WO2019064903A1

WO2019064903A1 - Medical pump, method for controlling medical pump, and medical pump system

Info

Publication number: WO2019064903A1
Application number: PCT/JP2018/028751
Authority: WO
Inventors: 隆幸勝沼
Original assignee: テルモ株式会社
Priority date: 2017-09-29
Filing date: 2018-07-31
Publication date: 2019-04-04
Also published as: JPWO2019064903A1

Abstract

Provided is a medical pump comprising: a storage unit for storing a medicine library including a plurality of medicine profiles; a reader capable of reading a data set stored in a communication device having a communication unit and a memory; and a control unit for setting, when a medicine profile corresponding to medicine specification information included in the data set read from the communication device is stored in the storage unit, information on administration on the basis of the medicine profile.

Description

MEDICAL PUMP, MEDICAL PUMP CONTROL METHOD, AND MEDICAL PUMP SYSTEM

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.

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. In the drug library, 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. Hereinafter, 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. Usually, 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.

JP, 2012-179099, A

In order to read a drug profile corresponding to a drug loaded in a syringe or the like attached to a medical pump, it is first necessary to select an appropriate drug profile from a drug library stored in the medical pump. However, if, for example, a drug library has thousands of drug profiles, it is laborious to select an appropriate drug profile.

Also, during the operation, a plurality of medical pumps are often used, but it takes time to select an appropriate drug profile for each medical pump.

In addition, when selecting a drug profile, 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 according to a first aspect of the present disclosure 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.

As one embodiment of the present disclosure, when the drug profile corresponding to the drug specifying information included in the data set is not stored in the storage unit, the control unit uses the drug specifying information in the data set. When it is determined whether the corresponding drug profile is included, and the data set includes the drug profile corresponding to the drug specifying information, administration related to administration based on the drug profile included in the data set Set the information.

As one embodiment of the present disclosure, 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.

In one embodiment of the present disclosure, the reader can read the data set stored in the communicator attached to a syringe attachable to the medical pump.

In one embodiment of the present disclosure, the communication device is an RF tag.

A control method of a medical pump according to a second aspect of the present disclosure 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 according to a third aspect of the present disclosure 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 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 set is stored in the storage unit.

In one embodiment of the present disclosure, 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.

According to a medical pump, a medical pump control method, and a medical pump system according to the present disclosure, an appropriate drug profile can be easily selected from a drug library.

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 | schematic front view of the medical pump shown in FIG. 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 | movement of the medical pump shown in FIG.

Hereinafter, embodiments of the present disclosure will be described with reference to the drawings. The dimensional proportions of the drawings may be exaggerated and differ from the actual proportions for the convenience of description. Moreover, in each figure, the same code | symbol is attached | subjected to a common member.

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.

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. When the drug library corresponding to the drug specifying information included in the read data set is included in the drug library, the medical pump 100 is information on administration based on the drug profile (hereinafter, also referred to simply as “administration information”) Set).

Here, 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.

Also, information on administration (administration information) 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. In addition, 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.

Next, a medical pump 100 according to an embodiment of the present disclosure will be described with reference to FIGS. 2 and 3. 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. 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. Examples of applicable intravenous anesthetics include propofol, mitazolam, remifentanil and the like. Examples of applicable vasoactive agents include epinephrine, noradrenaline, dobutamine, dopamine, isosorbide dinitrate, and nitroglycerin.

Hereinafter, an example of the device configuration of the medical pump 100 will be described in detail.

As shown in FIGS. 2 and 3, 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. At this time, 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.

As shown in FIGS. 2 and 3, the body cover 2 has an upper portion 2A and a lower portion 2B.

In the upper portion 2A, the display unit 3 and the operation panel unit 4 are disposed.

In the lower portion 2B, 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.

As shown in FIGS. 2 and 3, 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. As shown in FIG. 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. When 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. Provided to the institution. 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. When the syringe 200 is a prefilled syringe, 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. As shown in FIG. As described above, 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. In addition, the data set stored in the memory 320 may further include a drug profile.

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.

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. By this operation, 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.

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.

Next, with reference to FIG. 6, an example of an electrical configuration of the medical pump 100 shown in FIG. 1 will be described in detail.

In FIG. 6, 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.

In FIG. 6, 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.

In FIG. 6, 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. Thereby, 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.

In FIG. 6, 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. When the start switch button 4C is pressed, a control signal of liquid feeding start is input to the control unit 180. In addition, when the stop switch button 4D is pressed, a control signal of liquid feeding stop is input to the control unit 180.

In FIG. 6, 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.

In FIG. 6, 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. Moreover, when the control part 180 alert | reports the various alarm content by the display on the display part 3, the display part 3 may have a function as an alerting | reporting part.

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.

When the syringe 200 is attached to the medical pump 100, 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.

