WO2019064903A1 - Pompe médicale, procédé de commande de pompe médicale et système de pompe médicale - Google Patents

Pompe médicale, procédé de commande de pompe médicale et système de pompe médicale Download PDF

Info

Publication number
WO2019064903A1
WO2019064903A1 PCT/JP2018/028751 JP2018028751W WO2019064903A1 WO 2019064903 A1 WO2019064903 A1 WO 2019064903A1 JP 2018028751 W JP2018028751 W JP 2018028751W WO 2019064903 A1 WO2019064903 A1 WO 2019064903A1
Authority
WO
WIPO (PCT)
Prior art keywords
drug
medical pump
data set
syringe
unit
Prior art date
Application number
PCT/JP2018/028751
Other languages
English (en)
Japanese (ja)
Inventor
隆幸 勝沼
Original Assignee
テルモ株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by テルモ株式会社 filed Critical テルモ株式会社
Priority to JP2019544359A priority Critical patent/JPWO2019064903A1/ja
Publication of WO2019064903A1 publication Critical patent/WO2019064903A1/fr

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES 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
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/142—Pressure infusion, e.g. using pumps
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES 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
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES 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
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/172—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body electrical or electronic

Definitions

  • the present disclosure relates to a medical pump, a control method of the medical pump, and a medical pump system.
  • Medical pumps such as a syringe pump and an infusion pump are used, for example, in an operating room, an intensive care unit (ICU), and the like. Medical pumps are used, for example, in cases where drugs such as anti-cancer drugs, anesthetics, chemotherapeutic drugs, and nutrients are administered to patients with high accuracy and for a relatively long time.
  • drugs such as anti-cancer drugs, anesthetics, chemotherapeutic drugs, and nutrients are administered to patients with high accuracy and for a relatively long time.
  • Patent Document 1 There is known a method using a drug library in order to suppress administration of a drug in a wrong setting when administering a drug with a medical pump (see, for example, Patent Document 1).
  • the drug library is, for example, a database of setting information and the like at the time of administration for each of several thousands of drugs.
  • each drug has setting information such as a reference administration rate, an upper limit value / lower limit value of administration rate, a drug code, and a drug color.
  • a collection of setting information on one drug is also referred to as a “drug profile”.
  • the various settings of the drug profile in the drug library can be uniquely customized at the medical institution that owns the medical pump.
  • a drug library is stored in each medical pump.
  • a user of a medical pump can suppress misadministration due to a setting error by setting a dose of a drug after reading a drug profile corresponding to the drug filled in a syringe or the like attached to the medical pump. Can.
  • a human error may occur in which the user selects an incorrect drug profile.
  • An object of the present disclosure made in view of such point is to provide a medical pump, a medical pump control method, and a medical pump system capable of easily selecting an appropriate drug profile from a drug library. .
  • a medical pump includes: a storage unit storing a drug library including a plurality of drug profiles; a reader capable of reading a data set stored in a communication unit having a communication unit and a memory; And a controller configured to set information on administration based on the drug profile, when a drug profile corresponding to drug specifying information included in the data set read from the communication device is stored in the storage unit.
  • the control unit uses the drug specifying information in the data set.
  • administration related to administration based on the drug profile included in the data set Set the information.
  • the medical pump further includes a notification unit, and the control unit is configured to notify the notification unit when the data set does not include the medicine profile corresponding to the medicine identification information. To inform that the drug profile can not be selected.
  • the reader can read the data set stored in the communicator attached to a syringe attachable to the medical pump.
  • the communication device is an RF tag.
  • a control method of a medical pump is a control method of a medical pump including a storage unit storing a drug library including a plurality of drug profiles, which includes a communication unit and a communication unit including a memory. Reading a data set, and setting a drug-related information based on the drug profile, when a drug profile corresponding to drug specification information included in the data set is stored in the storage unit.
