WO2010013554A1 - Device for measuring blood pressure information - Google Patents
Device for measuring blood pressure information Download PDFInfo
- Publication number
- WO2010013554A1 WO2010013554A1 PCT/JP2009/061206 JP2009061206W WO2010013554A1 WO 2010013554 A1 WO2010013554 A1 WO 2010013554A1 JP 2009061206 W JP2009061206 W JP 2009061206W WO 2010013554 A1 WO2010013554 A1 WO 2010013554A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- blood pressure
- cuff
- tightening
- upper arm
- unit
- Prior art date
Links
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/02—Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
- A61B5/021—Measuring pressure in heart or blood vessels
- A61B5/022—Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skin; Ophthalmodynamometers
- A61B5/02233—Occluders specially adapted therefor
Definitions
- the present invention relates to a blood pressure information measuring device capable of measuring blood pressure information such as a blood pressure value, and more particularly, to a blood pressure information measuring device having a function of measuring the perimeter of a measurement site to which a cuff is attached.
- the blood pressure information measuring device is a device for obtaining indexes for health management based on the acquired blood pressure information, and is expected to be further utilized in the fields of early detection, prevention, treatment, etc. of cardiovascular diseases. Yes.
- the blood pressure information includes a wide variety of information related to the circulatory system such as systolic blood pressure value, diastolic blood pressure value, average blood pressure value, pulse wave, pulse, AI (Augmentation Index) value, and the like.
- a cuff containing a fluid bag is used for measuring blood pressure information.
- the cuff means a band-shaped structure having a lumen and can be wound around a part of a living body, and a fluid bag is formed by injecting a fluid such as gas or liquid into the lumen. It refers to what is used to measure blood pressure information after being inflated and deflated.
- a blood pressure information measuring device hereinafter also simply referred to as a sphygmomanometer
- a living body is provided with a cuff that contains a fluid bag for compressing an artery.
- the blood pressure value is measured by winding the wound fluid bag on the body surface and expanding / contracting the wound fluid bag to capture the arterial pressure pulse wave as a change in the internal pressure of the fluid bag.
- the cuff used by being wound around the arm is also called an armband or a manchette.
- the air bag as a fluid bag contained in the cuff is wound around the measurement site so as to cover the entire measurement site when the cuff is attached to the measurement site.
- a sphygmomanometer for measuring blood pressure values such as systolic blood pressure values and diastolic blood pressure values
- the upper arm and wrist are generally used as the measurement site, but there are large individual differences in the size of the upper arm and wrist . Therefore, when trying to deal with all people from thin arm to thick arm with a single size cuff, the length in the winding direction of the air bag contained in the cuff is constant.
- the wrapped state of the air bag varies depending on the size of the site to be measured.
- This difference in winding state may affect the blood pressure measurement results.
- the entire measurement site cannot be completely covered with the air bag in the wearing state, and the circumferential portion of the measurement site is not covered with the air bag. Can be.
- sufficient compression force cannot be obtained when the measurement site is compressed by the air bag, and the blood pressure value is measured slightly higher than the actual blood pressure value.
- a sphygmomanometer designed to solve such a problem for example, a sphygmomanometer disclosed in Japanese Patent Application Laid-Open No. 2004-154458 (Patent Document 1) or a blood pressure disclosed in Japanese Patent Application Laid-Open No. 7-59740 (Patent Document 2). There is a total.
- a discharge amount measuring mechanism for measuring the discharge amount of the pressurizing pump by detecting the rotation speed of the pressurizing pump for pressurizing the air bag is provided.
- the peripheral length of the measured region of the subject is estimated based on the discharge amount and the cuff pressure (inner pressure of the air bag) measured by the discharge amount measuring mechanism, and the blood pressure value measured based on the estimation result A configuration in which correction is performed as necessary is employed.
- a hook including a conductive terminal is provided at one end portion in the circumferential direction of the cuff, and the hook is disposed at a portion near the other end portion in the circumferential direction of the cuff.
- a plurality of hook receivers including conductive terminals that can be hooked are provided, and the perimeter of the part to be measured is measured by detecting which position of the hook receiver is hooked when the cuff is attached.
- a configuration is adopted in which the blood pressure value measured based on is corrected as necessary.
- the circumference of the measurement site is based on the discharge amount of the pressurizing pump and the cuff pressure until the cuff winding is completed.
- the discharge rate of the pressurizing pump is not uniquely determined by the circumference of the part to be measured and is also affected by the shape and softness of the part to be measured. Even if it exists, in the case where the body surface is softer, the estimated perimeter may be larger than the actual perimeter.
- the estimated peripheral length of the measurement site which is also estimated by the inflation state of the air bag that compresses the measurement site. If the air bag inflates into a balloon shape without inflating uniformly, etc. Also, there is a possibility that it is estimated to be larger than the actual perimeter.
- the conventional blood pressure monitor has the following problems.
- the optimal air bag is adjusted by controlling the operation of the pressurizing pump or the like to adjust the air flow rate. It is possible to adjust the inflating motion so that the inflated state is realized, and to adjust the inflating and deflating motion in order to reduce the time required for measurement. Such a control has not been performed in practice because the size of the film cannot be measured accurately and precisely. Therefore, a device for accurately and precisely measuring the size of the measurement site has been demanded.
- the present invention has been made in view of the above-described problems, and a first object of the present invention is to measure blood pressure information having a function capable of accurately and precisely measuring the circumference of a measurement site.
- a second object of the present invention is to provide an apparatus, and in addition to the first object, by effectively utilizing the information on the circumference of the measured region to be measured, it is possible to improve the performance and increase the performance.
- the object is to provide a functional blood pressure information measuring device.
- the blood pressure information measurement device includes a cuff, an expansion / contraction mechanism, a blood pressure information measurement unit, a tightening length adjustment mechanism, and a peripheral length measurement unit.
- the cuff includes a fluid bag for pressing the measurement site and a tightening belt wound around the fluid bag.
- the cuff has no cut in the circumferential direction and the measurement site can be inserted from the axial direction. It has the annular form comprised.
- the inflating and contracting mechanism is for inflating and deflating the fluid bag, and the blood pressure information measuring unit measures blood pressure information using the fluid bag.
- the tightening length adjusting mechanism is for variably adjusting the tightening length of the tightening belt with respect to the measurement site, and the perimeter measuring unit is for measuring the perimeter of the measurement site. is there.
- the circumference measuring unit determines the amount of movement of the tightening belt when the tightening belt is fastened and fixed to the measurement site using the tightening length adjusting mechanism. It is preferable to measure the perimeter of the measurement site by measuring.
- the circumference measurement unit preferably includes a marker provided on the fastening belt and a reading unit that reads the marker. It is preferable that the perimeter measurement unit is configured to measure the amount of movement of the fastening belt based on information read by the reading unit.
- the marker is preferably configured by a barcode, and in that case, the reading unit is configured by a photo interrupter for reading the barcode. It is preferable.
- the circumference measurement unit includes a rotating member that rotates as the fastening belt moves, and a rotation amount detection unit that detects the amount of rotation of the rotating member.
- the circumference measuring unit is configured to measure the movement amount of the fastening belt based on information detected by the rotation amount detection unit.
- the blood pressure information measurement device further includes a blood pressure information correction unit that corrects the blood pressure information measured by the blood pressure information measurement unit based on the circumference information of the measurement site detected by the circumference measurement unit. It is preferable to provide.
- the blood pressure information measurement device controls at least one of the inflating operation and the deflating operation of the fluid bag by the inflating and deflating mechanism based on the circumference information of the measurement site detected by the circumference measuring unit. It is preferable to further include an expansion / contraction operation control unit.
- the blood pressure information measurement device is based on the circumference information of the measurement site detected by the circumference measurement unit, and whether or not the circumference of the measurement site is within a predetermined measurable range. It is preferable to further include a determination unit that determines the above.
- the tightening length adjusting mechanism rotates the winding roller in the forward direction and the reverse direction, and the winding roller capable of winding and feeding the tightening belt. It preferably includes an electric motor to be driven and a brake that exerts a braking force on the winding roller when the electric motor is stopped.
- the cuff includes a cylindrical cuff main body including the fluid bag and the fastening belt, and a handle provided on the outer peripheral surface of the cuff main body. It is preferable that it contains.
- a winding operation unit for receiving a command to start the winding operation of the tightening belt by the winding roller is provided in the handle unit. Is preferred.
- the blood pressure information measuring device preferably further includes a tightening force detection mechanism for detecting the tightening force of the tightening belt with respect to the measurement site.
- the tightening length adjusting mechanism is It is preferable that the winding operation of the tightening belt by the winding roller is stopped when the tightening force detection mechanism detects a predetermined amount of tightening force.
- the tightening force detection mechanism winds the tightening belt by the winding roller in a state where a predetermined amount of fluid is injected into the fluid bag by the expansion / contraction mechanism. It is preferable that the tightening force of the tightening belt with respect to the measurement site is detected by detecting the internal pressure of the fluid bag during the taking operation.
- the tightening force detection mechanism detects the rotational torque applied to the take-up roller when it is rotationally driven by the electric motor, whereby the tightening to the measurement site is performed.
- the belt tightening force may be detected.
- the expansion / contraction mechanism performs the pressurizing operation of the fluid bag for blood pressure information measurement after stopping the winding operation of the tightening belt by the winding roller. It is preferably configured to start.
- the tightening length adjusting mechanism starts the feeding operation of the tightening belt by the winding roller after the measurement operation for blood pressure information measurement is completed. It is preferable to be configured.
- the cuff body further includes a flexible member configured to be elastically deformable in the radial direction outside the fluid bag and inside the fastening belt. It is preferable.
- a blood pressure information measuring device having a function capable of accurately and precisely measuring the peripheral length of a measurement site. Further, according to the present invention, it is possible to obtain a blood pressure information measuring device with high performance and high functionality by effectively utilizing the measured information on the circumference of the measured region.
- FIG. 4 is a cross-sectional view of the cuff in a non-mounted state along the line IV-IV shown in FIG. 3. It is a model top view which shows the structure of the fastening length adjustment mechanism of the sphygmomanometer in Embodiment 1 of this invention.
- FIG. 1 It is a schematic diagram which shows the structure of the upper arm circumference measurement part of the blood pressure meter in Embodiment 1 of this invention. It is a flowchart which shows the process sequence of the sphygmomanometer in Embodiment 1 of this invention. It is a timing chart which shows the operation state and operation state of each part of the blood pressure monitor in Embodiment 1 of this invention in time series. It is a schematic diagram for demonstrating the mounting
- a so-called upper arm type sphygmomanometer configured to measure a systolic blood pressure value and a diastolic blood pressure value
- the tightening operation for the upper arm of the cuff the tightening operation for the upper arm of the cuff, the blood pressure measurement operation performed after the tightening operation, and the tightening release operation for the upper arm of the cuff performed after the measuring operation are automatically continued. Further, the circumference of the upper arm is automatically measured during the tightening operation on the upper arm of the cuff.
- FIG. 1 is a diagram showing an external structure of a sphygmomanometer according to Embodiment 1 of the present invention. First, with reference to FIG. 1, the external structure of sphygmomanometer 1A in the present embodiment will be described.
- the sphygmomanometer 1A includes a main body 10, a cuff 20A, an air tube 90, and a connection cable 92.
- the main body 10 has a box-shaped housing, and a display unit 14 and an operation unit 16 are provided on an upper surface thereof.
- the main body 10 is used by being placed on a placement surface such as a table at the time of measurement.
- the cuff 20 ⁇ / b> A is configured in an annular shape having no cut in the circumferential direction, and includes a cylindrical cuff main body portion 30 including a hollow opening into which the upper arm can be inserted from the axial direction, and the cuff main body portion 30. And a grip portion 40 provided on the outer peripheral surface.
- an encoder strip 73 for specifying the perimeter of the upper arm to which the cuff 20A is to be attached is attached.
- the cuff 20A is attached to the upper arm during measurement.
- the air tube 90 and the connection cable 92 respectively connect the main body 10 and the cuff 20 ⁇ / b> A configured separately.
- FIG. 2 is a diagram showing a functional block configuration of the sphygmomanometer according to the present embodiment. Next, with reference to FIG. 2, the functional block configuration of sphygmomanometer 1A in the present embodiment will be described.
- the main body 10 includes a control unit 11, a memory unit 12, a power supply unit 18, a motor drive circuit 53, an electromagnetic brake drive circuit 54, in addition to the display unit 14 and the operation unit 16 described above.
- the cuff 20A mainly includes an air bag 35, a fastening belt 32, a push button 44, a geared motor 51, an electromagnetic brake 52, a winding roller 58, and a photoelectric sensor 71.
- the control part 11 is comprised by CPU (Central Processing Unit), for example, and is a means for controlling the whole sphygmomanometer 1A.
- the memory unit 12 is composed of, for example, a ROM (Read-Only Memory) or a RAM (Random-Access Memory), and stores a program for causing the control unit 11 or the like to execute a processing procedure for blood pressure measurement, This is a means for storing measurement results and the like.
- the display unit 14 is configured by, for example, an LCD (Liquid Crystal Display), and is a means for displaying measurement results and the like.
- the operation unit 16 is a means for receiving an operation by a subject or the like and inputting a command from the outside to the control unit 11 or the power supply unit 18.
- the power supply unit 18 is means for supplying power as a power source to the control unit 11.
- the control unit 11 sends control signals for driving the geared motor 51, the electromagnetic brake 52, the pressure pump 61, and the exhaust valve 62 to the motor drive circuit 53, the electromagnetic brake drive circuit 54, the pressure pump drive circuit 64, and the exhaust valve drive.
- the upper arm circumference length of the subject is measured based on information on the fastening lengths of fastening belts 31 and 32 (described later) detected by the photoelectric sensor 71, or the blood pressure value as a measurement result is stored in the memory unit. 12 or the display unit 14.
- the control unit 11 includes a determination unit that determines whether or not the measured upper arm circumference is within a predetermined applicable range of the cuff 20A.
- the control unit 11 includes a blood pressure information measurement unit that acquires the blood pressure value of the subject based on the pressure value detected by the pressure sensor 63, and the blood pressure value acquired by the blood pressure information measurement unit is the measurement result. Is input to the memory unit 12 and the display unit 14 described above.
- the sphygmomanometer 1A may further include an output unit that outputs a blood pressure value as a measurement result to an external device (for example, a PC (Personal Computer) or a printer).
- an external device for example, a PC (Personal Computer) or a printer.
- the output unit for example, a serial communication line or a writing device for various recording media can be used.
- the motor drive circuit 53 controls the operation of the geared motor 51 based on the control signal input from the control unit 11.
- the electromagnetic brake drive circuit 54 controls the operation of the electromagnetic brake 52 based on the control signal input from the control unit 11.
- the pressurization pump drive circuit 64 controls the operation of the pressurization pump 61 based on the control signal input from the control unit 11.
- the exhaust valve drive circuit 65 controls the opening / closing operation of the exhaust valve 62 based on the control signal input from the control unit 11.
- the air bag 35 is a fluid bag for pressing the upper arm in the mounted state, and is connected to an air system component 60 described later via the air tube 90 described above.
- the geared motor 51, the electromagnetic brake 52, and the take-up roller 58 correspond to a tightening length adjusting mechanism 50 that variably adjusts a tightening length with respect to upper arms of tightening belts 31 and 32 (see FIG. 3 and the like) described later.
- Electrical connection between the geared motor 51 and the motor drive circuit 53 and electrical connection between the electromagnetic brake 52 and the electromagnetic brake drive circuit 54 are performed by the connection cable 92 (see FIG. 1) described above.
- the geared motor 51 is an electric motor that rotationally drives the winding roller 58 in the forward direction and the reverse direction, and its operation is controlled by the motor drive circuit 53 described above.
- the electromagnetic brake 52 is a brake that applies a braking force to the winding roller 58, and its operation is controlled by the electromagnetic brake drive circuit 54 described above.
- the take-up roller 58 is a member for taking up and sending out tightening belts 31 and 32 described later.
- the push button 44 corresponds to a winding operation operation unit that receives a test subject's command for starting a winding operation by the tightening length adjusting mechanism 50 including the geared motor 51, the electromagnetic brake 52, and the winding roller 58. .
- the pressurizing pump 61 is for supplying air to the inner cavity of the air bladder 35, and its operation is controlled by the pressurizing pump driving circuit 64 described above.
- the exhaust valve 62 is used to maintain the pressure inside the air bladder 35 (hereinafter also referred to as “cuff pressure”) or to open the space inside the air bladder 35 to the outside. It is controlled by the exhaust valve drive circuit 65.
- the pressure sensor 63 inputs an output signal corresponding to the pressure inside the air bladder 35 to the amplifier 66.
- the amplifier 66 amplifies the output value of the pressure sensor 63 and inputs it to the A / D conversion circuit 67.
- the A / D conversion circuit 67 converts the analog signal input from the amplifier 66 into a digital signal and inputs the digital signal to the control unit 11.
- the pressurization pump 61, the exhaust valve 62, and the pressure sensor 63 correspond to the air system component 60 described above.
- the pressurization pump 61 and the exhaust valve 62 inflate and contract the air bladder 35. It corresponds to an expansion / contraction mechanism.
- the air bag 35 and the air system component 60 described above are used as a tightening force detection mechanism for detecting the tightening force of the tightening belt with respect to the upper arm. Will be described later.
- the photoelectric sensor 71 (more specifically, a photo interrupter) is a reading unit for reading a bar code as a marker provided on the tightening belts 31 and 32 described later, and an electric signal corresponding to the read information is transmitted around the upper arm. Output to the length measuring circuit 72.
- the upper arm circumference measurement circuit 72 measures the upper arm circumference based on the electric signal input from the photoelectric sensor 71 and outputs an output signal corresponding to the measured upper arm circumference to the control unit 11.
- the bar code as the marker and the photoelectric sensor 71 as the reading unit are used as a perimeter measuring unit for measuring the perimeter of the upper arm, which is a measurement target, and details thereof will be described later.
- FIG. 3 is a perspective view showing a detailed structure of the cuff of the sphygmomanometer according to the present embodiment
- FIG. 4 is a cross-sectional view of the cuff in a non-wearing state along line IV-IV shown in FIG.
- FIG. 5 is a schematic top view showing the configuration of the tightening length adjusting mechanism of the sphygmomanometer according to the present embodiment
- FIG. 6 shows the configuration of the upper arm circumference measuring unit of the sphygmomanometer according to the present embodiment. It is a schematic diagram.
- the cuff 20 ⁇ / b> A has a cylindrical cuff main body 30 that is attached to the upper arm, and a handle 40 that is provided on the outer peripheral surface of the cuff main body 30.
- the handle portion 40 includes a base portion 41 that is a portion that is attached to the cuff main body portion 30 and a handle 42 that is a portion that is gripped by hand when attached.
- the cuff main body 30 is formed in a cylindrical shape so that the upper arm can be inserted in the axial direction, and the handle 40 is a handle 42 in a direction parallel to the axial direction of the cylindrical cuff main body 30. Is fixed to the cuff body 30 so as to extend.
- a tightening length adjusting mechanism 50 is disposed at a position on the outer peripheral surface of the cuff main body portion 30 and inside the base portion 41 of the handle portion 40.
- a photoelectric sensor 71 is provided at a predetermined position inside the base portion 41 of the handle portion 40. Further, the push button 44 described above is provided at a predetermined position on the outer surface of the handle portion 40.
- the cuff main body 30 includes an annular winding belt 31, 32, an exterior cover 33 attached to the inside of the tightening belt 31, a curler 34 and an air bag 35 housed inside the exterior cover 33. Mainly prepared.
- the tightening belts 31 and 32 are made of a member such as a cloth that does not substantially stretch in the circumferential direction, and are connected to the wide first tightening belt 31 and the first tightening belt.
- a second tightening belt 32 having a narrow width.
- the first tightening belt 31 is composed of a belt-like member having one end 31a and the other end 31b in the circumferential direction, and the handle portion 40 described above is attached to a predetermined position on the outer peripheral surface, and on the inner peripheral surface.
- the exterior cover 33 described above is attached.
- the second tightening belt 32 has one end portion 32 a and the other end portion 32 b in the circumferential direction, and one end portion 32 a is connected to the other end portion 31 b of the first tightening belt 31.
- the portion of the second tightening belt 32 near the other end 32b is overlapped with the outer peripheral side of the portion near the one end 31a of the first tightening belt 31, and the other end 32b of the second tightening belt 32 is
- the first tightening belt 31 is fixed to a take-up roller 58 disposed in a handle portion 40 attached to the outer peripheral surface of the first tightening belt 31. Accordingly, the first tightening belt 31 and the second tightening belt 32 function as one member configured in an annular shape, thereby forming the cuff body 30 having a hollow opening.
- the length of the connected first tightening belt 31 and second tightening belt 32 is variably adjusted by the tightening length adjusting mechanism 50.
- the cuff main body portion 30 In the state where the circumferential lengths of the connected first tightening belt 31 and second tightening belt 32 are increased, the cuff main body portion 30 is in an expanded state (a state in which the diameter is increased).
- the cuff main body portion 30 takes a reduced diameter state (a state where the diameter is reduced).
- the exterior cover 33 is formed of a member such as a cloth made of a stretchable low friction material, for example, and is attached on the inner peripheral surface of the first tightening belt 31 described above. More specifically, the outer cover 33 is fixed to the first tightening belt 31 by bonding the outer peripheral surface of the outer cover 33 to the inner peripheral surface of the first tightening belt 31 by adhesion or welding.
- the curler 34 included in the exterior cover 33 is made of a flexible member formed by injection molding using a resin material such as polypropylene as a raw material. More specifically, the curler 34 is composed of an annular curved elastic plate having a cut 34a along the axial direction at a predetermined position in the circumferential direction, and when cut along a plane perpendicular to the axial direction, The shape is C-shaped or U-shaped.
- the curler 34 is configured to be elastically deformable in the radial direction while maintaining its own annular shape. Therefore, the curler 34 takes a state in which the diameter is greatly expanded in the above-described expanded diameter state, and conversely, takes a state in which the diameter is small and narrowed in the above-described reduced diameter state.
- the cuff main body portion 30 when the cuff main body portion 30 is in the expanded state, the cuff main body portion 30 is greatly expanded by the elastic force of the curler 34, so that the upper arm can be inserted into and removed from the hollow opening of the cuff main body portion 30. It becomes easy.
- the air bag 35 is made of a bag-shaped member that can be expanded and contracted, and is formed, for example, by laminating two resin films and welding the periphery thereof.
- the inner cavity of the air bladder 35 is connected to the air pipe 90 via a nipple (not shown).
- the inner cavity of the air bladder 35 is pressurized and decompressed by a pressurizing pump 61 and an exhaust valve 62 provided in the main body 10 at the time of measurement, whereby the air bladder 35 is expanded or contracted.
- the tightening length adjusting mechanism 50 includes a geared motor 51, an electromagnetic brake 52, and a take-up roller 58.
- the geared motor 51, the electromagnetic brake 52, and the take-up roller 58 are assembled to a support frame 46 that is disposed on the outer peripheral surface of the cuff body 30 and inside the base 41 of the handle 40. .
- the support frame 46 is fixed on the outer peripheral surface of the first tightening belt 31, for example. Further, gears 55, 56, and 57 as power transmission mechanisms are assembled at predetermined positions of the support frame 46.
- the geared motor 51 is a motor equipped with a reduction gear, and includes a motor portion 51a, a reduction portion 51b, and an output shaft 51c.
- a gear 55 is fixed to the output shaft 51 c of the geared motor 51.
- An electromagnetic brake 52 is disposed adjacent to the geared motor 51 at the axial end of the geared motor 51 opposite to the side where the output shaft 51c is located. The electromagnetic brake 52 exerts a braking force on the rotation shaft 51a1 by holding the rotation shaft 51a1 of the motor unit 51a.
- the take-up roller 58 is fixed to a shaft 57a that is pivotally supported by the support frame 46, and is rotated by the rotation of the shaft 57a.
- the other end portion 32 b of the second tightening belt 32 described above is fixed to the winding roller 58.
- a gear 57 is fixed to the shaft 57a to which the winding roller 58 is fixed.
- a gear 56 is fixed to the shaft 56 a that is pivotally supported by the support frame 46.
- the gear 56 meshes with the gear 55 and the gear 57 described above, and transmits the rotational force generated on the output shaft 51 c of the geared motor 51 to the take-up roller 58.
- the gears 55, 56, and 57 are configured by adjusting the outer diameter and the number of teeth, respectively, and function as a speed reducer as well as the speed reducing portion 51 b of the geared motor 51.
- a photoelectric sensor 71 is disposed at a predetermined position inside the base portion 41 of the handle portion 40 so as to face the winding roller 58.
- the photoelectric sensor 71 includes a first photoelectric sensor 71 ⁇ / b> A and a second photoelectric sensor 71 ⁇ / b> B, and both of the two photoelectric sensors 71 ⁇ / b> A and 71 ⁇ / b> B face the winding roller 58.
- an encoder strip 73 is adhered to the surface of the second tightening belt 32.
- the encoder strip 73 passes through the portion on the detection surface side of the photoelectric sensor 71 when the second fastening belt 32 is taken up by the take-up roller 58, so that one end portion 32a of the second fastening belt 32 is passed. It is provided so as to extend from the closer portion toward the other end 32b side.
- the encoder strip 73 has a barcode 74 as a marker on its main surface.
- the tightening operation for the upper arm of the cuff 20A and the tightening releasing operation for the upper arm of the cuff 20A are respectively described below, the winding operation of the tightening belts 31 and 32 by the tightening length adjusting mechanism 50, and the tightening length adjustment. This is performed by the feeding operation of the fastening belts 31 and 32 by the mechanism 50.
- the tightening belts 31 and 32 Due to the winding operation of the second tightening belt 32 by the winding roller 58, the tightening belts 31 and 32 have their tightening lengths reduced against the elastic force of the curler 34, and the hollow opening portion of the cuff main body portion 30. Is gradually reduced in diameter. That is, the winding operation realizes the tightening operation of the cuff 20A with respect to the upper arm.
- the electromagnetic brake 52 is not in a state of holding the rotating shaft 51a1 of the motor unit 51a of the geared motor 51, and the motor unit 51a is restricted in its operation. It will be driven without.
- the diameter of the hollow opening of the cuff body 30 is gradually increased based on the elastic force of the curler 34.
- the tightening release operation of the cuff 20A with respect to the upper arm is realized by the delivery operation.
- the electromagnetic brake 52 is not in a state of holding the rotating shaft 51a1 of the motor portion 51a of the geared motor 51, and the motor portion 51a is restricted in its operation. It will be driven without.
- the rotating shaft 51a1 of the motor portion 51a of the geared motor 51 is held by the electromagnetic brake 52. It will be in the state. In this state, the braking force by the electromagnetic brake 52 reaches the take-up roller 58 via the rotary shaft 51a1, the speed reducer 51b, the output shaft 51c, the gears 55, 56, 57 and the shaft 57a of the motor 51a. The rotation operation of 58 is limited. Therefore, in this state, both the winding and feeding operations of the second tightening belt 32 by the winding roller 58 are stopped, and the diameter of the hollow opening of the cuff body 30 is maintained constant. Become.
- the tightening force detection mechanism is for detecting the tightening force of the cuff 20A against the upper arm during the above-described tightening operation of the cuff 20A in order to optimize the tightening state with respect to the upper arm of the cuff 20A.
- the tightening force detection mechanism includes the air bag 35 and the air system component 60 shown in FIG.
- the tightening force detection mechanism is a mechanism for detecting the tightening force of the tightening belts 31 and 32 with respect to the upper arm, and captures the tightening force as the internal pressure of the air bladder 35.
