WO2023190627A1 - Lesion healing determination device, lesion healing determination method, lesion healing determination program, and computer-readable non-transitory storage medium - Google Patents

Lesion healing determination device, lesion healing determination method, lesion healing determination program, and computer-readable non-transitory storage medium Download PDF

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Publication number
WO2023190627A1
WO2023190627A1 PCT/JP2023/012712 JP2023012712W WO2023190627A1 WO 2023190627 A1 WO2023190627 A1 WO 2023190627A1 JP 2023012712 W JP2023012712 W JP 2023012712W WO 2023190627 A1 WO2023190627 A1 WO 2023190627A1
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Prior art keywords
affected area
recovery
subject
state
condition
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PCT/JP2023/012712
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French (fr)
Japanese (ja)
Inventor
美幸 児玉
千里 谷田
敏樹 永濱
良雄 酒井
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株式会社タニタ
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Publication of WO2023190627A1 publication Critical patent/WO2023190627A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/05Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fields; Measuring using microwaves or radio waves 
    • A61B5/053Measuring electrical impedance or conductance of a portion of the body
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/05Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fields; Measuring using microwaves or radio waves 
    • A61B5/053Measuring electrical impedance or conductance of a portion of the body
    • A61B5/0537Measuring body composition by impedance, e.g. tissue hydration or fat content

