WO2023176427A1 - Oxygen saturation value measurement device and oxygen saturation value measurement method - Google Patents

Oxygen saturation value measurement device and oxygen saturation value measurement method Download PDF

Info

Publication number
WO2023176427A1
WO2023176427A1 PCT/JP2023/007291 JP2023007291W WO2023176427A1 WO 2023176427 A1 WO2023176427 A1 WO 2023176427A1 JP 2023007291 W JP2023007291 W JP 2023007291W WO 2023176427 A1 WO2023176427 A1 WO 2023176427A1
Authority
WO
WIPO (PCT)
Prior art keywords
light
receiving element
pulse wave
wave signal
light emitting
Prior art date
Application number
PCT/JP2023/007291
Other languages
French (fr)
Japanese (ja)
Inventor
和夫 山本
優貴 松井
哲也 木口
健一 日沼
正行 荒川
卓 大橋
光明 久保
Original Assignee
オムロン株式会社
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 オムロン株式会社 filed Critical オムロン株式会社
Publication of WO2023176427A1 publication Critical patent/WO2023176427A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/1455Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using optical sensors, e.g. spectral photometrical oximeters

Definitions

  • the present disclosure relates to an oxygen saturation measuring device and an oxygen saturation measuring method.
  • Photoplethysmography is a well-known method that measures oxygen saturation (S PO 2 ) in arterial blood by percutaneously irradiating light onto arteries in the human body from above the skin. ing. Since pulsations appear strongly on the skin of the human body, especially on arteries under the skin of the wrist, when measuring oxygen saturation at the wrist, a pulse wave signal with a relatively large amplitude can be obtained.
  • Japanese Patent Publication No. 2017-516539 discloses a technique for measuring physiological data with a wristwatch-type measuring device worn on the wrist.
  • the measuring device of PCT International Publication No. 2017-516539 is a wearable system that includes a band wrapped around the wrist and a sensor unit provided on the band.
  • the sensor unit includes a light emitting element such as an LED that emits an optical signal, and a light receiving element such as a photodiode that serves as a sensor that receives the optical signal.
  • the sensor unit is arranged within a part of the plate surface of a plate-shaped sensor plate having approximately the same thickness overall.
  • Japanese Patent Publication No. 2017-516539 discloses a technique for rotating a circular sensor unit placed on the inner surface of the band, which is the surface that contacts the skin, as a method for changing the sensor placement position.
  • Japanese Patent Publication No. 2017-516539 also discloses a sensor slide that is arranged on the inner surface of the band and slides in the circumferential direction of the wrist.
  • a band is wrapped around the wrist and a sensor unit is placed on the skin on the inside of the wrist near an artery such as the brachioradial artery. Then, an optical signal is emitted from the light emitting element of the sensor unit to the pulsating arterial blood.
  • the irradiated optical signal is reflected by the arterial blood, and the reflected optical signal is acquired as a pulse wave signal by the light receiving element of the sensor unit.
  • a value obtained by calculating the intensity of the acquired pulse wave signal using a predetermined calculation formula can be used as a measured value of oxygen saturation. Note that in the present disclosure, "intensity of pulse wave signal” means the amplitude of the pulse wave signal.
  • Japanese Patent Laid-Open No. 2017-136182 discloses a wristwatch-type wearable system as a biological information acquisition device that includes a band that is wrapped around the wrist or arm, and a sensor module (i.e., a sensor unit) installed in the band. Disclosed.
  • a sensor module i.e., a sensor unit
  • the biological information acquisition device disclosed in Japanese Patent Application Laid-open No. 2017-136182 in order to measure blood sugar level, light is irradiated onto a blood vessel to be measured, and the transmitted light that has passed through the blood vessel is transmitted to a plurality of light receiving sections (i.e., a light receiving element). ) is received by the JP 2017-136182A states that oxygen saturation can be measured based on the intensity of transmitted light that has passed through an artery.
  • Patent Document 1 Japanese Patent Publication No. 2017-516539
  • Patent Document 2 Japanese Patent Application Publication No. 2017-136182
  • the sensor unit tends to move away from its initial position near the artery to be measured.
  • the band may shift on the skin surface due to sweaty skin at the area where the band is worn.
  • a person to be measured who feels uncomfortable wearing the band may temporarily remove the band from his wrist and then re-wrap it around his wrist.
  • the palmaris longus tendon tends to protrude relatively largely from the skin at the wrist. The raised palmaris longus tendon pushes the band or sensor unit outward, increasing the distance between the sensor unit and the skin surface of the wrist.
  • the optical element as a sensor is placed at the initial position on the wrist, after placement, the placement position of the sensor changes in each of the extending direction of the forearm, the circumferential direction of the wrist, and the radial direction of the wrist. , the position is likely to shift from the initial position. For this reason, the intensity of the pulse wave signal acquired by the light receiving element decreases due to the positional shift, resulting in a problem in that the measurement of oxygen saturation is likely to be interrupted.
  • JP-A-2017-136182 transmitted light that passes through an artery is used to measure oxygen saturation. For this reason, for example, when reflected light is used to measure oxygen saturation, it is difficult to apply the technique of JP-A-2017-136182 as is to the problem of sensor positional deviation.
  • the present disclosure has been made with a focus on the above-mentioned problems, and includes an oxygen saturation measuring device and an oxygen saturation measuring method that can reduce the frequency of measurement interruptions caused by misalignment of the sensor at the inner side of the wrist. I will provide a.
  • An oxygen saturation measurement device includes a band wrapped around the wrist of a subject, a light emitting element that irradiates light to an artery in the wrist, and a first light emitting element that receives reflected light from the artery in the wrist. a second light-receiving element that is placed apart from the first light-receiving element and receives the reflected light from the wrist artery; Among the pulse wave signal and the second pulse wave signal acquired from the reflected light received by the second light receiving element, the light receiving element that has received the pulse wave signal having a larger amplitude is used as the measuring light receiving element.
  • the apparatus includes a light receiving element determining section that determines the light receiving element, and a measuring section that measures the oxygen saturation level of the artery irradiated with light based on the pulse wave signal received by the determined measuring light receiving element.
  • the light receiving element that receives the pulse wave signal having the larger amplitude is selected from among the first light receiving element and the second light receiving element. It is determined as a light receiving element for measuring oxygen saturation. Then, the oxygen saturation level is measured based on the pulse wave signal received by the determined measurement light receiving element.
  • a plurality of reflected lights of light emitted from the same light emitting element are received, and the amplitudes of pulse wave signals of the plurality of received reflected lights are compared.
  • the pulse wave signal having the largest amplitude is quantitatively selected as the pulse wave signal for oxygen saturation measurement. Therefore, the frequency of interruptions in oxygen saturation measurement due to misalignment of the sensor at the inner side of the wrist can be reduced.
  • the first light receiving element and the second light receiving element may be arranged along the circumferential direction of the wrist.
  • a more appropriate measurement light receiving element can be determined between two different positions along the circumferential direction of the wrist.
  • the measuring device may further include a determination unit, and perform a process of determining a measuring light receiving element from among the light receiving elements that have received a pulse wave signal that satisfies the reference value.
  • the first pulse wave signal and the second pulse wave signal satisfy a preset reference value based on the viewpoint of achieving a preset measurement accuracy. . Then, a process is performed to determine a measuring light receiving element from among the light receiving elements that have received a pulse wave signal that satisfies the reference value. Among the acquired pulse wave signals, only the pulse wave signals that satisfy the reference value are extracted for measurement, so that the measurement accuracy of oxygen saturation can be further improved.
  • the light emitting element includes a first light emitting element that irradiates light to an artery in the wrist, and a first light emitting element that is arranged apart from the first light emitting element along the circumferential direction of the wrist and that irradiates light to the artery in the wrist.
  • a second light emitting element that emits light, the second light emitting element is arranged apart from the first light receiving element, and the second light receiving element is arranged apart from the second light receiving element, and the second light emitting element emits light.
  • the first light receiving element, the second light receiving element, and the third light receiving element are arranged along the circumferential direction of the wrist, and the first light receiving element receives reflected light from the artery.
  • a distribution creation unit that creates a second amplitude distribution based on the first pulse wave signal, the second pulse wave signal, and the third pulse wave signal acquired from reflected light; A criterion set using the first amplitude distribution and the second amplitude distribution to correspond to the fact that the light emitting element is located above the artery among the first light emitting element and the second light emitting element.
  • a light emitting element determination unit that determines the light emitting element for which a distribution satisfying the conditions has been created as the light emitting element for measurement, and determines the oxygen saturation based on the pulse wave signal of the reflected light of the determined light emitting element for measurement. may be measured.
  • the reflected light of the first light emitting element is received by each of the first light receiving element, the second light receiving element, and the third light receiving element, and the received reflected light is reflected by the wrist.
  • a first amplitude distribution along the circumferential direction is created.
  • the reflected light of the second light emitting element is received by each of the first light receiving element, the second light receiving element, and the third light receiving element, and the received reflected light is transmitted along the circumferential direction of the wrist.
  • a second amplitude distribution is created.
  • a light emitting element is created that satisfies the reference condition set in accordance with the fact that the light emitting element is located above the artery. is determined as the light emitting element for measurement. Then, the oxygen saturation level is measured based on the pulse wave signal of the reflected light from the determined light emitting element for measurement. That is, the light emitting element located above the artery from among the plurality of light emitting elements is determined as the light emitting element for measurement. Therefore, the measurement accuracy of oxygen saturation can be further improved.
  • the light emitting device may further include a control unit that stops energizing the light emitting element.
  • An oxygen saturation measuring method includes irradiating light onto an artery to be measured using the light-emitting element of the oxygen saturation measuring device according to the above-described one aspect, and emitting light from the artery irradiated with the light. From the reflected light, a first pulse wave signal is obtained using the first light receiving element, a second pulse wave signal is obtained using the second light receiving element, and the first pulse wave signal and the second pulse wave signal are combined. The pulse wave signal is monitored, and the light receiving element that receives the pulse wave signal having the larger amplitude between the monitored first pulse wave signal and the monitored second pulse wave signal is determined as the light receiving element.
  • the measuring section is used to determine the oxygen saturation as a measuring light receiving element, and the measuring section is used to measure oxygen saturation based on the pulse wave signal received by the determined measuring light receiving element.
  • the oxygen saturation is measured at the position on the inside of the wrist due to the positional deviation of the sensor.
  • the frequency of measurement interruptions can be reduced.
  • the oxygen saturation measuring device and the oxygen saturation measuring method according to the present disclosure it is possible to reduce the frequency of interruption of measurement due to positional deviation of the sensor at the inner side of the wrist.
  • FIG. 1 is a cross-sectional view illustrating an oxygen saturation measuring device according to a first embodiment of the present disclosure.
  • FIG. 1 is a perspective view illustrating an oxygen saturation measuring device according to a first embodiment.
  • FIG. 2 is a plan view illustrating a sensor unit of the oxygen saturation measuring device according to the first embodiment.
  • 4 is a sectional view taken along line 4-4 in FIG. 3.
  • FIG. It is a sectional view explaining the oxygen saturation measuring device concerning the modification (the 1st modification) of a 1st embodiment.
  • It is a perspective view explaining the oxygen saturation measuring device concerning the modification (the 2nd modification) of a 1st embodiment.
  • It is a top view explaining the slider part of the oxygen saturation measuring device based on 2nd Embodiment.
  • FIG. 8 is a sectional view taken along line 8-8 in FIG. 7.
  • FIG. 8 is a sectional view taken along line 9-9 in FIG. 7.
  • FIG. 7 is a plan view illustrating the arrangement of a light emitting element and a light receiving element of an oxygen saturation measuring device according to a third embodiment. It is a flow chart explaining the oxygen saturation measuring method using the oxygen saturation measuring device concerning a 3rd embodiment. It is a graph explaining the distribution of the amplitude of the reflected light of the light irradiated from the 1st light emitting element of the oxygen saturation measuring device concerning 3rd Embodiment.
  • FIG. 7 is a plan view illustrating another arrangement pattern of light emitting elements and light receiving elements.
  • the contact surface has a curved shape.
  • the first embodiment will be described below with reference to FIGS. 1 to 6.
  • the oxygen saturation measuring device 10A includes a band 12, a base 14, a contact section 16, a light emitting element, a light receiving element, and a measuring section 18.
  • the light receiving elements include a first light receiving element PD1, a second light receiving element PD2, a third light receiving element PD3, a fourth light receiving element PD4, and a fifth light receiving element PD1.
  • a light receiving element PD5 is provided.
  • a radius 20, a radial styloid process 20A, a flexor carpi radialis tendon 22, and a radial artery 24 are illustrated.
  • the band 12 is wrapped around the wrist of the subject.
  • the material of the band 12 is arbitrary, such as resin, cloth, metal, etc.
  • the band 12 is also provided with a clasp for adjusting and fixing the length when it is wrapped around the wrist.
  • the band 12 is provided with a calculation display section 26.
  • a base 14 is provided on the inner surface of the band 12.
  • the base 14 may be fixed to the band 12, for example by adhesive.
  • the fixing method is not limited to adhesion, and a fixing plate member may be interposed between the circuit board and the band 12, and the circuit board may be fixed to the plate member by screwing or the like.
  • the base 14 has a flat joint surface 14A between the band 12 and the contact portion 16.
  • both a light emitting element and a light receiving element are bonded to the bonding surface 14A of the base 14.
  • at least one of the light emitting element and the light receiving element may be bonded to the bonding surface 14A.
  • the base 14 may be the circuit board itself on which the light emitting element and the light receiving element are mounted, or a combination of the circuit board and a fixing plate member, or a combination of the circuit board and a buffer. It may also be a combination of other members. That is, the base 14 of the present disclosure only needs to have a bonding surface 14A to which at least one of the light emitting element and the light receiving element is bonded.
  • light emitting elements first light emitting element LED1, second light emitting element LED2, third light emitting element LED3
  • light receiving elements first light receiving element PD1, second light receiving element PD2, third light receiving element PD3, fourth light receiving element PD4, and fifth light receiving element PD5
  • the light emitting element is, for example, an electronic component such as a light emitting diode (LED).
  • the light emitting element is placed at a preset position with respect to the contact portion 16, and irradiates light to the artery of the wrist.
  • the first light emitting element LED1, the second light emitting element LED2, and the third light emitting element LED3 are arranged apart from each other and arranged along the circumferential direction C of the wrist. Note that in the present disclosure, the number of light emitting elements is one or more and arbitrary.
  • the first light emitting element LED1, the second light emitting element LED2, and the third light emitting element LED3 all have a set of light sources.
  • the set of light sources includes one or more red light sources RED and one or more infrared light sources IR. That is, in the first embodiment, two types of light are emitted from one light emitting element. Two types of reflected light received by one light receiving element are used to measure oxygen saturation. Note that in the present disclosure, the number of types of light sources is not limited to two types, and may be one type, or three or more types.
  • red light in a wavelength range of about 620 nm to about 700 nm has a characteristic that its absorbance greatly changes depending on the presence or absence of oxygen bonded to hemoglobin.
  • near-infrared light in the wavelength range of about 850 nm to about 960 nm has a characteristic that its absorbance does not change significantly depending on the presence or absence of oxygen bonded to hemoglobin.
  • a fluctuation component (AC) of the pulse wave signal included in the monitored pulse wave signal and a fixed component (DC) that does not fluctuate are calculated.
  • a red light perfusion index (PI) value is calculated as PI RED .
  • the PI value (PI IR ) of reflected near-infrared light is calculated by monitoring changes in the intensity of the pulse wave signal of reflected near-infrared light over time. be done.
  • the ratio (PI RED / PI IR ) between the PI value of red light (PI RED ) and the PI value of near-infrared light (PI IR ) is calculated.
  • the oxygen saturation level can be calculated.
  • Oxygen saturation [%] a ⁇ (PI RED / PI IR ) + b ...
  • Coefficients a and b in equation (1) can be determined by experiment. Note that in the present disclosure, the method for measuring oxygen saturation is not limited to this, and other methods may be used.
  • the light receiving element is, for example, an electronic component such as a photodiode (PD).
  • the light receiving element is arranged at a preset position with respect to the contact part 16, and receives reflected light from the artery of the wrist via the contact surface 16A of the contact part 16.
  • the first light receiving element PD1, the second light receiving element PD2, the third light receiving element PD3, the fourth light receiving element PD4, and the fifth light receiving element PD5 are arranged apart from each other and in the circumferential direction of the wrist. arranged along. Note that in the present disclosure, the number of light receiving elements is one or more and arbitrary.
  • one "sensor unit” is configured by one or more light emitting elements and one or more light receiving elements corresponding to the one or more light emitting elements.
  • multiple sensor units may be provided. Further, both the number of light emitting elements and the number of light receiving elements included in one "sensor unit” can be set arbitrarily.
  • the oxygen saturation measuring device 10A is a reflective type in which the intensity of the pulse wave signal is measured using reflected light, but the present disclosure is not limited to the reflective type, and the pulse wave signal is measured using transmitted light. It may also be a transmission type in which the intensity of is measured.
  • a light shielding portion 14B is provided between the light emitting element and the light receiving element in the base 14.
  • the light blocking portion 14B prevents the light receiving element from directly receiving light from the light emitting element. Note that it is preferable to make the distance between the light emitting element and the light receiving element as close as possible while using the light shielding part 14B, from the viewpoint of shortening the optical path length and improving measurement accuracy as a result.
  • Contact portion 16 is attached to band 12 . Further, the contact portion 16 has translucency for light irradiated onto the artery of the wrist and light reflected from the artery of the wrist. Specifically, for example, a light-transmitting member such as a lens may be used.
  • the contact portion 16 disposed above the light emitting element in FIG. 4 is, for example, a diffuser lens capable of enlarging the irradiation area.
  • a diffusing agent may be placed above the light emitting element together with the diffusing lens or instead of the diffusing lens.
  • the contact portion 16 disposed above the light receiving element in FIG. 4 may be, for example, a condenser lens capable of collecting reflected light.
  • the contact portion 16 has a contact surface 16A that protrudes from the band 12 toward the wrist.
  • the contact surface 16A has a curved shape. The contact surface 16A comes into contact with the skin of the wrist when measuring oxygen saturation.
  • the contact portion 16 has a dome shape.
  • the central part in the left-right direction in FIG. Curves smoothly without tension.
  • the curvature is preferably 0.167 or more, for example, from the viewpoint of improving wearability for the person being measured.
  • the center portion of the contact portion 16 in the circumferential direction C of the wrist is flat, and both left and right end portions are smoothly curved.
  • the contact surface 16A does not need to have a flat portion, as shown in FIGS. 8 and 9.
  • the contact surface 16A may have a curved shape with an overall constant curvature.
  • the forearm extending direction E overlaps with any of the directions in which the radius 20 extends, the ulna, and the artery.
  • the "direction E in which the forearm extends” strictly speaking differs depending on the subject. That is, the "extending direction E of the forearm” is not uniquely determined by coordinates in a three-dimensional space, but is determined based on the extending direction of the radius 20, the ulna extending direction, and the artery extending direction for each subject. can be determined individually.
  • the maximum width of the contact portion 16 is set to 3 mm or more and 7 mm or less.
  • the maximum width W of the contact portion 16 is determined by measuring the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22 along the circumferential direction C of the wrist. means the maximum width of the case.
  • the maximum width of the contact portion may be set based on a distance set by other parts of the wrist other than the gap between the radial styloid process and the flexor carpi radialis tendon.
  • the maximum width W of the contact portion 16 is set in consideration of the state in which the contact portion 16 is arranged inside the recess of the gap.
  • the width G of the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22 is the minimum value measured along the circumferential direction C on the surface of the wrist, and the width G of this minimum value is The maximum width W of the contact portion 16 is set so that the contact portion 16 can be placed inside the recess of the gap.
  • the lower limit of the maximum width W of the contact portion 16 is less than 3 mm, the electronic components such as the light emitting element and the light receiving element will become too small, so there is a concern that the manufacturing cost will increase or that it will not be possible to manufacture them.
  • the upper limit of the maximum width W of the contact portion 16 exceeds 7 mm, it is placed in the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22 in the wrist of a female child, where the width of the gap is relatively narrow. things become difficult.
  • the maximum width W of the contact portion 16 can be changed as appropriate. Further, the upper limit of the maximum width W of the contact portion 16 may be changed depending on the gender and age of the subject to be measured. For example, the height and weight of a 17-year-old boy or girl can be set to be approximately 30% larger than the height and weight of a 5-year-old child. Therefore, if the upper limit of the maximum width W of the contact portion 16 for female children is 7 mm, the upper limit of the maximum width W of the contact portion 16 for female children of 17 years or older can be set to about 10 mm, for example.
  • the height and weight of a man can be set to be about 10% larger than the height and weight of a woman, for example. Therefore, if the upper limit of the maximum width W of the contact section 16 for female children is 7 mm, the upper limit of the maximum width W of the contact section 16 for male children can be set to about 8 mm. Further, for example, the upper limit of the maximum width W of the contact portion 16 for men aged 17 or older can be set to about 11 mm.
  • the measurement unit 18 is provided in a calculation display unit 26 attached to the band 12.
  • the calculation display section 26 is located on the back side, which is the outside of the wrist.
  • a light receiving element is connected to the measuring section 18. Data of a pulse wave signal of reflected light is inputted to the measurement unit 18 over time from a light receiving element.
  • the measurement unit 18 is configured as a computer including, for example, a CPU (Central Processing Unit), a RAM (Random Access Memory), a storage device, an I/O port, and the like.
  • the RAM, storage device, I/O port, etc. are configured to be able to exchange data with the CPU via an internal bus.
  • the measurement unit 18 measures the oxygen saturation level of the radial artery 24 irradiated with light, based on the pulse wave signal acquired from the reflected light, by a method using a ratio of PI values, etc.
  • the calculation display unit 26 displays the calculation results by the measurement unit 18 to the outside.
  • the calculation display section 26 may be provided with a storage device that temporarily stores measurement results. Note that in the present disclosure, the calculation display section 26 is not essential. If the calculation display part 26 is not provided, the measurement part 18 can be arranged, for example, on the contact part 16 or the base part 14 as part of the calculation device.
  • the storage device can also be placed on a member other than the calculation display section 26, such as the contact section 16 or the base section 14. Even if the calculation display section 26 is not provided, it is possible to obtain the calculation results by the measurement section 18, for example, via a communication section that is connected to the calculation device and enables communication with the outside. be.
  • the light emitting element and the light receiving element may be arranged on the contact surface 16A of the contact portion 16.
  • a first light receiving element PD1, a second light receiving element PD2, a third light receiving element PD3, a fourth light receiving element PD4, and a fifth light receiving element PD5 are arranged on the joint surface 14A of the base 14.
  • a case where the contact surface 16A is arranged instead of the contact surface 16A is illustrated.
  • the distance between the light emitting element and the radial artery 24 and the distance between the light receiving element and the radial artery 24 can be determined by the distance between the light emitting element and the light receiving element. and can be made shorter than when they are arranged on the joint surface 14A of the base 14. Note that when the light emitting element and the light receiving element are arranged on the contact surface 16A of the contact part 16, as long as the light emitting element and the light receiving element are connected to the measuring part 18, the contact part 16 does not have translucency. Not required.
  • one contact portion 16 may be placed across both the first light emitting element LED1 and the first light receiving element PD1. Further, one contact portion 16 may be provided for all of the plurality of light emitting elements and the plurality of light receiving elements. In one contact portion 16 in FIG. 6, the number of contact portions 16 is one. Therefore, the structure of the oxygen saturation measuring device can be simplified, and as a result, the manufacturing burden can be reduced.
  • the band 12 of the oxygen saturation measuring device 10A is wrapped around the wrist of the person to be measured.
  • the artery to be measured is, for example, the radial artery 24. Note that in the present disclosure, the artery to be measured is not limited to the radial artery 24, and may be any other artery.
  • the contact surface 16A is then brought into contact with the skin near the radial styloid process 20A on the inside of the wrist.
  • the contact portion 16 is arranged inside the depression in the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22. Then, light is irradiated from the light emitting element to the radial artery 24 located below the depression. Then, the reflected light from the radial artery 24 is received by the light receiving element. Then, the oxygen saturation level is measured by the measurement unit 18 based on the pulse wave signal acquired from the reflected light.
  • the contact surface 16A of the contact portion 16 protruding from the band 12 toward the wrist has a curved shape. For this reason, for example, after bringing the curved contact surface 16A into contact with the vicinity of the radial styloid process 20A on the inside of the wrist, the contact portion 16 is placed in a depression in the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22. By moving the contact portion 16 toward the inside of the recess along the direction, it is easy to arrange the contact portion 16 inside the recess of the gap.
  • the contact part 16 can be brought into contact with the skin surface on the inside of the wrist, as in the case where the contact part 16 is plate-shaped. There is no need to grope the location of the artery beforehand.
  • the contact portion 16 has translucency for light irradiated onto the artery of the wrist and light reflected from the artery of the wrist. Further, a base 14 having a flat bonding surface 14A is provided between the band 12 and the contact portion 16, and at least one of a light emitting element and a light receiving element is bonded to the bonding surface 14A of the base 14.
  • At least one of the electronic components of the light emitting element and the light receiving element is bonded on the flat bonding surface 14A between the band 12 and the contact portion 16. , avoid direct contact with skin. Therefore, deterioration of electronic components can be prevented.
  • the maximum width W of the contact portion 16 is 3 mm or more and 7 mm or less.
  • the artery to be measured is the radial artery 24, it is particularly advantageous in measuring the oxygen saturation level in the radial artery 24.
  • the curved contact surface 16A contacts the skin near the radial styloid process 20A on the inside of the wrist. . Further, the contact portion 16 is arranged inside the depression in the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22. Then, the oxygen saturation level is measured based on the pulse wave signal obtained from the reflected light from the radial artery 24.
  • the contact surface 16A can be easily fed into the hollow along the curved surface of the hollow. Therefore, as in the case of the oxygen saturation measurement device 10A of the present disclosure, the arrangement position of the contact portion 16 on the inside of the wrist can be easily determined, and interruption of oxygen saturation measurement can be suppressed.