- a predetermined amount of air is introduced into the air bag 35 prior to driving the tightening length adjusting mechanism 50 to reduce the diameter of the hollow opening of the cuff body 30.
- the air bag is injected between the fastening belts 31 and 32 and the upper arm, and the fastening length is reduced as the fastening length adjusting mechanism 50 is driven.
- the pressure sensor 63 By detecting the internal pressure of the air bag 35 by the pressure sensor 63, the tightening force applied to the upper arm by the tightening belts 31 and 32 is detected based on the detected internal pressure of the air bladder 35.
- the control unit 11 monitors the internal pressure of the air bladder 35 during the tightening operation by the tightening length adjusting mechanism 50 described above, and stops the operation of the geared motor 51 when the predetermined pressure value is reached. At the same time, the electromagnetic brake 52 is operated to stop the rotation of the winding roller 58. As described above, the tightening state with respect to the upper arm of the cuff 20A can be set to the optimum state.
- the upper arm circumference measurement unit is for automatically measuring the circumference of the upper arm during the tightening operation on the upper arm of the cuff 20A.
- the upper arm circumference measurement unit includes a bar code 74 as a marker provided on the second fastening belt 32 and photoelectric sensors 71 ⁇ / b> A and 71 ⁇ / b> B provided in the base 41 of the handle 40. It is configured.
- the photoelectric sensors 71 ⁇ / b> A and 71 ⁇ / b> B are reading means for reading a bar code 74 provided on the encoder strip 73.
- Each of the photoelectric sensors 71A and 71B includes a light emitting portion and a light receiving portion, and the light emitted from the light emitting portion is applied to the encoder strip 73, and the reflected light is received by the light receiving portion, thereby reflecting the light.
- the presence / absence of the bar code 74 is detected based on the light amount difference.
- the photoelectric sensors 71 ⁇ / b> A and 71 ⁇ / b> B output an electrical signal by photoelectrically converting the received light, and the output electrical signal is input to the upper arm circumference measurement circuit 72.
- the upper arm circumference measurement circuit 72 identifies the circumference of the upper arm of the subject based on the input electrical signal, and inputs the identified circumference of the upper arm to the control unit 11.
- the bar code 74 provided on the encoder strip 73 has a bar code group of two columns of I column and II column shown in FIG.
- the bar codes included in the I column include an identifier for indicating the position information of the second tightening belt 32 in the portion to which the bar code is attached, and are detected by the photoelectric sensor 71A.
- the barcode included in the II column is an identifier for indicating the detection timing of the barcode included in the I column, and is detected by the photoelectric sensor 71B.
- the two row barcode groups of the I row and the II row each have a section equally divided by a predetermined distance in the longitudinal direction of the second fastening belt 32.
- the length of each of the sections is 10 mm.
- the barcode included in the I column of each section includes a header and a footer, and a position mark.
- the header is located on the other end 32b side of the second tightening belt 32 and indicates the beginning of the section.
- the footer is located on the one end portion 32a side of the second fastening belt 32, and indicates the end of the section.
- the position mark is located between the header and the footer, and indicates the position information of the second fastening belt 32 at the start position of each section.
- the barcodes included in the II column of each section are arranged with a predetermined interval so that the presence or absence of the barcode is alternately repeated in the reading direction indicated by the arrow in the drawing.
- the position mark is written in octal one-digit bit display, and the barcodes included in the II column are arranged every other bit.
- the position information of the second tightening belt 32 at the start position of each section is the position of the tightening belts 31 and 32 from the first tightening belt 31 corresponding to the position where the photoelectric sensors 71A and 71B are provided to the corresponding portion. Shows the length. Therefore, the length indicated by the bar code 74 corresponds to the circumferential length of the fastening belts 31 and 32. Therefore, in the state where the cuff 20A is fitted to the subject's upper arm without any gap using the above-described tightening length adjusting mechanism 50 and the tightening force detecting mechanism, the length detected by the upper arm circumference measuring unit is the subject. Represents the perimeter of the upper arm.
- the cuff main body 30 is wound around the upper arm when the second fastening belt 32 is wound around the winding roller 58, so that the photoelectric sensor 71A, 71B reads the barcode 74 along the reading direction indicated by the arrow in the drawing.
- the information on the presence / absence of the barcode included in the I column detected by the photoelectric sensor 71A and the information on the presence / absence of the barcode included in the II column detected by the photoelectric sensor 71B are synchronized, and the upper arm circumference length is synchronized. Input to the measurement circuit 72.
- the upper arm circumference measurement circuit 72 determines the timing for recognizing information detected by the photoelectric sensor 71A as position information based on the information detected by the photoelectric sensor 71B among the input information. Then, the upper arm perimeter measurement circuit 72 extracts information related to the position mark from the information detected by the photoelectric sensor 71A by associating the information detected by the photoelectric sensor 71A with the above-described timing, and based on the position mark. Specify location information. As a result, the upper arm perimeter measuring circuit 72 detects the tightening length of the tightening belts 31 and 32 to identify the upper arm perimeter of the subject. As described above, the circumference of the upper arm of the subject is automatically measured by the upper arm circumference measurement unit.
- FIG. 7 is a flowchart showing a processing procedure of the sphygmomanometer according to the present embodiment
- FIG. 8 is a timing chart showing the operation state and the operation state of each part of the sphygmomanometer according to the present embodiment in time series.
- FIG. 9 is a schematic diagram for explaining the mounting operation for mounting the cuff of the sphygmomanometer in the present embodiment on the upper arm
- FIG. 10 shows the mounting of the cuff of the sphygmomanometer in the present embodiment on the upper arm. It is sectional drawing of a mounting state.
- the processing procedure of the sphygmomanometer 1A in the present embodiment is the same as the operation status and operating state of each part of the sphygmomanometer 1A, the wearing work of the cuff 20A, the wearing of the cuff 20A. It will be described together with the later state.
- the program according to the flowchart shown in FIG. 7 is stored in advance in the memory unit 12 shown in FIG. 2, and the control unit 11 reads out the program from the memory unit 12 and executes the program, so that the process proceeds.
- step S101 when the test subject operates the operation unit 16 of the sphygmomanometer 1A to input a power-on command, power as a power source is supplied from the power supply unit 18 to the control unit 11.
- the controller 11 is driven to initialize the sphygmomanometer 1A (step S101).
- step S101 As shown in FIG. 8, at the time t0 when the sphygmomanometer 1A is initialized, the geared motor 51, the electromagnetic brake 52, the pressurizing pump 61, and the photoelectric sensor 71 are all in an off state in which the operation is stopped.
- the exhaust valve 62 is in an open state so that the space inside the air bag 35 communicates with the outside so that the cuff pressure is equal to the atmospheric pressure, and the cuff pressure detected by the pressure sensor 63 shows the same value as the atmospheric pressure. It will be.
- the subject holds the handle 42 of the cuff 20 ⁇ / b> A with the right hand 100 and holds the handle 42 toward the hollow opening of the cuff body 30 of the cuff 20 ⁇ / b> A in the direction of arrow C in the figure.
- the left hand 200 which is a different hand from the right hand 100 is inserted.
- the cuff 20A is moved to the upper arm of the left hand 200, and the handle 42 is provided on the handle 42 with the thumb 101 of the right hand 100, which is the hand holding the handle 42, while maintaining the state of being attached to the upper arm of the left hand 200. Press the push button 44.
- the control unit 11 that has received the pressing of the push button 44 by the subject performs pre-pressurization of the air bag 35 (step S ⁇ b> 102). Specifically, as shown in FIG. 8, the control unit 11 closes the exhaust valve 62 in order to make the space inside the air bladder 35 out of communication at the time t1 when the push button 44 is pressed, Subsequently, driving of the pressurizing pump 61 is started to inject air into the air bladder 35 at time t2. And the control part 11 stops the drive of the pressurization pump 61 at the time t3 after progress of predetermined time.
- the time for which the pressurizing pump 61 is driven is a time necessary for a predetermined amount of air to be injected into the space inside the air bladder 35.
- the pre-pressurization for the air bag 35 is completed (step S103).
- the control unit 11 drives the photoelectric sensor 71 to start detecting the tightening length of the tightening belts 31 and 32 (step S104). Specifically, as shown in FIG. 8, the control unit 11 drives the photoelectric sensor 71 at time t ⁇ b> 4 after the pressurization pump 61 stops, and the photoelectric sensor of the barcode 74 provided on the second tightening belt 32. Reading by the sensor 71 is started.
- the control unit 11 starts the tightening operation of the cuff 20A with respect to the upper arm (step S105). At that time, the control unit 11 determines whether or not the cuff 20A has been tightened with respect to the upper arm in a predetermined tightening state (step S106), and when the predetermined tightening state is not achieved (NO in step S106). Continues the tightening operation of the cuff 20A with respect to the upper arm, and when the predetermined tightening state is reached (YES in step S106), the tightening operation of the cuff 20A with respect to the upper arm is stopped (step S107).
- the control unit 11 starts the winding operation of the second tightening belt 32 by the winding roller 58 by rotationally driving the geared motor 51 in the forward direction at time t5.
- the control unit 11 detects the cuff pressure of the air bladder 35 during the winding operation by the pressure sensor 63, and the forward direction of the geared motor 51 at time t6 when the detected cuff pressure reaches a predetermined threshold value.
- the electromagnetic brake 52 is driven to stop the rotation of the take-up roller 58.
- the threshold value is determined in advance based on the tightening force of the cuff 20A with respect to the upper arm suitable for blood pressure value measurement.
- the air bag 35 is reliably pressed against the upper arm 202 by the fastening belts 31 and 32. Become. Therefore, in the subsequent measurement operation, the air bag 35 is inflated, so that the upper arm 202 is surely compressed by the cuff 20A, and the artery located inside the upper arm 202 can be reliably blocked.
- the tightening length of the tightening belts 31 and 32 in this state is determined as the perimeter of the upper arm by the upper arm perimeter measuring circuit 72, and the determined upper arm perimeter is input to the control unit 11.
- the control unit 11 outputs the input upper arm circumference to the memory unit 12, and the memory unit 12 temporarily stores the input upper arm circumference.
- the control unit 11 stops driving the photoelectric sensor 71 and ends the detection of the tightening length (step S108). Specifically, as shown in FIG. 8, the control unit 11 stops driving the photoelectric sensor 71 at time t ⁇ b> 7 and ends reading of the barcode 74 provided on the second tightening belt 32 by the photoelectric sensor 71. To do.
- the control unit 11 determines whether or not the measured upper arm circumference is within a predetermined applicable range of the cuff 20 ⁇ / b> A (step S ⁇ b> 109). . That is, the control unit 11 determines whether or not the measurement result when the blood pressure value is measured using the cuff 20A is the size of the upper arm within a range in which the accuracy can be ensured.
- the control unit 11 determines that the measured upper arm perimeter is within a predetermined applicable range of the cuff 20A (YES in step S109)
- the control unit 11 proceeds to step S110.
- the process proceeds to step S115.
- step S109 the control unit 11 starts pressurization of the air bladder 35 for blood pressure measurement (step S110). Specifically, as shown in FIG. 8, the control unit 11 drives the pressurizing pump 61 to increase the cuff pressure at time t8, and pressurizes the air bladder 35 so as to obtain a predetermined cuff pressure. .
- the control unit 11 starts the slow depressurization of the air bladder 35 for blood pressure measurement (step S111). Specifically, as shown in FIG. 7, the control unit 11 stops driving the pressure pump 61 at time t ⁇ b> 9 when the pressure sensor 63 detects that the internal pressure of the air bladder 35 has reached a predetermined internal pressure. Thereafter, the exhaust valve 62 is gradually opened while controlling the opening amount of the exhaust valve 62. At that time, the control unit 11 acquires the fluctuation of the cuff pressure detected by the pressure sensor 63.
- the control unit 11 calculates a blood pressure value based on the variation of the cuff pressure obtained in the slow depressurization process (step S112). Subsequently, the control unit 11 outputs the blood pressure value obtained in step S112 to the memory unit 12 and the display unit 14, and the memory unit 12 stores the blood pressure value as a measurement result (step S113). The blood pressure value as the measurement result is displayed (step S114).
- the display unit 14 displays the systolic blood pressure value and the diastolic blood pressure value as numerical values, for example.
- step S109 the control unit 11 opens the air bag 35 (step S115) and the cuff 20A with respect to the upper arm 202.
- a tightening release operation is performed (step S116). Specifically, as shown in FIG. 8, the control unit 11 completely opens the exhaust valve 62 at time t ⁇ b> 10 when the calculation of the blood pressure value ends, exhausts the air in the air bladder 35 to the outside, and then At time t11, the operation of the electromagnetic brake 52 is stopped, and at time t12, the geared motor 51 is rotationally driven in the reverse direction, and the second tightening belt 32 is sent from the winding roller 58.
- control unit 11 stops driving the geared motor 51 at time t13 when the second tightening belt 32 is completely delivered from the take-up roller 58.
- the sphygmomanometer 1 ⁇ / b> A enters a standby state, and waits for an input of a power-off command from the operation unit 16 of the subject, and stops supplying power as a power source.
- the bar code 74 as the marker provided on the second fastening belt 32 and the photoelectric sensor 71 as the reading unit provided on the base 41 are used. It becomes possible to accurately measure the perimeter of the upper arm 202 as a measurement site to which 20A is attached. In general, a photoelectric sensor is very small. Therefore, if the above configuration is adopted, a cuff capable of automatically measuring the circumference of the upper arm can be made small and simple. Further, the barcode as a marker indicating the position information can be simply configured by attaching an encoder strip to a predetermined position of the fastening belt, and the apparatus configuration is not complicated and the apparatus is not enlarged.
- the geared motor 51, the electromagnetic brake 52, the take-up roller 58, and the like as the tightening length adjusting mechanism 50 are housed in the base 41 of the handle portion 40.
- the cuff 20A can be made small and compact.
- grip 42 provided on cuff 20A is held by left hand 200, which is different from right hand 100 to which cuff 20A is attached, and cuff 20A is hollow in this state.
- the left hand 200 to which the cuff 20A is attached is inserted into the opening, the cuff 20A is directed to the upper arm 202, and then the push button 44 provided on the handle 42 is pressed down. It is possible to automatically perform the tightening operation and the upper arm circumference measurement operation thereafter. Therefore, the cuff 20A can be attached to the upper arm 202 very easily, and the upper arm perimeter can be easily obtained.
- the sphygmomanometer 1A In the sphygmomanometer 1A according to the present embodiment, not only the operation of attaching the cuff 20A but also the blood pressure measurement operation performed thereafter, and the tightening release operation for the upper arm 202 of the cuff 20A performed after the measurement operation. Are automatically and continuously performed. Therefore, by adopting the above configuration, it is possible to obtain a sphygmomanometer that is very convenient and can be attached to the cuff 20A, measured the blood pressure value, and removed the cuff 20A by a so-called one-touch operation.
- the measured upper arm circumference is within the applicable range of the cuff 20A (that is, the blood pressure value is measured using the cuff 20A).
- the control unit 11 determines whether the accuracy of the blood pressure value as the measurement result is within a range in which the measurement result can be ensured, so that the measured upper arm circumference is within the applicable range.
- the blood pressure value is measured thereafter.
- the operation is immediately terminated. It is configured as follows. Therefore, when the size of the upper arm of the subject is outside the applicable range, the blood pressure value is not measured in the first place, so blood pressure that does not provide the subject with inaccurate measurement results. It can be a total.
- the tightening force with respect to the upper arm 202 of the cuff 20A is detected using a tightening force detection mechanism, Since the tightening force adjustment mechanism 50 is used to maintain the optimum tightening force, the reliable winding of the cuff 20A around the upper arm 202 is reproduced every measurement.
- the sphygmomanometer 1A in the above-described embodiment the case where the length of each section, which is the minimum unit of the upper arm that can be measured, is 10 mm is exemplified. However, if the length of this section is made smaller, It is possible to measure the upper arm circumference more precisely. However, as the width of the bar code 74 attached to the second tightening belt 32 becomes smaller, the detection tends to be difficult.
- the barcode position mark included in the I column is indicated by a bit display of octal one digit, but can be measured by variously changing this. It becomes possible to widen the range or increase the measurable resolution.
- the sphygmomanometer 1A includes a position mark in the barcode 74 so that the barcode 74 itself has position information in a portion to which the barcode is attached. is doing.
- the bar code 74 is always detected from the end of the encoder strip 73 when measuring the upper arm circumference, only the II-line bar code group shown in FIG.
- the upper arm circumference measuring circuit 72 counts the number of barcodes detected by the photoelectric sensor 71B, whereby the movement amount of the tightening belts 31 and 32 is detected. It is possible to specify the upper arm circumference based on the amount. Therefore, since the reading unit can be configured with only one photoelectric sensor, the apparatus configuration is simplified, and it is not necessary to provide a position mark, header, or footer, so that it is possible to improve the resolution of the upper arm circumference measurement. become.
- a rotation amount detection unit represented by a rotary encoder or the like is provided in the cuff 20A, and the rotation amount (rotation angle) of the winding roller 58 is detected by the rotation amount detection unit.
- the bar code group that is, FIG. 6 that increases the resolution of the measurement of the upper arm circumference or indicates the timing of the measurement. It is also possible to omit the bar code group in column II shown in FIG.
- the position where the barcode 74 as the marker described above is provided is not limited to the fastening belts 31 and 32.
- a roller, a gear, or the like as a rotating member that rotates with the movement of the fastening belts 31 and 32 may be separately provided, and the same barcode as the barcode 74 described above may be provided on the roller or gear.
- a photoelectric sensor 71 as a reading unit is disposed so as to face these rollers and gears.
- the marker is not necessarily a bar-shaped barcode as described above, and a plurality of markers having the same shape such as a circular shape or a triangular shape may be provided on a fastening belt, a roller, a gear, or the like.
- the rotation amount detection unit represented by the above-described rotary encoder or the like
- the above-described configuration using the barcode 74 and the photoelectric sensor 71 can be eliminated.
- the cuff 20A is provided with a rotating member that rotates in accordance with the movement of the tightening belts 31 and 32, and the amount of rotation of the rotating member is detected by the above-described rotation amount detection unit. What is necessary is just to set it as the structure which measures 32 movement amount.
- the rotary encoder may be attached to the take-up roller 58 serving as a rotating member.
- the upper arm circumference measured by the upper arm circumference measurement unit is used for determining whether the size of the upper arm to which the cuff 20A is attached is within the applicable range of the cuff 20A.
- the measured circumference of the upper arm can be used in various other ways.
- the following first and second modifications of the present embodiment show other apparatus configuration examples using the measured upper arm circumference.
- the configuration of the sphygmomanometer according to the first and second modified examples is mainly different from the sphygmomanometer in the present embodiment described above only in the configuration of the control unit 11, and the description thereof is omitted except for the difference. Does not repeat here.
- the sphygmomanometer according to the first modification uses the upper arm circumference measured by the upper arm circumference measurement unit to determine the pressurizing condition and the depressurizing condition of the air bag 35 that is inflated and inflated for measuring the blood pressure value. is there.
- the controller 11 controls the inflating / deflating operation control unit (which controls at least one of the inflating and deflating operations of the air bladder 35 by the inflating / deflating mechanism) (Not shown).
- the expansion / contraction movement control unit is configured to measure the upper arm circumference measured from a plurality of expansion / contraction operation programs stored in advance in a memory unit or the like based on the information about the upper arm circumference measured from the upper arm circumference measurement circuit 72.
- a suitable expansion / contraction operation program is selected, and based on this, the operation of the pressurization pump 61 and / or the exhaust valve 62 is controlled via the pressurization pump drive circuit 64 and / or the exhaust valve drive circuit 65.
- the expansion / contraction operation program for example, for a subject with a small upper arm size, a program for slowly performing a pressure operation by reducing the discharge amount per unit time of the pressure pump 61, or conversely, the size of the upper arm It is assumed that a program for performing a pressurization operation quickly by increasing the discharge amount per unit time of the pressurization pump 61 for a subject having a large pressure.
- the expansion / contraction operation program is, for example, a program for reducing the amount of air discharged from the air bag 35 per unit time by adjusting the opening amount of the exhaust valve 62 to be small for a subject with a small upper arm size.
- the opening amount of the exhaust valve 62 is adjusted to be large and the amount of air discharged from the air bag 35 per unit time is increased.
- FIG. 11 is a flowchart showing a processing procedure of the sphygmomanometer according to the first modification. Note that the flowchart shown in FIG. 11 shows only the changes from the flowchart shown in FIG. As shown in FIG. 11, in the sphygmomanometer according to the present modification, prior to performing the processing of steps S110 to S112, which is processing for blood pressure measurement, based on the upper arm circumference information acquired in step S108, In step S109A, the pressurizing condition and / or the depressurizing condition of the air bladder 35 are determined.
- control unit 11 receives the output of the upper arm circumference measurement circuit 72 and accesses the memory unit 12 to read out the optimum expansion / contraction operation program, and is a process for blood pressure measurement performed thereafter.
- the expansion / contraction operation control unit included in the control unit 11 controls the operation of the pressurization pump 61 and / or the exhaust valve 62 via the pressurization pump drive circuit 64 and / or the exhaust valve drive circuit 65.
- the inflation operation and / or the contraction operation of the air bag 35 according to the size of the upper arm to which the cuff 20A is attached is realized.
- the sphygmomanometer according to the second modification uses the upper arm circumference measured by the upper arm circumference measurement unit as a correction factor when calculating the blood pressure value.
- blood pressure information for correcting the blood pressure value as the measured blood pressure information to the blood pressure information measuring unit (not shown) provided in the control unit 11.
- a correction unit (not shown) is further provided.
- the blood pressure information correction unit calculates a correction coefficient based on the information on the upper arm periphery length input from the upper arm periphery length measurement circuit 72, corrects the envelope used for blood pressure value calculation using the correction coefficient, Based on this, a parameter for calculating the blood pressure value is determined.
- the blood pressure information measurement unit calculates a blood pressure value as a measurement result based on the determined parameter.
- FIG. 12 is a flowchart showing a processing procedure of the sphygmomanometer according to the second modified example. Note that the flowchart shown in FIG. 12 shows only the changes from the flowchart shown in FIG. As shown in FIG. 12, in the sphygmomanometer according to the present modification, step S111A is performed based on the upper arm circumference information acquired in step S108 prior to performing the process of step S112, which is a process for calculating the blood pressure value. In S111C, the correction process for calculating the blood pressure value described above is performed.
- a correction coefficient is calculated based on the upper arm circumference measurement information input from the upper arm circumference measurement circuit 72 in step S111A, and an envelope used for blood pressure value calculation using the correction coefficient in step S111B.
- the line is corrected, and a parameter for calculating the blood pressure value is determined based on the envelope line corrected in step S111C.
- a necessary correction is added to the measured blood pressure value according to the size of the upper arm to which the cuff 20A is attached.
- the measured blood pressure value tends to be higher than the actual blood pressure. High-precision blood pressure measurement is possible.
- a sphygmomanometer uses a bar code 74 provided on the second fastening belt 32 and a photoelectric sensor 71 provided on the base 41 to It is the example comprised so that operation
- release operation might be performed.
- a configuration such as the sphygmomanometer 1A in the present embodiment described above is employed, it is preferable to configure the cuff 20A so that its circumferential length always returns to the same length after use.
- the return of the length of the cuff 20A in the circumferential direction to the initial length is realized.
- FIG. 13 is a flowchart showing the processing procedure of the sphygmomanometer according to the third modification. Note that the flowchart shown in FIG. 13 shows only the changes from the flowchart shown in FIG. As shown in FIG. 13, in the sphygmomanometer according to this modification, after opening the air bladder 35 in step S115, the operation of the electromagnetic brake 52 is stopped in step S116A and the geared motor 51 is rotated in the reverse direction. By releasing the second tightening belt 32 from the winding roller 58, the tightening releasing operation of the cuff 20A is started.
- the control unit 11 determines whether or not the circumferential length of the cuff 20A has returned to the pre-stored initial length based on the position information detected by the upper arm circumference measurement unit (Step S11). S116B) If it is not determined that it has returned (NO in step S116B), the cuff 20A continues to be tightened and if it is determined that it has returned (YES in step S116B), the cuff 20A The tightening release operation is stopped (step S116C).
- the circumferential length of the cuff 20A is always restored to the same length after use, so that the circumference of the upper arm is changed every time it is used.
- the length can be reliably measured with high accuracy.
- FIG. 14 is a diagram showing a functional block configuration of the sphygmomanometer according to the second embodiment of the present invention.
- the blood pressure monitor 1B in the present embodiment is the same in appearance as the blood pressure monitor 1A in the above-described first embodiment, and most of the functional blocks have a common configuration. Therefore, portions similar to those in the first embodiment described above are denoted by the same reference numerals in the drawing, and the description thereof will not be repeated here.
- the sphygmomanometer 1A uses the air bag 35 and the air system component 60 as a tightening force detection mechanism for detecting the tightening force of the tightening belts 31 and 32 with respect to the upper arm 202, and the tightening force is used as the air bag 35. It was configured to be understood as internal pressure.
- the sphygmomanometer 1B according to the present embodiment is added to the take-up roller 58 around which the second tightening belt 32 is wound as a tightening force detection mechanism for detecting the tightening force of the tightening belts 31 and 32 with respect to the upper arm 202. By using a torque sensor that detects rotational torque, the tightening force is regarded as rotational torque applied to the winding roller 58.
- a torque sensor 59 is provided in the cuff 20B.
- the torque sensor 59 is a means for detecting rotational torque applied to the take-up roller 58, and is attached to, for example, a shaft 57a (see FIG. 5) to which the take-up roller 58 is fixed.
- FIG. 15 is a flowchart showing the processing procedure of the sphygmomanometer in the present embodiment
- FIG. 16 is a timing chart showing the operation status and the operating state of each part of the sphygmomanometer in the present embodiment in time series.
- the processing procedure of the sphygmomanometer 1B in the present embodiment will be described together with the operating states and operating states of the respective parts of the sphygmomanometer 1B.
- the program according to the flowchart shown in FIG. 15 is stored in advance in the memory unit 12 shown in FIG. 14, and the control unit 11 reads out the program from the memory unit 12 and executes the program.
- step S201 when the test subject operates the operation unit 16 of the sphygmomanometer 1 ⁇ / b> B and inputs a power-on command, power as a power source is supplied from the power supply unit 18 to the control unit 11.
- Control unit 11 is driven to initialize sphygmomanometer 1B (step S201).
- the geared motor 51, the electromagnetic brake 52, the pressure pump 61, and the photoelectric sensor 71 are all in an off state in which the operation is stopped.
- the rotational torque detected by the torque sensor 59 is almost zero, and the exhaust valve 62 is open to communicate the space inside the air bladder 35 with the outside to make the cuff pressure equal to the atmospheric pressure.
- the cuff pressure detected by 63 shows the same value as the atmospheric pressure.
- the control unit 11 drives the photoelectric sensor 71 to start detecting the tightening length of the tightening belts 31 and 32 (step S202). Specifically, as shown in FIG. 16, the control unit 11 drives the photoelectric sensor 71 at time t ⁇ b> 1 after the end of initialization, and the photoelectric sensor 71 of the barcode 74 provided on the second fastening belt 32. Start reading.
- the subject grips the handle 42 of the cuff 20B with the right hand 100 and grips the handle 42 toward the hollow opening of the cuff main body 30 of the cuff 20B, as in the case of the first embodiment described above.
- the left hand 200 which is a different hand from the right hand 100, is inserted (see FIG. 9).
- the cuff 20B is moved to the upper arm of the left hand 200, and the handle 42 is provided on the handle 42 with the thumb 101 of the right hand 100, which is the hand holding the handle 42, while maintaining the state of being in contact with the upper arm of the left hand 200. Press the push button 44.