Definitions

  • the present disclosure relates to an affected area recovery determination device, an affected area recovery determination method, and an affected area recovery determination program.
  • the patient becomes unable to move freely due to inflammation in the affected area, or the patient's muscle mass decreases due to being bedridden for a long time. Furthermore, the patient may move as if to protect the affected area, resulting in fatigue in the area on the opposite side of the affected area. Therefore, a certain period of rehabilitation is required to return the patient's life to the same level as before the surgery. Therefore, in order to quickly return to the previous standard of living, a rehabilitation plan is drawn up based on the recovery status of the affected area and the overall muscle mass.
  • Non-Patent Document 1 (Hidetaka Wakabayashi, "Rehabilitation Nutrition Pocket Guide”, 1st edition, JEF Corporation, September 2014, p.9-10) states that blood tests are performed on patients. It is described that the value of CRP (C-reactive protein) is determined by this method, and that CRP is used as an indicator of acute inflammation such as surgery, trauma, bone fracture, and infection.
  • CRP C-reactive protein
  • the period can be divided into a catabolic period and an anabolic period. Specifically, when CRP is below a predetermined threshold, the affected area is determined to be in the anabolic phase, and when it exceeds the threshold, the affected area is determined to be in the catabolic phase.
  • the catabolic phase the affected body attempts to break down muscle or fat to obtain the energy it needs. For this reason, even if energy is administered to the patient during the catabolic phase, muscle decomposition cannot be suppressed, so the patient's muscle mass decreases and the patient becomes malnourished.
  • the assimilation period is a period of assimilation and wound repair during the recovery process when biological invasion occurs due to surgery or trauma.
  • CRP can determine the condition of the affected area, it cannot predict the recovery time of the affected area. Furthermore, since the determination based on CRP also reflects abnormalities in the entire body of the person to be measured, accuracy cannot be obtained from the viewpoint of determining the condition of the affected area.
  • an object of the present disclosure is to provide an affected area recovery determination device, an affected area recovery determination method, and an affected area recovery determination program that can predict the recovery time of the affected area.
  • An affected area recovery determination device includes an acquisition unit that acquires an affected area index that reflects the condition of the affected area of a subject, and a condition of the affected area based on the affected area index acquired by the acquisition unit. and a prediction means for predicting the recovery time of the affected area based on the condition of the affected area determined by the affected area status determining means and the whole body index of the subject.
  • the affected area recovery determination device of the second aspect may be the affected area recovery determination device of the first aspect, in which the affected area index may be the impedance of the part of the subject including the affected area.
  • the state of the affected area is determined based on the impedance obtained from the potential difference by passing a current through a local part of the subject, so that the position of the affected area and the state of the affected area can be determined.
  • the affected area recovery determining device of the third aspect may be the affected area recovery determining device of the first aspect or the second aspect, in which the whole body index may be the whole body muscle mass of the subject. According to this configuration, it is possible to accurately predict the recovery time of the affected area.
  • the prediction means may predict the recovery time so that the recovery speed becomes faster as the whole body muscle mass of the subject increases. . According to this configuration, it is possible to accurately predict the recovery time of the affected area.
  • the affected area recovery determining device is the affected area recovery determining device according to any one of the first to fourth aspects, and determines the predicted recovery state of the affected area and the affected area state based on the recovery time predicted by the prediction means in the past.
  • a recovery state determining means may be provided for determining the recovery state of the affected area based on a difference from the current state of the affected area determined by the means. According to this configuration, it can be determined whether the affected area is properly recovering.
  • the affected area recovery determining device of the sixth aspect is the affected area recovery determining device of the fifth aspect, wherein the recovery state determining means may determine the recovery state of the affected area and the recovery state of the whole body index.
  • the whole body index is, for example, whole body muscle mass or body weight. Depending on the condition of the affected area of the person being measured, the person being measured may need to rest. As a result, whole body indicators such as whole body muscle mass and body weight may decrease, so it is necessary to restore these whole body indicators as well. Therefore, according to this configuration, since the recovery state of the affected area and the recovery state of the whole body index are acquired at the same time, it is possible to determine whether or not the subject is appropriately recovering.
  • the affected area recovery determining device is the affected area recovery determining device according to the fifth or sixth aspect, and may further include an advice generation unit that generates advice regarding recovery of the affected area based on the determination result of the recovery state determining means. good. According to this configuration, it is possible to create a more appropriate rehabilitation plan.
  • the method for determining recovery of an affected area includes a first step of acquiring an affected area index that reflects the condition of the affected area of the subject, and determining the condition of the affected area based on the affected area index acquired in the first step.
  • the method includes a second step of determining, and a third step of predicting the recovery time of the affected area based on the condition of the affected area determined in the second step and the whole body index of the subject.
  • the affected area recovery determination program of the ninth aspect is configured to cause a computer of an information processing device that acquires an affected area index that reflects the condition of the affected area of the subject by an acquisition means to an affected area condition determining means for determining the condition of the affected area; and a prediction means for predicting the recovery time of the affected area based on the condition of the affected area determined by the affected area condition determining means and the whole body index of the subject. Make it work.
  • FIG. 1 is a schematic configuration diagram of an affected area recovery determination system according to an embodiment.
  • FIG. 2 is a functional block diagram of the affected area determination device according to the embodiment.
  • FIG. 3 is a functional block diagram of the information processing device according to the embodiment.
  • FIG. 4 is a schematic diagram showing the relationship between recovery of the affected area and whole body muscle mass according to the embodiment.
  • FIG. 5 is a schematic diagram showing the difference between the predicted recovery state and the current recovery state of whole body muscle mass and inflammation degree according to the embodiment.
  • FIG. 6 is a schematic diagram showing an example of advice according to the embodiment.
  • FIG. 7 is a schematic diagram showing an example of advice according to the embodiment.
  • FIG. 8 is a flowchart showing the flow of bioelectrical impedance/weight acquisition processing according to the embodiment.
  • FIG. 9 is a flowchart 10 showing the flow of local impedance acquisition processing according to the embodiment.
  • FIG. 10 is a flowchart showing the flow of the affected area state determination process according to the embodiment.
  • FIG. 1 is a schematic configuration diagram of the affected area recovery determination system 10 of this embodiment.
  • the affected area recovery determination system 10 includes an affected area determination device 12 , a body composition meter 14 , and an information processing device 16 . Note that the size of each device in FIG. 1 does not reflect the actual size.
  • the affected area determining device 12 determines the state of the affected area of the subject by passing a current through any part of the subject and locally measuring bioelectrical impedance, which is electrical resistance. For example, if inflammation, a tumor, a wound, or other abnormality occurs in a certain area of the subject, moisture may accumulate in the affected area, the temperature of the affected area may rise, or the state of the cells may change. It may be different from the normal part. Therefore, the bioelectrical impedance of a region including an affected region is different from that of a normal region without an affected region, so the presence or absence of an affected region and the state of the affected region can be determined based on the bioelectrical impedance. In the following description, the bioelectrical impedance calculated by the affected area determination device 12 will be referred to as local impedance.
  • the arbitrary part to which the current is applied is, for example, a part such as an arm, leg, abdomen, or chest, or a region narrower than these parts (for example, in the case of an arm, the forearm, elbow, shoulder, etc.). be. That is, in this embodiment, as an example, the current path length is about the length of an arm or a leg at most. Further, any part to which the current is applied, in other words, the part including the affected part, is estimated in advance by the person to be measured or a medical professional. Then, the affected area determining device 12 determines the exact position of the affected area and the state of the affected area by passing a current through such an arbitrary area.
  • the affected area determination device 12 of this embodiment includes a measurement section 20 and a main body section 22.
  • the measurer who measures the local impedance using the affected area determination device 12 is the person to be measured, a medical worker, or the like.
  • the measuring section 20 can be placed at any part of the subject, and is provided with two electrode sections 24, each consisting of a current electrode 24A and a voltage electrode 24B.
  • the measurement unit 20 of this embodiment can be worn by a person to be measured, and is, for example, a bandage wrapped around the person to be measured.
  • the measurement unit 20 is not limited to a bandage, but may be made of a highly flexible material that can be worn on the person to be measured, such as a belt, arm cover, leg cover, socks, innerwear, clothes, or a wristband-like wearable device. . Furthermore, the measuring section 20 may be shaped so that it is not worn on the body, but is held by a person who is measuring and presses the electrode section 24 against the body of the person to be measured.
  • the shape and material of the measurement unit 20 are not limited as long as it can measure the local impedance of any part of the person to be measured.
  • the shape and material of the measurement unit 20 are selected depending on the location of the affected area of the person to be measured, lifestyle, local impedance measurement method, and the like. Note that if the local impedance is to be periodically measured at the same position on the person being measured, for example, the measurement unit 20 may be a bandage or the like, and the electrode unit 24 may be fixed to the person being measured. It is preferable to prevent it from shifting.
  • the measurement unit 20 when measuring the local impedance of a person to be measured at a plurality of locations, it is preferable that the measurement unit 20 has a shape that allows the measurement person to grasp it and easily change the position of the electrode unit 24 with respect to the person to be measured.
  • the current electrode 24A and the voltage electrode 24B are arranged in the measurement section 20 so as to be in contact with the body of the person to be measured.
  • the current electrode 24A and the voltage electrode 24B are made of metal, for example, but are not limited to this, and may be made of any conductive material, such as gel or fiber.
  • the position of the electrode portions 24 in the measurement unit 20 may be adjustable, thereby making it possible to change the distance between the electrode portions 24 (hereinafter referred to as “inter-electrode distance”).
  • inter-electrode distance the distance between the electrode portions 24
  • the position and depth of the affected area can be determined in detail. That is, when the distance between the electrodes is short, a narrow area on the surface of the subject is measured, so the position of the affected area can be determined in more detail.
  • the shorter the distance between the electrodes the more the condition of the affected area at a shallow position on the body of the person to be measured can be determined.
  • the affected area determination device 12 stores the inter-electrode distance, and uses the inter-electrode distance to calculate local impedance and determine the depth of the affected area.
  • the main body section 22 measures the local impedance of any part of the body of the subject by passing a current through the current electrode 24A and detecting the voltage using the voltage electrode 24B. The main body section 22 then performs a process of determining the state of the affected area in the area based on the local impedance.
  • the measuring section 20 and the main body section 22 are electrically connected by a flexible cable 30. Thereby, the measurement unit 20 can be placed at any part of the body of the person to be measured. Further, the measuring section 20 and the cable 30 are detachably connected by a connector 32. This allows measurement sections 20 of various shapes to be connected to the main body section 22.
  • the main body 22 also includes a monitor 26 and a power switch 28.
  • the monitor 26 is, for example, a touch panel display, and accepts input of various setting values and displays measurement results and the like.
  • the power switch 28 accepts an operation to turn on and turn off the power to the main body section 22 .
  • the body composition meter 14 obtains the bioimpedance of the subject from the potential difference measured by passing a current through the subject, and calculates the body composition of the subject.
  • the body composition meter 14 is also equipped with a weight scale, and is capable of measuring the weight of the subject.
  • the body composition meter 14 of this embodiment includes a hand grip section 40 that the person to be measured holds with both hands, and a platform 42 on which the person to be measured stands.
  • the hand grip section 40 and the mounting table 42 are electrically connected by a cable 44, for example.
  • the hand grip section 40 includes a hand electrode 40R that is held with the right hand and a hand electrode 40L that is held with the left hand.
  • the platform 42 includes a sole electrode 46R that contacts the sole of the right foot and a sole electrode 46L that contacts the sole of the left foot.
  • the body composition meter 14 calculates the bioimpedance of the whole body and each body part of the person to be measured by measuring the potential difference generated in the current path of the hand electrodes 40R, 40L and the sole electrodes 46R, 46L. The body composition meter 14 then calculates the body composition of the subject based on user information such as the subject's bioimpedance, weight, age and gender of the subject.
  • the body composition calculated by the body composition meter 14 includes fat percentage, fat mass, fat-free mass, muscle mass, visceral fat mass, visceral fat level, visceral fat area, subcutaneous fat mass, basal metabolic rate, bone mass, These include body water percentage, BMI, intracellular fluid volume, and extracellular fluid volume.
  • the body composition meter 14 also includes a monitor 48 for displaying measurement results.
  • the information processing device 16 functions as an affected area recovery determination device that executes an affected area recovery determination process, as will be described in detail later.
  • the information processing device 16 is, for example, a laptop personal computer equipped with a monitor 49, but is not limited to this, and may be a portable information processing device such as a tablet terminal, a desktop personal computer, or the like.
  • the information processing device 16 of this embodiment is capable of transmitting and receiving data with the affected area determining device 12 and the body composition meter 14, and receives the results of impedance measurement by the affected area determining device 12 and body composition meter 14.
  • data transmission and reception is performed by, for example, short-range communication such as BLE (Bluetooth Low Energy).
  • FIG. 2 is a functional block diagram of the affected area determination device 12 of this embodiment.
  • the main body 22 of the affected area determination device 12 includes a frequency setting unit 50, a current application control unit 52, a voltage detection unit 54, a local impedance calculation unit 56, an affected area state determination unit 58, a monitor control unit 60, a storage unit 62, and a communication unit. 64.
  • Each function executed by each unit shown in FIG. 2 may be executed by a calculation unit included in the affected area determination device 12 by starting a program, for example, or by individual hardware such as an ASIC (Application Specific Integrated Circuit). It may also be realized by software.
  • ASIC Application Specific Integrated Circuit
  • the frequency setting section 50 sets the frequency of the current flowing between the electrode sections 24 (hereinafter referred to as "current frequency").
  • the current frequency in this embodiment can be arbitrarily set within a predetermined frequency width, and among the settable frequencies, a relatively low frequency is referred to as a low frequency, and a relatively high frequency is referred to as a high frequency. Note that the frequency range of this embodiment is, for example, about 1 kHz to 3 MHz.
  • the current application control unit 52 controls turning on and off of the current set by the frequency setting unit 50. Thereby, when the current is turned on, a current flows from the current electrode 24A in contact with the person to be measured to the person to be measured.
  • the voltage detection unit 54 detects the voltage generated by passing a current through the current electrode 24A via the voltage electrode 24B.
  • the local impedance calculation unit 56 calculates the local impedance, which is the electrical resistance between the electrode parts 24 in contact with the subject. This local impedance becomes an affected area index that reflects the condition of the affected area of the subject.
  • the affected area state determination section 58 determines the state of the region between the electrode sections 24 based on the local impedance calculated by the local impedance calculation section 56. Specifically, the affected area state determination unit 58 determines the state of the affected area based on the local impedance including the affected area and a predetermined reference value.
  • the predetermined reference value is, for example, the local impedance of a region of the subject that is not affected. For example, if the affected area is on the right arm, the local impedance of the left arm is measured as the reference value. Note that in the following explanation, the local impedance of the affected area will be referred to as affected area impedance.
  • the affected part state determination unit 58 does not obtain the reference value by measurement, but reads out the reference value corresponding to the affected part of the subject from a table showing the normal impedance of each part to be used as the reference value, for example. The condition of the affected area may also be determined. Note that the table is stored in the storage unit 62.
  • the affected area state determination unit 58 determines the state of the affected area based on the affected area impedance and the reference value. For example, if the affected area is an inflammation of a site where a surgery has been performed on the person to be measured, the affected area state determination unit 58 calculates the difference between the affected area impedance and the reference value, and sets the difference as the degree of inflammation of the affected area. That is, the larger the difference, the higher the degree of inflammation. On the other hand, the smaller the difference, the smaller the degree of inflammation, and if the difference is less than a predetermined value, it is determined that the inflammation has healed.
  • the monitor control unit 60 controls the monitor 26 to display the determination result etc. by the affected area state determination unit 58.
  • the storage unit 62 is, for example, a non-volatile memory, and stores various data, programs used for various processes, determination results by the affected area state determination unit 58, and the like.
  • the communication unit 64 transmits and receives data to and from the information processing device 16 and the like.
  • FIG. 3 is a functional block diagram of the information processing device 16 of this embodiment.
  • the information processing device 16 includes a communication section 70, a calculation section 72, and a storage section 74.
  • the communication unit 70 sends and receives data to and from the affected area determination device 12, body composition analyzer 14, other information processing devices, other devices, and the like. That is, the communication unit 70 of the present embodiment acquires the local impedance, which is the affected area index, of the part of the subject including the affected area measured by the affected area determination device 12. Furthermore, the communication unit 70 functions as an acquisition unit that acquires the bioimpedance and weight of the subject measured by the body composition meter as an overall index to be described later.
  • the calculation unit 72 is a CPU (Central Processing Unit) or the like, and controls the operation of the information processing device 16.
  • the storage unit 74 is a nonvolatile storage device or the like, and stores various data and programs used for various processes.