  • a contact portion 16 having a contact surface 16A that contacts the skin of the wrist and where a sensor is disposed can be slid by operating from the outside of the band 12.
  • the oxygen saturation measuring device 10B includes a band 12, a slider section 30, a contact section 16, an operation section 40, a light emitting element, a light receiving element, and a measuring section. 18.
  • the band 12 includes a first body part 12A, a second body part 12B provided apart from the first body part 12A in the circumferential direction C of the wrist, and a pair of guide parts. Ru.
  • the pair of guide parts is formed by a first guide part 12C and a second guide part 12D.
  • the pair of guide parts connect the first main body part 12A and the second main body part 12B, respectively, and are provided apart from each other in the direction E in which the forearm extends.
  • the pair of guide portions extend along the circumferential direction C of the wrist with the through hole 12E in between.
  • the through hole 12E is formed by being surrounded by the first body part, the second body part, the first guide part, and the second guide part.
  • the through hole 12E extends along the circumferential direction C of the wrist.
  • the four members consisting of the first body part 12A, the second body part 12B, the first guide part 12C, and the second guide part 12D are integrally made of the same material.
  • the disclosure is not limited to this. Some or all of the four members may be made individually and connected to each other.
  • the through hole 12E has a rectangular shape in plan view, but the second embodiment is not limited to this, and may have other shapes, such as a linear shape.
  • plan view means a state viewed along the thickness direction of the band 12 (that is, the radial direction D of the wrist).
  • the through hole 12E is not essential as long as the contact portion 16 can be slid from the outside of the band 12 while the band 12 is wrapped around the wrist.
  • the slider section 30 is arranged inside the through hole 12E of the band 12.
  • the slider section 30 includes a base section 32, a pair of clamping sections, and an operating section 40.
  • the pair of clamping parts are formed by a first clamping part 34A and a second clamping part 34B.
  • materials such as resin and metal can be appropriately adopted.
  • the base portion 32 is arranged inside the through hole 12E of the band 12. “The base portion 32 is disposed inside the through hole 12E” may be a state in which the base portion 32 is disposed inside the through hole 12E in plan view, as shown in FIG. In other words, as shown in FIG. 8, in the radial direction D of the wrist, a portion of the base portion 32 in the vertical direction is not prevented from protruding outside the through hole 12E.
  • the first holding part 34A is provided at one end (the left end in FIG. 7) of the base part 32 in the width direction of the band 12, and slidably holds the first guide part 12C in the radial direction D of the wrist.
  • the second holding portion 34B is provided at the other end of the base portion 32 in the width direction of the band 12 (the right end in FIG. 7).
  • the second holding part 34B slidably holds the second guide part 12D in the radial direction of the wrist (radial direction D in FIG. 8). That is, the first clamping part 34A and the second clamping part 34B are provided in a slidable state with respect to the first guide part 12C and the third guide part 12D.
  • the base portion 32 is located between the first holding portion 34A and the first guide portion 12C, and between the second holding portion 34B and the third guide portion 12D.
  • the first clamping part 34A and the second clamping part 34B may be provided so as to be slidable with a gap formed therebetween to prevent them from falling off.
  • the first clamping part 34A and the second clamping part 34B are in contact with each other. may be slidably provided.
  • each of the first guide portion 12C and the second guide portion 12D has a plurality of fastening portions along the circumferential direction C of the wrist. may be formed.
  • the plurality of fastening parts may be through holes formed with narrow hole widths, for example, like cuts.
  • the fasteners can be formed as a set of fasteners by being arranged on the first guide part 12C and the second guide part 12D, respectively, on a straight line along the direction E in which the forearm extends.
  • a plurality of sets of fasteners may be formed along the circumferential direction C of the wrist.
  • a set of fasteners corresponding to the set of fasteners may be provided at both ends of the base portion 32 in the direction E in which the forearm extends.
  • the fastener may have a shape in which the distal end is larger in diameter than the proximal end, for example, like a cufflink.
  • the distal end of the fastener can be inserted into the through hole, and can be detachably attached by being sandwiched between the cuts in the fastener at the base end position.
  • the operating section 40 is connected to the slider section 30 and arranged on the outside of the band 12 on the side opposite to the wrist.
  • the operation section 40 may be connected to the slider section 30 or the contact section 16. By operating the operating section 40, the slider section 30 can slide along the circumferential direction C of the wrist.
  • a void A is formed.
  • the void A is a part of the through hole 12E. Therefore, the slider portion 30 can also slide along the direction E in which the forearm extends inside the formed gap A.
  • the gap A may be formed between at least one of the base portion 32 and the first guide portion 12C and between the base portion 32 and the second guide portion 12D. Further, in the present disclosure, the void A is not essential.
  • the oxygen saturation measuring device 10B according to the second embodiment further includes a pressurizing device 50 that applies force to the contact portion 16 from the side opposite to the wrist toward the wrist. Note that in the present disclosure, the pressurizing device 50 is not essential.
  • the base portion 32 is provided with a hole 32A that penetrates along the radial direction D of the wrist, and a female screw portion is formed on the inner surface of the provided hole 32A.
  • a rod-shaped member 42 is provided on the wrist side of the operating portion 40, and a male threaded portion is formed on the surface of the rod-shaped member 42 in correspondence with a female threaded portion of the hole 32A of the base portion 32.
  • the pressurizing device 50 of the second embodiment is a screw feeding mechanism that adjusts the amount of protrusion from the slider portion 30 in the radial direction D of the wrist.
  • the pressurizing device is not limited to this.
  • the pressurizing device may be configured by another mechanism, such as a mechanism that applies a force toward the wrist to the contact portion 16 using a spring force.
  • a plate-shaped connecting member 44 is provided at the end of the rod-shaped member 42 on the wrist side, and a base 14 is provided on the wrist side of the connecting member 44.
  • a contact portion 16 is provided on the opposite side of the base portion 14 from the connecting member 44 .
  • the contact portion 16 is attached to the slider portion 30 via a pressure device 50. Therefore, the contact portion 16 slides along the circumferential direction C of the wrist together with the slider portion 30.
  • the determined sensor placement position is fixed by turning the screw to increase the amount of protrusion of the pressure device 50 from the slider portion 30. Further, even after the sensor placement position is once fixed, the fixation of the sensor placement position can be loosened by turning the screw of the pressurizing device 50 so as to reduce the amount of protrusion from the slider portion 30. At the same time, it is possible to slide the slider section 30 again. That is, the sensor arrangement position can be changed to a desired position without loosening or removing the band 12 while the band 12 remains wrapped around the wrist of the subject.
  • the contact portion 16 may be directly attached to the slider portion 30 without using the pressurizing device 50. Further, the contact portion 16 may be indirectly attached to the slider portion 30 via a member other than the pressure device 50. Further, in the second embodiment, the plate-shaped operation unit 40 is illustrated, but the present disclosure is not limited to this.
  • a protrusion that protrudes upward may be provided on the upper part of the base portion 32 in FIG. 8 so that the person to be measured can pinch it with his or her fingers.
  • ⁇ Oxygen saturation measurement method Next, a method for measuring oxygen saturation using the oxygen saturation measuring device 10B according to the second embodiment will be described.
  • the band 12 of the oxygen saturation measuring device 10B is wrapped around the wrist of the subject.
  • the artery to be measured is, for example, the radial artery 24.
  • the contact surface 16A is then brought into contact with the skin near the radial styloid process 20A on the inside of the wrist.
  • the contact part 16 before placing the contact part 16 in the recess of the gap, by sliding the slider part 30, the contact part 16 is brought to an initial position near the artery to be measured on the inner skin surface of the wrist. can be placed.
  • the contact part 16 after placing the contact part 16 at the initial position, by sliding the slider part 30 to adjust the position, the contact part 16 can be placed on the skin surface on the inside of the wrist near the artery to be measured. It can be placed in a different position.
  • the slider section 30 is arranged inside the through hole 12E of the band 12 and is slidable along the circumferential direction C of the wrist. Further, a contact portion 16 having a contact surface 16A that contacts the wrist is attached to the slider portion 30. Further, an operating section 40 is connected to the slider section 30 or the contact section 16 and arranged on the outside of the band 12 on the side opposite to the wrist. That is, even when the band 12 is wrapped around the wrist, it is possible to slide the slider section 30 by operating the operating section 40 from outside the band 12. Therefore, the subject can slide the contact part 16 attached to the slider part 30 along the circumferential direction C of the wrist without loosening the band 12 and without exposing the inner surface of the band 12. It becomes possible.
  • the placement position of the sensor relative to the artery to be measured can be easily adjusted.
  • the base portion 32 of the slider portion 30 is arranged inside the through hole 12E of the band 12.
  • the slider part 30 can slide inside the formed gap A along the direction E in which the forearm extends. Since the contact part 16 attached to the slider part 30 can be slid not only in the circumferential direction C of the wrist but also in the direction E in which the forearm extends, it is easier to adjust the position of the sensor.
  • the slider portion 30 is movable to any position within a plane defined by two directions, the circumferential direction C of the wrist and the extending direction E of the forearm, inside the through hole 12E formed in the band 12. .
  • the slider section 30 can slide independently in two directions without being influenced by each other in the two directions.
  • the adjustable range of the arrangement position is wider than when the arrangement position is changed only on the circumference having a constant radius from the center of rotation, as in PCT International Publication No. 2017-516539.
  • the second embodiment also includes a pressure device 50 that applies force to the contact portion 16 from the side opposite to the wrist toward the wrist. Therefore, the position of the contact portion 16 relative to the artery to be measured in the wrist can be stably maintained.
  • the sensor for the artery to be measured can be used.
  • the placement position can be easily adjusted.
  • a measuring light receiving element is quantitatively selected from the two or more light receiving elements.
  • the oxygen saturation measuring device 10C according to the third embodiment illustrated in FIG. 10 includes three light emitting elements and five light receiving elements as in the first embodiment, and the slider described in the second embodiment. A slider section similar to section 30 is provided. Note that illustrations of the base, contact portion, slider portion, etc. are omitted in FIG. 10 for ease of viewing.
  • the third embodiment differs from the second embodiment in that the measurement unit 18 includes a light receiving element determining unit, a determining unit, a distribution creating unit, a light emitting element determining unit, and a control unit.
  • the measurement unit 18 includes a light receiving element determining unit, a determining unit, a distribution creating unit, a light emitting element determining unit, and a control unit.
  • some or all of the light receiving element determining section, the determining section, the distribution creating section, the light emitting element determining section, and the control section may be arranged separately from the measuring section 18.
  • the "first pulse wave signal” is a pulse wave signal acquired from the reflected light received by the first light receiving element PD1.
  • the "second pulse wave signal” is a pulse wave signal acquired from the reflected light received by the second light receiving element PD2.
  • the "third pulse wave signal” is a pulse wave signal acquired from the reflected light received by the third light receiving element PD3.
  • the "fourth pulse wave signal” is a pulse wave signal acquired from the reflected light received by the fourth light receiving element PD4.
  • the "fifth pulse wave signal” is a pulse wave signal acquired from the reflected light received by the fifth light receiving element PD5.
  • the light receiving element determining section is connected to each light receiving element.
  • the light-receiving element determining unit selects one of the first pulse wave signal, the second pulse wave signal, the third pulse wave signal, the fourth pulse wave signal, and the fifth pulse wave signal.
  • the light receiving element that receives the pulse wave signal having the larger amplitude is determined as the measuring light receiving element.
  • the light-receiving element determining unit selects the light-receiving element that has received a pulse wave signal having a larger amplitude between the first pulse wave signal and the second pulse wave signal as the light-receiving element for measurement. It may be determined as an element. Furthermore, when determining the light receiving element for measurement, any type of light to be irradiated can be selected from among red light and infrared light. However, from the viewpoint of comparison, it is preferable that the same type of light is used.
  • the determination section is connected to each light receiving element.
  • the determination unit is configured such that the first pulse wave signal, the second pulse wave signal, the third pulse wave signal, the fourth pulse wave signal, and the fifth pulse wave signal are set in advance. It is determined whether a preset reference value is satisfied based on the viewpoint of achieving measurement accuracy. Note that in the present disclosure, the determination unit determines whether at least the first pulse wave signal and the second pulse wave signal satisfy a reference value based on the viewpoint of achieving a preset measurement accuracy. do it.
  • extraction conditions are set to extract a more appropriate pulse wave signal from among the multiple pulse wave signals, for example, from the perspective of increasing the measurement accuracy of oxygen saturation. May be set.
  • an extraction condition for example, a light receiving element from which a pulse wave signal having the largest amplitude among a plurality of pulse wave signals satisfying a reference value is acquired can be determined as a measurement light receiving element.
  • the distribution creation unit calculates the received reflection light.
  • the amplitude distribution along the circumferential direction C of the wrist of light is created as a "first amplitude distribution.”
  • the distribution creation unit determines whether the reflected light from the second light emitting element LED2 is received by each of the first light receiving element PD1, the second light receiving element PD2, and the third light receiving element PD3.
  • the amplitude distribution of the reflected light along the circumferential direction C of the wrist is created as a "second amplitude distribution”.
  • the distribution creation unit determines whether the reflected light of the third light emitting element LED3 is received by each of the first light receiving element PD1, the second light receiving element PD2, and the third light receiving element PD3.
  • the amplitude distribution of the reflected light along the circumferential direction C of the wrist is created as a "third amplitude distribution".
  • the distribution creation unit may create at least the first amplitude distribution and the second amplitude distribution.
  • the timing of light irradiation from each light emitting element may be staggered.
  • the light-emitting element determination unit selects for measurement the light-emitting element for which a distribution satisfying a preset standard condition is created among the created first amplitude distribution, second amplitude distribution, and third amplitude distribution. Determine it as a light emitting element.
  • the reference condition is set so that the light emitting element is located above the artery. Oxygen saturation is measured based on the determined pulse wave signal of the reflected light from the light emitting element for measurement.
  • the light emitting element determining unit may determine the light emitting element for measurement based on at least the first amplitude distribution and the second amplitude distribution.
  • control unit The control unit continues to energize only one light emitting element determined as the measurement light emitting element among the first light emitting element LED1, the second light emitting element LED2, and the third light receiving element PD3. On the other hand, the control unit stops energizing the other two light emitting elements that have not been determined as measurement light emitting elements. Note that in the present disclosure, the control unit may at least determine whether or not to energize between the first light emitting element LED1 and the second light emitting element LED2.
  • step S1 in FIG. 11 first, the band 12 of the oxygen saturation measuring device 10C is wrapped around the wrist of the subject.
  • the artery to be measured is, for example, the radial artery 24.
  • step S2 the sensor unit is placed inside the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22.
  • step S3 the arrangement position of the sensor unit is adjusted by moving the arrangement position of the sensor unit inside the gap using, for example, the slider section 30.
  • the adjustment determines the placement position of the sensor unit.
  • step S4 the determined placement position is fixed using a pressurizing device.
  • step S5 the distribution creation unit is used to create a first amplitude distribution due to the reflected light of the first light emitting element LED1 and a second amplitude distribution due to the reflected light of the second light emitting element LED2. , and a third amplitude distribution based on the reflected light of the third light emitting element LED3.
  • FIG. 12A five data points representing the first amplitude distribution acquired by five light receiving elements arranged along the circumferential direction C of the wrist are illustrated.
  • FIG. 12B five data points representing the second amplitude distribution acquired by five light receiving elements arranged along the circumferential direction C of the wrist are illustrated.
  • FIG. 12C five data points representing the third amplitude distribution acquired by five light receiving elements arranged along the circumferential direction C of the wrist are illustrated.
  • a first locus L1 of a broken line connecting the five data points is arranged to overlap the five data points.
  • a dashed second locus L2 and in FIG. 12C, a dashed third locus L3 are arranged overlapping the respective data points.
  • the three trajectories L1, L2, and L3 indicate that the first light emitting element LED1 and the second light emitting element are arranged in a state where a confirmation light receiving element having a constant length of about 1000 pixels is arranged along the circumferential direction C of the wrist.
  • a confirmation light receiving element having a constant length of about 1000 pixels is arranged along the circumferential direction C of the wrist.
  • Illustration of the confirmation light receiving element is omitted.
  • the conditions for creating the amplitude distribution using the confirmation light-receiving elements are the same as the conditions for creating the amplitude distribution using the five light-receiving elements.
  • the amplitude when the light emitting element is located above the artery is lower than the amplitude when the light emitting element is located shifted from above the artery in the circumferential direction C of the wrist.
  • the light emitting element is located above the artery means a state in which the light emitting element and the artery at least partially overlap in plan view, as shown in FIG.
  • the central three light-receiving elements In the arrangement direction, the amplitude decreases from the first light receiving element toward the second light receiving element adjacent to the first light receiving element. Further, the amplitude increases from the second light receiving element toward the third light receiving element adjacent to the second light receiving element.
  • the reference condition is that the amplitude decreases and increases along the circumferential direction C.
  • a concave portion that is concave toward the bottom is drawn.
  • the amplitude of the second light receiving element PD2 in the second amplitude distribution in FIG. 12B, the amplitude of the second light receiving element PD2, the amplitude of the third light receiving element PD3, and the amplitude of the fourth light receiving element PD4 are It can be determined that the reference condition is satisfied by drawing a concave portion with the amplitude of . As a result, the second light emitting element LED2 from which the second amplitude distribution in FIG. 12B was obtained is determined as the light emitting element for measurement.
  • the amplitude increases from the first light receiving element PD1 to the second light receiving element PD2, but from the second light receiving element PD2 to the fifth light receiving element PD5. Until then, the amplitude continues to decrease. Therefore, since no concave portion is drawn in the first amplitude distribution, it is determined that the reference condition is not satisfied.
  • the amplitude continues to increase from the first light receiving element PD1 to the fourth light receiving element PD4, but from the fourth light receiving element PD4 to the fifth light receiving element The amplitude decreases until PD5. Thereafter, the amplitude is approximately constant from the fifth light receiving element PD5 toward the end of the determination target range located at the other end of the wrist in the circumferential direction C. That is, the amplitude does not change from decreasing to increasing. Therefore, no concave portion is drawn in the third amplitude distribution, and as a result, it is determined that the reference condition is not satisfied.
  • extraction conditions may be set to extract a more appropriate distribution from among the multiple distributions, for example, from the perspective of increasing the measurement accuracy of oxygen saturation.
  • an extraction condition for example, the difference between the central amplitude value that makes up the bottom of the recess and the larger amplitude value among the amplitude values at both ends that are located on both sides of the bottom and make up the two tops of the recess is calculated. Ru. Then, among the plurality of amplitude distributions that satisfy the reference condition, a light emitting element in which a distribution with the largest calculated difference is formed can be determined as a light emitting element for measurement.
  • the power supply to the first light emitting element LED1 and the third light emitting element LED3 which have not been determined as the light emitting element for measurement is stopped, and the power to the second light emitting element LED2 which has been determined as the light emitting element for measurement is stopped. continues to be energized. Then, the reflected light of the light emitted by the second light emitting element LED2 is received by the five light receiving elements.
  • the five light-receiving elements produce five pulse waves consisting of a first pulse wave signal, a second pulse wave signal, a third pulse wave signal, a fourth pulse wave signal, and a fifth pulse wave signal.
  • I get a signal.
  • step S6 in FIG. 11 five pulse wave signals are monitored.
  • a PI value is calculated for each of the five pulse wave signals.
  • the PI value can be calculated for each of the PI value of red light (PI RED ) and the PI value of near-infrared light (PI IR ).
  • step S7 it is determined by comparison whether the calculated PI value is greater than or equal to a preset reference value.
  • the comparison can be performed, for example, by the light receiving element determining section.
  • the reference value can be set for each of the PI value of red light (PI RED ) and the PI value of near-infrared light (PI IR ). Note that in the present disclosure, comparison processing with a reference value is not essential.
  • step S3 If all the PI values are less than a preset reference value, it is determined that the placement position of the light receiving element is not suitable for measurement, that is, a positional shift of the light receiving element has occurred. Then, the process moves to step S3, and the arrangement position of the sensor unit is adjusted again.
  • the arrangement position can be adjusted, for example, by sliding the slider section 30.
  • step S8 the process moves to step S8. Then, among the one or more pulse wave signals from which a PI value equal to or higher than the reference value is obtained, the light receiving element that receives the pulse wave signal having the largest amplitude is determined as the measuring light receiving element using the light receiving element determination unit. be done.
  • step S9 a PI value is calculated using the measurement unit 18 based on the pulse wave signal received by the determined measurement light receiving element.
  • step S10 oxygen saturation is calculated based on the calculated PI value.
  • step S11 the calculated oxygen saturation data is stored in the storage device.
  • step S12 if the number of oxygen saturation data is less than a preset designated number, the process moves to step S13. Then, as in step S7, it is determined whether a positional shift of the light receiving element has occurred by comparing the PI value with a reference value.
  • step S13 if it is determined that no positional deviation of the sensor unit has occurred because the PI value is greater than or equal to the reference value, the process moves to step S9, and the subsequent processes are repeated. On the other hand, if it is determined that the positional shift of the sensor unit has occurred because the PI value is not equal to or greater than the reference value, the process moves to step S6, and the five pulse wave signals are monitored again. Then, a PI value is calculated for each of the five pulse wave signals. Thereafter, the process from step S7 onwards is repeated to determine the measurement light receiving element again. The oxygen saturation data is then stored in the storage device.
  • step S12 if the number of saved oxygen saturation data is equal to or greater than a preset designated number, the process ends.
  • the oxygen saturation measurement method according to the third embodiment is configured by executing the above series of processes until the number of stored oxygen saturation data satisfies the specified number that can be stored in the storage device. .
  • step S13 if it is determined in step S13 that a positional shift of the sensor unit has occurred, after the band 12 is once removed from the wrist, the process does not proceed to step S6 and, for example, proceeds to step S1. Migration is also not excluded. That is, the arrangement position of the sensor unit may be adjusted by rewinding the band 12. Alternatively, the process may proceed to step S3, and the arrangement position of the sensor unit may be adjusted using, for example, the slider section 30.
  • the light receiving element that has received the pulse wave signal having the largest amplitude among the five light receiving elements is used for measuring oxygen saturation. It is determined as a light receiving element. Then, the oxygen saturation level is measured based on the pulse wave signal received by the determined measuring light receiving element.
  • the oxygen saturation measuring device 10C it is possible to reduce the frequency of interruptions in oxygen saturation measurement due to misalignment of the sensor at the inner side of the wrist.
  • the first light receiving element PD1, the second light receiving element PD2, the third light receiving element PD3, the fourth light receiving element PD4, and the fifth light receiving element PD5 are defined in the circumferential direction C of the wrist. arranged along. Therefore, a more appropriate measurement light receiving element can be determined among five different positions along the circumferential direction of the wrist.
  • the third embodiment it is determined whether the five acquired pulse wave signals satisfy a preset reference value based on the viewpoint of achieving preset measurement accuracy. Then, a process is performed to determine a measuring light receiving element from among the light receiving elements that have received a pulse wave signal that satisfies the reference value. On the other hand, if all five pulse wave signals do not satisfy the reference value, the process of adjusting the arrangement position of the light receiving element is repeated until a pulse wave signal that satisfies the reference value appears. Among the acquired pulse wave signals, only the pulse wave signals that satisfy the reference value are extracted for measurement, so that the measurement accuracy of oxygen saturation can be further improved.
  • a first amplitude distribution, a second amplitude distribution, and a third amplitude distribution are created. Then, among the created first amplitude distribution, second amplitude distribution, and third amplitude distribution, a preset reference condition corresponding to the fact that the light emitting element is located above the artery is set. A light emitting element for which a satisfying distribution has been created is determined as a light emitting element for measurement. Then, the oxygen saturation level is measured based on the pulse wave signal of the reflected light from the determined light emitting element for measurement. That is, the light emitting element located above the artery from among the plurality of light emitting elements is determined as the light emitting element for measurement. Therefore, the measurement accuracy of oxygen saturation can be further improved.
  • the present disclosure is not limited to controlling the energization to the light emitting element, and the control of the energization to the measuring light receiving element may be performed together with the control of the energization to the light emitting element, or independently. That is, the power supply to the light receiving element that is not determined as the measuring light receiving element may be stopped, and the power supply may be continued only to the light receiving element determined as the measuring light receiving element. Power saving can also be achieved by controlling the power supply to the measuring light receiving element.
  • the oxygen saturation measurement method using the oxygen saturation measurement device 10C according to the third embodiment it is possible to suppress interruption of oxygen saturation measurement due to positional deviation of the sensor at the inner side of the wrist.
  • FIG. 13 illustrates a case where a group including two light emitting elements and a group including three light receiving elements are arranged along the circumferential direction C of the wrist. That is, in the present disclosure, the arrangement direction of the group including one or more light-emitting elements and the group including one or more light-receiving elements may be in the direction E in which the forearm extends, or in the direction E in which the forearm extends. It may be in direction C.
  • present disclosure may be configured by partially combining the respective configurations shown in FIGS. 1 to 13.
  • present disclosure includes various embodiments not described above, and the technical scope of the present disclosure is determined only by the matters specifying the invention in the claims that are reasonable from the above description.