  • a medical pump system is a medical pump system including a syringe to which a communication device including a communication unit and a memory is attached, and a medical pump, the medical pump system
  • a storage unit storing a drug library including a plurality of drug profiles, a reader capable of reading a data set stored in the memory of the communication unit via the communication unit, and the data read from the communication unit
  • a controller configured to set information on administration based on the drug profile, when a drug profile corresponding to drug specifying information included in the set is stored in the storage unit.
  • the syringe is a pre-filled syringe having a syringe body pre-filled with a drug containing an intravenous anesthetic or a vasoactive agent, and the communicator pre-attached to the syringe body.
  • the data set including the drug specifying information corresponding to the drug filled in the syringe body is stored in the memory of the communication device.
  • an appropriate drug profile can be easily selected from a drug library.
  • FIG. 1 is a schematic configuration view of a medical pump system according to an embodiment of the present disclosure.
  • FIG. 1 is a schematic perspective view of a medical pump according to an embodiment of the present disclosure with a syringe attached. It is a general
  • FIG. 2 is a schematic perspective view of the syringe shown in FIG.
  • It is a schematic block diagram of the communication apparatus shown in FIG. It is the schematic which shows the electric constitution of the medical pump shown in FIG. It is an example of a display of the display part of the medical pump shown in FIG. It is a flowchart which shows an example of operation
  • FIG. 1 is a schematic configuration diagram of a medical pump system 1 according to an embodiment of the present disclosure.
  • the medical pump system 1 includes a medical pump 100 and a syringe 200.
  • the syringe 200 is attachable to the medical pump 100.
  • the communication device 300 is attached to the syringe 200.
  • the communication device 300 is, for example, an RF tag.
  • the medical pump 100 and the communication device 300 can communicate by wireless communication with a short reach distance such as NFC (Near Field Communication), for example.
  • NFC Near Field Communication
  • the wireless communication between the medical pump 100 and the communicator 300 Since the wireless communication between the medical pump 100 and the communicator 300 has a short reach distance, it can be communicated when the syringe 200 is mounted on the medical pump 100, but the syringe 200 can be communicated from the medical pump 100.
  • the medical pump 100 can not communicate with the communicator 300 when it is separated by more than the above distance. Thereby, the medical pump 100 can suppress reading data from the communication device 300 attached to the syringe 200 which is not attached to the medical pump 100.
  • a communicator 300 storing a set of information (hereinafter, also simply referred to as a “data set”) corresponding to a drug filled in the syringe 200 is attached to the syringe 200.
  • the medical pump 100 stores a drug library including a plurality of drug profiles.
  • the medical pump 100 reads the data set stored in the communicator 300 from the communicator 300 when the syringe 200 is attached to the medical pump 100.
  • the medical pump 100 is information on administration based on the drug profile (hereinafter, also referred to simply as “administration information”) Set).
  • the drug specifying information is information that can specify a drug profile, and is, for example, a drug code.
  • the medicine code includes, for example, a so-called HOT code consisting of a 13-digit management number.
  • information on administration is, for example, a reference administration rate, and an upper limit value / lower limit value of the administration rate.
  • the medical pump 100 administers the drug based on the administration information customized by the medical institution that owns the medical pump 100 by setting administration information corresponding to the drug filled in the attached syringe 200. be able to.
  • the medical pump 100 can prevent administration of a drug at a dosing rate that is larger than the upper limit value set by the medical institution that owns the medical pump 100 or smaller than the lower limit value.
  • FIG. 2 is a schematic perspective view of a medical pump 100 according to an embodiment of the present disclosure.
  • FIG. 3 is a schematic front view of a medical pump 100 according to an embodiment of the present disclosure. 2 and 3 show, as an example, the case where the medical pump 100 is a syringe pump.