  • the storage unit 74 of this embodiment stores a program (application software) for executing the affected area recovery determination process, various data received from the affected area determination device 12 and body composition meter 14, the age, gender, height, and Stores user information such as body type.
  • the calculation unit 72 includes an affected area state determination unit 80, a body composition calculation unit 82, a recovery prediction unit 84, a recovery state determination unit 86, and an advice generation unit 88 in order to perform the affected area recovery determination process.
  • the affected area state determining unit 80 determines the state of the affected area of the subject based on the local impedance acquired by the communication unit 70.
  • the affected area state determination unit 80 has the same function as the affected area state determination unit 58 included in the affected area determination device 12, and the affected area state determination unit 80 of this embodiment calculates the degree of inflammation as a state determination of the affected area.
  • the state of inflammation can be determined (estimated) by the affected area determining device 12 measuring the local impedance including the affected area using currents of different frequencies.
  • variables such as Z5, Z250, Z5/Z250, and X/R are used as explanatory variables.
  • the affected area determination device 12 measures the affected area multiple times at different frequencies.
  • Z5 is a local impedance measured at a current frequency of 5 kHz
  • Z250 is a local impedance measured at a current frequency of 250 kHz
  • X is local resistance
  • R is reactance.
  • the body composition calculation unit 82 calculates the body composition of the subject based on user information such as bioimpedance, weight, age and gender of the subject received from the body composition meter 14.
  • the recovery prediction unit 84 predicts the recovery time of the affected area based on the condition of the affected area determined by the affected area status determination unit 80 and the subject's whole body index.
  • the condition of the affected area in this embodiment is, for example, the degree of inflammation as described above.
  • An example of the subject's whole body body composition used to predict the recovery time of the affected area is the whole body muscle mass. Note that other body compositions such as whole body fat amount or body weight may be used as the whole body index used to predict the recovery time of the affected area.
  • the recovery of the affected area is generally influenced by the patient's whole body composition (for example, whole body muscle mass) and whole body indicators such as body weight.
  • the patient's systemic indicators are less affected by locally occurring inflammation in the affected area. Therefore, in this embodiment, the recovery time of the affected area is predicted based on the current condition of the affected area and the whole body index. This makes it possible to accurately predict when the affected area will recover.
  • FIG. 4 is a schematic diagram showing the relationship between recovery of the affected area and whole body muscle mass.
  • the affected area of the subject is the surgical site, and the degree of inflammation in the affected area is the highest immediately after the surgery. As shown in FIG. 4, the greater the total body muscle mass, the faster the affected area will recover. Furthermore, the recovery of the affected area also differs depending on the age of the person to be measured, and the younger the person to be measured, the faster the recovery.
  • the recovery prediction unit 84 of the present embodiment predicts the recovery time based on the degree of inflammation of the affected area immediately after the occurrence of inflammation, the whole body muscle mass, and the age, for example.
  • Equation 1 is an example of a prediction equation for predicting recovery time, and is a regression equation.
  • constants a, b, and c can be determined by the least squares method, etc., and a regression equation can be calculated.
  • time a*injury/muscle+b*age+ c...(1) time: recovery period injury: degree of inflammation in the affected area immediately after the onset of inflammation muscle: mass of whole body muscle just before the onset of inflammation age: age a: constant b: constant c: constant
  • the recovery prediction line calculated using the prediction formula is not limited to a curve but may be a straight line.
  • the prediction formula may be created by other methods such as machine learning instead of the regression formula.
  • the most recent value obtained before the occurrence of inflammation may be used instead of immediately after the occurrence of inflammation.
  • the body weight of the subject may be used instead of the whole body muscle mass, or other body composition such as the whole body fat mass may be used.
  • the rehabilitation period can be predicted by referring to the recovery period of each rehabilitation patient, and a comprehensive rehabilitation plan for multiple patients can be drawn up. It's okay. For example, a patient cannot undergo rehabilitation until the catabolic phase of the affected area ends and the anabolic phase begins. Therefore, by predicting the timing at which the affected area will enter the assimilation period from the recovery prediction line, an appropriate rehabilitation start time and rehabilitation end time can be planned. This allows medical facilities to accept rehabilitation patients at an appropriate time. In addition, medical facilities can predict the number of rehabilitation patients they will accept, making it possible to optimize the number of staff.
  • the recovery state determination unit 86 determines the recovery state of the affected area based on the difference between the predicted recovery state of the affected area based on the recovery time predicted by the recovery prediction unit 84 in the past and the current state of the affected area determined by the affected area status determination unit 80. Determine the condition.
  • the recovery state here is a concept that includes the progress of recovery of the affected area.
  • the predicted recovery state is a time-series prediction of recovery of the affected area.
  • the recovery state determined by the recovery state determination unit 86 is an evaluation obtained by comparing the current recovery state and the predicted recovery state.
  • the current recovery state is the actual recovery state at the current time.
  • FIG. 5 is a schematic diagram showing the difference between the predicted recovery state and the current recovery state of whole body muscle mass and inflammation degree.
  • the vertical axis represents the whole body muscle mass
  • the horizontal axis represents the degree of inflammation in the affected area. Note that the double line in the assimilation period in FIG. 5 is the recovery prediction line mentioned above.
  • the degree of inflammation is generally higher after surgery than before surgery.
  • Rehabilitation begins after the catabolic phase of inflammation ends. Note that whether the affected area is in the catabolic phase or the anabolic phase may be determined based on local impedance.
  • the degree of inflammation had slightly improved at the start of rehabilitation, the subject was in a resting state during the catabolic phase, so his whole body muscle mass was at its lowest. After that, the subject underwent rehabilitation, and the current state of recovery is that the degree of inflammation in the affected area has recovered to near the level before surgery. Ideally, the current state of recovery should overlap with the predicted recovery line, and the whole body muscle mass should recover to near the pre-surgery level. However, there is a difference between the current recovery state and the predicted recovery line shown in FIG.
  • the recovery state determination unit 86 determines the recovery state of the affected area.
  • the determination of the recovery state may be output as, for example, a difference in numerical values or the like between the recovery prediction line and the current recovery state. This output is, for example, display on the monitor 49 of the information processing device 16 and storage in the storage unit 74. Further, the recovery state determining unit 86 may output a predetermined comment or the like according to the numerical value instead of a numerical value etc. as the determination result.
  • the recovery state determination unit 86 of this embodiment determines not only the recovery state of an affected area such as inflammation, but also the recovery state of whole body muscle mass, which is a whole body index.
  • the recovery state determination unit 86 of the present embodiment simultaneously acquires not only the recovery state of the affected area such as inflammation of the subject, but also the recovery state of the whole body muscle mass, which is a whole body index, so that the recovery state of the subject It can be determined whether or not the person is recovering appropriately.
  • the whole body index used to determine the recovery state may include other whole body body compositions such as whole body fat mass, body weight, basal metabolism of the subject, and internal body age.
  • a rehabilitation plan may be designed to recover whole body indicators other than these whole body muscle mass.
  • the determination of the recovery state is performed multiple times during the process of recovery of the patient's affected area. Continuous measurement of the affected area in this way allows for a better and more appropriate rehabilitation plan for the patient.
  • the advice generation unit 88 generates advice regarding recovery of the affected area based on the determination result of the recovery state determination unit 86.
  • the advice is based on the difference calculated by the recovery state determining unit 86, and includes, for example, "The inflammation has decreased, but the muscle mass has not recovered as much as expected.”, "The muscle mass has not recovered as much as expected.” However, the inflammation does not heal very well.''
  • advice if the current inflammation in the affected area has not recovered compared to the recovery prediction line, for example, ⁇ Let's focus on suppressing inflammation.To suppress inflammation, do not move, apply heat, Measures to help the affected area recover may also be included, such as repeated cooling.
  • an example of the advice we give is, ⁇ Focus on increasing your muscle mass. Review your food intake and do appropriate training.'' etc. may be output.
  • the generated advice is displayed on the monitor 49 of the information processing device 16 and stored in the storage unit 74. By outputting such advice, it is possible to create a more appropriate rehabilitation plan.
  • 6 and 7 are schematic diagrams showing examples of advice generated by the advice generation unit 88.
  • the matrix corresponds to the level of the inflammation level and the increase/decrease in the whole body muscle mass compared to the recovery prediction line, and examples of advice according to the level of the inflammation level and the increase/decrease in the whole body muscle mass are stored in advance in the storage unit 74. is memorized.
  • the degree of inflammation is high and the muscle mass of the whole body is increasing, the rehabilitation intensity is strong, and therefore advice is output that prompts the rehabilitation plan to be modified to weaken the rehabilitation intensity.
  • the degree of inflammation is low and the muscle mass of the whole body is increasing, rehabilitation is progressing smoothly, and therefore no advice is output that prompts modification of the rehabilitation plan.
  • the degree of inflammation is high and the muscle mass of the whole body is decreased, nutritional intake is insufficient, and advice is output to urge modification of the rehabilitation plan to ensure sufficient nutritional intake.
  • the degree of inflammation is low and the whole body muscle mass has decreased, the recovery is progressing smoothly, but the rehabilitation intensity is weak, so advice is output to prompt the correction of the rehabilitation plan to increase the rehabilitation intensity. .
  • the advice may include meal contents that include nutrients that should be ingested based on the total body fat amount, the total body muscle mass, and the state of recovery of the affected area.
  • FIG. 6 is an example of advice based on two axes: the degree of inflammation and the whole body muscle mass
  • FIG. 7 is an example of advice that takes into account changes over time in the state of recovery of the affected area.
  • FIG. 7 is a matrix of advice examples according to the actual degree of inflammation recovery and the slope of the actual recovery state. Note that the slope of the actual recovery state is obtained by determining the recovery state of the affected area multiple times at different times.
  • a case where the slope is large is a case where the slope is large compared to the recovery prediction line. In this case, the pace of muscle mass increase is faster than the recovery of inflammation.
  • the case where the slopes match is the case where the slopes match the slope of the recovery prediction line. In this case, the patient is recovering relatively smoothly.
  • a case where the slope is small is a case where the recovery from inflammation is faster than the pace of increase in muscle mass.
  • the affected area recovery determination process by the affected area recovery determination system 10 will be described.
  • the affected area recovery determination process is executed by the information processing device 16, but before that, bioelectrical impedance/body weight acquisition process and local impedance acquisition process are performed.
  • user information necessary for the affected area recovery determination process such as the subject's age, sex, height, and body shape, is input in advance to the affected area determination device 12, body composition meter 14, and information processing device 16.
  • the user information of the person to be measured may be stored in a server (not shown) and read from the server.
  • FIG. 8 is a flowchart showing the flow of bioelectrical impedance/weight acquisition processing executed by the body composition meter 14.
  • step 100 the person to be measured stands on the stage 42 and grips the hand grip part 40.
  • the bioimpedance of the subject is measured by passing current through the hand electrodes 40R, 40L and the sole electrodes 46R, 46L and measuring the potential difference.
  • the weight of the subject is measured.
  • the bioimpedance and body weight measurement results are output and the process ends.
  • the output of the measurement results includes sending the measurement results to the information processing device 16, displaying the measurement results on the monitor 48, and the like.
  • the body composition of the subject is not calculated, but the body composition is not limited to this, and the body composition may be calculated after measuring the bioelectrical impedance and weight. .
  • the calculated body composition may be transmitted to the information processing device 16.
  • the bioimpedance of the whole body is measured excluding the missing limb.
  • the bioimpedance of the whole body excluding the missing part can be measured by placing an electrode near the missing part of the left arm and grasping the hand electrode 40R with the right hand. .
  • FIG. 9 is a flowchart showing the flow of local impedance acquisition processing executed by the affected area determination device 12.
  • step 200 the measurement unit 20 is placed on the affected area of the person to be measured.
  • the affected area determination device 12 displays on the monitor 26 messages such as "Please touch the affected area.” and "Is it okay to use the same affected area as the previous measurement?"
  • the affected area determining device 12 prompts the measurer to grasp the position of the affected area in the person to be measured, and arranges the measuring section 20 at an appropriate position.
  • step 202 the current frequency and inter-electrode distance are set according to input by the measurer of the affected area determination device 12.
  • the current frequency and the inter-electrode distance are input via the monitor 26, which is a touch panel display, for example.
  • the frequency setting section 50 sets the input current frequency.
  • the current frequency to be set is a low frequency and a high frequency in order to determine the degree of inflammation of the affected area.
  • the current application control unit 52 applies a current of the set frequency to the current electrode 24A. As a result, a current flows between the electrode sections 24 that are in contact with the person to be measured.
  • the voltage detection section 54 detects the voltage generated by the current flowing through the voltage electrode 24B.
  • the local impedance calculation unit 56 calculates the local impedance based on the voltage detected by the voltage detection unit 54.
  • step 210 it is determined whether the measurement of local impedance at all predetermined parts of the subject and at different frequencies has been completed, and in the case of an affirmative determination, the process moves to step 204. On the other hand, if the determination is negative, steps 204 to 210 are repeated until the local impedance calculation is completed.
  • the predetermined site includes, in addition to the affected area of the person to be measured, a site that does not have an affected area for obtaining a reference value.
  • the measurement results of the local impedance and the measurement conditions such as the current frequency at the time of measurement are output, and the process ends.
  • the output of the measurement results includes sending the measurement results to the information processing device 16, displaying the measurement results on the monitor 26, and the like.
  • the state of the affected area is not determined by the affected part state determining unit 58 of the affected part determining device 12, but the present invention is not limited to this, and after measuring the local impedance, the affected part state determining unit 58 A state determination may be made. When the state of the affected area is determined, the determination result may be transmitted to the information processing device 16.
  • FIG. 10 is a flowchart showing the flow of the affected area recovery determination process executed by the information processing device 16. Note that each determination result and calculation result in the affected area recovery determination process is stored in the storage unit 74 in chronological order in association with the subject.
  • step 300 the communication unit 70 obtains the measured value of local impedance from the affected area determination device 12, and the measured values of biological impedance and body weight from the body composition meter 14. Each acquired measurement value is stored in the storage unit 74.
  • the affected area state determination unit 80 determines the state of the affected area based on the acquired local impedance.
  • the body composition calculation unit 82 calculates the whole body muscle mass of the subject based on the acquired bioelectrical impedance and body weight.
  • step 306 it is determined whether a recovery prediction line for the affected area of the subject has been calculated. If the determination is positive, the process moves to step 310, and if the determination is negative, the process moves to step 308.
  • step 308 the recovery prediction unit 84 calculates a recovery prediction line based on the condition of the affected area determined in step 302 and the whole body muscle mass calculated in step 304, and the process proceeds to step 316. Note that the calculated recovery prediction line and recovery time are stored in the storage unit 74 in association with the subject.
  • step 316 which is a transition from step 308, the monitor 49 displays the recovery prediction line and recovery time.
  • a rehabilitation plan for the person to be measured is drawn up while checking the displayed contents.
  • step 310 to which the transition is made when an affirmative determination is made in step 306, the already calculated predicted recovery line of the subject is read out from the storage unit 74, and the state of the affected area determined in step 302 and the predicted recovery line calculated in step 304 are read out.
  • the recovery state determining unit 86 calculates the difference between the whole body muscle mass and the predicted recovery line.
  • the recovery state determination unit 86 determines the recovery state of the affected area and the recovery state of the whole body muscle mass based on the difference calculated in step 310.
  • the advice generation unit 88 generates advice based on the determination result in step 310.
  • the monitor 49 displays the recovery state determination result and the generated advice. While checking the displayed contents, the rehabilitation plan of the subject is modified as necessary.
  • the state of the affected area of the subject is determined based on local impedance, but the present disclosure is not limited thereto.
  • the condition of the affected area may be determined based on an affected area index different from local impedance.
  • the affected area index may be any index that reflects the condition of the affected area of the subject, and may be, for example, CRP.
  • CRP CRP
  • information that can more accurately specify the condition of the affected area, such as the type of the affected area (wound) may also be used.
  • data indicating the location, type, and shape of the affected area may be inputted to the information processing device 16 as the affected area index, and the affected area state determining section 80 may determine the state of the affected area based on these data.
  • the present disclosure is not limited to this.
  • the body composition analyzer 14 and the information processing device 16 may not communicate with each other.
  • the measurement results of the body composition analyzer 14 are directly input to the information processing device 16 in order to perform the process of determining recovery of the affected area.
  • the information processing device 16 performs the affected part recovery determination process, but the present disclosure is not limited to this.
  • the server may receive (acquire) the measurement results of the affected area determining device 12 and the body composition meter 14, and the server may perform the affected area recovery determination process.
  • the results of the affected area recovery determination process can be viewed using a mobile terminal device or the like.
  • Affected area recovery determination system 16 Information processing device (affected area recovery determination device) 80 Affected area condition determination unit (affected area condition determination means) 84 Recovery prediction unit (prediction means) 86 Recovery state determination unit (Recovery state determination unit) 88 Advice generation unit (advice generation means)