Abstract

This oxygen saturation value measurement device comprises: a band to be wound around a wrist of a subject; a light-emitting element for emitting light to an artery in the wrist; a first light-receiving element and a second light-receiving element for receiving reflected light from the artery; a light-receiving element determination unit for determining, as a light-receiving element to be used for measurement, the light-receiving element which received a pulse wave signal having a larger amplitude between a first pulse wave signal acquired from reflected light received by the first light-receiving element and a second pulse wave signal acquired from reflected light received by the second light-receiving element; and a measurement unit for measuring, on the basis of the pulse wave signal received by the determined light-receiving element for measurement, an oxygen saturation value of the artery irradiated with the light.

Description

酸素飽和度測定装置及び酸素飽和度測定方法Oxygen saturation measurement device and oxygen saturation measurement method
 本開示は、酸素飽和度測定装置及び酸素飽和度測定方法に関する。 The present disclosure relates to an oxygen saturation measuring device and an oxygen saturation measuring method.
 人体内の動脈に対し皮膚上から光を経皮的に照射することによって動脈血中の酸素飽和度(S)を測定する光電式容積脈波記録法(Photo Plethysmography,PPG)が知られている。人体の皮膚のうち、特に手首の皮下の動脈上では拍動が強く現れるので、手首の位置で酸素飽和度を測定する場合、比較的大きな振幅を有する脈波信号を取得できる。 Photoplethysmography (PPG) is a well-known method that measures oxygen saturation (S PO 2 ) in arterial blood by percutaneously irradiating light onto arteries in the human body from above the skin. ing. Since pulsations appear strongly on the skin of the human body, especially on arteries under the skin of the wrist, when measuring oxygen saturation at the wrist, a pulse wave signal with a relatively large amplitude can be obtained.
 酸素飽和度の測定装置の一例として特表2017-516539には、手首に装着される腕時計型の測定装置によって生理学的データを測定する技術が開示されている。特表2017-516539の測定装置は、手首に巻かれるバンドと、バンドに設けられたセンサユニットとを備えるウェアラブルシステムである。センサユニットは、光信号を発光するLED等の発光素子と、光信号を受光するセンサとしてのフォトダイオード等の受光素子とを有する。センサユニットは、全体的にほぼ厚みが等しい板状のセンサプレートの板面上の一部の領域内に配置される。 As an example of an oxygen saturation measuring device, Japanese Patent Publication No. 2017-516539 discloses a technique for measuring physiological data with a wristwatch-type measuring device worn on the wrist. The measuring device of PCT International Publication No. 2017-516539 is a wearable system that includes a band wrapped around the wrist and a sensor unit provided on the band. The sensor unit includes a light emitting element such as an LED that emits an optical signal, and a light receiving element such as a photodiode that serves as a sensor that receives the optical signal. The sensor unit is arranged within a part of the plate surface of a plate-shaped sensor plate having approximately the same thickness overall.
 また、特表2017-516539には、センサの配置位置を変える方法として、皮膚と接触する側の表面であるバンドの内面上に配置された円形状のセンサユニットを回転させる技術が開示されている。また、特表2017-516539には、バンドの内面上に配置され、手首の周方向にスライドするセンサースライドも開示されている。 Additionally, Japanese Patent Publication No. 2017-516539 discloses a technique for rotating a circular sensor unit placed on the inner surface of the band, which is the surface that contacts the skin, as a method for changing the sensor placement position. . Furthermore, Japanese Patent Publication No. 2017-516539 also discloses a sensor slide that is arranged on the inner surface of the band and slides in the circumferential direction of the wrist.
 腕時計型の測定装置を用いて酸素飽和度を測定する際、バンドが手首に巻かれると共にセンサユニットが手首の内側の皮膚上で腕橈骨動脈等の動脈の近傍位置に配置される。そして、センサユニットの発光素子から、光信号が、拍動する動脈血に対して照射される。 When measuring oxygen saturation using a wristwatch-type measuring device, a band is wrapped around the wrist and a sensor unit is placed on the skin on the inside of the wrist near an artery such as the brachioradial artery. Then, an optical signal is emitted from the light emitting element of the sensor unit to the pulsating arterial blood.
 照射された光信号は、動脈血で反射し、反射した光信号は、センサユニットの受光素子によって脈波信号として取得される。取得された脈波信号の強度を所定の計算式に用いて算出することによって得られた値は、酸素飽和度の測定値として使用できる。なお、本開示では「脈波信号の強度」は、脈波信号の振幅を意味する。 The irradiated optical signal is reflected by the arterial blood, and the reflected optical signal is acquired as a pulse wave signal by the light receiving element of the sensor unit. A value obtained by calculating the intensity of the acquired pulse wave signal using a predetermined calculation formula can be used as a measured value of oxygen saturation. Note that in the present disclosure, "intensity of pulse wave signal" means the amplitude of the pulse wave signal.
 また、特開2017-136182号公報には、手首や腕等に巻かれるバンドと、バンドに設けられたセンサモジュール(すなわち、センサユニット)とを備える生体情報取得装置としての腕時計型のウェアラブルシステムが開示されている。特開2017-136182号公報の生体情報取得装置では、血糖値を測定するため、測定対象の血管に対して光が照射され、血管を透過した透過光が、複数の受光部(すなわち、受光素子)によって受光される。特開2017-136182号公報では、動脈を透過した透過光の強度に基づいて酸素飽和度の測定が可能であるとされている。 Furthermore, Japanese Patent Laid-Open No. 2017-136182 discloses a wristwatch-type wearable system as a biological information acquisition device that includes a band that is wrapped around the wrist or arm, and a sensor module (i.e., a sensor unit) installed in the band. Disclosed. In the biological information acquisition device disclosed in Japanese Patent Application Laid-open No. 2017-136182, in order to measure blood sugar level, light is irradiated onto a blood vessel to be measured, and the transmitted light that has passed through the blood vessel is transmitted to a plurality of light receiving sections (i.e., a light receiving element). ) is received by the JP 2017-136182A states that oxygen saturation can be measured based on the intensity of transmitted light that has passed through an artery.
  特許文献1:特表2017-516539号公報
  特許文献2:特開2017-136182号公報
Patent Document 1: Japanese Patent Publication No. 2017-516539 Patent Document 2: Japanese Patent Application Publication No. 2017-136182
 ここで、腕時計型の測定装置が被測定者の手首の内側に装着される場合、センサユニットが測定対象の動脈近傍の初期位置から離れ易いという問題がある。具体的には例えば、バンドが被測定者の手首に装着された後、装着部位の皮膚が汗ばむことによって、バンドが皮膚表面上でずれる場合がある。或いは、装着状態に違和感を覚えた被測定者がバンドを一旦手首から外し、再度手首に巻き直す場合がある。また、例えば僅かに手首を曲げただけでも、手首の位置では長掌筋腱が、皮膚から比較的大きく隆起し易い。隆起した長掌筋腱がバンド又はセンサユニットを外側に押すことによって、センサユニットと手首の皮膚表面との間隔が広がる。 Here, when a wristwatch-type measuring device is worn on the inside of the wrist of the person to be measured, there is a problem that the sensor unit tends to move away from its initial position near the artery to be measured. Specifically, for example, after the band is worn on the wrist of the person being measured, the band may shift on the skin surface due to sweaty skin at the area where the band is worn. Alternatively, a person to be measured who feels uncomfortable wearing the band may temporarily remove the band from his wrist and then re-wrap it around his wrist. Furthermore, even if the wrist is slightly bent, for example, the palmaris longus tendon tends to protrude relatively largely from the skin at the wrist. The raised palmaris longus tendon pushes the band or sensor unit outward, increasing the distance between the sensor unit and the skin surface of the wrist.
 すなわち、手首の位置では、センサとしての光素子が初期位置に一旦配置されても、配置後、前腕の延びる方向、手首の周方向、及び、手首の径方向のそれぞれにおいて、センサの配置位置が、初期位置から位置ずれし易い。このため、位置ずれに起因して受光素子によって取得される脈波信号の強度が低下し、結果、酸素飽和度の測定が中断され易いという問題が生じていた。 In other words, even if the optical element as a sensor is placed at the initial position on the wrist, after placement, the placement position of the sensor changes in each of the extending direction of the forearm, the circumferential direction of the wrist, and the radial direction of the wrist. , the position is likely to shift from the initial position. For this reason, the intensity of the pulse wave signal acquired by the light receiving element decreases due to the positional shift, resulting in a problem in that the measurement of oxygen saturation is likely to be interrupted.
 ここで、特表2017-516539の場合、センサユニットを回転させることによって、センサユニット内の光素子の位置を、回転中心から一定の半径を有する円周上でスライドさせることが可能である。しかし、光素子の位置の変化範囲は、回転中心から一定の半径を有する円周上のみに限定される。具体的には、位置の変化範囲は、前腕の延びる方向と手首の周方向との2方向で定義される平面の中における一定の円周上のみに限定される。このため、センサの位置ずれが生じた場合に調整可能な位置範囲が小さい。 Here, in the case of PCT International Publication No. 2017-516539, by rotating the sensor unit, it is possible to slide the position of the optical element within the sensor unit on the circumference having a constant radius from the center of rotation. However, the range of change in the position of the optical element is limited only to the circumference having a constant radius from the center of rotation. Specifically, the range of position change is limited only to a certain circumference within a plane defined by two directions: the extending direction of the forearm and the circumferential direction of the wrist. For this reason, the range of positions that can be adjusted in the event of positional deviation of the sensor is small.
 また、特開2017-136182号公報では、動脈を透過した透過光が、酸素飽和度の測定に用いられる。このため、例えば反射光が酸素飽和度の測定に用いられる場合、センサの位置ずれの問題に対し、特開2017-136182号公報の技術をそのまま適用することは難しい。 Furthermore, in Japanese Patent Application Publication No. 2017-136182, transmitted light that passes through an artery is used to measure oxygen saturation. For this reason, for example, when reflected light is used to measure oxygen saturation, it is difficult to apply the technique of JP-A-2017-136182 as is to the problem of sensor positional deviation.
 本開示は上記した問題に着目して為されたものであって、手首の内側の位置でセンサの位置ずれに起因する測定の中断の頻度を低減できる酸素飽和度測定装置及び酸素飽和度測定方法を提供する。 The present disclosure has been made with a focus on the above-mentioned problems, and includes an oxygen saturation measuring device and an oxygen saturation measuring method that can reduce the frequency of measurement interruptions caused by misalignment of the sensor at the inner side of the wrist. I will provide a.
 本開示の一態様に係る酸素飽和度測定装置は、被測定者の手首に巻かれるバンドと、手首の動脈に対し光を照射する発光素子と、手首の動脈からの反射光を受光する第1の受光素子と、第1の受光素子と離れて配置され手首の動脈からの反射光を受光する第2の受光素子と、第1の受光素子で受光された反射光から取得された第1の脈波信号と、第2の受光素子で受光された反射光から取得された第2の脈波信号とのうち、より大きな振幅を有する脈波信号が受光された受光素子を測定用受光素子として決定する受光素子決定部と、決定された測定用受光素子で受光された脈波信号に基づき、光が照射された動脈の酸素飽和度を測定する測定部と、を備える。 An oxygen saturation measurement device according to one aspect of the present disclosure includes a band wrapped around the wrist of a subject, a light emitting element that irradiates light to an artery in the wrist, and a first light emitting element that receives reflected light from the artery in the wrist. a second light-receiving element that is placed apart from the first light-receiving element and receives the reflected light from the wrist artery; Among the pulse wave signal and the second pulse wave signal acquired from the reflected light received by the second light receiving element, the light receiving element that has received the pulse wave signal having a larger amplitude is used as the measuring light receiving element. The apparatus includes a light receiving element determining section that determines the light receiving element, and a measuring section that measures the oxygen saturation level of the artery irradiated with light based on the pulse wave signal received by the determined measuring light receiving element.
 上記の一態様に係る酸素飽和度測定装置では、酸素飽和度の測定時、第1の受光素子と第2の受光素子とのうち、より大きな振幅を有する脈波信号が受光された受光素子が酸素飽和度の測定用受光素子として決定される。そして、決定された測定用受光素子で受光された脈波信号に基づき酸素飽和度を測定する。 In the oxygen saturation measurement device according to the above aspect, when measuring oxygen saturation, the light receiving element that receives the pulse wave signal having the larger amplitude is selected from among the first light receiving element and the second light receiving element. It is determined as a light receiving element for measuring oxygen saturation. Then, the oxygen saturation level is measured based on the pulse wave signal received by the determined measurement light receiving element.
 すなわち、同一の発光素子から照射された光の複数の反射光が受光されると共に、受光された複数の反射光の脈波信号の振幅が比較される。比較を通じて最大の振幅を有する脈波信号が、酸素飽和度測定用の脈波信号として定量的に選択される。このため、手首の内側の位置でセンサの位置ずれに起因する、酸素飽和度の測定の中断の頻度を低減できる。 That is, a plurality of reflected lights of light emitted from the same light emitting element are received, and the amplitudes of pulse wave signals of the plurality of received reflected lights are compared. Through the comparison, the pulse wave signal having the largest amplitude is quantitatively selected as the pulse wave signal for oxygen saturation measurement. Therefore, the frequency of interruptions in oxygen saturation measurement due to misalignment of the sensor at the inner side of the wrist can be reduced.
 また、上記の一態様では、第1の受光素子と第2の受光素子とは、手首の周方向に沿って並べられてよい。 Furthermore, in the above embodiment, the first light receiving element and the second light receiving element may be arranged along the circumferential direction of the wrist.
 上記の構成によれば、手首の周方向に沿った異なる2つの位置の間で、より適切な測定用受光素子を決定できる。 According to the above configuration, a more appropriate measurement light receiving element can be determined between two different positions along the circumferential direction of the wrist.
 また、上記の一態様では、第1の脈波信号と第2の脈波信号とが、予め設定された測定精度を達成する観点に基づいて予め設定された基準値を満たすかどうかを判定する判定部を更に備え、基準値を満たす脈波信号を受光した受光素子の中から測定用受光素子を決定する処理を行ってもよい。 Further, in the above aspect, it is determined whether the first pulse wave signal and the second pulse wave signal satisfy a preset reference value based on a viewpoint of achieving a preset measurement accuracy. The measuring device may further include a determination unit, and perform a process of determining a measuring light receiving element from among the light receiving elements that have received a pulse wave signal that satisfies the reference value.
 上記の構成によれば、第1の脈波信号と第2の脈波信号とが、予め設定された測定精度を達成する観点に基づいて予め設定された基準値を満たすかどうかが判定される。そして、基準値を満たす脈波信号を受光した受光素子の中から測定用受光素子を決定する処理が行われる。取得された脈波信号のうち、基準値を満たす脈波信号のみが測定用に抽出されるので、酸素飽和度の測定精度をより高めることができる。 According to the above configuration, it is determined whether the first pulse wave signal and the second pulse wave signal satisfy a preset reference value based on the viewpoint of achieving a preset measurement accuracy. . Then, a process is performed to determine a measuring light receiving element from among the light receiving elements that have received a pulse wave signal that satisfies the reference value. Among the acquired pulse wave signals, only the pulse wave signals that satisfy the reference value are extracted for measurement, so that the measurement accuracy of oxygen saturation can be further improved.
 また、上記の一態様では、発光素子として、手首の動脈に対し光を照射する第1の発光素子と、手首の周方向に沿って第1の発光素子と離れて配置され手首の動脈に対し光を照射する第2の発光素子と、を備え、第1の受光素子と離れて配置されると共に第2の受光素子と離れて配置され、第3の脈波信号を取得するために手首の動脈からの反射光を受光する第3の受光素子を備え、第1の受光素子と第2の受光素子と第3の受光素子とは、手首の周方向に沿って並べられ、第1の発光素子の光の反射光から取得された前記第1の脈波信号と前記第2の脈波信号と前記第3の脈波信号とに基づく第1の振幅の分布と、第2の発光素子の光の反射光から取得された前記第1の脈波信号と前記第2の脈波信号と前記第3の脈波信号とに基づく第2の振幅の分布とを作成する分布作成部と、第1の振幅の分布と第2の振幅の分布とを用いて、第1の発光素子と第2の発光素子とのうち、発光素子が動脈の上側に位置することに対応して設定された基準条件を満たす分布が作成された方の発光素子を測定用発光素子として決定する発光素子決定部と、を備え、決定された測定用発光素子の光の反射光の脈波信号に基づき酸素飽和度を測定してもよい。 Further, in the above aspect, the light emitting element includes a first light emitting element that irradiates light to an artery in the wrist, and a first light emitting element that is arranged apart from the first light emitting element along the circumferential direction of the wrist and that irradiates light to the artery in the wrist. a second light emitting element that emits light, the second light emitting element is arranged apart from the first light receiving element, and the second light receiving element is arranged apart from the second light receiving element, and the second light emitting element emits light. The first light receiving element, the second light receiving element, and the third light receiving element are arranged along the circumferential direction of the wrist, and the first light receiving element receives reflected light from the artery. a first amplitude distribution based on the first pulse wave signal, the second pulse wave signal, and the third pulse wave signal acquired from the reflected light of the light of the element; a distribution creation unit that creates a second amplitude distribution based on the first pulse wave signal, the second pulse wave signal, and the third pulse wave signal acquired from reflected light; A criterion set using the first amplitude distribution and the second amplitude distribution to correspond to the fact that the light emitting element is located above the artery among the first light emitting element and the second light emitting element. a light emitting element determination unit that determines the light emitting element for which a distribution satisfying the conditions has been created as the light emitting element for measurement, and determines the oxygen saturation based on the pulse wave signal of the reflected light of the determined light emitting element for measurement. may be measured.
 上記の構成によれば、第1の発光素子の光の反射光が、第1の受光素子と第2の受光素子と第3の受光素子とのそれぞれによって受光され、受光した反射光の手首の周方向に沿った第1の振幅の分布が作成される。また、第2の発光素子の光の反射光が、第1の受光素子と第2の受光素子と第3の受光素子とのそれぞれによって受光され、受光された反射光の手首の周方向に沿った第2の振幅の分布が作成される。 According to the above configuration, the reflected light of the first light emitting element is received by each of the first light receiving element, the second light receiving element, and the third light receiving element, and the received reflected light is reflected by the wrist. A first amplitude distribution along the circumferential direction is created. Further, the reflected light of the second light emitting element is received by each of the first light receiving element, the second light receiving element, and the third light receiving element, and the received reflected light is transmitted along the circumferential direction of the wrist. A second amplitude distribution is created.
 そして、作成された第1の振幅の分布と第2の振幅の分布とのうち、発光素子が動脈の上側に位置することに対応して設定された基準条件を満たす分布が作成された発光素子が、測定用発光素子として決定される。そして、決定された測定用発光素子の光の反射光の脈波信号に基づき酸素飽和度が測定される。すなわち、複数の発光素子の中から動脈の上側に位置する発光素子が、測定用発光素子として決定される。このため、酸素飽和度の測定精度を更に高めることができる。 Then, out of the created first amplitude distribution and second amplitude distribution, a light emitting element is created that satisfies the reference condition set in accordance with the fact that the light emitting element is located above the artery. is determined as the light emitting element for measurement. Then, the oxygen saturation level is measured based on the pulse wave signal of the reflected light from the determined light emitting element for measurement. That is, the light emitting element located above the artery from among the plurality of light emitting elements is determined as the light emitting element for measurement. Therefore, the measurement accuracy of oxygen saturation can be further improved.
 また、上記の一態様では、第1の発光素子と第2の発光素子とのうち測定用発光素子として決定された発光素子にのみ通電を継続し、かつ、測定用発光素子として決定されなかった発光素子への通電を停止する制御部を更に備えてもよい。 Further, in the above embodiment, current is continued to be applied only to the light emitting element determined as the measurement light emitting element among the first light emitting element and the second light emitting element, and the light emitting element is not determined as the measurement light emitting element. The light emitting device may further include a control unit that stops energizing the light emitting element.
 上記の構成によれば、測定用発光素子として決定されなかった発光素子への通電が停止されるので、省電力を図ることができる。 According to the above configuration, power supply to the light emitting elements that have not been determined as measurement light emitting elements is stopped, so power saving can be achieved.
 本開示の他の態様に係る酸素飽和度測定方法は、上記の一態様に係る酸素飽和度測定装置の発光素子を用いて測定対象の動脈に光を照射し、光が照射された動脈からの反射光から、第1の受光素子を用いて第1の脈波信号を取得すると共に第2の受光素子を用いて第2の脈波信号を取得し、第1の脈波信号と第2の脈波信号とをモニタし、モニタされた第1の脈波信号とモニタされた第2の脈波信号とのうち、より大きな振幅を有する脈波信号が受光された受光素子を、受光素子決定部を用いて測定用受光素子として決定し、決定された測定用受光素子で受光された脈波信号に基づき、測定部を用いて酸素飽和度を測定する。 An oxygen saturation measuring method according to another aspect of the present disclosure includes irradiating light onto an artery to be measured using the light-emitting element of the oxygen saturation measuring device according to the above-described one aspect, and emitting light from the artery irradiated with the light. From the reflected light, a first pulse wave signal is obtained using the first light receiving element, a second pulse wave signal is obtained using the second light receiving element, and the first pulse wave signal and the second pulse wave signal are combined. The pulse wave signal is monitored, and the light receiving element that receives the pulse wave signal having the larger amplitude between the monitored first pulse wave signal and the monitored second pulse wave signal is determined as the light receiving element. The measuring section is used to determine the oxygen saturation as a measuring light receiving element, and the measuring section is used to measure oxygen saturation based on the pulse wave signal received by the determined measuring light receiving element.
 上記の他の態様に係る酸素飽和度測定方法によれば、本開示の一態様に係る酸素飽和度測定装置の場合と同様、手首の内側の位置でセンサの位置ずれに起因する酸素飽和度の測定の中断の頻度を低減できる。 According to the oxygen saturation measuring method according to the other aspect described above, as in the case of the oxygen saturation measuring device according to one aspect of the present disclosure, the oxygen saturation is measured at the position on the inside of the wrist due to the positional deviation of the sensor. The frequency of measurement interruptions can be reduced.
 よって、本開示に係る酸素飽和度測定装置及び酸素飽和度測定方法によれば、手首の内側の位置でセンサの位置ずれに起因する測定の中断の頻度を低減できる。 Therefore, according to the oxygen saturation measuring device and the oxygen saturation measuring method according to the present disclosure, it is possible to reduce the frequency of interruption of measurement due to positional deviation of the sensor at the inner side of the wrist.
本開示の第1実施形態に係る酸素飽和度測定装置を説明する断面図である。FIG. 1 is a cross-sectional view illustrating an oxygen saturation measuring device according to a first embodiment of the present disclosure. 第1実施形態に係る酸素飽和度測定装置を説明する斜視図である。FIG. 1 is a perspective view illustrating an oxygen saturation measuring device according to a first embodiment. 第1実施形態に係る酸素飽和度測定装置のセンサユニットを説明する平面図である。FIG. 2 is a plan view illustrating a sensor unit of the oxygen saturation measuring device according to the first embodiment. 図3中の4-4線断面図である。4 is a sectional view taken along line 4-4 in FIG. 3. FIG. 第1実施形態の変形例(第1変形例)に係る酸素飽和度測定装置を説明する断面図である。It is a sectional view explaining the oxygen saturation measuring device concerning the modification (the 1st modification) of a 1st embodiment. 第1実施形態の変形例(第2変形例)に係る酸素飽和度測定装置を説明する斜視図である。It is a perspective view explaining the oxygen saturation measuring device concerning the modification (the 2nd modification) of a 1st embodiment. 第2実施形態に係る酸素飽和度測定装置のスライダー部を説明する平面図である。It is a top view explaining the slider part of the oxygen saturation measuring device based on 2nd Embodiment. 図7中の8-8線断面図である。8 is a sectional view taken along line 8-8 in FIG. 7. FIG. 図7中の9-9線断面図である。8 is a sectional view taken along line 9-9 in FIG. 7. FIG. 第3実施形態に係る酸素飽和度測定装置の発光素子と受光素子との配置を説明する平面図である。FIG. 7 is a plan view illustrating the arrangement of a light emitting element and a light receiving element of an oxygen saturation measuring device according to a third embodiment. 第3実施形態に係る酸素飽和度測定装置を用いた酸素飽和度測定方法を説明するフローチャートである。It is a flow chart explaining the oxygen saturation measuring method using the oxygen saturation measuring device concerning a 3rd embodiment. 第3実施形態に係る酸素飽和度測定装置の第1の発光素子から照射された光の反射光の振幅の分布を説明するグラフである。It is a graph explaining the distribution of the amplitude of the reflected light of the light irradiated from the 1st light emitting element of the oxygen saturation measuring device concerning 3rd Embodiment. 第3実施形態に係る酸素飽和度測定装置の第2の発光素子から照射された光の反射光の振幅の分布を説明するグラフである。It is a graph explaining the distribution of the amplitude of the reflected light of the light irradiated from the 2nd light emitting element of the oxygen saturation measuring device based on 3rd Embodiment. 第3実施形態に係る酸素飽和度測定装置の第3の発光素子から照射された光の反射光の振幅の分布を説明するグラフである。It is a graph explaining the distribution of the amplitude of the reflected light of the light irradiated from the 3rd light emitting element of the oxygen saturation measuring device based on 3rd Embodiment. 発光素子と受光素子との他の配置パターンを説明する平面図である。FIG. 7 is a plan view illustrating another arrangement pattern of light emitting elements and light receiving elements.
 以下に本開示の第1~第3実施形態を説明する。以下の図面の記載において、同一の部分及び類似の部分には、同一の符号又は類似の符号を付している。ただし、図面は模式的なものであり、厚みと平面寸法との関係、各装置や各部材の厚みの比率等は現実のものとは異なる。したがって、具体的な厚みや寸法は以下の説明を参酌して判定すべきものである。また、図面相互間においても互いの寸法の関係や比率が異なる部分が含まれている。また、明細書中に特段の断りが無い限り、本開示の各構成要素の個数は、1つに限定されず、複数存在してもよい。 First to third embodiments of the present disclosure will be described below. In the description of the drawings below, the same or similar parts are denoted by the same or similar symbols. However, the drawings are schematic, and the relationship between the thickness and planar dimensions, the ratio of the thickness of each device and each member, etc. differ from the reality. Therefore, specific thickness and dimensions should be determined with reference to the following explanation. Furthermore, the drawings include portions that differ in dimensional relationships and ratios. Further, unless otherwise specified in the specification, the number of each component of the present disclosure is not limited to one, and a plurality may exist.
-第1実施形態-
 第1実施形態では、センサが配置されると共に皮膚に接触する接触面を有する接触部において、接触面が、湾曲形状である。以下、第1実施形態を、図1~図6を参照して説明する。
-First embodiment-
In the first embodiment, in the contact section where the sensor is disposed and has a contact surface that contacts the skin, the contact surface has a curved shape. The first embodiment will be described below with reference to FIGS. 1 to 6.
<酸素飽和度測定装置>
 図1に示すように、第1実施形態に係る酸素飽和度測定装置10Aは、バンド12と、基部14と、接触部16と、発光素子と、受光素子と、測定部18と、を備える。図1中に例示された酸素飽和度測定装置10Aでは、受光素子として、第1の受光素子PD1と第2の受光素子PD2と第3の受光素子PD3と第4の受光素子PD4と第5の受光素子PD5とが設けられる。また、図1中の手首の内部には、橈骨20、橈骨茎状突起20A、橈側手根屈筋腱22及び橈骨動脈24が例示されている。
<Oxygen saturation measuring device>
As shown in FIG. 1, the oxygen saturation measuring device 10A according to the first embodiment includes a band 12, a base 14, a contact section 16, a light emitting element, a light receiving element, and a measuring section 18. In the oxygen saturation measuring device 10A illustrated in FIG. 1, the light receiving elements include a first light receiving element PD1, a second light receiving element PD2, a third light receiving element PD3, a fourth light receiving element PD4, and a fifth light receiving element PD1. A light receiving element PD5 is provided. Further, inside the wrist in FIG. 1, a radius 20, a radial styloid process 20A, a flexor carpi radialis tendon 22, and a radial artery 24 are illustrated.
(バンド)
 バンド12は、被測定者の手首に巻かれる。バンド12の素材は、例えば樹脂、布地、金属等、任意である。また、バンド12には手首に巻かれた際の長さを調節しかつ固定するための留め金が設けられる。図2に示すように、バンド12には演算表示部26が設けられる。
(band)
The band 12 is wrapped around the wrist of the subject. The material of the band 12 is arbitrary, such as resin, cloth, metal, etc. The band 12 is also provided with a clasp for adjusting and fixing the length when it is wrapped around the wrist. As shown in FIG. 2, the band 12 is provided with a calculation display section 26.
(基部)
 基部14は、バンド12の内面上に設けられる。具体的には第1実施形態では、基部14は、バンド12に例えば接着によって固定され得る。ただし、固定方法は接着に限定されず、バンド12との間に固定用の板状部材を介在させ、回路基板が板状部材にネジ止め等によって固定されてもよい。
(base)
A base 14 is provided on the inner surface of the band 12. Specifically, in the first embodiment, the base 14 may be fixed to the band 12, for example by adhesive. However, the fixing method is not limited to adhesion, and a fixing plate member may be interposed between the circuit board and the band 12, and the circuit board may be fixed to the plate member by screwing or the like.
 基部14は、バンド12と接触部16との間に平坦な接合面14Aを有する。第1実施形態では、基部14の接合面14Aには、発光素子及び受光素子の両方が接合される。本開示では、接合面14Aに、発光素子及び受光素子のうち少なくとも一方が接合されればよい。 The base 14 has a flat joint surface 14A between the band 12 and the contact portion 16. In the first embodiment, both a light emitting element and a light receiving element are bonded to the bonding surface 14A of the base 14. In the present disclosure, at least one of the light emitting element and the light receiving element may be bonded to the bonding surface 14A.
 また、本開示では、基部14は、発光素子及び受光素子が搭載される回路基板そのものであってもよいし、或いは、回路基板と固定用の板状部材との組み合わせ、或いは、回路基板と緩衝部材との組み合わせ等であってもよい。すなわち、本開示の基部14は、発光素子及び受光素子のうち少なくとも一方が接合される接合面14Aを有すればよい。 Further, in the present disclosure, the base 14 may be the circuit board itself on which the light emitting element and the light receiving element are mounted, or a combination of the circuit board and a fixing plate member, or a combination of the circuit board and a buffer. It may also be a combination of other members. That is, the base 14 of the present disclosure only needs to have a bonding surface 14A to which at least one of the light emitting element and the light receiving element is bonded.
 図3に示すように、基部14の接合面14A上には、発光素子(第1の発光素子LED1,第2の発光素子LED2,第3の発光素子LED3)及び受光素子(第1の受光素子PD1,第2の受光素子PD2,第3の受光素子PD3,第4の受光素子PD4,第5の受光素子PD5)が配置される。なお、発光素子及び受光素子が搭載される回路基板の図示は省略する。 As shown in FIG. 3, on the joint surface 14A of the base 14, light emitting elements (first light emitting element LED1, second light emitting element LED2, third light emitting element LED3) and light receiving elements (first light receiving element PD1, second light receiving element PD2, third light receiving element PD3, fourth light receiving element PD4, and fifth light receiving element PD5) are arranged. Note that illustration of the circuit board on which the light emitting element and the light receiving element are mounted is omitted.
(発光素子)
 発光素子は、例えば発光ダイオード(LED)等の電子部品である。発光素子は、接触部16に対し予め設定された位置に配置され、手首の動脈に対し光を照射する。第1の発光素子LED1と第2の発光素子LED2と第3の発光素子LED3とは、互いに離れて配置されると共に、手首の周方向Cに沿って並べられる。なお、本開示では、発光素子の個数は、1つ以上、任意である。
(Light emitting element)
The light emitting element is, for example, an electronic component such as a light emitting diode (LED). The light emitting element is placed at a preset position with respect to the contact portion 16, and irradiates light to the artery of the wrist. The first light emitting element LED1, the second light emitting element LED2, and the third light emitting element LED3 are arranged apart from each other and arranged along the circumferential direction C of the wrist. Note that in the present disclosure, the number of light emitting elements is one or more and arbitrary.
 図3に示すように、第1の発光素子LED1と第2の発光素子LED2と第3の発光素子LED3とは、いずれも、一組の光源を有する。一組の光源には、1つ以上の赤色光源REDと1つ以上の赤外光源IRとが含まれる。すなわち、第1実施形態では、1つの発光素子から2種類の光が照射される。そして、1つの受光素子が受光する2種類の反射光が、酸素飽和度の測定に用いられる。なお、本開示では、光源の種類は2種類に限定されず、1種類であってもよいし、或いは、3種類以上であってもよい。 As shown in FIG. 3, the first light emitting element LED1, the second light emitting element LED2, and the third light emitting element LED3 all have a set of light sources. The set of light sources includes one or more red light sources RED and one or more infrared light sources IR. That is, in the first embodiment, two types of light are emitted from one light emitting element. Two types of reflected light received by one light receiving element are used to measure oxygen saturation. Note that in the present disclosure, the number of types of light sources is not limited to two types, and may be one type, or three or more types.
(酸素飽和度の測定原理)
 ここで、2種類の照射光及び2種類の反射光が用いられる第1実施形態における酸素飽和度の測定原理を説明する。具体的には、例えば、620nm程度~700nm程度の波長領域の赤色光は、ヘモグロビンに結合する酸素の有無によって、吸光度が大きく変わるという特性を有する。一方、850nm程度~960nm程度の波長領域の近赤外光は、ヘモグロビンに結合する酸素の有無によって、吸光度が大きく変わらないという特性を有する。
(Measurement principle of oxygen saturation)
Here, the principle of measuring oxygen saturation in the first embodiment in which two types of irradiation light and two types of reflected light are used will be explained. Specifically, for example, red light in a wavelength range of about 620 nm to about 700 nm has a characteristic that its absorbance greatly changes depending on the presence or absence of oxygen bonded to hemoglobin. On the other hand, near-infrared light in the wavelength range of about 850 nm to about 960 nm has a characteristic that its absorbance does not change significantly depending on the presence or absence of oxygen bonded to hemoglobin.
 このため、赤色光の反射光の脈波信号の強度の変化は、経時的にモニタされる。そして、モニタされた脈波信号に含まれる脈波信号の変動成分(AC)と、変動しない固定成分(DC)とが算出される。そして、変動成分を固定成分で除す(AC/DC)ことによって、赤色光の灌流指標(Perfusion Index,PI)値が、PIREDとして算出される。また、赤色光の場合と同様に、近赤外光の反射光の脈波信号の強度の変化を経時的にモニタすることによって、近赤外光の反射光のPI値(PIIR)が算出される。 Therefore, changes in the intensity of the pulse wave signal of the reflected red light are monitored over time. Then, a fluctuation component (AC) of the pulse wave signal included in the monitored pulse wave signal and a fixed component (DC) that does not fluctuate are calculated. Then, by dividing the variable component by the fixed component (AC/DC), a red light perfusion index (PI) value is calculated as PI RED . In addition, as in the case of red light, the PI value (PI IR ) of reflected near-infrared light is calculated by monitoring changes in the intensity of the pulse wave signal of reflected near-infrared light over time. be done.
 そして、赤色光のPI値(PIRED)と近赤外光のPI値(PIIR)との比(PIRED/PIIR)が算出される。そして、算出された比(PIRED/PIIR)を以下の式(1)に用いることによって、酸素飽和度を算出することができる。
 
