WO2021090531A1 - Artificial pancreas - Google Patents

Artificial pancreas Download PDF

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Publication number
WO2021090531A1
WO2021090531A1 PCT/JP2020/025580 JP2020025580W WO2021090531A1 WO 2021090531 A1 WO2021090531 A1 WO 2021090531A1 JP 2020025580 W JP2020025580 W JP 2020025580W WO 2021090531 A1 WO2021090531 A1 WO 2021090531A1
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WO
WIPO (PCT)
Prior art keywords
venous blood
main body
blood
artificial pancreas
unit
Prior art date
Application number
PCT/JP2020/025580
Other languages
French (fr)
Japanese (ja)
Inventor
孝 浅香
仁是 佐藤
Original Assignee
テルモ株式会社
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Publication of WO2021090531A1 publication Critical patent/WO2021090531A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/1455Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using optical sensors, e.g. spectral photometrical oximeters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/1486Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using enzyme electrodes, e.g. with immobilised oxidase
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/142Pressure infusion, e.g. using pumps

Definitions

  • the present invention relates to an artificial pancreas that realizes stable blood glucose control in patients after highly invasive surgery.
  • Factor (1) is excessive secretion of hormones that raise blood glucose levels due to invasive stress caused by general anesthesia or surgery.
  • the factor (2) is a decrease in the blood glucose level suppressing function due to an increase in insulin resistance due to the physiological stress of surgery.
  • the blood glucose level rises, and depending on the degree of invasiveness, the blood glucose level becomes higher than usual for 3 to 7 days.
  • hyperglycemic symptoms become more prominent. Hyperglycemic conditions reduce the patient's protective function against infection, resulting in a high postoperative infectious complication rate and mortality rate.
  • the patient group when strict blood glucose control of 80 to 120 mg / dl by intensive insulin therapy (frequent insulin injection) is performed is 180 to 200 mg / dl. It was reported that the mortality rate was reduced, bloodstream infection was suppressed, dialysis treatment was suppressed, and the length of hospital stay in the ICU was shortened for the group of patients with relatively loose glycemic control.
  • the risk of hypoglycemia caused by demanding strict glycemic control was pointed out, and the validity of strict glycemic control was controversial. against this background, we want to strictly control blood glucose, but because of the high risk of frequent hypoglycemia, the trend is to loosely control blood glucose for diabetic patients after surgery, which is currently highly invasive. There is.
  • the blood glucose control of patients after surgery is classified into three types, which are the widely used sliding scale method, continuous insulin administration method, and artificial pancreas.
  • the implementation of the sliding scale method and the continuous insulin administration method is actually difficult to carry out strict glycemic control (for example, glycemic control of 80 to 120 mg / dl).
  • the reason for the difficulty is as follows.
  • healthcare professionals are always responsible for multiple patients. It is practically impossible for a healthcare professional to frequently measure the blood glucose level and administer insulin to each patient in order to keep track of the blood glucose level trend of each patient.
  • blood glucose measurement does not necessarily measure blood gas with an accuracy of ⁇ 2 to 3%, but there are variations in measured values due to measurement performed by a self-measuring machine with an accuracy of about ⁇ 10%.
  • the device performs all of blood glucose measurement, drug dose calculation, and drug administration work. Therefore, the artificial pancreas can realize strict blood glucose control from the viewpoints of risk reduction, cost reduction, and effective utilization of resources.
  • Patent Document 1 discloses an artificial pancreas.
  • This artificial pancreas is suitable for a drug solution that causes fluctuations in blood glucose level such as insulin when a patient falls into a hypoglycemic state due to injury or illness of a patient or the like who is in a surgically hyperglycemic state invaded by surgery or injury or illness. Can be administered to.
  • the conventional artificial pancreas has a large device and requires complicated operations, and is mounted on a stand for movement.
  • Conventional artificial pancreas is used by moving the stand on the floor so that it is placed near the patient.
  • conventional artificial pancreas is capable of strict blood glucose control after surgery, it is difficult to use clinically because it requires large and complicated operations. Also, it is not easy to move a large artificial pancreas as the patient moves.
  • the present invention has been made to solve the above problems, and provides an easy-to-use artificial pancreas that can easily and surely realize stable blood glucose control of a diabetic patient after a highly invasive surgery.
  • the purpose is to do.
  • the subject is an artificial pancreas that controls blood glucose in a living body according to the present invention, and is arranged in a main body portion, a control unit arranged in the main body portion, and the main body portion.
  • a venous blood feeding section that passes venous blood obtained from the living body through the main body and returns the venous blood to the living body, and a venous blood feeding section that is arranged in the main body and passes through the main body by the venous blood feeding section.
  • a blood glucose level measuring unit that measures the blood glucose level of the venous blood and notifies the control unit of the blood glucose level
  • a connecting portion that is arranged in the main body and connects a drug solution cartridge for storing the drug solution, and the blood glucose level.
  • control unit When notified to the control unit, the control unit is characterized by comprising a drug solution administration operation unit for administering a predetermined amount of the drug solution according to the blood glucose level to the venous blood from the drug solution cartridge. Achieved by the artificial pancreas.
  • the main body portion only needs to be attached to a suitable place of a living body part of a patient, for example.
  • the blood glucose level measuring unit measures the blood glucose level of the venous blood passing through the main body and controls the blood glucose level.
  • the control unit operates the drug solution administration operation unit to administer a predetermined amount of the drug solution according to the blood glucose level from the drug solution cartridge to the venous blood in the venous blood flow path portion.
  • the blood glucose level can be measured and the drug solution can be administered according to the blood glucose level simply by passing venous blood through the main body. Therefore, the artificial pancreas can easily and surely realize stable glycemic control of highly invasive post-surgery patients, especially diabetic patients, and is easy to use, even if the medical staff does not always manage it. become.
  • the drug solution cartridge is an insulin cartridge that administers insulin to the venous blood in the venous blood flow path when the blood glucose level is larger than a predetermined value, and the above. It is characterized by having a glucose cartridge for administering glucose to the venous blood in the venous blood flow path portion when the blood glucose level is smaller than a predetermined value.
  • the main body is attached to a suitable place in the living body of the patient, insulin is added to the venous blood in the venous blood flow path when the blood glucose level is larger than a predetermined value.
  • insulin is added to the venous blood in the venous blood flow path when the blood glucose level is larger than a predetermined value.
  • Can be administered, and glucose can be administered to venous blood in the venous blood flow path when the blood glucose level is smaller than a predetermined value. Therefore, the artificial pancreas can easily and surely realize stable glycemic control of diabetic patients after highly invasive surgery.
  • the venous blood pumping portion is arranged along the main body portion to guide the venous blood, and the venous blood obtained from the living body is described as described above. It is characterized by having a liquid feeding pump that returns to the living body after passing through a guide line portion.
  • venous blood can be passed along the main body portion through this guide conduit portion. In this way, the blood glucose level measurement work and the drug solution administration work can be reliably performed while the venous blood is passed through the guide tube portion.
  • the main body portion is formed in a ring shape, and the main body portion is held at an appropriate position of the living body through a part of the living body.
  • the main body portion is formed in a ring shape, the main body portion can be held by the arm through, for example, a hand, which is a part of the patient's living body at an appropriate position. Therefore, the main body can be easily and surely held in the living body.
  • the invention according to claim 5 is preferably characterized in that a battery for supplying power to the control unit, the drug solution administration operation unit, and the liquid delivery pump is arranged in the main body unit.
  • the guide line portion is arranged so as to make substantially a circle in the main body portion, and the control unit is the vein when the venous blood passes through the guide line portion. It is characterized by completing the measurement of the blood glucose level of blood, the determination of the dose of the drug solution to the venous blood, and the operation of administering the drug solution to the venous blood.
  • the venous blood control unit measures the blood glucose level of the venous blood, determines the dose of the drug solution to the venous blood, and administers the drug solution to the venous blood when the venous blood passes through the guide tube. Can be completed.
  • the guide conduit portion returns the first lumen through which the venous blood has passed from the living body into the main body and the venous blood having passed through the main body into the living body. It has a second lumen, and the first lumen and the second lumen are arranged in parallel and connected to an indwelling needle.
  • the route for flowing venous blood is to obtain venous blood from a living body using one indwelling needle and the first and second lumens, measure the blood glucose level, and if necessary, a drug solution. Can be returned to the living body after administration of.
  • the antithrombotic drug solution supply unit for supplying the antithrombotic drug to the venous blood and the physiological saline supply unit for supplying the physiological saline to the venous blood are the main bodies. It is characterized by being connected to a unit.
  • the main body portion to be attached to a suitable part of the living body is C-shaped.
  • the main body portion when the main body portion is C-shaped, it can be attached or detached from a direction intersecting with the arm, for example, as compared with the case where the main body portion is a ring type. This makes it even easier to attach and remove the artificial pancreas.
  • the power supply unit for supplying power to the control unit, the chemical solution administration operation unit, and the liquid supply pump is arranged outside the main body unit. And.
  • the artificial pancreas can be operated by receiving the power supply from the power supply unit arranged outside the main body.
  • the present invention it is possible to provide an easy-to-use artificial pancreas that can easily and surely realize stable blood glucose control of a diabetic patient after a highly invasive surgical operation.
  • FIG. 1st Embodiment of the artificial pancreas of this invention It is a figure which shows the state which actually uses the preferable 1st Embodiment of the artificial pancreas of this invention. It is a front view which shows the artificial pancreas shown in FIG. It is a figure which shows the internal composition example of the artificial pancreas shown in FIG. It is a figure which shows the internal composition example of the artificial pancreas shown in FIG. It is a figure which shows the preferable 2nd Embodiment of the artificial pancreas of this invention. It is a figure which shows the preferable 3rd Embodiment of the artificial pancreas of this invention.
  • FIG. 1 is a diagram showing a state in which a preferred first embodiment of the artificial pancreas of the present invention is actually used.
  • FIG. 2 is a front view showing the artificial pancreas 1 shown in FIG.
  • FIG. 3 is a diagram showing an example of the internal configuration of the artificial pancreas 1 shown in FIG.
  • the artificial pancreas 1 shown in FIGS. 1 to 3 performs stable blood glucose control of patients after highly invasive surgery, particularly stable blood glucose control of diabetic patients.
  • the artificial pancreas 1 is a so-called disposable compact medical device that is preferably used only once. However, the artificial pancreas 1 may be regenerated and reusable.
  • the artificial pancreas 1 can also be referred to as a ring-type artificial pancreas set.
  • the artificial pancreas 1 is easily attached to a suitable part of the patient's body, for example, as shown in FIG. 1, on the patient's arm 300, and the artificial pancreas 1 is integrated with the patient.
  • the artificial pancreas 1 can be expected to solve the problem of tube handling when the patient moves from place to place.
  • the therapy with artificial pancreas 1 performs all blood glucose measurement, drug dose calculation and drug administration work.
  • healthcare professionals are often in charge of multiple patients at all times.
  • the medical staff can always easily and surely grasp the blood glucose level trend of each patient. Therefore, the artificial pancreas 1 is suitable for highly invasive post-surgical patients, especially diabetic patients, from the viewpoints of risk reduction by strict blood glucose control, cost reduction by miniaturization, and effective utilization of resources. , Stable and strict blood glucose control is feasible.
  • the artificial pancreas 1 is roughly composed of a main body portion 2, a venous blood feeding unit 3, a blood glucose level measuring unit 4, a connecting unit 5, and a drug solution administration operating unit 6A. , 6B and a control unit 10.
  • the main body 2 also has a battery 9.
  • the battery 9 is built in the main body 2, and a primary battery such as a button battery can be used. For example, power is supplied to each element described later for at least 5 to 6 hours or more.
  • the type of the battery 9 is not particularly limited, and the duration of the battery 9 is not particularly limited and can be set arbitrarily.
  • the main body 2 shown in FIGS. 1 to 3 is made of, for example, a material such as plastic or silicon that does not cause any problem even if it comes into contact with a living body.
  • the main body portion 2 is, for example, a ring-shaped member having no break along the circumferential direction and having a hollow portion 2H along the circumferential direction as shown in FIG. That is, the artificial pancreas 1 is a bracelet-shaped pancreas device.
  • the main body 2 is preferably transparent or translucent so that the medical staff can see the state of venous blood passing through the inside, but may be opaque if it is not necessary.
  • the inner diameter D1 of the main body 2 shown in FIG. 1 is preferably set in the range of 40 mm to 80 mm so that the main body 2 can be held through the patient's arm 300.
  • the outer diameter D2 is preferably set in the range of 70 mm to 120 mm. It is preferable to prepare several sizes of the main body 2 in advance so that the inner diameter D1 and the outer diameter D2 of the main body 2 can be selected according to the physique and age of the patient.
  • the main body 2 is formed by an outer peripheral surface 2A, an inner peripheral surface 2B, and left and right side surfaces 2C and 2C.
  • the outer peripheral surface 2A, the inner peripheral surface 2B, and the left and right side surfaces 2C and 2C have a ring-shaped hollow portion 2H inside.
  • a non-slip sheet can be arranged on the inner peripheral surface 2B, if necessary, so that the main body 2 does not rotate with respect to the arm 300.
  • FIG. 4 is a diagram showing an example of the venous blood feeding unit 3.
  • the venous blood feeding unit 3 shown in FIGS. 3 and 4 is arranged in the main body 2, and the venous blood obtained from the arm 300 of the patient who is a living body is passed through the main body 2 for almost one round, and the venous blood is passed through the arm 300. It has a function to return to.
  • the venous blood feeding unit 3 has a guide line portion 11 and a liquid feeding pump 12.
  • the guide pipeline portion 11 is arranged substantially once along the circular hollow portion 2H of the main body portion 2, and the guide pipeline portion 11 is arranged in a circular shape along the hollow portion 2H.
  • One end portion 11P of the guide conduit portion 11 extends from the hollow portion 2H of the main body portion 2 to the outside of the main body portion 2 as a flexible first lumen 11A formed of a thermoplastic resin or the like.
  • the other end 11Q of the guide conduit portion 11 extends from the hollow portion 2H of the main body portion 2 to the outside of the main body portion 2 as a flexible second lumen 11B formed of a thermoplastic resin or the like.
  • a flexible first lumen 11A formed of a thermoplastic resin or the like
  • the other end 11Q of the guide conduit portion 11 extends from the hollow portion 2H of the main body portion 2 to the outside of the main body portion 2 as a flexible second lumen 11B formed of a thermoplastic resin or the like.
  • Such a venous blood feeding route has a double lumen structure having a first lumen 11A and a second lumen 11B.
  • FIG. 4 shows a preferable structural example of the indwelling needle (indwelling catheter) 13.
  • the indwelling needle 13 has two lumens, an intake side tube portion 13A for taking in blood from the vein and a return side tube portion 13B for returning blood to the vein.
  • One end side of the intake side tube portion 13A is liquidtight by being fitted inside the first lumen 11A by providing a rib of a predetermined height or a groove of a predetermined depth in the circumferential direction of the outer circumference thereof. It is connected to the.
  • one end side of the return side tube portion 13B is liquidtightly connected by being fitted inside the second lumen 11B by providing a rib or a groove in the circumferential direction of the outer circumference thereof.
  • the intake side tube portion 13A has an intake flow path 13C shown by a broken line, and this intake flow path 13C is connected to the first lumen 11A and reaches the tip opening 13D of the indwelling needle 13.
  • the return side tube portion 13B has a return flow path 13E as shown by a broken line, and the return flow path 13E is connected to the second lumen 11B and reaches the return opening 13F. ing.