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Abstract

An information processing device (16) acquires the local impedance at a lesion of a subject, and determines the state of the lesion, such as inflammation, on the basis of the local impedance. The healing of a lesion is typically affected by the muscle mass of the patient. Meanwhile, the muscle mass of the patient is unlikely to be affected by a change in a locally occurring lesion. Accordingly, the information processing device (16) predicts a healing time for the lesion on the basis of the determined state of the lesion and the muscle mass of the subject.

Description

患部回復判定装置、患部回復判定方法、患部回復判定プログラム、及びコンピュータ読み取り可能な非一時的記憶媒体Affected area recovery determination device, affected area recovery determination method, affected area recovery determination program, and computer-readable non-temporary storage medium 関連出願の相互参照Cross-reference of related applications
 本出願では、2022年3月31日に日本国に出願された特許出願番号2022-59075の利益を主張し、当該出願の内容は引用することによりここに組み込まれているものとする。 This application claims the benefit of patent application number 2022-59075 filed in Japan on March 31, 2022, and the contents of that application are incorporated herein by reference.
 本開示は、患部回復判定装置、患部回復判定方法、及び患部回復判定プログラムに関する。 The present disclosure relates to an affected area recovery determination device, an affected area recovery determination method, and an affected area recovery determination program.
 外科手術を実施した際、患者は患部の炎症が生じて体を自由に動かせない、又は寝たきりの生活が長く続くことで患者の筋肉量の低下が生じる。また、患者は患部をかばうように動いてしまい、患部とは逆側の部位に疲労が生じてしまう場合もある。このため、患者の生活を手術前と同水準に戻すためには、一定期間のリハビリを要する。そこで、早期に元の生活水準に戻すために、患部の回復具合を把握して回復具合と全身筋肉量に応じたリハビリ計画が立案される。 When a surgical operation is performed, the patient becomes unable to move freely due to inflammation in the affected area, or the patient's muscle mass decreases due to being bedridden for a long time. Furthermore, the patient may move as if to protect the affected area, resulting in fatigue in the area on the opposite side of the affected area. Therefore, a certain period of rehabilitation is required to return the patient's life to the same level as before the surgery. Therefore, in order to quickly return to the previous standard of living, a rehabilitation plan is drawn up based on the recovery status of the affected area and the overall muscle mass.
 ここで、非特許文献1(若林秀隆著,「リハビリテーション栄養 ポケットガイド」,第1版,株式会社ジェフコーポレーション,2014年9月,p.9-10)には、患者に対して血液検査を行うことでCRP(C-リアクディブ・プロテイン)の値を求め、CRPを手術、外傷、骨折、感染症等の急性の炎症の指標として用いることが記載されている。 Here, Non-Patent Document 1 (Hidetaka Wakabayashi, "Rehabilitation Nutrition Pocket Guide", 1st edition, JEF Corporation, September 2014, p.9-10) states that blood tests are performed on patients. It is described that the value of CRP (C-reactive protein) is determined by this method, and that CRP is used as an indicator of acute inflammation such as surgery, trauma, bone fracture, and infection.
 炎症等の侵襲が身体に生じている状態では、その時期が異化期と同化期に分けられる。具体的には、CRPが所定のしきい値以下となった場合に患部は同化期と判定され、しきい値を超えた場合に患部は異化期と判定される。異化期では、患部は筋肉又は脂肪を分解して必要なエネルギーを得ようとする。このため、異化期に患者にエネルギーを投与しても筋肉の分解を抑制することはできないため、患者の筋肉量は減少し低栄養となる。なお、同化期とは、手術や外傷などで生体侵襲が生じた際の回復過程のうち、同化と創傷の修復をする期間である。 When the body is undergoing an invasion such as inflammation, the period can be divided into a catabolic period and an anabolic period. Specifically, when CRP is below a predetermined threshold, the affected area is determined to be in the anabolic phase, and when it exceeds the threshold, the affected area is determined to be in the catabolic phase. During the catabolic phase, the affected body attempts to break down muscle or fat to obtain the energy it needs. For this reason, even if energy is administered to the patient during the catabolic phase, muscle decomposition cannot be suppressed, so the patient's muscle mass decreases and the patient becomes malnourished. The assimilation period is a period of assimilation and wound repair during the recovery process when biological invasion occurs due to surgery or trauma.
 しかしながら、CRPによる判定は、患部の状態を判定できても、患部の回復時期まで予測できるものではない。また、CRPによる判定は、被測定者の体全体の異常も反映してしまうため、患部の状態の判定という観点では精度が得られない。 However, although CRP can determine the condition of the affected area, it cannot predict the recovery time of the affected area. Furthermore, since the determination based on CRP also reflects abnormalities in the entire body of the person to be measured, accuracy cannot be obtained from the viewpoint of determining the condition of the affected area.
 そこで、本開示は、患部の回復時期を予測できる、患部回復判定装置、患部回復判定方法、及び患部回復判定プログラムを提供することを目的とする。 Therefore, an object of the present disclosure is to provide an affected area recovery determination device, an affected area recovery determination method, and an affected area recovery determination program that can predict the recovery time of the affected area.
 本開示の第1態様の患部回復判定装置は、被測定者の患部の状態を反映した患部指標を取得する取得手段と、前記取得手段によって取得された前記患部指標に基づいて、前記患部の状態を判定する患部状態判定手段と、前記患部状態判定手段によって判定された前記患部の状態と被測定者の全身指標とに基づいて、患部の回復時期を予測する予測手段と、を備える。 An affected area recovery determination device according to a first aspect of the present disclosure includes an acquisition unit that acquires an affected area index that reflects the condition of the affected area of a subject, and a condition of the affected area based on the affected area index acquired by the acquisition unit. and a prediction means for predicting the recovery time of the affected area based on the condition of the affected area determined by the affected area status determining means and the whole body index of the subject.
 患部の回復には、患者の全身指標である全身の体組成や体重等が影響するという研究結果が知られている。一方で、患者の全身指標は局所的に生じている患部の変化の影響を受け難い。そこで、本構成は、現在の患部の状態と全身指標とに基づいて患部の回復時期を予測する。これにより、本構成は、正確に患部の回復時期を予測できる。 Research has shown that the recovery of the affected area is influenced by the patient's overall body composition and weight, which are indicators of the patient's whole body. On the other hand, the patient's systemic index is not easily affected by locally occurring changes in the affected area. Therefore, this configuration predicts the recovery time of the affected area based on the current condition of the affected area and the whole body index. Thereby, this configuration can accurately predict the recovery time of the affected area.
 第2態様の患部回復判定装置は第1態様の患部回復判定装置において、前記患部指標を被測定者の患部を含む部位のインピーダンスとしてもよい。本構成によれば、被測定者の局所的な部位に電流を流し、電位差から取得するインピーダンスに基づいて患部の状態を判定するので、患部の位置及び患部の状態を判定できる。 The affected area recovery determination device of the second aspect may be the affected area recovery determination device of the first aspect, in which the affected area index may be the impedance of the part of the subject including the affected area. According to this configuration, the state of the affected area is determined based on the impedance obtained from the potential difference by passing a current through a local part of the subject, so that the position of the affected area and the state of the affected area can be determined.
 第3態様の患部回復判定装置は第1態様又は第2態様の患部回復判定装置において、前記全身指標を被測定者の全身筋肉量としてもよい。本構成によれば、正確に患部の回復時期を予測できる。 The affected area recovery determining device of the third aspect may be the affected area recovery determining device of the first aspect or the second aspect, in which the whole body index may be the whole body muscle mass of the subject. According to this configuration, it is possible to accurately predict the recovery time of the affected area.
 第4態様の患部回復判定装置は第3態様の患部回復判定装置において、前記予測手段は、被測定者の全身筋肉量が多いほど回復速度が速くなるように前記回復時期を予測してもよい。本構成によれば、正確に患部の回復時期を予測できる。 In the affected area recovery determining device according to the fourth aspect, in the affected area recovery determining device according to the third aspect, the prediction means may predict the recovery time so that the recovery speed becomes faster as the whole body muscle mass of the subject increases. . According to this configuration, it is possible to accurately predict the recovery time of the affected area.
 第5態様の患部回復判定装置は第1態様から第4態様の何れか1つの患部回復判定装置において、過去に前記予測手段によって予測した前記回復時期に基づく患部の予測回復状態と前記患部状態判定手段によって判定された現在の前記患部の状態との差異に基づいて、患部の回復状態を判定する回復状態判定手段を備えてもよい。本構成によれば、患部が適切に回復しているか否かを判定できる。 The affected area recovery determining device according to a fifth aspect is the affected area recovery determining device according to any one of the first to fourth aspects, and determines the predicted recovery state of the affected area and the affected area state based on the recovery time predicted by the prediction means in the past. A recovery state determining means may be provided for determining the recovery state of the affected area based on a difference from the current state of the affected area determined by the means. According to this configuration, it can be determined whether the affected area is properly recovering.
 第6態様の患部回復判定装置は第5態様の患部回復判定装置において、前記回復状態判定手段は、前記患部の回復状態及び前記全身指標の回復状態を判定してもよい。全身指標は、例えば、全身筋肉量又は体重等である。被測定者の患部の状態によっては、被測定者は安静にする必要がある。その結果、全身筋肉量や体重等の全身指標が減少する場合もあるので、この全身指標も回復させる必要がある。このため、本構成によれば、患部の回復状態と全身指標の回復状態を同時に取得するので、被測定者が適切に回復しているか否かを判定できる。 The affected area recovery determining device of the sixth aspect is the affected area recovery determining device of the fifth aspect, wherein the recovery state determining means may determine the recovery state of the affected area and the recovery state of the whole body index. The whole body index is, for example, whole body muscle mass or body weight. Depending on the condition of the affected area of the person being measured, the person being measured may need to rest. As a result, whole body indicators such as whole body muscle mass and body weight may decrease, so it is necessary to restore these whole body indicators as well. Therefore, according to this configuration, since the recovery state of the affected area and the recovery state of the whole body index are acquired at the same time, it is possible to determine whether or not the subject is appropriately recovering.
 第7態様の患部回復判定装置は第5態様又は第6態様の患部回復判定装置において、前記回復状態判定手段の判定結果に基づいて、患部の回復に関するアドバイスを生成するアドバイス生成部を備えてもよい。本構成によれば、より適切なリハビリ計画の作成が可能となる。 The affected area recovery determining device according to the seventh aspect is the affected area recovery determining device according to the fifth or sixth aspect, and may further include an advice generation unit that generates advice regarding recovery of the affected area based on the determination result of the recovery state determining means. good. According to this configuration, it is possible to create a more appropriate rehabilitation plan.
 第8態様の患部回復判定方法は、被測定者の患部の状態を反映した患部指標を取得する第1工程と、前記第1工程によって取得された前記患部指標に基づいて、前記患部の状態を判定する第2工程と、前記第2工程によって判定された前記患部の状態と被測定者の全身指標とに基づいて、患部の回復時期を予測する第3工程と、を有する。 The method for determining recovery of an affected area according to the eighth aspect includes a first step of acquiring an affected area index that reflects the condition of the affected area of the subject, and determining the condition of the affected area based on the affected area index acquired in the first step. The method includes a second step of determining, and a third step of predicting the recovery time of the affected area based on the condition of the affected area determined in the second step and the whole body index of the subject.
 第9態様の患部回復判定プログラムは、被測定者の患部の状態を反映した患部指標を取得手段によって取得する情報処理装置のコンピュータを、前記取得手段によって取得された前記患部指標に基づいて、前記患部の状態を判定する患部状態判定手段と、前記患部状態判定手段によって判定された前記患部の状態と被測定者の全身指標とに基づいて、患部の回復時期を予測する予測手段と、して機能させる。 The affected area recovery determination program of the ninth aspect is configured to cause a computer of an information processing device that acquires an affected area index that reflects the condition of the affected area of the subject by an acquisition means to an affected area condition determining means for determining the condition of the affected area; and a prediction means for predicting the recovery time of the affected area based on the condition of the affected area determined by the affected area condition determining means and the whole body index of the subject. Make it work.
 本開示によれば、患部の回復時期を予測できる。 According to the present disclosure, it is possible to predict the recovery time of the affected area.
図1は、実施形態の患部回復判定システムの概略構成図である。FIG. 1 is a schematic configuration diagram of an affected area recovery determination system according to an embodiment. 図2は、実施形態の患部判定装置の機能ブロック図である。FIG. 2 is a functional block diagram of the affected area determination device according to the embodiment. 図3は、実施形態の情報処理装置の機能ブロック図である。FIG. 3 is a functional block diagram of the information processing device according to the embodiment. 図4は、実施形態の患部の回復と全身筋肉量との関係を示す模式図である。FIG. 4 is a schematic diagram showing the relationship between recovery of the affected area and whole body muscle mass according to the embodiment. 図5は、実施形態の全身筋肉量と炎症度の予測回復状態と現在回復状態との差異を示す模式図である。FIG. 5 is a schematic diagram showing the difference between the predicted recovery state and the current recovery state of whole body muscle mass and inflammation degree according to the embodiment. 図6は、実施形態のアドバイス例を示す模式図である。FIG. 6 is a schematic diagram showing an example of advice according to the embodiment. 図7は、実施形態のアドバイス例を示す模式図である。FIG. 7 is a schematic diagram showing an example of advice according to the embodiment. 図8は、実施形態の生体インピーダンス・体重取得処理の流れを示すフローチャートである。FIG. 8 is a flowchart showing the flow of bioelectrical impedance/weight acquisition processing according to the embodiment. 図9は、実施形態の局所インピーダンス取得処理の流れを示すフローチャート10ある。FIG. 9 is a flowchart 10 showing the flow of local impedance acquisition processing according to the embodiment. 図10は、実施形態の患部状態判定処理の流れを示すフローチャートである。FIG. 10 is a flowchart showing the flow of the affected area state determination process according to the embodiment.
 以下、図面を参照して本開示の実施形態を説明する。なお、以下に説明する実施形態は、本開示を実施する場合の一例を示すものであって、本開示を以下に説明する具体的構成に限定するものではない。本開示の実施にあたっては、実施形態に応じた具体的構成が適宜採用されてよい。 Hereinafter, embodiments of the present disclosure will be described with reference to the drawings. Note that the embodiment described below shows an example of implementing the present disclosure, and the present disclosure is not limited to the specific configuration described below. In implementing the present disclosure, specific configurations depending on the embodiments may be adopted as appropriate.
 図1は、本実施形態の患部回復判定システム10の概略構成図である。患部回復判定システム10は、患部判定装置12、体組成計14、及び情報処理装置16を備える。なお、図1における各装置の大きさは実際の大きさを反映したものではない。 FIG. 1 is a schematic configuration diagram of the affected area recovery determination system 10 of this embodiment. The affected area recovery determination system 10 includes an affected area determination device 12 , a body composition meter 14 , and an information processing device 16 . Note that the size of each device in FIG. 1 does not reflect the actual size.
 患部判定装置12は、被測定者の任意の部位に電流を流し、電気抵抗である生体インピーダンスを局所的に測定することで、被測定者の患部の状態を判定する。例えば、患部として炎症、腫瘍、傷、及びその他の異常が被測定者の所定の部位に生じている場合には、患部に水分が蓄積されたり、患部の温度が高くなったり、細胞の状態が正常な部位に比べて異なっていたりする。このため、患部を含む部位の生体インピーダンスは、患部が生じていない正常な部位に比べて差異が生じるので、生体インピーダンスに基づいて患部の有無及び患部の状態を判定できる。なお、以下の説明では、患部判定装置12によって算出される生体インピーダンスを局所インピーダンスという。 The affected area determining device 12 determines the state of the affected area of the subject by passing a current through any part of the subject and locally measuring bioelectrical impedance, which is electrical resistance. For example, if inflammation, a tumor, a wound, or other abnormality occurs in a certain area of the subject, moisture may accumulate in the affected area, the temperature of the affected area may rise, or the state of the cells may change. It may be different from the normal part. Therefore, the bioelectrical impedance of a region including an affected region is different from that of a normal region without an affected region, so the presence or absence of an affected region and the state of the affected region can be determined based on the bioelectrical impedance. In the following description, the bioelectrical impedance calculated by the affected area determination device 12 will be referred to as local impedance.
 なお、電流を流す任意の部位とは、例えば、腕、脚、腹部、胸部等の部位、又はこれらの部位よりもよりも狭い領域(例えば、腕であれば、前腕、肘、肩等)である。すなわち、本実施形態では、一例として、電流経路長は長くても腕又は脚の長さ程度である。また、電流を流す任意の部位、換言すると患部を含む部位は、被測定者自身又は医療従事者によって予め見当が付けられている。そして、患部判定装置12は、このような任意の部位に電流を流すことで、患部の正確な位置及び患部の状態を判定する。 Note that the arbitrary part to which the current is applied is, for example, a part such as an arm, leg, abdomen, or chest, or a region narrower than these parts (for example, in the case of an arm, the forearm, elbow, shoulder, etc.). be. That is, in this embodiment, as an example, the current path length is about the length of an arm or a leg at most. Further, any part to which the current is applied, in other words, the part including the affected part, is estimated in advance by the person to be measured or a medical professional. Then, the affected area determining device 12 determines the exact position of the affected area and the state of the affected area by passing a current through such an arbitrary area.
 本実施形態の患部判定装置12は、測定部20及び本体部22を備える。なお、患部判定装置12を用いて局所インピーダンスを測定する測定者は、被測定者自身又は医療従事者等である。 The affected area determination device 12 of this embodiment includes a measurement section 20 and a main body section 22. Note that the measurer who measures the local impedance using the affected area determination device 12 is the person to be measured, a medical worker, or the like.
 測定部20は、被測定者の任意の部位に配置可能とされ、電流電極24A及び電圧電極24Bで構成される電極部24が2つ設けられる。本実施形態の測定部20は、被測定者に装着可能とされ、例えば被測定者に巻き付けられる包帯である。 The measuring section 20 can be placed at any part of the subject, and is provided with two electrode sections 24, each consisting of a current electrode 24A and a voltage electrode 24B. The measurement unit 20 of this embodiment can be worn by a person to be measured, and is, for example, a bandage wrapped around the person to be measured.