When the syringe 200 is attached to the medical pump 100 and the reader 170 reads a data set from the communication device 300, 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.

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. In the example shown in FIG. 7, 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.

In the medicine name display column 701, for example, a medicine name such as "nitroglycerin" is displayed. In 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. In the example shown in FIG. 7, 1.00 [μg / kg / min] is displayed as the reference administration rate, and 1.20 [mL / h] is displayed as the reference flow rate. The user can, for example, change the reference dosing rate as needed. However, when the value set by the user exceeds the upper limit value of the administration rate defined in the drug profile or falls below the lower limit value, the control unit 180 causes the notification unit 131 to notify the warning. When 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.

When the control unit 180 reads a drug profile, a message such as “The drug has been recognized” is displayed in the message field 704, for example.

When the start switch button 4C is pressed, the control unit 180 controls the pump unit 160 so as to administer the medicine to the patient according to the set administration information.

When the drug profile corresponding to the drug specifying information acquired from the data set read by the reader 170 is not stored in the storage unit 110, 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.

If the drug profile corresponding to the drug specifying information acquired from the data set read by the reader 170 is not stored in the storage unit 110 and is not included in the data set, the control unit 180 can not select the drug profile Is notified to the notification unit 131. When the display unit 3 is made to function as a notification unit, 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.

An example of the operation of the medical pump 100 will be described with reference to the flowchart shown in FIG.

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).

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).

When the drug profile corresponding to the drug specifying information is not stored in the storage unit 110 (No in step S102), the 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).

When the drug profile corresponding to the drug specifying information is included in the data set read by the reader 170 (Yes in step S104), the control unit 180 reads the drug profile included in the data set (step S105). .

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).

Thus, in the medical pump 100 according to the present embodiment, 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.

Further, in the present embodiment, 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 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.

Further, in the medical pump 100 according to the present embodiment, 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 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.

Further, in the present embodiment, the 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 present invention is not limited to the embodiment described above, and various modifications can be made by one skilled in the art within the technical concept of the present invention. For example, 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.

1 Medical pump system 2 Body cover 2A Upper part of body cover 2B Lower part of body cover 3 Display 4 Operation panel 4A Power ON / OFF button 4B Fast-forward switch button 4C Start switch button 4D Stop switch button 4E Menu selection button 4F Operation indicator 5 Clamp 6 Syringe installation unit 7 Syringe pusher drive unit 8 Housing unit 8E Right end of the housing unit 9 Tube fixing unit 10 Slider 100 Medical pump 110 Storage unit 111 Switch 112 Power supply converter unit (Power supply unit)
113 rechargeable battery 114 outlet 115 commercial AC power supply 120 detection switch 121 detection switch 122 clamp sensor 130 display unit driver 131 notification unit 133 motor 134 motor driver 135 feed screw 140 communication unit 160 pump unit 170 reader 180 control unit 200 syringe 201 syringe body 202 Syringe presser 203 Tube 204 Indwelling needle 205 Presser flange 209 Body flange 210 Scale of medicine 211 Syringe outlet 300 Communication unit 310 Communication unit 320 Memory 701 Drug name display column of display unit 702 Drug color display column of display unit 703 Display Administration setting display section of part 704 Message section of display part P Patient

Claims

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 related to 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. Pump.
In the medical pump according to claim 1,
The control unit
If the drug profile corresponding to the drug specifying information included in the data set is not stored in the storage unit, it is determined whether the data set includes the drug profile corresponding to the drug specifying information;
A medical pump, wherein, when the data set includes the drug profile corresponding to the drug specifying information, information on administration is set based on the drug profile included in the data set.
In the medical pump according to claim 2,
Further comprising a notification unit;
The medical pump, wherein the control unit causes the notification unit to notify that the drug profile can not be selected when the data set does not include the drug profile corresponding to the drug specifying information.
The medical pump according to any one of claims 1 to 3.
The medical pump, wherein the reader is capable of reading the data set stored in the communicator attached to a syringe attachable to the medical pump.
The medical pump according to any one of claims 1 to 4.
The medical communication pump is an RF tag.
A control method of a medical pump including a storage unit storing a drug library including a plurality of drug profiles, the control method comprising:
Reading a data set from a communicator having a communicator and a memory;
And controlling information on administration based on the drug profile, when the drug profile corresponding to the drug specifying information included in the data set is stored in the storage unit.
A medical pump system comprising: a syringe to which a communication unit having a communication unit and a memory is attached; and a medical pump,
The medical pump is
A storage unit storing a drug library including a plurality of drug profiles;
A reader capable of reading the data set stored in the memory of the communication device via the communication unit;
And a controller configured to set information related to 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. Pump system.
In the medical pump system according to claim 7,
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 attached to the syringe body in advance.
The medical pump system, wherein the data set including the medicine specifying information corresponding to the medicine filled in the syringe body is stored in the memory of the communication device.