WO2015198584A1 - 測定装置及び測定方法 - Google Patents

測定装置及び測定方法 Download PDF

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Publication number
WO2015198584A1
WO2015198584A1 PCT/JP2015/003117 JP2015003117W WO2015198584A1 WO 2015198584 A1 WO2015198584 A1 WO 2015198584A1 JP 2015003117 W JP2015003117 W JP 2015003117W WO 2015198584 A1 WO2015198584 A1 WO 2015198584A1
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WO
WIPO (PCT)
Prior art keywords
contact
control unit
unit
test site
information
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/JP2015/003117
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English (en)
French (fr)
Japanese (ja)
Inventor
欣也 杉本
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Kyocera Corp
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Kyocera Corp
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Publication date
Application filed by Kyocera Corp filed Critical Kyocera Corp
Priority to US15/320,161 priority Critical patent/US20170119257A1/en
Publication of WO2015198584A1 publication Critical patent/WO2015198584A1/ja
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
    • A61B5/026—Measuring blood flow
    • A61B5/0261—Measuring blood flow using optical means, e.g. infrared light
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
    • A61B5/6813—Specially adapted to be attached to a specific body part
    • A61B5/6825—Hand
    • A61B5/6826—Finger
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
    • A61B5/6843—Monitoring or controlling sensor contact pressure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6887—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient mounted on external non-worn devices, e.g. non-medical devices
    • A61B5/6898—Portable consumer electronic devices, e.g. music players, telephones, tablet computers

Definitions

  • the present invention relates to a measuring apparatus and a measuring method.
  • a measuring device that acquires biological output information from a test site such as a fingertip of a subject (user) and measures the biological information is known.
  • a blood flow measuring device that measures blood flow as biological information irradiates a fingertip with a laser beam and measures blood flow based on scattered light from blood flow of capillaries at the fingertip (see, for example, Patent Document 1). ).
  • the measurement accuracy of biological information depends on the state of capillaries at the site to be examined. For this reason, it is desirable that the measurement apparatus causes the user to contact the test site in an appropriate contact state in order to measure biological information with high accuracy.
  • An object of the present invention made in view of such circumstances is to provide a measuring apparatus and a measuring method capable of improving the measurement accuracy of biological information.
  • a measuring apparatus provides: A measuring device for measuring biological information by bringing a test site into contact with a contact part, A biosensor for obtaining biometric output from the test site; A color information acquisition unit that acquires color information of the test site in contact with the contact unit; A notification unit; A control unit, The controller is Based on the color information, information on the contact state of the test site in the contact portion is notified from the notification portion, The biological information is measured based on the biological measurement output.
  • the control unit may determine the contact state based on a ratio of a red component in the color information.
  • the control unit may determine the contact state based on a change in the ratio of the red component.
  • a pressure detection unit for detecting a contact pressure of the test site in the contact unit may determine the change in the ratio based on the ratio of the red component when the pressure detection unit detects the contact pressure.
  • the control unit may notify from the notification unit when the ratio of the red component is lower than a predetermined lower limit threshold and / or higher than a predetermined upper limit threshold.
  • the control unit may control acquisition of the biological measurement output in the biological sensor based on the color information.
  • the present invention can be realized as a method substantially corresponding to the measurement apparatus described above, and these are also included in the scope of the present invention.
  • the measuring method is: In measuring biological information by bringing the test site into contact with the contact part, Obtaining color information of the test site in contact with the contact part by a color information obtaining unit; Obtaining a biometric output from the test site by a biometric sensor; The control unit notifies the information on the contact state of the test site in the contact unit based on the color information from the notification unit, and measures the biological information based on the biometric output. Including.
  • the measurement apparatus and measurement method according to the present invention can improve the measurement accuracy of biological information.
  • FIG. 1 It is a functional block diagram which shows schematic structure of the measuring apparatus which concerns on one embodiment of this invention. It is a figure which shows an example of the use condition of the measuring apparatus of FIG. It is a flowchart which shows an example of the measurement process of the blood flow rate which the control part of FIG. 1 performs. It is a figure which shows an example of the mobile telephone carrying the measuring apparatus of FIG.