- the control unit 11 that has received the pressing of the push button 44 by the subject starts the tightening operation of the cuff 20B with respect to the upper arm (step S203). At that time, the control unit 11 determines whether or not the cuff 20B has been tightened with respect to the upper arm in a predetermined tightening state (step S204), and when it is not in the predetermined tightening state (NO in step S204). Continues the tightening operation of the cuff 20B with respect to the upper arm and stops the tightening operation of the cuff 20B with respect to the upper arm when the predetermined tightening state is reached (YES in step S204) (step S205).
- the control unit 11 starts the winding operation of the second tightening belt 32 by the winding roller 58 by rotationally driving the geared motor 51 in the forward direction at time t2.
- the control unit 11 detects the rotational torque applied to the winding roller 58 during the winding operation by the torque sensor 59, and at time t3 when the detected rotational torque reaches a predetermined threshold value, the geared motor 51 The forward rotation is stopped, and at the same time, the electromagnetic brake 52 is driven to stop the winding roller 58 from rotating.
- the threshold value is determined in advance based on the tightening force of the cuff 20B on the upper arm suitable for blood pressure value measurement.
- the air bag 35 is securely attached to the upper arm 202 by the fastening belts 31 and 32. It will be in the state pressed (refer FIG. 10). Therefore, in the subsequent measurement operation, the air bag 35 is inflated, so that the upper arm 202 is surely compressed by the cuff 20B, and the artery located inside the upper arm 202 can be surely blocked.
- the tightening length of the tightening belts 31 and 32 in this state is determined as the perimeter of the upper arm by the upper arm perimeter measuring circuit 72, and the determined upper arm perimeter is input to the control unit 11.
- the control unit 11 outputs the input upper arm circumference to the memory unit 12, and the memory unit 12 temporarily stores the input upper arm circumference.
- the control unit 11 stops driving the photoelectric sensor 71 and ends the detection of the tightening length (step S206). Specifically, as shown in FIG. 16, the control unit 11 stops driving the photoelectric sensor 71 at time t ⁇ b> 4 and ends reading of the barcode 74 provided on the second fastening belt 32 by the photoelectric sensor 71. To do.
- the control unit 11 determines whether or not the measured upper arm circumference is within a predetermined applicable range of the cuff 20 ⁇ / b> B (step S ⁇ b> 207). . That is, the control unit 11 determines whether or not the measurement result when the blood pressure value is measured using the cuff 20B is the size of the upper arm within a range in which the accuracy can be ensured.
- the control unit 11 determines that the measured upper arm circumference is within a predetermined applicable range of the cuff 20B (YES in step S207)
- the control unit 11 proceeds to step S208.
- the process proceeds to step S213.
- the control unit 11 starts pressurization of the air bladder 35 for blood pressure measurement (step S208). Specifically, as shown in FIG. 16, the control unit 11 closes the exhaust valve 62 in order to make the space inside the air bag 35 out of communication with the outside at time t5, and then at time t6, the air bag. In order to inject air into the air 35, driving of the pressurizing pump 61 is started to increase the cuff pressure, and the air bag 35 is pressurized so as to become a predetermined cuff pressure.
- the control unit 11 starts the slow depressurization of the air bladder 35 for blood pressure measurement (step S209). Specifically, as shown in FIG. 16, the control unit 11 stops driving the pressure pump 61 at time t7 when the pressure sensor 63 detects that the internal pressure of the air bladder 35 has reached a predetermined internal pressure. Thereafter, the exhaust valve 62 is gradually opened while controlling the opening amount of the exhaust valve 62. At that time, the control unit 11 acquires the fluctuation of the cuff pressure detected by the pressure sensor 63.
- the control unit 11 calculates a blood pressure value based on the variation of the cuff pressure obtained in the slow depressurization process (step S210). Subsequently, the control unit 11 outputs the blood pressure value obtained in step S210 to the memory unit 12 and the display unit 14, and the blood pressure value is stored as a measurement result in the memory unit 12 (step S211). The blood pressure value as the measurement result is displayed (step S212).
- the display unit 14 displays the systolic blood pressure value and the diastolic blood pressure value as numerical values, for example.
- step S207 the control unit 11 opens the air bag 35 (step S213) and the cuff 20B with respect to the upper arm 202.
- a tightening release operation is performed (step S214). Specifically, as shown in FIG. 16, the control unit 11 completely opens the exhaust valve 62 at time t8 when the calculation of the blood pressure value is finished, exhausts the air in the air bag 35 to the outside, and then At time t9, the operation of the electromagnetic brake 52 is stopped, and at time t10, the geared motor 51 is rotationally driven in the reverse direction, and the second tightening belt 32 is sent from the winding roller 58.
- control unit 11 stops driving the geared motor 51 at time t11 when the second tightening belt 32 is completely delivered from the take-up roller 58. Thereafter, the sphygmomanometer 1B is in a standby state, and waits for an input of a power-off command from the operation unit 16 of the subject, and stops supplying power as a power source.
- the winding operation operation unit for starting the winding operation of the second tightening belt 32 is configured by the push button 44.
- the winding operation operation unit it is not always necessary to configure the winding operation operation unit with a push button, and it is configured with a slide type button, a dial type button, a touch sensor, a voice recognition sensor, or the like. Also good.
- the position at which the winding operation operation unit is provided is not limited to the position at which the handle unit 40 can be operated with the thumb, but may be provided at another position of the handle unit 40 or the main body 10.
- the non-wearing part is the upper arm of the left hand and the hand holding the handle is the right hand has been described as an example. It is also possible to use the part as the upper arm of the right hand and the left hand as the hand holding the handle.
- a so-called upper arm type sphygmomanometer cuff that is attached to the upper arm when measuring blood pressure values has been described as an example of the sphygmomanometer cuff.
- the present invention is not limited to this, such as a so-called wrist-type sphygmomanometer cuff that is worn on the wrist when measuring blood pressure values, or a so-called ankle-type sphygmomanometer cuff that is worn on the ankle when measuring blood pressure values.
- the invention can also be applied.
- the present invention is applied to a sphygmomanometer capable of measuring a systolic blood pressure value and a diastolic blood pressure value has been described as an example.
- the present invention can also be applied to a blood pressure information measuring device capable of measuring blood pressure information other than blood pressure values and diastolic blood pressure values.
- 1A, 1B Blood pressure monitor 10 main body, 11 control unit, 12 memory unit, 14 display unit, 16 operation unit, 18 power supply unit, 20A, 20B cuff, 30 cuff main unit, 31 first tightening belt, 31a one end, 31b other end, 32 second clamping belt, 32a one end, 32b other end, 33 exterior cover, 34 curler, 34a cut, 35 air bag, 40 handle part, 41 base part, 42 handle, 44 push button, 46 Support frame, 50 tightening length adjustment mechanism, 51 geared motor, 51a motor part, 51a1 rotating shaft, 51b deceleration part, 51c output shaft, 52 electromagnetic brake, 53 motor drive circuit, 54 electromagnetic brake drive circuit, 55, 56, 57 Gear, 56a, 57a shaft, 58 take-up roller, 59 ton Sensor, 60 air system components, 61 pressure pump, 62 exhaust valve, 63 pressure sensor, 64 pressure pump drive circuit, 65 exhaust valve drive circuit, 66 amplifier, 67 A / D conversion circuit, 71, 71A, 71B photo
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Engineering & Computer Science (AREA)
- Medical Informatics (AREA)
- Physics & Mathematics (AREA)
- Ophthalmology & Optometry (AREA)
- Biophysics (AREA)
- Pathology (AREA)
- Dentistry (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Physiology (AREA)
- Molecular Biology (AREA)
- Surgery (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
Abstract
A blood pressure meter is provided with a cuff (20A) having therein an air bag and also with an expanding and contracting mechanism for expanding and contracting the air bag. The cuff (20A) has a tubular cuff body section (30), and the cuff body section (30) is provided with fastening belts (31, 32) wrapped around the outside of the air bag and also with a fastening length adjusting mechanism (50) for variably adjusting the fastening length of the fastening belts (31, 32) relative to an upper arm. The blood pressure meter is also provided with an upper arm circumference measuring section for measuring the circumferential length of the upper arm by using the fastening belts (31, 32). The fastening belts (31, 32) have a barcode (74) for specifying the circumferential length of the upper arm. The circumference measuring section includes a photoelectric sensor for specifying the circumferential length of the upper arm by reading the marker (74). Thus, the blood pressure meter has a function capable of accurately and precisely measuring the circumferential length of the upper arm which is a portion to be measured.
Description
本発明は、血圧値等の血圧情報を測定可能な血圧情報測定装置に関し、より特定的には、カフが装着される被測定部位の周囲長を計測する機能を備えた血圧情報測定装置に関する。
The present invention relates to a blood pressure information measuring device capable of measuring blood pressure information such as a blood pressure value, and more particularly, to a blood pressure information measuring device having a function of measuring the perimeter of a measurement site to which a cuff is attached.
被験者の血圧情報を取得することは、被験者の健康状態を知る上で非常に重要なことである。近年では、従来から健康管理の代表的な指標として広くその有用性が認められている収縮期血圧値(最高血圧値)、拡張期血圧値(最低血圧値)等を取得することに限られず、被験者の脈波を取得することによって心臓負荷や動脈の硬さの変化を捉える試み等がなされている。血圧情報測定装置は、取得した血圧情報に基づいてこれら健康管理のための指標を得るための装置であり、循環器系の疾患の早期発見や予防、治療等の分野においてさらなる活用が期待されている。なお、血圧情報には、収縮期血圧値、拡張期血圧値、平均血圧値、脈波、脈拍、AI(Augmentation Index)値等、循環器系に関連する種々の情報が広く含まれる。
It is very important to acquire the blood pressure information of the subject in order to know the health status of the subject. In recent years, it is not limited to acquiring systolic blood pressure values (maximum blood pressure values), diastolic blood pressure values (minimum blood pressure values), etc., which have been widely recognized as useful indicators of health care. Attempts have been made to capture changes in cardiac load and arterial stiffness by acquiring a subject's pulse wave. The blood pressure information measuring device is a device for obtaining indexes for health management based on the acquired blood pressure information, and is expected to be further utilized in the fields of early detection, prevention, treatment, etc. of cardiovascular diseases. Yes. The blood pressure information includes a wide variety of information related to the circulatory system such as systolic blood pressure value, diastolic blood pressure value, average blood pressure value, pulse wave, pulse, AI (Augmentation Index) value, and the like.
一般に、血圧情報の測定には、流体袋を内包するカフが利用される。ここで、カフとは、内腔を有する帯状の構造物であって生体の一部に巻付けが可能なものを意味し、気体や液体等の流体を内腔に注入することにより流体袋を膨張・収縮させて血圧情報の測定に利用されるもののことを指す。たとえば、収縮期血圧値や拡張期血圧値等の血圧値を測定するための血圧情報測定装置(以下、単に血圧計とも称する)においては、動脈を圧迫するための流体袋を内包するカフを生体の体表面に巻付け、巻付けられた流体袋を膨張・収縮させて動脈圧脈波を流体袋の内圧の変化として捉えることにより、血圧値の測定が行なわれる。なお、特に腕に巻き付けられて使用されるカフは、腕帯あるいはマンシェットとも呼ばれる。
Generally, a cuff containing a fluid bag is used for measuring blood pressure information. Here, the cuff means a band-shaped structure having a lumen and can be wound around a part of a living body, and a fluid bag is formed by injecting a fluid such as gas or liquid into the lumen. It refers to what is used to measure blood pressure information after being inflated and deflated. For example, in a blood pressure information measuring device (hereinafter also simply referred to as a sphygmomanometer) for measuring a blood pressure value such as a systolic blood pressure value or a diastolic blood pressure value, a living body is provided with a cuff that contains a fluid bag for compressing an artery. The blood pressure value is measured by winding the wound fluid bag on the body surface and expanding / contracting the wound fluid bag to capture the arterial pressure pulse wave as a change in the internal pressure of the fluid bag. In particular, the cuff used by being wound around the arm is also called an armband or a manchette.
カフに内包される流体袋としての空気袋は、被測定部位へのカフの装着時において被測定部位の全体を覆うように被測定部位の周方向に巻き付けられる。収縮期血圧値や拡張期血圧値等の血圧値を測定するための血圧計の場合、一般に被測定部位としては上腕や手首が採用されるが、これら上腕や手首のサイズには個体差が大きい。そのため、細い腕の人から太い腕の人まですべての人を単一のサイズのカフで対応しようとした場合には、カフに内包された空気袋の巻付け方向の長さが一定であるのに対し、被測定部位の周囲長は被験者ごとに異なるため、空気袋の巻付け状態は被測定部位のサイズに応じて異なることとなる。
The air bag as a fluid bag contained in the cuff is wound around the measurement site so as to cover the entire measurement site when the cuff is attached to the measurement site. In the case of a sphygmomanometer for measuring blood pressure values such as systolic blood pressure values and diastolic blood pressure values, the upper arm and wrist are generally used as the measurement site, but there are large individual differences in the size of the upper arm and wrist . Therefore, when trying to deal with all people from thin arm to thick arm with a single size cuff, the length in the winding direction of the air bag contained in the cuff is constant. On the other hand, since the circumference of the site to be measured is different for each subject, the wrapped state of the air bag varies depending on the size of the site to be measured.
この巻付け状態の違いは、血圧値の測定結果に影響を与える場合がある。特に、被験者の腕が太い場合には、装着状態において被測定部位の全体を空気袋にて完全に覆うことができず、被測定部位の周方向の一部が空気袋で覆われていない状態となり得る。この場合には、空気袋による被測定部位への圧迫の際に十分な圧迫力が得られず、実際の血圧値よりもやや高めに血圧値が測定されることとなってしまう。
This difference in winding state may affect the blood pressure measurement results. In particular, when the subject's arm is thick, the entire measurement site cannot be completely covered with the air bag in the wearing state, and the circumferential portion of the measurement site is not covered with the air bag. Can be. In this case, sufficient compression force cannot be obtained when the measurement site is compressed by the air bag, and the blood pressure value is measured slightly higher than the actual blood pressure value.
このような問題の解決が企図された血圧計として、たとえば特開2004-154458号公報(特許文献1)に開示の血圧計や、特開平7-59740号公報(特許文献2)に開示の血圧計がある。上記特開2004-154458号公報に開示の血圧計においては、空気袋を加圧するための加圧ポンプの回転数を検出することにより加圧ポンプの吐出量を計測する吐出量計測機構が設けられており、当該吐出量計測機構によって計測された吐出量とカフ圧(空気袋の内圧)とに基づいて被験者の被測定部位の周囲長が推定され、当該推定結果に基づいて測定された血圧値に必要に応じて補正が施される構成が採用されている。また、上記特開平7-59740号公報に開示の血圧計においては、カフの周方向の一端部に導電端子を含むフックが設けられるとともに、カフの周方向の他端部寄りの部分に上記フックが引っ掛け可能な導電端子を含むフック受けが複数設けられており、カフの装着に際してどの位置のフック受けにフックが引っ掛けられたかを検出することによって被測定部位の周囲長が計測され、当該計測結果に基づいて測定された血圧値に必要に応じて補正が施される構成が採用されている。
As a sphygmomanometer designed to solve such a problem, for example, a sphygmomanometer disclosed in Japanese Patent Application Laid-Open No. 2004-154458 (Patent Document 1) or a blood pressure disclosed in Japanese Patent Application Laid-Open No. 7-59740 (Patent Document 2). There is a total. In the sphygmomanometer disclosed in the above Japanese Patent Application Laid-Open No. 2004-154458, a discharge amount measuring mechanism for measuring the discharge amount of the pressurizing pump by detecting the rotation speed of the pressurizing pump for pressurizing the air bag is provided. The peripheral length of the measured region of the subject is estimated based on the discharge amount and the cuff pressure (inner pressure of the air bag) measured by the discharge amount measuring mechanism, and the blood pressure value measured based on the estimation result A configuration in which correction is performed as necessary is employed. In the sphygmomanometer disclosed in the above-mentioned Japanese Patent Application Laid-Open No. 7-59740, a hook including a conductive terminal is provided at one end portion in the circumferential direction of the cuff, and the hook is disposed at a portion near the other end portion in the circumferential direction of the cuff. A plurality of hook receivers including conductive terminals that can be hooked are provided, and the perimeter of the part to be measured is measured by detecting which position of the hook receiver is hooked when the cuff is attached. A configuration is adopted in which the blood pressure value measured based on is corrected as necessary.
しかしながら、上記特開2004-154458号公報に開示の構成を採用した場合にも、被測定部位の周囲長を正確に推定することが困難であるという課題が残る。上述したように、上記特開2004-154458号公報に開示の血圧計においては、カフの巻付けが完了するまでの加圧ポンプの吐出量とカフ圧とに基づいて被測定部位の周囲長が推定されるが、加圧ポンプの吐出量は被測定部位の周囲長によって一意に決まるものではなく、被測定部位の形状や柔らかさによっても影響を受けるため、たとえば同じ周囲長の被測定部位であったとしても体表面がより柔らかい被測定部位の場合には、推定された周囲長が実際の周囲長よりも大きくなってしまうおそれがある。また、被測定部位を圧迫する空気袋の膨張状態によっても推定される被測定部位の周囲長に誤差が生じる可能性があり、空気袋が均一に膨らむことなく風船状に膨らんだ場合等には、やはり実際の周囲長よりも大きく推定されてしまうおそれがある。
However, even when the configuration disclosed in Japanese Patent Application Laid-Open No. 2004-154458 is adopted, there remains a problem that it is difficult to accurately estimate the perimeter of the measurement site. As described above, in the sphygmomanometer disclosed in Japanese Patent Application Laid-Open No. 2004-154458, the circumference of the measurement site is based on the discharge amount of the pressurizing pump and the cuff pressure until the cuff winding is completed. Although it is estimated, the discharge rate of the pressurizing pump is not uniquely determined by the circumference of the part to be measured and is also affected by the shape and softness of the part to be measured. Even if it exists, in the case where the body surface is softer, the estimated perimeter may be larger than the actual perimeter. Also, there may be an error in the estimated peripheral length of the measurement site, which is also estimated by the inflation state of the air bag that compresses the measurement site.If the air bag inflates into a balloon shape without inflating uniformly, etc. Also, there is a possibility that it is estimated to be larger than the actual perimeter.
また、上記特開平7-59740号公報に開示の構成を採用した場合にも、計測された被測定部位の周囲長に誤差が生じる場合がある。上述したように、上記特開平7-59740号公報に開示の血圧計においては、カフの巻付けの際にカフの周方向の一端部に設けられたフックがカフの周方向の他端部に設けられたフック受けのいずれかに引っ掛けられることになるが、カフの装着自体は人手に委ねられているため、巻付け状態の如何によって計測される被測定部位の周囲長に差が生じることになる。すなわち、カフが隙間なくぴったりと上腕に宛がわれて装着された場合には、正しく被測定部位の周囲長が計測されることになるが、カフが緩めに被測定部位に巻き付けられた場合には、実際の周囲長よりも大きく計測されてしまうことになり、カフが必要以上にきつく被測定部位に巻き付けられた場合には、実際の周囲長よりも小さく計測されてしまうことになる。また、上記特開平7-59740号公報に開示の構成を採用した場合により精緻に被測定部位の周囲長を計測するためには、カフの他端部に非常に多くのフック受けを密に設けることが必要になるため、実際には製造が困難になるという問題もある。
Further, even when the configuration disclosed in the above-mentioned Japanese Patent Application Laid-Open No. 7-59740 is adopted, an error may occur in the circumference of the measured site to be measured. As described above, in the sphygmomanometer disclosed in Japanese Patent Application Laid-Open No. 7-59740, the hook provided at one end portion in the circumferential direction of the cuff is attached to the other end portion in the circumferential direction of the cuff when the cuff is wound. Although it will be hooked on one of the hook receivers provided, since the cuff attachment itself is left to human hands, there will be a difference in the perimeter of the measured site depending on the winding state Become. In other words, when the cuff is attached to the upper arm exactly without gaps, the circumference of the measurement site is correctly measured, but when the cuff is loosely wrapped around the measurement site Will be measured larger than the actual perimeter, and if the cuff is wound around the measurement site that is tighter than necessary, it will be measured smaller than the actual perimeter. In addition, when the configuration disclosed in the above-mentioned Japanese Patent Application Laid-Open No. 7-59740 is adopted, in order to measure the circumference of the measurement site more precisely, a very large number of hook receivers are densely provided at the other end of the cuff. In other words, it is actually difficult to manufacture.
また、上述した測定誤差の問題とは別に、従来の血圧計においては、以下のような問題もあった。
In addition to the above-described measurement error problem, the conventional blood pressure monitor has the following problems.
第1に、被測定部位が非常に大きいサイズの人や極端に小さい人の場合には、そもそも予め想定された被測定部位の周囲長の範囲を逸脱しているにも拘らず、カフ自体の装着は行なえ、その結果、適正な測定結果が得られないにも拘らず血圧値の測定がそのまま行なえてしまうという問題があった。このような状況においては、被測定部位のサイズが当該カフの適用可能範囲外であることを知らずに被験者が測定結果を適正なものと思い込むおそれがあり、正確でない測定結果を被験者に提供しないための工夫が求められていた。
First, in the case of a person with a very large size or an extremely small person to be measured, the cuff itself is in spite of the fact that it deviates from the range of the perimeter of the part to be measured that was assumed in the first place. As a result, there is a problem that blood pressure values can be measured as they are even though proper measurement results cannot be obtained. In such a situation, the subject may think that the measurement result is appropriate without knowing that the size of the part to be measured is outside the applicable range of the cuff, and not provide the subject with an inaccurate measurement result. Ingenuity was required.
第2に、実際にカフが装着される被測定部位のサイズが予め判明している場合には、加圧ポンプ等の動作を制御して空気の流量を調節することにより、最適な空気袋の膨張状態が実現されるように膨張動作を調節したり、測定に要する時間を短縮するために膨張および収縮動作を調節したりすることが可能になるが、従来の血圧計においては、被測定部位のサイズを正確にかつ精緻に測定することができず、このような制御は実際には行なわれていなかった。そのため、被測定部位のサイズを正確にかつ精緻に測定するための工夫が求められていた。
Secondly, when the size of the part to be measured where the cuff is actually attached is known in advance, the optimal air bag is adjusted by controlling the operation of the pressurizing pump or the like to adjust the air flow rate. It is possible to adjust the inflating motion so that the inflated state is realized, and to adjust the inflating and deflating motion in order to reduce the time required for measurement. Such a control has not been performed in practice because the size of the film cannot be measured accurately and precisely. Therefore, a device for accurately and precisely measuring the size of the measurement site has been demanded.
本発明は、上述の問題点に鑑みてなされたものであり、本発明の第1の目的は、被測定部位の周囲長を正確にかつ精緻に計測することができる機能を備えた血圧情報測定装置を提供することにあり、また本発明の第2の目的は、上記第1の目的に加え、計測された被測定部位の周囲長の情報を有効に活用することにより、高性能化、高機能化された血圧情報測定装置を提供することにある。
The present invention has been made in view of the above-described problems, and a first object of the present invention is to measure blood pressure information having a function capable of accurately and precisely measuring the circumference of a measurement site. A second object of the present invention is to provide an apparatus, and in addition to the first object, by effectively utilizing the information on the circumference of the measured region to be measured, it is possible to improve the performance and increase the performance. The object is to provide a functional blood pressure information measuring device.
本発明に基づく血圧情報測定装置は、カフと、膨縮機構と、血圧情報測定部と、締付け長さ調節機構と、周囲長計測部とを備えている。上記カフは、被測定部位を圧迫するための流体袋と、上記流体袋の外側に巻き回された締付けベルトとを含み、周方向に切れ目を有さず、軸方向から被測定部位が挿入可能に構成された環状の形態を有している。上記膨縮機構は、上記流体袋を膨張および収縮させるためのものであり、上記血圧情報測定部は、上記流体袋を利用して血圧情報を測定する。上記締付け長さ調節機構は、上記締付けベルトの被測定部位に対する締付け長さを可変に調節するためのものであり、上記周囲長計測部は、被測定部位の周囲長を計測するためのものである。
The blood pressure information measurement device according to the present invention includes a cuff, an expansion / contraction mechanism, a blood pressure information measurement unit, a tightening length adjustment mechanism, and a peripheral length measurement unit. The cuff includes a fluid bag for pressing the measurement site and a tightening belt wound around the fluid bag. The cuff has no cut in the circumferential direction and the measurement site can be inserted from the axial direction. It has the annular form comprised. The inflating and contracting mechanism is for inflating and deflating the fluid bag, and the blood pressure information measuring unit measures blood pressure information using the fluid bag. The tightening length adjusting mechanism is for variably adjusting the tightening length of the tightening belt with respect to the measurement site, and the perimeter measuring unit is for measuring the perimeter of the measurement site. is there.
上記本発明に基づく血圧情報測定装置にあっては、上記周囲長計測部が、上記締付け長さ調節機構を用いて上記締付けベルトを被測定部位に締付け固定する際の上記締付けベルトの移動量を計測することにより、被測定部位の周囲長を計測することが好ましい。
In the blood pressure information measuring device according to the present invention, the circumference measuring unit determines the amount of movement of the tightening belt when the tightening belt is fastened and fixed to the measurement site using the tightening length adjusting mechanism. It is preferable to measure the perimeter of the measurement site by measuring.
上記本発明に基づく血圧情報測定装置にあっては、上記周囲長計測部が、上記締付けベルトに設けられたマーカーと、上記マーカーを読み取る読み取り部とを含んでいることが好ましく、その場合に、上記周囲長計測部が、上記読み取り部によって読み取られた情報に基づいて上記締付けベルトの上記移動量を計測するように構成されていることが好ましい。
In the blood pressure information measurement device according to the present invention, the circumference measurement unit preferably includes a marker provided on the fastening belt and a reading unit that reads the marker. It is preferable that the perimeter measurement unit is configured to measure the amount of movement of the fastening belt based on information read by the reading unit.
上記本発明に基づく血圧情報測定装置にあっては、上記マーカーがバーコードにて構成されていることが好ましく、その場合に、上記読み取り部が上記バーコードを読み取るためのフォトインタラプタにて構成されていることが好ましい。
In the blood pressure information measurement device according to the present invention, the marker is preferably configured by a barcode, and in that case, the reading unit is configured by a photo interrupter for reading the barcode. It is preferable.
上記本発明に基づく血圧情報測定装置にあっては、上記周囲長計測部が、上記締付けベルトの移動に伴って回転する回転部材と、上記回転部材の回転量を検出する回転量検出部とを含んでいることが好ましく、その場合に、上記周囲長計測部が、上記回転量検出部によって検出された情報に基づいて上記締付けベルトの上記移動量を計測するように構成されていることが好ましい。
In the blood pressure information measurement device according to the present invention, the circumference measurement unit includes a rotating member that rotates as the fastening belt moves, and a rotation amount detection unit that detects the amount of rotation of the rotating member. In that case, it is preferable that the circumference measuring unit is configured to measure the movement amount of the fastening belt based on information detected by the rotation amount detection unit. .
上記本発明に基づく血圧情報測定装置は、上記周囲長計測部によって検出された被測定部位の周囲長情報に基づき、上記血圧情報測定部によって測定された血圧情報を補正する血圧情報補正部をさらに備えていることが好ましい。
The blood pressure information measurement device according to the present invention further includes a blood pressure information correction unit that corrects the blood pressure information measured by the blood pressure information measurement unit based on the circumference information of the measurement site detected by the circumference measurement unit. It is preferable to provide.
