[go: up one dir, main page]

WO2020149045A1 - Medical pump - Google Patents

Medical pump Download PDF

Info

Publication number
WO2020149045A1
WO2020149045A1 PCT/JP2019/047700 JP2019047700W WO2020149045A1 WO 2020149045 A1 WO2020149045 A1 WO 2020149045A1 JP 2019047700 W JP2019047700 W JP 2019047700W WO 2020149045 A1 WO2020149045 A1 WO 2020149045A1
Authority
WO
WIPO (PCT)
Prior art keywords
unit
medical pump
power
battery
sub
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/JP2019/047700
Other languages
French (fr)
Japanese (ja)
Inventor
裕一 筒井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Terumo Corp
Original Assignee
Terumo Corp
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 Terumo Corp filed Critical Terumo Corp
Priority to JP2020566142A priority Critical patent/JPWO2020149045A1/en
Publication of WO2020149045A1 publication Critical patent/WO2020149045A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • 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 disclosure relates to a medical pump used for delivering a liquid into a living body.
  • Medical pumps are electric devices that consume electric power to operate. Many medical pumps are capable of both being operated by receiving AC power from an external power source such as a commercial power system and operating by being supplied with power from a built-in battery. ..
  • the medical pump cannot receive power from both the external power source and the built-in battery due to some abnormality, the medical pump cannot operate. In that case, it is desirable to be able to inform a medical staff or the like that an abnormality of the power source has occurred in the medical pump.
  • IEC60601-2-24:2012 which is a standard for medical pumps, etc., gives a high-priority alarm when a medical pump cannot be supplied with power from both an external power source and a built-in battery. Is required to be notified for 3 minutes or more.
  • Patent Document 1 discloses a medical pump that includes a main battery and a sub battery, and the sub battery can notify an alarm.
  • An object of the present disclosure is to provide a medical pump that can improve the convenience of a configuration including a main battery and a sub battery.
  • the medical pump according to the first aspect of the present disclosure can supply electric power in a state in which the external electric power acquisition unit that acquires electric power from the external electric power source and the electric power supply from the external electric power acquisition unit are not received.
  • a first power supply unit and a second power supply unit, and the first power supply unit is capable of charging the second power supply unit.
  • the first power supply unit charges the second power supply unit when the external power acquisition unit is not acquiring power from an external power source. To do.
  • a medical pump further includes an alarm notification unit that notifies an alarm, and the second power supply unit is configured such that both the external power acquisition unit and the first power supply unit supply power. When it is not possible to supply the power, it is possible to supply power to the alarm notification unit for the first predetermined time.
  • the medical pump as one embodiment of the present disclosure further includes a control unit, and the control unit has any two of the external power acquisition unit, the first power supply unit, and the second power supply unit.
  • the alarm informing unit is informed of the alarm.
  • control unit controls the external power acquisition unit, the first power supply unit, and the external power acquisition unit for a second predetermined time after the medical pump is activated. Even if any two of the second power supply units cannot supply power to the medical pump, the alarm notification unit is not notified of an alarm.
  • the first power supply unit is a battery that can be charged with the power supplied from the external power acquisition unit.
  • the second power supply unit is a capacitor.
  • the convenience of the configuration including the main battery and the sub battery can be improved.
  • FIG. 1 is a front view of a medical pump according to an embodiment of the present disclosure. It is a front view of the medical pump shown in FIG. 1 in which the syringe is mounted. It is a functional block diagram of the medical pump shown in FIG. It is a figure which shows a mode that an external power acquisition part charges a main battery and a sub-battery, when the external power acquisition part is acquiring power from an external power source. It is a figure which shows a mode that a sub battery is charged with a main battery, when the external electric power acquisition part has not acquired electric power from an external electric power source. 5 is a flowchart showing an example of operation of the medical pump according to the embodiment of the present disclosure.
  • FIG. 1 is a front view of a medical pump 1 according to an embodiment of the present disclosure.
  • the medical pump 1 is described as a syringe pump, but the medical pump 1 is not limited to a syringe pump.
  • the medical pump 1 may be an infusion pump, a nutrition pump, or a blood pump.
  • FIG. 2 is a front view of the medical pump 1 with the syringe 50 placed thereon. As shown in FIG. 2, the medical pump 1 is configured as a pump that feeds the liquid contained in the hollow portion 52 of the syringe 50.