 酸素飽和度[%]=a×(PIRED/PIIR)+b   ・・・式(1)
 
 式(1)中の係数a,bは、実験によって求めることができる。なお、本開示では、酸素飽和度の測定方法は、これに限定されず、他の方法であってもよい。
Then, the ratio (PI RED / PI IR ) between the PI value of red light (PI RED ) and the PI value of near-infrared light (PI IR ) is calculated. Then, by using the calculated ratio (PI RED /PI IR ) in the following equation (1), the oxygen saturation level can be calculated.

Oxygen saturation [%] = a × (PI RED / PI IR ) + b ... Formula (1)

Coefficients a and b in equation (1) can be determined by experiment. Note that in the present disclosure, the method for measuring oxygen saturation is not limited to this, and other methods may be used.
(受光素子)
 受光素子は、例えばフォトダイオード(PD)等の電子部品である。受光素子は、接触部16に対し予め設定された位置に配置され、接触部16の接触面16Aを介して手首の動脈からの反射光を受光する。第1の受光素子PD1と第2の受光素子PD2と第3の受光素子PD3と第4の受光素子PD4と第5の受光素子PD5とは、互いに離れて配置されると共に、手首の周方向に沿って並べられる。なお、本開示では、受光素子の個数は、1つ以上、任意である。
(Light receiving element)
The light receiving element is, for example, an electronic component such as a photodiode (PD). The light receiving element is arranged at a preset position with respect to the contact part 16, and receives reflected light from the artery of the wrist via the contact surface 16A of the contact part 16. The first light receiving element PD1, the second light receiving element PD2, the third light receiving element PD3, the fourth light receiving element PD4, and the fifth light receiving element PD5 are arranged apart from each other and in the circumferential direction of the wrist. arranged along. Note that in the present disclosure, the number of light receiving elements is one or more and arbitrary.
 第1実施形態では、1つ以上の発光素子と、1つ以上の発光素子に対応する1つ以上の受光素子とによって、1つの「センサユニット」が構成される。本開示では、複数のセンサユニットが設けられてよい。また、1つの「センサユニット」中に含まれる発光素子の個数と、受光素子の個数とは、いずれも任意に設定できる。 In the first embodiment, one "sensor unit" is configured by one or more light emitting elements and one or more light receiving elements corresponding to the one or more light emitting elements. In the present disclosure, multiple sensor units may be provided. Further, both the number of light emitting elements and the number of light receiving elements included in one "sensor unit" can be set arbitrarily.
 また、第1実施形態に係る酸素飽和度測定装置10Aは、反射光によって脈波信号の強度が測定される反射型であるが、本開示では反射型に限定されず、透過光によって脈波信号の強度が測定される透過型であってもよい。 Further, the oxygen saturation measuring device 10A according to the first embodiment is a reflective type in which the intensity of the pulse wave signal is measured using reflected light, but the present disclosure is not limited to the reflective type, and the pulse wave signal is measured using transmitted light. It may also be a transmission type in which the intensity of is measured.
(遮光部)
 図4に示すように、基部14における発光素子と受光素子との間には、遮光部14Bが設けられる。遮光部14Bによって、受光素子が発光素子からの光を直接受光することが防止される。なお、遮光部14Bを用いつつ発光素子と受光素子との間隔を可能な限り近づけることが、光路長が短くなり、結果、測定精度を高められる観点から、好ましい。
(light shielding part)
As shown in FIG. 4, a light shielding portion 14B is provided between the light emitting element and the light receiving element in the base 14. The light blocking portion 14B prevents the light receiving element from directly receiving light from the light emitting element. Note that it is preferable to make the distance between the light emitting element and the light receiving element as close as possible while using the light shielding part 14B, from the viewpoint of shortening the optical path length and improving measurement accuracy as a result.
(接触部)
 接触部16は、バンド12に取り付けられる。また、接触部16は、手首の動脈に対して照射される光と手首の動脈からの反射光とに対する透光性を有する。具体的には例えば、レンズ等の透光性を有する部材が採用され得る。図4中で発光素子の上側に配置される接触部16は、例えば、照射領域を拡大可能な拡散レンズである。また、図示を省略するが、発光素子の上側に、拡散レンズと共に、又は拡散レンズの代わりに、拡散剤が配置されてもよい。また、図4中で受光素子の上側に配置される接触部16は、例えば、反射光を集めることが可能な集光レンズであってよい。
(contact part)
Contact portion 16 is attached to band 12 . Further, the contact portion 16 has translucency for light irradiated onto the artery of the wrist and light reflected from the artery of the wrist. Specifically, for example, a light-transmitting member such as a lens may be used. The contact portion 16 disposed above the light emitting element in FIG. 4 is, for example, a diffuser lens capable of enlarging the irradiation area. Further, although not shown, a diffusing agent may be placed above the light emitting element together with the diffusing lens or instead of the diffusing lens. Further, the contact portion 16 disposed above the light receiving element in FIG. 4 may be, for example, a condenser lens capable of collecting reflected light.
 また、接触部16は、バンド12から手首側に突出する接触面16Aを有する。第1実施形態では、接触面16Aは、湾曲形状を有する。接触面16Aは、酸素飽和度の測定時、手首の皮膚に接触する。 Furthermore, the contact portion 16 has a contact surface 16A that protrudes from the band 12 toward the wrist. In the first embodiment, the contact surface 16A has a curved shape. The contact surface 16A comes into contact with the skin of the wrist when measuring oxygen saturation.
 図3及び図4に示すように、接触部16は、ドーム状である。ドームの外面に相当する接触面では、図4中の左右方向(すなわち、前腕の延びる方向E)における中央部は平坦であると共に、左右の両端部はそれぞれ、一定の曲率を有することによって、角張ることなく円滑に湾曲する。曲率は、例えば0.167以上であることが、被測定者の装着性向上の観点から好ましい。なお、図示を省略するが、同様に、接触部16の手首の周方向Cにおける中央部は、平坦であると共に、左右の両端部はそれぞれ円滑に湾曲する。 As shown in FIGS. 3 and 4, the contact portion 16 has a dome shape. In the contact surface corresponding to the outer surface of the dome, the central part in the left-right direction in FIG. Curves smoothly without tension. The curvature is preferably 0.167 or more, for example, from the viewpoint of improving wearability for the person being measured. Although not shown in the drawings, similarly, the center portion of the contact portion 16 in the circumferential direction C of the wrist is flat, and both left and right end portions are smoothly curved.
 また、本開示では、後で第2実施形態において説明するが、図8及び図9に示すように、接触面16Aは、平坦な部分を有しなくてもよい。接触面16Aは、全体的に一定の曲率を有する状態で、湾曲形状を有してもよい。 Furthermore, in the present disclosure, as will be described later in the second embodiment, the contact surface 16A does not need to have a flat portion, as shown in FIGS. 8 and 9. The contact surface 16A may have a curved shape with an overall constant curvature.
 なお、本明細書では「前腕の延びる方向E」は、橈骨20の延びる方向、尺骨の延びる方向及び動脈の延びる方向のいずれの方向とも重なる。また「前腕の延びる方向E」は、厳密には被測定者毎に異なる。すなわち、「前腕の延びる方向E」は、3次元空間内で座標によって一義的に決定されるものではなく、被測定者毎の橈骨20の延びる方向、尺骨の延びる方向及び動脈の延びる方向に基づいて個別に決定され得る。 Note that in this specification, "the forearm extending direction E" overlaps with any of the directions in which the radius 20 extends, the ulna, and the artery. Moreover, the "direction E in which the forearm extends" strictly speaking differs depending on the subject. That is, the "extending direction E of the forearm" is not uniquely determined by coordinates in a three-dimensional space, but is determined based on the extending direction of the radius 20, the ulna extending direction, and the artery extending direction for each subject. can be determined individually.
(接触部の最大幅)
 第1実施形態では、接触部16の最大幅は、3mm以上、7mm以下に設定される。ここで、本実施形態では図1に示すように、接触部16の最大幅Wは、手首の周方向Cに沿って、橈骨茎状突起20Aと橈側手根屈筋腱22との隙間を測った場合の最大幅を意味する。なお、本開示では、接触部の最大幅は、橈骨茎状突起と橈側手根屈筋腱との隙間以外の、手首における他の部位によって設定される距離に基づいて設定されてよい。
(Maximum width of contact part)
In the first embodiment, the maximum width of the contact portion 16 is set to 3 mm or more and 7 mm or less. In this embodiment, as shown in FIG. 1, the maximum width W of the contact portion 16 is determined by measuring the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22 along the circumferential direction C of the wrist. means the maximum width of the case. Note that in the present disclosure, the maximum width of the contact portion may be set based on a distance set by other parts of the wrist other than the gap between the radial styloid process and the flexor carpi radialis tendon.
 すなわち、本実施形態では、接触部16の最大幅Wは、接触部16が隙間の窪みの内側に配置される状態を考慮して設定される。換言すると、橈骨茎状突起20Aと橈側手根屈筋腱22との隙間の幅Gは、手首の表面上で周方向Cに沿って測定された最小値であると共に、この最小値の幅Gの隙間の窪みの内側に配置できるように、接触部16の最大幅Wが設定される。 That is, in this embodiment, the maximum width W of the contact portion 16 is set in consideration of the state in which the contact portion 16 is arranged inside the recess of the gap. In other words, the width G of the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22 is the minimum value measured along the circumferential direction C on the surface of the wrist, and the width G of this minimum value is The maximum width W of the contact portion 16 is set so that the contact portion 16 can be placed inside the recess of the gap.
 第1実施形態では、接触部16の最大幅Wの下限値が3mm未満の場合、発光素子及び受光素子等の電子部品が小さくなり過ぎるため、製造コストが上昇する、又は製造できない懸念がある。一方、接触部16の最大幅Wの上限値が7mmを超える場合、隙間の幅が比較的狭い、小児の女性の手首における橈骨茎状突起20Aと橈側手根屈筋腱22との隙間に配置することが難しくなる。 In the first embodiment, if the lower limit of the maximum width W of the contact portion 16 is less than 3 mm, the electronic components such as the light emitting element and the light receiving element will become too small, so there is a concern that the manufacturing cost will increase or that it will not be possible to manufacture them. On the other hand, if the upper limit of the maximum width W of the contact portion 16 exceeds 7 mm, it is placed in the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22 in the wrist of a female child, where the width of the gap is relatively narrow. things become difficult.
 なお、本開示では、接触部16の最大幅Wは、適宜変更できる。また、接触部16の最大幅Wの上限値は、測定対象の性別及び年齢に応じて変化させてもよい。例えば、17歳の少年少女の身長及び体重は、5歳の児童のときの身長及び体重と比べ、30%程度増大すると設定できる。このため、小児の女性用の接触部16の最大幅Wの上限値が7mmである場合、例えば17歳以上の女性用の接触部16の最大幅Wの上限値は、10mm程度に設定できる。 Note that in the present disclosure, the maximum width W of the contact portion 16 can be changed as appropriate. Further, the upper limit of the maximum width W of the contact portion 16 may be changed depending on the gender and age of the subject to be measured. For example, the height and weight of a 17-year-old boy or girl can be set to be approximately 30% larger than the height and weight of a 5-year-old child. Therefore, if the upper limit of the maximum width W of the contact portion 16 for female children is 7 mm, the upper limit of the maximum width W of the contact portion 16 for female children of 17 years or older can be set to about 10 mm, for example.
 また、男性の身長及び体重は、女性の身長及び体重と比べ、例えば、10%程度増大すると設定できる。このため、小児の女性用の接触部16の最大幅Wの上限値が7mmである場合、小児の男性用の接触部16の最大幅Wの上限値は、8mm程度に設定できる。また、例えば17歳以上の男性用の接触部16の最大幅Wの上限値は、11mm程度に設定できる。 Furthermore, the height and weight of a man can be set to be about 10% larger than the height and weight of a woman, for example. Therefore, if the upper limit of the maximum width W of the contact section 16 for female children is 7 mm, the upper limit of the maximum width W of the contact section 16 for male children can be set to about 8 mm. Further, for example, the upper limit of the maximum width W of the contact portion 16 for men aged 17 or older can be set to about 11 mm.
(測定部)
 第1実施形態では、測定部18は、バンド12に取り付けられた演算表示部26に設けられる。演算表示部26は、手首の外側である甲側に位置する。測定部18には受光素子が接続される。測定部18には、反射光の脈波信号のデータが受光素子から経時的に入力される。
(Measurement section)
In the first embodiment, the measurement unit 18 is provided in a calculation display unit 26 attached to the band 12. The calculation display section 26 is located on the back side, which is the outside of the wrist. A light receiving element is connected to the measuring section 18. Data of a pulse wave signal of reflected light is inputted to the measurement unit 18 over time from a light receiving element.
 測定部18は、例えば、CPU(Central Processing Unit)、RAM(Random Access Memory)、記憶装置、I/Oポート等を備えたコンピュータとして構成される。RAM、記憶装置、I/Oポート等は内部バスを介してCPUとデータ交換可能に構成される。 The measurement unit 18 is configured as a computer including, for example, a CPU (Central Processing Unit), a RAM (Random Access Memory), a storage device, an I/O port, and the like. The RAM, storage device, I/O port, etc. are configured to be able to exchange data with the CPU via an internal bus.
 測定部18は、反射光から取得された脈波信号に基づき、光が照射された橈骨動脈24の酸素飽和度を、PI値の比を用いる方法等によって、測定する。 The measurement unit 18 measures the oxygen saturation level of the radial artery 24 irradiated with light, based on the pulse wave signal acquired from the reflected light, by a method using a ratio of PI values, etc.
(演算表示部)
 演算表示部26は、測定部18による演算結果を外部に対して表示する。演算表示部26には、測定結果を一時的に保存する記憶装置が設けられてもよい。なお、本開示では、演算表示部26は必須でない。演算表示部26が設けられない場合、測定部18は、例えば接触部16又は基部14に、演算装置の一部として配置できる。
(Calculation display section)
The calculation display unit 26 displays the calculation results by the measurement unit 18 to the outside. The calculation display section 26 may be provided with a storage device that temporarily stores measurement results. Note that in the present disclosure, the calculation display section 26 is not essential. If the calculation display part 26 is not provided, the measurement part 18 can be arranged, for example, on the contact part 16 or the base part 14 as part of the calculation device.
 また、記憶装置も同様に接触部16又は基部14等、演算表示部26以外の部材に配置できる。そして、演算表示部26が設けられない場合であっても、例えば、演算装置に接続され且つ外部との通信を可能とする通信部を介して、測定部18による算出結果を得ることが可能である。 Furthermore, the storage device can also be placed on a member other than the calculation display section 26, such as the contact section 16 or the base section 14. Even if the calculation display section 26 is not provided, it is possible to obtain the calculation results by the measurement section 18, for example, via a communication section that is connected to the calculation device and enables communication with the outside. be.
<第1変形例>
 図5に示すように、発光素子と受光素子とは、接触部16の接触面16A上に配置されてもよい。図5中には、第1の受光素子PD1と第2の受光素子PD2と第3の受光素子PD3と第4の受光素子PD4と第5の受光素子PD5とが、基部14の接合面14A上ではなく、接触面16A上に配置された場合が例示されている。
<First modification example>
As shown in FIG. 5, the light emitting element and the light receiving element may be arranged on the contact surface 16A of the contact portion 16. In FIG. 5, a first light receiving element PD1, a second light receiving element PD2, a third light receiving element PD3, a fourth light receiving element PD4, and a fifth light receiving element PD5 are arranged on the joint surface 14A of the base 14. A case where the contact surface 16A is arranged instead of the contact surface 16A is illustrated.
 発光素子と受光素子とが接触部16の接触面16A上に配置されることによって、発光素子と橈骨動脈24との距離、及び、受光素子と橈骨動脈24との距離を、発光素子と受光素子とが基部14の接合面14A上に配置される場合より短くできる。なお、発光素子と受光素子とが接触部16の接触面16A上に配置される場合、発光素子と受光素子とが測定部18に接続される限り、接触部16が透光性を有することは必須ではない。 By disposing the light emitting element and the light receiving element on the contact surface 16A of the contact portion 16, the distance between the light emitting element and the radial artery 24 and the distance between the light receiving element and the radial artery 24 can be determined by the distance between the light emitting element and the light receiving element. and can be made shorter than when they are arranged on the joint surface 14A of the base 14. Note that when the light emitting element and the light receiving element are arranged on the contact surface 16A of the contact part 16, as long as the light emitting element and the light receiving element are connected to the measuring part 18, the contact part 16 does not have translucency. Not required.
<第2変形例>
 図6に示すように、1つの接触部16が、第1の発光素子LED1と第1の受光素子PD1との両方に跨って配置されてもよい。また、複数の発光素子と複数の受光素子とのすべてに対して1つの接触部16が設けられてもよい。図6中の1つの接触部16では、接触部16の個数が1つである。このため、酸素飽和度測定装置の構造を簡易にでき、結果、製造負担を低減できる。
<Second modification example>
As shown in FIG. 6, one contact portion 16 may be placed across both the first light emitting element LED1 and the first light receiving element PD1. Further, one contact portion 16 may be provided for all of the plurality of light emitting elements and the plurality of light receiving elements. In one contact portion 16 in FIG. 6, the number of contact portions 16 is one. Therefore, the structure of the oxygen saturation measuring device can be simplified, and as a result, the manufacturing burden can be reduced.
<酸素飽和度測定方法>
 次に、第1実施形態に係る酸素飽和度測定装置10Aを用いた酸素飽和度測定方法を説明する。まず、酸素飽和度測定装置10Aのバンド12が、被測定者の手首に巻かれる。測定対象の動脈は、例えば橈骨動脈24である。なお、本開示では、測定対象の動脈は、橈骨動脈24に限定されず、他の任意の動脈であってもよい。そして、接触面16Aが、手首の内側の橈骨茎状突起20Aの近傍の皮膚に接触させられる。
<Oxygen saturation measurement method>
Next, a method for measuring oxygen saturation using the oxygen saturation measuring device 10A according to the first embodiment will be described. First, the band 12 of the oxygen saturation measuring device 10A is wrapped around the wrist of the person to be measured. The artery to be measured is, for example, the radial artery 24. Note that in the present disclosure, the artery to be measured is not limited to the radial artery 24, and may be any other artery. The contact surface 16A is then brought into contact with the skin near the radial styloid process 20A on the inside of the wrist.
 そして、図1に示すように、接触部16が、橈骨茎状突起20Aと橈側手根屈筋腱22との隙間の窪みの内側に配置される。そして、窪みの下側に位置する橈骨動脈24に対し発光素子から光が照射される。そして、橈骨動脈24からの反射光が、受光素子によって受光される。そして、反射光から取得された脈波信号に基づき、測定部18によって酸素飽和度が測定される。 As shown in FIG. 1, the contact portion 16 is arranged inside the depression in the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22. Then, light is irradiated from the light emitting element to the radial artery 24 located below the depression. Then, the reflected light from the radial artery 24 is received by the light receiving element. Then, the oxygen saturation level is measured by the measurement unit 18 based on the pulse wave signal acquired from the reflected light.
(第1実施形態の作用効果)
 第1実施形態に係る酸素飽和度測定装置10Aによれば、バンド12から手首側に突出する接触部16の接触面16Aが、湾曲形状である。このため、例えば、湾曲形状の接触面16Aを手首の内側の橈骨茎状突起20Aの近傍に接触させた後、接触部16を橈骨茎状突起20Aと橈側手根屈筋腱22との隙間の窪みに沿って窪みの内側に向かって移動させれば、接触部16を隙間の窪みの内側に配置させ易い。すなわち、人体の骨、筋及び腱によって形成される構造上の窪みの形状を活用することによって、接触部16が板状である場合のように、接触部16を手首の内側の皮膚表面に接触させる前に、動脈の位置を予め手探りする必要がない。
(Operations and effects of the first embodiment)
According to the oxygen saturation measurement device 10A according to the first embodiment, the contact surface 16A of the contact portion 16 protruding from the band 12 toward the wrist has a curved shape. For this reason, for example, after bringing the curved contact surface 16A into contact with the vicinity of the radial styloid process 20A on the inside of the wrist, the contact portion 16 is placed in a depression in the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22. By moving the contact portion 16 toward the inside of the recess along the direction, it is easy to arrange the contact portion 16 inside the recess of the gap. That is, by utilizing the shape of the structural depressions formed by the bones, muscles, and tendons of the human body, the contact part 16 can be brought into contact with the skin surface on the inside of the wrist, as in the case where the contact part 16 is plate-shaped. There is no need to grope the location of the artery beforehand.
 また、第1実施形態では、接触部16は、手首の動脈に対して照射される光と手首の動脈からの反射光とに対する透光性を有する。また、バンド12と接触部16との間に平坦な接合面14Aを有する基部14が設けられ、かつ、基部14の接合面14Aに発光素子及び受光素子のうち少なくとも一方が接合される。 Furthermore, in the first embodiment, the contact portion 16 has translucency for light irradiated onto the artery of the wrist and light reflected from the artery of the wrist. Further, a base 14 having a flat bonding surface 14A is provided between the band 12 and the contact portion 16, and at least one of a light emitting element and a light receiving element is bonded to the bonding surface 14A of the base 14.
 ここで、発光素子及び受光素子の電子部品を、湾曲形状を有する接触面16A上に搭載する場合、電子部品が、測定の際に皮膚に直接接触する。このため、電子部品に皮膚から皮脂や汚れ等が付着し易くなり、結果、電子部品の劣化が進む。 Here, when electronic components such as a light emitting element and a light receiving element are mounted on the curved contact surface 16A, the electronic components come into direct contact with the skin during measurement. Therefore, sebum, dirt, and the like from the skin tend to adhere to the electronic components, resulting in accelerated deterioration of the electronic components.
 一方、第1実施形態では、バンド12と接触部16との間の平坦な接合面14A上に発光素子及び受光素子のうち少なくとも一方の電子部品が接合されるので、測定の際、電子部品が、皮膚に直接接触しない。このため、電子部品の劣化を防止できる。 On the other hand, in the first embodiment, at least one of the electronic components of the light emitting element and the light receiving element is bonded on the flat bonding surface 14A between the band 12 and the contact portion 16. , avoid direct contact with skin. Therefore, deterioration of electronic components can be prevented.
 また、第1実施形態では、接触部16の最大幅Wは、3mm以上、7mm以下である。このため、接触部16を橈骨茎状突起20Aと橈側手根屈筋腱22との隙間に配置した状態で、橈骨動脈24の酸素飽和度を測定する際における、装着者の装着時の不快感の抑制と測定の継続とを効率よく両立できる。 Furthermore, in the first embodiment, the maximum width W of the contact portion 16 is 3 mm or more and 7 mm or less. For this reason, when measuring the oxygen saturation level of the radial artery 24 with the contact portion 16 disposed in the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22, the wearer may feel uncomfortable when wearing it. It is possible to efficiently achieve both suppression and continuation of measurement.
 また、第1実施形態では、測定対象の動脈が橈骨動脈24であるため、橈骨動脈24中の酸素飽和度の測定において特に有利である。 Furthermore, in the first embodiment, since the artery to be measured is the radial artery 24, it is particularly advantageous in measuring the oxygen saturation level in the radial artery 24.
 また、第1実施形態に係る酸素飽和度測定装置10Aを用いた酸素飽和度測定方法によれば、湾曲形状の接触面16Aが、手首の内側の橈骨茎状突起20Aの近傍の皮膚に接触する。また、接触部16が、橈骨茎状突起20Aと橈側手根屈筋腱22との隙間の窪みの内側に配置される。そして、橈骨動脈24からの反射光から取得された脈波信号に基づき酸素飽和度が測定される。 Further, according to the oxygen saturation measuring method using the oxygen saturation measuring device 10A according to the first embodiment, the curved contact surface 16A contacts the skin near the radial styloid process 20A on the inside of the wrist. . Further, the contact portion 16 is arranged inside the depression in the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22. Then, the oxygen saturation level is measured based on the pulse wave signal obtained from the reflected light from the radial artery 24.
 例えば、接触面16Aを橈骨茎状突起20Aの近傍に接触させた時点では接触面16Aが窪みの最深部に到達していない場合であっても、接触面16Aが湾曲形状であるので、接触面16Aを窪みの表面の湾曲面に沿って窪みの内側に送り込み易い。このため、本開示の酸素飽和度測定装置10Aの場合と同様、手首の内側における接触部16の配置位置を容易に決定できると共に、酸素飽和度の測定の中断を抑制することができる。 For example, even if the contact surface 16A has not reached the deepest part of the recess when the contact surface 16A is brought into contact with the vicinity of the radial styloid process 20A, since the contact surface 16A has a curved shape, the contact surface 16A can be easily fed into the hollow along the curved surface of the hollow. Therefore, as in the case of the oxygen saturation measurement device 10A of the present disclosure, the arrangement position of the contact portion 16 on the inside of the wrist can be easily determined, and interruption of oxygen saturation measurement can be suppressed.
-第2実施形態-
 第2実施形態では、センサが配置されると共に手首の皮膚に接触する接触面16Aを有する接触部16が、バンド12の外側からの操作でスライド可能である。以下、本開示の第2実施形態を、図7~図9を参照して説明する。
-Second embodiment-
In the second embodiment, a contact portion 16 having a contact surface 16A that contacts the skin of the wrist and where a sensor is disposed can be slid by operating from the outside of the band 12. A second embodiment of the present disclosure will be described below with reference to FIGS. 7 to 9.
 なお、以下、第2実施形態において第1実施形態における部材と同名の部材について、第1実施形態の場合と同様の機能を有するため重複説明を省略すると共に、第1実施形態との構成上の相違点に関し主に説明する。また、第2実施形態の構成から導かれる作用効果について、第1実施形態の場合と同様の作用効果である場合、重複説明を省略すると共に、第1実施形態と異なる作用効果に関し主に説明する。 Note that, in the following, members in the second embodiment having the same names as members in the first embodiment have the same functions as in the first embodiment, so redundant explanations will be omitted, and there are differences in structure with the first embodiment. I will mainly explain the differences. Further, if the effects derived from the configuration of the second embodiment are similar to those of the first embodiment, duplicate explanations will be omitted, and the effects that are different from the first embodiment will be mainly explained. .
<酸素飽和度測定装置>
 図7に示すように、第2実施形態に係る酸素飽和度測定装置10Bは、バンド12と、スライダー部30と、接触部16と、操作部40と、発光素子と、受光素子と、測定部18と、を備える。
<Oxygen saturation measuring device>
As shown in FIG. 7, the oxygen saturation measuring device 10B according to the second embodiment includes a band 12, a slider section 30, a contact section 16, an operation section 40, a light emitting element, a light receiving element, and a measuring section. 18.
(バンド)
 第2実施形態では、バンド12は、第1本体部12Aと、第1本体部12Aと手首の周方向Cにおいて離れて設けられた第2本体部12Bと、一対のガイド部と、で構成される。一対のガイド部は、第1ガイド部12Cと第2ガイド部12Dとによって形成される。一対のガイド部は、第1本体部12Aと第2本体部12Bとをそれぞれ接続すると共に、前腕の延びる方向Eにおいて互いに離れて設けられる。一対のガイド部は、貫通孔12Eを挟んで、手首の周方向Cに沿って延びる。貫通孔12Eは、第1本体部と第2本体部と第1ガイド部と第2ガイド部とで囲まれることによって形成される。貫通孔12Eは、手首の周方向Cに沿って延びる。
(band)
In the second embodiment, the band 12 includes a first body part 12A, a second body part 12B provided apart from the first body part 12A in the circumferential direction C of the wrist, and a pair of guide parts. Ru. The pair of guide parts is formed by a first guide part 12C and a second guide part 12D. The pair of guide parts connect the first main body part 12A and the second main body part 12B, respectively, and are provided apart from each other in the direction E in which the forearm extends. The pair of guide portions extend along the circumferential direction C of the wrist with the through hole 12E in between. The through hole 12E is formed by being surrounded by the first body part, the second body part, the first guide part, and the second guide part. The through hole 12E extends along the circumferential direction C of the wrist.
 第2実施形態では、第1本体部12Aと第2本体部12Bと第1ガイド部12Cと第2ガイド部12Dとからなる4つの部材は、同じ素材によって一体的に作製されているが、本開示では、これに限定されない。4つの部材の一部又はすべてが個別に作成され、かつ、互いに連結されてもよい。 In the second embodiment, the four members consisting of the first body part 12A, the second body part 12B, the first guide part 12C, and the second guide part 12D are integrally made of the same material. The disclosure is not limited to this. Some or all of the four members may be made individually and connected to each other.
(貫通孔)
 第2実施形態では、貫通孔12Eは、平面視で矩形状であるが、第2実施形態では、これに限定されず、例えば線状等、他の形状で構成されてもよい。なお、本開示では「平面視」は、バンド12の厚み方向(すなわち、手首の径方向D)に沿って見た状態を意味する。また、本開示では、バンド12が手首に巻かれた状態で、接触部16をバンド12の外側からスライド可能であれば、貫通孔12Eは必須ではない。
(through hole)
In the second embodiment, the through hole 12E has a rectangular shape in plan view, but the second embodiment is not limited to this, and may have other shapes, such as a linear shape. Note that in the present disclosure, "plan view" means a state viewed along the thickness direction of the band 12 (that is, the radial direction D of the wrist). Further, in the present disclosure, the through hole 12E is not essential as long as the contact portion 16 can be slid from the outside of the band 12 while the band 12 is wrapped around the wrist.
(スライダー部)
 図7に示すように、スライダー部30は、バンド12の貫通孔12Eの内側に配置される。スライダー部30は、基体部32と、一対の挟持部と、操作部40と、を有する。一対の挟持部は、第1挟持部34Aと、第2挟持部34Bとによって形成される。スライダー部30の素材としては、樹脂や金属等の材料を適宜採用できる。
(slider section)