上記本発明に基づく血圧情報測定装置は、上記周囲長計測部によって検出された被測定部位の周囲長情報に基づき、上記膨縮機構による流体袋の膨張動作および収縮動作の少なくともいずれか一方を制御する膨縮動作制御部をさらに備えていることが好ましい。
The blood pressure information measurement device according to the present invention controls at least one of the inflating operation and the deflating operation of the fluid bag by the inflating and deflating mechanism based on the circumference information of the measurement site detected by the circumference measuring unit. It is preferable to further include an expansion / contraction operation control unit.
上記本発明に基づく血圧情報測定装置は、上記周囲長計測部によって検出された被測定部位の周囲長情報に基づき、予め定められた測定可能範囲内に被測定部位の周囲長があるか否かを判断する判断部をさらに備えていることが好ましい。
The blood pressure information measurement device according to the present invention is based on the circumference information of the measurement site detected by the circumference measurement unit, and whether or not the circumference of the measurement site is within a predetermined measurable range. It is preferable to further include a determination unit that determines the above.
上記本発明に基づく血圧情報測定装置にあっては、上記締付け長さ調節機構が、上記締付けベルトを巻取りおよび送出し可能な巻取りローラと、上記巻取りローラを順方向および逆方向に回転駆動する電動機と、上記電動機の停止時に上記巻取りローラに対して制動力を及ぼす制動機とを含んでいることが好ましい。
In the blood pressure information measuring device according to the present invention, the tightening length adjusting mechanism rotates the winding roller in the forward direction and the reverse direction, and the winding roller capable of winding and feeding the tightening belt. It preferably includes an electric motor to be driven and a brake that exerts a braking force on the winding roller when the electric motor is stopped.
上記本発明に基づく血圧情報測定装置にあっては、上記カフが、上記流体袋および上記締付けベルトを含む筒状のカフ本体部と、上記カフ本体部の外周面上に設けられた把手部とを含んでいることが好ましい。
In the blood pressure information measuring device according to the present invention, the cuff includes a cylindrical cuff main body including the fluid bag and the fastening belt, and a handle provided on the outer peripheral surface of the cuff main body. It is preferable that it contains.
上記本発明に基づく血圧情報測定装置にあっては、上記巻取りローラによる上記締付けベルトの巻取り動作の開始の命令を受付けるための巻取り動作操作部が、上記把手部に設けられていることが好ましい。
In the blood pressure information measurement device according to the present invention, a winding operation unit for receiving a command to start the winding operation of the tightening belt by the winding roller is provided in the handle unit. Is preferred.
上記本発明に基づく血圧情報測定装置は、被測定部位に対する上記締付けベルトの締付け力を検出する締付け力検出機構をさらに備えていることが好ましく、その場合に、上記締付け長さ調節機構が、上記締付け力検出機構が所定の大きさの締付け力を検出した場合に上記巻取りローラによる上記締付けベルトの巻取り動作を停止するように構成されていることが好ましい。
The blood pressure information measuring device according to the present invention preferably further includes a tightening force detection mechanism for detecting the tightening force of the tightening belt with respect to the measurement site. In this case, the tightening length adjusting mechanism is It is preferable that the winding operation of the tightening belt by the winding roller is stopped when the tightening force detection mechanism detects a predetermined amount of tightening force.
上記本発明に基づく血圧情報測定装置にあっては、上記締付け力検出機構が、上記膨縮機構によって上記流体袋に所定量の流体が注入された状態で上記巻取りローラによる上記締付けベルトの巻取り動作の際の上記流体袋の内圧を検出することにより、被測定部位に対する上記締付けベルトの締付け力を検出するように構成されていることが好ましい。
In the blood pressure information measuring device according to the present invention, the tightening force detection mechanism winds the tightening belt by the winding roller in a state where a predetermined amount of fluid is injected into the fluid bag by the expansion / contraction mechanism. It is preferable that the tightening force of the tightening belt with respect to the measurement site is detected by detecting the internal pressure of the fluid bag during the taking operation.
上記本発明に基づく血圧情報測定装置にあっては、上記締付け力検出機構が、上記電動機によって回転駆動される際の上記巻取りローラに加わる回転トルクを検出することにより、被測定部位に対する上記締付けベルトの締付け力を検出するように構成されていてもよい。
In the blood pressure information measuring device according to the present invention, the tightening force detection mechanism detects the rotational torque applied to the take-up roller when it is rotationally driven by the electric motor, whereby the tightening to the measurement site is performed. The belt tightening force may be detected.
上記本発明に基づく血圧情報測定装置にあっては、上記膨縮機構が、上記巻取りローラによる上記締付けベルトの巻取り動作の停止後において血圧情報測定のための上記流体袋の加圧動作を開始するように構成されていることが好ましい。
In the blood pressure information measuring device according to the present invention, the expansion / contraction mechanism performs the pressurizing operation of the fluid bag for blood pressure information measurement after stopping the winding operation of the tightening belt by the winding roller. It is preferably configured to start.
上記本発明に基づく血圧情報測定装置にあっては、上記締付け長さ調節機構が、血圧情報測定のための測定動作の終了後に上記巻取りローラによる上記締付けベルトの送出し動作を開始するように構成されていることが好ましい。
In the blood pressure information measuring device according to the present invention, the tightening length adjusting mechanism starts the feeding operation of the tightening belt by the winding roller after the measurement operation for blood pressure information measurement is completed. It is preferable to be configured.
上記本発明に基づく血圧情報測定装置にあっては、上記カフ本体部が、上記流体袋の外側でかつ上記締付けベルトの内側に径方向に弾性変形可能に構成された可撓性部材をさらに有していることが好ましい。
In the blood pressure information measuring device according to the present invention, the cuff body further includes a flexible member configured to be elastically deformable in the radial direction outside the fluid bag and inside the fastening belt. It is preferable.
本発明によれば、被測定部位の周囲長を正確にかつ精緻に計測することができる機能を備えた血圧情報測定装置とすることができる。また、本発明によれば、計測された被測定部位の周囲長の情報を有効に活用することにより、高性能化、高機能化された血圧情報測定装置とすることができる。
According to the present invention, it is possible to provide a blood pressure information measuring device having a function capable of accurately and precisely measuring the peripheral length of a measurement site. Further, according to the present invention, it is possible to obtain a blood pressure information measuring device with high performance and high functionality by effectively utilizing the measured information on the circumference of the measured region.
以下、本発明の実施の形態について、図を参照して詳細に説明する。以下に示す実施の形態においては、血圧情報測定装置として、収縮期血圧値および拡張期血圧値を測定することが可能に構成されたいわゆる上腕式の血圧計を例示して説明を行なう。なお、以下に示す血圧計は、カフの上腕に対する締付け動作と、当該締付け動作後に行なわれる血圧値の測定動作と、当該測定動作後に行なわれるカフの上腕に対する締付け解除動作とが自動的に連続して行なわれるように構成されたものであり、さらには、上記カフの上腕に対する締付け動作中において、上腕の周囲長が自動で計測されるように構成されたものである。
Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. In the following embodiment, a so-called upper arm type sphygmomanometer configured to measure a systolic blood pressure value and a diastolic blood pressure value will be described as an example of the blood pressure information measuring device. In the sphygmomanometer shown below, the tightening operation for the upper arm of the cuff, the blood pressure measurement operation performed after the tightening operation, and the tightening release operation for the upper arm of the cuff performed after the measuring operation are automatically continued. Further, the circumference of the upper arm is automatically measured during the tightening operation on the upper arm of the cuff.
(実施の形態1)
図1は、本発明の実施の形態1における血圧計の外観構造を示す図である。まず、図1を参照して、本実施の形態における血圧計1Aの外観構造について説明する。 (Embodiment 1)
FIG. 1 is a diagram showing an external structure of a sphygmomanometer according toEmbodiment 1 of the present invention. First, with reference to FIG. 1, the external structure of sphygmomanometer 1A in the present embodiment will be described.
図1は、本発明の実施の形態1における血圧計の外観構造を示す図である。まず、図1を参照して、本実施の形態における血圧計1Aの外観構造について説明する。 (Embodiment 1)
FIG. 1 is a diagram showing an external structure of a sphygmomanometer according to
図1に示すように、本実施の形態における血圧計1Aは、本体10と、カフ20Aと、エア管90と、接続ケーブル92とを備えている。本体10は、箱状の筐体を有しており、その上面に表示部14および操作部16が設けられている。本体10は、測定時においてテーブル等の載置面に載置されて使用される。カフ20Aは、周方向に切れ目を有さない環状の形態にて構成されており、上腕を軸方向から挿入可能な中空開口部を含む筒状のカフ本体部30と、このカフ本体部30の外周面上に設けられた把手部40とを有している。カフ20Aのカフ本体部30の所定位置には、カフ20Aが装着されることとなる上腕の周囲長を特定するためのエンコーダストリップ73が取り付けられている。カフ20Aは、測定時において上腕に装着されて使用される。エア管90および接続ケーブル92は、分離されて構成された本体10とカフ20Aとをそれぞれ接続している。
As shown in FIG. 1, the sphygmomanometer 1A according to the present embodiment includes a main body 10, a cuff 20A, an air tube 90, and a connection cable 92. The main body 10 has a box-shaped housing, and a display unit 14 and an operation unit 16 are provided on an upper surface thereof. The main body 10 is used by being placed on a placement surface such as a table at the time of measurement. The cuff 20 </ b> A is configured in an annular shape having no cut in the circumferential direction, and includes a cylindrical cuff main body portion 30 including a hollow opening into which the upper arm can be inserted from the axial direction, and the cuff main body portion 30. And a grip portion 40 provided on the outer peripheral surface. At a predetermined position of the cuff body 30 of the cuff 20A, an encoder strip 73 for specifying the perimeter of the upper arm to which the cuff 20A is to be attached is attached. The cuff 20A is attached to the upper arm during measurement. The air tube 90 and the connection cable 92 respectively connect the main body 10 and the cuff 20 </ b> A configured separately.
図2は、本実施の形態における血圧計の機能ブロックの構成を示す図である。次に、この図2を参照して、本実施の形態における血圧計1Aの機能ブロックの構成について説明する。
FIG. 2 is a diagram showing a functional block configuration of the sphygmomanometer according to the present embodiment. Next, with reference to FIG. 2, the functional block configuration of sphygmomanometer 1A in the present embodiment will be described.
図2に示すように、本体10は、上述した表示部14および操作部16に加え、制御部11と、メモリ部12と、電源部18と、モータ駆動回路53と、電磁ブレーキ駆動回路54と、加圧ポンプ61と、排気弁62と、圧力センサ63と、加圧ポンプ駆動回路64と、排気弁駆動回路65と、増幅器66と、A/D(Analog/Digital)変換回路67と、上腕周囲長計測回路72とを有している。一方、カフ20Aは、空気袋35と、締付けベルト32と、押し釦44と、ギヤードモータ51と、電磁ブレーキ52と、巻取りローラ58と、光電センサ71とを主として有している。
As shown in FIG. 2, the main body 10 includes a control unit 11, a memory unit 12, a power supply unit 18, a motor drive circuit 53, an electromagnetic brake drive circuit 54, in addition to the display unit 14 and the operation unit 16 described above. , Pressure pump 61, exhaust valve 62, pressure sensor 63, pressure pump drive circuit 64, exhaust valve drive circuit 65, amplifier 66, A / D (Analog / Digital) conversion circuit 67, upper arm And a peripheral length measuring circuit 72. On the other hand, the cuff 20A mainly includes an air bag 35, a fastening belt 32, a push button 44, a geared motor 51, an electromagnetic brake 52, a winding roller 58, and a photoelectric sensor 71.
制御部11は、たとえばCPU(Central Processing Unit)にて構成され、血圧計1Aの全体を制御するための手段である。メモリ部12は、たとえばROM(Read-Only Memory)やRAM(Random-Access Memory)にて構成され、血圧値測定のための処理手順を制御部11等に実行させるためのプログラムを記憶したり、測定結果等を記憶したりするための手段である。表示部14は、たとえばLCD(Liquid Crystal Display)にて構成され、測定結果等を表示するための手段である。操作部16は、被験者等による操作を受付けてこの外部からの命令を制御部11や電源部18に入力するための手段である。電源部18は、制御部11に電源としての電力を供給するための手段である。
The control part 11 is comprised by CPU (Central Processing Unit), for example, and is a means for controlling the whole sphygmomanometer 1A. The memory unit 12 is composed of, for example, a ROM (Read-Only Memory) or a RAM (Random-Access Memory), and stores a program for causing the control unit 11 or the like to execute a processing procedure for blood pressure measurement, This is a means for storing measurement results and the like. The display unit 14 is configured by, for example, an LCD (Liquid Crystal Display), and is a means for displaying measurement results and the like. The operation unit 16 is a means for receiving an operation by a subject or the like and inputting a command from the outside to the control unit 11 or the power supply unit 18. The power supply unit 18 is means for supplying power as a power source to the control unit 11.
制御部11は、ギヤードモータ51、電磁ブレーキ52、加圧ポンプ61および排気弁62を駆動するための制御信号をモータ駆動回路53、電磁ブレーキ駆動回路54、加圧ポンプ駆動回路64および排気弁駆動回路65にそれぞれ入力したり、光電センサ71によって検出された後述する締付けベルト31,32の締付け長さの情報に基づいて被験者の上腕周囲長を計測したり、測定結果としての血圧値をメモリ部12や表示部14に入力したりする。また、制御部11は、計測された上腕周囲長が予め定められた当該カフ20Aの適用可能範囲内であるか否かを判断する判断部を含んでおり、当該判断部での判断の結果に基づき、以降の血圧値測定動作に移行すべきか否かを決定する機能も有している。また、制御部11は、圧力センサ63によって検出された圧力値に基づいて被験者の血圧値を取得する血圧情報測定部を含んでおり、この血圧情報測定部によって取得された血圧値が、測定結果として上述したメモリ部12や表示部14に入力される。なお、血圧計1Aは、測定結果としての血圧値を外部の機器(たとえばPC(Personal Computer)やプリンタ等)に出力する出力部を別途有していてもよい。出力部としては、たとえばシリアル通信回線や各種の記録媒体への書き込み装置等が利用可能である。
The control unit 11 sends control signals for driving the geared motor 51, the electromagnetic brake 52, the pressure pump 61, and the exhaust valve 62 to the motor drive circuit 53, the electromagnetic brake drive circuit 54, the pressure pump drive circuit 64, and the exhaust valve drive. The upper arm circumference length of the subject is measured based on information on the fastening lengths of fastening belts 31 and 32 (described later) detected by the photoelectric sensor 71, or the blood pressure value as a measurement result is stored in the memory unit. 12 or the display unit 14. In addition, the control unit 11 includes a determination unit that determines whether or not the measured upper arm circumference is within a predetermined applicable range of the cuff 20A. Based on this, it also has a function of determining whether or not to shift to the subsequent blood pressure value measurement operation. Further, the control unit 11 includes a blood pressure information measurement unit that acquires the blood pressure value of the subject based on the pressure value detected by the pressure sensor 63, and the blood pressure value acquired by the blood pressure information measurement unit is the measurement result. Is input to the memory unit 12 and the display unit 14 described above. The sphygmomanometer 1A may further include an output unit that outputs a blood pressure value as a measurement result to an external device (for example, a PC (Personal Computer) or a printer). As the output unit, for example, a serial communication line or a writing device for various recording media can be used.
モータ駆動回路53は、制御部11から入力された制御信号に基づいてギヤードモータ51の動作を制御する。電磁ブレーキ駆動回路54は、制御部11から入力された制御信号に基づいて電磁ブレーキ52の動作を制御する。加圧ポンプ駆動回路64は、制御部11から入力された制御信号に基づいて加圧ポンプ61の動作を制御する。排気弁駆動回路65は、制御部11から入力された制御信号に基づいて排気弁62の開閉動作を制御する。
The motor drive circuit 53 controls the operation of the geared motor 51 based on the control signal input from the control unit 11. The electromagnetic brake drive circuit 54 controls the operation of the electromagnetic brake 52 based on the control signal input from the control unit 11. The pressurization pump drive circuit 64 controls the operation of the pressurization pump 61 based on the control signal input from the control unit 11. The exhaust valve drive circuit 65 controls the opening / closing operation of the exhaust valve 62 based on the control signal input from the control unit 11.
空気袋35は、装着状態において上腕を圧迫するための流体袋であり、上述したエア管90を介して後述するエア系コンポーネント60に接続されている。ギヤードモータ51、電磁ブレーキ52および巻取りローラ58は、後述する締付けベルト31,32(図3等参照)の上腕に対する締付け長さを可変に調節する締付け長さ調節機構50に相当する。ギヤードモータ51とモータ駆動回路53との電気的な接続および電磁ブレーキ52と電磁ブレーキ駆動回路54との電気的な接続は、それぞれ上述した接続ケーブル92(図1参照)によって行なわれている。
The air bag 35 is a fluid bag for pressing the upper arm in the mounted state, and is connected to an air system component 60 described later via the air tube 90 described above. The geared motor 51, the electromagnetic brake 52, and the take-up roller 58 correspond to a tightening length adjusting mechanism 50 that variably adjusts a tightening length with respect to upper arms of tightening belts 31 and 32 (see FIG. 3 and the like) described later. Electrical connection between the geared motor 51 and the motor drive circuit 53 and electrical connection between the electromagnetic brake 52 and the electromagnetic brake drive circuit 54 are performed by the connection cable 92 (see FIG. 1) described above.
ギヤードモータ51は、巻取りローラ58を順方向および逆方向に回転駆動する電動機であり、その動作が上述したモータ駆動回路53によって制御される。電磁ブレーキ52は、巻取りローラ58に対して制動力を及ぼす制動機であり、その動作が上述した電磁ブレーキ駆動回路54によって制御される。巻取りローラ58は、後述する締付けベルト31,32を巻取ったり送出したりするための部材である。押し釦44は、ギヤードモータ51、電磁ブレーキ52および巻取りローラ58にて構成される締付け長さ調節機構50による巻付け動作を開始するための被験者の命令を受付ける巻付け動作操作部に相当する。
The geared motor 51 is an electric motor that rotationally drives the winding roller 58 in the forward direction and the reverse direction, and its operation is controlled by the motor drive circuit 53 described above. The electromagnetic brake 52 is a brake that applies a braking force to the winding roller 58, and its operation is controlled by the electromagnetic brake drive circuit 54 described above. The take-up roller 58 is a member for taking up and sending out tightening belts 31 and 32 described later. The push button 44 corresponds to a winding operation operation unit that receives a test subject's command for starting a winding operation by the tightening length adjusting mechanism 50 including the geared motor 51, the electromagnetic brake 52, and the winding roller 58. .
加圧ポンプ61は、空気袋35の内腔に空気を供給するためのものであり、その動作が上述した加圧ポンプ駆動回路64によって制御される。排気弁62は、空気袋35の内部の圧力(以下、「カフ圧」とも称する)を維持したり、空気袋35の内部の空間を外部に開放するためのものであり、その動作が上述した排気弁駆動回路65によって制御される。圧力センサ63は、空気袋35の内部の圧力に応じた出力信号を増幅器66に入力する。増幅器66は、圧力センサ63の出力値を増幅し、A/D変換回路67に入力する。A/D変換回路67は、増幅器66から入力されたアナログ信号をデジタル信号に変換して制御部11に入力する。なお、これら構成要素のうち、加圧ポンプ61、排気弁62および圧力センサ63が上述したエア系コンポーネント60に相当し、特に、加圧ポンプ61と排気弁62とが空気袋35を膨縮させる膨縮機構に相当する。
The pressurizing pump 61 is for supplying air to the inner cavity of the air bladder 35, and its operation is controlled by the pressurizing pump driving circuit 64 described above. The exhaust valve 62 is used to maintain the pressure inside the air bladder 35 (hereinafter also referred to as “cuff pressure”) or to open the space inside the air bladder 35 to the outside. It is controlled by the exhaust valve drive circuit 65. The pressure sensor 63 inputs an output signal corresponding to the pressure inside the air bladder 35 to the amplifier 66. The amplifier 66 amplifies the output value of the pressure sensor 63 and inputs it to the A / D conversion circuit 67. The A / D conversion circuit 67 converts the analog signal input from the amplifier 66 into a digital signal and inputs the digital signal to the control unit 11. Of these components, the pressurization pump 61, the exhaust valve 62, and the pressure sensor 63 correspond to the air system component 60 described above. In particular, the pressurization pump 61 and the exhaust valve 62 inflate and contract the air bladder 35. It corresponds to an expansion / contraction mechanism.
また、本実施の形態における血圧計1Aにおいては、上述した空気袋35およびエア系コンポーネント60が上腕に対する締付けベルトの締付け力を検出する締付け力検出機構として利用されることになるが、その詳細については後述することとする。
In the sphygmomanometer 1A according to the present embodiment, the air bag 35 and the air system component 60 described above are used as a tightening force detection mechanism for detecting the tightening force of the tightening belt with respect to the upper arm. Will be described later.
光電センサ71(より特定的にはフォトインタラプタ)は、後述する締付けベルト31,32に設けられたマーカーとしてのバーコードを読み取るための読み取り部であり、読み取った情報に応じた電気信号を上腕周囲長計測回路72に出力する。上腕周囲長計測回路72は、光電センサ71から入力された電気信号に基づいて上腕周囲長を計測し、計測した上腕周囲長に応じた出力信号を制御部11に出力する。なお、これらマーカーとしてのバーコードおよび読み取り部としての光電センサ71が被測定部位である上腕の周囲長を計測する周囲長計測部として利用されるが、その詳細については後述することとする。
The photoelectric sensor 71 (more specifically, a photo interrupter) is a reading unit for reading a bar code as a marker provided on the tightening belts 31 and 32 described later, and an electric signal corresponding to the read information is transmitted around the upper arm. Output to the length measuring circuit 72. The upper arm circumference measurement circuit 72 measures the upper arm circumference based on the electric signal input from the photoelectric sensor 71 and outputs an output signal corresponding to the measured upper arm circumference to the control unit 11. The bar code as the marker and the photoelectric sensor 71 as the reading unit are used as a perimeter measuring unit for measuring the perimeter of the upper arm, which is a measurement target, and details thereof will be described later.
図3は、本実施の形態における血圧計のカフの詳細な構造を示す斜視図であり、図4は、図3中に示すIV-IV線に沿ったカフの非装着状態における断面図である。また、図5は、本実施の形態における血圧計の締付け長さ調節機構の構成を示す模式上面図でり、図6は、本実施の形態における血圧計の上腕周囲長計測部の構成を示す模式図である。次に、これら図3ないし図6を参照して、本実施の形態における血圧計1Aのカフ20Aの詳細な構造について説明する。
FIG. 3 is a perspective view showing a detailed structure of the cuff of the sphygmomanometer according to the present embodiment, and FIG. 4 is a cross-sectional view of the cuff in a non-wearing state along line IV-IV shown in FIG. . FIG. 5 is a schematic top view showing the configuration of the tightening length adjusting mechanism of the sphygmomanometer according to the present embodiment, and FIG. 6 shows the configuration of the upper arm circumference measuring unit of the sphygmomanometer according to the present embodiment. It is a schematic diagram. Next, the detailed structure of the cuff 20A of the sphygmomanometer 1A according to the present embodiment will be described with reference to FIGS.
図3および図4に示すように、カフ20Aは、上腕に装着される筒状のカフ本体部30と、このカフ本体部30の外周面上に設けられた把手部40とを有している。把手部40は、カフ本体部30に取付けられる部分である基部41と、装着に際して手で把持するための部分である把手42とを含んでいる。カフ本体部30は、上腕が軸方向ら挿入可能となるように筒状に形成されており、把手部40は、筒状に形成されたカフ本体部30の軸方向と平行な方向に把手42が延在するようにカフ本体部30に固定されている。カフ本体部30の外周面上の位置でかつ把手部40の基部41の内部には、締付け長さ調節機構50が配設されている。また、把手部40の基部41の内部の所定位置には、光電センサ71が設けられている。さらに、把手部40の外表面の所定位置には、上述した押し釦44が設けられている。
As shown in FIGS. 3 and 4, the cuff 20 </ b> A has a cylindrical cuff main body 30 that is attached to the upper arm, and a handle 40 that is provided on the outer peripheral surface of the cuff main body 30. . The handle portion 40 includes a base portion 41 that is a portion that is attached to the cuff main body portion 30 and a handle 42 that is a portion that is gripped by hand when attached. The cuff main body 30 is formed in a cylindrical shape so that the upper arm can be inserted in the axial direction, and the handle 40 is a handle 42 in a direction parallel to the axial direction of the cylindrical cuff main body 30. Is fixed to the cuff body 30 so as to extend. A tightening length adjusting mechanism 50 is disposed at a position on the outer peripheral surface of the cuff main body portion 30 and inside the base portion 41 of the handle portion 40. A photoelectric sensor 71 is provided at a predetermined position inside the base portion 41 of the handle portion 40. Further, the push button 44 described above is provided at a predetermined position on the outer surface of the handle portion 40.
カフ本体部30は、環状に巻き回された締付けベルト31,32と、締付けベルト31の内側に取付けられた外装カバー33と、外装カバー33の内部に収容されたカーラ34および空気袋35とを主として備えている。締付けベルト31,32は、実質的に周方向に伸縮性を有しない布等の部材にて構成されており、幅の広い第1の締付けベルト31と、この第1の締付けベルトに連結された幅の狭い第2の締付けベルト32とを含んでいる。
The cuff main body 30 includes an annular winding belt 31, 32, an exterior cover 33 attached to the inside of the tightening belt 31, a curler 34 and an air bag 35 housed inside the exterior cover 33. Mainly prepared. The tightening belts 31 and 32 are made of a member such as a cloth that does not substantially stretch in the circumferential direction, and are connected to the wide first tightening belt 31 and the first tightening belt. A second tightening belt 32 having a narrow width.
第1の締付けベルト31は、周方向に一端部31aおよび他端部31bを有する帯状の部材からなり、その外周面上の所定位置に上述した把手部40が取付けられ、その内周面上に上述した外装カバー33が取付けられている。第2の締付けベルト32は、周方向に一端部32aおよび他端部32bを有しており、このうちの一端部32aが第1の締付けベルト31の他端部31bに連結されている。第2の締付けベルト32の他端部32b寄りの部分は、第1の締付けベルト31の一端部31a寄りの部分の外周側に重ね合わされており、第2の締付けベルト32の他端部32bは、第1の締付けベルト31の外周面上に取付けられた把手部40内に配設された巻取りローラ58に固定されている。これにより、第1の締付けベルト31および第2の締付けベルト32は、環状に構成された一つの部材として機能し、これによって中空開口部を有するカフ本体部30が形作られている。
The first tightening belt 31 is composed of a belt-like member having one end 31a and the other end 31b in the circumferential direction, and the handle portion 40 described above is attached to a predetermined position on the outer peripheral surface, and on the inner peripheral surface. The exterior cover 33 described above is attached. The second tightening belt 32 has one end portion 32 a and the other end portion 32 b in the circumferential direction, and one end portion 32 a is connected to the other end portion 31 b of the first tightening belt 31. The portion of the second tightening belt 32 near the other end 32b is overlapped with the outer peripheral side of the portion near the one end 31a of the first tightening belt 31, and the other end 32b of the second tightening belt 32 is The first tightening belt 31 is fixed to a take-up roller 58 disposed in a handle portion 40 attached to the outer peripheral surface of the first tightening belt 31. Accordingly, the first tightening belt 31 and the second tightening belt 32 function as one member configured in an annular shape, thereby forming the cuff body 30 having a hollow opening.