  • FIG. 1 is a functional block diagram showing a schematic configuration of a measuring apparatus according to an embodiment of the present invention.
  • the measuring device 10 includes a camera 11, a white light source 12, a pressure detection unit 13, a notification unit 14, a biosensor 15, a contact unit 16, a control unit 17, a storage unit 18, and a display unit 19. Prepare.
  • the measuring device 10 uses the biological sensor 15 to acquire a biological measurement output of a subject who contacts the contact unit 16 and measures biological information based on the biological measurement output.
  • FIG. 2 is a diagram illustrating an example of a usage state of the measuring device 10, and is a diagram illustrating a state in which the subject presses the finger of the hand that is the test site against the contact portion 16 of the measuring device 10. In the state where the finger is pressed against the contact portion 16 as shown in FIG. 2, the measuring device 10 uses the biological sensor 15 to acquire a biological measurement output and measure biological information.
  • the biological information measured by the measuring apparatus 10 can be any biological information that can be measured using the biological sensor 15.
  • the measurement device 10 will be described below as an example of measuring the blood flow of a subject, which is information related to blood flow.
  • the camera 11 acquires color information of a region to be examined that contacts the contact portion 16.
  • the camera 11 is an example of a color information acquisition unit, and is, for example, a digital video camera in the present embodiment.
  • the color information acquisition unit is not limited to the camera 11 and may have any configuration capable of acquiring color information, such as a color sensor using an LED (Light Emitting Diode).
  • the color information acquisition unit may acquire the color information of the red component among the colors of the region to be examined.
  • the white light source 12 irradiates the test site with white light.
  • the camera 11 acquires color information in the reflected light from the test site irradiated with white light from the white light source 12. If the camera 11 can acquire color information without irradiating the test site with white light due to the performance of the camera 11, the measuring device 10 may not include the white light source 12.
  • the pressure detection unit 13 detects the contact pressure of the test site in the contact unit 16.
  • the pressure detection unit 13 is configured by, for example, a piezoelectric element.
  • the pressure detection unit 13 is connected to the control unit 17 and transmits the detected contact pressure to the control unit 17 as a pressure signal. Therefore, when the test part is in contact with the contact part 16, the pressure detection unit 13 detects the contact pressure acting on the contact part 16 from the test part, and uses the detected contact pressure as a pressure signal to the control unit 17. Send.
  • the control unit 17 can determine whether or not the test site is in contact with the contact unit 16 based on the pressure signal.
  • the notification unit 14 notifies information related to the contact state of the test site in the contact unit 16 based on the control of the control unit 17.
  • the information on the contact state is, for example, information on whether or not the test site is in contact with the contact portion 16 so that the capillary blood vessel at the test site is in a state suitable for measurement of biological information.
  • reporting part 14 can alert
  • the notification unit 14 performs notification by a visual method, for example, the notification unit 14 performs notification by displaying an image or a character on the display unit 19.
  • reporting part 14 may alert
  • the notification unit 14 performs notification by outputting an alarm sound, a voice guide, or the like from a sound generating device such as a speaker.
  • the notification performed by the notification unit 14 is not limited to a visual or auditory method, and may be any method that can be recognized by the subject. Specific control of the notification unit 14 by the control unit 17 will be described later.
  • the biological sensor 15 acquires a biological measurement output from the test site.
  • the biological sensor 15 includes a laser light source 21 and a light receiving unit 22.
  • the laser light source 21 emits laser light based on the control of the control unit 17.
  • the laser light source 21 irradiates, for example, a laser beam having a wavelength capable of detecting a predetermined component contained in blood as measurement light, and is configured by, for example, an LD (laser diode: Laser Diode). .
  • LD laser diode: Laser Diode
  • the light receiving unit 22 receives the scattered light of the measurement light from the test site as a biometric measurement output.