 測定部20は、包帯に限らず、ベルト、アームカバー、レッグカバー、靴下、インナー、洋服、リストバンド状のウェアラブルデバイス等、被測定者に装着可能でフレキシブル性の高い材質で構成されてもよい。また、測定部20は、身体に装着するものではなく、測定者が把持して被測定者の身体に電極部24を押し当てる形状とされてもよい。 The measurement unit 20 is not limited to a bandage, but may be made of a highly flexible material that can be worn on the person to be measured, such as a belt, arm cover, leg cover, socks, innerwear, clothes, or a wristband-like wearable device. . Furthermore, the measuring section 20 may be shaped so that it is not worn on the body, but is held by a person who is measuring and presses the electrode section 24 against the body of the person to be measured.
 測定部20は、被測定者の任意の部位の局所インピーダンスを測定可能であれば、形状及び材質は限定されない。測定部20の形状及び材質は、被測定者の患部の位置、生活態様、又は局所インピーダンスの測定方法等に応じて選択される。なお、被測定者に対して定期的に同じ位置の局所インピーダンスを測定するのであれば、例えば、測定部20を包帯等とすることで、被測定者に対して電極部24を固定して位置がずれないようにすることが好ましい。一方で、被測定者の局所インピーダンスを複数個所で測定する場合には、測定部20は測定者によって把持され、被測定者に対する電極部24の位置を変更し易い形状とすること好ましい。 The shape and material of the measurement unit 20 are not limited as long as it can measure the local impedance of any part of the person to be measured. The shape and material of the measurement unit 20 are selected depending on the location of the affected area of the person to be measured, lifestyle, local impedance measurement method, and the like. Note that if the local impedance is to be periodically measured at the same position on the person being measured, for example, the measurement unit 20 may be a bandage or the like, and the electrode unit 24 may be fixed to the person being measured. It is preferable to prevent it from shifting. On the other hand, when measuring the local impedance of a person to be measured at a plurality of locations, it is preferable that the measurement unit 20 has a shape that allows the measurement person to grasp it and easily change the position of the electrode unit 24 with respect to the person to be measured.
 電流電極24A及び電圧電極24Bは、被測定者の身体に接触するように測定部20に配置される。電流電極24A及び電圧電極24Bは、一例として、金属であるが、これに限らず、導電性部材であれば、例えばジェル状又は繊維状でもよい。 The current electrode 24A and the voltage electrode 24B are arranged in the measurement section 20 so as to be in contact with the body of the person to be measured. The current electrode 24A and the voltage electrode 24B are made of metal, for example, but are not limited to this, and may be made of any conductive material, such as gel or fiber.
 なお、測定部20において電極部24の位置が調整可能とされ、これにより電極部24間の距離(以下「電極間距離」という。)が変更可能とされてもよい。電極間距離を変更することにより、患部の位置や深さを詳細に判定できる。すなわち、電極間距離が短い場合には、被測定者の表面の狭い領域を測定することになるため患部の位置をより詳細に判定できる。また、電極間距離が短いほど、被測定者の身体の浅い位置における患部の状態を判定できる。一方、電極間距離が長い場合には、被測定者の表面の広い領域を測定することになるため、少ない測定回数で患部の状態を判定できる。また、電極間距離が長いほど、身体の深い位置における患部の状態を判定できる。なお、患部判定装置12は、電極間距離を記憶し、局所インピーダンスの算出及び患部の深さ判定に電極間距離を用いる。 Note that the position of the electrode portions 24 in the measurement unit 20 may be adjustable, thereby making it possible to change the distance between the electrode portions 24 (hereinafter referred to as “inter-electrode distance”). By changing the distance between the electrodes, the position and depth of the affected area can be determined in detail. That is, when the distance between the electrodes is short, a narrow area on the surface of the subject is measured, so the position of the affected area can be determined in more detail. Moreover, the shorter the distance between the electrodes, the more the condition of the affected area at a shallow position on the body of the person to be measured can be determined. On the other hand, when the distance between the electrodes is long, a wide area of the surface of the subject is measured, so the condition of the affected area can be determined with fewer measurements. Furthermore, the longer the distance between the electrodes, the more the condition of the affected area at a deeper position in the body can be determined. The affected area determination device 12 stores the inter-electrode distance, and uses the inter-electrode distance to calculate local impedance and determine the depth of the affected area.
 本体部22は、電流電極24Aに電流を流し、電圧電極24Bによって電圧を検出することで、被測定者の身体における任意の部位の局所インピーダンスを測定する。そして、本体部22は、局所インピーダンスに基づいて当該部位に生じた患部の状態を判定する処理を行う。 The main body section 22 measures the local impedance of any part of the body of the subject by passing a current through the current electrode 24A and detecting the voltage using the voltage electrode 24B. The main body section 22 then performs a process of determining the state of the affected area in the area based on the local impedance.
 測定部20と本体部22とは、柔軟なケーブル30で電気的に接続される。これにより、測定部20は、被測定者の身体の任意に部位に配置可能とされる。また、測定部20とケーブル30とはコネクタ32で着脱可能なように接続されている。これにより、様々な形状の測定部20が本体部22に接続可能とされる。 The measuring section 20 and the main body section 22 are electrically connected by a flexible cable 30. Thereby, the measurement unit 20 can be placed at any part of the body of the person to be measured. Further, the measuring section 20 and the cable 30 are detachably connected by a connector 32. This allows measurement sections 20 of various shapes to be connected to the main body section 22.
 また、本体部22は、モニタ26及び電源スイッチ28を備える。モニタ26は、一例として、タッチパネルディスプレイであり、各種設定値の入力を受け付けたり、測定結果等を表示する。電源スイッチ28は、本体部22の電源のオン操作及びオフ操作を受け付ける。 The main body 22 also includes a monitor 26 and a power switch 28. The monitor 26 is, for example, a touch panel display, and accepts input of various setting values and displays measurement results and the like. The power switch 28 accepts an operation to turn on and turn off the power to the main body section 22 .
 体組成計14は、被測定者に電流を流して測定する電位差から被測定者の生体インピーダンスを取得し、被測定者の体組成を算出する。また、体組成計14は、体重計も備え、被測定者の体重も測定可能とされている。 The body composition meter 14 obtains the bioimpedance of the subject from the potential difference measured by passing a current through the subject, and calculates the body composition of the subject. The body composition meter 14 is also equipped with a weight scale, and is capable of measuring the weight of the subject.
 本実施形態の体組成計14は、被測定者が両手で握るハンドグリップ部40と被測定者が載る載台42とを備える。ハンドグリップ部40と載台42とは一例としてケーブル44によって電気的に接続されている。 The body composition meter 14 of this embodiment includes a hand grip section 40 that the person to be measured holds with both hands, and a platform 42 on which the person to be measured stands. The hand grip section 40 and the mounting table 42 are electrically connected by a cable 44, for example.
 ハンドグリップ部40は、右手で把持される手電極40Rと左手で把持される手電極40Lを備える。載台42には、右足裏と接触する足裏電極46Rと左足裏と接触する足裏電極46Lを備える。 The hand grip section 40 includes a hand electrode 40R that is held with the right hand and a hand electrode 40L that is held with the left hand. The platform 42 includes a sole electrode 46R that contacts the sole of the right foot and a sole electrode 46L that contacts the sole of the left foot.
 体組成計14は、手電極40R,40L及び足裏電極46R,46Lの電流経路に生じる電位差を測定することで、被計測者の全身及び各身体部位の生体インピーダンスを算出する。そして体組成計14は、被測定者の生体インピーダンス、体重、被測定者の年齢及び性別等のユーザ情報に基づいて、被測定者の体組成を算出する。なお、体組成計14で算出される体組成は、脂肪率、脂肪量、除脂肪量、筋肉量、内臓脂肪量、内臓脂肪レベル、内臓脂肪面積、皮下脂肪量、基礎代謝量、骨量、体水分率、BMI、細胞内液量、細胞外液量等である。 The body composition meter 14 calculates the bioimpedance of the whole body and each body part of the person to be measured by measuring the potential difference generated in the current path of the hand electrodes 40R, 40L and the sole electrodes 46R, 46L. The body composition meter 14 then calculates the body composition of the subject based on user information such as the subject's bioimpedance, weight, age and gender of the subject. The body composition calculated by the body composition meter 14 includes fat percentage, fat mass, fat-free mass, muscle mass, visceral fat mass, visceral fat level, visceral fat area, subcutaneous fat mass, basal metabolic rate, bone mass, These include body water percentage, BMI, intracellular fluid volume, and extracellular fluid volume.
 また、体組成計14は、測定結果を表示するためのモニタ48を備えている。 The body composition meter 14 also includes a monitor 48 for displaying measurement results.
 情報処理装置16は、詳細を後述するように患部回復判定処理を実行する患部回復判定装置として機能する。情報処理装置16は、一例として、モニタ49を備えたラップトップ型のパーソナルコンピュータであるが、これに限らず、タブレット端末等の可搬型の情報処理装置、及びデスクトップ型のパーソナルコンピュータ等でもよい。 The information processing device 16 functions as an affected area recovery determination device that executes an affected area recovery determination process, as will be described in detail later. The information processing device 16 is, for example, a laptop personal computer equipped with a monitor 49, but is not limited to this, and may be a portable information processing device such as a tablet terminal, a desktop personal computer, or the like.
 本実施形態の情報処理装置16は、患部判定装置12及び体組成計14とデータの送受信が可能とされており、患部判定装置12及び体組成計14によるインピーダンスの測定結果を受信する。なお、データの送受信は、例えばBLE(Bluetooth Low Energy)等の近距離通信によって行われる。 The information processing device 16 of this embodiment is capable of transmitting and receiving data with the affected area determining device 12 and the body composition meter 14, and receives the results of impedance measurement by the affected area determining device 12 and body composition meter 14. Note that data transmission and reception is performed by, for example, short-range communication such as BLE (Bluetooth Low Energy).
 図2は、本実施形態の患部判定装置12の機能ブロック図である。患部判定装置12の本体部22は、周波数設定部50、電流印可制御部52、電圧検出部54、局所インピーダンス算出部56、患部状態判定部58、モニタ制御部60、記憶部62、及び通信部64を備える。図2に示される各部で実行される各機能は、一例としてプログラムが起動することによって患部判定装置12が備える演算部で実行されてもよいし、ASIC(Application Specific Integrated Circuit)等の個別のハードウェアによって実現されてもよい。 FIG. 2 is a functional block diagram of the affected area determination device 12 of this embodiment. The main body 22 of the affected area determination device 12 includes a frequency setting unit 50, a current application control unit 52, a voltage detection unit 54, a local impedance calculation unit 56, an affected area state determination unit 58, a monitor control unit 60, a storage unit 62, and a communication unit. 64. Each function executed by each unit shown in FIG. 2 may be executed by a calculation unit included in the affected area determination device 12 by starting a program, for example, or by individual hardware such as an ASIC (Application Specific Integrated Circuit). It may also be realized by software.
 周波数設定部50は、電極部24間に流す電流の周波数(以下「電流周波数」という。)を設定する。本実施形態の電流周波数は、所定の周波数幅の間で任意に設定可能とされ、設定可能な周波数のうち相対的に低い周波数を低周波数といい、相対的に高い周波数を高周波数という。なお、本実施形態の周波数領域は、一例として、1kHz~3MHz程度である。 The frequency setting section 50 sets the frequency of the current flowing between the electrode sections 24 (hereinafter referred to as "current frequency"). The current frequency in this embodiment can be arbitrarily set within a predetermined frequency width, and among the settable frequencies, a relatively low frequency is referred to as a low frequency, and a relatively high frequency is referred to as a high frequency. Note that the frequency range of this embodiment is, for example, about 1 kHz to 3 MHz.
 電流印可制御部52は、周波数設定部50で設定された電流のオン、オフを制御する。これにより、電流がオンとされると、被測定者に接触している電流電極24Aから被測定者に対して電流が流れる。 The current application control unit 52 controls turning on and off of the current set by the frequency setting unit 50. Thereby, when the current is turned on, a current flows from the current electrode 24A in contact with the person to be measured to the person to be measured.
 電圧検出部54は、電流電極24Aに電流を流すことで生じた電圧を電圧電極24Bを介して検出する。 The voltage detection unit 54 detects the voltage generated by passing a current through the current electrode 24A via the voltage electrode 24B.
 局所インピーダンス算出部56は、電圧検出部54で検出した電圧に基づいて、被測定者に接触する電極部24間の電気抵抗である局所インピーダンスを算出する。この局所インピーダンスが、被測定者の患部の状態を反映した患部指標となる。 Based on the voltage detected by the voltage detection unit 54, the local impedance calculation unit 56 calculates the local impedance, which is the electrical resistance between the electrode parts 24 in contact with the subject. This local impedance becomes an affected area index that reflects the condition of the affected area of the subject.
 患部状態判定部58は、局所インピーダンス算出部56によって算出された局所インピーダンスに基づいて、電極部24間における部位の状態を判定する。具体的には、患部状態判定部58は、患部を含む局所インピーダンスと所定の基準値とに基づいて、患部の状態を判定する。所定の基準値は、例えば、被測定者に対して患部が生じていない部位の局所インピーダンスである。例えば、患部が右腕に存在する場合には、左腕の局所インピーダンスを基準値として測定する。なお、以下の説明では、患部の局所インピーダンスを患部インピーダンスという。 The affected area state determination section 58 determines the state of the region between the electrode sections 24 based on the local impedance calculated by the local impedance calculation section 56. Specifically, the affected area state determination unit 58 determines the state of the affected area based on the local impedance including the affected area and a predetermined reference value. The predetermined reference value is, for example, the local impedance of a region of the subject that is not affected. For example, if the affected area is on the right arm, the local impedance of the left arm is measured as the reference value. Note that in the following explanation, the local impedance of the affected area will be referred to as affected area impedance.
 なお、患部状態判定部58は基準値を測定によって求めるのではなく、例えば、基準値とする部位毎の通常のインピーダンスを示したテーブルから、被測定者の患部に対応する基準値を読み出して、患部の状態を判定してもよい。なお、テーブルは記憶部62に記憶される。 It should be noted that the affected part state determination unit 58 does not obtain the reference value by measurement, but reads out the reference value corresponding to the affected part of the subject from a table showing the normal impedance of each part to be used as the reference value, for example. The condition of the affected area may also be determined. Note that the table is stored in the storage unit 62.
 そして、患部状態判定部58は、患部インピーダンスと基準値とに基づいて、患部の状態を判定する。例えば、患部が被測定者に対する手術が行われた部位の炎症であると、患部状態判定部58は、患部インピーダンスと基準値との差異を算出し、当該差異を患部の炎症度とする。すなわち、差異が大きいほど炎症度は高い。一方、差異が小さいほど炎症度は小さく、差異が所定値以下の場合には炎症は治っていると判定される。 Then, the affected area state determination unit 58 determines the state of the affected area based on the affected area impedance and the reference value. For example, if the affected area is an inflammation of a site where a surgery has been performed on the person to be measured, the affected area state determination unit 58 calculates the difference between the affected area impedance and the reference value, and sets the difference as the degree of inflammation of the affected area. That is, the larger the difference, the higher the degree of inflammation. On the other hand, the smaller the difference, the smaller the degree of inflammation, and if the difference is less than a predetermined value, it is determined that the inflammation has healed.
 モニタ制御部60は、患部状態判定部58による判定結果等を表示するようにモニタ26を制御する。 The monitor control unit 60 controls the monitor 26 to display the determination result etc. by the affected area state determination unit 58.
 記憶部62は、例えば、不揮発性メモリであり、各種データ及び各種処理に用いられるプログラム、及び患部状態判定部58による判定結果等を保存する。 The storage unit 62 is, for example, a non-volatile memory, and stores various data, programs used for various processes, determination results by the affected area state determination unit 58, and the like.
 通信部64は、情報処理装置16等との間でデータの送受信を行なう。 The communication unit 64 transmits and receives data to and from the information processing device 16 and the like.
 図3は、本実施形態の情報処理装置16の機能ブロック図である。 FIG. 3 is a functional block diagram of the information processing device 16 of this embodiment.
 情報処理装置16は、通信部70、演算部72、及び記憶部74を備える。 The information processing device 16 includes a communication section 70, a calculation section 72, and a storage section 74.
 通信部70は、患部判定装置12、体組成計14、他の情報処理装置、及び他の機器等とのデータの送受信を行なう。すなわち、本実施形態の通信部70は、患部判定装置12が測定した被測定者の患部を含む部位の患部指標である局所インピーダンスを取得する。また、通信部70は、体組成計で測定した被測定者の生体インピーダンス及び体重を後述する全体指標として取得する取得手段として機能する。 The communication unit 70 sends and receives data to and from the affected area determination device 12, body composition analyzer 14, other information processing devices, other devices, and the like. That is, the communication unit 70 of the present embodiment acquires the local impedance, which is the affected area index, of the part of the subject including the affected area measured by the affected area determination device 12. Furthermore, the communication unit 70 functions as an acquisition unit that acquires the bioimpedance and weight of the subject measured by the body composition meter as an overall index to be described later.
 演算部72は、CPU(Central Processing Unit)等であり、情報処理装置16の動作を制御する。 The calculation unit 72 is a CPU (Central Processing Unit) or the like, and controls the operation of the information processing device 16.
 記憶部74は、不揮発性の記憶装置等であり、各種データ及び各種処理に用いられるプログラムを記憶する。本実施形態の記憶部74は、患部回復判定処理を実行するためのプログラム(アプリケーションソフトウェア)、患部判定装置12及び体組成計14から受信した各種データ、被測定者の年齢、性別、身長、及び体型等のユーザ情報等を記憶する。 The storage unit 74 is a nonvolatile storage device or the like, and stores various data and programs used for various processes. The storage unit 74 of this embodiment stores a program (application software) for executing the affected area recovery determination process, various data received from the affected area determination device 12 and body composition meter 14, the age, gender, height, and Stores user information such as body type.
 演算部72は、患部回復判定処理を行うために、患部状態判定部80、体組成算出部82、回復予測部84、回復状態判定部86、及びアドバイス生成部88を備える。 The calculation unit 72 includes an affected area state determination unit 80, a body composition calculation unit 82, a recovery prediction unit 84, a recovery state determination unit 86, and an advice generation unit 88 in order to perform the affected area recovery determination process.
 患部状態判定部80は、通信部70によって取得された局所インピーダンスに基づいて、被測定者の患部の状態を判定する。なお、患部状態判定部80は、患部判定装置12が備える患部状態判定部58と同様の機能であり、本実施形態の患部状態判定部80は、患部の状態判定として炎症度を算出する。 The affected area state determining unit 80 determines the state of the affected area of the subject based on the local impedance acquired by the communication unit 70. The affected area state determination unit 80 has the same function as the affected area state determination unit 58 included in the affected area determination device 12, and the affected area state determination unit 80 of this embodiment calculates the degree of inflammation as a state determination of the affected area.