連結された第1の締付けベルト31および第2の締付けベルト32は、締付け長さ調節機構50によってその周方向の長さが可変に調節される。連結された第1の締付けベルト31および第2の締付けベルト32の周方向の長さが長くされた状態においては、カフ本体部30が拡径状態(径が大きくされた状態)をとることになり、周方向の長さが短くされた状態においては、カフ本体部30が縮径状態(径が小さくされた状態)をとることになる。
The length of the connected first tightening belt 31 and second tightening belt 32 is variably adjusted by the tightening length adjusting mechanism 50. In the state where the circumferential lengths of the connected first tightening belt 31 and second tightening belt 32 are increased, the cuff main body portion 30 is in an expanded state (a state in which the diameter is increased). Thus, in a state where the length in the circumferential direction is shortened, the cuff main body portion 30 takes a reduced diameter state (a state where the diameter is reduced).
外装カバー33は、たとえば伸縮性のある低摩擦材料かなる布等の部材にて構成されており、上述した第1の締付けベルト31の内周面上に取付けられている。より詳細には、外装カバー33の外周面が第1の締付けベルト31の内周面に接着または溶着等によって接合されることにより、外装カバー33が第1の締付けベルト31に固定されている。
The exterior cover 33 is formed of a member such as a cloth made of a stretchable low friction material, for example, and is attached on the inner peripheral surface of the first tightening belt 31 described above. More specifically, the outer cover 33 is fixed to the first tightening belt 31 by bonding the outer peripheral surface of the outer cover 33 to the inner peripheral surface of the first tightening belt 31 by adhesion or welding.
外装カバー33に内包されたカーラ34は、たとえばポリプロピレン等の樹脂材料を原料として射出成形によって形成された可撓性部材からなる。より詳細には、カーラ34は、周方向の所定位置に軸方向に沿った切れ目34aを有する環状の湾曲弾性板にて構成されており、軸方向と直交する平面に沿って切断した場合にその形状がC字状またはU字状となっている。カーラ34は、自身の環状形態を保持するとともに、径方向に弾性変形可能に構成されている。したがって、カーラ34は、上述した拡径状態においてその径が大きく広がった状態をとることになり、反対に上述した縮径状態においてその径が小さく狭まった状態をとることになる。なお、カフ本体部30が拡径状態をとった場合には、カーラ34の弾性力によってカフ本体部30が大きく広がることになるため、カフ本体部30の中空開口部内に上腕を抜き差しすることが容易となる。
The curler 34 included in the exterior cover 33 is made of a flexible member formed by injection molding using a resin material such as polypropylene as a raw material. More specifically, the curler 34 is composed of an annular curved elastic plate having a cut 34a along the axial direction at a predetermined position in the circumferential direction, and when cut along a plane perpendicular to the axial direction, The shape is C-shaped or U-shaped. The curler 34 is configured to be elastically deformable in the radial direction while maintaining its own annular shape. Therefore, the curler 34 takes a state in which the diameter is greatly expanded in the above-described expanded diameter state, and conversely, takes a state in which the diameter is small and narrowed in the above-described reduced diameter state. In addition, when the cuff main body portion 30 is in the expanded state, the cuff main body portion 30 is greatly expanded by the elastic force of the curler 34, so that the upper arm can be inserted into and removed from the hollow opening of the cuff main body portion 30. It becomes easy.
空気袋35は、膨縮可能な袋状の部材からなり、たとえば2枚の樹脂フィルムを重ね合わせてその周縁を溶着することによって形成されている。空気袋35の内腔は、図示しないニップルを介してエア管90に接続されている。空気袋35の内腔は、測定時において本体10に設けられた加圧ポンプ61および排気弁62によって加減圧され、これによって空気袋35が膨張または収縮する。
The air bag 35 is made of a bag-shaped member that can be expanded and contracted, and is formed, for example, by laminating two resin films and welding the periphery thereof. The inner cavity of the air bladder 35 is connected to the air pipe 90 via a nipple (not shown). The inner cavity of the air bladder 35 is pressurized and decompressed by a pressurizing pump 61 and an exhaust valve 62 provided in the main body 10 at the time of measurement, whereby the air bladder 35 is expanded or contracted.
図3ないし図5に示すように、締付け長さ調節機構50は、ギヤードモータ51、電磁ブレーキ52および巻取りローラ58を含んでいる。これらギヤードモータ51、電磁ブレーキ52および巻取りローラ58は、カフ本体部30の外周面上の位置でかつ把手部40の基部41の内部に配設された支持枠46にそれぞれ組付けられている。支持枠46は、たとえば第1の締付けベルト31の外周面上に固定されている。また、支持枠46の所定位置には、動力伝達機構としてのギヤ55,56,57が組付けられている。
3 to 5, the tightening length adjusting mechanism 50 includes a geared motor 51, an electromagnetic brake 52, and a take-up roller 58. The geared motor 51, the electromagnetic brake 52, and the take-up roller 58 are assembled to a support frame 46 that is disposed on the outer peripheral surface of the cuff body 30 and inside the base 41 of the handle 40. . The support frame 46 is fixed on the outer peripheral surface of the first tightening belt 31, for example. Further, gears 55, 56, and 57 as power transmission mechanisms are assembled at predetermined positions of the support frame 46.
ギヤードモータ51は、減速機を具備したモータであり、モータ部51a、減速部51bおよび出力シャフト51cを含んでいる。ギヤードモータ51の出力シャフト51cには、ギヤ55が固着されている。ギヤードモータ51の出力シャフト51cが位置する側とは反対側の軸方向端部には、当該ギヤードモータ51と隣接して電磁ブレーキ52が配設されている。電磁ブレーキ52は、モータ部51aの回転シャフト51a1を拘持することによって回転シャフト51a1に対して制動力を発揮する。
The geared motor 51 is a motor equipped with a reduction gear, and includes a motor portion 51a, a reduction portion 51b, and an output shaft 51c. A gear 55 is fixed to the output shaft 51 c of the geared motor 51. An electromagnetic brake 52 is disposed adjacent to the geared motor 51 at the axial end of the geared motor 51 opposite to the side where the output shaft 51c is located. The electromagnetic brake 52 exerts a braking force on the rotation shaft 51a1 by holding the rotation shaft 51a1 of the motor unit 51a.
巻取りローラ58は、支持枠46に軸支されたシャフト57aに固着されており、シャフト57aが回転することによって従動して回転する。巻取りローラ58には、上述した第2の締付けベルト32の他端部32bが固定されている。巻取りローラ58が固着されたシャフト57aには、ギヤ57が固着されている。また、支持枠46に軸支されたシャフト56aには、ギヤ56が固着されている。ギヤ56は、上述したギヤ55およびギヤ57にそれぞれ歯合しており、ギヤードモータ51の出力シャフト51cに生じる回転力を巻取りローラ58に伝達する。なお、これらギヤ55,56,57は、それぞれその外径や歯数が調節されて構成されており、ギヤードモータ51の減速部51b同様、減速機としても機能する。
The take-up roller 58 is fixed to a shaft 57a that is pivotally supported by the support frame 46, and is rotated by the rotation of the shaft 57a. The other end portion 32 b of the second tightening belt 32 described above is fixed to the winding roller 58. A gear 57 is fixed to the shaft 57a to which the winding roller 58 is fixed. A gear 56 is fixed to the shaft 56 a that is pivotally supported by the support frame 46. The gear 56 meshes with the gear 55 and the gear 57 described above, and transmits the rotational force generated on the output shaft 51 c of the geared motor 51 to the take-up roller 58. The gears 55, 56, and 57 are configured by adjusting the outer diameter and the number of teeth, respectively, and function as a speed reducer as well as the speed reducing portion 51 b of the geared motor 51.
図4に示すように、把手部40の基部41の内部の所定位置には、巻取りローラ58に対面するように光電センサ71が配設されている。ここで、図6に示すように光電センサ71は、第1光電センサ71Aと第2光電センサ71Bとを含んでおり、これら2つの光電センサ71A,71Bのいずれもが巻取りローラ58に対面するように配置されている。
As shown in FIG. 4, a photoelectric sensor 71 is disposed at a predetermined position inside the base portion 41 of the handle portion 40 so as to face the winding roller 58. Here, as shown in FIG. 6, the photoelectric sensor 71 includes a first photoelectric sensor 71 </ b> A and a second photoelectric sensor 71 </ b> B, and both of the two photoelectric sensors 71 </ b> A and 71 </ b> B face the winding roller 58. Are arranged as follows.
一方、図3および図5に示すように、第2の締付けベルト32の表面には、エンコーダストリップ73が貼着されている。エンコーダストリップ73は、巻取りローラ58によって第2の締付けベルト32が巻き取られる際に光電センサ71の検出面側の部分を通過することとなるように、第2の締付けベルト32の一端部32a寄りの部分から他端部32b側に向けて延在するように設けられている。なお、エンコーダストリップ73は、その主面にマーカーとしてのバーコード74を有している。
On the other hand, as shown in FIGS. 3 and 5, an encoder strip 73 is adhered to the surface of the second tightening belt 32. The encoder strip 73 passes through the portion on the detection surface side of the photoelectric sensor 71 when the second fastening belt 32 is taken up by the take-up roller 58, so that one end portion 32a of the second fastening belt 32 is passed. It is provided so as to extend from the closer portion toward the other end 32b side. The encoder strip 73 has a barcode 74 as a marker on its main surface.
次に、図5を参照して、本実施の形態における血圧計1Aのカフ20Aの締付け長さ調節機構50の動作について説明する。本実施の形態における血圧計1Aにおいては、上述したように、カフ20Aの上腕に対する締付け動作と、当該締付け動作後に行なわれる血圧値の測定動作と、当該測定動作後に行なわれるカフ20Aの上腕に対する締付け解除動作とが自動的に連続して行なわれるように構成されている。このうち、カフ20Aの上腕に対する締付け動作と、カフ20Aの上腕に対する締付け解除動作は、それぞれ以下において説明する、締付け長さ調節機構50による締付けベルト31,32の巻取り動作と、締付け長さ調節機構50による締付けベルト31,32の送出し動作とによって行なわれる。
Next, the operation of the tightening length adjustment mechanism 50 of the cuff 20A of the sphygmomanometer 1A according to the present embodiment will be described with reference to FIG. In sphygmomanometer 1A according to the present embodiment, as described above, tightening operation on upper arm of cuff 20A, measurement operation of blood pressure value performed after the tightening operation, and tightening on upper arm of cuff 20A performed after the measuring operation. The release operation is automatically and continuously performed. Among them, the tightening operation for the upper arm of the cuff 20A and the tightening releasing operation for the upper arm of the cuff 20A are respectively described below, the winding operation of the tightening belts 31 and 32 by the tightening length adjusting mechanism 50, and the tightening length adjustment. This is performed by the feeding operation of the fastening belts 31 and 32 by the mechanism 50.
図5を参照して、ギヤードモータ51が順方向に回転駆動された状態においては、ギヤードモータ51の出力シャフト51cが順方向に回転し、その回転力がギヤ55,56,57を介してシャフト57aに伝達され、巻取りローラ58が順方向に回転する。巻取りローラ58が順方向に回転することにより、巻取りローラ58にその他端部32bが固定された第2の締付けベルト32は、巻取りローラ58によって図中矢印A方向に巻取られる。この巻取りローラ58による第2の締付けベルト32の巻取り動作により、締付けベルト31,32は、カーラ34の弾性力に抗してその締付け長さが減少し、カフ本体部30の中空開口部が徐々に縮径することになる。すなわち、当該巻取り動作により、上腕に対するカフ20Aの締付け動作が実現されることになる。なお、ギヤードモータ51の順方向への回転駆動時においては、電磁ブレーキ52は、ギヤードモータ51のモータ部51aの回転シャフト51a1を拘持した状態にはなく、モータ部51aはその動作を制限されることなく駆動されることになる。
Referring to FIG. 5, when geared motor 51 is rotationally driven in the forward direction, output shaft 51c of geared motor 51 rotates in the forward direction, and the rotational force is transmitted through gears 55, 56, 57 to the shaft. 57a and the winding roller 58 rotates in the forward direction. As the take-up roller 58 rotates in the forward direction, the second tightening belt 32 having the other end 32b fixed to the take-up roller 58 is taken up by the take-up roller 58 in the direction of arrow A in the figure. Due to the winding operation of the second tightening belt 32 by the winding roller 58, the tightening belts 31 and 32 have their tightening lengths reduced against the elastic force of the curler 34, and the hollow opening portion of the cuff main body portion 30. Is gradually reduced in diameter. That is, the winding operation realizes the tightening operation of the cuff 20A with respect to the upper arm. When the geared motor 51 is driven to rotate in the forward direction, the electromagnetic brake 52 is not in a state of holding the rotating shaft 51a1 of the motor unit 51a of the geared motor 51, and the motor unit 51a is restricted in its operation. It will be driven without.
一方、ギヤードモータ51が逆方向に回転駆動された状態においては、ギヤードモータ51の出力シャフト51cが逆方向に回転し、その回転力がギヤ55,56,57を介してシャフト57aに伝達され、巻取りローラ58が逆方向に回転する。巻取りローラ58が逆方向に回転することにより、巻取りローラ58に巻取られていた部分の第2の締付けベルト32は、巻取りローラ58から図中矢印B方向に向かって送出される。この巻取りローラ58による第2の締付けベルト32の送出し動作により、締付けベルト31,32は、その締付け長さが増加することになる。その際、カーラ34の弾性力に基づいてカフ本体部30の中空開口部は、徐々に拡径することになる。すなわち、当該送出し動作により、上腕に対するカフ20Aの締付け解除動作が実現されることになる。なお、ギヤードモータ51の逆方向への回転駆動時においては、電磁ブレーキ52は、ギヤードモータ51のモータ部51aの回転シャフト51a1を拘持した状態にはなく、モータ部51aはその動作を制限されることなく駆動されることになる。
On the other hand, in the state where the geared motor 51 is rotationally driven in the reverse direction, the output shaft 51c of the geared motor 51 rotates in the reverse direction, and the rotational force is transmitted to the shaft 57a via the gears 55, 56, 57, The winding roller 58 rotates in the reverse direction. When the winding roller 58 rotates in the reverse direction, the portion of the second tightening belt 32 that has been wound around the winding roller 58 is fed from the winding roller 58 in the direction of arrow B in the figure. By the feeding operation of the second tightening belt 32 by the winding roller 58, the tightening length of the tightening belts 31 and 32 is increased. At that time, the diameter of the hollow opening of the cuff body 30 is gradually increased based on the elastic force of the curler 34. In other words, the tightening release operation of the cuff 20A with respect to the upper arm is realized by the delivery operation. When the geared motor 51 is driven to rotate in the reverse direction, the electromagnetic brake 52 is not in a state of holding the rotating shaft 51a1 of the motor portion 51a of the geared motor 51, and the motor portion 51a is restricted in its operation. It will be driven without.
また、ギヤードモータ51が順方向または逆方向のいずれにも回転駆動されていない状態、すなわちギヤードモータ51の停止時においては、ギヤードモータ51のモータ部51aの回転シャフト51a1が電磁ブレーキ52によって拘持された状態となる。当該状態においては、電磁ブレーキ52による制動力がモータ部51aの回転シャフト51a1、減速部51b、出力シャフト51c、ギヤ55,56,57およびシャフト57aを介して巻取りローラ58に及び、巻取りローラ58の回転動作が制限されることになる。したがって、当該状態においては、巻取りローラ58による第2の締付けベルト32の巻取りおよび送出し動作のいずれもが停止され、カフ本体部30の中空開口部の径が一定に維持されることになる。
Further, when the geared motor 51 is not rotationally driven in either the forward direction or the reverse direction, that is, when the geared motor 51 is stopped, the rotating shaft 51a1 of the motor portion 51a of the geared motor 51 is held by the electromagnetic brake 52. It will be in the state. In this state, the braking force by the electromagnetic brake 52 reaches the take-up roller 58 via the rotary shaft 51a1, the speed reducer 51b, the output shaft 51c, the gears 55, 56, 57 and the shaft 57a of the motor 51a. The rotation operation of 58 is limited. Therefore, in this state, both the winding and feeding operations of the second tightening belt 32 by the winding roller 58 are stopped, and the diameter of the hollow opening of the cuff body 30 is maintained constant. Become.
次に、図2を参照して、本実施の形態における血圧計1Aに設けられる締付け力検出機構について説明する。当該締付け力検出機構は、カフ20Aの上腕に対する締付け状態を最適な状態とするために、上述したカフ20Aの締付け動作中において上腕に対するカフ20Aの締付け力を検出するためのものである。
Next, with reference to FIG. 2, a tightening force detection mechanism provided in the sphygmomanometer 1A in the present embodiment will be described. The tightening force detection mechanism is for detecting the tightening force of the cuff 20A against the upper arm during the above-described tightening operation of the cuff 20A in order to optimize the tightening state with respect to the upper arm of the cuff 20A.
本実施の形態における血圧計1Aにおいては、締付け力検出機構が図2に示す空気袋35およびエア系コンポーネント60によって構成されている。この締付け力検出機構は、上腕に対する締付けベルト31,32の締付け力を検出するための機構であり、その締付け力を空気袋35の内圧として捉えるものである。
In the sphygmomanometer 1A according to the present embodiment, the tightening force detection mechanism includes the air bag 35 and the air system component 60 shown in FIG. The tightening force detection mechanism is a mechanism for detecting the tightening force of the tightening belts 31 and 32 with respect to the upper arm, and captures the tightening force as the internal pressure of the air bladder 35.
具体的には、本実施の形態における血圧計1Aにおいては、締付け長さ調節機構50を駆動させてカフ本体部30の中空開口部を縮径させるに先立ち、所定量の空気を空気袋35内に加圧ポンプ61によって注入しておき、上記締付け長さ調節機構50の駆動に伴って締付け長さが減少することとなる締付けベルト31,32と上腕との間で挟まれることとなる空気袋35の内圧を圧力センサ63によって検出することにより、検出された空気袋35の内圧に基づいて締付けベルト31,32による上腕への締付け力を検出する。
Specifically, in the sphygmomanometer 1A according to the present embodiment, a predetermined amount of air is introduced into the air bag 35 prior to driving the tightening length adjusting mechanism 50 to reduce the diameter of the hollow opening of the cuff body 30. The air bag is injected between the fastening belts 31 and 32 and the upper arm, and the fastening length is reduced as the fastening length adjusting mechanism 50 is driven. By detecting the internal pressure of the air bag 35 by the pressure sensor 63, the tightening force applied to the upper arm by the tightening belts 31 and 32 is detected based on the detected internal pressure of the air bladder 35.
制御部11は、上述した締付け長さ調節機構50による締付け動作中において上記空気袋35の内圧を監視し、予め定めた所定の圧力値となった時点でギヤードモータ51の動作を停止させ、これと同時に電磁ブレーキ52を動作させて巻取りローラ58の回転を停止させる。以上により、カフ20Aの上腕に対する締付け状態を最適な状態とすることができる。
The control unit 11 monitors the internal pressure of the air bladder 35 during the tightening operation by the tightening length adjusting mechanism 50 described above, and stops the operation of the geared motor 51 when the predetermined pressure value is reached. At the same time, the electromagnetic brake 52 is operated to stop the rotation of the winding roller 58. As described above, the tightening state with respect to the upper arm of the cuff 20A can be set to the optimum state.
次に、図6を参照して、本実施の形態における血圧計1Aの上腕周囲長計測部によって上腕の周囲長が計測される仕組みについて詳説する。当該上腕周囲長計測部は、カフ20Aの上腕に対する締付け動作中において上腕の周囲長を自動計測するためのものである。
Next, with reference to FIG. 6, a detailed description will be given of a mechanism in which the perimeter of the upper arm is measured by the upper arm perimeter measurement unit of the sphygmomanometer 1A according to the present embodiment. The upper arm circumference measurement unit is for automatically measuring the circumference of the upper arm during the tightening operation on the upper arm of the cuff 20A.
図6に示すように、上腕周囲長計測部は、第2の締付けベルト32に設けられたマーカーとしてのバーコード74と、把手部40の基部41内に設けられた光電センサ71A,71Bとによって構成されている。光電センサ71A,71Bは、エンコーダストリップ73に設けられたバーコード74を読み取るための読み取り手段である。光電センサ71A,71Bのそれぞれは、発光部と受光部とを備えており、発光部から出射された光がエンコーダストリップ73に照射され、その反射光が受光部によって受光されることにより、その反射光の光量差に基づいてバーコード74の有無を検出する。光電センサ71A,71Bは、受光した光を光電変換することによって電気信号を出力し、出力された電気信号は、上腕周囲長計測回路72に入力される。上腕周囲長計測回路72は、入力された電気信号に基づいて被験者の上腕の周囲長を特定し、特定した上腕の周囲長を制御部11に入力する。
As shown in FIG. 6, the upper arm circumference measurement unit includes a bar code 74 as a marker provided on the second fastening belt 32 and photoelectric sensors 71 </ b> A and 71 </ b> B provided in the base 41 of the handle 40. It is configured. The photoelectric sensors 71 </ b> A and 71 </ b> B are reading means for reading a bar code 74 provided on the encoder strip 73. Each of the photoelectric sensors 71A and 71B includes a light emitting portion and a light receiving portion, and the light emitted from the light emitting portion is applied to the encoder strip 73, and the reflected light is received by the light receiving portion, thereby reflecting the light. The presence / absence of the bar code 74 is detected based on the light amount difference. The photoelectric sensors 71 </ b> A and 71 </ b> B output an electrical signal by photoelectrically converting the received light, and the output electrical signal is input to the upper arm circumference measurement circuit 72. The upper arm circumference measurement circuit 72 identifies the circumference of the upper arm of the subject based on the input electrical signal, and inputs the identified circumference of the upper arm to the control unit 11.
より詳細には、エンコーダストリップ73に設けられたバーコード74は、図6中に示すI列およびII列の2列のバーコード群を有している。I列に含まれるバーコードは、当該バーコードが付された部分における第2の締付けベルト32の位置情報を示すための識別子を含んでおり、光電センサ71Aによって検知される。II列に含まれるバーコードは、上記I列に含まれるバーコードの検知のタイミングを示すための識別子であり、光電センサ71Bによって検知される。
More specifically, the bar code 74 provided on the encoder strip 73 has a bar code group of two columns of I column and II column shown in FIG. The bar codes included in the I column include an identifier for indicating the position information of the second tightening belt 32 in the portion to which the bar code is attached, and are detected by the photoelectric sensor 71A. The barcode included in the II column is an identifier for indicating the detection timing of the barcode included in the I column, and is detected by the photoelectric sensor 71B.
上記I列およびII列の2列のバーコード群は、それぞれ第2の締付けベルト32の長尺方向において所定の距離で等分された区間を有している。本実施の形態におけるカフ20Aにおいては、上記各区間の長さがそれぞれ10mmとされている。各区間のI列に含まれるバーコードは、ヘッダおよびフッタと、位置マークとをそれぞれ含んでいる。ヘッダは、第2の締付けベルト32の他端部32b側に位置し、当該区間の始まりを示している。フッタは、第2の締付けベルト32の一端部32a側に位置し、当該区間の終わりを示している。位置マークは、これらヘッダとフッタの間に位置し、各区間の始まりの位置における第2の締付けベルト32の位置情報を示している。これに対し、各区間のII列に含まれるバーコードは、図中に矢印で示す読み取り方向において交互にバーコードの有無が繰り返されるように、各バーコードが所定の間隔をもって配置されている。なお、本実施の形態におけるカフ20Aにおいては、上記位置マークが8進1桁のビット表示で記されており、II列に含まれるバーコードは、1ビット置きに配置されている。
The two row barcode groups of the I row and the II row each have a section equally divided by a predetermined distance in the longitudinal direction of the second fastening belt 32. In the cuff 20A in the present embodiment, the length of each of the sections is 10 mm. The barcode included in the I column of each section includes a header and a footer, and a position mark. The header is located on the other end 32b side of the second tightening belt 32 and indicates the beginning of the section. The footer is located on the one end portion 32a side of the second fastening belt 32, and indicates the end of the section. The position mark is located between the header and the footer, and indicates the position information of the second fastening belt 32 at the start position of each section. On the other hand, the barcodes included in the II column of each section are arranged with a predetermined interval so that the presence or absence of the barcode is alternately repeated in the reading direction indicated by the arrow in the drawing. In the cuff 20A according to the present embodiment, the position mark is written in octal one-digit bit display, and the barcodes included in the II column are arranged every other bit.
各区間の始まりの位置における第2の締付けベルト32の位置情報は、光電センサ71A,71Bが設けられた位置に対応する部分の第1の締付けベルト31から当該部分までの締付けベルト31,32の長さを示している。そのため、バーコード74によって示された当該長さは、締付けベルト31,32の周方向長さに相当することになる。したがって、上述した締付け長さ調節機構50および締付け力検出機構を用いてカフ20Aを被験者の上腕に隙間なくぴったりとフィットさせた状態において、上記上腕周囲長計測部によって検出された上記長さが被験者の上腕周囲長を表すことになる。
The position information of the second tightening belt 32 at the start position of each section is the position of the tightening belts 31 and 32 from the first tightening belt 31 corresponding to the position where the photoelectric sensors 71A and 71B are provided to the corresponding portion. Shows the length. Therefore, the length indicated by the bar code 74 corresponds to the circumferential length of the fastening belts 31 and 32. Therefore, in the state where the cuff 20A is fitted to the subject's upper arm without any gap using the above-described tightening length adjusting mechanism 50 and the tightening force detecting mechanism, the length detected by the upper arm circumference measuring unit is the subject. Represents the perimeter of the upper arm.
上述したように、本実施の形態におけるカフ20Aにおいては、第2の締付けベルト32が巻取りローラ58によって巻き取られることによってカフ本体部30が上腕に巻き付けられることになるため、光電センサ71A,71Bは、図中に矢印で示す読み取り方向に沿ってバーコード74を読み取ることになる。その際、光電センサ71Aによって検出されたI列に含まれるバーコードの有無の情報と、光電センサ71Bによって検出されたII列に含まれるバーコードの有無の情報とが、同期されて上腕周囲長計測回路72に入力される。
As described above, in the cuff 20A according to the present embodiment, the cuff main body 30 is wound around the upper arm when the second fastening belt 32 is wound around the winding roller 58, so that the photoelectric sensor 71A, 71B reads the barcode 74 along the reading direction indicated by the arrow in the drawing. At that time, the information on the presence / absence of the barcode included in the I column detected by the photoelectric sensor 71A and the information on the presence / absence of the barcode included in the II column detected by the photoelectric sensor 71B are synchronized, and the upper arm circumference length is synchronized. Input to the measurement circuit 72.
上腕周囲長計測回路72は、入力された上記情報のうち光電センサ71Bによって検出された情報に基づいて光電センサ71Aによって検出された情報を位置情報として認識するためのタイミングを決定する。そして、上腕周囲長計測回路72は、光電センサ71Aによって検出された情報を上述のタイミングと関連付けることにより、光電センサ71Aによって検出された情報から位置マークに関する情報を抽出し、当該位置マークに基づいて位置情報を特定する。これにより、上腕周囲長計測回路72によって締付けベルト31,32の締付け長さが検出され、被験者の上腕の周囲長が特定される。以上により、被験者の上腕の周囲長が上腕周囲長計測部によって自動計測されることになる。
The upper arm circumference measurement circuit 72 determines the timing for recognizing information detected by the photoelectric sensor 71A as position information based on the information detected by the photoelectric sensor 71B among the input information. Then, the upper arm perimeter measurement circuit 72 extracts information related to the position mark from the information detected by the photoelectric sensor 71A by associating the information detected by the photoelectric sensor 71A with the above-described timing, and based on the position mark. Specify location information. As a result, the upper arm perimeter measuring circuit 72 detects the tightening length of the tightening belts 31 and 32 to identify the upper arm perimeter of the subject. As described above, the circumference of the upper arm of the subject is automatically measured by the upper arm circumference measurement unit.