  • the light receiving unit 22 is configured by, for example, a PD (photodiode: Photo Diode).
  • the biological sensor 15 transmits a photoelectric conversion signal of scattered light received by the light receiving unit 22 to the control unit 17.
  • the contact unit 16 is a part that contacts a test site such as a finger in order for the subject to measure biological information.
  • the contact part 16 can be comprised by a plate-shaped member, for example.
  • the contact portion 16 is made of a transparent member with respect to at least the measurement light from the laser light source 21, the white light from the white light source 12, and the scattered light of the measurement light and the reflected light of the white light from the contacted test site. Composed.
  • the control unit 17 is a processor that controls and manages the entire measurement apparatus 10 including each functional block of the measurement apparatus 10.
  • the control unit 17 includes a processor such as a CPU (Central Processing Unit) that executes a program that defines a control procedure, and the program is stored in, for example, the storage unit 18 or an external storage medium.
  • a processor such as a CPU (Central Processing Unit) that executes a program that defines a control procedure, and the program is stored in, for example, the storage unit 18 or an external storage medium.
  • a CPU Central Processing Unit
  • the control part 17 notifies the information regarding the contact state of the test site in the contact part 16 from the notification part 14.
  • the control unit 17 performs notification so that the subject can adjust the contact state so that the capillary blood vessel at the site to be examined is in a state suitable for measurement of biological information. For example, when the contact pressure at which the test site comes into contact with the contact portion 16 is strong, the capillaries in the test site are crushed, and the blood does not flow through the capillaries or is difficult to flow. Even if the blood flow is measured in this state, a highly accurate blood flow measurement result is not output. In this case, the control unit 17 gives a notification from the notification unit 14 so that the subject weakens the contact pressure of the test site.
  • the control unit 17 determines the contact state based on the color information acquired from the camera 11.
  • the control unit 17 determines the contact state based on the ratio of the red component in the color information using the color property of the finger.
  • the red component is a component whose wavelength is included in, for example, 610 nm to 780 nm.
  • the control part 17 of the measuring apparatus 10 which concerns on this Embodiment judges a contact state using this characteristic especially based on the change of the ratio of a red component.
  • the control unit 17 determines the contact state based on the change in the ratio of the red component in this way, the subject contacts the contact unit 16 after setting the measuring apparatus 10 in a state in which biological information can be measured.
  • a change in the ratio of the red component during contact with the test site is determined using the ratio of the red component of the test site as a reference.
  • the control unit 17 determines whether or not the test site has contacted the contact unit 16 based on whether or not the pressure detection unit 13 has detected pressure.
  • the control unit 17 acquires an image (initial image) acquired by the camera 11 when the pressure detection unit 13 detects pressure.
  • the control unit 17 calculates the ratio of the red component included in the image by analyzing the color information of the acquired initial image. Thereafter, the control unit 17 continuously acquires the image acquired by the camera 11 while the biometric sensor 15 acquires the biometric measurement output, and analyzes the color information of the image, thereby the red component included in the image. The ratio is calculated.
  • the control unit 17 outputs, from the notification unit 14, a notification instructing to reduce the contact pressure when the calculated ratio of the red component is decreased by a predetermined ratio or more with respect to the ratio of the red component of the initial image.
  • a predetermined ratio that is a criterion for determining whether to perform notification is stored in advance in the storage unit 18, for example.
  • the control unit 17 may determine whether or not the blood flow rate can be measured based on the image acquired by the camera 11 when starting measurement of biological information. For example, when the ratio of the red component calculated based on the initial image is equal to or less than a predetermined threshold, the control unit 17 determines that blood is not flowing to the test site to the extent that blood flow can be measured. In this case, the control unit 17 displays on the display unit 19 that the blood flow rate cannot be measured. The control unit 17 may list and display on the display unit 19 what is assumed as a cause that blood does not flow to the test site to such an extent that blood flow can be measured. Possible causes include, for example, that the subject has white wax disease, and that the site to be examined is not at the same height as the heart.