As shown in FIG. 7, the slider section 30 is arranged inside the through hole 12E of the band 12. The slider section 30 includes a base section 32, a pair of clamping sections, and an operating section 40. The pair of clamping parts are formed by a first clamping part 34A and a second clamping part 34B. As the material of the slider section 30, materials such as resin and metal can be appropriately adopted.
(基体部)
 基体部32は、バンド12の貫通孔12Eの内側に配置される。「基体部32が貫通孔12Eの内側に配置される」とは、図7に示すように、平面視で、基体部32が貫通孔12Eの内側に配置される状態であり得る。換言すると、図8に示すように、手首の径方向Dにおいては、基体部32の上下方向の一部が、貫通孔12Eの外側に突出することは、妨げられない。
(base part)
The base portion 32 is arranged inside the through hole 12E of the band 12. “The base portion 32 is disposed inside the through hole 12E” may be a state in which the base portion 32 is disposed inside the through hole 12E in plan view, as shown in FIG. In other words, as shown in FIG. 8, in the radial direction D of the wrist, a portion of the base portion 32 in the vertical direction is not prevented from protruding outside the through hole 12E.
(挟持部)
 図7に示すように、第1挟持部34Aと第2挟持部34Bとによって形成される一対の挟持部は、基体部32のバンドの幅方向(すなわち、前腕の延びる方向E)における両端に設けられる。第1挟持部34Aは、基体部32のバンド12の幅方向における一端(図7中の左端)に設けられると共に、第1ガイド部12Cをスライド可能に手首の径方向Dで挟む。
(Holding part)
As shown in FIG. 7, a pair of clamping parts formed by the first clamping part 34A and the second clamping part 34B are provided at both ends of the band of the base part 32 in the width direction (i.e., the direction E in which the forearm extends). It will be done. The first holding part 34A is provided at one end (the left end in FIG. 7) of the base part 32 in the width direction of the band 12, and slidably holds the first guide part 12C in the radial direction D of the wrist.
 第2挟持部34Bは、基体部32のバンド12の幅方向における他端(図7中の右端)に設けられる。第2挟持部34Bは、第2ガイド部12Dをスライド可能に、手首の径方向(図8中の径方向D)において挟む。すなわち、第1挟持部34Aと第2挟持部34Bとは、第1ガイド部12Cと第3ガイド部12Dとに対してスライド可能な状態で設けられる。また、第1挟持部34Aと第1ガイド部12Cとの間、及び、第2挟持部34Bと第3ガイド部12Dとの間に、基体部32が第1ガイド部12Cと第3ガイド部12Dとから脱落しない程度の隙間が形成された状態で、第1挟持部34Aと第2挟持部34Bとは、スライド可能に設けられ得る。又は、第1挟持部34Aと第1ガイド部12Cとが接触し、かつ、第2挟持部34Bと第3ガイド部12Dとが接触した状態で、第1挟持部34Aと第2挟持部34Bとは、スライド可能に設けられ得る。 The second holding portion 34B is provided at the other end of the base portion 32 in the width direction of the band 12 (the right end in FIG. 7). The second holding part 34B slidably holds the second guide part 12D in the radial direction of the wrist (radial direction D in FIG. 8). That is, the first clamping part 34A and the second clamping part 34B are provided in a slidable state with respect to the first guide part 12C and the third guide part 12D. In addition, the base portion 32 is located between the first holding portion 34A and the first guide portion 12C, and between the second holding portion 34B and the third guide portion 12D. The first clamping part 34A and the second clamping part 34B may be provided so as to be slidable with a gap formed therebetween to prevent them from falling off. Alternatively, in a state where the first clamping part 34A and the first guide part 12C are in contact with each other, and the second clamping part 34B and the third guide part 12D are in contact with each other, the first clamping part 34A and the second clamping part 34B are in contact with each other. may be slidably provided.
 なお、第2実施形態では、一対のガイド部と一対の挟持部とによって基体部32を貫通孔12Eの内側でスライドさせる構成が例示されたが、本開示では、これに限定されない。本開示では、基体部32を貫通孔12Eの内側でスライドさせる構成として、例えば、第1ガイド部12Cと第2ガイド部12Dとのそれぞれに、手首の周方向Cに沿って複数の留め部が形成されてもよい。 Although the second embodiment exemplifies a configuration in which the base portion 32 is slid inside the through hole 12E by a pair of guide portions and a pair of clamping portions, the present disclosure is not limited to this. In the present disclosure, as a configuration in which the base portion 32 is slid inside the through hole 12E, for example, each of the first guide portion 12C and the second guide portion 12D has a plurality of fastening portions along the circumferential direction C of the wrist. may be formed.
 複数の留め部は、例えば切れ目のように孔幅が狭く形成された貫通孔であってよい。留め部は、例えば、前腕の延びる方向Eに沿った直線上に、第1ガイド部12Cと第2ガイド部12Dとにそれぞれ配置されることによって、一組の留め部として形成できる。そして、一組の留め部が複数、手首の周方向Cに沿って形成されてよい。 The plurality of fastening parts may be through holes formed with narrow hole widths, for example, like cuts. For example, the fasteners can be formed as a set of fasteners by being arranged on the first guide part 12C and the second guide part 12D, respectively, on a straight line along the direction E in which the forearm extends. A plurality of sets of fasteners may be formed along the circumferential direction C of the wrist.
 また、一組の留め部に対応する一組の留め具が、基体部32における前腕の延びる方向Eの両端にそれぞれ設けられてよい。留め具は、例えば、カフスボタンのように先端が基端より拡径された形状を有してよい。留め具の先端は、貫通孔に差し込み可能であると共に、基端の位置で留め部の切れ目に挟まれることによって着脱自在に取り付けることができる。手首の周方向Cに沿って複数設けられた留め部の中で留め具の取り付け位置を変更することによって、基体部32を貫通孔12Eの内側でスライドさせることが可能である。 Furthermore, a set of fasteners corresponding to the set of fasteners may be provided at both ends of the base portion 32 in the direction E in which the forearm extends. The fastener may have a shape in which the distal end is larger in diameter than the proximal end, for example, like a cufflink. The distal end of the fastener can be inserted into the through hole, and can be detachably attached by being sandwiched between the cuts in the fastener at the base end position. By changing the mounting position of the fasteners among the plurality of fasteners provided along the circumferential direction C of the wrist, it is possible to slide the base portion 32 inside the through hole 12E.
(操作部)
 図8に示すように、第2実施形態では、操作部40は、スライダー部30に連結され、手首と反対側におけるバンド12の外側に配置される。なお、本開示では、操作部40は、スライダー部30又は接触部16に連結されればよい。操作部40が操作されることによって、スライダー部30は、手首の周方向Cに沿ってスライド可能である。
(Operation unit)
As shown in FIG. 8, in the second embodiment, the operating section 40 is connected to the slider section 30 and arranged on the outside of the band 12 on the side opposite to the wrist. Note that in the present disclosure, the operation section 40 may be connected to the slider section 30 or the contact section 16. By operating the operating section 40, the slider section 30 can slide along the circumferential direction C of the wrist.
 図9に示すように、第2実施形態では、前腕の延びる方向Eにおいて、基体部32と第1ガイド部12Cとの間、及び、基体部32と第2ガイド部12Dとの間の両方に、空隙Aが形成される。空隙Aは、貫通孔12Eの一部である。このため、形成された空隙Aの内側で、スライダー部30は、前腕の延びる方向Eに沿ってスライドすることも可能である。 As shown in FIG. 9, in the second embodiment, both between the base portion 32 and the first guide portion 12C and between the base portion 32 and the second guide portion 12D in the direction E in which the forearm extends. , a void A is formed. The void A is a part of the through hole 12E. Therefore, the slider portion 30 can also slide along the direction E in which the forearm extends inside the formed gap A.
 なお、本開示では、基体部32と第1ガイド部12Cとの間、及び、基体部32と第2ガイド部12Dとの間のうち少なくとも一方の間に空隙Aが形成されればよい。また、本開示では、空隙Aは必須ではない。 Note that in the present disclosure, the gap A may be formed between at least one of the base portion 32 and the first guide portion 12C and between the base portion 32 and the second guide portion 12D. Further, in the present disclosure, the void A is not essential.
(加圧装置)
 第2実施形態に係る酸素飽和度測定装置10Bは、更に、接触部16に対し手首と反対側から手首に向かう力を加える加圧装置50を備える。なお、本開示では、加圧装置50は必須ではない。
(pressure device)
The oxygen saturation measuring device 10B according to the second embodiment further includes a pressurizing device 50 that applies force to the contact portion 16 from the side opposite to the wrist toward the wrist. Note that in the present disclosure, the pressurizing device 50 is not essential.
 具体的には、図8に示すように、基体部32には手首の径方向Dに沿って貫通する孔32Aが設けられ、設けられた孔32Aの内面に雌ネジ部が形成される。また、操作部40の手首側には棒状部材42が設けられ、棒状部材42の表面には雄ネジ部が、基体部32の孔32Aの雌ネジ部に対応して形成される。 Specifically, as shown in FIG. 8, the base portion 32 is provided with a hole 32A that penetrates along the radial direction D of the wrist, and a female screw portion is formed on the inner surface of the provided hole 32A. Further, a rod-shaped member 42 is provided on the wrist side of the operating portion 40, and a male threaded portion is formed on the surface of the rod-shaped member 42 in correspondence with a female threaded portion of the hole 32A of the base portion 32.
 すなわち、第2実施形態の加圧装置50は、手首の径方向Dにおけるスライダー部30からの突出量を調整するねじ送り機構である。なお、本開示では、加圧装置としては、これに限定されない。例えば、ばね力を用いて接触部16に対し手首に向かう力が加えられる機構等、他の機構によって加圧装置が構成されてもよい。 That is, the pressurizing device 50 of the second embodiment is a screw feeding mechanism that adjusts the amount of protrusion from the slider portion 30 in the radial direction D of the wrist. Note that in the present disclosure, the pressurizing device is not limited to this. For example, the pressurizing device may be configured by another mechanism, such as a mechanism that applies a force toward the wrist to the contact portion 16 using a spring force.
 また、棒状部材42の手首側の端部には、板状の連結部材44が設けられ、連結部材44の手首側には基部14が設けられる。基部14の連結部材44と反対側には、接触部16が設けられる。第2実施形態では、スライダー部30には加圧装置50を介して、接触部16が取り付けられる。このため、接触部16は、スライダー部30と共に手首の周方向Cに沿ってスライドする。 Furthermore, a plate-shaped connecting member 44 is provided at the end of the rod-shaped member 42 on the wrist side, and a base 14 is provided on the wrist side of the connecting member 44. A contact portion 16 is provided on the opposite side of the base portion 14 from the connecting member 44 . In the second embodiment, the contact portion 16 is attached to the slider portion 30 via a pressure device 50. Therefore, the contact portion 16 slides along the circumferential direction C of the wrist together with the slider portion 30.
 スライダー部30のスライドによってセンサの配置位置が決定された後、加圧装置50のスライダー部30からの突出量を増やすようにねじを回すことによって、決定されたセンサの配置位置が固定される。また、センサの配置位置が一旦固定された後であっても、スライダー部30からの突出量を減らすように加圧装置50のねじを回すことによって、センサの配置位置の固定を緩めることができると共に、再度、スライダー部30をスライドさせることが可能である。すなわち、バンド12を緩める又は外すことなく、バンド12が被測定者の手首に巻かれた状態のまま、センサの配置位置を所望の位置に変更できる。 After the sensor placement position is determined by sliding the slider portion 30, the determined sensor placement position is fixed by turning the screw to increase the amount of protrusion of the pressure device 50 from the slider portion 30. Further, even after the sensor placement position is once fixed, the fixation of the sensor placement position can be loosened by turning the screw of the pressurizing device 50 so as to reduce the amount of protrusion from the slider portion 30. At the same time, it is possible to slide the slider section 30 again. That is, the sensor arrangement position can be changed to a desired position without loosening or removing the band 12 while the band 12 remains wrapped around the wrist of the subject.
 なお、本開示では、接触部16は、加圧装置50を介することなくスライダー部30に直接取り付けられてもよい。また、接触部16は、加圧装置50以外の部材を介してスライダー部30に間接的に取り付けられてもよい。また、第2実施形態では、板状の操作部40が例示されたが、本開示では、これに限定されない。例えば、図8中の基体部32の上部に、上側に突出する突出部が、被測定者が手指で摘まむことが可能であるように設けられてもよい。 Note that in the present disclosure, the contact portion 16 may be directly attached to the slider portion 30 without using the pressurizing device 50. Further, the contact portion 16 may be indirectly attached to the slider portion 30 via a member other than the pressure device 50. Further, in the second embodiment, the plate-shaped operation unit 40 is illustrated, but the present disclosure is not limited to this. For example, a protrusion that protrudes upward may be provided on the upper part of the base portion 32 in FIG. 8 so that the person to be measured can pinch it with his or her fingers.
<酸素飽和度測定方法>
 次に、第2実施形態に係る酸素飽和度測定装置10Bを用いた酸素飽和度測定方法を説明する。第1実施形態の場合と同様、まず、酸素飽和度測定装置10Bのバンド12が被測定者の手首に巻かれる。測定対象の動脈は、例えば橈骨動脈24である。そして、接触面16Aが、手首の内側の橈骨茎状突起20Aの近傍の皮膚に接触させられる。
<Oxygen saturation measurement method>
Next, a method for measuring oxygen saturation using the oxygen saturation measuring device 10B according to the second embodiment will be described. As in the case of the first embodiment, first, the band 12 of the oxygen saturation measuring device 10B is wrapped around the wrist of the subject. The artery to be measured is, for example, the radial artery 24. The contact surface 16A is then brought into contact with the skin near the radial styloid process 20A on the inside of the wrist.
 第2実施形態では、接触部16を隙間の窪みに配置する前に、スライダー部30をスライドさせることによって、接触部16を手首の内側の皮膚表面の上で測定対象の動脈近傍の初期位置に配置することができる。或いは、接触部16を初期位置に配置した後、配置位置の調整のため、スライダー部30をスライドさせることによって、接触部16を手首の内側の皮膚表面の上で測定対象の動脈近傍で、初期位置とは異なる位置に配置することができる。 In the second embodiment, before placing the contact part 16 in the recess of the gap, by sliding the slider part 30, the contact part 16 is brought to an initial position near the artery to be measured on the inner skin surface of the wrist. can be placed. Alternatively, after placing the contact part 16 at the initial position, by sliding the slider part 30 to adjust the position, the contact part 16 can be placed on the skin surface on the inside of the wrist near the artery to be measured. It can be placed in a different position.
(第2実施形態の作用効果)
 第2実施形態に係る酸素飽和度測定装置10Bでは、スライダー部30は、バンド12の貫通孔12Eの内側に配置されると共に、手首の周方向Cに沿ってスライド可能である。また、手首に接触する接触面16Aを有する接触部16が、スライダー部30に取り付けられる。また、スライダー部30又は接触部16に連結され手首と反対側におけるバンド12の外側に、操作部40が配置される。すなわち、バンド12が手首に巻かれた状態であっても、バンド12の外側から操作部40を操作してスライダー部30をスライドさせることが可能である。このため、被測定者は、バンド12を緩めることなく、かつ、バンド12の内面を露出させることなく、スライダー部30に取り付けられた接触部16を手首の周方向Cに沿ってスライドさせることが可能になる。
(Operations and effects of the second embodiment)
In the oxygen saturation measuring device 10B according to the second embodiment, the slider section 30 is arranged inside the through hole 12E of the band 12 and is slidable along the circumferential direction C of the wrist. Further, a contact portion 16 having a contact surface 16A that contacts the wrist is attached to the slider portion 30. Further, an operating section 40 is connected to the slider section 30 or the contact section 16 and arranged on the outside of the band 12 on the side opposite to the wrist. That is, even when the band 12 is wrapped around the wrist, it is possible to slide the slider section 30 by operating the operating section 40 from outside the band 12. Therefore, the subject can slide the contact part 16 attached to the slider part 30 along the circumferential direction C of the wrist without loosening the band 12 and without exposing the inner surface of the band 12. It becomes possible.
 このため、第2実施形態によれば、手首に装着された状態であっても、測定対象の動脈に対するセンサの配置位置を容易に調整できる。 Therefore, according to the second embodiment, even when the sensor is worn on the wrist, the placement position of the sensor relative to the artery to be measured can be easily adjusted.
 また、第2実施形態では、スライダー部30の基体部32が、バンド12の貫通孔12Eの内側に配置される。また、スライダー部30の基体部32の両端には、一対のガイド部のそれぞれを手首の径方向Dにおいてスライド可能に挟む挟持部が、対応して設けられる。このため、一対のガイド部に対して一対の挟持部をスライドさせることによって、スライダー部30をスライドさせることが可能になる。 Furthermore, in the second embodiment, the base portion 32 of the slider portion 30 is arranged inside the through hole 12E of the band 12. In addition, at both ends of the base portion 32 of the slider portion 30, there are correspondingly provided holding portions that slidably sandwich each of the pair of guide portions in the radial direction D of the wrist. Therefore, by sliding the pair of clamping parts with respect to the pair of guide parts, it becomes possible to slide the slider part 30.
 また、第2実施形態では、バンドの幅方向(すなわち、前腕の延びる方向E)において、基体部32と第1ガイド部12Cとの間、及び、基体部32と第2ガイド部12Dとの間のうち少なくとも一方の間に空隙Aが形成される。また、形成された空隙Aの内側でスライダー部30が、前腕の延びる方向Eに沿ってスライド可能である。スライダー部30に取り付けられた接触部16を、手首の周方向Cに加え、前腕の延びる方向Eに沿ってもスライド可能になるため、センサの配置位置をより調整し易い。 Further, in the second embodiment, in the width direction of the band (that is, the direction E in which the forearm extends), between the base portion 32 and the first guide portion 12C, and between the base portion 32 and the second guide portion 12D. A gap A is formed between at least one of them. Moreover, the slider part 30 can slide inside the formed gap A along the direction E in which the forearm extends. Since the contact part 16 attached to the slider part 30 can be slid not only in the circumferential direction C of the wrist but also in the direction E in which the forearm extends, it is easier to adjust the position of the sensor.
 また、スライダー部30は、バンド12に形成された貫通孔12Eの内側で、手首の周方向Cと前腕の延びる方向Eとの2方向によって定義される平面内の任意の位置に移動可能である。換言すると、スライダー部30は、2方向において互いに影響を受けることなく、2方向において互いに独立してスライド可能である。このため、特表2017-516539のように、回転中心から一定の半径を有する円周上でのみ配置位置を変える場合と比べ、配置位置の調整可能範囲が広い。 Furthermore, the slider portion 30 is movable to any position within a plane defined by two directions, the circumferential direction C of the wrist and the extending direction E of the forearm, inside the through hole 12E formed in the band 12. . In other words, the slider section 30 can slide independently in two directions without being influenced by each other in the two directions. For this reason, the adjustable range of the arrangement position is wider than when the arrangement position is changed only on the circumference having a constant radius from the center of rotation, as in PCT International Publication No. 2017-516539.
 また、第2実施形態は、接触部16に対し手首と反対側から手首に向かう力を加える加圧装置50を備える。このため、手首の測定対象の動脈に対する接触部16の配置位置を安定的に維持できる。 The second embodiment also includes a pressure device 50 that applies force to the contact portion 16 from the side opposite to the wrist toward the wrist. Therefore, the position of the contact portion 16 relative to the artery to be measured in the wrist can be stably maintained.
 また、第2実施形態に係る酸素飽和度測定装置10Bを用いた酸素飽和度測定方法によれば、酸素飽和度測定装置10Bが手首に装着された状態であっても、測定対象の動脈に対するセンサの配置位置を容易に調整できる。 Further, according to the oxygen saturation measuring method using the oxygen saturation measuring device 10B according to the second embodiment, even when the oxygen saturation measuring device 10B is worn on the wrist, the sensor for the artery to be measured can be used. The placement position can be easily adjusted.
-第3実施形態-
 第3実施形態では、酸素飽和度を測定するための受光素子が2つ以上設けられると共に、2つ以上の受光素子の中から測定用受光素子が、定量的に選択される。以下、本開示の第3実施形態を、図10~図12を参照して説明する。
-Third embodiment-
In the third embodiment, two or more light receiving elements for measuring oxygen saturation are provided, and a measuring light receiving element is quantitatively selected from the two or more light receiving elements. A third embodiment of the present disclosure will be described below with reference to FIGS. 10 to 12.
 なお、以下、第3実施形態において第1又は第2実施形態における部材と同名の部材について、第1又は第2実施形態の場合と同様の機能を有するため重複説明を省略すると共に、第1又は第2実施形態との構成上の相違点に関し主に説明する。また、第3実施形態の構成から導かれる作用効果について、第1又は第2実施形態の場合と同様の作用効果である場合、重複説明を省略すると共に、第1又は第2実施形態と異なる作用効果に関し主に説明する。 Note that, in the third embodiment, members having the same names as members in the first or second embodiment have the same functions as those in the first or second embodiment, so redundant explanation will be omitted, and The differences in configuration from the second embodiment will be mainly explained. Regarding the effects derived from the configuration of the third embodiment, if the effects are similar to those of the first or second embodiment, redundant explanation will be omitted, and effects different from those of the first or second embodiment will be omitted. I will mainly explain the effects.
<酸素飽和度測定装置>
 図10中に例示された第3実施形態に係る酸素飽和度測定装置10Cは、第1実施形態と同様に3つの発光素子と5つの受光素子とを備えると共に、第2実施形態で説明したスライダー部30と同様のスライダー部を備える。なお、基部、接触部及びスライダー部等の図示は、図10中では見易さのため省略する。
<Oxygen saturation measuring device>
The oxygen saturation measuring device 10C according to the third embodiment illustrated in FIG. 10 includes three light emitting elements and five light receiving elements as in the first embodiment, and the slider described in the second embodiment. A slider section similar to section 30 is provided. Note that illustrations of the base, contact portion, slider portion, etc. are omitted in FIG. 10 for ease of viewing.
 一方、第3実施形態では、測定部18が、受光素子決定部と、判定部と、分布作成部と、発光素子決定部と、制御部と、を有する点が、第2実施形態と異なる。なお、本開示では、受光素子決定部と、判定部と、分布作成部と、発光素子決定部と、制御部とのうち一部又はすべてが、測定部18とは別に配置されてもよい。 On the other hand, the third embodiment differs from the second embodiment in that the measurement unit 18 includes a light receiving element determining unit, a determining unit, a distribution creating unit, a light emitting element determining unit, and a control unit. Note that in the present disclosure, some or all of the light receiving element determining section, the determining section, the distribution creating section, the light emitting element determining section, and the control section may be arranged separately from the measuring section 18.
(脈波信号)
 第3実施形態では、「第1の脈波信号」は、第1の受光素子PD1で受光された反射光から取得された脈波信号である。また、「第2の脈波信号」は、第2の受光素子PD2で受光された反射光から取得された脈波信号である。また、「第3の脈波信号」は、第3の受光素子PD3で受光された反射光から取得された脈波信号である。また、「第4の脈波信号」は、第4の受光素子PD4で受光された反射光から取得された脈波信号である。また、「第5の脈波信号」は、第5の受光素子PD5で受光された反射光から取得された脈波信号である。
(pulse wave signal)
In the third embodiment, the "first pulse wave signal" is a pulse wave signal acquired from the reflected light received by the first light receiving element PD1. Moreover, the "second pulse wave signal" is a pulse wave signal acquired from the reflected light received by the second light receiving element PD2. Moreover, the "third pulse wave signal" is a pulse wave signal acquired from the reflected light received by the third light receiving element PD3. Moreover, the "fourth pulse wave signal" is a pulse wave signal acquired from the reflected light received by the fourth light receiving element PD4. Moreover, the "fifth pulse wave signal" is a pulse wave signal acquired from the reflected light received by the fifth light receiving element PD5.
(受光素子決定部)
 受光素子決定部は、それぞれの受光素子に接続される。第3実施形態では、受光素子決定部は、第1の脈波信号と第2の脈波信号と第3の脈波信号と第4の脈波信号と第5の脈波信号とのうち、より大きな振幅を有する脈波信号が受光された受光素子を、測定用受光素子として決定する。
(Light receiving element determining section)
The light receiving element determining section is connected to each light receiving element. In the third embodiment, the light-receiving element determining unit selects one of the first pulse wave signal, the second pulse wave signal, the third pulse wave signal, the fourth pulse wave signal, and the fifth pulse wave signal. The light receiving element that receives the pulse wave signal having the larger amplitude is determined as the measuring light receiving element.
 なお、本開示では、少なくとも2つの受光素子が用いられればよい。すなわち、本開示では、受光素子決定部が、第1の脈波信号と第2の脈波信号とのうち、より大きな振幅を有する方の脈波信号が受光された受光素子を、測定用受光素子として決定すればよい。また、測定用受光素子の決定に際し、照射する光の種類としては、赤色光及び赤外光のうち任意の光を選択できる。ただし、対比の観点から、同じ種類の光が用いられることが好ましい。 Note that in the present disclosure, at least two light receiving elements may be used. That is, in the present disclosure, the light-receiving element determining unit selects the light-receiving element that has received a pulse wave signal having a larger amplitude between the first pulse wave signal and the second pulse wave signal as the light-receiving element for measurement. It may be determined as an element. Furthermore, when determining the light receiving element for measurement, any type of light to be irradiated can be selected from among red light and infrared light. However, from the viewpoint of comparison, it is preferable that the same type of light is used.
(判定部)
 判定部は、それぞれの受光素子に接続される。第3実施形態では、判定部は、第1の脈波信号と第2の脈波信号と第3の脈波信号と第4の脈波信号と第5の脈波信号とが、予め設定された測定精度を達成する観点に基づいて予め設定された基準値を満たすどうかを判定する。なお、本開示では、判定部は、少なくとも、第1の脈波信号と第2の脈波信号とが、予め設定された測定精度を達成する観点に基づいて、基準値を満たすかどうかを判定すればよい。
(Judgment Department)
The determination section is connected to each light receiving element. In the third embodiment, the determination unit is configured such that the first pulse wave signal, the second pulse wave signal, the third pulse wave signal, the fourth pulse wave signal, and the fifth pulse wave signal are set in advance. It is determined whether a preset reference value is satisfied based on the viewpoint of achieving measurement accuracy. Note that in the present disclosure, the determination unit determines whether at least the first pulse wave signal and the second pulse wave signal satisfy a reference value based on the viewpoint of achieving a preset measurement accuracy. do it.
 なお、基準値を満たす脈波信号が複数取得される場合には、例えば酸素飽和度の測定精度を高める観点から、複数の脈波信号のうちでより適切な脈波信号を抽出する抽出条件が設定されてよい。抽出条件としては、例えば、基準値を満たす複数の脈波信号のうち、最も大きい振幅を有する脈波信号が取得された受光素子を、測定用受光素子として決定することができる。 Note that when multiple pulse wave signals that meet the standard value are acquired, extraction conditions are set to extract a more appropriate pulse wave signal from among the multiple pulse wave signals, for example, from the perspective of increasing the measurement accuracy of oxygen saturation. May be set. As an extraction condition, for example, a light receiving element from which a pulse wave signal having the largest amplitude among a plurality of pulse wave signals satisfying a reference value is acquired can be determined as a measurement light receiving element.
(分布作成部)
 分布作成部は、第1の発光素子LED1の光の反射光が第1の受光素子PD1と第2の受光素子PD2と第3の受光素子PD3とのそれぞれによって受光された場合、受光された反射光の手首の周方向Cに沿った振幅の分布を「第1の振幅の分布」として作成する。また、分布作成部は、第2の発光素子LED2の光の反射光が第1の受光素子PD1と第2の受光素子PD2と第3の受光素子PD3とのそれぞれによって受光された場合、受光された反射光の手首の周方向Cに沿った振幅の分布を「第2の振幅の分布」として作成する。
(Distribution creation department)
When the reflected light of the light of the first light emitting element LED1 is received by each of the first light receiving element PD1, the second light receiving element PD2, and the third light receiving element PD3, the distribution creation unit calculates the received reflection light. The amplitude distribution along the circumferential direction C of the wrist of light is created as a "first amplitude distribution." Further, the distribution creation unit determines whether the reflected light from the second light emitting element LED2 is received by each of the first light receiving element PD1, the second light receiving element PD2, and the third light receiving element PD3. The amplitude distribution of the reflected light along the circumferential direction C of the wrist is created as a "second amplitude distribution".
 また、分布作成部は、第3の発光素子LED3の光の反射光が第1の受光素子PD1と第2の受光素子PD2と第3の受光素子PD3とのそれぞれによって受光された場合、受光された反射光の手首の周方向Cに沿った振幅の分布を「第3の振幅の分布」として作成する。なお、本開示では、分布作成部は、少なくとも、第1の振幅の分布と第2の振幅の分布を作成すればよい。また、振幅の分布の作成の際、それぞれの発光素子の光の照射のタイミングは、ずらせばよい。 Further, the distribution creation unit determines whether the reflected light of the third light emitting element LED3 is received by each of the first light receiving element PD1, the second light receiving element PD2, and the third light receiving element PD3. The amplitude distribution of the reflected light along the circumferential direction C of the wrist is created as a "third amplitude distribution". Note that in the present disclosure, the distribution creation unit may create at least the first amplitude distribution and the second amplitude distribution. Furthermore, when creating the amplitude distribution, the timing of light irradiation from each light emitting element may be staggered.
(発光素子決定部)
 発光素子決定部は、作成された第1の振幅の分布と第2の振幅の分布と第3の振幅の分布のうち、予め設定された基準条件を満たす分布が作成された発光素子を測定用発光素子として決定する。基準条件は、発光素子が動脈の上側に位置することに対応して設定される。決定された測定用発光素子の光の反射光の脈波信号に基づき、酸素飽和度が測定される。なお、本開示では、発光素子決定部は、少なくとも、第1の振幅の分布と第2の振幅の分布とに基づき、測定用発光素子を決定すればよい。
(Light emitting element determining section)