図7は、本実施の形態における血圧計の処理手順を示すフローチャートであり、図8は、本実施の形態における血圧計の各部の動作状況や動作状態を時系列的に示すタイミングチャートである。また、図9は、本実施の形態における血圧計のカフを上腕に装着する装着作業を説明するための模式図であり、図10は、本実施の形態における血圧計のカフを上腕に装着した装着状態の断面図である。次に、これら図7ないし図10を参照して、本実施の形態における血圧計1Aの処理手順を、当該血圧計1Aの各部の動作状況や動作状態あるいはカフ20Aの装着作業、カフ20Aの装着後の状態とあわせて説明する。なお、図7に示すフローチャートに従うプログラムは、図2において示したメモリ部12に予め記憶されており、制御部11がメモリ部12からこのプログラムを読み出して実行することにより、その処理が進められる。
FIG. 7 is a flowchart showing a processing procedure of the sphygmomanometer according to the present embodiment, and FIG. 8 is a timing chart showing the operation state and the operation state of each part of the sphygmomanometer according to the present embodiment in time series. FIG. 9 is a schematic diagram for explaining the mounting operation for mounting the cuff of the sphygmomanometer in the present embodiment on the upper arm, and FIG. 10 shows the mounting of the cuff of the sphygmomanometer in the present embodiment on the upper arm. It is sectional drawing of a mounting state. Next, referring to FIG. 7 to FIG. 10, the processing procedure of the sphygmomanometer 1A in the present embodiment is the same as the operation status and operating state of each part of the sphygmomanometer 1A, the wearing work of the cuff 20A, the wearing of the cuff 20A. It will be described together with the later state. The program according to the flowchart shown in FIG. 7 is stored in advance in the memory unit 12 shown in FIG. 2, and the control unit 11 reads out the program from the memory unit 12 and executes the program, so that the process proceeds.
まず、図7に示すように、被験者が血圧計1Aの操作部16を操作して電源オンの命令を入力すると、電源部18から制御部11に対して電源としての電力が供給され、これにより制御部11が駆動し、血圧計1Aの初期化が行なわれる(ステップS101)。図8に示すように、血圧計1Aの初期化が行なわれた時刻t0においては、ギヤードモータ51、電磁ブレーキ52、加圧ポンプ61および光電センサ71はいずれも動作が停止したオフ状態にあり、排気弁62は空気袋35の内部の空間を外部と連通させてカフ圧を大気圧と等しくすべく開放された状態にあり、圧力センサ63によって検出されるカフ圧は大気圧と同じ値を示すことになる。
First, as shown in FIG. 7, when the test subject operates the operation unit 16 of the sphygmomanometer 1A to input a power-on command, power as a power source is supplied from the power supply unit 18 to the control unit 11. The controller 11 is driven to initialize the sphygmomanometer 1A (step S101). As shown in FIG. 8, at the time t0 when the sphygmomanometer 1A is initialized, the geared motor 51, the electromagnetic brake 52, the pressurizing pump 61, and the photoelectric sensor 71 are all in an off state in which the operation is stopped. The exhaust valve 62 is in an open state so that the space inside the air bag 35 communicates with the outside so that the cuff pressure is equal to the atmospheric pressure, and the cuff pressure detected by the pressure sensor 63 shows the same value as the atmospheric pressure. It will be.
次に、被験者は、図9に示すように、カフ20Aの把手42を右手100で把持し、カフ20Aのカフ本体部30の中空開口部に図中矢印C方向に向けて、把手42を把持した右手100とは異なる方の手である左手200を挿入する。そして、カフ20Aを左手200の上腕にまで移動させ、左手200の上腕に宛がった状態を維持しつつ、把手42を把持した方の手である右手100の親指101で把手42に設けられた押し釦44を押下する。
Next, as shown in FIG. 9, the subject holds the handle 42 of the cuff 20 </ b> A with the right hand 100 and holds the handle 42 toward the hollow opening of the cuff body 30 of the cuff 20 </ b> A in the direction of arrow C in the figure. The left hand 200 which is a different hand from the right hand 100 is inserted. Then, the cuff 20A is moved to the upper arm of the left hand 200, and the handle 42 is provided on the handle 42 with the thumb 101 of the right hand 100, which is the hand holding the handle 42, while maintaining the state of being attached to the upper arm of the left hand 200. Press the push button 44.
図7に示すように、上記被験者による押し釦44の押下を受付けた制御部11は、空気袋35の予備加圧を行なう(ステップS102)。具体的には、図8に示すように、制御部11は、押し釦44が押下された時刻t1において空気袋35の内部の空間を外部と非連通とするために排気弁62を閉鎖させ、つづいて時刻t2において空気袋35内に空気を注入するために加圧ポンプ61の駆動を開始する。そして、制御部11は、所定時間経過後の時刻t3において加圧ポンプ61の駆動を停止する。ここで、加圧ポンプ61が駆動される時間は、予め定められた所定量の空気が空気袋35の内部の空間に注入されることとなるために必要な時間である。以上により、空気袋35に対する予備加圧が終了する(ステップS103)。
As shown in FIG. 7, the control unit 11 that has received the pressing of the push button 44 by the subject performs pre-pressurization of the air bag 35 (step S <b> 102). Specifically, as shown in FIG. 8, the control unit 11 closes the exhaust valve 62 in order to make the space inside the air bladder 35 out of communication at the time t1 when the push button 44 is pressed, Subsequently, driving of the pressurizing pump 61 is started to inject air into the air bladder 35 at time t2. And the control part 11 stops the drive of the pressurization pump 61 at the time t3 after progress of predetermined time. Here, the time for which the pressurizing pump 61 is driven is a time necessary for a predetermined amount of air to be injected into the space inside the air bladder 35. Thus, the pre-pressurization for the air bag 35 is completed (step S103).
次に、図7に示すように、制御部11は、光電センサ71を駆動し、締付けベルト31,32の締付け長さの検出を開始する(ステップS104)。具体的には、図8に示すように、制御部11は、加圧ポンプ61の停止後の時刻t4において光電センサ71を駆動し、第2の締付けベルト32に設けられたバーコード74の光電センサ71による読み取りを開始する。
Next, as shown in FIG. 7, the control unit 11 drives the photoelectric sensor 71 to start detecting the tightening length of the tightening belts 31 and 32 (step S104). Specifically, as shown in FIG. 8, the control unit 11 drives the photoelectric sensor 71 at time t <b> 4 after the pressurization pump 61 stops, and the photoelectric sensor of the barcode 74 provided on the second tightening belt 32. Reading by the sensor 71 is started.
次に、図7に示すように、制御部11は、上腕に対するカフ20Aの締付け動作を開始する(ステップS105)。その際、制御部11は、上腕に対するカフ20Aの締付けが所定の締付け状態となったか否かを判断し(ステップS106)、所定の締付け状態となっていない場合(ステップS106においてNOの場合)には、上腕に対するカフ20Aの締付け動作を継続し、所定の締付け状態となった場合(ステップS106においてYESの場合)には、上腕に対するカフ20Aの締付け動作を停止する(ステップS107)。
Next, as shown in FIG. 7, the control unit 11 starts the tightening operation of the cuff 20A with respect to the upper arm (step S105). At that time, the control unit 11 determines whether or not the cuff 20A has been tightened with respect to the upper arm in a predetermined tightening state (step S106), and when the predetermined tightening state is not achieved (NO in step S106). Continues the tightening operation of the cuff 20A with respect to the upper arm, and when the predetermined tightening state is reached (YES in step S106), the tightening operation of the cuff 20A with respect to the upper arm is stopped (step S107).
具体的には、図8に示すように、制御部11は、時刻t5においてギヤードモータ51を順方向に回転駆動することにより、巻取りローラ58による第2の締付けベルト32の巻取り動作を開始させる。そして、制御部11は、当該巻取り動作中において空気袋35のカフ圧を圧力センサ63によって検出し、検出されたカフ圧が予め定められた閾値に達した時刻t6においてギヤードモータ51の順方向への回転駆動を停止し、これと同時に電磁ブレーキ52を駆動して巻取りローラ58の回転を停止する。ここで、上記閾値は、血圧値測定に適した上腕に対するカフ20Aの締付け力に基づいて予め決定される。
Specifically, as shown in FIG. 8, the control unit 11 starts the winding operation of the second tightening belt 32 by the winding roller 58 by rotationally driving the geared motor 51 in the forward direction at time t5. Let Then, the control unit 11 detects the cuff pressure of the air bladder 35 during the winding operation by the pressure sensor 63, and the forward direction of the geared motor 51 at time t6 when the detected cuff pressure reaches a predetermined threshold value. At the same time, the electromagnetic brake 52 is driven to stop the rotation of the take-up roller 58. Here, the threshold value is determined in advance based on the tightening force of the cuff 20A with respect to the upper arm suitable for blood pressure value measurement.
ここで、図10に示すように、カフ20Aが上腕202に最適締付け力にて締付けられた状態においては、締付けベルト31,32によって空気袋35が上腕202に対して確実に押圧された状態となる。そのため、以降の測定動作において空気袋35が膨張することにより、上腕202がカフ20Aによって確実に圧迫されることになり、上腕202の内部に位置する動脈に対する阻血が確実に行なえるようになる。なお、当該状態における締付けベルト31,32の締付け長さが上腕周囲長計測回路72によって上腕の周囲長として決定され、当該決定された上腕周囲長が制御部11に入力されることになる。制御部11は、入力された上腕周囲長をメモリ部12に対して出力し、メモリ部12は、入力された上腕周囲長を一時的に記憶する。
Here, as shown in FIG. 10, when the cuff 20A is fastened to the upper arm 202 with the optimum tightening force, the air bag 35 is reliably pressed against the upper arm 202 by the fastening belts 31 and 32. Become. Therefore, in the subsequent measurement operation, the air bag 35 is inflated, so that the upper arm 202 is surely compressed by the cuff 20A, and the artery located inside the upper arm 202 can be reliably blocked. Note that the tightening length of the tightening belts 31 and 32 in this state is determined as the perimeter of the upper arm by the upper arm perimeter measuring circuit 72, and the determined upper arm perimeter is input to the control unit 11. The control unit 11 outputs the input upper arm circumference to the memory unit 12, and the memory unit 12 temporarily stores the input upper arm circumference.
次に、図7に示すように、制御部11は、光電センサ71の駆動を停止し、締付け長さの検出を終了する(ステップS108)。具体的には、図8に示すように、制御部11は、時刻t7において光電センサ71の駆動を停止し、第2の締付けベルト32に設けられたバーコード74の光電センサ71による読み取りを終了する。
Next, as shown in FIG. 7, the control unit 11 stops driving the photoelectric sensor 71 and ends the detection of the tightening length (step S108). Specifically, as shown in FIG. 8, the control unit 11 stops driving the photoelectric sensor 71 at time t <b> 7 and ends reading of the barcode 74 provided on the second tightening belt 32 by the photoelectric sensor 71. To do.
次に、図7に示すように、制御部11は、計測された上腕周囲長が予め定められた当該カフ20Aの適用可能範囲内の大きさであるか否かの判断を行なう(ステップS109)。すなわち、制御部11は、当該カフ20Aを用いて血圧値の測定を行なった場合の測定結果がその精度を保障できる範囲内の上腕の大きさであるか否かの判断を行なう。制御部11は、計測された上腕周囲長が予め定められた当該カフ20Aの適用可能範囲内の大きさであると判断した場合(ステップS109においてYESの場合)に、ステップS110へと移行し、計測された上腕周囲長が予め定められた当該カフ20Aの適用可能範囲内の大きさでないと判断した場合(ステップS109においてNOの場合)に、ステップS115へと移行する。
Next, as shown in FIG. 7, the control unit 11 determines whether or not the measured upper arm circumference is within a predetermined applicable range of the cuff 20 </ b> A (step S <b> 109). . That is, the control unit 11 determines whether or not the measurement result when the blood pressure value is measured using the cuff 20A is the size of the upper arm within a range in which the accuracy can be ensured. When the control unit 11 determines that the measured upper arm perimeter is within a predetermined applicable range of the cuff 20A (YES in step S109), the control unit 11 proceeds to step S110. When it is determined that the measured upper arm perimeter is not within a predetermined range of the applicable range of the cuff 20A (NO in step S109), the process proceeds to step S115.
ステップS109においてYESと判断された場合には、図7に示すように、制御部11は、血圧値測定のために空気袋35の加圧を開始する(ステップS110)。具体的には、図8に示すように、制御部11は、時刻t8において加圧ポンプ61を駆動してカフ圧を上昇させ、所定のカフ圧となるように空気袋35の加圧を行なう。
If it is determined YES in step S109, as shown in FIG. 7, the control unit 11 starts pressurization of the air bladder 35 for blood pressure measurement (step S110). Specifically, as shown in FIG. 8, the control unit 11 drives the pressurizing pump 61 to increase the cuff pressure at time t8, and pressurizes the air bladder 35 so as to obtain a predetermined cuff pressure. .
次に、図7に示すように、制御部11は、血圧値測定のために空気袋35の微速減圧を開始する(ステップS111)。具体的には、図7に示すように、制御部11は、圧力センサ63によって空気袋35の内圧が所定の内圧に達したことが検出された時刻t9において加圧ポンプ61の駆動を停止し、その後排気弁62の開放量を制御しつつ徐々に排気弁62を開放させる。また、その際、制御部11は、圧力センサ63によって検出されるカフ圧の変動を取得する。
Next, as shown in FIG. 7, the control unit 11 starts the slow depressurization of the air bladder 35 for blood pressure measurement (step S111). Specifically, as shown in FIG. 7, the control unit 11 stops driving the pressure pump 61 at time t <b> 9 when the pressure sensor 63 detects that the internal pressure of the air bladder 35 has reached a predetermined internal pressure. Thereafter, the exhaust valve 62 is gradually opened while controlling the opening amount of the exhaust valve 62. At that time, the control unit 11 acquires the fluctuation of the cuff pressure detected by the pressure sensor 63.
次に、図7に示すように、制御部11は、微速減圧過程において得られたカフ圧の変動に基づいて血圧値を算出する(ステップS112)。つづいて、制御部11は、ステップS112において得られた血圧値をメモリ部12および表示部14に出力し、メモリ部12において当該血圧値が測定結果として記憶され(ステップS113)、表示部14において上記測定結果としての血圧値が表示される(ステップS114)。ここで、表示部14は、収縮期血圧値および拡張期血圧値をたとえば数値として表示する。
Next, as shown in FIG. 7, the control unit 11 calculates a blood pressure value based on the variation of the cuff pressure obtained in the slow depressurization process (step S112). Subsequently, the control unit 11 outputs the blood pressure value obtained in step S112 to the memory unit 12 and the display unit 14, and the memory unit 12 stores the blood pressure value as a measurement result (step S113). The blood pressure value as the measurement result is displayed (step S114). Here, the display unit 14 displays the systolic blood pressure value and the diastolic blood pressure value as numerical values, for example.
ステップS109においてNOと判断された場合、あるいはステップS114が終了した場合には、図7に示すように、制御部11は、空気袋35を開放する(ステップS115)とともに、上腕202に対するカフ20Aの締付け解除動作を行う(ステップS116)。具体的には、図8に示すように、制御部11は、血圧値の算出が終了した時刻t10において排気弁62を完全に開放し、空気袋35内の空気を外部へと排気させ、その後時刻t11において電磁ブレーキ52の動作を停止させるとともに、時刻t12においてギヤードモータ51を逆方向に回転駆動し、巻取りローラ58から第2の締付けベルト32を送出させる。その後、制御部11は、第2の締付けベルト32が完全に巻取りローラ58から送出された時刻t13においてギヤードモータ51の駆動を停止する。この後、血圧計1Aは待機状態をとり、被験者の操作部16による電源オフの命令の入力を待って電源としての電力の供給を停止する。
If NO is determined in step S109, or if step S114 is completed, as shown in FIG. 7, the control unit 11 opens the air bag 35 (step S115) and the cuff 20A with respect to the upper arm 202. A tightening release operation is performed (step S116). Specifically, as shown in FIG. 8, the control unit 11 completely opens the exhaust valve 62 at time t <b> 10 when the calculation of the blood pressure value ends, exhausts the air in the air bladder 35 to the outside, and then At time t11, the operation of the electromagnetic brake 52 is stopped, and at time t12, the geared motor 51 is rotationally driven in the reverse direction, and the second tightening belt 32 is sent from the winding roller 58. Thereafter, the control unit 11 stops driving the geared motor 51 at time t13 when the second tightening belt 32 is completely delivered from the take-up roller 58. Thereafter, the sphygmomanometer 1 </ b> A enters a standby state, and waits for an input of a power-off command from the operation unit 16 of the subject, and stops supplying power as a power source.
以上において説明した本実施の形態における血圧計1Aにおいては、第2の締付けベルト32に設けられたマーカーとしてのバーコード74と、基部41に設けられた読み取り部としての光電センサ71とによって、カフ20Aが装着された被測定部位としての上腕202の周囲長を精度よく測定することが可能になる。一般に光電センサは非常に小型であり、そのため上記構成を採用すれば小型で簡便に上腕周囲長を自動計測することが可能なカフとすることができる。また、位置情報を示すマーカーとしてのバーコードについても、締付けベルトの所定位置にエンコーダストリップを取付けることで簡便に構成可能であり、装置構成が複雑化したり装置が大型化することもない。
In the sphygmomanometer 1 </ b> A according to the present embodiment described above, the bar code 74 as the marker provided on the second fastening belt 32 and the photoelectric sensor 71 as the reading unit provided on the base 41 are used. It becomes possible to accurately measure the perimeter of the upper arm 202 as a measurement site to which 20A is attached. In general, a photoelectric sensor is very small. Therefore, if the above configuration is adopted, a cuff capable of automatically measuring the circumference of the upper arm can be made small and simple. Further, the barcode as a marker indicating the position information can be simply configured by attaching an encoder strip to a predetermined position of the fastening belt, and the apparatus configuration is not complicated and the apparatus is not enlarged.
また、本実施の形態における血圧計1Aにおいては、締付け長さ調節機構50としてのギヤードモータ51、電磁ブレーキ52および巻取りローラ58等が把手部40の基部41に収容された構成であるため、カフ20Aを小型にかつコンパクトに構成することができる。
Further, in the sphygmomanometer 1A according to the present embodiment, the geared motor 51, the electromagnetic brake 52, the take-up roller 58, and the like as the tightening length adjusting mechanism 50 are housed in the base 41 of the handle portion 40. The cuff 20A can be made small and compact.
また、本実施の形態における血圧計1Aにあっては、カフ20Aが装着される右手100とは異なる方の左手200でカフ20Aに設けられた把手42を把持し、その状態でカフ20Aの中空開口部内にカフ20Aが装着される左手200を差し込んでカフ20Aを上腕202に宛がい、その後把手42に設けられた押し釦44を押下するという非常に簡単な操作により、カフ20Aの上腕202に対する締付け動作および上腕周囲長の計測動作がその後自動的に行なわれるようにすることができる。したがって、非常に容易にカフ20Aを上腕202に対して装着することができるとともに上腕周囲長を簡便に得ることができる。
Further, in sphygmomanometer 1A according to the present embodiment, grip 42 provided on cuff 20A is held by left hand 200, which is different from right hand 100 to which cuff 20A is attached, and cuff 20A is hollow in this state. The left hand 200 to which the cuff 20A is attached is inserted into the opening, the cuff 20A is directed to the upper arm 202, and then the push button 44 provided on the handle 42 is pressed down. It is possible to automatically perform the tightening operation and the upper arm circumference measurement operation thereafter. Therefore, the cuff 20A can be attached to the upper arm 202 very easily, and the upper arm perimeter can be easily obtained.
また、本実施の形態における血圧計1Aにおいては、上記カフ20Aの装着作業のみならず、その後に行なわれる血圧値の測定動作と、当該測定動作後に行なわれるカフ20Aの上腕202に対する締付け解除動作とがすべて自動的に連続して行なわれるように構成されている。したがって、上記構成を採用することにより、いわゆるワンタッチ動作でカフ20Aの装着、血圧値の測定およびカフ20Aの取り外しが行なえる非常に利便性に優れた血圧計とすることができる。
In the sphygmomanometer 1A according to the present embodiment, not only the operation of attaching the cuff 20A but also the blood pressure measurement operation performed thereafter, and the tightening release operation for the upper arm 202 of the cuff 20A performed after the measurement operation. Are automatically and continuously performed. Therefore, by adopting the above configuration, it is possible to obtain a sphygmomanometer that is very convenient and can be attached to the cuff 20A, measured the blood pressure value, and removed the cuff 20A by a so-called one-touch operation.
さらには、上述の本実施の形態における血圧計1Aにおいては、計測された上腕周囲長が予め定められた当該カフ20Aの適用可能範囲内(すなわち、当該カフ20Aを用いて血圧値の測定を行なった場合にその測定結果としての血圧値の精度が保障できる範囲内)にあるか否かの判断が制御部11によって行なわれるように構成することにより、計測された上腕周囲長が上記適用可能範囲内にあると判断された場合にはその後に血圧値測定が行なわれるように構成し、計測された上腕周囲長が上記適用可能範囲外にあると判断された場合には直ちにその動作を終了するように構成している。したがって、被験者の上腕のサイズが上記適用可能範囲外にある場合には、そもそも血圧値測定自体が行なえないように構成されることになるため、正確でない測定結果を被験者に提供することのない血圧計とすることができる。
Furthermore, in the sphygmomanometer 1A in the above-described embodiment, the measured upper arm circumference is within the applicable range of the cuff 20A (that is, the blood pressure value is measured using the cuff 20A). In such a case, the control unit 11 determines whether the accuracy of the blood pressure value as the measurement result is within a range in which the measurement result can be ensured, so that the measured upper arm circumference is within the applicable range. When it is determined that the blood pressure value is measured, the blood pressure value is measured thereafter. When it is determined that the measured upper arm circumference is outside the applicable range, the operation is immediately terminated. It is configured as follows. Therefore, when the size of the upper arm of the subject is outside the applicable range, the blood pressure value is not measured in the first place, so blood pressure that does not provide the subject with inaccurate measurement results. It can be a total.
また、上述した本実施の形態における血圧計1Aにおいては、締付けベルト31,32を用いて上腕202を締付ける際に、締付け力検出機構を用いてカフ20Aの上腕202に対する締付け力を検出し、当該締付け力が最適となった状態を締付け長さ調節機構50を用いて維持するように構成されているため、上腕202に対するカフ20Aの確実な巻付けが測定の都度再現されるようになる。
Further, in the sphygmomanometer 1A according to the present embodiment described above, when the upper arm 202 is tightened using the tightening belts 31 and 32, the tightening force with respect to the upper arm 202 of the cuff 20A is detected using a tightening force detection mechanism, Since the tightening force adjustment mechanism 50 is used to maintain the optimum tightening force, the reliable winding of the cuff 20A around the upper arm 202 is reproduced every measurement.
なお、上述の本実施の形態における血圧計1Aにおいては、計測可能な上腕の最小単位である各区間の長さを10mmとした場合を例示したが、この区間の長さをより小さくすれば、より精緻に上腕周囲長を計測することが可能である。しかしながら、第2の締付けベルト32に付されるバーコード74の幅が小さくなればなるほど、その検出は困難になる傾向にある。上述の本実施の形態における血圧計1Aにおいては、I列に含まれるバーコードの位置マークが8進1桁のビット表示で示された場合としたが、これを種々変更することにより、測定可能範囲を広げたりあるいは測定可能な分解能を高めたりすることが可能になる。たとえば、位置マークを8進2桁表示や8進3桁表示とすることにより、より精緻な上腕周囲長の計測が可能になる。また、読み取り方向における位置マークの前後にヘッダおよびフッタを配置しない構成とすることも可能であり、そのように構成した場合にもより精緻な上腕周囲長の計測が可能になる。
In the sphygmomanometer 1A in the above-described embodiment, the case where the length of each section, which is the minimum unit of the upper arm that can be measured, is 10 mm is exemplified. However, if the length of this section is made smaller, It is possible to measure the upper arm circumference more precisely. However, as the width of the bar code 74 attached to the second tightening belt 32 becomes smaller, the detection tends to be difficult. In the sphygmomanometer 1A according to the above-described embodiment, the barcode position mark included in the I column is indicated by a bit display of octal one digit, but can be measured by variously changing this. It becomes possible to widen the range or increase the measurable resolution. For example, by displaying the position mark in octal 2-digit display or octal 3-digit display, more precise measurement of the upper arm circumference can be performed. Further, it is possible to adopt a configuration in which the header and the footer are not arranged before and after the position mark in the reading direction, and even in such a configuration, a more precise measurement of the upper arm circumference can be performed.
また、上述の本実施の形態における血圧計1Aにおいては、バーコード74自体が当該バーコードが付された部分における位置情報を有することとなるように、当該バーコード74に位置マークを含めて構成している。しかしながら、上腕周囲長の計測に際して必ずエンコーダストリップ73の端からバーコード74が検出されるように構成した場合には、図6に示すII列のバーコード群のみをエンコーダストリップ73に設け、図6に示すI列のバーコード群を設けない構成とすることも可能である。このように構成した場合には、光電センサ71Bによって検出されたバーコードの数を上腕周囲長計測回路72がカウントすることにより締付けベルト31,32の移動量が検出されることになり、当該移動量に基づいて上腕周囲長を特定することが可能になる。したがって、1個の光電センサのみで読み取り部が構成可能となるため装置構成が簡素化するとともに、位置マークやヘッダおよびフッタを設ける必要がなくなるため上腕周囲長の計測の分解能を向上させることが可能になる。
In addition, the sphygmomanometer 1A according to the present embodiment described above includes a position mark in the barcode 74 so that the barcode 74 itself has position information in a portion to which the barcode is attached. is doing. However, when the bar code 74 is always detected from the end of the encoder strip 73 when measuring the upper arm circumference, only the II-line bar code group shown in FIG. It is also possible to adopt a configuration in which the I-line barcode group shown in FIG. When configured in this way, the upper arm circumference measuring circuit 72 counts the number of barcodes detected by the photoelectric sensor 71B, whereby the movement amount of the tightening belts 31 and 32 is detected. It is possible to specify the upper arm circumference based on the amount. Therefore, since the reading unit can be configured with only one photoelectric sensor, the apparatus configuration is simplified, and it is not necessary to provide a position mark, header, or footer, so that it is possible to improve the resolution of the upper arm circumference measurement. become.
さらには、上述の光電センサ71を用いた読み取り部に加え、ロータリエンコーダ等に代表される回転量検出部をカフ20Aに設け、当該回転量検出部にて巻取りローラ58の回転量(回転角度)を検出し、これを用いて締付けベルト31,32の締付け長さを計測することとすれば、上腕周囲長の計測の分解能を高めたりあるいは計測のタイミングを示すバーコード群(すなわち、図6に示したII列のバーコード群)を省略したりすることも可能である。
Further, in addition to the reading unit using the photoelectric sensor 71 described above, a rotation amount detection unit represented by a rotary encoder or the like is provided in the cuff 20A, and the rotation amount (rotation angle) of the winding roller 58 is detected by the rotation amount detection unit. ) And using this to measure the tightening length of the tightening belts 31 and 32, the bar code group (that is, FIG. 6) that increases the resolution of the measurement of the upper arm circumference or indicates the timing of the measurement. It is also possible to omit the bar code group in column II shown in FIG.
また、上述したマーカーとしてのバーコード74が設けられる位置は、締付けベルト31,32に限定されるものではない。たとえば、締付けベルト31,32の移動に伴って回転する回転部材としてのコロやギア等を別途設け、当該コロやギアに上述したバーコード74と同様のバーコードを設けることとしてもよい。なお、その場合には、これらコロやギアに対面するように読み取り部としての光電センサ71が配設されることになる。
Further, the position where the barcode 74 as the marker described above is provided is not limited to the fastening belts 31 and 32. For example, a roller, a gear, or the like as a rotating member that rotates with the movement of the fastening belts 31 and 32 may be separately provided, and the same barcode as the barcode 74 described above may be provided on the roller or gear. In this case, a photoelectric sensor 71 as a reading unit is disposed so as to face these rollers and gears.