  • White wax disease is a disease in which blood does not flow into arteries due to convulsive contraction of blood vessels.
  • the control unit 17 determines that the blood flow rate cannot be measured.
  • the test site is not at the same height as the heart, for example, when the test site is in contact with the contact portion 16 with the hand raised, the test site As a result, the hydrostatic pressure decreases and the blood flow rate at the test site decreases. In this case, the control unit 17 determines that blood is not flowing to such an extent that blood flow can be measured.
  • control unit 17 may display the solution on the display unit 19 when the problem due to the cause can be solved.
  • the display unit 19 may perform a measurement with, for example, “finger height is the same as the heart height. Please display ".
  • the control unit 17 When the control unit 17 displays that the blood flow volume cannot be measured, the control unit 17 causes the display unit 19 to display a selection screen for selecting whether or not to measure biological information again.
  • the selection screen when the subject selects to measure again using the input unit provided in the measurement device 10, the control unit 17 can measure the blood flow based on the image acquired by the camera 11. It is determined again whether or not.
  • the control unit 17 ends without measuring the biological information.
  • the control unit 17 ends the measurement when the subject recognizes that the subject has white wax disease, for example, by causing the subject to determine whether or not to perform the biometric measurement again. When the cause that the subject is supposed to solve is solved, the measurement can be performed again.
  • the control unit 17 causes the laser light source 21 to emit laser light when it is determined that the blood flow rate can be measured based on the image acquired by the camera 11. After the biosensor 15 starts acquiring the biometric output by the emission of the laser light, the control unit 17 determines whether acquisition of the biometric output by the biosensor 15 is finished. For example, the control unit 17 may determine that the acquisition of the biometric output is completed after a predetermined time has elapsed since the biosensor 15 starts acquiring the biometric output. In addition, for example, the control unit 17 may determine that the acquisition of the biometric output is completed when the biometric sensor 15 acquires a sufficient biometric output for measuring the biometric information. When the control unit 17 determines that the acquisition of the biometric output is completed, the control unit 17 stops the output of the laser light from the laser light source 21. In this way, the control unit 17 controls the acquisition of the biological measurement output in the biological sensor 15.
  • the control unit 17 measures the biological information based on the biological measurement output acquired by the biological sensor 15. Specifically, the control unit 17 generates biological information based on the output (biological information output) of the light receiving unit 22.
  • the control unit 17 irradiates the living tissue (test site) with laser light from the laser light source 21 and receives the scattered light scattered from the living tissue by the light receiving unit 22. . And the control part 17 calculates a blood flow rate based on the output regarding the received scattered light.
  • the control unit 17 detects a beat signal (also referred to as a beat signal) generated by light interference between scattered light from a stationary tissue and scattered light from a moving blood cell.
  • This beat signal represents the intensity as a function of time.
  • the control part 17 makes this beat signal the power spectrum which represented power as a function of frequency.
  • the Doppler shift frequency is proportional to the blood cell velocity, and the power corresponds to the amount of blood cells.
  • the control part 17 calculates
  • the control unit 17 causes the display unit 19 to display the measured biological information.
  • the storage unit 18 can be composed of a semiconductor memory, a magnetic memory, or the like, and stores various information, a program for operating the measuring apparatus 10, and the like, and also functions as a work memory.
  • the storage unit 18 stores, for example, a threshold value and a ratio that are a reference for the determination performed by the control unit 17.
  • storage part 18 may memorize
  • the storage unit 18 may store the ratio of the red component of the test site when the control unit 17 comes into contact with the contact unit 16, which serves as a reference for determining the rate of change of the red component of the test site.
  • the display unit 19 is a display device configured by a known display such as a liquid crystal display, an organic EL display, or an inorganic EL display.
  • the display unit 19 can display various information based on the control of the control unit 17, for example, displays measured biological information.
  • control unit 17 starts the flow of FIG. 3 when the subject operates the measuring device 10 so that the measuring device 10 can measure biological information.