The light-emitting element determination unit selects for measurement the light-emitting element for which a distribution satisfying a preset standard condition is created among the created first amplitude distribution, second amplitude distribution, and third amplitude distribution. Determine it as a light emitting element. The reference condition is set so that the light emitting element is located above the artery. Oxygen saturation is measured based on the determined pulse wave signal of the reflected light from the light emitting element for measurement. Note that in the present disclosure, the light emitting element determining unit may determine the light emitting element for measurement based on at least the first amplitude distribution and the second amplitude distribution.
(制御部)
 制御部は、第1の発光素子LED1と第2の発光素子LED2と第3の受光素子PD3とのうち、測定用発光素子として決定された1つの発光素子にのみ通電を継続する。一方、制御部は、測定用発光素子として決定されなかった他の2つの発光素子への通電を停止する。なお、本開示では、制御部は、少なくとも、第1の発光素子LED1と第2の発光素子LED2との間で通電の有無を決定すればよい。
(control unit)
The control unit continues to energize only one light emitting element determined as the measurement light emitting element among the first light emitting element LED1, the second light emitting element LED2, and the third light receiving element PD3. On the other hand, the control unit stops energizing the other two light emitting elements that have not been determined as measurement light emitting elements. Note that in the present disclosure, the control unit may at least determine whether or not to energize between the first light emitting element LED1 and the second light emitting element LED2.
<酸素飽和度測定方法>
 次に、第3実施形態に係る酸素飽和度測定装置10Cを用いた酸素飽和度測定方法を説明する。第1及び第2実施形態の場合と同様、図11中のステップS1において、まず、酸素飽和度測定装置10Cのバンド12が、被測定者の手首に巻かれる。測定対象の動脈は、例えば橈骨動脈24である。
<Oxygen saturation measurement method>
Next, a method for measuring oxygen saturation using the oxygen saturation measuring device 10C according to the third embodiment will be described. As in the first and second embodiments, in step S1 in FIG. 11, first, the band 12 of the oxygen saturation measuring device 10C is wrapped around the wrist of the subject. The artery to be measured is, for example, the radial artery 24.
 次に、接触面16Aが、手首の内側の橈骨茎状突起20Aの近傍の皮膚に接触させられる。そして、ステップS2において、センサユニットが、橈骨茎状突起20Aと橈側手根屈筋腱22との隙間の内側に配置される。 Next, the contact surface 16A is brought into contact with the skin near the radial styloid process 20A on the inside of the wrist. Then, in step S2, the sensor unit is placed inside the gap between the radial styloid process 20A and the flexor carpi radialis tendon 22.
 次に、ステップS3において、例えばスライダー部30を用いて、隙間の内側でセンサユニットの配置位置を移動させることによって、センサユニットの配置位置が調整される。調整によって、センサユニットの配置位置が決定される。次に、ステップS4において、加圧装置を用いて、決定された配置位置が固定される。 Next, in step S3, the arrangement position of the sensor unit is adjusted by moving the arrangement position of the sensor unit inside the gap using, for example, the slider section 30. The adjustment determines the placement position of the sensor unit. Next, in step S4, the determined placement position is fixed using a pressurizing device.
(測定用発光素子の決定処理)
 次に、ステップS5において、分布作成部を用いて、第1の発光素子LED1の光の反射光による第1の振幅の分布と、第2の発光素子LED2の光の反射光による第2の振幅の分布と、第3の発光素子LED3の光の反射光による第3の振幅の分布とが作成される。
(Determination process of light emitting element for measurement)
Next, in step S5, the distribution creation unit is used to create a first amplitude distribution due to the reflected light of the first light emitting element LED1 and a second amplitude distribution due to the reflected light of the second light emitting element LED2. , and a third amplitude distribution based on the reflected light of the third light emitting element LED3.
 そして、発光素子決定部を用いて、作成された第1の振幅の分布と第2の振幅の分布と第3の振幅の分布とのうち、基準条件を満たす分布が作成された発光素子が、測定用発光素子として決定される。 Then, using the light emitting element determining unit, a light emitting element for which a distribution satisfying the reference condition is created among the created first amplitude distribution, second amplitude distribution, and third amplitude distribution, It is determined as a light emitting element for measurement.
 図12A中には、手首の周方向Cに沿って並ぶ5つの受光素子によって取得された第1の振幅の分布を表す5つのデータ点が例示されている。また、図12B中には、手首の周方向Cに沿って並ぶ5つの受光素子によって取得された第2の振幅の分布を表す5つのデータ点が例示されている。また、図12C中には、手首の周方向Cに沿って並ぶ5つの受光素子によって取得された第3の振幅の分布を表す5つのデータ点が例示されている。 In FIG. 12A, five data points representing the first amplitude distribution acquired by five light receiving elements arranged along the circumferential direction C of the wrist are illustrated. Further, in FIG. 12B, five data points representing the second amplitude distribution acquired by five light receiving elements arranged along the circumferential direction C of the wrist are illustrated. Further, in FIG. 12C, five data points representing the third amplitude distribution acquired by five light receiving elements arranged along the circumferential direction C of the wrist are illustrated.
 また、図12A中には、5つのデータ点を結ぶ破線の第1の軌跡L1が、5つのデータ点と重ねて配置されている。同様に、図12B中には、破線の第2の軌跡L2が、また、図12C中には、破線の第3の軌跡L3が、それぞれのデータ点と重ねて配置されている。3つの軌跡L1,L2,L3は、手首の周方向Cに沿って1000ピクセル程度の一定の長さを有する確認用受光素子が配置された状態で、第1の発光素子LED1、第2の発光素子LED2及び第3の発光素子LED3を用いて作成された、それぞれの振幅の分布である。確認用受光素子の図示は省略する。また、確認用受光素子によって振幅の分布を作成する際の作成条件は、5つの受光素子によって振幅の分布を作成する際の作成条件と同様である。 Furthermore, in FIG. 12A, a first locus L1 of a broken line connecting the five data points is arranged to overlap the five data points. Similarly, in FIG. 12B, a dashed second locus L2 and in FIG. 12C, a dashed third locus L3 are arranged overlapping the respective data points. The three trajectories L1, L2, and L3 indicate that the first light emitting element LED1 and the second light emitting element are arranged in a state where a confirmation light receiving element having a constant length of about 1000 pixels is arranged along the circumferential direction C of the wrist. These are respective amplitude distributions created using the element LED2 and the third light emitting element LED3. Illustration of the confirmation light receiving element is omitted. Further, the conditions for creating the amplitude distribution using the confirmation light-receiving elements are the same as the conditions for creating the amplitude distribution using the five light-receiving elements.
 ここで、手首の周方向Cにおいて、発光素子が動脈の上側に位置する場合の振幅は、発光素子が動脈の上側から手首の周方向Cにずれて位置する場合の振幅より低くなる。なお、「発光素子が動脈の上側に位置する」とは、図10に示すように、平面視で、発光素子と動脈とが少なくとも部分的に重なる状態を意味する。 Here, in the circumferential direction C of the wrist, the amplitude when the light emitting element is located above the artery is lower than the amplitude when the light emitting element is located shifted from above the artery in the circumferential direction C of the wrist. Note that "the light emitting element is located above the artery" means a state in which the light emitting element and the artery at least partially overlap in plan view, as shown in FIG.
 このため、手首の周方向Cに沿った一端側(例えば図12B中の左側)から他端側(例えば図12B中の右側)に向かって並ぶ5つの受光素子のうち、中央の3つの受光素子において、配置方向に沿って1番目の受光素子から、1番目の受光素子に隣接する2番目の受光素子に向かって振幅が減少する。また、2番目の受光素子から、2番目の受光素子に隣接する3番目の受光素子に向かって振幅が増大する。 Therefore, among the five light-receiving elements arranged from one end side (for example, the left side in FIG. 12B) to the other end side (for example, the right side in FIG. 12B) along the circumferential direction C of the wrist, the central three light-receiving elements In the arrangement direction, the amplitude decreases from the first light receiving element toward the second light receiving element adjacent to the first light receiving element. Further, the amplitude increases from the second light receiving element toward the third light receiving element adjacent to the second light receiving element.
 すなわち、周方向Cに沿って振幅が減少し、かつ、増大することが、基準条件として設定される。換言すると、図12B中の振幅の分布の中で、下側に向かって窪むような凹部が描かれる。 That is, the reference condition is that the amplitude decreases and increases along the circumferential direction C. In other words, in the amplitude distribution in FIG. 12B, a concave portion that is concave toward the bottom is drawn.
 具体的には第3実施形態では、図12B中の第2の振幅の分布の中で、第2の受光素子PD2の振幅と、第3の受光素子PD3の振幅と、第4の受光素子PD4の振幅とによって凹部が描かれることによって、基準条件が満たされると判定できる。結果、図12B中の第2の振幅の分布が得られた、第2の発光素子LED2が、測定用発光素子として決定される。 Specifically, in the third embodiment, in the second amplitude distribution in FIG. 12B, the amplitude of the second light receiving element PD2, the amplitude of the third light receiving element PD3, and the amplitude of the fourth light receiving element PD4 are It can be determined that the reference condition is satisfied by drawing a concave portion with the amplitude of . As a result, the second light emitting element LED2 from which the second amplitude distribution in FIG. 12B was obtained is determined as the light emitting element for measurement.
 一方、図12Aの第1の振幅の分布の中では、第1の受光素子PD1から第2の受光素子PD2に向かって振幅が増大するが、第2の受光素子PD2から第5の受光素子PD5までの間、振幅が減少し続ける。このため、第1の振幅の分布の中で凹部が描かれないことによって、基準条件が満たされないと判定される。 On the other hand, in the first amplitude distribution in FIG. 12A, the amplitude increases from the first light receiving element PD1 to the second light receiving element PD2, but from the second light receiving element PD2 to the fifth light receiving element PD5. Until then, the amplitude continues to decrease. Therefore, since no concave portion is drawn in the first amplitude distribution, it is determined that the reference condition is not satisfied.
 また、図12Cの第3の振幅の分布の中では、第1の受光素子PD1から第4の受光素子PD4に向かって振幅が増大し続けるが、第4の受光素子PD4から第5の受光素子PD5までの間、振幅が減少する。その後、振幅は、第5の受光素子PD5から、手首の周方向Cの他端に位置する判定対象範囲の端部に向かって、ほぼ一定である。すなわち、振幅は、減少から増加に転じない。このため、第3の振幅の分布の中で凹部が描かれず、結果、基準条件が満たされないと判定される。 In addition, in the third amplitude distribution in FIG. 12C, the amplitude continues to increase from the first light receiving element PD1 to the fourth light receiving element PD4, but from the fourth light receiving element PD4 to the fifth light receiving element The amplitude decreases until PD5. Thereafter, the amplitude is approximately constant from the fifth light receiving element PD5 toward the end of the determination target range located at the other end of the wrist in the circumferential direction C. That is, the amplitude does not change from decreasing to increasing. Therefore, no concave portion is drawn in the third amplitude distribution, and as a result, it is determined that the reference condition is not satisfied.
 なお、基準条件を満たす振幅の分布が複数形成される場合には、例えば酸素飽和度の測定精度を高める観点から、複数の分布のうちでより適切な分布を抽出する抽出条件が設定されてよい。抽出条件としては、例えば、凹部の底部を構成する中央の振幅値と、底部の両側に位置し凹部の2つの頂部を構成する両端の振幅値の中でより大きな振幅値との差が算出される。そして、基準条件を満たす複数の振幅の分布のうち、算出された差が最も大きい分布が形成される発光素子を、測定用発光素子として決定することができる。 Note that when multiple amplitude distributions that meet the standard conditions are formed, extraction conditions may be set to extract a more appropriate distribution from among the multiple distributions, for example, from the perspective of increasing the measurement accuracy of oxygen saturation. . As an extraction condition, for example, the difference between the central amplitude value that makes up the bottom of the recess and the larger amplitude value among the amplitude values at both ends that are located on both sides of the bottom and make up the two tops of the recess is calculated. Ru. Then, among the plurality of amplitude distributions that satisfy the reference condition, a light emitting element in which a distribution with the largest calculated difference is formed can be determined as a light emitting element for measurement.
 次に、測定用発光素子として決定されなかった第1の発光素子LED1と第3の発光素子LED3とへの通電が停止されると共に、測定用発光素子として決定された第2の発光素子LED2への通電が継続される。そして、第2の発光素子LED2が照射した光の反射光が、5つの受光素子によって受光される。 Next, the power supply to the first light emitting element LED1 and the third light emitting element LED3 which have not been determined as the light emitting element for measurement is stopped, and the power to the second light emitting element LED2 which has been determined as the light emitting element for measurement is stopped. continues to be energized. Then, the reflected light of the light emitted by the second light emitting element LED2 is received by the five light receiving elements.
 このため、5つの受光素子によって、第1の脈波信号と第2の脈波信号と第3の脈波信号と第4の脈波信号と第5の脈波信号とからなる5つの脈波信号が得られる。そして、図11中のステップS6において、5つの脈波信号がモニタされる。そして、5つの脈波信号のそれぞれについてPI値が算出される。PI値は、赤色光のPI値(PIRED)と近赤外光のPI値(PIIR)とのそれぞれについて算出できる。 Therefore, the five light-receiving elements produce five pulse waves consisting of a first pulse wave signal, a second pulse wave signal, a third pulse wave signal, a fourth pulse wave signal, and a fifth pulse wave signal. I get a signal. Then, in step S6 in FIG. 11, five pulse wave signals are monitored. Then, a PI value is calculated for each of the five pulse wave signals. The PI value can be calculated for each of the PI value of red light (PI RED ) and the PI value of near-infrared light (PI IR ).
(PI値と基準値との比較処理)
 次に、ステップS7において、算出されたPI値が、予め設定された基準値以上であるかどうかが、比較によって判定される。比較は、例えば受光素子決定部によって実行できる。また、基準値は、赤色光のPI値(PIRED)と近赤外光のPI値(PIIR)とのそれぞれについて設定できる。なお、本開示では、基準値との比較処理は必須ではない。
(Comparison process between PI value and reference value)
Next, in step S7, it is determined by comparison whether the calculated PI value is greater than or equal to a preset reference value. The comparison can be performed, for example, by the light receiving element determining section. Further, the reference value can be set for each of the PI value of red light (PI RED ) and the PI value of near-infrared light (PI IR ). Note that in the present disclosure, comparison processing with a reference value is not essential.
 すべてのPI値が予め設定された基準値未満である場合、受光素子の配置位置が測定に適していない、すなわち、受光素子の位置ずれが生じている、と判定される。そして、処理は、ステップS3に移行し、センサユニットの配置位置が、再度調整される。配置位置の調整は、例えば、スライダー部30をスライドさせることによって実行できる。 If all the PI values are less than a preset reference value, it is determined that the placement position of the light receiving element is not suitable for measurement, that is, a positional shift of the light receiving element has occurred. Then, the process moves to step S3, and the arrangement position of the sensor unit is adjusted again. The arrangement position can be adjusted, for example, by sliding the slider section 30.
(測定用発受光素子の決定処理)
 一方、1つ以上のPI値が予め設定された基準値以上である場合、処理は、ステップS8に移行する。そして、基準値以上のPI値が得られる1つ以上の脈波信号のうち、最も大きな振幅を有する脈波信号が受光された受光素子が、受光素子決定部を用いて測定用受光素子として決定される。
(Determination process of light emitting and receiving elements for measurement)
On the other hand, if one or more PI values are equal to or greater than a preset reference value, the process moves to step S8. Then, among the one or more pulse wave signals from which a PI value equal to or higher than the reference value is obtained, the light receiving element that receives the pulse wave signal having the largest amplitude is determined as the measuring light receiving element using the light receiving element determination unit. be done.
(酸素飽和度測定処理)
 次に、決定された測定用受光素子で受光された脈波信号に基づき、ステップS9において、測定部18を用いてPI値が算出される。次に、ステップS10において、算出されたPI値に基づき、酸素飽和度が算出される。次に、ステップS11において、算出された酸素飽和度のデータは、記憶装置に保存される。
(Oxygen saturation measurement process)
Next, in step S9, a PI value is calculated using the measurement unit 18 based on the pulse wave signal received by the determined measurement light receiving element. Next, in step S10, oxygen saturation is calculated based on the calculated PI value. Next, in step S11, the calculated oxygen saturation data is stored in the storage device.
 次に、ステップS12において、酸素飽和度のデータの個数が、予め設定された指定数未満である場合、処理は、ステップS13に移行する。そして、ステップS7と同様、受光素子の位置ずれが生じているかどうかが、PI値と基準値との比較によって判定される。 Next, in step S12, if the number of oxygen saturation data is less than a preset designated number, the process moves to step S13. Then, as in step S7, it is determined whether a positional shift of the light receiving element has occurred by comparing the PI value with a reference value.
 ステップS13において、PI値が基準値以上であることによって、センサユニットの位置ずれが生じていないと判定される場合、処理は、ステップS9に移行すると共に、以降の処理が繰り返される。一方、PI値が基準値以上でないことによって、センサユニットの位置ずれが生じていると判定される場合、処理は、ステップS6に移行し、再度、5つの脈波信号がモニタされる。そして、5つの脈波信号のそれぞれについてPI値が算出される。以下、ステップS7以降の処理が繰り返されることによって、測定用受光素子が再度決定される。そして、酸素飽和度のデータが、記憶装置に保存される。 In step S13, if it is determined that no positional deviation of the sensor unit has occurred because the PI value is greater than or equal to the reference value, the process moves to step S9, and the subsequent processes are repeated. On the other hand, if it is determined that the positional shift of the sensor unit has occurred because the PI value is not equal to or greater than the reference value, the process moves to step S6, and the five pulse wave signals are monitored again. Then, a PI value is calculated for each of the five pulse wave signals. Thereafter, the process from step S7 onwards is repeated to determine the measurement light receiving element again. The oxygen saturation data is then stored in the storage device.
 一方、ステップS12において、保存された酸素飽和度のデータの個数が、予め設定された指定数以上である場合、処理は、終了する。上記の一連の処理を、保存された酸素飽和度のデータの個数が、記憶装置が保存可能な指定数を満たすまで実行することにより、第3実施形態に係る酸素飽和度測定方法が構成される。 On the other hand, in step S12, if the number of saved oxygen saturation data is equal to or greater than a preset designated number, the process ends. The oxygen saturation measurement method according to the third embodiment is configured by executing the above series of processes until the number of stored oxygen saturation data satisfies the specified number that can be stored in the storage device. .
 なお、本開示では、ステップS13において、センサユニットの位置ずれが生じていると判定される場合、バンド12が手首から一旦外された後、処理がステップS6に移行することなく、例えばステップS1に移行することも排除されない。すなわち、バンド12が巻き直されることによって、センサユニットの配置位置を調整してもよい。或いは、処理がステップS3に移行して、例えばスライダー部30を用いて、センサユニットの配置位置が調整されてもよい。 Note that in the present disclosure, if it is determined in step S13 that a positional shift of the sensor unit has occurred, after the band 12 is once removed from the wrist, the process does not proceed to step S6 and, for example, proceeds to step S1. Migration is also not excluded. That is, the arrangement position of the sensor unit may be adjusted by rewinding the band 12. Alternatively, the process may proceed to step S3, and the arrangement position of the sensor unit may be adjusted using, for example, the slider section 30.
(第3実施形態の作用効果)
 第3実施形態に係る酸素飽和度測定装置10Cでは、酸素飽和度の測定時、5つの受光素子のうち、最も大きな振幅を有する脈波信号が受光された受光素子が、酸素飽和度の測定用受光素子として決定される。そして、決定された測定用受光素子で受光された脈波信号に基づき、酸素飽和度が測定される。
(Operations and effects of the third embodiment)
In the oxygen saturation measuring device 10C according to the third embodiment, when measuring oxygen saturation, the light receiving element that has received the pulse wave signal having the largest amplitude among the five light receiving elements is used for measuring oxygen saturation. It is determined as a light receiving element. Then, the oxygen saturation level is measured based on the pulse wave signal received by the determined measuring light receiving element.
 すなわち、同一の発光素子から照射された光の複数の反射光が受光されると共に、受光された複数の反射光の脈波信号の振幅が比較される。比較を通じて最大の振幅を有する脈波信号が、酸素飽和度測定用の脈波信号として定量的に選択される。このため、第3実施形態に係る酸素飽和度測定装置10Cによれば、手首の内側の位置でセンサの位置ずれに起因する酸素飽和度の測定の中断の頻度を低減できる。 That is, a plurality of reflected lights of light emitted from the same light emitting element are received, and the amplitudes of pulse wave signals of the plurality of received reflected lights are compared. Through the comparison, the pulse wave signal having the largest amplitude is quantitatively selected as the pulse wave signal for oxygen saturation measurement. Therefore, according to the oxygen saturation measuring device 10C according to the third embodiment, it is possible to reduce the frequency of interruptions in oxygen saturation measurement due to misalignment of the sensor at the inner side of the wrist.
 また、第3実施形態では、第1の受光素子PD1と第2の受光素子PD2と第3の受光素子PD3と第4の受光素子PD4と第5の受光素子PD5とは、手首の周方向Cに沿って並べられる。このため、手首の周方向に沿った異なる5つの位置の間で、より適切な測定用受光素子を決定できる。 Further, in the third embodiment, the first light receiving element PD1, the second light receiving element PD2, the third light receiving element PD3, the fourth light receiving element PD4, and the fifth light receiving element PD5 are defined in the circumferential direction C of the wrist. arranged along. Therefore, a more appropriate measurement light receiving element can be determined among five different positions along the circumferential direction of the wrist.
 また、第3実施形態では、取得された5つの脈波信号が、予め設定された測定精度を達成する観点に基づいて予め設定された基準値を満たすかどうかが判定される。そして、基準値を満たす脈波信号を受光した受光素子の中から測定用受光素子を決定する処理が行われる。一方、5つの脈波信号のすべてが基準値を満たさない場合、基準値を満たす脈波信号が表れるまで、受光素子の配置位置を調整する処理が繰り返される。取得された脈波信号のうち、基準値を満たす脈波信号のみが測定用に抽出されるので、酸素飽和度の測定精度をより高めることができる。 Furthermore, in the third embodiment, it is determined whether the five acquired pulse wave signals satisfy a preset reference value based on the viewpoint of achieving preset measurement accuracy. Then, a process is performed to determine a measuring light receiving element from among the light receiving elements that have received a pulse wave signal that satisfies the reference value. On the other hand, if all five pulse wave signals do not satisfy the reference value, the process of adjusting the arrangement position of the light receiving element is repeated until a pulse wave signal that satisfies the reference value appears. Among the acquired pulse wave signals, only the pulse wave signals that satisfy the reference value are extracted for measurement, so that the measurement accuracy of oxygen saturation can be further improved.
 また、第3実施形態では、第1の振幅の分布と第2の振幅の分布と第3の振幅の分布とが作成される。そして、作成された第1の振幅の分布と第2の振幅の分布と第3の振幅の分布とのうち、発光素子が動脈の上側に位置することに対応して予め設定された基準条件を満たす分布が作成された発光素子が、測定用発光素子として決定される。そして、決定された測定用発光素子の光の反射光の脈波信号に基づき、酸素飽和度が測定される。すなわち、複数の発光素子の中から動脈の上側に位置する発光素子が、測定用発光素子として決定される。このため、酸素飽和度の測定精度を更に高めることができる。 Furthermore, in the third embodiment, a first amplitude distribution, a second amplitude distribution, and a third amplitude distribution are created. Then, among the created first amplitude distribution, second amplitude distribution, and third amplitude distribution, a preset reference condition corresponding to the fact that the light emitting element is located above the artery is set. A light emitting element for which a satisfying distribution has been created is determined as a light emitting element for measurement. Then, the oxygen saturation level is measured based on the pulse wave signal of the reflected light from the determined light emitting element for measurement. That is, the light emitting element located above the artery from among the plurality of light emitting elements is determined as the light emitting element for measurement. Therefore, the measurement accuracy of oxygen saturation can be further improved.
 また、第3実施形態では、測定用発光素子として決定されなかった発光素子への通電が停止されるので、省電力を図ることができる。なお、本開示では、発光素子への通電の制御に限定されず、測定用受光素子への通電の制御も、発光素子への通電の制御と共に、或いは単独で実行されてよい。すなわち、測定用受光素子として決定されなかった受光素子への通電が停止されると共に、測定用受光素子として決定された受光素子へのみ通電が継続されてもよい。測定用受光素子への通電の制御が実行されることによっても、省電力を図ることができる。 Furthermore, in the third embodiment, power supply to light emitting elements that have not been determined as measurement light emitting elements is stopped, so power can be saved. Note that the present disclosure is not limited to controlling the energization to the light emitting element, and the control of the energization to the measuring light receiving element may be performed together with the control of the energization to the light emitting element, or independently. That is, the power supply to the light receiving element that is not determined as the measuring light receiving element may be stopped, and the power supply may be continued only to the light receiving element determined as the measuring light receiving element. Power saving can also be achieved by controlling the power supply to the measuring light receiving element.
 また、第3実施形態に係る酸素飽和度測定装置10Cを用いた酸素飽和度測定方法によれば、手首の内側の位置でセンサの位置ずれに起因する酸素飽和度の測定の中断を抑制できる。 Furthermore, according to the oxygen saturation measurement method using the oxygen saturation measurement device 10C according to the third embodiment, it is possible to suppress interruption of oxygen saturation measurement due to positional deviation of the sensor at the inner side of the wrist.
<その他の実施形態>
 本開示は上記の開示された実施の形態によって説明したが、この開示の一部をなす論述及び図面は、本開示を限定するものであると理解すべきではない。例えば、第1実施形態では、図3に示したように、1つ以上の発光素子が含まれるグループと1つ以上の受光素子が含まれるグループとが、前腕の延びる方向Eに沿って配置された場合が例示された。しかし、本開示では、1つ以上の発光素子が含まれるグループと1つ以上の受光素子が含まれるグループとの配置方向は、これに限定されない。
<Other embodiments>
Although the present disclosure has been described with reference to the disclosed embodiments above, the discussion and drawings forming a part of this disclosure should not be understood to limit the present disclosure. For example, in the first embodiment, as shown in FIG. 3, a group including one or more light emitting elements and a group including one or more light receiving elements are arranged along the direction E in which the forearm extends. An example was given. However, in the present disclosure, the arrangement direction of the group including one or more light emitting elements and the group including one or more light receiving elements is not limited to this.
 図13中には、2つの発光素子が含まれるグループと3つの受光素子が含まれるグループとが、手首の周方向Cに沿って配置された場合が例示されている。すなわち、本開示では、1つ以上の発光素子が含まれるグループと1つ以上の受光素子が含まれるグループとの配置方向は、前腕の延びる方向Eであってもよいし、或いは、手首の周方向Cであってもよい。 FIG. 13 illustrates a case where a group including two light emitting elements and a group including three light receiving elements are arranged along the circumferential direction C of the wrist. That is, in the present disclosure, the arrangement direction of the group including one or more light-emitting elements and the group including one or more light-receiving elements may be in the direction E in which the forearm extends, or in the direction E in which the forearm extends. It may be in direction C.
 また、図1~図13中に示したそれぞれの構成を部分的に組み合わせて本開示を構成してもよい。本開示は、上記に記載していない様々な実施の形態等を含むと共に、本開示の技術的範囲は、上記の説明から妥当な特許請求の範囲の発明特定事項によってのみ定められるものである。 Additionally, the present disclosure may be configured by partially combining the respective configurations shown in FIGS. 1 to 13. The present disclosure includes various embodiments not described above, and the technical scope of the present disclosure is determined only by the matters specifying the invention in the claims that are reasonable from the above description.
 2022年3月14日に出願した日本国特許出願2022-039713号の開示は、その全体が参照により本明細書に取り込まれる。 The disclosure of Japanese Patent Application No. 2022-039713 filed on March 14, 2022 is incorporated herein by reference in its entirety.
 また、本明細書に記載されたすべての文献、特許出願及び技術規格は、個々の文献、特許出願及び技術規格が参照により取り込まれることが具体的かつ個々に記された場合と同程度に、本明細書中に参照により取り込まれる。 In addition, all documents, patent applications, and technical standards mentioned herein are incorporated by reference to the same extent as if each individual document, patent application, and technical standard were specifically and individually indicated to be incorporated by reference. Incorporated herein by reference.