  • the tip opening 13D is formed at the tip of the indwelling needle 13, whereas the return opening 13F is formed at a position in the middle of the indwelling needle 13. That is, the tip opening 13D and the return opening 13F are located at positions separated by a predetermined distance in the axial direction of the indwelling needle 13. However, the tip opening 13D and the return opening 13F are both located in the blood vessel of the vein when the indwelling needle 13 is pierced into the blood vessel.
  • the liquid feed pump 12 is arranged in the main body 2.
  • the liquid feed pump 12 is configured to sequentially press the elastically deformable guide pipe portion 11 by, for example, a plurality of fingers (not shown) pulsating in the middle of the guide pipe portion 11.
  • the liquid feed pump 12 can send a predetermined amount (mL / h) of venous blood from the vein to the main body 2.
  • a peristaltic type peripheral type
  • the control unit 10 has a blood glucose control start button 40 for venous blood.
  • the indwelling needle 13 is pierced into the vein of the arm 300 and indwelled.
  • an indwelling needle having an outer cylinder made of flexible plastic and an inner cylinder of a metal needle for puncture is used and made of flexible plastic in the vein.
  • the outer cylinder (not shown) of the above the inner cylinder of the metal needle for puncture is pulled out, and then the indwelling needle 13 using the outer cylinder made of flexible plastic (not shown) as a guide portion. Is placed in the vein of the arm 300 by inserting.
  • the liquid feeding pump 12 is operated by the command of the control unit 10.
  • the liquid feeding pump 12 is activated, the patient's venous blood is fed from the indwelling needle 13 in the feeding direction M, as shown in FIGS. 1 and 4.
  • Venous blood is guided around the guide line portion 11 in the main body portion 2 in the R direction through the intake side tube portion 13A and the first lumen 11A.
  • Venous blood is sent once in the main body 2, and the blood glucose level is measured during the delivery, and insulin or a predetermined concentration of glucose (predetermined concentration of glucose solution) is administered in a small amount according to the blood glucose level.
  • Examples of the applicable insulin include fast-acting insulin of human insulin preparation, super-fast-acting insulin analog of mixed human insulin and insulin analogy preparation, biphasic insulin analog, combined dissolved insulin analog and the like.
  • the blood glucose level measuring unit 4 shown in FIG. 3 is arranged in the main body 2 near the guide tube portion 11 of the venous blood feeding unit 3.
  • the blood glucose level of the venous blood that is sent by going around the guide tube portion 11 of the venous blood feeding section 3 is preferably continuously non-invasive and for venous blood. Measure without contact.
  • the blood glucose level measuring unit 4 notifies the control unit 10 of the blood glucose level measurement data DT.
  • the blood glucose level measuring unit 4 exerts a continuous blood glucose monitoring function for continuously measuring the blood glucose level of venous blood.
  • the glucose sensor as the detection means of the blood glucose level measuring unit 4
  • near infrared (700 to 1050 nm) spectroscopy is preferably used.
  • this near-infrared spectroscopy when measuring changes in blood glucose level over time, the measured values of blood glucose level are obtained at a plurality of elapsed times, and the veins are irradiated with near-infrared light to obtain the measured values from the veins.
  • the absorbance for each of a plurality of wavelengths is obtained in the near infrared set wavelength range, the wavelength having a high correlation with the measured value is specified, and the absorbance at the specified wavelength is used.
  • a calculation formula for calculating the measured value is derived, and at another elapsed time, the vein is irradiated with near-infrared light, the diffused reflected light or transmitted light from the vein is received, and the absorbance at the specified wavelength is obtained.
  • the blood glucose level is calculated from the above formula, but the near-infrared spectroscopy is not particularly limited. Further, as the glucose sensor which is the detecting means of the blood glucose level measuring unit 4, for example, an enzyme electrode or the like may be used.
  • connection unit 5 and the drug solution administration operation units 6A and 6B will be described.
  • the connecting portion 5 is attached with the chemical solution administration operating portions 6A and 6B side by side.
  • a diaphragm type microinjection pump can be adopted.
  • the connecting portion 5 is provided on the side surface 2C of the main body portion 2, and is preferably made of the same plastic material as the main body portion 2.
  • the main body 2 detachably connects the insulin cartridge 21 and the glucose cartridge 22 in order to increase or decrease the blood glucose level of venous blood.
  • the insulin cartridge 21 and the glucose cartridge 22 are examples of chemical cartridges.
  • Insulin is stored in the insulin cartridge 21.
  • insulin When insulin is administered in small amounts to venous blood, it lowers the blood sugar level in venous blood.
  • Glucose is stored in the glucose cartridge 22.
  • glucol When glucol is administered in small amounts to venous blood, it raises the blood sugar level in venous blood.
  • the insulin cartridge 21 and the glucose cartridge 22 are the same size, but for example, the insulin cartridge 21 is colored red and the glucose cartridge 22 is colored blue so that they can be easily distinguished visually.
  • the insulin cartridge 21 is detachably connected to the drug solution administration operation unit 6A at the connection unit 5.
  • the glucose cartridge 22 is detachably connected to the drug solution administration operation unit 6B at the connection unit 5.
  • the control unit 10 shown in FIG. 3 is a drug solution administration operation unit 6A on the insulin cartridge 21 side based on the blood glucose level measurement data DT of venous blood that substantially goes around the guide tube portion 11 obtained by the blood glucose level measurement unit 4. Or drive the drug solution administration operation unit 6B on the glucose cartridge 22 side.
  • the control unit 10 has a memory 10M, and the memory 10M stores software of an algorithm for calculating an insulin dose and a glucose dose from the blood glucose level measurement data DT.
  • the control unit 10 drives the drug solution administration operation unit 6A. Then, the insulin of the insulin cartridge 21 is administered in a small amount into the venous blood passing through the guide tube portion 11 to lower the blood glucose level of the venous blood. Further, when the blood glucose level measurement data DT of venous blood that substantially goes around the guide tube portion 11 is smaller than the predetermined blood glucose level data, the control unit 10 drives the drug solution administration operation unit 6B.
  • Glucose of the glucose cartridge 22 is administered in a small amount into the venous blood passing through the guide tube portion 11 to raise the blood glucose level of the venous blood.
  • the control unit 10 receives a predetermined amount of insulin or a predetermined amount of glucose according to the magnitude of the blood glucose level of venous blood. Is administered in a small amount to the venous blood in the venous blood flow path to control the blood glucose level.
  • the display unit 30 may be arranged in the main body unit 2.
  • the display unit 30 can display the blood glucose level of venous blood, the amount of insulin administered in a small amount, and the amount of glucose administered in a small amount.
  • the battery 9 supplies power to the control unit 10, the blood glucose level measuring unit 4, and the liquid feeding pump 12.
  • the antithrombotic drug supply unit 41 is connected to the bag 41B containing the antithrombotic drug.
  • the saline supply unit 42 is connected to a bag 42B containing the saline solution.
  • the antithrombotic drug supply unit 41 is a drug solution supply unit that supplies an antithrombotic drug into venous blood passing through the guide tube portion 11 of the main body 2 as needed.
  • the physiological saline supply unit 42 smoothly flows an antithrombotic drug, for example, heparin, into the venous blood passing through the guide tube portion 11 of the main body 2 as needed. Supply.
  • valve 41G By opening the valve 41G, the antithrombotic drug in the bag 42B can be administered into the venous blood passing through the guide tube section 11 via the antithrombotic drug supply section 41.
  • the valve 42G By opening the valve 42G, the saline solution in the bag 42B can be administered into the venous blood passing through the guide tube portion 11 via the saline solution supply unit 42.
  • the valves 41G and 42G can be opened and closed manually. However, as shown in FIG. 3, the valves 41G and 42G may be opened and closed by a command from the control unit 10.
  • FIGS. 1 and 2 show an example of blood glucose control of venous blood by the artificial pancreas 1 described above with reference to FIGS. 1 to 4.
  • the insulin cartridge 21 is detachably connected to the drug solution administration operation unit 6A at the connection unit 5.
  • the glucose cartridge 22 is detachably connected to the drug solution administration operation unit 6B at the connection unit 5.
  • the inner peripheral surface 2B of the main body 2 is held at an appropriate position of the arm 300 when the main body 2 is inserted from the patient's hand.
  • the indwelling needle 13 is pierced into the vein of the arm 300, and the indwelling needle 13 is indwelled in the vein so as not to move, for example, using a tape.
  • an indwelling needle (not shown) having an outer cylinder made of flexible plastic and an inner cylinder of a metal needle for puncture can be used intravenously.
  • the inner cylinder of the metal needle for puncture is pulled out, and then the indwelling needle 13 using the outer cylinder made of flexible plastic (not shown) as a guide portion. Is placed in the vein of the arm 300 by inserting.
  • the tip opening 13D and the return opening 13F shown in FIG. 4 are both located in the vein of the vein.
  • the venous blood is taken into the intake flow path 13C from the tip opening 13D along the feeding direction M, and is taken into the first lumen 11A via the intake flow path 13C as the collected venous blood.
  • the venous blood returned after passing through the second lumen 11B venous blood whose blood glucose level is adjusted by containing insulin and / or glucose
  • the return opening 13F is located at a position separated from the indwelling needle 13 in the axial direction.
  • the liquid feed pump 12 is operated by the command of the control unit 10.
  • a predetermined amount of venous blood is fed in the feeding direction M as shown in FIGS. 1 and 4.
  • Venous blood is guided through the first lumen 11A through the guide conduit portion 11 in the main body portion 2 for substantially one round in the R direction.
  • the venous blood whose blood glucose level has been measured is returned to the vein of the arm along the return direction N through the indwelling needle 13 through the second lumen 11B and the same route.
  • the intake side tube portion 13A and the first lumen 11A of the indwelling needle 13 are used. Due to the double lumen structure using 13B, the first lumen 11A and the second lumen 11B, venous blood discharged from the body is returned to the body through the indwelling needle 13 by the same route.
  • the antithrombotic drug supply unit 41 supplies the antithrombotic drug into the venous blood passing through the guide tube portion 11 of the main body 2 as needed. Further, the physiological saline supply unit 42 supplies the physiological saline solution, if necessary, in order to smoothly flow the antithrombotic drug into the venous blood passing through the guide tube portion 11 of the main body portion 2.
  • the blood glucose level measuring unit 4 continuously measures the blood glucose level of the venous blood to be delivered in a non-invasive and non-contact manner on the way around the guide tube portion 11 of the venous blood feeding unit 3.
  • the blood glucose level measuring unit 4 notifies the control unit 10 of the blood glucose level measurement data DT while continuously measuring the blood glucose level of venous blood.
  • control unit 10 is a drug solution administration operation unit on the insulin cartridge 21 side based on the blood glucose level measurement data DT of venous blood that substantially goes around the guide tube portion 11 obtained by the blood glucose level measurement unit 4. 6A is driven, or the drug solution administration operation unit 6B on the glucose cartridge 22 side is driven.
  • the control unit 10 calculates the insulin dose and the glucose dose from the blood glucose level measurement data DT.
  • the control unit 10 drives the drug solution administration operation unit 6A. Then, the insulin of the insulin cartridge 21 is administered in a small amount into the venous blood passing through the guide tube portion 11 to lower the blood glucose level of the venous blood. Further, when the blood glucose level measurement data DT of venous blood that substantially goes around the guide tube portion 11 is smaller than the predetermined blood glucose level data, the control unit 10 drives the drug solution administration operation unit 6B. , Glucose of the glucose cartridge 22 is administered in a small amount into the venous blood passing through the guide tube portion 11 to raise the blood glucose level of the venous blood.
  • the control unit 10 applies a predetermined amount of insulin or a predetermined amount of glucose according to the magnitude of the blood glucose level of venous blood to the insulin cartridge 21 or glucose.
  • Blood glucose is controlled by injecting venous blood in the venous blood flow path from the cartridge 22.
  • the display unit 30 shown in FIG. 2 preferably displays the blood glucose level of venous blood, the amount of insulin administered in a small amount, and the amount of glucose administered in a small amount, so that the medical staff can confirm these values. it can.
  • the main body portion only needs to be attached to the part of the living body of the patient.
  • the blood glucose level measuring unit measures the blood glucose level of the venous blood passing through the main body and controls the blood glucose level.
  • the control unit operates the drug solution administration operation unit to administer a predetermined amount of the drug solution according to the blood glucose level from the drug solution cartridge to the venous blood in the venous blood flow path portion.
  • the blood glucose level can be measured and the drug solution can be administered according to the blood glucose level simply by passing venous blood through the main body. Therefore, even if the medical staff does not always manage it, it is possible to prevent poor blood sampling and easily and easily perform stable glycemic control of highly invasive patients after surgery, especially stable glycemic control of diabetic patients. It can be realized reliably and is easy to use.
  • the artificial pancreas of the first embodiment only needs to be attached to the patient's arm, for example.
  • the artificial pancreas is lightweight, small in size, inexpensive to manufacture, and easy to manage. Therefore, the artificial pancreas is easily available, and the artificial pancreas can be easily set or removed from the patient.
  • the venous blood from the patient can be taken out of the living body, the blood glucose level of the venous blood can be measured, and the venous blood feeding route for the minute administration of the drug solution can be easily secured.
  • the artificial pancreas is attached to the patient's arm, it can easily move with the patient when the patient moves.
  • the mortality rate can be improved by improving the blood glucose control of patients, improving the incidence of infection at the surgical site, and preventing the prognosis from deteriorating. It is possible to reduce the risk of hyperglycemia / hypoglycemia in medical staff, reduce the amount of work required for measuring blood glucose level and administering insulin and glycosyl, and unify the criteria for drug administration. For hospitals, the number of beds can be improved by improving the prognosis of patients.
  • the main body of the artificial pancreas of the first embodiment is a so-called ring type, it can be easily attached to the arm, which is one of the appropriate places for attaching the main body, by passing the patient's arm through the main body. Therefore, by using the artificial pancreas, the medical staff is freed from the complicated handling of the tube, which has been a problem when applying the artificial pancreas to the patient.
  • Venous blood can be completed with a small dose of insulin or a small dose of glucose.
  • the conventional artificial pancreas is mounted on a stand for movement because the device is large and requires complicated operations.
  • the conventional artificial pancreas is used by arranging it near the patient by moving the floor surface, and a large-scale and complicated operation is performed by a medical worker such as a nurse.
  • the artificial pancreas of the first embodiment when the artificial pancreas is attached to a part of the patient, for example, the arm, the measurement of the blood glucose level of venous blood is started and the vein is venous according to the blood glucose level.
  • a small amount of insulin or a small amount of glucose can be automatically, easily and surely administered to blood.
  • FIG. 5 shows a second embodiment of the artificial pancreas of the present invention.
  • the artificial pancreas 101 shown in FIG. 5 is different from the artificial pancreas 1 shown in FIG. 1 in the following points.
  • the main body 2 of the artificial pancreas 1 shown in FIG. 1 is a ring type, and when the main body 2 is attached to the arm 300, it moves to the arm 300 after putting a hand in the inner peripheral surface 2B of the main body 2. To do.
  • the main body 102 of the artificial pancreas 101 shown in FIG. 5 is made of elastically deformable plastic or the like, and the main body 102 forms a C shape instead of a ring shape. Therefore, the main body 2 has a notched portion 150.
  • the main body 102 is elastically deformed when the arm 300 is passed through the notch 150.
  • the main body 102 can be easily attached to the arm 300 from the side of the arm 300, and the inner peripheral surface 2B of the main body 102 can be brought into close contact with the peripheral surface of the arm 300.