  • the control unit 17 acquires a pressure signal output by the pressure detection unit 13 when the subject brings the test site into contact with the contact unit 16 (step S101). Thereby, the control unit 17 recognizes that the test site has contacted the contact unit 16.
  • the control unit 17 acquires an image captured by the camera 11 when the test site comes into contact with the contact unit 16 (step S102).
  • the control unit 17 analyzes the color information of the image acquired in step S102, and calculates the ratio of the red component included in the image (step S103).
  • the control unit 17 determines whether or not the calculated ratio of the red component is equal to or less than a predetermined threshold stored in the storage unit 18 (step S104).
  • control unit 17 determines that the ratio of the red component is equal to or less than the predetermined threshold (Yes in step S104)
  • the control unit 17 determines that the blood is not flowing to the extent that the blood flow can be measured, and the blood flow cannot be measured. Is displayed on the display unit 19 (step S105).
  • the control unit 17 may display on the display unit 19 what is assumed as a cause that blood is not flowing to such an extent that blood flow can be measured and a solution to the problem caused by the cause.
  • the control unit 17 displays on the display unit 19 a selection screen for selecting whether or not to measure the blood flow again, that is, whether or not to continue measuring the blood flow in this flow.
  • the control unit 17 determines whether or not to continue the blood flow measurement based on the input of the subject to this display (step S106).
  • control unit 17 ends this flow without measuring the blood flow rate.
  • Step S106 When it is determined that the measurement of the blood flow is continued based on the input of the subject (Yes in Step S106), the control unit 17 proceeds to Step S101, and the pressure when the test site comes into contact with the contact unit 16 is determined. The pressure signal output from the detector 13 is acquired.
  • control unit 17 determines in step S104 that the red component ratio is larger than the predetermined threshold (No in step S104), the control unit 17 stores the red component ratio calculated in step S103 in the storage unit 18 (step S107). .
  • the controller 17 emits laser light from the laser light source 21 (step S108). In this way, the control unit 17 starts the acquisition of the biological measurement output in the biological sensor 15.
  • the control unit 17 analyzes the color information of the image acquired by the camera 11, and the ratio of the red component is equal to or greater than the predetermined ratio stored in the storage unit 18. It is determined whether or not the number has decreased (step S109).
  • step S109 When the control unit 17 determines that the ratio of the red component has decreased by a predetermined rate or more (Yes in step S109), the control unit 17 determines that the capillary is crushed because the contact pressure at the test site in the contact unit 16 is strong. Then, a notification for instructing to weaken the contact pressure is issued from the notification unit 14 (step S110). When the subject recognizes this notification, the subject weakens the pressure at the site to be examined. And the control part 17 transfers to step S109, and judges whether the ratio of the red component in a test site
  • control unit 17 determines whether or not the acquisition of the biological measurement output by the biological sensor 15 is completed (Step S111). ).
  • control unit 17 determines that the acquisition of the biometric output is not completed (No in Step S111)
  • the control unit 17 proceeds to Step S109.
  • the control unit 17 stops the emission of the laser beam from the laser light source 21 when it is determined that the acquisition of the biometric measurement output is completed (Yes in Step S111) (Step S112).
  • Control part 17 measures living body information based on living body measurement output which living body sensor 15 acquired (Step S113).
  • the control unit 17 displays the measurement result of the biological information measured in step S113 on the display unit 19 (step S114).
  • the subject can know the blood flow volume by confirming the displayed measurement result.
  • the color information acquisition unit acquires the color information of the region to be examined that is in contact with the contact unit 16, and the control unit 17 performs the detection based on the color information. It is determined whether or not the capillaries at the test site are in an appropriate state for measuring biological information, that is, whether or not they are collapsed.