また、マーカーとしては、必ずしも上述の如くの棒状のバーコードである必要はなく、たとえば円形状や三角形状等の同じ形状の複数のマーカーを締付けベルトやコロ、ギア等に設けることとしてもよい。
Also, the marker is not necessarily a bar-shaped barcode as described above, and a plurality of markers having the same shape such as a circular shape or a triangular shape may be provided on a fastening belt, a roller, a gear, or the like.
また、上述のロータリエンコーダ等に代表される回転量検出部を用いる構成とする場合には、上述したバーコード74および光電センサ71を用いた構成自体を廃止することも可能である。その場合には、締付けベルト31,32の移動に伴って回転する回転部材をカフ20Aに設け、当該回転部材の回転量を上述した回転量検出部によって検出し、これに基づいて締付けベルト31,32の移動量を計測する構成とすればよい。なお、回転量検出部としてロータリエンコーダを採用する場合には、当該ロータリエンコーダを回転部材としての巻取りローラ58に付設することとすればよい。
Further, when the rotation amount detection unit represented by the above-described rotary encoder or the like is used, the above-described configuration using the barcode 74 and the photoelectric sensor 71 can be eliminated. In that case, the cuff 20A is provided with a rotating member that rotates in accordance with the movement of the tightening belts 31 and 32, and the amount of rotation of the rotating member is detected by the above-described rotation amount detection unit. What is necessary is just to set it as the structure which measures 32 movement amount. When a rotary encoder is employed as the rotation amount detection unit, the rotary encoder may be attached to the take-up roller 58 serving as a rotating member.
以上の本実施の形態においては、上腕周囲長計測部によって計測された上腕周囲長が、カフ20Aが装着された上腕のサイズが当該カフ20Aの適用可能範囲内にあるか否かの判断に利用されるように構成した場合を例示したが、計測された上腕周囲長はこの他にも種々利用が可能である。以下に示す本実施の形態の第1および第2変形例は、計測された上腕周囲長を利用した他の装置構成例を示すものである。なお、これら第1および第2変形例に係る血圧計の構成は、主として制御部11の構成においてのみ上述の本実施の形態における血圧計と相違するものであるため、当該相違部分を除きその説明はここでは繰り返さない。
In the above embodiment, the upper arm circumference measured by the upper arm circumference measurement unit is used for determining whether the size of the upper arm to which the cuff 20A is attached is within the applicable range of the cuff 20A. However, the measured circumference of the upper arm can be used in various other ways. The following first and second modifications of the present embodiment show other apparatus configuration examples using the measured upper arm circumference. The configuration of the sphygmomanometer according to the first and second modified examples is mainly different from the sphygmomanometer in the present embodiment described above only in the configuration of the control unit 11, and the description thereof is omitted except for the difference. Does not repeat here.
第1変形例に係る血圧計は、上腕周囲長計測部によって計測された上腕周囲長を、血圧値測定のために膨縮する空気袋35の加圧条件および減圧条件の決定に利用するものである。具体的には、図2に示すブロック構成の血圧計1Aにおいて、制御部11に、膨縮機構による空気袋35の膨張動作および収縮動作の少なくもいずれか一方を制御する膨縮動作制御部(不図示)を設ける。膨縮動作制御部は、上腕周囲長計測回路72から入力された上腕周囲長の情報に基づき、予めメモリ部等に記憶されている複数の膨縮動作プログラムの中から当該計測された上腕周囲長に適した膨縮動作プログラムを選択し、これに基づいて加圧ポンプ駆動回路64および/または排気弁駆動回路65を介して加圧ポンプ61および/または排気弁62の動作を制御する。
The sphygmomanometer according to the first modification uses the upper arm circumference measured by the upper arm circumference measurement unit to determine the pressurizing condition and the depressurizing condition of the air bag 35 that is inflated and inflated for measuring the blood pressure value. is there. Specifically, in the sphygmomanometer 1A having the block configuration shown in FIG. 2, the controller 11 controls the inflating / deflating operation control unit (which controls at least one of the inflating and deflating operations of the air bladder 35 by the inflating / deflating mechanism) (Not shown). The expansion / contraction movement control unit is configured to measure the upper arm circumference measured from a plurality of expansion / contraction operation programs stored in advance in a memory unit or the like based on the information about the upper arm circumference measured from the upper arm circumference measurement circuit 72. A suitable expansion / contraction operation program is selected, and based on this, the operation of the pressurization pump 61 and / or the exhaust valve 62 is controlled via the pressurization pump drive circuit 64 and / or the exhaust valve drive circuit 65.
上記膨縮動作プログラムとしては、たとえば上腕のサイズが小さい被験者に対しては加圧ポンプ61の単位時間あたりの吐出量を小さくして加圧動作をゆっくりと行うプログラムとしたり、逆に上腕のサイズが大きい被験者に対して加圧ポンプ61の単位時間当たりの吐出量を大きくして加圧動作を迅速に行なうプログラムとしたりすることが想定される。また、上記膨縮動作プログラムとしては、たとえば上腕のサイズ小さい被験者に対しては排気弁62の開放量を小さく調節し、単位時間当たりに空気袋35から排出される空気の量を少なくするプログラムとしたり、逆に上腕のサイズが大きい被験者に対しては排気弁62の開放量を大きく調節し、単位時間当たりに空気袋35から排出される空気の量を大きくするプログラムとしたりすることが想定される。
As the expansion / contraction operation program, for example, for a subject with a small upper arm size, a program for slowly performing a pressure operation by reducing the discharge amount per unit time of the pressure pump 61, or conversely, the size of the upper arm It is assumed that a program for performing a pressurization operation quickly by increasing the discharge amount per unit time of the pressurization pump 61 for a subject having a large pressure. The expansion / contraction operation program is, for example, a program for reducing the amount of air discharged from the air bag 35 per unit time by adjusting the opening amount of the exhaust valve 62 to be small for a subject with a small upper arm size. On the contrary, for a subject with a large upper arm size, it is assumed that the opening amount of the exhaust valve 62 is adjusted to be large and the amount of air discharged from the air bag 35 per unit time is increased. The
図11は、第1変形例に係る血圧計の処理手順を示すフローチャートである。なお、図11に示すフローチャートは、図7に示したフローチャートに対する変更点のみを抜き出して図示したものである。図11に示すように、本変形例に係る血圧計においては、血圧値測定のための処理であるステップS110~S112の処理を行なうに先立ち、ステップS108において取得した上腕周囲長の情報に基づき、ステップS109Aにおいて空気袋35の加圧条件および/または減圧条件が決定される。具体的には、制御部11が上腕周囲長計測回路72の出力を受けてメモリ部12にアクセスし、最適な膨縮動作プログラムを読み出し、その後に行なわれる血圧値測定のための処理であるステップS110~S112において、制御部11に含まれる膨縮動作制御部が加圧ポンプ駆動回路64および/または排気弁駆動回路65を介して加圧ポンプ61および/または排気弁62の動作を制御する。
FIG. 11 is a flowchart showing a processing procedure of the sphygmomanometer according to the first modification. Note that the flowchart shown in FIG. 11 shows only the changes from the flowchart shown in FIG. As shown in FIG. 11, in the sphygmomanometer according to the present modification, prior to performing the processing of steps S110 to S112, which is processing for blood pressure measurement, based on the upper arm circumference information acquired in step S108, In step S109A, the pressurizing condition and / or the depressurizing condition of the air bladder 35 are determined. Specifically, the control unit 11 receives the output of the upper arm circumference measurement circuit 72 and accesses the memory unit 12 to read out the optimum expansion / contraction operation program, and is a process for blood pressure measurement performed thereafter. In S110 to S112, the expansion / contraction operation control unit included in the control unit 11 controls the operation of the pressurization pump 61 and / or the exhaust valve 62 via the pressurization pump drive circuit 64 and / or the exhaust valve drive circuit 65.
以上において説明した第1変形例に係る構成を採用することにより、カフ20Aが装着された上腕のサイズに応じた空気袋35の膨張動作および/または収縮動作が実現されることになるため、従来に比してより高精度に血圧値を測定することが可能となったり、従来に比してより迅速に血圧値の測定が行なえたりするようになる。
By adopting the configuration according to the first modification described above, the inflation operation and / or the contraction operation of the air bag 35 according to the size of the upper arm to which the cuff 20A is attached is realized. Thus, it becomes possible to measure the blood pressure value with higher accuracy than in the past, and it is possible to measure the blood pressure value more quickly than in the past.
第2変形例に係る血圧計は、上腕周囲長計測部によって計測された上腕周囲長を、血圧値算出の際の補正要素として利用するものである。具体的には、図2に示すブロック構成の血圧計1Aにおいて、制御部11に設けられた血圧情報測定部(不図示)に、測定された血圧情報としての血圧値を補正するための血圧情報補正部(不図示)をさらに設ける。血圧情報補正部は、上腕周囲長計測回路72から入力された上腕周囲長の情報に基づき、補正係数を算出し、当該補正係数を用いて血圧値算出に利用される包落線を補正し、これに基づいて血圧値算出のためのパラメータを決定する。血圧情報測定部は、当該決定されたパラメータに基づいて測定結果としての血圧値を算出する。
The sphygmomanometer according to the second modification uses the upper arm circumference measured by the upper arm circumference measurement unit as a correction factor when calculating the blood pressure value. Specifically, in the sphygmomanometer 1A having the block configuration shown in FIG. 2, blood pressure information for correcting the blood pressure value as the measured blood pressure information to the blood pressure information measuring unit (not shown) provided in the control unit 11. A correction unit (not shown) is further provided. The blood pressure information correction unit calculates a correction coefficient based on the information on the upper arm periphery length input from the upper arm periphery length measurement circuit 72, corrects the envelope used for blood pressure value calculation using the correction coefficient, Based on this, a parameter for calculating the blood pressure value is determined. The blood pressure information measurement unit calculates a blood pressure value as a measurement result based on the determined parameter.
図12は、第2変形例に係る血圧計の処理手順を示すフローチャートである。なお、図12に示すフローチャートは、図7に示したフローチャートに対する変更点のみを抜き出して図示したものである。図12に示すように、本変形例に係る血圧計においては、血圧値算出のための処理であるステップS112の処理を行なうに先立ち、ステップS108において取得した上腕周囲長の情報に基づき、ステップS111A~S111Cにおいて上述した血圧値算出のための補正処理が行なわれる。具体的には、ステップS111Aにおいて上腕周囲長計測回路72から入力された上腕周囲長の情報に基づいて補正係数が算出され、ステップS111Bにおいて上記補正係数を用いて血圧値算出に利用される包落線が補正され、ステップS111Cにおいて補正された包落線に基づいて血圧値算出のためのパラメータが決定される。
FIG. 12 is a flowchart showing a processing procedure of the sphygmomanometer according to the second modified example. Note that the flowchart shown in FIG. 12 shows only the changes from the flowchart shown in FIG. As shown in FIG. 12, in the sphygmomanometer according to the present modification, step S111A is performed based on the upper arm circumference information acquired in step S108 prior to performing the process of step S112, which is a process for calculating the blood pressure value. In S111C, the correction process for calculating the blood pressure value described above is performed. Specifically, a correction coefficient is calculated based on the upper arm circumference measurement information input from the upper arm circumference measurement circuit 72 in step S111A, and an envelope used for blood pressure value calculation using the correction coefficient in step S111B. The line is corrected, and a parameter for calculating the blood pressure value is determined based on the envelope line corrected in step S111C.
以上において説明した第2変形例に係る構成を採用することにより、カフ20Aが装着された上腕のサイズに応じて必要な補正が測定された血圧値に加えられることになる。たとえば、一般に上腕のサイズが大きい被験者が血圧値を測定した場合には、測定された血圧値が実際よりも高めになる傾向があるため、上記血圧情報補正部による補正処理を経ることにより、より高精度の血圧値測定が可能になる。
By adopting the configuration according to the second modification described above, a necessary correction is added to the measured blood pressure value according to the size of the upper arm to which the cuff 20A is attached. For example, in general, when a subject whose upper arm size is large measures a blood pressure value, the measured blood pressure value tends to be higher than the actual blood pressure. High-precision blood pressure measurement is possible.
また、以下に示す本実施の形態の第3変形例に係る血圧計は、第2の締付けベルト32に設けられたバーコード74と基部41に設けられた光電センサ71を用いて、カフ20Aの締付け解除動作時の締付け長さ調節機構の動作制御を行なうように構成した例である。上述の本実施の形態における血圧計1Aの如くの構成を採用した場合には、使用後においてカフ20Aの周方向の長さが常に同じ長さに復帰するように構成することが好ましい。そのため、本変形例に係る血圧計においては、上述の如くバーコード74と光電センサ71とを含む上腕周囲長計測部を利用してカフ20Aの締付け解除動作時の締付け長さ調節機構の動作制御を行なうことで上述したカフ20Aの周方向の長さの初期長さへの復帰を実現している。
In addition, a sphygmomanometer according to a third modification of the present embodiment shown below uses a bar code 74 provided on the second fastening belt 32 and a photoelectric sensor 71 provided on the base 41 to It is the example comprised so that operation | movement control of the fastening length adjustment mechanism at the time of fastening cancellation | release operation might be performed. When a configuration such as the sphygmomanometer 1A in the present embodiment described above is employed, it is preferable to configure the cuff 20A so that its circumferential length always returns to the same length after use. Therefore, in the sphygmomanometer according to the present modification, the operation control of the tightening length adjusting mechanism during the tightening release operation of the cuff 20A using the upper arm circumference measuring unit including the barcode 74 and the photoelectric sensor 71 as described above. By performing the above, the return of the length of the cuff 20A in the circumferential direction to the initial length is realized.
図13は、第3変形例に係る血圧計の処理手順を示すフローチャートである。なお、図13に示すフローチャートは、図7に示したフローチャートに対する変更点のみを抜き出して図示したものである。図13に示すように、本変形例に係る血圧計においては、ステップS115の空気袋35の開放後に、ステップS116Aにおいて電磁ブレーキ52の動作を停止させるとともにギヤードモータ51を逆方向に回転駆動して巻取りローラ58から第2の締付けベルト32を送出させることで、カフ20Aの締付け解除動作が開始される。その際、制御部11は、カフ20Aの周方向の長さが予め記憶されている初期長さに復帰したか否かを上腕周囲長計測部によって検出された位置情報に基づいて判断し(ステップS116B)、復帰したと判断されない場合(ステップS116BにおいてNOの場合)には、カフ20Aの締付け解除動作を継続し、復帰したと判断した場合(ステップS116BにおいてYESの場合)には、カフ20Aの締付け解除動作を停止する(ステップS116C)。
FIG. 13 is a flowchart showing the processing procedure of the sphygmomanometer according to the third modification. Note that the flowchart shown in FIG. 13 shows only the changes from the flowchart shown in FIG. As shown in FIG. 13, in the sphygmomanometer according to this modification, after opening the air bladder 35 in step S115, the operation of the electromagnetic brake 52 is stopped in step S116A and the geared motor 51 is rotated in the reverse direction. By releasing the second tightening belt 32 from the winding roller 58, the tightening releasing operation of the cuff 20A is started. At that time, the control unit 11 determines whether or not the circumferential length of the cuff 20A has returned to the pre-stored initial length based on the position information detected by the upper arm circumference measurement unit (Step S11). S116B) If it is not determined that it has returned (NO in step S116B), the cuff 20A continues to be tightened and if it is determined that it has returned (YES in step S116B), the cuff 20A The tightening release operation is stopped (step S116C).
以上において説明した第3変形例に係る構成を採用することにより、使用後においてカフ20Aの周方向の長さが常に同じ長さに復帰するように構成されるため、使用の度毎に上腕周囲長を確実に高精度に計測することが可能になる。
By adopting the configuration according to the third modification described above, the circumferential length of the cuff 20A is always restored to the same length after use, so that the circumference of the upper arm is changed every time it is used. The length can be reliably measured with high accuracy.
(実施の形態2)
図14は、本発明の実施の形態2における血圧計の機能ブロックの構成を示す図である。まず、図14を参照して、本実施の形態における血圧計1Bの機能ブロックの構成について説明する。なお、本実施の形態における血圧計1Bは、上述の実施の形態1における血圧計1Aと外観構造において同一であり、また機能ブロックの構成についてもその大部分が共通の構成である。したがって、上述の実施の形態1と同様の部分については、図中同一の符号を付し、その説明はここでは繰り返さない。 (Embodiment 2)
FIG. 14 is a diagram showing a functional block configuration of the sphygmomanometer according to the second embodiment of the present invention. First, with reference to FIG. 14, the structure of the functional block of thesphygmomanometer 1B in the present embodiment will be described. The blood pressure monitor 1B in the present embodiment is the same in appearance as the blood pressure monitor 1A in the above-described first embodiment, and most of the functional blocks have a common configuration. Therefore, portions similar to those in the first embodiment described above are denoted by the same reference numerals in the drawing, and the description thereof will not be repeated here.
図14は、本発明の実施の形態2における血圧計の機能ブロックの構成を示す図である。まず、図14を参照して、本実施の形態における血圧計1Bの機能ブロックの構成について説明する。なお、本実施の形態における血圧計1Bは、上述の実施の形態1における血圧計1Aと外観構造において同一であり、また機能ブロックの構成についてもその大部分が共通の構成である。したがって、上述の実施の形態1と同様の部分については、図中同一の符号を付し、その説明はここでは繰り返さない。 (Embodiment 2)
FIG. 14 is a diagram showing a functional block configuration of the sphygmomanometer according to the second embodiment of the present invention. First, with reference to FIG. 14, the structure of the functional block of the
上述の実施の形態1における血圧計1Aは、上腕202に対する締付けベルト31,32の締付け力を検出する締付け力検出機構として空気袋35およびエア系コンポーネント60を利用し、その締付け力を空気袋35の内圧として捉えるように構成されていた。これに対し、本実施の形態における血圧計1Bは、上腕202に対する締付けベルト31,32の締付け力を検出する締付け力検出機構として、第2の締付けベルト32が巻付けられる巻取りローラ58に加わる回転トルクを検出するトルクセンサを用いることにより、その締付け力を巻取りローラ58に加わる回転トルクとして捉えるように構成している。
The sphygmomanometer 1A according to the first embodiment uses the air bag 35 and the air system component 60 as a tightening force detection mechanism for detecting the tightening force of the tightening belts 31 and 32 with respect to the upper arm 202, and the tightening force is used as the air bag 35. It was configured to be understood as internal pressure. On the other hand, the sphygmomanometer 1B according to the present embodiment is added to the take-up roller 58 around which the second tightening belt 32 is wound as a tightening force detection mechanism for detecting the tightening force of the tightening belts 31 and 32 with respect to the upper arm 202. By using a torque sensor that detects rotational torque, the tightening force is regarded as rotational torque applied to the winding roller 58.
図14に示すように、本実施の形態における血圧計1Bにおいては、カフ20Bにトルクセンサ59が設けられている。トルクセンサ59は、巻取りローラ58に加わる回転トルクを検出するための手段であり、たとえば巻取りローラ58が固着されたシャフト57a(図5参照)に取付けられる。
As shown in FIG. 14, in the sphygmomanometer 1B according to the present embodiment, a torque sensor 59 is provided in the cuff 20B. The torque sensor 59 is a means for detecting rotational torque applied to the take-up roller 58, and is attached to, for example, a shaft 57a (see FIG. 5) to which the take-up roller 58 is fixed.
図15は、本実施の形態における血圧計の処理手順を示すフローチャートであり、図16は、本実施の形態における血圧計の各部の動作状況や動作状態を時系列的に示すタイミングチャートである。次に、これら図15および図16を参照して、本実施の形態における血圧計1Bの処理手順を、当該血圧計1Bの各部の動作状況や動作状態とあわせて説明する。なお、図15に示すフローチャートに従うプログラムは、図14において示したメモリ部12に予め記憶されており、制御部11がメモリ部12からこのプログラムを読み出して実行することにより、その処理が進められる。
FIG. 15 is a flowchart showing the processing procedure of the sphygmomanometer in the present embodiment, and FIG. 16 is a timing chart showing the operation status and the operating state of each part of the sphygmomanometer in the present embodiment in time series. Next, with reference to these FIG. 15 and FIG. 16, the processing procedure of the sphygmomanometer 1B in the present embodiment will be described together with the operating states and operating states of the respective parts of the sphygmomanometer 1B. Note that the program according to the flowchart shown in FIG. 15 is stored in advance in the memory unit 12 shown in FIG. 14, and the control unit 11 reads out the program from the memory unit 12 and executes the program.
まず、図15に示すように、被験者が血圧計1Bの操作部16を操作して電源オンの命令を入力すると、電源部18から制御部11に対して電源としての電力が供給され、これにより制御部11が駆動し、血圧計1Bの初期化が行なわれる(ステップS201)。図16に示すように、血圧計1Bの初期化が行なわれた時刻t0においては、ギヤードモータ51、電磁ブレーキ52、加圧ポンプ61および光電センサ71はいずれも動作が停止したオフ状態にあり、トルクセンサ59によって検出される回転トルクはほぼゼロであり、排気弁62は空気袋35の内部の空間を外部と連通させてカフ圧を大気圧と等しくすべく開放された状態にあり、圧力センサ63によって検出されるカフ圧は大気圧と同じ値を示すことになる。
First, as shown in FIG. 15, when the test subject operates the operation unit 16 of the sphygmomanometer 1 </ b> B and inputs a power-on command, power as a power source is supplied from the power supply unit 18 to the control unit 11. Control unit 11 is driven to initialize sphygmomanometer 1B (step S201). As shown in FIG. 16, at the time t0 when the sphygmomanometer 1B is initialized, the geared motor 51, the electromagnetic brake 52, the pressure pump 61, and the photoelectric sensor 71 are all in an off state in which the operation is stopped. The rotational torque detected by the torque sensor 59 is almost zero, and the exhaust valve 62 is open to communicate the space inside the air bladder 35 with the outside to make the cuff pressure equal to the atmospheric pressure. The cuff pressure detected by 63 shows the same value as the atmospheric pressure.
次に、図15に示すように、制御部11は、光電センサ71を駆動し、締付けベルト31,32の締付け長さの検出を開始する(ステップS202)。具体的には、図16に示すように、制御部11は、初期化終了後の時刻t1において光電センサ71を駆動し、第2の締付けベルト32に設けられたバーコード74の光電センサ71による読み取りを開始する。
Next, as shown in FIG. 15, the control unit 11 drives the photoelectric sensor 71 to start detecting the tightening length of the tightening belts 31 and 32 (step S202). Specifically, as shown in FIG. 16, the control unit 11 drives the photoelectric sensor 71 at time t <b> 1 after the end of initialization, and the photoelectric sensor 71 of the barcode 74 provided on the second fastening belt 32. Start reading.
次に、被験者は、上述した実施の形態1における場合と同様に、カフ20Bの把手42を右手100で把持し、カフ20Bのカフ本体部30の中空開口部に向けて、把手42を把持した右手100とは異なる方の手である左手200を挿入する(図9参照)。そして、カフ20Bを左手200の上腕にまで移動させ、左手200の上腕に宛がった状態を維持しつつ、把手42を把持した方の手である右手100の親指101で把手42に設けられた押し釦44を押下する。
Next, the subject grips the handle 42 of the cuff 20B with the right hand 100 and grips the handle 42 toward the hollow opening of the cuff main body 30 of the cuff 20B, as in the case of the first embodiment described above. The left hand 200, which is a different hand from the right hand 100, is inserted (see FIG. 9). Then, the cuff 20B is moved to the upper arm of the left hand 200, and the handle 42 is provided on the handle 42 with the thumb 101 of the right hand 100, which is the hand holding the handle 42, while maintaining the state of being in contact with the upper arm of the left hand 200. Press the push button 44.
図15に示すように、上記被験者による押し釦44の押下を受付けた制御部11は、上腕に対するカフ20Bの締付け動作を開始する(ステップS203)。その際、制御部11は、上腕に対するカフ20Bの締付けが所定の締付け状態となったか否かを判断し(ステップS204)、所定の締付け状態となっていない場合(ステップS204においてNOの場合)には、上腕に対するカフ20Bの締付け動作を継続し、所定の締付け状態となった場合(ステップS204においてYESの場合)には、上腕に対するカフ20Bの締付け動作を停止する(ステップS205)。
As shown in FIG. 15, the control unit 11 that has received the pressing of the push button 44 by the subject starts the tightening operation of the cuff 20B with respect to the upper arm (step S203). At that time, the control unit 11 determines whether or not the cuff 20B has been tightened with respect to the upper arm in a predetermined tightening state (step S204), and when it is not in the predetermined tightening state (NO in step S204). Continues the tightening operation of the cuff 20B with respect to the upper arm and stops the tightening operation of the cuff 20B with respect to the upper arm when the predetermined tightening state is reached (YES in step S204) (step S205).
具体的には、図16に示すように、制御部11は、時刻t2においてギヤードモータ51を順方向に回転駆動することにより、巻取りローラ58による第2の締付けベルト32の巻取り動作を開始させる。そして、制御部11は、当該巻取り動作中において巻取りローラ58に加わる回転トルクをトルクセンサ59によって検出し、検出された回転トルクが予め定められた閾値に達した時刻t3においてギヤードモータ51の順方向への回転駆動を停止し、これと同時に電磁ブレーキ52を駆動して巻取りローラ58の回転を停止する。ここで、上記閾値は、血圧値測定に適した上腕に対するカフ20Bの締付け力に基づいて予め決定される。
Specifically, as shown in FIG. 16, the control unit 11 starts the winding operation of the second tightening belt 32 by the winding roller 58 by rotationally driving the geared motor 51 in the forward direction at time t2. Let Then, the control unit 11 detects the rotational torque applied to the winding roller 58 during the winding operation by the torque sensor 59, and at time t3 when the detected rotational torque reaches a predetermined threshold value, the geared motor 51 The forward rotation is stopped, and at the same time, the electromagnetic brake 52 is driven to stop the winding roller 58 from rotating. Here, the threshold value is determined in advance based on the tightening force of the cuff 20B on the upper arm suitable for blood pressure value measurement.
ここで、上述した実施の形態1における場合と同様に、カフ20Bが上腕202に最適締付け力にて締付けられた状態においては、締付けベルト31,32によって空気袋35が上腕202に対して確実に押圧された状態となる(図10参照)。そのため、以降の測定動作において空気袋35が膨張することにより、上腕202がカフ20Bによって確実に圧迫されることになり、上腕202の内部に位置する動脈に対する阻血が確実に行なえるようになる。なお、当該状態における締付けベルト31,32の締付け長さが上腕周囲長計測回路72によって上腕の周囲長として決定され、当該決定された上腕周囲長が制御部11に入力されることになる。制御部11は、入力された上腕周囲長をメモリ部12に対して出力し、メモリ部12は、入力された上腕周囲長を一時的に記憶する。
Here, as in the case of the first embodiment described above, when the cuff 20B is fastened to the upper arm 202 with the optimum tightening force, the air bag 35 is securely attached to the upper arm 202 by the fastening belts 31 and 32. It will be in the state pressed (refer FIG. 10). Therefore, in the subsequent measurement operation, the air bag 35 is inflated, so that the upper arm 202 is surely compressed by the cuff 20B, and the artery located inside the upper arm 202 can be surely blocked. Note that the tightening length of the tightening belts 31 and 32 in this state is determined as the perimeter of the upper arm by the upper arm perimeter measuring circuit 72, and the determined upper arm perimeter is input to the control unit 11. The control unit 11 outputs the input upper arm circumference to the memory unit 12, and the memory unit 12 temporarily stores the input upper arm circumference.