 ここで、患部として炎症が生じている場合の状態判定について説明する。 Here, we will explain how to determine the condition when inflammation is occurring as the affected area.
 まず、患部が炎症していると、炎症の箇所に水分が蓄積されるため、局所インピーダンスが小さくなる。そして、炎症が回復するにつれて、蓄積されていた水分が減少するため、局所インピーダンスは次第に大きくなる。 First, when the affected area is inflamed, moisture accumulates in the inflamed area, which reduces local impedance. Then, as the inflammation recovers, the accumulated water decreases, so the local impedance gradually increases.
 また、炎症が生じると、患部には局所性浮腫が生じる。局所性浮腫が生じると、細胞外液量が増加するので、細胞内液量と細胞外液量との比率が変化する。低周波数の電流によって測定した局所インピーダンスは特に細胞外液量を反映する。一方で、高周波数の電流によって測定した局所インピーダンスは細胞外液量及び細胞内液量を反映する。 Additionally, when inflammation occurs, local edema occurs in the affected area. When local edema occurs, the amount of extracellular fluid increases, so the ratio between the amount of intracellular fluid and the amount of extracellular fluid changes. The local impedance measured by low-frequency current particularly reflects the extracellular fluid volume. On the other hand, local impedance measured by high-frequency current reflects the extracellular and intracellular fluid volumes.
 従って、患部判定装置12が周波数の異なる電流によって患部を含む局所インピーダンスを測定することで、炎症の状態を判定(推定)できる。具体的には、Z5、Z250、Z5/Z250、X/Rといった変数が説明変数として用いられる。このため、患部判定装置12は、患部を異なる周波数で複数回測定する。なお、Z5は、5kHzの電流周波数で測定された局所インピーダンス、Z250は250kHzの電流周波数で測定された局所インピーダンスである。また、Xは局所レジスタンスであり、Rはリアクタンスである。 Therefore, the state of inflammation can be determined (estimated) by the affected area determining device 12 measuring the local impedance including the affected area using currents of different frequencies. Specifically, variables such as Z5, Z250, Z5/Z250, and X/R are used as explanatory variables. For this reason, the affected area determination device 12 measures the affected area multiple times at different frequencies. Note that Z5 is a local impedance measured at a current frequency of 5 kHz, and Z250 is a local impedance measured at a current frequency of 250 kHz. Also, X is local resistance and R is reactance.
 体組成算出部82は、体組成計14から受信した生体インピーダンス、体重、被測定者の年齢及び性別等のユーザ情報に基づいて、被測定者の体組成を算出する。 The body composition calculation unit 82 calculates the body composition of the subject based on user information such as bioimpedance, weight, age and gender of the subject received from the body composition meter 14.
 回復予測部84は、患部状態判定部80によって判定された患部の状態と被測定者の全身指標とに基づいて、患部の回復時期を予測する。本実施形態の患部の状態とは、上述のように一例として炎症度である。患部の回復時期を予測するために用いられる被測定者の全身の体組成は、一例として、全身筋肉量である。なお、患部の回復時期を予測するために用いられる全身指標として、例えば全身の脂肪量等の他の体組成又は体重が用いられてもよい。 The recovery prediction unit 84 predicts the recovery time of the affected area based on the condition of the affected area determined by the affected area status determination unit 80 and the subject's whole body index. The condition of the affected area in this embodiment is, for example, the degree of inflammation as described above. An example of the subject's whole body body composition used to predict the recovery time of the affected area is the whole body muscle mass. Note that other body compositions such as whole body fat amount or body weight may be used as the whole body index used to predict the recovery time of the affected area.
 ここで、患部の回復には、一般的に患者の全身の体組成(例えば全身筋肉量)や体重等の全身指標が影響する。一方で、患者の全身指標は局所的に生じる患部の炎症等の影響を受け難い。このため、本実施形態では、現在の患部の状態と全身指標とに基づいて患部の回復時期を予測する。これにより、正確に患部の回復時期が予測可能となる。 Here, the recovery of the affected area is generally influenced by the patient's whole body composition (for example, whole body muscle mass) and whole body indicators such as body weight. On the other hand, the patient's systemic indicators are less affected by locally occurring inflammation in the affected area. Therefore, in this embodiment, the recovery time of the affected area is predicted based on the current condition of the affected area and the whole body index. This makes it possible to accurately predict when the affected area will recover.
 図4は、患部の回復と全身筋肉量との関係を示す模式図である。図4では、被測定者の患部を手術個所とし、手術直後の患部の炎症度が最も高い。そして図4に示されるように、全身筋肉量が多いほど患部の回復は早くなる。また、患部の回復は、被測定者の年齢によっても異なり、被測定者が若いほど回復は早い。 FIG. 4 is a schematic diagram showing the relationship between recovery of the affected area and whole body muscle mass. In FIG. 4, the affected area of the subject is the surgical site, and the degree of inflammation in the affected area is the highest immediately after the surgery. As shown in FIG. 4, the greater the total body muscle mass, the faster the affected area will recover. Furthermore, the recovery of the affected area also differs depending on the age of the person to be measured, and the younger the person to be measured, the faster the recovery.
 そこで、本実施形態の回復予測部84は、一例として、炎症発生直後における患部の炎症度、全身筋肉量、及び年齢から回復時期を予測する。 Therefore, the recovery prediction unit 84 of the present embodiment predicts the recovery time based on the degree of inflammation of the affected area immediately after the occurrence of inflammation, the whole body muscle mass, and the age, for example.
 下記数式1は、回復時期を予測するための予測式の一例であり、回帰式としている。変数であるinjury、muscle、age、timeはデータベースとして蓄積することで、最小二乗法等により定数a,b,cを求めることができ、回帰式が算出される。 Equation 1 below is an example of a prediction equation for predicting recovery time, and is a regression equation. By storing the variables injury, muscle, age, and time as a database, constants a, b, and c can be determined by the least squares method, etc., and a regression equation can be calculated.
 time=a*injury/muscle+b*age+ c ・・・(1)
  time: 回復時期
  injury:炎症発生直後の患部の炎症度
  muscle:炎症発生直前の全身筋肉量
  age: 年齢
  a:定数
  b:定数
  c:定数
time=a*injury/muscle+b*age+ c...(1)
time: recovery period injury: degree of inflammation in the affected area immediately after the onset of inflammation muscle: mass of whole body muscle just before the onset of inflammation age: age a: constant b: constant c: constant
 なお、予測式で算出される回復予測線は、曲線に限らず直線でもよい。また、予測式は、回帰式ではなく機械学習等、他の手法によって作成されてもよい。また、全身筋肉量は、炎症発生直後ではなく炎症発生前に取得した直近の値を用いてもよい。また、予測式に用いられる変数として、全身筋肉量ではなく、被測定者の体重を用いてもよいし、全身脂肪量等の他の体組成を用いてもよい。 Note that the recovery prediction line calculated using the prediction formula is not limited to a curve but may be a straight line. Moreover, the prediction formula may be created by other methods such as machine learning instead of the regression formula. Further, for the whole body muscle mass, the most recent value obtained before the occurrence of inflammation may be used instead of immediately after the occurrence of inflammation. Moreover, as a variable used in the prediction formula, the body weight of the subject may be used instead of the whole body muscle mass, or other body composition such as the whole body fat mass may be used.
 このように回復予測線を用いた患部の回復時期の予測が行われることで、医療従事者は、被測定者に対する適切なリハビリ計画を立案できる。 By predicting the recovery time of the affected area using the recovery prediction line in this way, medical personnel can formulate an appropriate rehabilitation plan for the subject.
 また、多数のリハビリ患者が入院又は通院している病院やクリニック等の医療施設では、リハビリ患者毎の回復時期を参照してリハビリ期間を予測し、複数の患者に対する総合的なリハビリ計画を立案してもよい。例えば、患部の異化期が終了して同化期に至るまでの間は、患者はリハビリができない。このため、回復予測線から患部が同化期となるタイミングを予測することで、適切なリハビリ開始時期とリハビリ終了時期とが計画される。これにより、医療施設は、適切なタイミングでリハビリ患者を受け入れることができる。また、医療施設は、施設で受け入れるリハビリ患者の数を予測でき、スタッフの人数の最適化等が可能となる。 In addition, in medical facilities such as hospitals and clinics where a large number of rehabilitation patients are hospitalized or attend, the rehabilitation period can be predicted by referring to the recovery period of each rehabilitation patient, and a comprehensive rehabilitation plan for multiple patients can be drawn up. It's okay. For example, a patient cannot undergo rehabilitation until the catabolic phase of the affected area ends and the anabolic phase begins. Therefore, by predicting the timing at which the affected area will enter the assimilation period from the recovery prediction line, an appropriate rehabilitation start time and rehabilitation end time can be planned. This allows medical facilities to accept rehabilitation patients at an appropriate time. In addition, medical facilities can predict the number of rehabilitation patients they will accept, making it possible to optimize the number of staff.
 回復状態判定部86は、過去に回復予測部84によって予測した回復時期に基づく患部の予測回復状態と患部状態判定部80によって判定された現在の患部の状態との差異に基づいて、患部の回復状態を判定する。 The recovery state determination unit 86 determines the recovery state of the affected area based on the difference between the predicted recovery state of the affected area based on the recovery time predicted by the recovery prediction unit 84 in the past and the current state of the affected area determined by the affected area status determination unit 80. Determine the condition.
 なお、ここでいう回復状態とは、患部の回復の進行状況を含む概念である。また、予測回復状態は、患部の回復の時系列予測である。そして、回復状態判定部86によって判定される回復状態とは、現在回復状態と予測回復状態とを比較することで得られる評価である。現在回復状態とは、現時点における実際の回復状態である。 Note that the recovery state here is a concept that includes the progress of recovery of the affected area. Furthermore, the predicted recovery state is a time-series prediction of recovery of the affected area. The recovery state determined by the recovery state determination unit 86 is an evaluation obtained by comparing the current recovery state and the predicted recovery state. The current recovery state is the actual recovery state at the current time.
 図5は、全身筋肉量と炎症度の予測回復状態と現在回復状態との差異を示す模式図である。図5は、一例として、縦軸を全身筋肉量とし、横軸を患部の炎症度とする。なお、図5の同化期における二重線が上述した回復予測線である。 FIG. 5 is a schematic diagram showing the difference between the predicted recovery state and the current recovery state of whole body muscle mass and inflammation degree. In FIG. 5, as an example, the vertical axis represents the whole body muscle mass, and the horizontal axis represents the degree of inflammation in the affected area. Note that the double line in the assimilation period in FIG. 5 is the recovery prediction line mentioned above.
 図5に示されるように、一般的に、炎症度は手術前に比べて手術後の方が高くなる。そして、炎症の異化期が終了してからリハビリが開始される。なお、患部が異化期又は同化期であるかは、局所インピーダンスに基づいて判定されてもよい。 As shown in Figure 5, the degree of inflammation is generally higher after surgery than before surgery. Rehabilitation begins after the catabolic phase of inflammation ends. Note that whether the affected area is in the catabolic phase or the anabolic phase may be determined based on local impedance.
 そして、リハビリ開始時には炎症度が若干改善しているものの、被測定者は異化期の間は安静状態とされていたため、全身筋肉量は最も低下している。その後、被測定者がリハビリを行った結果である現在回復状態は、患部の炎症度が手術前近くにまで回復している。本来であれば、現在回復状態は、回復予測線に重なり、全身筋肉量も手術前近くにまで回復することが理想的である。しかしながら、図5に示される現在回復状態と回復予測線とに差異が生じている。 Although the degree of inflammation had slightly improved at the start of rehabilitation, the subject was in a resting state during the catabolic phase, so his whole body muscle mass was at its lowest. After that, the subject underwent rehabilitation, and the current state of recovery is that the degree of inflammation in the affected area has recovered to near the level before surgery. Ideally, the current state of recovery should overlap with the predicted recovery line, and the whole body muscle mass should recover to near the pre-surgery level. However, there is a difference between the current recovery state and the predicted recovery line shown in FIG.
 この差異に基づいて、回復状態判定部86は患部の回復状態を判定する。なお、回復状態の判定は、例えば、回復予測線と現在回復状態との数値等の差異として出力されてもよい。この出力とは、例えば、情報処理装置16のモニタ49への表示、及び記憶部74による記憶である。また、回復状態判定部86は、判定結果として数値等ではなく、数値に応じて予め定められたコメント等を出力してもよい。 Based on this difference, the recovery state determination unit 86 determines the recovery state of the affected area. Note that the determination of the recovery state may be output as, for example, a difference in numerical values or the like between the recovery prediction line and the current recovery state. This output is, for example, display on the monitor 49 of the information processing device 16 and storage in the storage unit 74. Further, the recovery state determining unit 86 may output a predetermined comment or the like according to the numerical value instead of a numerical value etc. as the determination result.
 なお、本実施形態の回復状態判定部86は、炎症等の患部の回復状態だけでなく、全身指標である全身筋肉量等の回復状態を判定する。 Note that the recovery state determination unit 86 of this embodiment determines not only the recovery state of an affected area such as inflammation, but also the recovery state of whole body muscle mass, which is a whole body index.
 すなわち、上述のように、患部を回復させるために被測定者を安静状態にした結果、全身筋肉量が減少する場合もある。したがって、被測定者は全身筋肉量も回復させる必要がある。このように、本実施形態の回復状態判定部86は、被測定者の炎症等の患部の回復状態だけでなく、全身指標である全身筋肉量等の回復状態を同時に取得するので、被測定者が適切に回復しているか否かを判定できる。 That is, as mentioned above, as a result of placing the subject in a resting state in order to recover the affected area, the whole body muscle mass may decrease. Therefore, the subject also needs to recover muscle mass throughout the body. In this way, the recovery state determination unit 86 of the present embodiment simultaneously acquires not only the recovery state of the affected area such as inflammation of the subject, but also the recovery state of the whole body muscle mass, which is a whole body index, so that the recovery state of the subject It can be determined whether or not the person is recovering appropriately.
 なお、回復状態の判定に用いられる全身指標は、全身筋肉量の他に、全身の脂肪量等の他の全身の体組成、体重、被測定者の基礎代謝、及び体内年齢等でもよい。また、リハビリ計画も、これら全身筋肉量以外の全身指標を回復させるためのものが立案されてもよい。 In addition to the whole body muscle mass, the whole body index used to determine the recovery state may include other whole body body compositions such as whole body fat mass, body weight, basal metabolism of the subject, and internal body age. Furthermore, a rehabilitation plan may be designed to recover whole body indicators other than these whole body muscle mass.
 また、回復状態の判定は、患者の患部が回復する過程で複数回行われる。このような患部の継続的な測定で、患者のリハビリ計画を良い適切なものにできる。 Further, the determination of the recovery state is performed multiple times during the process of recovery of the patient's affected area. Continuous measurement of the affected area in this way allows for a better and more appropriate rehabilitation plan for the patient.
 アドバイス生成部88は、回復状態判定部86の判定結果に基づいて、患部の回復に関するアドバイスを生成する。アドバイスは、回復状態判定部86によって算出された差異に基づくものであり、例えば“炎症は小さくなっていますが、筋肉量が思ったほど回復していません。”、“筋肉量は回復していますが、炎症の直りがあまりよくありません。”等である。 The advice generation unit 88 generates advice regarding recovery of the affected area based on the determination result of the recovery state determination unit 86. The advice is based on the difference calculated by the recovery state determining unit 86, and includes, for example, "The inflammation has decreased, but the muscle mass has not recovered as much as expected.", "The muscle mass has not recovered as much as expected." However, the inflammation does not heal very well.''
 また、アドバイスの例として、回復予測線に対して現在の患部の炎症が回復していない場合には、例えば、“炎症を抑える方に注力しましょう。炎症を抑えるには、動かさない、温め、冷やしを繰り返す等の対策があります。”とのように、患部を回復させるための対策が含まれてもよい。また、回復予測線に対して現在の全身筋肉量が回復していない場合には、アドバイスの例として“筋肉を増やす方向に注力しましょう。食事量を見直し、適度なトレーニングを行いましょう。”等が出力されてもよい。生成されたアドバイスは、情報処理装置16のモニタ49へ表示され、記憶部74に記憶される。このようなアドバイスの出力によって、より適切なリハビリ計画の作成が可能となる。 In addition, as an example of advice, if the current inflammation in the affected area has not recovered compared to the recovery prediction line, for example, ``Let's focus on suppressing inflammation.To suppress inflammation, do not move, apply heat, Measures to help the affected area recover may also be included, such as repeated cooling. In addition, if your current total body muscle mass has not recovered in line with the recovery prediction line, an example of the advice we give is, ``Focus on increasing your muscle mass. Review your food intake and do appropriate training.'' etc. may be output. The generated advice is displayed on the monitor 49 of the information processing device 16 and stored in the storage unit 74. By outputting such advice, it is possible to create a more appropriate rehabilitation plan.
 図6,7は、アドバイス生成部88が生成するアドバイスの例を示す模式図である。 6 and 7 are schematic diagrams showing examples of advice generated by the advice generation unit 88.
 図6の例では、回復予測線と比較した炎症度の高低と全身筋肉量の増減とに応じたマトリクスであり、炎症度の高低及び全身筋肉量の増減に応じたアドバイス例が予め記憶部74に記憶される。 In the example of FIG. 6, the matrix corresponds to the level of the inflammation level and the increase/decrease in the whole body muscle mass compared to the recovery prediction line, and examples of advice according to the level of the inflammation level and the increase/decrease in the whole body muscle mass are stored in advance in the storage unit 74. is memorized.
 例えば、炎症度が高く、全身筋肉量が増加している場合には、リハビリ強度が強いため、リハビリ強度を弱めるようにリハビリ計画の修正を促すアドバイスが出力される。一方、炎症度が低く、全身筋肉量が増加している場合には、リハビリは順調に推移しているため、リハビリ計画の修正を促すようなアドバイスは出力されない。また、炎症度が高く、全身筋肉量が減少している場合には、栄養摂取が不十分であるため、栄養を十分に摂取するようにリハビリ計画の修正を促すアドバイスが出力される。また、炎症度が低く、全身筋肉量が減少している場合には、順調に回復しているが、リハビリ強度が弱いため、リハビリ強度を強めるようにリハビリ計画の修正を促すアドバイスが出力される。 For example, if the degree of inflammation is high and the muscle mass of the whole body is increasing, the rehabilitation intensity is strong, and therefore advice is output that prompts the rehabilitation plan to be modified to weaken the rehabilitation intensity. On the other hand, if the degree of inflammation is low and the muscle mass of the whole body is increasing, rehabilitation is progressing smoothly, and therefore no advice is output that prompts modification of the rehabilitation plan. Further, if the degree of inflammation is high and the muscle mass of the whole body is decreased, nutritional intake is insufficient, and advice is output to urge modification of the rehabilitation plan to ensure sufficient nutritional intake. In addition, if the degree of inflammation is low and the whole body muscle mass has decreased, the recovery is progressing smoothly, but the rehabilitation intensity is weak, so advice is output to prompt the correction of the rehabilitation plan to increase the rehabilitation intensity. .