  • the medical pump 100 is, for example, an intravenous anesthetic filled in the syringe 200 in an intensive care unit such as an operating room or an intensive care unit (ICU), a coronal care unit (CCU), or a neonatal intensive care unit (NICU). It is used to continuously deliver drugs such as vasoactive agents to the patient's body.
  • ICU intensive care unit
  • CCU coronal care unit
  • NICU neonatal intensive care unit
  • Intravenous anesthetics include drugs that act on the nervous system to exert sedative or analgesic effects.
  • the medical pump 100 can deliver various medicines including a venous anesthetic and a blood vessel agonist etc. filled in the syringe 200 into the patient's body.
  • a venous anesthetic examples include propofol, mitazolam, remifentanil and the like.
  • applicable vasoactive agents include epinephrine, noradrenaline, dobutamine, dopamine, isosorbide dinitrate, and nitroglycerin.
  • the medical pump 100 presses the syringe presser 202 of the syringe 200 as a medicine container filled with a medicine in the T direction to make the medicine in the syringe body 201 a tube.
  • the fluid is accurately delivered to the patient P via the indwelling needle 203 and the indwelling needle 204.
  • the syringe body 201 of the syringe 200 is set so as not to move to the medical pump 100 by the clamp 5.
  • the medical pump 100 has a main body cover 2.
  • the main body cover 2 is integrally molded of a molded resin material having chemical resistance. Thereby, the main body cover 2 has a protection processing structure. Even if a drug etc. are applied to the medical pump 100, the prevention processing structure can suppress the drug etc. from invading the inside of the medical pump 100.
  • the reason for having the antifungal treatment structure is that the medicine in the syringe main body 201 is spilled, the dripping solution disposed above the medical pump 100 is spilled out, and the antiseptic solution used in the periphery is scattered. It is because it may adhere.
  • the body cover 2 has an upper portion 2A and a lower portion 2B.
  • the display unit 3 and the operation panel unit 4 are disposed.
  • a syringe setting unit 6 and a syringe pressing unit driving unit 7 for pressing the syringe pressing unit 202 are disposed.
  • the display unit 3 is an image display device capable of color display.
  • the display unit 3 can be configured by, for example, a color liquid crystal display device.
  • the display unit 3 can display information in a plurality of foreign languages as needed, in addition to information description in Japanese.
  • the display unit 3 is disposed at the upper left position of the upper portion 2A of the main body cover 2 and above the syringe installation unit 6 and the syringe pusher driving unit 7.
  • the display unit 3 includes an input device such as a touch sensor, and may receive an input from a user.
  • the operation panel unit 4 is disposed on the right side of the display unit 3 in the upper portion 2A of the main body cover 2.
  • the operation panel unit 4 is provided with a power ON / OFF button 4A, an operation indicator 4F, and an operation button.
  • FIGS. 2 and 3 show an example in which the minimum necessary fast forward switch button 4B, start switch button 4C, stop switch button 4D, and menu selection button 4E are arranged as operation buttons.
  • the syringe installation unit 6 and the syringe presser drive unit 7 are arranged side by side along the X direction.
  • the syringe installation part 6 can insert and fix the syringe 200 detachably.
  • the syringe installation unit 6 can fix different types of syringes 200 of different sizes.
  • FIG. 4 shows an external perspective view of the syringe 200.
  • the syringe 200 has a syringe body 201 and a syringe pusher 202.
  • the syringe body 201 has a body flange 209, and the syringe presser 202 has a presser flange 205.
  • On the syringe body 201 a scale 210 of medicine is formed.
  • One end of a flexible tube 203 is detachably connected to the outlet portion 211 of the syringe body 201.
  • the syringe 200 is a prefilled syringe in which a drug is pre-filled in the syringe body 201
  • the syringe 200 is a medical device with the cap for sealing the opening of the outlet portion 211 attached to the outlet portion 211 of the syringe body 201.
  • Drugs pre-filled in the syringe body 201 include intravenous anesthetics such as propofol, mitazolam, and remifentanil, and vasoactive drugs such as epinephrine, noradrenaline, dobutamine, dopamine, isosorbide nitrate, and nitroglycerin.
  • a communicator 300 storing a data set corresponding to a drug filled in the syringe 200 is attached to the syringe body 201.
  • the syringe 300 is in a state in which the communication device 300 having a memory storing a data set including drug specifying information corresponding to the drug filled in the syringe body 201 is attached to the syringe body 201 in advance. 200 are provided to medical institutions.