  • the main body 2 When the main body 2 is C-shaped, it can be attached or detached from the direction where it intersects with the arm 300, for example, as compared with the case where the main body 2 is ring-shaped. Therefore, the attachment and detachment of the artificial pancreas 101 becomes easier. It also increases the width of the patient's arm thickness that can be applied.
  • FIG. 6 shows a third embodiment of the artificial pancreas of the present invention.
  • the difference between the artificial pancreas 201 of the second embodiment shown in FIG. 6 and the artificial pancreas 1 shown in FIG. 2 is as follows.
  • the artificial pancreas 201 has a connection portion 230 for an external power supply for connecting to the commercial power supply 220.
  • the connection unit 230 for an external power supply is electrically connected to a control unit 10 or the like that requires power supply via a detachable connector 231.
  • the connection unit 230 for the external power supply converts the commercial power supply 220 into a direct current having a predetermined voltage and supplies the commercial power supply 220 to the control unit 10 and the like. In this case, the built-in battery 9 may be omitted.
  • an external monitor display unit 330 may be connected to the control unit 10 by wire or wirelessly.
  • the external monitor display unit 330 is arranged at a place away from the patient's bed, such as a nurse center.
  • medical staff such as nurses can perform stable glycemic control of highly invasive patients after surgery, especially stable glycemic control of diabetic patients, on the external monitor display unit 330. You can definitely do it.
  • the same effects as those in the first embodiment are exhibited.
  • the venous blood flow path is obtained when the blood glucose level is larger than a predetermined value.
  • Insulin can be administered to the venous blood in the part, and glucose can be administered to the venous blood in the venous blood flow path when the blood glucose level is smaller than a predetermined value. Therefore, the artificial pancreas can easily and surely realize stable blood glucose control of patients after highly invasive surgery, particularly stable blood glucose control of diabetic patients.
  • the battery Since the battery is located in the main body, there is no need to supply power from the outside, and the artificial pancreas can be used independently even without an external power supply.
  • the venous blood control unit measures the blood glucose level of the venous blood, determines the dose of the drug solution to the venous blood, and administers the drug solution to the venous blood when the venous blood passes through the guide tube. Can be completed.
  • the route for venous blood flow is to obtain venous blood from the living body using one indwelling needle and the first and second lumens, measure the blood glucose level, administer a drug solution if necessary, and then return it to the living body. Can be done.
  • physiological saline to the venous blood together with an antithrombotic drug for preventing the thrombus of the venous blood, the generation of the thrombus due to the passage of the venous blood is prevented.
  • the present invention has been described above. However, the present invention is not limited to the above embodiment, and various modifications can be made without departing from the scope of claims.
  • the configuration of the above embodiment may be partially omitted or may be arbitrarily combined so as to be different from the above.
  • the main body portions 2, 102 are of the bracelet type so that they can be worn through the patient's arm 300.
  • the present invention is not limited to this, and the main body portion 2 may be a ring type or a C-shaped ankle type so that it can be attached to a patient's leg or ankle.
  • the main body may be formed in a slightly thick flat plate or sheet shape, for example, according to the outer shape of the arm 300, and elements such as a venous blood feeding portion may be arranged in the main body.
  • the main body may be attached to the surface of the skin of the arm so as to be detachably attached with an adhesive, or may be attached to the arm detachably using an attachment. You can also do it.
  • the artificial pancreas according to the present embodiment may be capable of acquiring other vital information in addition to the function of measuring the blood glucose level.
  • the artificial pancreas may not be disposable but may be washed and sterilized after use.
  • the artificial pancreas may be provided with a sensor that detects the body movement of the patient by using an acceleration sensor or the like.
  • the main body is not limited to being attached to the arms and legs that are a part of the patient's living body, but may be attached to a part other than the living body, for example, the frame of the bed on which the patient is sleeping.
  • liquid feed pump 13 ⁇ ⁇ ⁇ Indwelling needle, 13A ⁇ ⁇ ⁇ Intake side tube part, 13B ⁇ ⁇ ⁇ Return side tube part, 13C ⁇ ⁇ ⁇ Intake flow path, 13D ⁇ ⁇ ⁇ Tip opening, 13E ⁇ ⁇ ⁇ Return flow path, 13F ⁇ .. Opening for return, 21 ... Insulin cartridge (example of chemical cartridge), 22 ... Glucose cartridge (example of chemical cartridge), 30 ... Display, 40 ... Start of blood glucose control Button, 41 ... Anti-thrombotic drug supply unit, 41B ... Bag, 41G ... Valve, 42 ... Saline supply unit, 42B ... Bag, 42G ...

Abstract

[Problem] To provide a usable artificial pancreas making it possible to easily and reliably achieve stable blood sugar management for a patient after a highly invasive surgical operation. [Solution] An artificial pancreas 1 comprises a body unit 2; a control unit 10 disposed in the body unit 2; a venous blood transporting unit 3 disposed in the body unit 2, passing venous blood obtained from a living body through the body unit 2, and returning the venous blood to the living body; a blood sugar level measuring unit 4 disposed in the body unit 2, measuring the blood sugar level of the venous blood passed through the body unit 2 by the venous blood transporting unit 3, and notifying the control unit 10 of the blood sugar level; a connecting unit 5 disposed in the body unit 2 and connecting pharmaceutical liquid cartridges (21, 22) for storing a pharmaceutical liquid; and pharmaceutical liquid administration operation units 6A, 6B with which, when the control unit 10 is notified of the blood sugar level, the control unit 10 allows a predetermined amount of pharmaceutical liquid corresponding to the value of the blood sugar level to be administered to the venous blood from the pharmaceutical liquid cartridges (21, 22).

Description

人工膵臓Artificial pancreas
 本発明は、侵襲度の高い外科手術後の患者の安定的な血糖管理を実現する人工膵臓に関する。 The present invention relates to an artificial pancreas that realizes stable blood glucose control in patients after highly invasive surgery.
 一般的に、侵襲性のある外科手術後の患者では、血糖値が上昇の傾向にある。その血糖値が上昇する要因としては、次のようなことが知られている。要因(1)としては、全身麻酔や手術による侵襲ストレスで、血糖値を上昇させるホルモンの過剰分泌である。要因(2)としては、手術の生理学的ストレスによるインスリン抵抗性の上昇による血糖値抑制機能の低下である。術後直後から血糖値は上昇し、侵襲度によるが、3日~7日間は通常よりも高血糖状態となる。特に、糖尿病患者では、高血糖症状がさらに顕著になる。高血糖状態は、患者の感染防御機能を低下させてしまうので、術後の感染性合併症率や死亡率が高くなる。 Generally, blood glucose levels tend to rise in patients after invasive surgery. The following are known as factors that increase the blood glucose level. Factor (1) is excessive secretion of hormones that raise blood glucose levels due to invasive stress caused by general anesthesia or surgery. The factor (2) is a decrease in the blood glucose level suppressing function due to an increase in insulin resistance due to the physiological stress of surgery. Immediately after the operation, the blood glucose level rises, and depending on the degree of invasiveness, the blood glucose level becomes higher than usual for 3 to 7 days. Especially in diabetic patients, hyperglycemic symptoms become more prominent. Hyperglycemic conditions reduce the patient's protective function against infection, resulting in a high postoperative infectious complication rate and mortality rate.
 そこで、外科系ICU(集中治療室)患者に対して、強化インスリン療法(頻回インスリン注射)による80~120mg/dlの厳格な血糖管理を行った場合の患者群は、180~200mg/dlの比較的緩く血糖管理を行った場合の患者群に対して、死亡率の減少、血流感染の抑制、透析治療の抑制、ICU入院日数の短縮等が報告された。
 しかし、一方では、厳格な血糖管理を求めることで生じる低血糖リスクが指摘され、厳格な血糖管理の妥当性に議論が生じた。このような背景から、厳格な血糖管理をしたいが、低血糖頻発のリスクが高いために、現状は侵襲度の高い外科手術後の糖尿病患者には、緩く血糖管理をするのがトレンドになっている。
Therefore, for surgical ICU (intensive care unit) patients, the patient group when strict blood glucose control of 80 to 120 mg / dl by intensive insulin therapy (frequent insulin injection) is performed is 180 to 200 mg / dl. It was reported that the mortality rate was reduced, bloodstream infection was suppressed, dialysis treatment was suppressed, and the length of hospital stay in the ICU was shortened for the group of patients with relatively loose glycemic control.
However, on the other hand, the risk of hypoglycemia caused by demanding strict glycemic control was pointed out, and the validity of strict glycemic control was controversial. Against this background, we want to strictly control blood glucose, but because of the high risk of frequent hypoglycemia, the trend is to loosely control blood glucose for diabetic patients after surgery, which is currently highly invasive. There is.
 外科手術後の患者の血糖管理は、3種類に分類され、広く普及しているスライディングスケール法と、持続インスリン投与法と、そして人工膵臓である。スライディングスケール法と持続インスリン投与法との実施は、厳格な血糖管理(例えば80~120mg/dlの血糖管理)を行うのには、実情としては困難である。 The blood glucose control of patients after surgery is classified into three types, which are the widely used sliding scale method, continuous insulin administration method, and artificial pancreas. The implementation of the sliding scale method and the continuous insulin administration method is actually difficult to carry out strict glycemic control (for example, glycemic control of 80 to 120 mg / dl).
 その困難な理由は、次の通りである。血糖管理のリソース面では、医療従事者は常に複数の患者を担当している。医療従事者が、各患者の血糖値トレンドを常に把握するために、頻繁に血糖値測定を行い、各患者に対してインスリン投与を行うことは、現実に不可能である。血糖管理のデバイス面では、血糖測定には必ずしも精度±2~3%の血液ガス測定ではなく、精度±10%程度の自己測定機で行うことによる測定値のバラツキがある。 The reason for the difficulty is as follows. In terms of glycemic control resources, healthcare professionals are always responsible for multiple patients. It is practically impossible for a healthcare professional to frequently measure the blood glucose level and administer insulin to each patient in order to keep track of the blood glucose level trend of each patient. In terms of blood glucose control devices, blood glucose measurement does not necessarily measure blood gas with an accuracy of ± 2 to 3%, but there are variations in measured values due to measurement performed by a self-measuring machine with an accuracy of about ± 10%.
 一方、現在の手法で厳格な血糖コントロールを実現できるのは、人工膵臓のみである。人工膵臓による療法は、血糖測定と、薬剤投与量計算と、薬剤投与作業と、をすべて装置が行う。このため、人工膵臓は、リスク低減と、コストの削減と、リソースの有効活用と、の観点から、厳格な血糖管理が実現可能である。 On the other hand, only artificial pancreas can achieve strict glycemic control with the current method. In the therapy with the artificial pancreas, the device performs all of blood glucose measurement, drug dose calculation, and drug administration work. Therefore, the artificial pancreas can realize strict blood glucose control from the viewpoints of risk reduction, cost reduction, and effective utilization of resources.
 特許文献1には、人工膵臓が開示されている。この人工膵臓は、手術または傷病により侵襲を受けた外科的高血糖状態にある患者等の傷病により、患者が低血糖状態に陥った場合に、インスリン等の血糖値変動を生じさせる薬液等を適正に投与できる。 Patent Document 1 discloses an artificial pancreas. This artificial pancreas is suitable for a drug solution that causes fluctuations in blood glucose level such as insulin when a patient falls into a hypoglycemic state due to injury or illness of a patient or the like who is in a surgically hyperglycemic state invaded by surgery or injury or illness. Can be administered to.
特開2008-183250号公報Japanese Unexamined Patent Publication No. 2008-183250
 ところが、従来の人工膵臓は、装置が大型で複雑な操作を行う必要があり、移動用のスタンドに搭載されている。従来の人工膵臓は、スタンドを床面上で移動することで患者の近くに配置して用いられる。従来の人工膵臓は、外科手術後の厳格な血糖管理が可能なものの、大型で複雑な操作を必要とするので、実際には臨床では使いにくい。また、患者の移動に伴って、大型の人工膵臓を移動するのが容易ではない。 However, the conventional artificial pancreas has a large device and requires complicated operations, and is mounted on a stand for movement. Conventional artificial pancreas is used by moving the stand on the floor so that it is placed near the patient. Although conventional artificial pancreas is capable of strict blood glucose control after surgery, it is difficult to use clinically because it requires large and complicated operations. Also, it is not easy to move a large artificial pancreas as the patient moves.
 本発明は、前記課題を解決するためになされたものであり、侵襲度の高い外科手術後の糖尿病患者の安定的な血糖管理を、容易にしかも確実に実現できる使い勝手の良好な人工膵臓を提供することを目的とする。 The present invention has been made to solve the above problems, and provides an easy-to-use artificial pancreas that can easily and surely realize stable blood glucose control of a diabetic patient after a highly invasive surgery. The purpose is to do.
 前記課題は、本発明によれば、請求項1の発明では、生体の血糖管理を行う人工膵臓であって、本体部と、前記本体部に配置される制御部と、前記本体部に配置され、前記生体から得られる静脈血を前記本体部に通して、前記静脈血を前記生体に戻す静脈血送液部と、前記本体部に配置され、前記静脈血送液部により前記本体部を通る前記静脈血の血糖値を測定して前記血糖値を前記制御部に通知する血糖値測定部と、前記本体部に配置され、薬液を貯留する薬液カートリッジを接続する接続部と、前記血糖値を前記制御部に通知すると、前記制御部の指令により前記血糖値の値に応じた所定量の前記薬液を、前記薬液カートリッジから前記静脈血に投与させる薬液投与操作部と、を備えることを特徴とする人工膵臓により、達成される。 According to the present invention, the subject is an artificial pancreas that controls blood glucose in a living body according to the present invention, and is arranged in a main body portion, a control unit arranged in the main body portion, and the main body portion. , A venous blood feeding section that passes venous blood obtained from the living body through the main body and returns the venous blood to the living body, and a venous blood feeding section that is arranged in the main body and passes through the main body by the venous blood feeding section. A blood glucose level measuring unit that measures the blood glucose level of the venous blood and notifies the control unit of the blood glucose level, a connecting portion that is arranged in the main body and connects a drug solution cartridge for storing the drug solution, and the blood glucose level. When notified to the control unit, the control unit is characterized by comprising a drug solution administration operation unit for administering a predetermined amount of the drug solution according to the blood glucose level to the venous blood from the drug solution cartridge. Achieved by the artificial pancreas.
 請求項1の発明の構成では、本体部は、例えば患者の生体の部位の適所に対して装着するだけで良い。静脈血送液部は、生体から得られる静脈血を本体部内に通しながら生体に戻す際に、血糖値測定部は、本体部を通る静脈血の血糖値を測定してその血糖値を制御部に通知する。制御部は、薬液投与操作部を作動させて、血糖値の値に応じた所定量の薬液を、薬液カートリッジから静脈血流路部内の静脈血に投与させる。これにより、人工膵臓では、本体部に静脈血を通すだけで、血糖値を測定して血糖値の値に応じて薬液を投与できる。従って、医療従事者が常に管理をしなくても、人工膵臓は、侵襲度の高い外科手術後の患者、特に糖尿病患者の安定的な血糖管理を、容易にしかも確実に実現でき、使い勝手が良好になる。 In the configuration of the invention of claim 1, the main body portion only needs to be attached to a suitable place of a living body part of a patient, for example. When the venous blood delivery unit returns the venous blood obtained from the living body to the living body while passing it through the main body, the blood glucose level measuring unit measures the blood glucose level of the venous blood passing through the main body and controls the blood glucose level. Notify to. The control unit operates the drug solution administration operation unit to administer a predetermined amount of the drug solution according to the blood glucose level from the drug solution cartridge to the venous blood in the venous blood flow path portion. As a result, in the artificial pancreas, the blood glucose level can be measured and the drug solution can be administered according to the blood glucose level simply by passing venous blood through the main body. Therefore, the artificial pancreas can easily and surely realize stable glycemic control of highly invasive post-surgery patients, especially diabetic patients, and is easy to use, even if the medical staff does not always manage it. become.
