends the series of processes without performing an alert (display of the vibration of the casing and the degree of risk) for the measurement subject. .
  • the control unit 21 vibrates the housing (main body) with the vibration unit 26 by the function of the vibration control unit 53 (S58), and the risk level display unit.
  • the color corresponding to the degree of danger is displayed (lighted) on the display 25a by the function 54 (S59).
  • the control unit 21 vibrates the housing and causes the display 25a to emit light in red.
  • the wearable device 2 alerts the measurement result to the person to be measured when getting up if the degree of risk determined from the measurement result is a predetermined value or more, and is determined from the measurement result. If the risk level is less than a predetermined value, the alert to the measurement subject at the time of getting up is not performed.
  • the measured person can confirm the measurement result by an alert at the time of waking up when the blood pressure value continuously measured during sleep is determined to be dangerous, and continuously measured during sleep. If the blood pressure value is not in a dangerous state, an alert or the like can be prevented.
  • the wearable device as the blood pressure measurement device performs the continuous measurement of the blood pressure value in the sleep of the measurement subject using the blood pressure sensor capable of continuously measuring the blood pressure value.
  • the blood pressure measurement device detects that the measurement subject wakes up during the continuous measurement of the blood pressure value during sleep, the blood pressure measurement device displays information indicating the measurement result of the continuous measurement of the blood pressure value on the display unit.
  • the measurement subject who has measured the blood pressure while sleeping by the blood pressure measurement device can easily confirm the measurement result when waking up without performing a specific operation instruction.
  • the person to be measured can make a daily action plan according to blood pressure data at bedtime, which can be used for health maintenance.
  • the present invention is not limited to the above-described embodiment as it is, and can be embodied by modifying the constituent elements without departing from the scope of the invention in the implementation stage. Further, various inventions can be formed by appropriately combining a plurality of constituent elements disclosed in the embodiment. For example, some components may be deleted from all the components shown in the embodiment. Furthermore, you may combine suitably the component covering different embodiment.
  • Appendix 1 An information processing apparatus, Memory, And at least one processor cooperating with the memory;
  • the processor is Measure blood pressure at bedtime of the person being measured using the blood pressure sensor, Determining that the person to be measured has woken up,
  • An information processing apparatus configured to display, on a display unit, information indicating a measurement result of continuous measurement of blood pressure values performed while sleeping when it is determined that the measurement subject has woken up.

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Abstract

La présente invention concerne un dispositif d'affichage d'informations et un programme qui permettent de notifier à un sujet des données concernant des résultats mesurés pendant le sommeil, de telle sorte que le sujet peut facilement reconnaître les données. Le dispositif d'affichage d'informations de la présente invention comprend : une unité d'acquisition de données de mesure qui acquiert un résultat de mesure d'une valeur de pression artérielle mesurée pendant qu'un sujet est endormi; une unité de détermination de réveil qui détermine le réveil du sujet; et une unité de commande d'affichage qui permet à des informations indiquant le résultat de mesure acquis par l'unité d'acquisition de données de mesure d'être affichées sur une unité d'affichage, lorsque l'unité de détermination de réveil détermine que le sujet est éveillé.
PCT/JP2018/017365 2017-05-15 2018-05-01 Dispositif d'affichage d'informations et programme Ceased WO2018211963A1 (fr)

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JP7614679B1 (ja) 2024-04-26 2025-01-16 福田 博美 健康モニタリングシステム及び健康モニタリング方法
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JP2005198829A (ja) * 2004-01-15 2005-07-28 Seiko Epson Corp 生体情報解析装置、生体情報解析方法、制御プログラムおよび記録媒体
JP2006212218A (ja) * 2005-02-03 2006-08-17 Toshiba Corp 健康管理装置、健康管理システム、健康管理方法および健康管理プログラム
JP2016007492A (ja) * 2014-06-26 2016-01-18 オムロンヘルスケア株式会社 動作情報測定装置とその装着し忘れ防止支援方法及びプログラム

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Publication number Priority date Publication date Assignee Title
JP2005198829A (ja) * 2004-01-15 2005-07-28 Seiko Epson Corp 生体情報解析装置、生体情報解析方法、制御プログラムおよび記録媒体
JP2006212218A (ja) * 2005-02-03 2006-08-17 Toshiba Corp 健康管理装置、健康管理システム、健康管理方法および健康管理プログラム
JP2016007492A (ja) * 2014-06-26 2016-01-18 オムロンヘルスケア株式会社 動作情報測定装置とその装着し忘れ防止支援方法及びプログラム

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