  • FIG. 5 shows a schematic configuration diagram of the communication device 300.
  • the communication device 300 is, for example, an RF tag.
  • the communication device 300 includes a communication unit 310 and a memory 320.
  • the communication unit 310 performs wireless communication with the reader 170 (see FIG. 6) included in the medical pump 100.
  • the communication unit 310 communicates with the medical pump 100 by short distance wireless communication such as NFC.
  • the memory 320 stores information such as a data set corresponding to a drug filled in the syringe 200.
  • the data set stored in the memory 320 includes drug identification information such as a drug code.
  • the data set stored in the memory 320 may further include a drug profile.
  • the communication unit 310 When the communication unit 310 receives a request for transmission of a data set from the medical pump 100, the communication unit 310 transmits the data set stored in the memory 320 to the medical pump 100.
  • the apparatus configuration of the medical pump 100 will be described with reference to FIGS. 2 and 3 again.
  • the syringe setting unit 6 includes a storage unit 8 for storing the syringe body 201 and a clamp 5.
  • the housing portion 8 is a recess having a substantially semicircular cross section and is formed along the X direction in order to store the syringe body 201.
  • a tube fixing portion 9 for detachably holding the tube 203 is formed on the wall portion of the end portion of the housing portion 8.
  • the clamp 5 When operating the clamp 5 to remove the syringe 200 from the syringe setting portion 6, the clamp 5 is pulled in the Y1 direction (front direction) against the force of a spring (not shown) and further turned 90 degrees in the R1 direction. By this operation, the fixing of the syringe body 201 by the clamp 5 is released, and the syringe 200 can be removed from the housing portion 8. Further, when the clamp 5 is operated to attach the syringe 200 to the syringe setting portion 6, the clamp 5 is pulled in the Y1 direction against the force of a spring (not shown) and rotated 90 degrees in the R2 direction by the spring force. Return to the Y2 direction.
  • the syringe body 201 can be housed in the housing portion 8 and fixed by the clamp 5.
  • the right end 8E of the storage unit 8 of the syringe installation unit 6 is partially cut away so that the syringe 200 of various capacities such as 5 mL, 10 mL, 20 mL, 30 mL, 50 mL, etc. can be fixed by the clamp 5 It has become.
  • the syringe pusher 202 When the syringe body 201 is housed and fixed in the housing portion 8, the syringe pusher 202 is disposed in the syringe pusher driving unit 7.
  • the syringe presser driving unit 7 has a slider 10. The slider 10 pushes the pusher flange 205 of the syringe pusher 202 little by little along the T direction relative to the syringe main body 201 according to a command from the control unit 180 shown in FIG.
  • the X direction, the Y direction, and the Z direction in FIG. 2 and FIG. 3 are orthogonal to each other, and the Z direction is the vertical direction.
  • the medical pump 100 has a control unit (computer) 180 that determines and controls the overall operation.
  • the control unit 180 is, for example, a one-chip microcomputer.
  • the control unit 180 is connected to the power ON / OFF button 4A and the switch 111.
  • the switch 111 supplies power to the control unit 180 from any one of the power converter unit 112 and the rechargeable battery 113 by switching between the power converter unit (power source unit) 112 and the rechargeable battery 113 such as a lithium ion battery, for example. Do.
  • the power supply converter unit 112 is connected to the commercial AC power supply 115 via the outlet 114.
  • the pump unit 160 is electrically connected to the control unit 180.
  • the pump unit 160 administers the drug to the patient according to the administration information set based on the drug profile according to an instruction from the control unit 180.
  • a pair of detection switches 120 and 121 are disposed in the housing portion 8 of the pump portion 160.
  • the detection switches 120 and 121 detect whether or not the syringe body 201 of the syringe 200 is correctly disposed in the storage unit 8 and notify the control unit 180.
  • the clamp sensor 122 of the pump unit 160 detects the position state of the clamp 5 to notify the control unit 180 whether or not the syringe body 201 is reliably clamped by the clamp 5.
  • the motor 133 of the syringe pusher driving unit 7 of the pump unit 160 rotates the feed screw 135 to move the slider 10 in the T direction when driven by the motor driver 134 by an instruction of the control unit 180.
  • the slider 10 presses the presser flange 205 of the syringe presser 202 in the T direction, and the medicine in the syringe main body 201 shown in FIG. Send the fluid correctly.