Claims (6)

  1.  被測定者の手首に巻かれるバンドと、
     前記手首の動脈に対し光を照射する発光素子と、
     前記手首の前記動脈からの反射光を受光する第1の受光素子と、
     前記第1の受光素子と離れて配置され前記手首の前記動脈からの反射光を受光する第2の受光素子と、
     前記第1の受光素子で受光された前記反射光から取得された第1の脈波信号と前記第2の受光素子で受光された前記反射光から取得された第2の脈波信号とのうち、より大きな振幅を有する前記脈波信号が受光された前記受光素子を測定用受光素子として決定する受光素子決定部と、
     決定された前記測定用受光素子で受光された前記脈波信号に基づき、前記光が照射された前記動脈の酸素飽和度を測定する測定部と、
     を備える酸素飽和度測定装置。
    A band wrapped around the wrist of the person to be measured;
    a light emitting element that irradiates light to the wrist artery;
    a first light receiving element that receives reflected light from the artery of the wrist;
    a second light receiving element that is placed apart from the first light receiving element and receives reflected light from the artery of the wrist;
    A first pulse wave signal obtained from the reflected light received by the first light receiving element and a second pulse wave signal obtained from the reflected light received by the second light receiving element. , a light-receiving element determining unit that determines the light-receiving element that has received the pulse wave signal having a larger amplitude as a measurement light-receiving element;
    a measurement unit that measures the oxygen saturation of the artery irradiated with the light based on the pulse wave signal received by the determined measurement light receiving element;
    Oxygen saturation measuring device equipped with.
  2.  前記第1の受光素子と前記第2の受光素子とは、前記手首の周方向に沿って並べられる、
     請求項1に記載の酸素飽和度測定装置。
    the first light receiving element and the second light receiving element are arranged along the circumferential direction of the wrist;
    The oxygen saturation measuring device according to claim 1.
  3.  前記第1の脈波信号と前記第2の脈波信号とが、予め設定された測定精度を達成する観点に基づいて予め設定された基準値を満たすかどうかを判定する判定部を更に備え、
     前記基準値を満たす前記脈波信号を受光した前記受光素子の中から前記測定用受光素子を決定する処理を行う、
     請求項1又は2に記載の酸素飽和度測定装置。
    further comprising a determination unit that determines whether the first pulse wave signal and the second pulse wave signal satisfy a preset reference value based on a viewpoint of achieving a preset measurement accuracy;
    performing a process of determining the measurement light receiving element from among the light receiving elements that have received the pulse wave signal that satisfies the reference value;
    The oxygen saturation measuring device according to claim 1 or 2.
  4.  前記発光素子として、前記手首の前記動脈に対し前記光を照射する第1の発光素子と、前記手首の周方向に沿って前記第1の発光素子と離れて配置され前記手首の前記動脈に対し前記光を照射する第2の発光素子と、を備え、
     前記第1の受光素子と離れて配置されると共に前記第2の受光素子と離れて配置され、第3の脈波信号を取得するために前記手首の前記動脈からの前記反射光を受光する第3の受光素子を備え、
     前記第1の受光素子と前記第2の受光素子と前記第3の受光素子とは、前記手首の前記周方向に沿って並べられ、
     前記第1の発光素子の前記光の前記反射光から取得された前記第1の脈波信号と前記第2の脈波信号と前記第3の脈波信号とに基づく第1の振幅の分布と、前記第2の発光素子の前記光の前記反射光から取得された前記第1の脈波信号と前記第2の脈波信号と前記第3の脈波信号とに基づく第2の振幅の分布とを作成する分布作成部と、
     前記第1の振幅の分布と前記第2の振幅の分布とを用いて、前記第1の発光素子と前記第2の発光素子とのうち、前記発光素子が前記動脈の上側に位置することに対応して設定された基準条件を満たす前記分布が作成された方の前記発光素子を測定用発光素子として決定する発光素子決定部と、を備え、
     決定された前記測定用発光素子の前記光の前記反射光の前記脈波信号に基づき前記酸素飽和度を測定する、
     請求項1~3のいずれか一項に記載の酸素飽和度測定装置。
    The light emitting element includes a first light emitting element that irradiates the light to the artery of the wrist, and a first light emitting element that is arranged apart from the first light emitting element along the circumferential direction of the wrist and that irradiates the artery of the wrist. a second light emitting element that irradiates the light,
    a third light-receiving element, which is disposed apart from the first light-receiving element and also apart from the second light-receiving element, and which receives the reflected light from the artery of the wrist in order to obtain a third pulse wave signal; Equipped with 3 light receiving elements,
    The first light receiving element, the second light receiving element, and the third light receiving element are arranged along the circumferential direction of the wrist,
    a first amplitude distribution based on the first pulse wave signal, the second pulse wave signal, and the third pulse wave signal acquired from the reflected light of the light of the first light emitting element; , a second amplitude distribution based on the first pulse wave signal, the second pulse wave signal, and the third pulse wave signal acquired from the reflected light of the light of the second light emitting element; a distribution creation unit that creates
    Using the first amplitude distribution and the second amplitude distribution, it is determined that the light emitting element is located above the artery among the first light emitting element and the second light emitting element. a light emitting element determining unit that determines the light emitting element for which the distribution satisfying the correspondingly set reference condition is created as the light emitting element for measurement;
    Measuring the oxygen saturation based on the pulse wave signal of the reflected light of the determined light emitting element for measurement;
    The oxygen saturation measuring device according to any one of claims 1 to 3.
  5.  前記第1の発光素子と前記第2の発光素子とのうち前記測定用発光素子として決定された前記発光素子にのみ通電を継続し、かつ、前記測定用発光素子として決定されなかった前記発光素子への通電を停止する制御部を更に備える、
     請求項4に記載の酸素飽和度測定装置。
    Of the first light emitting element and the second light emitting element, only the light emitting element determined as the light emitting element for measurement continues to be energized, and the light emitting element not determined as the light emitting element for measurement further comprising a control unit that stops energizing the
    The oxygen saturation measuring device according to claim 4.
  6.  請求項1~5のいずれか一項に記載の酸素飽和度測定装置の前記発光素子を用いて測定対象の前記動脈に前記光を照射し、
     前記光が照射された前記動脈からの前記反射光から、前記第1の受光素子を用いて前記第1の脈波信号を取得すると共に前記第2の受光素子を用いて前記第2の脈波信号を取得し、
     前記第1の脈波信号と前記第2の脈波信号とをモニタし、
     モニタされた前記第1の脈波信号とモニタされた前記第2の脈波信号とのうち、より大きな前記振幅を有する前記脈波信号が受光された前記受光素子を、前記受光素子決定部を用いて前記測定用受光素子として決定し、
     決定された前記測定用受光素子で受光された前記脈波信号に基づき、前記測定部を用いて前記酸素飽和度を測定する、
     酸素飽和度測定方法。
    Irradiating the light to the artery to be measured using the light emitting element of the oxygen saturation measuring device according to any one of claims 1 to 5,
    The first pulse wave signal is obtained using the first light receiving element from the reflected light from the artery irradiated with the light, and the second pulse wave signal is obtained using the second light receiving element. get the signal,
    monitoring the first pulse wave signal and the second pulse wave signal;
    The light receiving element that has received the pulse wave signal having the larger amplitude of the monitored first pulse wave signal and the monitored second pulse wave signal is selected by the light receiving element determining section. is used to determine the light receiving element for measurement,
    Measuring the oxygen saturation using the measurement unit based on the pulse wave signal received by the determined measurement light receiving element;
    How to measure oxygen saturation.
PCT/JP2023/007291 2022-03-14 2023-02-28 Oxygen saturation value measurement device and oxygen saturation value measurement method WO2023176427A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2022039713A JP2023134265A (en) 2022-03-14 2022-03-14 Oxygen saturation degree measuring device and oxygen saturation degree measuring method
JP2022-039713 2022-03-14