 請求項2の発明では、好ましくは、前記薬液カートリッジは、前記血糖値の値が予め定めた値よりも大きい場合に前記静脈血流路部内の前記静脈血にインスリンを投与するインスリンカートリッジと、前記血糖値の値が予め定めた値よりも小さい場合に前記静脈血流路部内の前記静脈血にグルコースを投与するグルコースカートリッジと、を有することを特徴とする。 In the invention of claim 2, preferably, the drug solution cartridge is an insulin cartridge that administers insulin to the venous blood in the venous blood flow path when the blood glucose level is larger than a predetermined value, and the above. It is characterized by having a glucose cartridge for administering glucose to the venous blood in the venous blood flow path portion when the blood glucose level is smaller than a predetermined value.
 請求項2の発明の構成では、本体部を患者の生体の部位の適所に対して装着すれば、血糖値の値が予め定めた値よりも大きい場合に静脈血流路部内の静脈血にインスリンを投与でき、血糖値の値が予め定めた値よりも小さい場合に静脈血流路部内の静脈血にグルコースを投与できる。このため、人工膵臓は、侵襲度の高い外科手術後の糖尿病患者の安定的な血糖管理を、容易にしかも確実に実現できる。 In the configuration of the invention of claim 2, if the main body is attached to a suitable place in the living body of the patient, insulin is added to the venous blood in the venous blood flow path when the blood glucose level is larger than a predetermined value. Can be administered, and glucose can be administered to venous blood in the venous blood flow path when the blood glucose level is smaller than a predetermined value. Therefore, the artificial pancreas can easily and surely realize stable glycemic control of diabetic patients after highly invasive surgery.
 請求項3の発明では、好ましくは、前記静脈血送液部は、前記本体部に沿って配置されて前記静脈血を案内する案内管路部と、前記生体から得られる前記静脈血を、前記案内管路部に通した後に前記生体に戻す送液ポンプと、を有することを特徴とする。 In the invention of claim 3, preferably, the venous blood pumping portion is arranged along the main body portion to guide the venous blood, and the venous blood obtained from the living body is described as described above. It is characterized by having a liquid feeding pump that returns to the living body after passing through a guide line portion.
 請求項3の発明の構成では、静脈血送液部の案内管路部は、本体部に沿って配置するので、静脈血はこの案内管路部を通じて本体部に沿って通すことができる。このように、案内管路部に静脈血を通す間に、血糖値の測定作業と、薬液の投与作業を確実に行える。 In the configuration of the invention of claim 3, since the guide conduit portion of the venous blood feeding portion is arranged along the main body portion, venous blood can be passed along the main body portion through this guide conduit portion. In this way, the blood glucose level measurement work and the drug solution administration work can be reliably performed while the venous blood is passed through the guide tube portion.
 請求項4の発明では、好ましくは、前記本体部は、リング型に形成され、前記本体部は、前記生体の一部分を通して前記生体の適所の部位に保持させることを特徴とする。 In the invention of claim 4, preferably, the main body portion is formed in a ring shape, and the main body portion is held at an appropriate position of the living body through a part of the living body.
 請求項4の発明の構成では、本体部がリング型に形成されているので、本体部には、患者の生体の適所の一部分である例えば手を通して、本体部は腕に保持できる。このため、本体部の生体への保持が容易にしかも確実に行える。 In the configuration of the invention of claim 4, since the main body portion is formed in a ring shape, the main body portion can be held by the arm through, for example, a hand, which is a part of the patient's living body at an appropriate position. Therefore, the main body can be easily and surely held in the living body.
 請求項5の発明では、好ましくは、前記制御部と、前記薬液投与操作部と、前記送液ポンプと、に電源供給するバッテリが、前記本体部に配置されていることを特徴とする。 The invention according to claim 5 is preferably characterized in that a battery for supplying power to the control unit, the drug solution administration operation unit, and the liquid delivery pump is arranged in the main body unit.
 請求項5の発明の構成では、バッテリが本体部に配置されているので、外部から電源供給をする必要がなく、外部電源が無くても、人工膵臓は単独で使用することができる。 In the configuration of the invention of claim 5, since the battery is arranged in the main body, it is not necessary to supply power from the outside, and the artificial pancreas can be used independently even without an external power supply.
 請求項6の発明では、好ましくは、前記案内管路部は、前記本体部内においてほぼ一周するように配置され、前記制御部は、前記静脈血が前記案内管路部内を通る際に、前記静脈血の前記血糖値の測定と、前記静脈血への前記薬液の投与量の決定と、前記静脈血に前記薬液を投与する動作と、を完了させることを特徴とする。 In the invention of claim 6, preferably, the guide line portion is arranged so as to make substantially a circle in the main body portion, and the control unit is the vein when the venous blood passes through the guide line portion. It is characterized by completing the measurement of the blood glucose level of blood, the determination of the dose of the drug solution to the venous blood, and the operation of administering the drug solution to the venous blood.
 請求項6の発明の構成では、案内管路部は、本体部内においてほぼ一周するように配置されているので、静脈血が本体部内を流れる長さをできる限り確保できる。このため、静脈血制御部は、静脈血が案内管路部内を通る際に、静脈血の血糖値の測定と、静脈血への薬液の投与量の決定と、静脈血に薬液を投与する動作を完了できる。 In the configuration of the invention of claim 6, since the guide conduit portion is arranged so as to make substantially one circumference in the main body portion, the length of venous blood flowing in the main body portion can be secured as much as possible. Therefore, the venous blood control unit measures the blood glucose level of the venous blood, determines the dose of the drug solution to the venous blood, and administers the drug solution to the venous blood when the venous blood passes through the guide tube. Can be completed.
 請求項7の発明では、好ましくは、前記案内管路部は、前記生体内から前記静脈血を前記本体内へ通す第1ルーメンと、前記本体内を通った前記静脈血を前記生体内に戻す第2ルーメンと、を有し、前記第1ルーメンと前記第2ルーメンは、平行に配置され、留置針に接続されていることを特徴とする。 In the invention of claim 7, preferably, the guide conduit portion returns the first lumen through which the venous blood has passed from the living body into the main body and the venous blood having passed through the main body into the living body. It has a second lumen, and the first lumen and the second lumen are arranged in parallel and connected to an indwelling needle.
 請求項7の発明の構成では、静脈血を流す経路は、1つの留置針と、第1ルーメンと第2ルーメンを用いて、生体から静脈血を得て、血糖値を測定して必要なら薬液を投与した後に、生体に戻すことができる。 In the configuration of the invention of claim 7, the route for flowing venous blood is to obtain venous blood from a living body using one indwelling needle and the first and second lumens, measure the blood glucose level, and if necessary, a drug solution. Can be returned to the living body after administration of.
 請求項8の発明では、好ましくは、前記静脈血に抗血栓用薬剤を供給する抗血栓用薬液供給部と、前記静脈血に生理食塩水を供給する生理食塩水供給部と、が、前記本体部に接続されることを特徴とする。 In the invention of claim 8, preferably, the antithrombotic drug solution supply unit for supplying the antithrombotic drug to the venous blood and the physiological saline supply unit for supplying the physiological saline to the venous blood are the main bodies. It is characterized by being connected to a unit.
 請求項8の発明の構成では、静脈血の血栓を防ぐための抗血栓用薬剤とともに生理食塩水を、静脈血に供給することで、静脈血が通ることによる血栓の発生を防止する。 In the configuration of the invention of claim 8, by supplying physiological saline to the venous blood together with an antithrombotic drug for preventing the thrombus of the venous blood, the generation of the thrombus due to the passage of the venous blood is prevented.
 請求項9の発明では、好ましくは、前記生体の適所の部位に装着される前記本体部は、C字型であることを特徴とする。 In the invention of claim 9, preferably, the main body portion to be attached to a suitable part of the living body is C-shaped.
 請求項9の発明の構成では、本体部がC字型であると、本体部がリング型である場合に比べて、例えば腕に対して交差する方向から取り付けたり、取り外したりできる。このため、人工膵臓の取り付けと取り外しがさらに容易になる。 In the configuration of the invention of claim 9, when the main body portion is C-shaped, it can be attached or detached from a direction intersecting with the arm, for example, as compared with the case where the main body portion is a ring type. This makes it even easier to attach and remove the artificial pancreas.
 請求項10の発明では、好ましくは、前記制御部と、前記薬液投与操作部と、前記送液ポンプと、に電源供給する電源供給部が、前記本体部の外部に配置されていることを特徴とする。 In the invention of claim 10, preferably, the power supply unit for supplying power to the control unit, the chemical solution administration operation unit, and the liquid supply pump is arranged outside the main body unit. And.
 請求項10の発明の構成では、本体部の外部に配置された電源供給部から電源の供給を受けることで、人工膵臓の動作を行わせることができる。 In the configuration of the invention of claim 10, the artificial pancreas can be operated by receiving the power supply from the power supply unit arranged outside the main body.
 本発明によれば、侵襲度の高い外科手術後の糖尿病患者の安定的な血糖管理を、容易にしかも確実に実現できる使い勝手の良好な人工膵臓を提供することができる。 According to the present invention, it is possible to provide an easy-to-use artificial pancreas that can easily and surely realize stable blood glucose control of a diabetic patient after a highly invasive surgical operation.
本発明の人工膵臓の好ましい第1実施形態を実際に使用している状態を示す図である。It is a figure which shows the state which actually uses the preferable 1st Embodiment of the artificial pancreas of this invention. 図1に示す人工膵臓を示す正面図である。It is a front view which shows the artificial pancreas shown in FIG. 図1に示す人工膵臓の内部構成例を示す図である。It is a figure which shows the internal composition example of the artificial pancreas shown in FIG. 図1に示す人工膵臓の内部構成例を示す図である。It is a figure which shows the internal composition example of the artificial pancreas shown in FIG. 本発明の人工膵臓の好ましい第2実施形態を示す図である。It is a figure which shows the preferable 2nd Embodiment of the artificial pancreas of this invention. 本発明の人工膵臓の好ましい第3実施形態を示す図である。It is a figure which shows the preferable 3rd Embodiment of the artificial pancreas of this invention.
 以下に、本発明の好ましい実施形態を、図面を参照して詳しく説明する。
 なお、以下に説明する実施形態は、本発明の好適な具体例であるから、技術的に好ましい種々の限定が付されているが、本発明の範囲は、以下の説明において特に本発明を限定する旨の記載がない限り、これらの態様に限られるものではない。また、各図面中、同様の構成要素には同一の符号を付して詳細な説明は適宜省略する。
Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the drawings.
Since the embodiments described below are suitable specific examples of the present invention, various technically preferable limitations are added, but the scope of the present invention particularly limits the present invention in the following description. Unless otherwise stated, the present invention is not limited to these aspects. Further, in each drawing, the same components are designated by the same reference numerals, and detailed description thereof will be omitted as appropriate.
<第1実施形態>
(人工膵臓1の全体構成)
 図1は、本発明の人工膵臓の好ましい第1実施形態を実際に使用している状態を示す図である。図2は、図1に示す人工膵臓1を示す正面図である。図3は、図1に示す人工膵臓1の内部構成例を示す図である。
 図1から図3に示す人工膵臓1は、侵襲度の高い外科手術後の患者の安定的な血糖管理を行う、特に糖尿病患者の安定的な血糖管理を行う。この人工膵臓1は、好ましくは1回だけ使用する、いわゆる使い捨て型のコンパクトな医療装置である。しかし、人工膵臓1は、再生して再利用可能なものであっても良い。人工膵臓1は、リング式人工膵臓セットとも呼ぶことができる。人工膵臓1は、患者の生体の適所の部位、例えば図1に示すように、患者の腕300への装着が容易であり、人工膵臓1は患者に一体化されている。人工膵臓1は、患者が場所を移動する場合に、チューブの取り回しの問題の解消が期待できる。
<First Embodiment>
(Overall composition of artificial pancreas 1)
FIG. 1 is a diagram showing a state in which a preferred first embodiment of the artificial pancreas of the present invention is actually used. FIG. 2 is a front view showing the artificial pancreas 1 shown in FIG. FIG. 3 is a diagram showing an example of the internal configuration of the artificial pancreas 1 shown in FIG.
The artificial pancreas 1 shown in FIGS. 1 to 3 performs stable blood glucose control of patients after highly invasive surgery, particularly stable blood glucose control of diabetic patients. The artificial pancreas 1 is a so-called disposable compact medical device that is preferably used only once. However, the artificial pancreas 1 may be regenerated and reusable. The artificial pancreas 1 can also be referred to as a ring-type artificial pancreas set. The artificial pancreas 1 is easily attached to a suitable part of the patient's body, for example, as shown in FIG. 1, on the patient's arm 300, and the artificial pancreas 1 is integrated with the patient. The artificial pancreas 1 can be expected to solve the problem of tube handling when the patient moves from place to place.
 人工膵臓1による療法は、血糖測定と、薬剤投与量計算と薬剤投与作業を、すべて行う。血糖管理のリソース面では、医療従事者は常に複数の患者を担当していることが多い。しかし、各患者が小型の人工膵臓1を装着していることで、医療従事者は各患者の血糖値トレンドを常に容易にしかも確実に把握できる。このため、人工膵臓1は、厳重な血糖値管理によるリスク低減と、小型化によるコストの削減と、リソースの有効活用の観点から、侵襲度の高い外科手術後の患者、特に糖尿病患者に対して、安定的で厳格な血糖管理が実現可能である。 The therapy with artificial pancreas 1 performs all blood glucose measurement, drug dose calculation and drug administration work. In terms of glycemic control resources, healthcare professionals are often in charge of multiple patients at all times. However, since each patient wears a small artificial pancreas 1, the medical staff can always easily and surely grasp the blood glucose level trend of each patient. Therefore, the artificial pancreas 1 is suitable for highly invasive post-surgical patients, especially diabetic patients, from the viewpoints of risk reduction by strict blood glucose control, cost reduction by miniaturization, and effective utilization of resources. , Stable and strict blood glucose control is feasible.
 図1と図2に示すように、人工膵臓1は、概略的には、本体部2と、静脈血送液部3と、血糖値測定部4と、接続部5と、薬液投与操作部6A,6Bと、制御部10と、を有する。図2と図3に示すように、本体部2は、その他にバッテリ9を有する。バッテリ9は、本体部2に内蔵されており、例えばボタン電池のような一次電池を用いることができ、例えば後で説明する各要素に対して、少なくとも5~6時間以上電源供給する。しかし、バッテリ9の種類は特に限定されず、バッテリ9の持続時間は、特に限定されず、任意に設定できる。 As shown in FIGS. 1 and 2, the artificial pancreas 1 is roughly composed of a main body portion 2, a venous blood feeding unit 3, a blood glucose level measuring unit 4, a connecting unit 5, and a drug solution administration operating unit 6A. , 6B and a control unit 10. As shown in FIGS. 2 and 3, the main body 2 also has a battery 9. The battery 9 is built in the main body 2, and a primary battery such as a button battery can be used. For example, power is supplied to each element described later for at least 5 to 6 hours or more. However, the type of the battery 9 is not particularly limited, and the duration of the battery 9 is not particularly limited and can be set arbitrarily.