次に、図15に示すように、制御部11は、光電センサ71の駆動を停止し、締付け長さの検出を終了する(ステップS206)。具体的には、図16に示すように、制御部11は、時刻t4において光電センサ71の駆動を停止し、第2の締付けベルト32に設けられたバーコード74の光電センサ71による読み取りを終了する。
Next, as shown in FIG. 15, the control unit 11 stops driving the photoelectric sensor 71 and ends the detection of the tightening length (step S206). Specifically, as shown in FIG. 16, the control unit 11 stops driving the photoelectric sensor 71 at time t <b> 4 and ends reading of the barcode 74 provided on the second fastening belt 32 by the photoelectric sensor 71. To do.
次に、図15に示すように、制御部11は、計測された上腕周囲長が予め定められた当該カフ20Bの適用可能範囲内の大きさであるか否かの判断を行なう(ステップS207)。すなわち、制御部11は、当該カフ20Bを用いて血圧値の測定を行なった場合の測定結果がその精度を保障できる範囲内の上腕の大きさであるか否かの判断を行なう。制御部11は、計測された上腕周囲長が予め定められた当該カフ20Bの適用可能範囲内の大きさであると判断した場合(ステップS207においてYESの場合)に、ステップS208へと移行し、計測された上腕周囲長が予め定められた当該カフ20Bの適用可能範囲内の大きさでないと判断した場合(ステップS207においてNOの場合)に、ステップS213へと移行する。
Next, as shown in FIG. 15, the control unit 11 determines whether or not the measured upper arm circumference is within a predetermined applicable range of the cuff 20 </ b> B (step S <b> 207). . That is, the control unit 11 determines whether or not the measurement result when the blood pressure value is measured using the cuff 20B is the size of the upper arm within a range in which the accuracy can be ensured. When the control unit 11 determines that the measured upper arm circumference is within a predetermined applicable range of the cuff 20B (YES in step S207), the control unit 11 proceeds to step S208. When it is determined that the measured upper arm perimeter is not within a predetermined range of the applicable range of the cuff 20B (NO in step S207), the process proceeds to step S213.
次に、図15に示すように、制御部11は、血圧値測定のために空気袋35の加圧を開始する(ステップS208)。具体的には、図16に示すように、制御部11は、時刻t5において空気袋35の内部の空間を外部と非連通とするために排気弁62を閉鎖させ、つづいて時刻t6において空気袋35内に空気を注入するために加圧ポンプ61の駆動を開始してカフ圧を上昇させ、所定のカフ圧となるように空気袋35の加圧を行なう。
Next, as shown in FIG. 15, the control unit 11 starts pressurization of the air bladder 35 for blood pressure measurement (step S208). Specifically, as shown in FIG. 16, the control unit 11 closes the exhaust valve 62 in order to make the space inside the air bag 35 out of communication with the outside at time t5, and then at time t6, the air bag. In order to inject air into the air 35, driving of the pressurizing pump 61 is started to increase the cuff pressure, and the air bag 35 is pressurized so as to become a predetermined cuff pressure.
次に、図15に示すように、制御部11は、血圧値測定のために空気袋35の微速減圧を開始する(ステップS209)。具体的には、図16に示すように、制御部11は、圧力センサ63によって空気袋35の内圧が所定の内圧に達したことが検出された時刻t7において加圧ポンプ61の駆動を停止し、その後排気弁62の開放量を制御しつつ徐々に排気弁62を開放させる。また、その際、制御部11は、圧力センサ63によって検出されるカフ圧の変動を取得する。
Next, as shown in FIG. 15, the control unit 11 starts the slow depressurization of the air bladder 35 for blood pressure measurement (step S209). Specifically, as shown in FIG. 16, the control unit 11 stops driving the pressure pump 61 at time t7 when the pressure sensor 63 detects that the internal pressure of the air bladder 35 has reached a predetermined internal pressure. Thereafter, the exhaust valve 62 is gradually opened while controlling the opening amount of the exhaust valve 62. At that time, the control unit 11 acquires the fluctuation of the cuff pressure detected by the pressure sensor 63.
次に、図15に示すように、制御部11は、微速減圧過程において得られたカフ圧の変動に基づいて血圧値を算出する(ステップS210)。つづいて、制御部11は、ステップS210において得られた血圧値をメモリ部12および表示部14に出力し、メモリ部12において当該血圧値が測定結果として記憶され(ステップS211)、表示部14において上記測定結果としての血圧値が表示される(ステップS212)。ここで、表示部14は、収縮期血圧値および拡張期血圧値をたとえば数値として表示する。
Next, as shown in FIG. 15, the control unit 11 calculates a blood pressure value based on the variation of the cuff pressure obtained in the slow depressurization process (step S210). Subsequently, the control unit 11 outputs the blood pressure value obtained in step S210 to the memory unit 12 and the display unit 14, and the blood pressure value is stored as a measurement result in the memory unit 12 (step S211). The blood pressure value as the measurement result is displayed (step S212). Here, the display unit 14 displays the systolic blood pressure value and the diastolic blood pressure value as numerical values, for example.
ステップS207においてNOと判断された場合、あるいはステップS212が終了した場合には、図15に示すように、制御部11は、空気袋35を開放する(ステップS213)とともに、上腕202に対するカフ20Bの締付け解除動作を行う(ステップS214)。具体的には、図16に示すように、制御部11は、血圧値の算出が終了した時刻t8において排気弁62を完全に開放し、空気袋35内の空気を外部へと排気させ、その後時刻t9において電磁ブレーキ52の動作を停止させるとともに、時刻t10においてギヤードモータ51を逆方向に回転駆動し、巻取りローラ58から第2の締付けベルト32を送出させる。その後、制御部11は、第2の締付けベルト32が完全に巻取りローラ58から送出された時刻t11においてギヤードモータ51の駆動を停止する。この後、血圧計1Bは待機状態をとり、被験者の操作部16による電源オフの命令の入力を待って電源としての電力の供給を停止する。
If NO is determined in step S207, or if step S212 is completed, as shown in FIG. 15, the control unit 11 opens the air bag 35 (step S213) and the cuff 20B with respect to the upper arm 202. A tightening release operation is performed (step S214). Specifically, as shown in FIG. 16, the control unit 11 completely opens the exhaust valve 62 at time t8 when the calculation of the blood pressure value is finished, exhausts the air in the air bag 35 to the outside, and then At time t9, the operation of the electromagnetic brake 52 is stopped, and at time t10, the geared motor 51 is rotationally driven in the reverse direction, and the second tightening belt 32 is sent from the winding roller 58. Thereafter, the control unit 11 stops driving the geared motor 51 at time t11 when the second tightening belt 32 is completely delivered from the take-up roller 58. Thereafter, the sphygmomanometer 1B is in a standby state, and waits for an input of a power-off command from the operation unit 16 of the subject, and stops supplying power as a power source.
以上において説明した如くの血圧計1Bとした場合にも、上述の実施の形態1における血圧計1Aとした場合と同様の効果を得ることができる。
Even when the sphygmomanometer 1B as described above is used, the same effect as that obtained when the sphygmomanometer 1A in the first embodiment described above can be obtained.
なお、上述した本発明の実施の形態1および2における血圧計1A,1Bにおいては、第2の締付けベルト32の巻取り動作を開始させるための巻付け動作操作部を押し釦44によって構成した場合を例示して説明を行なったが、必ずしも当該巻付け動作操作部を押し釦にて構成する必要はなく、スライド式の釦やダイヤル式の釦、タッチセンサ、音声認識センサ等にて構成してもよい。また、巻付け動作操作部が設けられる位置も把手部40の親指で操作できる位置に限られるものではなく、把手部40の他の位置や本体10に設けることとしてよい。
In the above-described sphygmomanometers 1A and 1B according to the first and second embodiments of the present invention, the winding operation operation unit for starting the winding operation of the second tightening belt 32 is configured by the push button 44. However, it is not always necessary to configure the winding operation operation unit with a push button, and it is configured with a slide type button, a dial type button, a touch sensor, a voice recognition sensor, or the like. Also good. Further, the position at which the winding operation operation unit is provided is not limited to the position at which the handle unit 40 can be operated with the thumb, but may be provided at another position of the handle unit 40 or the main body 10.
また、上述した本発明の実施の形態1および2における血圧計1A,1Bにおいては、カフの上腕に対する締付け動作と、当該締付け動作後に行なわれる血圧値の測定動作と、当該測定動作後に行なわれるカフの上腕に対する締付け解除動作とが自動的に連続して行なわれるように構成した場合を例示して説明を行なったが、これら一連の動作がすべて連続して自動で行なわれるように構成する必要は必ずしもなく、各動作がそれぞれ操作部の操作に基づいて順次行なわれるように構成してもよい。
In sphygmomanometers 1A and 1B according to Embodiments 1 and 2 of the present invention described above, the cuff upper arm tightening operation, the blood pressure value measuring operation performed after the tightening operation, and the cuff performed after the measuring operation are performed. Although the description has been given by exemplifying the case where the tightening release operation with respect to the upper arm is automatically performed continuously, it is necessary to configure so that all of these series of operations are automatically performed continuously. It is not always necessary, and each operation may be sequentially performed based on the operation of the operation unit.
また、上述した本発明の実施の形態1および2においては、非装着部位を左手の上腕とし、把手部を把持する手を右手とした場合を例示して説明を行なったが、当然に非装着部位を右手の上腕とし、把手部を把持する手を左手とすることも可能である。また、上述の実施の形態1および2においては、血圧計のカフとして、血圧値の測定に際して上腕に装着されるいわゆる上腕式の血圧計用カフを例示して説明を行なったが、特にこれに限定されるものではなく、血圧値の測定に際して手首に装着されるいわゆる手首式の血圧計用カフや、血圧値の測定際して足首に装着されるいわゆる足首式の血圧計用カフ等に本発明を適用することも当然に可能である。
In the first and second embodiments of the present invention described above, the case where the non-wearing part is the upper arm of the left hand and the hand holding the handle is the right hand has been described as an example. It is also possible to use the part as the upper arm of the right hand and the left hand as the hand holding the handle. In the first and second embodiments described above, a so-called upper arm type sphygmomanometer cuff that is attached to the upper arm when measuring blood pressure values has been described as an example of the sphygmomanometer cuff. The present invention is not limited to this, such as a so-called wrist-type sphygmomanometer cuff that is worn on the wrist when measuring blood pressure values, or a so-called ankle-type sphygmomanometer cuff that is worn on the ankle when measuring blood pressure values. Of course, the invention can also be applied.
さらには、上述した本発明の実施の形態1および2においては、本体とカフとが分離されて構成された血圧計に本発明を適用した場合を例示して説明を行なったが、本体とカフとが一体化された血圧計に本発明を適用することも当然に可能である。
Further, in the first and second embodiments of the present invention described above, the case where the present invention is applied to a sphygmomanometer in which the main body and the cuff are separated has been described as an example. Naturally, it is also possible to apply the present invention to a sphygmomanometer integrated with and.
また、上述した本発明の実施の形態1および2においては、収縮期血圧値および拡張期血圧値が測定可能な血圧計に本発明を適用した場合を例示して説明を行なったが、収縮期血圧値および拡張期血圧値以外の他の血圧情報が測定可能な血圧情報測定装置に本発明を適用することも可能である。
In the first and second embodiments of the present invention described above, the case where the present invention is applied to a sphygmomanometer capable of measuring a systolic blood pressure value and a diastolic blood pressure value has been described as an example. The present invention can also be applied to a blood pressure information measuring device capable of measuring blood pressure information other than blood pressure values and diastolic blood pressure values.
このように、今回開示した上記各実施の形態およびその変形例はすべての点で例示であって、制限的なものではない。本発明の技術的範囲は請求の範囲によって画定され、また請求の範囲の記載と均等の意味および範囲内でのすべての変更を含むものである。
As described above, the above-described embodiments and modifications thereof disclosed herein are illustrative in all respects and are not restrictive. The technical scope of the present invention is defined by the scope of the claims, and is intended to include any modifications within the scope and meaning equivalent to the terms of the claims.
1A,1B 血圧計、10 本体、11 制御部、12 メモリ部、14 表示部、16 操作部、18 電源部、20A,20B カフ、30 カフ本体部、31 第1の締付けベルト、31a 一端部、31b 他端部、32 第2の締付けベルト、32a 一端部、32b 他端部、33 外装カバー、34 カーラ、34a 切れ目、35 空気袋、40 把手部、41 基部、42 把手、44 押し釦、46 支持枠、50 締付け長さ調節機構、51 ギヤードモータ、51a モータ部、51a1 回転シャフト、51b 減速部、51c 出力シャフト、52 電磁ブレーキ、53 モータ駆動回路、54 電磁ブレーキ駆動回路、55,56,57 ギヤ、56a,57a シャフト、58 巻取りローラ、59 トルクセンサ、60 エア系コンポーネント、61 加圧ポンプ、62 排気弁、63 圧力センサ、64 加圧ポンプ駆動回路、65 排気弁駆動回路、66 増幅器、67 A/D変換回路、71,71A,71B 光電センサ、72 上腕周囲長計測回路、73 エンコーダストリップ、74 バーコード、90 エア管、92 接続ケーブル、100 右手、101 親指、200 左手、202 上腕。
1A, 1B Blood pressure monitor, 10 main body, 11 control unit, 12 memory unit, 14 display unit, 16 operation unit, 18 power supply unit, 20A, 20B cuff, 30 cuff main unit, 31 first tightening belt, 31a one end, 31b other end, 32 second clamping belt, 32a one end, 32b other end, 33 exterior cover, 34 curler, 34a cut, 35 air bag, 40 handle part, 41 base part, 42 handle, 44 push button, 46 Support frame, 50 tightening length adjustment mechanism, 51 geared motor, 51a motor part, 51a1 rotating shaft, 51b deceleration part, 51c output shaft, 52 electromagnetic brake, 53 motor drive circuit, 54 electromagnetic brake drive circuit, 55, 56, 57 Gear, 56a, 57a shaft, 58 take-up roller, 59 ton Sensor, 60 air system components, 61 pressure pump, 62 exhaust valve, 63 pressure sensor, 64 pressure pump drive circuit, 65 exhaust valve drive circuit, 66 amplifier, 67 A / D conversion circuit, 71, 71A, 71B photoelectric sensor 72, upper arm circumference measurement circuit, 73 encoder strip, 74 bar code, 90 air tube, 92 connection cable, 100 right hand, 101 thumb, 200 left hand, 202 upper arm.
Claims (12)
- 被測定部位を圧迫するための流体袋(35)および前記流体袋(35)の外側に巻き回された締付けベルト(31,32)を含み、周方向に切れ目を有さず、軸方向から被測定部位が挿入可能に構成された環状のカフと、
前記流体袋(35)を膨張および収縮させる膨縮機構(61,62)と、
前記流体袋(35)を利用して血圧情報を測定する血圧情報測定部と、
前記締付けベルト(31,32)の被測定部位に対する締付け長さを可変に調節する締付け長さ調節機構(50)と、
被測定部位の周囲長を計測する周囲長計測部とを備えた、血圧情報測定装置。 It includes a fluid bag (35) for compressing the measurement site and a tightening belt (31, 32) wound around the fluid bag (35), has no cut in the circumferential direction, and is covered from the axial direction. An annular cuff configured to allow insertion of a measurement site;
An expansion / contraction mechanism (61, 62) for expanding and contracting the fluid bag (35);
A blood pressure information measuring unit for measuring blood pressure information using the fluid bag (35);
A tightening length adjusting mechanism (50) that variably adjusts the tightening length of the tightening belt (31, 32) with respect to the measurement site;
A blood pressure information measurement device comprising a circumference measurement unit that measures the circumference of a measurement site. - 前記周囲長計測部は、前記締付け長さ調節機構(50)を用いて前記締付けベルト(31,32)を被測定部位に締付け固定する際の前記締付けベルト(31,32)の移動量を計測することにより、被測定部位の周囲長を計測する、請求の範囲第1項に記載の血圧情報測定装置。 The perimeter measuring unit measures the amount of movement of the tightening belt (31, 32) when the tightening belt (31, 32) is fastened and fixed to the measurement site using the tightening length adjusting mechanism (50). The blood pressure information measuring device according to claim 1, wherein the peripheral length of the part to be measured is measured.
- 前記周囲長計測部は、前記締付けベルト(31,32)に設けられたマーカーと、前記マーカーを読み取る読み取り部とを含み、前記読み取り部によって読み取られた情報に基づいて前記締付けベルト(31,32)の前記移動量を計測する、請求の範囲第2項に記載の血圧情報測定装置。 The perimeter measuring unit includes a marker provided on the tightening belt (31, 32) and a reading unit for reading the marker, and the tightening belt (31, 32) based on information read by the reading unit. The blood pressure information measurement device according to claim 2, wherein the movement amount is measured.
- 前記マーカーは、バーコード(74)であり、
前記読み取り部は、前記バーコード(74)を読み取るためのフォトインタラプタ(71)である、請求の範囲第3項に記載の血圧情報測定装置。 The marker is a barcode (74);
The blood pressure information measuring device according to claim 3, wherein the reading unit is a photo interrupter (71) for reading the barcode (74). - 前記周囲長計測部は、前記締付けベルト(31,32)の移動に伴って回転する回転部材と、前記回転部材の回転量を検出する回転量検出部とを含み、前記回転量検出部によって検出された情報に基づいて前記締付けベルト(31,32)の前記移動量を計測する、請求の範囲第2項に記載の血圧情報測定装置。 The perimeter measuring unit includes a rotating member that rotates as the fastening belts (31, 32) move, and a rotation amount detecting unit that detects a rotation amount of the rotating member, and is detected by the rotation amount detecting unit. The blood pressure information measuring device according to claim 2, wherein the movement amount of the tightening belt (31, 32) is measured based on the obtained information.
- 前記周囲長計測部によって検出された被測定部位の周囲長情報に基づき、前記血圧情報測定部によって測定された血圧情報を補正する血圧情報補正部をさらに備えた、請求の範囲第1項に記載の血圧情報測定装置。 2. The blood pressure information correction unit according to claim 1, further comprising a blood pressure information correction unit that corrects blood pressure information measured by the blood pressure information measurement unit based on the circumference length information of the measurement site detected by the circumference measurement unit. Blood pressure information measuring device.
- 前記周囲長計測部によって検出された被測定部位の周囲長情報に基づき、前記膨縮機構(61,62)による流体袋(35)の膨張動作および収縮動作の少なくともいずれか一方を制御する膨縮動作制御部をさらに備えた、請求の範囲第1項に記載の血圧情報測定装置。 Inflation / deflation for controlling at least one of the inflating and deflating operations of the fluid bag (35) by the inflating / deflating mechanism (61, 62) based on the perimeter information of the measurement site detected by the perimeter measuring unit The blood pressure information measurement device according to claim 1, further comprising an operation control unit.
- 前記周囲長計測部によって検出された被測定部位の周囲長情報に基づき、予め定められた測定可能範囲内に被測定部位の周囲長があるか否かを判断する判断部をさらに備えた、請求の範囲第1項に記載の血圧情報測定装置。 The apparatus further comprises a determination unit that determines whether or not the circumference of the measurement site is within a predetermined measurable range based on the circumference information of the measurement site detected by the circumference measurement unit. The blood pressure information measuring device according to claim 1,
- 前記締付け長さ調節機構(50)は、前記締付けベルト(31,32)を巻取りおよび送出し可能な巻取りローラ(58)と、前記巻取りローラ(58)を順方向および逆方向に回転駆動する電動機(51)と、前記電動機(51)の停止時に前記巻取りローラ(58)に対して制動力を及ぼす制動機(52)とを含む、請求の範囲第1項に記載の血圧情報測定装置。 The tightening length adjusting mechanism (50) rotates the wind-up roller (58) capable of winding and feeding the tightening belt (31, 32) and the wind-up roller (58) in the forward direction and the reverse direction. The blood pressure information according to claim 1, comprising: an electric motor (51) to be driven; and a brake (52) that applies a braking force to the winding roller (58) when the electric motor (51) is stopped. measuring device.
- 前記カフは、前記流体袋(35)および前記締付けベルト(31,32)を含む筒状のカフ本体部(30)と、前記カフ本体部(30)の外周面上に設けられた把手部(40)とを含む、請求の範囲第1項に記載の血圧情報測定装置。 The cuff includes a cylindrical cuff main body portion (30) including the fluid bag (35) and the fastening belts (31, 32), and a handle portion provided on an outer peripheral surface of the cuff main body portion (30) ( 40). The blood pressure information measuring device according to claim 1, further comprising:
- 前記巻取りローラ(58)による前記締付けベルト(31,32)の巻取り動作の開始の命令を受付けるための巻取り動作操作部(44)が、前記把手部(40)に設けられている、請求の範囲第10項に記載の血圧情報測定装置。 A winding operation unit (44) for receiving a command to start the winding operation of the tightening belt (31, 32) by the winding roller (58) is provided in the handle unit (40). The blood pressure information measuring device according to claim 10.
- 前記カフは、前記流体袋(35)の外側でかつ前記締付けベルト(31,32)の内側に径方向に弾性変形可能に構成された可撓性部材(34)をさらに有している、請求の範囲第1項に記載の血圧情報測定装置。 The cuff further includes a flexible member (34) configured to be elastically deformable in a radial direction outside the fluid bag (35) and inside the tightening belt (31, 32). The blood pressure information measuring device according to claim 1,
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008-195021 | 2008-07-29 | ||
JP2008195021A JP2010029458A (en) | 2008-07-29 | 2008-07-29 | Blood pressure information measuring device |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2010013554A1 true WO2010013554A1 (en) | 2010-02-04 |
Family
ID=41610259
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2009/061206 WO2010013554A1 (en) | 2008-07-29 | 2009-06-19 | Device for measuring blood pressure information |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP2010029458A (en) |
WO (1) | WO2010013554A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012043485A1 (en) * | 2010-09-27 | 2012-04-05 | 日本精密測器株式会社 | Electronic blood pressure meter, method for estimating circumference length of measurement portion, and method for measuring blood pressure |
WO2015141786A1 (en) * | 2014-03-20 | 2015-09-24 | テルモ株式会社 | Hemostatic instrument |
CN112971747A (en) * | 2019-12-13 | 2021-06-18 | 华为技术有限公司 | Wrist-worn electronic device, method for measuring wrist size, and method for measuring blood pressure |
CN118303860A (en) * | 2024-04-08 | 2024-07-09 | 深圳市景新浩科技有限公司 | Blood pressure measuring instrument with contraction function and measuring method thereof |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5659347B2 (en) * | 2010-11-22 | 2015-01-28 | 株式会社パラマ・テック | Sphygmomanometer |
JP6019592B2 (en) * | 2012-01-23 | 2016-11-02 | オムロンヘルスケア株式会社 | Blood pressure measurement device |
KR101784484B1 (en) * | 2016-05-24 | 2017-10-11 | 이동화 | Wristband type blood pressure measuring apparatus |
KR101791495B1 (en) * | 2016-05-27 | 2017-10-30 | 주식회사 라이프시맨틱스 | Device for measuring edema |
KR102605835B1 (en) | 2018-11-14 | 2023-11-27 | 삼성전자주식회사 | Method, electronic device, and storage medium for detecting biometric information |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6116730A (en) * | 1984-07-03 | 1986-01-24 | コーリン電子株式会社 | Blood pressure measuring apparatus equipped with automatic correction function |
JPS6148339A (en) * | 1984-08-14 | 1986-03-10 | オムロン株式会社 | Electronic hemomanometer |
JPS63186625A (en) * | 1987-01-28 | 1988-08-02 | オムロン株式会社 | Electronic hemomanometer |
JPH06245911A (en) * | 1993-02-23 | 1994-09-06 | Matsushita Electric Works Ltd | Sphygmomanometer |
JP2001017409A (en) * | 1999-07-09 | 2001-01-23 | Aloka Co Ltd | Respiration sensor |
-
2008
- 2008-07-29 JP JP2008195021A patent/JP2010029458A/en not_active Withdrawn
-
2009
- 2009-06-19 WO PCT/JP2009/061206 patent/WO2010013554A1/en active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6116730A (en) * | 1984-07-03 | 1986-01-24 | コーリン電子株式会社 | Blood pressure measuring apparatus equipped with automatic correction function |
JPS6148339A (en) * | 1984-08-14 | 1986-03-10 | オムロン株式会社 | Electronic hemomanometer |
JPS63186625A (en) * | 1987-01-28 | 1988-08-02 | オムロン株式会社 | Electronic hemomanometer |
JPH06245911A (en) * | 1993-02-23 | 1994-09-06 | Matsushita Electric Works Ltd | Sphygmomanometer |
JP2001017409A (en) * | 1999-07-09 | 2001-01-23 | Aloka Co Ltd | Respiration sensor |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012043485A1 (en) * | 2010-09-27 | 2012-04-05 | 日本精密測器株式会社 | Electronic blood pressure meter, method for estimating circumference length of measurement portion, and method for measuring blood pressure |
WO2015141786A1 (en) * | 2014-03-20 | 2015-09-24 | テルモ株式会社 | Hemostatic instrument |
CN112971747A (en) * | 2019-12-13 | 2021-06-18 | 华为技术有限公司 | Wrist-worn electronic device, method for measuring wrist size, and method for measuring blood pressure |
CN118303860A (en) * | 2024-04-08 | 2024-07-09 | 深圳市景新浩科技有限公司 | Blood pressure measuring instrument with contraction function and measuring method thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2010029458A (en) | 2010-02-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2010013554A1 (en) | Device for measuring blood pressure information | |
JP5076996B2 (en) | Blood pressure information measuring device | |
JP5169552B2 (en) | Cuff for blood pressure information measuring device and blood pressure information measuring device provided with the same | |
US7862514B2 (en) | Blood pressure measurement | |
KR102017067B1 (en) | Wrist wearable blood pressure monitor | |
US20090118628A1 (en) | System for measuring blood pressure featuring a blood pressure cuff comprising size information | |
JP2009284967A (en) | Cuff for blood pressure data measuring instrument and blood pressure data measuring instrument equipped with it | |
EP1075846A2 (en) | Cuff for blood pressure manometer | |
JP2007244837A (en) | Blood pressure measuring device | |
WO2007072647A1 (en) | Electronic blood pressure meter having blood pressure calculation system | |
JP5151801B2 (en) | Cuff for blood pressure information measuring device and blood pressure information measuring device provided with the same | |
JP4240034B2 (en) | Blood pressure measurement device | |
JP5251447B2 (en) | Cuff for blood pressure information measuring device and blood pressure information measuring device provided with the same | |
KR100661385B1 (en) | Electronic blood pressure measurement device and blood pressure measuring method | |
TW200803788A (en) | Device for measuring blood pressure | |
JP2012210374A (en) | Cuff for blood pressure information measurement device and the blood pressure information measurement device including the same | |
JP2012024197A (en) | Electronic sphygmomanometer | |
KR20150092465A (en) | Wrist wearable blood pressure monitor | |
KR100961158B1 (en) | Blood pressure measuring apparatus and method thereof | |
US7427267B2 (en) | Blood pressure determining method | |
CN115334960A (en) | Blood pressure measurement system and blood pressure measurement method using same | |
JP2010131247A (en) | Blood pressure measuring apparatus | |
CN113543701A (en) | Blood pressure measurement system and blood pressure measurement method using same | |
JP5366704B2 (en) | Biological information measuring device | |
KR20190063143A (en) | Wearable wrist-type sphygmomanometer with dual sensor |
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: 09802799 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 09802799 Country of ref document: EP Kind code of ref document: A1 |