  • the control unit 17 determines that the capillary is crushed, the control unit 17 notifies the subject to weaken the contact pressure from the notification unit 14, and therefore the subject is suitable for measuring the biological information. It becomes easy to adjust a contact pressure so that it may be in a state. Therefore, the measurement apparatus 10 can improve the measurement accuracy of the biological information because the capillary blood vessel can easily measure the biological information in a state suitable for the measurement of the biological information.
  • each component, each step, etc. can be rearranged so that there is no logical contradiction, and multiple components, steps, etc. can be combined or divided into one It is.
  • the control unit 17 determines that the test site is in contact with the contact unit 16 when the pressure detection unit 13 detects pressure.
  • the determination of whether or not the contact has occurred is not limited to the detection based on the detection by the pressure detection unit 13.
  • the control unit 17 may determine contact of the test site with the contact unit 16 based on an image acquired by the camera 11.
  • the camera 11 acquires the scenery around the measuring apparatus 10 as an image before the test site comes into contact with the contact unit 16, but when the test site is in contact with the contact unit 16, the test site is obtained. Get the image. In this way, the image acquired by the camera 11 changes abruptly before and after contact with the contact portion 16 of the test site.
  • the control unit 17 determines whether or not the test site has contacted the contact unit 16 based on the image acquired by the camera 11. Specifically, the control unit 17 performs image analysis of the image acquired by the camera 11. The control unit 17 determines that the test site has come into contact with the contact unit 16 when the image changes rapidly. In this case, the measuring apparatus 10 may not include the pressure detection unit 13.
  • reports from the alerting
  • the notification from the notification unit 14 is not limited to this case.
  • the control unit 17 may perform notification from the notification unit 14.
  • the control unit 17 determines that the capillaries are crushed and blood is not flowing through the test site to the extent that blood flow can be measured. Based on this determination, the control unit 17 performs a notification from the notification unit 14 instructing to weaken the contact pressure.
  • control unit 17 may perform notification from the notification unit 14 when the ratio of the red component of the test site is higher than a predetermined upper limit threshold.
  • the contact pressure from the test site to the contact unit 16 is weak, for example, the biometric measurement output acquired by the biosensor 15 includes noise, and the control unit 17
  • the measurement accuracy of biological information to be measured may decrease.
  • the control unit 17 may perform notification based on the upper limit threshold value in order to prevent a decrease in the measurement accuracy of the biological information. Specifically, the control unit 17 performs a notification from the notification unit 14 instructing to increase the contact pressure when the ratio of the red component of the test site is higher than a predetermined upper limit threshold.
  • control part 17 performs notification which adjusts a contact pressure to an appropriate pressure from the alerting
  • the predetermined lower limit threshold and the predetermined upper limit threshold are stored in advance in the storage unit 18, for example.
  • the predetermined lower threshold and the predetermined upper threshold may be determined by the control unit 17 by performing calibration for each subject.
  • the predetermined lower threshold and the predetermined upper threshold reflect individual differences for each subject, such as the thickness of the skin of the subject's test site and the thickness of the capillary vessel, for example.
  • the measurement apparatus 10 can measure the biological information with higher accuracy.
  • the measuring device 10 includes a temperature sensor that measures the temperature (air temperature) around the measuring device 10, and based on the temperature measured by the temperature sensor, a predetermined lower threshold and a predetermined threshold regarding the ratio of the red component of the test site At least one of the upper thresholds may be changed. For example, when the ambient temperature of the measuring device 10 is lower than a predetermined temperature threshold, the blood circulation of the subject may deteriorate, so the measuring device 10 sets at least one of a predetermined lower threshold and a predetermined upper threshold, The temperature may be set lower than the lower threshold and the upper threshold set when the temperature is equal to or higher than a predetermined temperature threshold.
  • the control unit 17 may control the emission of the laser light from the laser light source 21 based on the contact state determined based on the ratio of the red component of the test site. For example, when the control unit 17 determines that the part to be examined is in contact with the contact unit 16 in a state suitable for measurement of biological information, the control unit 17 emits laser light, and the contact state is in a state suitable for measurement of biological information. When it is determined that the laser beam has disappeared (for example, Yes in step S109 in the flow of FIG. 3), the emission of the laser beam may be stopped. As described above, the control unit 17 can suppress unnecessary power consumption by controlling the emission of the laser light in accordance with the contact state.