(本体部2)
 まず、本体部2について、説明する。
 図1~図3に示す本体部2は、例えば生体に接触しても問題のないプラスチック製やシリコン製等の材質で作られている。本体部2は、例えば円周方向に沿って切れ目がなく、図3に示すように円周方向に沿って中空部2Hを有するリング型の部材である。すなわち、人工膵臓1は、腕輪型の膵臓装置である。この本体部2は、医療従事者が内部を通る静脈血の様子を見ることができるように、好ましくは透明あるいは半透明であるが、その必要がない場合には不透明であっても良い。
(Main body 2)
First, the main body 2 will be described.
The main body 2 shown in FIGS. 1 to 3 is made of, for example, a material such as plastic or silicon that does not cause any problem even if it comes into contact with a living body. The main body portion 2 is, for example, a ring-shaped member having no break along the circumferential direction and having a hollow portion 2H along the circumferential direction as shown in FIG. That is, the artificial pancreas 1 is a bracelet-shaped pancreas device. The main body 2 is preferably transparent or translucent so that the medical staff can see the state of venous blood passing through the inside, but may be opaque if it is not necessary.
 本体部2は、図1の例では、患者の腕300に通して保持できるように、図1に示す本体部2の内径D1は、好ましくは40mm~80mmの範囲で設定され、本体部2の外径D2は、好ましくは70mm~120mmの範囲で設定される。本体部2の内径D1と外径D2は、患者の体格や年齢に応じて、選択できるように、本体部2はいくつかのサイズのものをあらかじめ用意するのが好ましい。 In the example of FIG. 1, the inner diameter D1 of the main body 2 shown in FIG. 1 is preferably set in the range of 40 mm to 80 mm so that the main body 2 can be held through the patient's arm 300. The outer diameter D2 is preferably set in the range of 70 mm to 120 mm. It is preferable to prepare several sizes of the main body 2 in advance so that the inner diameter D1 and the outer diameter D2 of the main body 2 can be selected according to the physique and age of the patient.
 図1に示すように、本体部2は、外周面2Aと、内周面2Bと、左右の側面2C,2Cにより形成されている。外周面2Aと内周面2Bと左右の側面2C,2Cは、内部にリング型の中空部2Hを有している。本体部2が腕300に対して回転しないようにするために、必要に応じて内周面2Bには滑り止めのシートを配置することができる。 As shown in FIG. 1, the main body 2 is formed by an outer peripheral surface 2A, an inner peripheral surface 2B, and left and right side surfaces 2C and 2C. The outer peripheral surface 2A, the inner peripheral surface 2B, and the left and right side surfaces 2C and 2C have a ring-shaped hollow portion 2H inside. A non-slip sheet can be arranged on the inner peripheral surface 2B, if necessary, so that the main body 2 does not rotate with respect to the arm 300.
(静脈血送液部3)
 次に、静脈血送液部3について、説明する。図4は、静脈血送液部3の例を示す図である。
 図3と図4に示す静脈血送液部3は、本体部2に配置され、生体である患者の腕300から得られる静脈血を本体部2においてほぼ一周分通して、静脈血を腕300に戻す機能を有する。静脈血送液部3は、案内管路部11と、送液ポンプ12を有する。案内管路部11は、可撓性を有する透明なチューブを用いることができる。透明なチューブを用いることで、医療従事者は、内部を通る静脈血の様子を確認し易い。
(Venous blood delivery unit 3)
Next, the venous blood feeding unit 3 will be described. FIG. 4 is a diagram showing an example of the venous blood feeding unit 3.
The venous blood feeding unit 3 shown in FIGS. 3 and 4 is arranged in the main body 2, and the venous blood obtained from the arm 300 of the patient who is a living body is passed through the main body 2 for almost one round, and the venous blood is passed through the arm 300. It has a function to return to. The venous blood feeding unit 3 has a guide line portion 11 and a liquid feeding pump 12. As the guide line portion 11, a transparent tube having flexibility can be used. By using a transparent tube, it is easy for the medical staff to check the state of venous blood passing through the inside.
 図4に示すように、案内管路部11は、本体部2の円形の中空部2Hに沿ってほぼ一周分配置されており、案内管路部11は中空部2Hに沿って円形状に配置されている。案内管路部11の一端部11Pは、本体部2の中空部2Hから本体部2の外部へ、熱可塑性樹脂などで形成され可撓性を有する第1ルーメン11Aとして延設されている。同様にして、案内管路部11の他端部11Qは、本体部2の中空部2Hから本体部2の外部へ、熱可塑性樹脂などで形成され可撓性を有する第2ルーメン11Bとして延設されている。第1ルーメン11Aと第2ルーメン11Bは、平行になっており、連結部11Cを介して留置針13に接続されている。図3に示すように、このような静脈血の送液ルートは、第1ルーメン11Aと第2ルーメン11Bを有するダブルルーメン構造になっている。 As shown in FIG. 4, the guide pipeline portion 11 is arranged substantially once along the circular hollow portion 2H of the main body portion 2, and the guide pipeline portion 11 is arranged in a circular shape along the hollow portion 2H. Has been done. One end portion 11P of the guide conduit portion 11 extends from the hollow portion 2H of the main body portion 2 to the outside of the main body portion 2 as a flexible first lumen 11A formed of a thermoplastic resin or the like. Similarly, the other end 11Q of the guide conduit portion 11 extends from the hollow portion 2H of the main body portion 2 to the outside of the main body portion 2 as a flexible second lumen 11B formed of a thermoplastic resin or the like. Has been done. The first lumen 11A and the second lumen 11B are parallel to each other and are connected to the indwelling needle 13 via the connecting portion 11C. As shown in FIG. 3, such a venous blood feeding route has a double lumen structure having a first lumen 11A and a second lumen 11B.
 図4には、留置針(留置カテーテル)13の好ましい構造例を示している。図4に拡大して示すように、留置針13は、血液を静脈の血管内から取り入れる取り入れ側チューブ部分13Aと、血液を静脈の血管内に戻す戻し側チューブ部分13Bと、の2つのルーメンを有する。取り入れ側チューブ部分13Aの一端部側は、その外周の円周方向に所定の高さのリブまたは所定の深さの溝を設けるなどして第1ルーメン11Aの内側に嵌合させることで液密に接続されている。また、戻し側チューブ部分13Bの一端部側は、その外周の円周方向にリブまたは溝を設けるなどして第2ルーメン11Bの内側に嵌合させることで液密に接続されている。取り入れ側チューブ部分13Aは、破線で示す取入れ流路13Cを有しており、この取入れ流路13Cは、第1ルーメン11Aにつながっていて、しかも留置針13の先端開口部13Dに達している。また、戻し側チューブ部分13Bは、破線で示すように、戻し流路13Eを有しており、この戻し流路13Eは、第2ルーメン11Bにつながっていて、しかも戻し用の開口部13Fに達している。先端開口部13Dは、留置針13の先端部に形成されているのに対して、戻し用の開口部13Fは、留置針13の途中の位置に形成されている。すなわち、先端開口部13Dと戻し用の開口部13Fは、留置針13の軸方向について所定距離離間した位置にある。しかし、先端開口部13Dと戻し用の開口部13Fは、留置針13を血管に刺した状態では、共に静脈の血管内に位置されることになる。 FIG. 4 shows a preferable structural example of the indwelling needle (indwelling catheter) 13. As shown enlarged in FIG. 4, the indwelling needle 13 has two lumens, an intake side tube portion 13A for taking in blood from the vein and a return side tube portion 13B for returning blood to the vein. Have. One end side of the intake side tube portion 13A is liquidtight by being fitted inside the first lumen 11A by providing a rib of a predetermined height or a groove of a predetermined depth in the circumferential direction of the outer circumference thereof. It is connected to the. Further, one end side of the return side tube portion 13B is liquidtightly connected by being fitted inside the second lumen 11B by providing a rib or a groove in the circumferential direction of the outer circumference thereof. The intake side tube portion 13A has an intake flow path 13C shown by a broken line, and this intake flow path 13C is connected to the first lumen 11A and reaches the tip opening 13D of the indwelling needle 13. Further, the return side tube portion 13B has a return flow path 13E as shown by a broken line, and the return flow path 13E is connected to the second lumen 11B and reaches the return opening 13F. ing. The tip opening 13D is formed at the tip of the indwelling needle 13, whereas the return opening 13F is formed at a position in the middle of the indwelling needle 13. That is, the tip opening 13D and the return opening 13F are located at positions separated by a predetermined distance in the axial direction of the indwelling needle 13. However, the tip opening 13D and the return opening 13F are both located in the blood vessel of the vein when the indwelling needle 13 is pierced into the blood vessel.
 図3,図4に示すように、送液ポンプ12は、本体部2に配置されている。送液ポンプ12は、案内管路部11の途中において、例えば複数のフィンガ(不図示)が脈動することにより、弾性変形可能な案内管路部11を順次押圧する構成にする。これにより、案内管路部11内の静脈血は、案内管路部11を通じて、図4に示すR方向に送液する。送液ポンプ12は、静脈から所定量(mL/h)の静脈血を、本体部2からに送液することができる。こうして、送液ポンプ12は、例えば蠕動式(ペリスタルティック式)のポンプを用いることができる。図3に示すように、制御部10は、静脈血の血糖管理開始ボタン40を有する。 As shown in FIGS. 3 and 4, the liquid feed pump 12 is arranged in the main body 2. The liquid feed pump 12 is configured to sequentially press the elastically deformable guide pipe portion 11 by, for example, a plurality of fingers (not shown) pulsating in the middle of the guide pipe portion 11. As a result, the venous blood in the guide line portion 11 is sent through the guide line portion 11 in the R direction shown in FIG. The liquid feed pump 12 can send a predetermined amount (mL / h) of venous blood from the vein to the main body 2. In this way, as the liquid feed pump 12, for example, a peristaltic type (peristaltic type) pump can be used. As shown in FIG. 3, the control unit 10 has a blood glucose control start button 40 for venous blood.
 これにより、図1に示すように、留置針13を腕300の静脈内に刺して留置する。留置針13を腕300の静脈内に留置するには、例えば、可撓性プラスチック製の外筒と穿刺用の金属針の内筒とを有する留置針を用いて静脈内に可撓性プラスチック製の外筒(不図示)を留置(不図示)させてから、穿刺用の金属針の内筒を抜いた後、可撓性プラスチック製の外筒(不図示)を案内部として、留置針13を挿入することで腕300の静脈内に留置する。そして、医療従事者が、この静脈血の血糖管理開始ボタン40を押すことにより、制御部10の指令により送液ポンプ12が作動する。送液ポンプ12が作動すると、図1と図4に示すように、患者の静脈血は、留置針13から送り方向Mに送液される。静脈血は、取り入れ側チューブ部分13Aと第1ルーメン11Aとを通じて、本体部2内の案内管路部11をR方向に一周分案内される。静脈血は、本体部2において一周分送られ、その送られている間に血糖値を測定し、血糖値の値に応じてインスリンまたは所定濃度のグルコース(所定濃度のブドウ糖溶液)が微量投与された後、第2ルーメン11Bと戻し側チューブ部分13Bとを通じて、同一ルートで、腕300の静脈に戻されるようになっている。
 適用されるインスリンとしては、ヒトインスリン製剤の速効型インスリン,混合型ヒトインスリンやインスリンアナロジ製剤の超速効型インスリンアナログ,二相性インスリンアナログ,配合溶解インスリンアナログ等が挙げられる。
As a result, as shown in FIG. 1, the indwelling needle 13 is pierced into the vein of the arm 300 and indwelled. To place the indwelling needle 13 in the vein of the arm 300, for example, an indwelling needle having an outer cylinder made of flexible plastic and an inner cylinder of a metal needle for puncture is used and made of flexible plastic in the vein. After indwelling (not shown) the outer cylinder (not shown) of the above, the inner cylinder of the metal needle for puncture is pulled out, and then the indwelling needle 13 using the outer cylinder made of flexible plastic (not shown) as a guide portion. Is placed in the vein of the arm 300 by inserting. Then, when the medical worker presses the blood glucose control start button 40 of the venous blood, the liquid feeding pump 12 is operated by the command of the control unit 10. When the liquid feeding pump 12 is activated, the patient's venous blood is fed from the indwelling needle 13 in the feeding direction M, as shown in FIGS. 1 and 4. Venous blood is guided around the guide line portion 11 in the main body portion 2 in the R direction through the intake side tube portion 13A and the first lumen 11A. Venous blood is sent once in the main body 2, and the blood glucose level is measured during the delivery, and insulin or a predetermined concentration of glucose (predetermined concentration of glucose solution) is administered in a small amount according to the blood glucose level. After that, it is returned to the vein of the arm 300 by the same route through the second lumen 11B and the return side tube portion 13B.
Examples of the applicable insulin include fast-acting insulin of human insulin preparation, super-fast-acting insulin analog of mixed human insulin and insulin analogy preparation, biphasic insulin analog, combined dissolved insulin analog and the like.
(血糖値測定部4)
 次に、血糖値測定部4について、説明する。
 図3に示す血糖値測定部4は、本体部2において静脈血送液部3の案内管路部11の近くに配置されている。静脈血送液部3の案内管路部11をほぼ一周することで送液される静脈血の血糖値を、患者の負担が軽減するために、好ましくは連続的に非侵襲、静脈血に対して非接触で測定する。血糖値測定部4は、血糖値の測定データDTを、制御部10に通知する。血糖値測定部4は、静脈血の血糖値を、連続して測定する連続血糖モニタリング機能を発揮する。血糖値測定部4の検出手段であるグルコースセンサとしては、好ましくは例えば、近赤外(700~1050nm)分光法を用いるものである。この近赤外分光法とは、血糖値の時間経過に伴う変化を測定するに際して、複数の経過時間において、血糖値の実測値を得ると共に、静脈に近赤外光を照射し、静脈からの拡散反射光又は透過光を受光して、近赤外の設定波長範囲で複数の波長毎の吸光度を求め、前記実測値に対して吸光度の相関が高い波長を特定し、特定した波長の吸光度から前記実測値を算出する計算式を導出し、他の経過時間において、静脈に近赤外光を照射し、静脈からの拡散反射光又は透過光を受光して、特定した波長の吸光度を求めて、前記計算式から血糖値を算出するものであるが、この近赤外分光法には特に限定されない。また、血糖値測定部4の検出手段であるグルコースセンサとしては、例えば酵素電極等を用いても良い。
(Blood glucose measurement unit 4)
Next, the blood glucose level measuring unit 4 will be described.
The blood glucose level measuring unit 4 shown in FIG. 3 is arranged in the main body 2 near the guide tube portion 11 of the venous blood feeding unit 3. In order to reduce the burden on the patient, the blood glucose level of the venous blood that is sent by going around the guide tube portion 11 of the venous blood feeding section 3 is preferably continuously non-invasive and for venous blood. Measure without contact. The blood glucose level measuring unit 4 notifies the control unit 10 of the blood glucose level measurement data DT. The blood glucose level measuring unit 4 exerts a continuous blood glucose monitoring function for continuously measuring the blood glucose level of venous blood. As the glucose sensor as the detection means of the blood glucose level measuring unit 4, for example, near infrared (700 to 1050 nm) spectroscopy is preferably used. In this near-infrared spectroscopy, when measuring changes in blood glucose level over time, the measured values of blood glucose level are obtained at a plurality of elapsed times, and the veins are irradiated with near-infrared light to obtain the measured values from the veins. By receiving diffused reflected light or transmitted light, the absorbance for each of a plurality of wavelengths is obtained in the near infrared set wavelength range, the wavelength having a high correlation with the measured value is specified, and the absorbance at the specified wavelength is used. A calculation formula for calculating the measured value is derived, and at another elapsed time, the vein is irradiated with near-infrared light, the diffused reflected light or transmitted light from the vein is received, and the absorbance at the specified wavelength is obtained. , The blood glucose level is calculated from the above formula, but the near-infrared spectroscopy is not particularly limited. Further, as the glucose sensor which is the detecting means of the blood glucose level measuring unit 4, for example, an enzyme electrode or the like may be used.