  • the fast forward switch button 4B, the start switch button 4C, the stop switch button 4D, and the menu selection button 4E are electrically connected to the control unit 180.
  • the start switch button 4C is pressed, a control signal of liquid feeding start is input to the control unit 180.
  • the stop switch button 4D is pressed, a control signal of liquid feeding stop is input to the control unit 180.
  • the display unit driver 130 is electrically connected to the control unit 180.
  • the display driver 130 drives the display 3 according to an instruction of the controller 180 to display various information on the display 3.
  • the notification unit 131 is electrically connected to the control unit 180.
  • the notification unit 131 notifies various alarm contents by voice, light, vibration, or the like according to an instruction of the control unit 180.
  • reports the various alarm content by the display on the display part 3
  • the display part 3 may have a function as an alerting
  • the communication unit 140 transmits and receives data to and from a server of a medical institution or the like via a network. Also, the communication unit 140 may be connected locally to a computer such as a desktop computer, for example, to transmit and receive data.
  • the reader 170 communicates with the communication unit 310 of the communication device 300 attached to the syringe 200 by wireless communication with a short reach distance, such as NFC.
  • the reader 170 transmits a data set transmission request to the communication device 300.
  • the reader 170 reads the data set transmitted from the communicator 300 in response to the transmission request from the reader 170.
  • the storage unit 110 may be configured using, for example, a semiconductor memory and a magnetic memory.
  • the storage unit 110 stores various information and programs necessary for the operation of the medical pump 100.
  • the storage unit 110 stores a drug library including a plurality of drug profiles.
  • the storage unit 110 can store a drug library customized by a medical institution that owns the medical pump 100. For example, when the control unit 180 downloads the drug library stored in the server of the medical institution to the storage unit 110 via the communication unit 140, the storage unit 110 stores the drug library customized by the medical institution. can do.
  • the control unit 180 acquires the drug specifying information included in the data set.
  • the drug specifying information is, for example, a drug code, but is not limited to the drug code and may be any information that can specify a drug.
  • the control unit 180 determines whether or not a drug profile corresponding to the acquired drug specifying information is stored in the storage unit 110, and if stored, reads information on the drug profile and sets administration information and the like. Do.
  • the administration information includes the reference administration rate and the upper limit / lower limit of the administration rate, as described above.
  • control unit 180 When the control unit 180 reads a drug profile corresponding to the drug filled in the syringe 200 mounted on the medical pump 100, the control unit 180 reflects the information included in the drug profile and updates the display content of the display unit 3. .
  • FIG. 7 shows an example of display on the display unit 3 when the control unit 180 reads a drug profile.
  • a drug name display field 701 a drug color display field 702, and an administration setting display field 703 are displayed. Also, if there is a message, a message is displayed in the message column 704.
  • the medicine name display column 701 for example, a medicine name such as "nitroglycerin" is displayed.
  • the medicine color display column 702 colors preset for the medicine are displayed.
  • the administration setting display column 703 displays, for example, a reference administration rate and a reference flow rate.
  • 1.00 [ ⁇ g / kg / min] is displayed as the reference administration rate
  • 1.20 [mL / h] is displayed as the reference flow rate.
  • the user can, for example, change the reference dosing rate as needed.
  • the control unit 180 causes the notification unit 131 to notify the warning.
  • the display unit 3 functions as a notification unit, the control unit 180 may notify a warning by changing the display of the display unit 3.
  • the medical pump 100 can thereby prevent the user from administering the drug at a dosing rate that is greater than the upper limit value of the dosing rate defined in the drug profile or less than the lower limit value.
  • a message such as “The drug has been recognized” is displayed in the message field 704, for example.
  • control unit 180 controls the pump unit 160 so as to administer the medicine to the patient according to the set administration information.