Publications (1)

Publication Number Publication Date
WO2023176427A1 true WO2023176427A1 (en) 2023-09-21

Family

ID=88023541

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2023/007291 WO2023176427A1 (en) 2022-03-14 2023-02-28 Oxygen saturation value measurement device and oxygen saturation value measurement method

Country Status (2)

Country Link
JP (1) JP2023134265A (en)
WO (1) WO2023176427A1 (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11318840A (en) * 1998-05-14 1999-11-24 Omron Corp Pulse wave detector
JP2006325766A (en) * 2005-05-24 2006-12-07 Sharp Corp Biological signal measuring instrument
JP2009254522A (en) * 2008-04-15 2009-11-05 Sharp Corp Optical biological information measuring instrument, and light emitting/receiving unit for measuring biological information
JP2010051790A (en) * 2008-08-28 2010-03-11 Korea Electronics Telecommun Instrument and method for measuring pulse wave
JP2013121420A (en) * 2011-12-09 2013-06-20 Sony Corp Measuring apparatus, measuring method, program, and recording medium
US20200229743A1 (en) * 2019-01-23 2020-07-23 Samsung Electronics Co., Ltd. Apparatus and method for measuring bio-signal

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11318840A (en) * 1998-05-14 1999-11-24 Omron Corp Pulse wave detector
JP2006325766A (en) * 2005-05-24 2006-12-07 Sharp Corp Biological signal measuring instrument
JP2009254522A (en) * 2008-04-15 2009-11-05 Sharp Corp Optical biological information measuring instrument, and light emitting/receiving unit for measuring biological information
JP2010051790A (en) * 2008-08-28 2010-03-11 Korea Electronics Telecommun Instrument and method for measuring pulse wave
JP2013121420A (en) * 2011-12-09 2013-06-20 Sony Corp Measuring apparatus, measuring method, program, and recording medium
US20200229743A1 (en) * 2019-01-23 2020-07-23 Samsung Electronics Co., Ltd. Apparatus and method for measuring bio-signal

Also Published As

Publication number Publication date
JP2023134265A (en) 2023-09-27

Similar Documents

Publication Publication Date Title
US20230172545A1 (en) Multi-site noninvasive measurement of a physiological parameter
US10362974B2 (en) Systems, devices, and methods for performing trans-abdominal fetal oximetry and/or trans-abdominal fetal pulse oximetry using a heartbeat signal for a pregnant mammal
US8311601B2 (en) Reflectance and/or transmissive pulse oximeter
EP1322216B1 (en) A pulse oximeter and a method of its operation
KR102434701B1 (en) Apparatus and method for acquiring bio- information and apparatus for detecting bio- information
US6553242B1 (en) Physiological stress detector device and method
US7613490B2 (en) Physiological stress detector device and system
JP2001149349A (en) Sensor for living body
JP2018000930A (en) Blood oxygen saturation measuring apparatus
EP2112902B1 (en) Pad for measuring systolic blood pressure in the ankle using ppg
US20220296136A1 (en) Systems, devices, and methods for performing trans-abdominal fetal oximetry and/or trans-abdominal fetal pulse oximetry using a fetal heartbeat signal for a pregnant mammal
JP2019513035A (en) Optical measurement device for cardiovascular diagnosis
WO2023176427A1 (en) Oxygen saturation value measurement device and oxygen saturation value measurement method
WO2023176429A1 (en) Oxygen saturation level measurement device and oxygen saturation level measurement method
WO2023176428A1 (en) Oxygen saturation measurement device and oxygen saturation measurement method
JPH10295676A (en) Sensor and device for measuring interruption in blood circulation
JP2024013142A (en) Oxygen saturation measuring device and oxygen saturation measuring method
US20220142494A1 (en) Optical sensor modules with selective optical pathways
KR20010078429A (en) Saturation Measuring System Using Pulse Oximetry

Legal Events

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

Ref document number: 23770385

Country of ref document: EP

Kind code of ref document: A1