(接続部5と薬液投与操作部6A,6B)
 次に、接続部5と、薬液投与操作部6A,6Bについて、説明する。
 図1と図2に示すように、接続部5は、薬液投与操作部6A,6Bを並べて取り付けている。薬液投与操作部6A,6Bとしては、例えばダイアフラム型微量注入ポンプを採用することができる。接続部5は、本体部2の側面2Cに設けられており、好ましくは本体部2と同じプラスチック製の材質で作られている。本体部2は、静脈血の血糖値を増加させる操作あるいは減少させる操作をするために、インスリンカートリッジ21と、グルコースカートリッジ22を、着脱可能に接続する。インスリンカートリッジ21とグルコースカートリッジ22は、薬液カートリッジの例である。
(Connecting part 5 and drug solution administration operation part 6A, 6B)
Next, the connection unit 5 and the drug solution administration operation units 6A and 6B will be described.
As shown in FIGS. 1 and 2, the connecting portion 5 is attached with the chemical solution administration operating portions 6A and 6B side by side. As the drug solution administration operation units 6A and 6B, for example, a diaphragm type microinjection pump can be adopted. The connecting portion 5 is provided on the side surface 2C of the main body portion 2, and is preferably made of the same plastic material as the main body portion 2. The main body 2 detachably connects the insulin cartridge 21 and the glucose cartridge 22 in order to increase or decrease the blood glucose level of venous blood. The insulin cartridge 21 and the glucose cartridge 22 are examples of chemical cartridges.
 インスリンカートリッジ21内には、インスリンが貯留されている。インスリンが静脈血に微量投与されると、静脈血の血糖値を下げる。グルコースカートリッジ22内には、グルコースが貯留されている。グルコールが静脈血に微量投与されると、静脈血の血糖値を上げる。インスリンカートリッジ21とグルコースカートリッジ22のサイズは、同じであるが、目視で容易に区別できるようにするために、例えばインスリンカートリッジ21は赤色に、グルコースカートリッジ22は青色に、それぞれ着色されている。インスリンカートリッジ21は、接続部5において、薬液投与操作部6Aに対して着脱可能に接続される。グルコースカートリッジ22は、接続部5において、薬液投与操作部6Bに対して着脱可能に接続される。 Insulin is stored in the insulin cartridge 21. When insulin is administered in small amounts to venous blood, it lowers the blood sugar level in venous blood. Glucose is stored in the glucose cartridge 22. When glucol is administered in small amounts to venous blood, it raises the blood sugar level in venous blood. The insulin cartridge 21 and the glucose cartridge 22 are the same size, but for example, the insulin cartridge 21 is colored red and the glucose cartridge 22 is colored blue so that they can be easily distinguished visually. The insulin cartridge 21 is detachably connected to the drug solution administration operation unit 6A at the connection unit 5. The glucose cartridge 22 is detachably connected to the drug solution administration operation unit 6B at the connection unit 5.
 図3に示す制御部10は、血糖値測定部4により得られた案内管路部11をほぼ一周する静脈血の血糖値の測定データDTに基づいて、インスリンカートリッジ21側の薬液投与操作部6Aを駆動するか、グルコースカートリッジ22側の薬液投与操作部6Bを駆動する。制御部10は、メモリ10Mを有し、このメモリ10Mは、血糖値の測定データDTから、インスリン投与量、グルコース投与量を算出するアルゴリズムのソフトウェアを記憶している。 The control unit 10 shown in FIG. 3 is a drug solution administration operation unit 6A on the insulin cartridge 21 side based on the blood glucose level measurement data DT of venous blood that substantially goes around the guide tube portion 11 obtained by the blood glucose level measurement unit 4. Or drive the drug solution administration operation unit 6B on the glucose cartridge 22 side. The control unit 10 has a memory 10M, and the memory 10M stores software of an algorithm for calculating an insulin dose and a glucose dose from the blood glucose level measurement data DT.
 これにより、案内管路部11をほぼ一周する静脈血の血糖値の測定データDTが予め定めた血糖値のデータに比べて大きい場合には、制御部10は、薬液投与操作部6Aを駆動して、インスリンカートリッジ21のインスリンを、案内管路部11内を通る静脈血中に、微量投与して静脈血の血糖値を下げる。また、案内管路部11をほぼ一周する静脈血の血糖値の測定データDTが予め定めた血糖値のデータに比べて小さい場合には、制御部10は、薬液投与操作部6Bを駆動して、グルコースカートリッジ22のグルコースを、案内管路部11内を通る静脈血中に、微量投与して静脈血の血糖値を上げる。このように、薬液投与操作部6A,6Bは、静脈血の血糖値を制御部10に通知すると、制御部10は、静脈血の血糖値の大小に応じた所定量のインスリンあるいは所定量のグルコースを、静脈血流路部内の静脈血に微量投与させて、血糖値の制御を行う。 As a result, when the measurement data DT of the blood glucose level of venous blood that substantially goes around the guide tube portion 11 is larger than the blood glucose level data determined in advance, the control unit 10 drives the drug solution administration operation unit 6A. Then, the insulin of the insulin cartridge 21 is administered in a small amount into the venous blood passing through the guide tube portion 11 to lower the blood glucose level of the venous blood. Further, when the blood glucose level measurement data DT of venous blood that substantially goes around the guide tube portion 11 is smaller than the predetermined blood glucose level data, the control unit 10 drives the drug solution administration operation unit 6B. , Glucose of the glucose cartridge 22 is administered in a small amount into the venous blood passing through the guide tube portion 11 to raise the blood glucose level of the venous blood. As described above, when the drug solution administration operation units 6A and 6B notify the control unit 10 of the blood glucose level of venous blood, the control unit 10 receives a predetermined amount of insulin or a predetermined amount of glucose according to the magnitude of the blood glucose level of venous blood. Is administered in a small amount to the venous blood in the venous blood flow path to control the blood glucose level.
 図2に例示するように、好ましくは表示部30が本体部2に配置されるようにしても良い。この表示部30は、静脈血の血糖値や、微量投与したインスリンの量や、微量投与したグルコースの量を表示できる。例えば、バッテリ9は、図3に示すように、制御部10、血糖値測定部4、送液ポンプ12に電源供給する。 As illustrated in FIG. 2, preferably, the display unit 30 may be arranged in the main body unit 2. The display unit 30 can display the blood glucose level of venous blood, the amount of insulin administered in a small amount, and the amount of glucose administered in a small amount. For example, as shown in FIG. 3, the battery 9 supplies power to the control unit 10, the blood glucose level measuring unit 4, and the liquid feeding pump 12.
(抗血栓用薬剤供給部41と生理食塩水供給部42)
 次に、図2と図3を参照して、本体部2に接続されるチューブ状の抗血栓用薬剤供給部41と、チューブ状の生理食塩水供給部42について説明する。抗血栓用薬剤供給部41は、抗血栓用薬剤を収容しているバッグ41Bに接続されている。生理食塩水供給部42は、生理食塩水を収容しているバッグ42Bに接続されている。抗血栓用薬剤供給部41は、必要に応じて、本体部2の案内管路部11内を通る静脈血中に、抗血栓用薬剤を供給する薬液供給部である。また、生理食塩水供給部42は、必要に応じて、本体部2の案内管路部11内を通る静脈血中に、抗血栓用薬剤、例えばヘパリンをスムーズに流すために、生理食塩水を供給する。
(Antithrombotic drug supply unit 41 and physiological saline supply unit 42)
Next, with reference to FIGS. 2 and 3, a tubular antithrombotic drug supply unit 41 connected to the main body 2 and a tubular physiological saline supply unit 42 will be described. The antithrombotic drug supply unit 41 is connected to the bag 41B containing the antithrombotic drug. The saline supply unit 42 is connected to a bag 42B containing the saline solution. The antithrombotic drug supply unit 41 is a drug solution supply unit that supplies an antithrombotic drug into venous blood passing through the guide tube portion 11 of the main body 2 as needed. Further, the physiological saline supply unit 42 smoothly flows an antithrombotic drug, for example, heparin, into the venous blood passing through the guide tube portion 11 of the main body 2 as needed. Supply.
 バルブ41Gを開けることにより、バッグ42B内の抗血栓用薬剤は、抗血栓用薬剤供給部41を介して、案内管路部11内を通る静脈血中に投与できる。バルブ42Gを開けることにより、バッグ42B内の生理食塩水は、生理食塩水供給部42を介して、案内管路部11内を通る静脈血中に投与できる。バルブ41G,42Gは、手動で開閉可能である。しかし、図3に示すように、バルブ41G,42Gの開閉は、制御部10からの指令により行っても良い。 By opening the valve 41G, the antithrombotic drug in the bag 42B can be administered into the venous blood passing through the guide tube section 11 via the antithrombotic drug supply section 41. By opening the valve 42G, the saline solution in the bag 42B can be administered into the venous blood passing through the guide tube portion 11 via the saline solution supply unit 42. The valves 41G and 42G can be opened and closed manually. However, as shown in FIG. 3, the valves 41G and 42G may be opened and closed by a command from the control unit 10.
(人工膵臓1による静脈血の血糖管理)
 次に、上述した人工膵臓1による静脈血の血糖管理例について、図1~図4を参照して説明する。
 図1と図2に示すように、本体部2では、インスリンカートリッジ21が、接続部5において、薬液投与操作部6Aに対して着脱可能に接続される。グルコースカートリッジ22が、接続部5において、薬液投与操作部6Bに対して着脱可能に接続される。図1に示すように、本体部2の内周面2Bには、患者の手から入れると、本体部2は腕300の適切な位置に保持される。
(Blood glucose control of venous blood by artificial pancreas 1)
Next, an example of blood glucose control of venous blood by the artificial pancreas 1 described above will be described with reference to FIGS. 1 to 4.
As shown in FIGS. 1 and 2, in the main body 2, the insulin cartridge 21 is detachably connected to the drug solution administration operation unit 6A at the connection unit 5. The glucose cartridge 22 is detachably connected to the drug solution administration operation unit 6B at the connection unit 5. As shown in FIG. 1, the inner peripheral surface 2B of the main body 2 is held at an appropriate position of the arm 300 when the main body 2 is inserted from the patient's hand.
 図1に示すように、留置針13を腕300の静脈に刺して、例えばテープを用いて、留置針13が動かないように静脈内に留置する。留置針13を腕300の静脈内に留置するには、例えば、可撓性プラスチック製の外筒と穿刺用の金属針の内筒とを有する留置針(不図示)を用いて静脈内に可撓性プラスチック製の外筒(不図示)を留置させてから、穿刺用の金属針の内筒を抜いた後、可撓性プラスチック製の外筒(不図示)を案内部として、留置針13を挿入することで腕300の静脈内に留置する。 As shown in FIG. 1, the indwelling needle 13 is pierced into the vein of the arm 300, and the indwelling needle 13 is indwelled in the vein so as not to move, for example, using a tape. In order to place the indwelling needle 13 in the vein of the arm 300, for example, an indwelling needle (not shown) having an outer cylinder made of flexible plastic and an inner cylinder of a metal needle for puncture can be used intravenously. After indwelling the outer cylinder made of flexible plastic (not shown), the inner cylinder of the metal needle for puncture is pulled out, and then the indwelling needle 13 using the outer cylinder made of flexible plastic (not shown) as a guide portion. Is placed in the vein of the arm 300 by inserting.
 留置針13を挿入することで腕300の静脈内に留置すると、図4に示す先端開口部13Dと戻し用の開口部13Fは、共に静脈の血管内に位置される。静脈血は、送り方向Mに沿って先端開口部13Dから取入れ流路13C内に取り入れられ、採血した静脈血として、取入れ流路13Cを経て、第1ルーメン11Aへ取り入れられる。一方、第2ルーメン11Bを経て、戻ってきた静脈血(インスリンおよび/またはグルコースを含むことで血糖値が調整された静脈血)は、戻し方向Nに沿って、戻し側チューブ部分13Bの戻し流路13Eを経て、戻し用の開口部13Fから、静脈内に戻される。戻し用の開口部13Fは、留置針13の軸方向について離した位置にある。これにより、静脈から取り入れる血液と静脈に戻される血液とが、混濁しない。 When the indwelling needle 13 is inserted and placed in the vein of the arm 300, the tip opening 13D and the return opening 13F shown in FIG. 4 are both located in the vein of the vein. The venous blood is taken into the intake flow path 13C from the tip opening 13D along the feeding direction M, and is taken into the first lumen 11A via the intake flow path 13C as the collected venous blood. On the other hand, the venous blood returned after passing through the second lumen 11B (venous blood whose blood glucose level is adjusted by containing insulin and / or glucose) flows back from the return tube portion 13B along the return direction N. It is returned intravenously through the return opening 13F via the road 13E. The return opening 13F is located at a position separated from the indwelling needle 13 in the axial direction. As a result, the blood taken in from the vein and the blood returned to the vein are not turbid.
 そして、医療従事者が、図3に示す静脈血の血糖管理開始ボタン40を押すことにより、制御部10の指令により送液ポンプ12が作動する。送液ポンプ12が作動すると、図1と図4に示すように、所定量の静脈血が、送り方向Mに送液される。静脈血は、第1ルーメン11Aを通じて、本体部2内の案内管路部11をR方向にほぼ一周分案内される。そして、血糖値を測定した静脈血は、第2ルーメン11Bを通じて、同一ルートで留置針13を通じて、戻し方向Nに沿って腕の静脈に戻される。このように、本体部2内をほぼ一周した静脈血の送液ルートとしては、留置針13の取り入れ側チューブ部分13Aと第1ルーメン11Aと、第2ルーメン11Bと留置針13の戻し側チューブ部分13Bと、第1ルーメン11Aと第2ルーメン11Bを用いたダブルルーメン構造により、体内から出た静脈血は、同一ルートで留置針13を通じて体内に戻される。 Then, when the medical worker presses the blood glucose control start button 40 for venous blood shown in FIG. 3, the liquid feed pump 12 is operated by the command of the control unit 10. When the liquid feeding pump 12 is operated, a predetermined amount of venous blood is fed in the feeding direction M as shown in FIGS. 1 and 4. Venous blood is guided through the first lumen 11A through the guide conduit portion 11 in the main body portion 2 for substantially one round in the R direction. Then, the venous blood whose blood glucose level has been measured is returned to the vein of the arm along the return direction N through the indwelling needle 13 through the second lumen 11B and the same route. As described above, as the venous blood delivery route that has substantially circled the inside of the main body 2, the intake side tube portion 13A and the first lumen 11A of the indwelling needle 13, the second lumen 11B and the return side tube portion of the indwelling needle 13 are used. Due to the double lumen structure using 13B, the first lumen 11A and the second lumen 11B, venous blood discharged from the body is returned to the body through the indwelling needle 13 by the same route.