  • the control unit 180 corresponds the acquired drug specifying information to the data set read by the reader 170. It is determined whether the drug profile to be included is included. When the drug set is included in the data set, the control unit 180 reads the information of the drug profile and sets administration information and the like.
  • the control unit 180 can not select the drug profile Is notified to the notification unit 131.
  • the control unit 180 causes the message column 704 to display “drug profile not found” on the display shown in FIG. 7, for example. Further, in this case, the control unit 180 may display a color indicating an abnormality in the drug color display field 702 without displaying the drug name in the drug name display field 701 in FIG. 7.
  • the reader 170 of the medical pump 100 reads the data set stored in the communicator 300 from the communicator 300 when the syringe 200 is attached to the medical pump 100.
  • the control unit 180 acquires drug specifying information included in the data set read by the reader 170 (step S101).
  • the control unit 180 determines whether or not the medicine profile corresponding to the acquired medicine identification information is stored in the storage unit 110 (step S102).
  • step S102 When the drug profile corresponding to the drug specifying information is stored in the storage unit 110 (Yes in step S102), the control unit 180 reads the drug profile stored in the storage unit 110 (step S103).
  • control unit 180 causes the drug profile corresponding to the acquired drug specifying information to be the data set read by the reader 170. It is determined whether it is included (step S104).
  • the control unit 180 reads the drug profile included in the data set (step S105). .
  • control unit 180 When the drug profile corresponding to the drug specifying information is not included in the data set read by the reader 170 (No in step S104), the control unit 180 notifies the notifying unit 131 that the drug profile can not be selected as a warning. (Step S106).
  • the reader 170 can read the data set stored in the communicator 300. Further, when the drug profile corresponding to the drug specifying information included in the data set read from the communication device 300 is stored in the storage unit 110, the control unit 180 sets information on administration based on the drug profile. Thereby, the medical pump 100 according to the present embodiment can easily select an appropriate drug profile from the drug library. Further, by storing the drug profile customized by the medical institution that owns the medical pump 100 in the storage unit 110, the medical pump 100 can read the drug profile customized by the medical institution.
  • the control unit 180 corresponds to the drug specifying information to the data set. If the drug profile is included, information on administration is set based on the drug profile. As a result, the medical pump 100 can read a general-purpose drug profile even when the drug profile corresponding to the drug specifying information included in the data set read from the communication device 300 is not stored. Medical institutions can use this universal drug profile to perform dosing, but may change it as needed.
  • the control unit 180 determines the drug Set information on dosing based on the profile. Further, when the drug profile corresponding to the drug specifying information included in the data set read from the communication device 300 is not stored in the storage unit 110, the control unit 180 includes the drug profile corresponding to the drug specifying information in the data set. If a drug profile is included, information on administration is set based on the drug profile. Therefore, when the drug profile corresponding to the drug specifying information included in the data set read from the communicator 300 is stored in both the memory 110 and the communicator 300, the controller 180 stores the drug profile in the memory 110. Set up information on dosing based on the drug profile being used. Thereby, the user can easily set desired administration information in the medical pump 100.
  • control unit 180 does not store the drug profile corresponding to the drug specifying information included in the data set read from the communication unit 300 in the storage unit 110, and the drug specifying information is not stored in the data set. If the medicine profile corresponding to is not included, the notification unit 131 or the display unit 3 is informed that the medicine profile can not be selected. As a result, the medical pump 100 can inform the user that the drug profile can not be selected and that caution is required.
  • the medical pump is not limited to a syringe pump, and may be another type of medical pump such as an infusion pump that delivers a drug contained in an infusion bag.
  • the present disclosure relates to a medical pump, a control method of the medical pump, and a medical pump system.