  • FIG. 4 is a diagram showing an example of a mobile phone equipped with the measuring apparatus 10 of FIG. As shown in FIG. 4A, the mobile phone 30 includes a measuring device 10 on the back side thereof.
  • FIG. 4B is a diagram illustrating an example in which the subject performs measurement of biological information using the mobile phone 30 including the measuring device 10.
  • the subject causes the measuring device 10 to measure biological information by bringing a finger into contact with the contact portion 16 of the measuring device 10.
  • the measuring device 10 When the subject measures the biological information using the mobile phone 30 provided with the measuring device 10, the measuring device 10 is dedicated for the subject to measure the biological information using the mobile phone 30. Measurement of biological information may be started by starting an application. The measuring device 10 may automatically start measuring biological information when the contact pressure is detected at the contact portion 16. In this case, the subject can start measurement of biological information by bringing his / her finger into contact with the contact unit 16 without activating the application.
  • the functions of the functional units of the measuring device 10 shown in FIG. 1 may be included in the functional units of the electronic device.
  • the measuring apparatus 10 may use a camera included in the mobile phone 30 as the camera 11 or use a display included in the mobile phone 30 as the display unit 19.
  • the arrangement of the measuring device 10 in the mobile phone 30 is not limited to that shown in FIG.
  • the measuring device 10 may be disposed on another part of the back surface of the mobile phone 30, or may be disposed on the surface or side surface of the mobile phone 30.
  • the electronic device on which the measuring apparatus 10 is mounted is not limited to the mobile phone 30.
  • the measuring apparatus 10 can be mounted on a wide variety of electronic devices such as a portable music player, a notebook computer, a wristwatch, a tablet terminal, and a game machine.
  • the control part 17 with which the measuring apparatus 10 is provided produces
  • the control part 17 with which the measuring apparatus 10 is provided produces
  • a server device connected to the measuring device 10 via a wired or wireless network or a combination thereof includes a functional unit corresponding to the control unit 17, and biometric information is generated by the server device having this functional unit. It may be done.
  • the measuring apparatus 10 acquires the biometric information output by the biometric sensor 15, and transmits the acquired biometric information output to the server apparatus from a separately provided communication unit.
  • the server device generates biometric information based on the biometric information output, and transmits the generated biometric information to the measurement device 10.
  • the subject can view the biological information received by the measuring apparatus 10 by displaying the information on the display unit 19.
  • the server device when the server device generates biometric information, the measurement device 10 can be reduced in size and the like as compared with the case where all the functional units illustrated in FIG. 1 are realized on one measurement device 10. .

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  • Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
  • Measuring And Recording Apparatus For Diagnosis (AREA)
PCT/JP2015/003117 2014-06-24 2015-06-22 測定装置及び測定方法 Ceased WO2015198584A1 (ja)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003505133A (ja) * 1999-07-26 2003-02-12 カルディオセンス リミテッド ショックおよびプレショックの医学的状態を検出するための改良された方法および装置
JP2003075135A (ja) * 2001-08-31 2003-03-12 Nec Corp 指紋画像入力装置および指紋画像による生体識別方法
WO2006030781A1 (ja) * 2004-09-13 2006-03-23 The Ritsumeikan Trust 指先からの生体情報の抽出方法およびその装置

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003505133A (ja) * 1999-07-26 2003-02-12 カルディオセンス リミテッド ショックおよびプレショックの医学的状態を検出するための改良された方法および装置
JP2003075135A (ja) * 2001-08-31 2003-03-12 Nec Corp 指紋画像入力装置および指紋画像による生体識別方法
WO2006030781A1 (ja) * 2004-09-13 2006-03-23 The Ritsumeikan Trust 指先からの生体情報の抽出方法およびその装置

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