 抗血栓用薬剤供給部41は、必要に応じて、本体部2の案内管路部11内を通る静脈血中に、抗血栓用薬剤を供給する。また、生理食塩水供給部42は、必要に応じて、本体部2の案内管路部11内を通る静脈血中に、抗血栓用薬剤をスムーズに流すために、生理食塩水を供給する。 The antithrombotic drug supply unit 41 supplies the antithrombotic drug into the venous blood passing through the guide tube portion 11 of the main body 2 as needed. Further, the physiological saline supply unit 42 supplies the physiological saline solution, if necessary, in order to smoothly flow the antithrombotic drug into the venous blood passing through the guide tube portion 11 of the main body portion 2.
 血糖値測定部4は、静脈血送液部3の案内管路部11をほぼ一周する途中で、送液される静脈血の血糖値を、非侵襲でしかも非接触で連続的に測定する。血糖値測定部4は、血糖値の測定データDTを、静脈血の血糖値を、連続して測定しながら制御部10に通知する。 The blood glucose level measuring unit 4 continuously measures the blood glucose level of the venous blood to be delivered in a non-invasive and non-contact manner on the way around the guide tube portion 11 of the venous blood feeding unit 3. The blood glucose level measuring unit 4 notifies the control unit 10 of the blood glucose level measurement data DT while continuously measuring the blood glucose level of venous blood.
 制御部10は、制御部10は、血糖値測定部4により得られた案内管路部11をほぼ一周する静脈血の血糖値の測定データDTに基づいて、インスリンカートリッジ21側の薬液投与操作部6Aを駆動するか、グルコースカートリッジ22側の薬液投与操作部6Bを駆動する。制御部10は、血糖値の測定データDTから、インスリン投与量、グルコース投与量を算出する。 In the control unit 10, the control unit 10 is a drug solution administration operation unit on the insulin cartridge 21 side based on the blood glucose level measurement data DT of venous blood that substantially goes around the guide tube portion 11 obtained by the blood glucose level measurement unit 4. 6A is driven, or the drug solution administration operation unit 6B on the glucose cartridge 22 side is driven. The control unit 10 calculates the insulin dose and the glucose dose from the blood glucose level measurement data DT.
 これにより、案内管路部11をほぼ一周する静脈血の血糖値の測定データDTが予め定めた血糖値のデータに比べて大きい場合には、制御部10は、薬液投与操作部6Aを駆動して、インスリンカートリッジ21のインスリンを、案内管路部11内を通る静脈血中に、微量投与して静脈血の血糖値を下げる。また、案内管路部11をほぼ一周する静脈血の血糖値の測定データDTが予め定めた血糖値のデータに比べて小さい場合には、制御部10は、薬液投与操作部6Bを駆動して、グルコースカートリッジ22のグルコースを、案内管路部11内を通る静脈血中に、微量投与して静脈血の血糖値を上げる。 As a result, when the measurement data DT of the blood glucose level of venous blood that substantially goes around the guide tube portion 11 is larger than the blood glucose level data determined in advance, the control unit 10 drives the drug solution administration operation unit 6A. Then, the insulin of the insulin cartridge 21 is administered in a small amount into the venous blood passing through the guide tube portion 11 to lower the blood glucose level of the venous blood. Further, when the blood glucose level measurement data DT of venous blood that substantially goes around the guide tube portion 11 is smaller than the predetermined blood glucose level data, the control unit 10 drives the drug solution administration operation unit 6B. , Glucose of the glucose cartridge 22 is administered in a small amount into the venous blood passing through the guide tube portion 11 to raise the blood glucose level of the venous blood.
 このように、静脈血の血糖値が制御部10に通知されると、制御部10は、静脈血の血糖値の大小に応じた所定量のインスリンあるいは所定量のグルコースを、インスリンカートリッジ21あるいはグルコースカートリッジ22から、静脈血流路部内の静脈血に注入させて、血糖制御を行う。
 なお、図2に示す表示部30は、好ましくは、静脈血の血糖値や、微量投与したインスリンの量や、微量投与したグルコースの量を表示することで、医療従事者はこれらの数値を確認できる。
In this way, when the blood glucose level of venous blood is notified to the control unit 10, the control unit 10 applies a predetermined amount of insulin or a predetermined amount of glucose according to the magnitude of the blood glucose level of venous blood to the insulin cartridge 21 or glucose. Blood glucose is controlled by injecting venous blood in the venous blood flow path from the cartridge 22.
The display unit 30 shown in FIG. 2 preferably displays the blood glucose level of venous blood, the amount of insulin administered in a small amount, and the amount of glucose administered in a small amount, so that the medical staff can confirm these values. it can.
 以上説明したように、図示した第1実施形態の人工膵臓では、本体部は、患者の生体の部位に対して装着するだけで良い。静脈血送液部は、生体から得られる静脈血を本体部内に通しながら生体に戻す際に、血糖値測定部は、本体部を通る静脈血の血糖値を測定してその血糖値を制御部に通知する。制御部は、薬液投与操作部を作動させて、血糖値の値に応じた所定量の薬液を、薬液カートリッジから静脈血流路部内の静脈血に投与させる。 As described above, in the artificial pancreas of the first embodiment shown in the figure, the main body portion only needs to be attached to the part of the living body of the patient. When the venous blood delivery unit returns the venous blood obtained from the living body to the living body while passing it through the main body, the blood glucose level measuring unit measures the blood glucose level of the venous blood passing through the main body and controls the blood glucose level. Notify to. The control unit operates the drug solution administration operation unit to administer a predetermined amount of the drug solution according to the blood glucose level from the drug solution cartridge to the venous blood in the venous blood flow path portion.
 これにより、第1実施形態の人工膵臓では、本体部に静脈血を通すだけで、血糖値を測定して血糖値の値に応じて薬液を投与できる。従って、医療従事者が常に管理をしなくても、採血不良を防いで、侵襲度の高い外科手術後の患者の安定的な血糖管理、特に糖尿病患者の安定的な血糖管理を、容易にしかも確実に実現でき、使い勝手が良好である。 As a result, in the artificial pancreas of the first embodiment, the blood glucose level can be measured and the drug solution can be administered according to the blood glucose level simply by passing venous blood through the main body. Therefore, even if the medical staff does not always manage it, it is possible to prevent poor blood sampling and easily and easily perform stable glycemic control of highly invasive patients after surgery, especially stable glycemic control of diabetic patients. It can be realized reliably and is easy to use.
 第1実施形態の人工膵臓は、患者の例えば腕に装着するだけで済む。しかも人工膵臓は軽量であり、サイズも小さく、安価に製造でき、管理が容易である。このため、人工膵臓の入手がし易く、人工膵臓を患者にセッティングしたり、取り外したりするのが容易である。また、患者からの静脈血を生体から外に出して、静脈血の血糖値の測定と、薬液の微量投与のための静脈血の送液ルートの確保が容易にできる。しかも、人工膵臓は、患者の腕に装着されているので、患者が移動する時には、患者とともに容易に移動することができる。 The artificial pancreas of the first embodiment only needs to be attached to the patient's arm, for example. Moreover, the artificial pancreas is lightweight, small in size, inexpensive to manufacture, and easy to manage. Therefore, the artificial pancreas is easily available, and the artificial pancreas can be easily set or removed from the patient. In addition, the venous blood from the patient can be taken out of the living body, the blood glucose level of the venous blood can be measured, and the venous blood feeding route for the minute administration of the drug solution can be easily secured. Moreover, since the artificial pancreas is attached to the patient's arm, it can easily move with the patient when the patient moves.
 第1実施形態の人工膵臓を用いることで、次のメリットがある。患者の血糖管理の改善、手術部位の感染の発症率の改善、予後悪化を防ぐことで死亡率の改善が図れる。医療従事者における高血糖・低血糖のリスクの低減、血糖値の測定作業やインスリン、グリコ―スの投与作業の業務量の削減、薬剤の投与判断基準の統一を図ることができる。病院については、患者の予後向上による病床回転数の改善が図れる。 Using the artificial pancreas of the first embodiment has the following merits. The mortality rate can be improved by improving the blood glucose control of patients, improving the incidence of infection at the surgical site, and preventing the prognosis from deteriorating. It is possible to reduce the risk of hyperglycemia / hypoglycemia in medical staff, reduce the amount of work required for measuring blood glucose level and administering insulin and glycosyl, and unify the criteria for drug administration. For hospitals, the number of beds can be improved by improving the prognosis of patients.
 第1実施形態の人工膵臓の本体部がいわゆるリング型であるので、本体部に対して患者の腕を通せば、本体部の装着部位の適所の1つである腕に容易に装着できる。このため、人工膵臓を用いることにより、従来、医療従事者が、人工膵臓を患者に適用する際に問題としていたチューブの取り回しの煩雑さから解放される。 Since the main body of the artificial pancreas of the first embodiment is a so-called ring type, it can be easily attached to the arm, which is one of the appropriate places for attaching the main body, by passing the patient's arm through the main body. Therefore, by using the artificial pancreas, the medical staff is freed from the complicated handling of the tube, which has been a problem when applying the artificial pancreas to the patient.
 患者の静脈血は、本体部内をほぼ一周分循環して通過する中で、血糖値の非侵襲による測定作業と、血糖値の値に応じてインスリンの投与量あるいはグルコースの投与量の決定を行い、静脈血にインスリンの微量投与あるいはグルコースの微量投与を完了できる。 While the patient's venous blood circulates and passes through the main body for almost one round, the measurement work is performed by non-invasive blood glucose level, and the insulin dose or glucose dose is determined according to the blood glucose level. , Venous blood can be completed with a small dose of insulin or a small dose of glucose.
 従来の人工膵臓は、装置が大型で複雑な操作を行う必要があり、移動用のスタンドに搭載されている。従来の人工膵臓は、床面を移動することで患者の近くに配置して用いられ、大型で複雑な操作を必要看護師等の医療従事者が、行っていた。 The conventional artificial pancreas is mounted on a stand for movement because the device is large and requires complicated operations. The conventional artificial pancreas is used by arranging it near the patient by moving the floor surface, and a large-scale and complicated operation is performed by a medical worker such as a nurse.
 しかし、第1実施形態の人工膵臓を用いることにより、人工膵臓は患者の一部分、例えば腕に対して装着すれば、静脈血の血糖値の測定を開始して、血糖値の値に応じて静脈血にインスリンの微量投与あるいはグルコースの微量投与を、自動的に容易にしかも確実に行うことができる。 However, by using the artificial pancreas of the first embodiment, when the artificial pancreas is attached to a part of the patient, for example, the arm, the measurement of the blood glucose level of venous blood is started and the vein is venous according to the blood glucose level. A small amount of insulin or a small amount of glucose can be automatically, easily and surely administered to blood.
(他の実施形態)
 次に、本発明の人工膵臓の別の好ましい実施形態を説明する。以下に説明する別の実施形態の構成要素が、上述した第1実施形態の構成要素と実質的に同じ場合には、同じ符号を記してその説明を省略する。
<第2実施形態>
 まず、本発明の人工膵臓の好ましい第2実施形態を、図5を参照して説明する。図5は、本発明の人工膵臓の第2実施形態を示している。
 図5に示す人工膵臓101が、図1に示す人工膵臓1と異なるのは、次の点である。図1に示す人工膵臓1の本体部2は、リング型であり、本体部2を腕300に装着する際には、本体部2の内周面2B内に手を入れてから腕300まで移動する。
(Other embodiments)
Next, another preferred embodiment of the artificial pancreas of the present invention will be described. When the components of another embodiment described below are substantially the same as the components of the first embodiment described above, the same reference numerals are given and the description thereof will be omitted.
<Second Embodiment>
First, a preferred second embodiment of the artificial pancreas of the present invention will be described with reference to FIG. FIG. 5 shows a second embodiment of the artificial pancreas of the present invention.
The artificial pancreas 101 shown in FIG. 5 is different from the artificial pancreas 1 shown in FIG. 1 in the following points. The main body 2 of the artificial pancreas 1 shown in FIG. 1 is a ring type, and when the main body 2 is attached to the arm 300, it moves to the arm 300 after putting a hand in the inner peripheral surface 2B of the main body 2. To do.
 これに対して、図5に示す人工膵臓101の本体部102は、弾性変形可能なプラスチック等により作られており、本体部102はリング型ではなくC字型を形成している。このため、本体部2は、切り欠き部分150を有している。これにより、本体部102を腕300に装着する場合には、この切り欠き部分150を通じて腕300を通す際に、本体部102が弾性変形する。本体部102は、腕300に対して、腕300の側方から容易に装着でき、本体部102の内周面2Bは腕300の周囲面に密着することができる。 On the other hand, the main body 102 of the artificial pancreas 101 shown in FIG. 5 is made of elastically deformable plastic or the like, and the main body 102 forms a C shape instead of a ring shape. Therefore, the main body 2 has a notched portion 150. As a result, when the main body 102 is attached to the arm 300, the main body 102 is elastically deformed when the arm 300 is passed through the notch 150. The main body 102 can be easily attached to the arm 300 from the side of the arm 300, and the inner peripheral surface 2B of the main body 102 can be brought into close contact with the peripheral surface of the arm 300.
 本体部2がC字型であると、本体部2がリング型である場合に比べて、例えば腕300に対して交差する方向から取り付けたり、取り外したりできる。このため、人工膵臓101の取り付けと取り外しが、さらに容易になる。また、適用できる患者の腕の太さの幅が大きくなる。 When the main body 2 is C-shaped, it can be attached or detached from the direction where it intersects with the arm 300, for example, as compared with the case where the main body 2 is ring-shaped. Therefore, the attachment and detachment of the artificial pancreas 101 becomes easier. It also increases the width of the patient's arm thickness that can be applied.
<第3実施形態>
 次に、本発明の人工膵臓の好ましい第3実施形態を、図6を参照して説明する。図6は、本発明の人工膵臓の第3実施形態を示している。
 図6に示す第2実施形態の人工膵臓201が、図2に示す人工膵臓1と異なる点は、次の通りである。人工膵臓201は、内蔵のバッテリ9の他に、商用電源220に接続するための外部電源用の接続部230を有する。外部電源用の接続部230は、着脱可能なコネクタ231を介して、電源供給を必要とする制御部10等に電気的に接続されている。外部電源用の接続部230は、商用電源220を所定の電圧の直流に変換して、制御部10等に供給される。この場合には、内蔵のバッテリ9の搭載を省略することもできる。
 また、図6に示すように、制御部10には、外部のモニタ用表示部330が、有線または無線により接続するようにしても良い。この外部のモニタ用表示部330は、患者のベッドから離れた場所、例えばナースセンタ等に配置する。これにより、看護師等の医療従事者は、外部のモニタ用表示部330上で、侵襲度の高い外科手術後の患者の安定的な血糖管理、特に糖尿病患者の安定的な血糖管理を、より確実に行える。
 上述した第2実施形態と第3実施形態においても、第1実施形態と同様の作用効果を発揮する。
<Third Embodiment>
Next, a preferred third embodiment of the artificial pancreas of the present invention will be described with reference to FIG. FIG. 6 shows a third embodiment of the artificial pancreas of the present invention.
The difference between the artificial pancreas 201 of the second embodiment shown in FIG. 6 and the artificial pancreas 1 shown in FIG. 2 is as follows. In addition to the built-in battery 9, the artificial pancreas 201 has a connection portion 230 for an external power supply for connecting to the commercial power supply 220. The connection unit 230 for an external power supply is electrically connected to a control unit 10 or the like that requires power supply via a detachable connector 231. The connection unit 230 for the external power supply converts the commercial power supply 220 into a direct current having a predetermined voltage and supplies the commercial power supply 220 to the control unit 10 and the like. In this case, the built-in battery 9 may be omitted.