Landscapes

  • Health & Medical Sciences (AREA)
  • Vascular Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Infusion, Injection, And Reservoir Apparatuses (AREA)

Abstract

L'invention concerne une pompe médicale comprenant : une unité de stockage pour stocker une bibliothèque de médicaments comprenant une pluralité de profils de médicaments ; un lecteur capable de lire un ensemble de données stocké dans un dispositif de communication comportant une unité de communication et une mémoire ; et une unité de commande pour paramétrer, lorsqu'un profil de médicament correspondant à des informations de spécification de médicament figurant dans l'ensemble de données lu à partir du dispositif de communication est stocké dans l'unité de stockage, des informations concernant l'administration sur la base du profil du médicament.
PCT/JP2018/028751 2017-09-29 2018-07-31 Pompe médicale, procédé de commande de pompe médicale et système de pompe médicale WO2019064903A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2019544359A JPWO2019064903A1 (ja) 2017-09-29 2018-07-31 医療用ポンプ、医療用ポンプの制御方法、及び医療用ポンプシステム

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2017191866 2017-09-29
JP2017-191866 2017-09-29

Publications (1)

Publication Number Publication Date
WO2019064903A1 true WO2019064903A1 (fr) 2019-04-04

Family

ID=65901605

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2018/028751 WO2019064903A1 (fr) 2017-09-29 2018-07-31 Pompe médicale, procédé de commande de pompe médicale et système de pompe médicale

Country Status (2)

Country Link
JP (1) JPWO2019064903A1 (fr)
WO (1) WO2019064903A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021085135A1 (fr) 2019-10-29 2021-05-06 テルモ株式会社 Pompe médicale, procédé de commande de pompe médicale et système de pompe médicale

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008529675A (ja) * 2005-02-11 2008-08-07 カーディナル ヘルス ３０３、インコーポレイテッド 薬剤管理用識別システム及び方法

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008529675A (ja) * 2005-02-11 2008-08-07 カーディナル ヘルス ３０３、インコーポレイテッド 薬剤管理用識別システム及び方法

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021085135A1 (fr) 2019-10-29 2021-05-06 テルモ株式会社 Pompe médicale, procédé de commande de pompe médicale et système de pompe médicale
US11969575B2 (en) 2019-10-29 2024-04-30 Terumo Kabushiki Kaisha Medical infusion pump, method of controlling medical infusion pump, and medical infusion pump system

Also Published As

Publication number Publication date
JPWO2019064903A1 (ja) 2020-09-10

Similar Documents

Publication Publication Date Title
JP7162604B2 (ja) 医療用ポンプ、医療用ポンプの制御方法、及び医療用ポンプシステム
JP6360332B2 (ja) 送液ポンプ
US20210146036A1 (en) Infusion system, device, and method having advanced infusion features
JP6207516B2 (ja) 輸液ポンプ
JP4942658B2 (ja) キャップ付き注入装置
US20160259913A1 (en) Drug delivery dose indicator
JP5881299B2 (ja) 医療用ポンプ
JP6441076B2 (ja) シリンジポンプ
WO2019064903A1 (fr) Pompe médicale, procédé de commande de pompe médicale et système de pompe médicale
JP2017131675A (ja) シリンジポンプ
JP2019069289A (ja) シリンジポンプ
CN114585403B (zh) 医疗用泵、医疗用泵的控制方法及医疗用泵***
JP7183169B2 (ja) 医療用ポンプ、医療用ポンプの制御方法、及び医療用ポンプシステム
JP6397893B2 (ja) 送液ポンプ
JP2015181555A (ja) 送液ポンプ
WO2014049657A1 (fr) Pompe à usage médical
CA3223991A1 (fr) Pompes de perfusion intraveineuse avec systeme et ajustement de modele pharmacodynamique pour affichage et fonctionnement

Legal Events

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

Ref document number: 18863548

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2019544359

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 18863548

Country of ref document: EP

Kind code of ref document: A1