 また、患部の状態が良好な場合にはその旨を表示して、リハビリを一時的に休憩してもよいとのアドバイスが出力されてもよい。一方で、患部の回復の進捗が順調な場合でも、筋肉量の回復の進捗が順調でない場合には、運動を続けることを促すアドバイスが出力されてもよい。 Furthermore, if the condition of the affected area is good, a message to that effect may be displayed and advice may be output that it is okay to take a temporary break from rehabilitation. On the other hand, even if the recovery of the affected area is progressing smoothly, if the recovery of muscle mass is not progressing smoothly, advice to continue exercising may be output.
 なお、アドバイスには、全身脂肪量と全身筋肉量と患部の回復状態に基づいて、摂取するべき栄養素が含まれる食事内容等が含まれてもよい。 Note that the advice may include meal contents that include nutrients that should be ingested based on the total body fat amount, the total body muscle mass, and the state of recovery of the affected area.
 図6の例は、炎症度と全身筋肉量との2軸に基づくアドバイス例であるが、図7の例は、患部の回復状態の時間変化を加味したアドバイス例である。具体的には、図7は現実の炎症回復の程度と現実の回復状態の傾きとに応じたアドバイス例のマトリクスである。なお、現実の回復状態の傾きは、患部の回復状態を異なる時期に複数回判定することで取得される。 The example in FIG. 6 is an example of advice based on two axes: the degree of inflammation and the whole body muscle mass, whereas the example in FIG. 7 is an example of advice that takes into account changes over time in the state of recovery of the affected area. Specifically, FIG. 7 is a matrix of advice examples according to the actual degree of inflammation recovery and the slope of the actual recovery state. Note that the slope of the actual recovery state is obtained by determining the recovery state of the affected area multiple times at different times.
 傾きが大きい場合とは、回復予測線と比較して傾きが大きい場合である。この場合は、炎症の回復より、筋肉量増加のペースが早い。傾きが一致する場合とは、回復予測線の傾きと一致する場合である。この場合は、比較的順調に回復している場合である。傾きが小さい場合とは、炎症の回復が筋肉量増加のペースより早い場合である。 A case where the slope is large is a case where the slope is large compared to the recovery prediction line. In this case, the pace of muscle mass increase is faster than the recovery of inflammation. The case where the slopes match is the case where the slopes match the slope of the recovery prediction line. In this case, the patient is recovering relatively smoothly. A case where the slope is small is a case where the recovery from inflammation is faster than the pace of increase in muscle mass.
 そして、図7に示されるように、炎症回復が早い場合には、傾きにかかわらず、リハビリ計画の修正を促すようなアドバイスは出力されない。一方、炎症回復が予測通りの場合には、傾きが大きいと炎症回復を早めるような修正を促すアドバイスが出力される。傾きが一致していると修正を促すようなアドバイスは出力されない。傾きが小さいと筋肉量を増加するような修正を促すアドバイスが出力される。また、炎症回復が遅い場合には、傾きにかかわらず、炎症回復を早めるような修正を促すアドバイスが出力される。 As shown in FIG. 7, if the inflammation recovers quickly, no advice is output that prompts correction of the rehabilitation plan, regardless of the slope. On the other hand, if the inflammation recovery is as predicted and the slope is large, advice is output that prompts corrections that will speed up the inflammation recovery. If the slopes match, no advice will be output that prompts correction. If the slope is small, advice is output that prompts corrections such as increasing muscle mass. Furthermore, if the recovery from inflammation is slow, advice is output that urges corrections that will speed up the recovery from inflammation, regardless of the slope.
 次に、図8~10を参照して、患部回復判定システム10による患部回復判定処理について説明する。なお、患部回復判定処理は、情報処理装置16で実行されるが、その前に生体インピーダンス・体重取得処理及び局所インピーダンス取得処理が行われる。また、患部判定装置12、体組成計14、及び情報処理装置16には、被測定者の年齢、性別、身長、及び体型等の患部回復判定処理に必要なユーザ情報が予め入力されている。なお、被測定者のユーザ情報は、サーバ(不図示)に記憶され、サーバから読み出されてもよい。 Next, with reference to FIGS. 8 to 10, the affected area recovery determination process by the affected area recovery determination system 10 will be described. Note that the affected area recovery determination process is executed by the information processing device 16, but before that, bioelectrical impedance/body weight acquisition process and local impedance acquisition process are performed. In addition, user information necessary for the affected area recovery determination process, such as the subject's age, sex, height, and body shape, is input in advance to the affected area determination device 12, body composition meter 14, and information processing device 16. Note that the user information of the person to be measured may be stored in a server (not shown) and read from the server.
 図8は、体組成計14によって実行される生体インピーダンス・体重取得処理の流れを示すフローチャートである。 FIG. 8 is a flowchart showing the flow of bioelectrical impedance/weight acquisition processing executed by the body composition meter 14.
 まず、ステップ100では、被測定者が載台42に載り、ハンドグリップ部40を把持する。 First, in step 100, the person to be measured stands on the stage 42 and grips the hand grip part 40.
 次のステップ102では、手電極40R,40L及び足裏電極46R,46Lに電流を流し、電位差を測定することで、被測定者の生体インピーダンスを測定する。 In the next step 102, the bioimpedance of the subject is measured by passing current through the hand electrodes 40R, 40L and the sole electrodes 46R, 46L and measuring the potential difference.
 次のステップ104では、被測定者の体重を測定する。 In the next step 104, the weight of the subject is measured.
 次のステップ106では、生体インピーダンス及び体重の測定結果を出力して処理を終了する。測定結果の出力は、情報処理装置16への測定結果の送信、モニタ48による測定結果の表示等である。 In the next step 106, the bioimpedance and body weight measurement results are output and the process ends. The output of the measurement results includes sending the measurement results to the information processing device 16, displaying the measurement results on the monitor 48, and the like.
 なお、本実施形態による生体インピーダンス・体重取得処理では、被測定者の体組成の算出は行わないが、これに限らず、生体インピーダンス及び体重を測定した後に体組成の算出が行われてもよい。算出された体組成は、情報処理装置16へ送信されてもよい。 Note that in the bioelectrical impedance/weight acquisition process according to the present embodiment, the body composition of the subject is not calculated, but the body composition is not limited to this, and the body composition may be calculated after measuring the bioelectrical impedance and weight. . The calculated body composition may be transmitted to the information processing device 16.
 また、被測定者に四肢の欠損がある場合には、欠損箇所を除いて全身の生体インピーダンスが測定される。例えば、左腕を欠損している被測定者であれば、左腕の欠損箇所の近辺に電極を配置し、右手で手電極40Rを把持することで、欠損部分を除いた全身の生体インピーダンスを測定できる。 Additionally, if the subject has a missing limb, the bioimpedance of the whole body is measured excluding the missing limb. For example, if a subject has a missing left arm, the bioimpedance of the whole body excluding the missing part can be measured by placing an electrode near the missing part of the left arm and grasping the hand electrode 40R with the right hand. .
 図9は、患部判定装置12によって実行される局所インピーダンス取得処理の流れを示すフローチャートである。 FIG. 9 is a flowchart showing the flow of local impedance acquisition processing executed by the affected area determination device 12.
 まず、ステップ200では、測定部20を被測定者の患部に配置する。このとき、患部判定装置12は、モニタ26に「患部をタッチしてください。」及び「測定箇所は前回と同じ患部でいいですか?」等の表示を行う。これにより、患部判定装置12は、測定者に被測定者における患部の位置の把握を促し、適切な位置に測定部20を配置させる。 First, in step 200, the measurement unit 20 is placed on the affected area of the person to be measured. At this time, the affected area determination device 12 displays on the monitor 26 messages such as "Please touch the affected area." and "Is it okay to use the same affected area as the previous measurement?" Thereby, the affected area determining device 12 prompts the measurer to grasp the position of the affected area in the person to be measured, and arranges the measuring section 20 at an appropriate position.
 ステップ202では、患部判定装置12の測定者による入力に応じて電流周波数及び電極間距離の設定を行う。電流周波数及び電極間距離は、例えば、タッチパネルディスプレイであるモニタ26を介して入力される。周波数設定部50は入力された電流周波数を設定する。設定される電流周波数は、患部の炎症度を判定するために、低周波数及び高周波数が設定される。 In step 202, the current frequency and inter-electrode distance are set according to input by the measurer of the affected area determination device 12. The current frequency and the inter-electrode distance are input via the monitor 26, which is a touch panel display, for example. The frequency setting section 50 sets the input current frequency. The current frequency to be set is a low frequency and a high frequency in order to determine the degree of inflammation of the affected area.
 次のステップ204では、設定された周波数の電流を電流印可制御部52が電流電極24Aに印可する。これにより、被測定者に接触している電極部24間に電流が流れる。 In the next step 204, the current application control unit 52 applies a current of the set frequency to the current electrode 24A. As a result, a current flows between the electrode sections 24 that are in contact with the person to be measured.
 次のステップ206では、電流が流れることによって生じる電圧を電圧電極24Bを介して電圧検出部54が検出する。 In the next step 206, the voltage detection section 54 detects the voltage generated by the current flowing through the voltage electrode 24B.
 次のステップ208では、電圧検出部54によって検出された電圧に基づいて、局所インピーダンス算出部56が局所インピーダンスを算出する。 In the next step 208, the local impedance calculation unit 56 calculates the local impedance based on the voltage detected by the voltage detection unit 54.
 次のステップ210では、被測定者の全ての所定部位及び異なる周波数による局所インピーダンスの測定が完了したか否かを判定し、肯定判定の場合はステップ204へ移行する。一方、否定判定の場合は局所インピーダンスの算出が完了するまで、ステップ204からステップ210を繰り返す。なお、所定部位には、被測定者の患部の他に、基準値を取得するための患部が生じていない部位が含まれる。 In the next step 210, it is determined whether the measurement of local impedance at all predetermined parts of the subject and at different frequencies has been completed, and in the case of an affirmative determination, the process moves to step 204. On the other hand, if the determination is negative, steps 204 to 210 are repeated until the local impedance calculation is completed. Note that the predetermined site includes, in addition to the affected area of the person to be measured, a site that does not have an affected area for obtaining a reference value.
 次のステップ212では、局所インピーダンスの測定結果及び測定時の電流周波数等の測定条件を出力して処理を終了する。測定結果の出力は、情報処理装置16への測定結果の送信、モニタ26による測定結果の表示等である。 In the next step 212, the measurement results of the local impedance and the measurement conditions such as the current frequency at the time of measurement are output, and the process ends. The output of the measurement results includes sending the measurement results to the information processing device 16, displaying the measurement results on the monitor 26, and the like.
 なお、本実施形態による局所インピーダンス取得処理では、患部判定装置12の患部状態判定部58による患部の状態判定は行わないが、これに限らず、局所インピーダンスを測定した後に患部状態判定部58による患部の状態判定が行われてもよい。患部の状態判定を行った場合、その判定結果が情報処理装置16へ送信されてもよい。 Note that in the local impedance acquisition process according to the present embodiment, the state of the affected area is not determined by the affected part state determining unit 58 of the affected part determining device 12, but the present invention is not limited to this, and after measuring the local impedance, the affected part state determining unit 58 A state determination may be made. When the state of the affected area is determined, the determination result may be transmitted to the information processing device 16.
 図10は、情報処理装置16で実行される患部回復判定処理の流れを示すフローチャートである。なお、患部回復判定処理における各判定結果及ぶ算出結果は、被測定者に関連付けて時系列で記憶部74に記憶される。 FIG. 10 is a flowchart showing the flow of the affected area recovery determination process executed by the information processing device 16. Note that each determination result and calculation result in the affected area recovery determination process is stored in the storage unit 74 in chronological order in association with the subject.
 まず、ステップ300では、患部判定装置12から局所インピーダンスの測定値、体組成計14から生体インピーダンス及び体重の測定値を通信部70が取得する。取得した各測定値は、記憶部74に記憶される。 First, in step 300, the communication unit 70 obtains the measured value of local impedance from the affected area determination device 12, and the measured values of biological impedance and body weight from the body composition meter 14. Each acquired measurement value is stored in the storage unit 74.
 次のステップ302では、取得した局所インピーダンスに基づいて、患部状態判定部80が患部の状態を判定する。 In the next step 302, the affected area state determination unit 80 determines the state of the affected area based on the acquired local impedance.
 次のステップ304では、取得した生体インピーダンス及び体重に基づいて、体組成算出部82が被測定者の全身筋肉量を算出する。 In the next step 304, the body composition calculation unit 82 calculates the whole body muscle mass of the subject based on the acquired bioelectrical impedance and body weight.
 次のステップ306では、当該被測定者の患部に対する回復予測線が算出されているか否かを判定し、肯定判定の場合はステップ310へ移行し、否定判定の場合はステップ308へ移行する。 In the next step 306, it is determined whether a recovery prediction line for the affected area of the subject has been calculated. If the determination is positive, the process moves to step 310, and if the determination is negative, the process moves to step 308.
 ステップ308では、ステップ302で判定した患部の状態とステップ304で算出した全身筋肉量とに基づいて、回復予測部84が回復予測線を算出し、ステップ316へ移行する。なお、算出された回復予測線及び回復時期は、被測定者に対応付けられて記憶部74に記憶される。 In step 308, the recovery prediction unit 84 calculates a recovery prediction line based on the condition of the affected area determined in step 302 and the whole body muscle mass calculated in step 304, and the process proceeds to step 316. Note that the calculated recovery prediction line and recovery time are stored in the storage unit 74 in association with the subject.
 ステップ308から移行したステップ316では、回復予測線及び回復時期をモニタ49が表示する。表示内容を確認しながら、被測定者のリハビリ計画が立案される。 In step 316, which is a transition from step 308, the monitor 49 displays the recovery prediction line and recovery time. A rehabilitation plan for the person to be measured is drawn up while checking the displayed contents.
 一方、ステップ306で肯定判定となった場合に移行するステップ310では、既に算出されている被測定者の回復予測線を記憶部74から読み出し、ステップ302で判定した患部の状態とステップ304で算出した全身筋肉量との回復予測線からの差異を回復状態判定部86が算出する。 On the other hand, in step 310 to which the transition is made when an affirmative determination is made in step 306, the already calculated predicted recovery line of the subject is read out from the storage unit 74, and the state of the affected area determined in step 302 and the predicted recovery line calculated in step 304 are read out. The recovery state determining unit 86 calculates the difference between the whole body muscle mass and the predicted recovery line.
 次のステップ312では、ステップ310で算出した差異に基づいて、回復状態判定部86が患部の回復状態及び全身筋肉量の回復状態を判定する。 In the next step 312, the recovery state determination unit 86 determines the recovery state of the affected area and the recovery state of the whole body muscle mass based on the difference calculated in step 310.
 次のステップ314では、ステップ310の判定結果に基づいて、アドバイス生成部88がアドバイスを生成する。 In the next step 314, the advice generation unit 88 generates advice based on the determination result in step 310.
 次のステップ316では、回復状態の判定結果及び生成されたアドバイスをモニタ49が表示する。この表示内容を確認しながら、必要に応じて、被測定者のリハビリ計画の修正が行われる。 In the next step 316, the monitor 49 displays the recovery state determination result and the generated advice. While checking the displayed contents, the rehabilitation plan of the subject is modified as necessary.
 以上、本開示を、上記実施形態を用いて説明したが、本開示の技術的範囲は上記実施形態に記載の範囲には限定されない。開示の要旨を逸脱しない範囲で上記実施形態に多様な変更又は改良を加えることができ、該変更又は改良を加えた形態も本開示の技術的範囲に含まれる。 Although the present disclosure has been described above using the above embodiments, the technical scope of the present disclosure is not limited to the range described in the above embodiments. Various changes or improvements can be made to the embodiments described above without departing from the gist of the disclosure, and forms with such changes or improvements are also included within the technical scope of the present disclosure.
 上記実施形態では、被測定者の患部の状態を局所インピーダンスに基づいて判定する形態について説明したが、本開示はこれに限らない。例えば、患部の状態を局所インピーダンスとは異なる患部指標に基づいて判定してもよい。 In the above embodiment, the state of the affected area of the subject is determined based on local impedance, but the present disclosure is not limited thereto. For example, the condition of the affected area may be determined based on an affected area index different from local impedance.
 すなわち患部指標は、被測定者の患部の状態を反映した指標であればよく、例えば、CRPとしてもよい。なお、CRPを患部指標として用いる場合には、例えば、患部(傷)の種類等、患部の状態をより正確に特定できる情報をさらに用いてもよい。また、患部指標として患部の場所、種類、及び形状を示すデータを情報処理装置16に入力し、患部状態判定部80がこれらのデータに基づいて患部の状態を判定してもよい。 In other words, the affected area index may be any index that reflects the condition of the affected area of the subject, and may be, for example, CRP. Note that when CRP is used as an index of the affected area, information that can more accurately specify the condition of the affected area, such as the type of the affected area (wound), may also be used. Alternatively, data indicating the location, type, and shape of the affected area may be inputted to the information processing device 16 as the affected area index, and the affected area state determining section 80 may determine the state of the affected area based on these data.
 上記実施形態では、体組成計14と情報処理装置16とが通信可能とされている形態について説明したが、本開示はこれに限らない。体組成計14と情報処理装置16とは通信しない形態としてもよい。この形態の場合、患部回復判定処理を行うために、体組成計14の計測結果を情報処理装置16に直接入力する。 In the embodiment described above, a configuration in which the body composition analyzer 14 and the information processing device 16 are able to communicate has been described, but the present disclosure is not limited to this. The body composition analyzer 14 and the information processing device 16 may not communicate with each other. In this case, the measurement results of the body composition analyzer 14 are directly input to the information processing device 16 in order to perform the process of determining recovery of the affected area.
 上記実施形態では、情報処理装置16が患部回復判定処理を行う形態について説明したが、本開示はこれに限らない。患部判定装置12及び体組成計14の測定結果をサーバが受信(取得)し、サーバが患部回復判定処理を行ってもよい。この形態の場合、患部回復判定処理の結果は、携帯端末装置等によって閲覧可能とされる。 In the above embodiment, the information processing device 16 performs the affected part recovery determination process, but the present disclosure is not limited to this. The server may receive (acquire) the measurement results of the affected area determining device 12 and the body composition meter 14, and the server may perform the affected area recovery determination process. In this case, the results of the affected area recovery determination process can be viewed using a mobile terminal device or the like.
 10  患部回復判定システム
 16  情報処理装置(患部回復判定装置)
 80  患部状態判定部(患部状態判定手段)
 84  回復予測部(予測手段)
 86  回復状態判定部(回復状態判定部)
 88  アドバイス生成部(アドバイス生成手段)
10 Affected area recovery determination system 16 Information processing device (affected area recovery determination device)
80 Affected area condition determination unit (affected area condition determination means)
84 Recovery prediction unit (prediction means)
86 Recovery state determination unit (Recovery state determination unit)
88 Advice generation unit (advice generation means)