Further, as shown in FIG. 6, an external monitor display unit 330 may be connected to the control unit 10 by wire or wirelessly. The external monitor display unit 330 is arranged at a place away from the patient's bed, such as a nurse center. As a result, medical staff such as nurses can perform stable glycemic control of highly invasive patients after surgery, especially stable glycemic control of diabetic patients, on the external monitor display unit 330. You can definitely do it.
Also in the second embodiment and the third embodiment described above, the same effects as those in the first embodiment are exhibited.
 以上説明したように、本発明の人工膵臓の各実施形態では、本体部を患者の生体の部位に対して装着すれば、血糖値の値が予め定めた値よりも大きい場合に静脈血流路部内の静脈血にインスリンを投与でき、血糖値の値が予め定めた値よりも小さい場合に静脈血流路部内の静脈血にグルコースを投与できる。このため、人工膵臓は、侵襲度の高い外科手術後の患者の安定的な血糖管理、特に糖尿病患者の安定的な血糖管理を、容易にしかも確実に実現できる。 As described above, in each embodiment of the artificial pancreas of the present invention, if the main body is attached to a part of the living body of the patient, the venous blood flow path is obtained when the blood glucose level is larger than a predetermined value. Insulin can be administered to the venous blood in the part, and glucose can be administered to the venous blood in the venous blood flow path when the blood glucose level is smaller than a predetermined value. Therefore, the artificial pancreas can easily and surely realize stable blood glucose control of patients after highly invasive surgery, particularly stable blood glucose control of diabetic patients.
 バッテリが本体部に配置されているので、外部から電源供給をする必要がなく、外部電源が無くても、人工膵臓は単独で使用することができる。 Since the battery is located in the main body, there is no need to supply power from the outside, and the artificial pancreas can be used independently even without an external power supply.
 案内管路部は、本体部内においてほぼ一周するように配置されているので、静脈血が本体部内を流れる長さをできる限り確保できる。このため、静脈血制御部は、静脈血が案内管路部内を通る際に、静脈血の血糖値の測定と、静脈血への薬液の投与量の決定と、静脈血に薬液を投与する動作を完了することができる。 Since the guide line section is arranged so as to make a round in the main body, the length of venous blood flowing in the main body can be secured as much as possible. Therefore, the venous blood control unit measures the blood glucose level of the venous blood, determines the dose of the drug solution to the venous blood, and administers the drug solution to the venous blood when the venous blood passes through the guide tube. Can be completed.
 静脈血を流す経路は、1つの留置針と、第1ルーメンと第2ルーメンを用いて、生体から静脈血を得て、血糖値を測定して必要なら薬液を投与した後に、生体に戻すことができる。静脈血の血栓を防ぐための抗血栓用薬剤とともに生理食塩水を、静脈血に供給することで、静脈血が通ることによる血栓の発生を防止する。 The route for venous blood flow is to obtain venous blood from the living body using one indwelling needle and the first and second lumens, measure the blood glucose level, administer a drug solution if necessary, and then return it to the living body. Can be done. By supplying physiological saline to the venous blood together with an antithrombotic drug for preventing the thrombus of the venous blood, the generation of the thrombus due to the passage of the venous blood is prevented.
 以上、本発明の実施形態について説明した。しかし、本発明は、上記実施形態に限定されず、特許請求の範囲を逸脱しない範囲で種々の変更を行うことができる。上記実施形態の構成は、その一部を省略したり、上記とは異なるように任意に組み合わせたりすることができる。
 例えば、本体部2,102は、図1の例では、患者の腕300に通して装着できるように腕輪タイプになっている。しかし、これに限らず、本体部2は、患者の脚部や足首等に装着できるように、リング型あるいはC字型の脚輪タイプにしても良い。
The embodiment of the present invention has been described above. However, the present invention is not limited to the above embodiment, and various modifications can be made without departing from the scope of claims. The configuration of the above embodiment may be partially omitted or may be arbitrarily combined so as to be different from the above.
For example, in the example of FIG. 1, the main body portions 2, 102 are of the bracelet type so that they can be worn through the patient's arm 300. However, the present invention is not limited to this, and the main body portion 2 may be a ring type or a C-shaped ankle type so that it can be attached to a patient's leg or ankle.
 また、本体部は、例えば腕300の外形状に合わせた少し厚みのある平板状あるいはシート状に形成して、本体部内に、静脈血送液部等の要素を配置するようにしても良い。この場合には、本体部は、例えば腕の皮膚の表面に対して、粘着剤により着脱可能に貼り付けるようにして装着したり、取付具を用いて腕に対して着脱可能に装着したりすることもできる。 Further, the main body may be formed in a slightly thick flat plate or sheet shape, for example, according to the outer shape of the arm 300, and elements such as a venous blood feeding portion may be arranged in the main body. In this case, the main body may be attached to the surface of the skin of the arm so as to be detachably attached with an adhesive, or may be attached to the arm detachably using an attachment. You can also do it.
 本実施形態に係る人工膵臓は、血糖値を測定する機能に加えて、他のバイタル情報を取得できるようにしても良い。人工膵臓は使い捨てでなく使用後に洗浄・滅菌できるようにしても良い。人工膵臓には加速度センサ等を用いて患者の体動を検知するセンサを設けても良い。本体部は、患者の生体の一部である腕や足に装着することに限らず、生体以外の部位である、例えば患者の寝ているベッドの枠体等に装着しても良い。 The artificial pancreas according to the present embodiment may be capable of acquiring other vital information in addition to the function of measuring the blood glucose level. The artificial pancreas may not be disposable but may be washed and sterilized after use. The artificial pancreas may be provided with a sensor that detects the body movement of the patient by using an acceleration sensor or the like. The main body is not limited to being attached to the arms and legs that are a part of the patient's living body, but may be attached to a part other than the living body, for example, the frame of the bed on which the patient is sleeping.
 1・・・人工膵臓、2・・・本体部、2A・・・外周面、2B・・・内周面、2C・・・左右の側面、2H・・・中空部、3・・・静脈血送液部、4・・・血糖値測定部、5・・・接続部、6A,6B・・・薬液投与操作部、9・・・バッテリ、10・・・制御部、11・・・案内管路部、11A・・・第1ルーメン、11B・・・第2ルーメン、11C・・・連結部、11P・・・一端部、11Q・・・他端部、12・・・送液ポンプ、13・・・留置針、13A・・・取り入れ側チューブ部分、13B・・・戻し側チューブ部分、13C・・・取入れ流路、13D・・・先端開口部、13E・・・戻し流路、13F・・・戻し用の開口部、21・・・インスリンカートリッジ(薬液カートリッジンの例)、22・・・グルコースカートリッジ(薬液カートリッジンの例)、30・・・表示部、40・・・血糖管理開始ボタン、41・・・抗血栓用薬剤供給部、41B・・・バッグ、41G・・・バルブ、42・・・生理食塩水供給用部、42B・・・バッグ、42G・・・バルブ、101・・・人工膵臓、102・・・本体部、150・・・切り欠き部分、201・・・人工膵臓、220・・・商用電源、230・・・接続部、231・・・コネクタ、300・・・患者の腕、330・・・モニタ用表示部、DT・・・静脈血の血糖値の測定データ 1 ... Artificial pancreas, 2 ... Main body, 2A ... Outer surface, 2B ... Inner peripheral surface, 2C ... Left and right sides, 2H ... Hollow part, 3 ... Venous blood Liquid transfer unit, 4 ... Blood glucose level measurement unit, 5 ... Connection unit, 6A, 6B ... Chemical solution administration operation unit, 9 ... Battery, 10 ... Control unit, 11 ... Guide tube Road section, 11A ... 1st lumen, 11B ... 2nd lumen, 11C ... connecting section, 11P ... one end, 11Q ... other end, 12 ... liquid feed pump, 13・ ・ ・ Indwelling needle, 13A ・ ・ ・ Intake side tube part, 13B ・ ・ ・ Return side tube part, 13C ・ ・ ・ Intake flow path, 13D ・ ・ ・ Tip opening, 13E ・ ・ ・ Return flow path, 13F ・.. Opening for return, 21 ... Insulin cartridge (example of chemical cartridge), 22 ... Glucose cartridge (example of chemical cartridge), 30 ... Display, 40 ... Start of blood glucose control Button, 41 ... Anti-thrombotic drug supply unit, 41B ... Bag, 41G ... Valve, 42 ... Saline supply unit, 42B ... Bag, 42G ... Valve, 101.・ ・ Artificial pancreas, 102 ・ ・ ・ Main body, 150 ・ ・ ・ Notch, 201 ・ ・ ・ Artificial pancreas, 220 ・ ・ ・ Commercial power supply, 230 ・ ・ ・ Connection part, 231 ・ ・ ・ Connector, 300 ・ ・・ Patient's arm, 330 ・ ・ ・ Monitor display, DT ・ ・ ・ Measurement data of blood glucose level of venous blood

Claims (10)

  1.  生体の血糖管理を行う人工膵臓であって、
     本体部と、
     前記本体部に配置される制御部と、
     前記本体部に配置され、前記生体から得られる静脈血を前記本体部に通して、前記静脈血を前記生体に戻す静脈血送液部と、
     前記本体部に配置され、前記静脈血送液部により前記本体部を通る前記静脈血の血糖値を測定して前記血糖値を前記制御部に通知する血糖値測定部と、
     前記本体部に配置され、薬液を貯留する薬液カートリッジを接続する接続部と、
     前記血糖値を前記制御部に通知すると、前記制御部の指令により前記血糖値の値に応じた所定量の前記薬液を、前記薬液カートリッジから前記静脈血に投与させる薬液投与操作部と、
     を備えることを特徴とする人工膵臓。
    An artificial pancreas that controls blood sugar in the body
    With the main body
    A control unit arranged in the main body and
    A venous blood delivery section arranged in the main body, passing venous blood obtained from the living body through the main body, and returning the venous blood to the living body.
    A blood glucose level measuring unit arranged in the main body, measuring the blood glucose level of the venous blood passing through the main body by the venous blood feeding unit, and notifying the control unit of the blood glucose level.
    A connection portion arranged in the main body portion and connecting a chemical solution cartridge for storing the chemical solution, and a connection portion.
    When the blood glucose level is notified to the control unit, a drug solution administration operation unit that administers a predetermined amount of the drug solution according to the blood glucose level value to the venous blood from the drug solution cartridge according to a command from the control unit.
    An artificial pancreas characterized by being equipped with.
  2.  前記薬液カートリッジは、前記血糖値の値が予め定めた値よりも大きい場合に前記静脈血流路部内の前記静脈血にインスリンを投与するインスリンカートリッジと、前記血糖値の値が予め定めた値よりも小さい場合に前記静脈血流路部内の前記静脈血にグルコースを投与するグルコースカートリッジと、を有することを特徴とする請求項1に記載の人工膵臓。 The drug solution cartridge is a combination of an insulin cartridge that administers insulin to the venous blood in the venous blood flow path when the blood glucose level is larger than a predetermined value, and a blood glucose level value that is predetermined. The artificial pancreas according to claim 1, further comprising a glucose cartridge that administers glucose to the venous blood in the venous blood flow path when the size is small.
  3.  前記静脈血送液部は、前記本体部に沿って配置されて前記静脈血を案内する案内管路部と、前記生体から得られる前記静脈血を、前記案内管路部に通した後に前記生体に戻す送液ポンプと、を有することを特徴とする請求項1または2に記載の人工膵臓。 The venous blood pumping portion is arranged along the main body portion to guide the venous blood, and the venous blood obtained from the living body is passed through the guiding duct portion and then the living body. The artificial pancreas according to claim 1 or 2, characterized in that it has a liquid feeding pump that returns to.
  4.  前記本体部は、リング型に形成され、前記本体部は、前記生体の一部分を通して前記生体の適所の部位に保持させることを特徴とする請求項1~3のいずれか1項に記載の人工膵臓。 The artificial pancreas according to any one of claims 1 to 3, wherein the main body portion is formed in a ring shape, and the main body portion is held at an appropriate position of the living body through a part of the living body. ..
  5.  前記制御部と、前記薬液投与操作部と、前記送液ポンプと、に電源供給するバッテリが、前記本体部に配置されていることを特徴とする請求項3に記載の人工膵臓。 The artificial pancreas according to claim 3, wherein a battery for supplying power to the control unit, the drug solution administration operation unit, and the liquid delivery pump is arranged in the main body unit.
  6.  前記案内管路部は、前記本体部内においてほぼ一周するように配置され、前記制御部は、前記静脈血が前記案内管路部内を通る際に、前記静脈血の前記血糖値の測定と、前記静脈血への前記薬液の投与量の決定と、前記静脈血に前記薬液を投与する動作と、を完了させることを特徴とする請求項3または5に記載の人工膵臓。 The guide tube portion is arranged so as to make substantially a circle in the main body portion, and the control unit measures the blood glucose level of the venous blood and the blood glucose level of the venous blood when the venous blood passes through the guide tube portion. The artificial pancreas according to claim 3 or 5, wherein the determination of the dose of the drug solution to the venous blood and the operation of administering the drug solution to the venous blood are completed.
  7.  前記案内管路部は、前記生体内から前記静脈血を前記本体内へ通す第1ルーメンと、前記本体内を通った前記静脈血を前記生体内に戻す第2ルーメンと、を有し、前記第1ルーメンと前記第2ルーメンは、平行に配置され、留置針に接続されていることを特徴とする請求項3または5に記載の人工膵臓。 The guide conduit portion has a first lumen for passing the venous blood from the living body into the main body and a second lumen for returning the venous blood passing through the main body to the main body. The artificial pancreas according to claim 3 or 5, wherein the first lumen and the second lumen are arranged in parallel and connected to an indwelling needle.
  8.  前記静脈血に抗血栓用薬剤を供給する抗血栓用薬液供給部と、前記静脈血に生理食塩水を供給する生理食塩水供給部と、が、前記本体部に接続されることを特徴とする請求項1~7のいずれか1項に記載の人工膵臓。 An antithrombotic drug solution supply unit that supplies an antithrombotic drug to the venous blood and a physiological saline supply unit that supplies physiological saline to the venous blood are connected to the main body. The artificial pancreas according to any one of claims 1 to 7.
  9.  前記生体の部位に装着される前記本体部は、C字型であることを特徴とする請求項1~8のいずれか1項に記載の人工膵臓。 The artificial pancreas according to any one of claims 1 to 8, wherein the main body portion attached to the part of the living body is C-shaped.
  10.  前記制御部と、前記薬液投与操作部と、前記送液ポンプと、に電源供給する電源供給部が、前記本体部の外部に配置されていることを特徴とする請求項3に記載の人工膵臓。 The artificial pancreas according to claim 3, wherein a power supply unit for supplying power to the control unit, the drug solution administration operation unit, and the liquid supply pump is arranged outside the main body unit. ..
PCT/JP2020/025580 2019-11-05 2020-06-29 Artificial pancreas WO2021090531A1 (en)

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07213604A (en) * 1994-02-04 1995-08-15 Yoshihiko Suzuki Controller of blood sugar value
JP2006271839A (en) * 2005-03-30 2006-10-12 Toray Ind Inc Auxiliary appliance for medical column for extracorporeal circulation
JP2017113144A (en) * 2015-12-22 2017-06-29 日機装株式会社 Clamp device

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07213604A (en) * 1994-02-04 1995-08-15 Yoshihiko Suzuki Controller of blood sugar value
JP2006271839A (en) * 2005-03-30 2006-10-12 Toray Ind Inc Auxiliary appliance for medical column for extracorporeal circulation
JP2017113144A (en) * 2015-12-22 2017-06-29 日機装株式会社 Clamp device

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