Claims (10)

  1.  被測定者の患部の状態を反映した患部指標を取得する取得手段と、
     前記取得手段によって取得された前記患部指標に基づいて、前記患部の状態を判定する患部状態判定手段と、
     前記患部状態判定手段によって判定された前記患部の状態と被測定者の全身指標とに基づいて、患部の回復時期を予測する予測手段と、
    を備えた患部回復判定装置。
    an acquisition means for acquiring an affected area index that reflects the condition of the affected area of the subject;
    Affected area condition determination means for determining the condition of the affected area based on the affected area index acquired by the acquisition means;
    prediction means for predicting recovery time of the affected area based on the condition of the affected area determined by the affected area condition determination means and the whole body index of the subject;
    An affected area recovery determination device.
  2.  前記患部指標は、被測定者の患部を含む部位のインピーダンスである、請求項1に記載の患部回復判定装置。 The affected area recovery determination device according to claim 1, wherein the affected area index is an impedance of a part of the subject including the affected area.
  3.  前記全身指標は、被測定者の全身筋肉量である、請求項1又は請求項2に記載の患部回復判定装置。 The affected area recovery determination device according to claim 1 or 2, wherein the whole body index is the whole body muscle mass of the subject.
  4.  前記予測手段は、被測定者の全身筋肉量が多いほど回復速度が速くなるように前記回復時期を予測する、請求項3に記載の患部回復判定装置。 The affected area recovery determination device according to claim 3, wherein the prediction means predicts the recovery time so that the greater the whole body muscle mass of the subject, the faster the recovery speed.
  5.  過去に前記予測手段によって予測した前記回復時期に基づく患部の予測回復状態と前記患部状態判定手段によって判定された現在の前記患部の状態との差異に基づいて、患部の回復状態を判定する回復状態判定手段を備えた、請求項1から請求項4の何れか1項に記載の患部回復判定装置。 A recovery state in which the recovery state of the affected area is determined based on the difference between the predicted recovery state of the affected area based on the recovery time predicted by the prediction means in the past and the current state of the affected area determined by the affected area state determination means. The affected area recovery determining device according to any one of claims 1 to 4, comprising determining means.
  6.  前記回復状態判定手段は、前記患部の回復状態及び前記全身指標の回復状態を判定する、請求項5に記載の患部回復判定装置。 The affected area recovery determining device according to claim 5, wherein the recovery state determining means determines the recovery state of the affected area and the recovery state of the whole body index.
  7.  前記回復状態判定手段の判定結果に基づいて、患部の回復に関するアドバイスを生成するアドバイス生成部を備える、請求項5又は請求項6に記載の患部回復判定装置。 The affected area recovery determining device according to claim 5 or 6, further comprising an advice generation unit that generates advice regarding recovery of the affected area based on the determination result of the recovery state determining means.
  8.  被測定者の患部の状態を反映した患部指標を取得する第1工程と、
     前記第1工程によって取得された前記患部指標に基づいて、前記患部の状態を判定する第2工程と、
     前記第2工程によって判定された前記患部の状態と被測定者の全身指標とに基づいて、患部の回復時期を予測する第3工程と、
    を有する患部回復判定方法。
    A first step of obtaining an affected area index that reflects the condition of the affected area of the subject;
    a second step of determining the state of the affected area based on the affected area index obtained in the first step;
    a third step of predicting the recovery time of the affected area based on the condition of the affected area determined in the second step and the whole body index of the subject;
    A method for determining recovery of an affected area.
  9.  被測定者の患部の状態を反映した患部指標を取得手段によって取得する情報処理装置のコンピュータを、
     前記取得手段によって取得された前記患部指標に基づいて、前記患部の状態を判定する患部状態判定手段と、
     前記患部状態判定手段によって判定された前記患部の状態と被測定者の全身指標とに基づいて、患部の回復時期を予測する予測手段と、
    して機能させるための患部回復判定プログラム。
    A computer of an information processing device that uses an acquisition means to acquire an affected area index that reflects the condition of the affected area of the subject;
    Affected area condition determination means for determining the condition of the affected area based on the affected area index acquired by the acquisition means;
    prediction means for predicting recovery time of the affected area based on the condition of the affected area determined by the affected area condition determination means and the whole body index of the subject;
    A program to determine the recovery of the affected area so that it can function properly.
  10.  請求項9に記載の患部回復判定プログラムを記憶した、コンピュータ読取可能な非一時的記憶媒体。
     

     
    A computer-readable non-temporary storage medium storing the affected area recovery determination program according to claim 9.


PCT/JP2023/012712 2022-03-31 2023-03-28 Lesion healing determination device, lesion healing determination method, lesion healing determination program, and computer-readable non-transitory storage medium WO2023190627A1 (en)

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001187035A (en) * 1999-12-28 2001-07-10 Tanita Corp Lesion recovery degree judging device
JP2005095384A (en) * 2003-09-25 2005-04-14 Yamato Scale Co Ltd Affected part recovery condition determination apparatus and program
WO2019132013A1 (en) * 2017-12-28 2019-07-04 株式会社タニタ Condition evaluation device, condition evaluation method, and program
JP2022062321A (en) * 2020-10-08 2022-04-20 株式会社タニタ Measuring apparatus

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001187035A (en) * 1999-12-28 2001-07-10 Tanita Corp Lesion recovery degree judging device
JP2005095384A (en) * 2003-09-25 2005-04-14 Yamato Scale Co Ltd Affected part recovery condition determination apparatus and program
WO2019132013A1 (en) * 2017-12-28 2019-07-04 株式会社タニタ Condition evaluation device, condition evaluation method, and program
JP2022062321A (en) * 2020-10-08 2022-04-20 株式会社タニタ Measuring apparatus

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