  • the medical pump 1 includes a body cover 2.
  • the body cover 2 is integrally molded with a molding resin material having chemical resistance.
  • the main body cover 2 has a splash-proof treatment structure. Even if the medical pump 1 is exposed to a drug or the like, the splash-proof treatment structure can prevent the drug or the like from entering the inside of the medical pump 1.
  • the medical pump 1 includes a mounting portion 11 on which a syringe 50 can be mounted.
  • the syringe 50 that can be mounted on the mounting portion 11 has a cylindrical outer cylinder 51 that defines a hollow portion 52 therein, and a syringe 50 that is inserted into the hollow portion 52 from the proximal end side of the outer cylinder 51.
  • the hollow portion 52 can be moved along the extending direction A of the outer cylinder 51 (hereinafter, simply referred to as “extending direction A”) while closely contacting the inner peripheral surface of the outer cylinder 51 without a gap.
  • extending direction A extending direction of the outer cylinder 51
  • the outer cylinder 51 has an outer cylinder flange 53 at the base end, and defines an outlet hole 54 that communicates the hollow portion 52 with the outside at the tip.
  • a flexible tube 60 is attached to the outlet hole 54.
  • the pusher 55 has a pusher flange 56 at the base end.
  • a liquid such as a drug solution is stored in the hollow portion 52 of the syringe 50.
  • the mounting portion 11 can mount the outer cylinder 51 of the syringe 50.
  • the medical pump 1 accommodates a part of the outer cylinder flange 53 to accommodate the outer cylinder 51. Is provided in the extending direction A with respect to the medical pump 1.
  • the medical pump 1 includes a slider 12.
  • the slider 12 is movable along the extension direction A together with the pusher 55 of the syringe 50 mounted on the mounting unit 11.
  • the slider 12 includes a pusher fixing portion 13.
  • the pusher fixing section 13 fixes the pusher 55 of the syringe 50 placed on the placing section 11 to the slider 12.
  • the pusher fixing portion 13 can fix the pusher flange 56 to the slider 12 by sandwiching the pusher flange 56 of the mounted syringe 50.
  • the pusher flange 56 is fixed to the slider 12 by the pusher fixing portion 13, the pusher 55 moves integrally with the slider 12 as the slider 12 moves in the extending direction A.
  • the outer cylinder 51 mounted on the mounting portion 11 is fixed to the medical pump 1 in the extending direction A because a part of the outer cylinder flange 53 is housed in the slit 15. .. Therefore, when the slider 12 moves to the tip side of the syringe 50, the pusher 55 moves to the tip side with respect to the outer cylinder 51, and the liquid contained in the hollow portion 52 is discharged from the outlet hole 54. Therefore, the liquid contained in the hollow portion 52 can be sent to the inside of the living body through the tube 60.
  • the medical pump 1 includes a syringe clamp 14 that fixes an outer cylinder 51 of the syringe 50 mounted on the mounting portion 11.
  • the syringe clamp 14 is movable along the direction B orthogonal to the extending direction A, and the outer cylinder 51 of the syringe 50 mounted on the mounting unit 11 is replaced with the mounting unit 11. It is possible to fix it by sandwiching it between them. Further, fixing the outer cylinder 51 with the syringe clamp 14 makes it difficult for a part of the outer cylinder flange 53 to come off the slit 15, so that the outer cylinder 51 is firmly fixed to the medical pump 1.
  • the medical pump 1 includes a notched tube guide portion 16 at a position closer to the tip side than the syringe 50 when the syringe 50 is placed on the placing portion 11. I have it.
  • the tube guide portion 16 is used for allowing the tube 60 attached to the tip of the syringe 50 to pass therethrough while positioning the syringe 50 placed on the placing portion 11.
  • FIG. 3 is a functional block diagram of the medical pump 1.
  • the medical pump 1 includes, as functional blocks, a circuit unit 20, an operation input unit 31, a display unit 32, an alarm notification unit 33, a pump drive unit 34, and an external power monitoring unit 70. And a main battery monitoring unit 72 and a sub battery monitoring unit 73.
  • the medical pump 1 serves as an electric power supply unit capable of supplying electric power to the medical pump 1, an external electric power acquisition unit 40, a main battery 42 as a first electric power supply unit, and a second electric power supply unit. Sub battery 43 of.
  • the circuit unit 20 includes a clock unit 21, a storage unit 22, and a control unit 23.
  • the clock unit 21 measures time, ticks the time, and can be realized by, for example, RTC (Real Time Clock: real time clock).
  • the clock unit 21 may be realized as a function of the control unit 23.
  • the storage unit 22 stores various information and programs.
  • the storage unit 22 is, for example, a HDD (Hard Disk Drive), SSD (Solid State Drive), EEPROM (Electrically Erasable Programmable Read-Only AnyMemory), ROM (Read-Only Any), ROM (Read-Only Any), and ROM (Read-Only Any). It has a storage device.
  • the control unit 23 realizes a specific function by reading, for example, specific information and a program stored in the storage unit 22, and controls the operation of the medical pump 1 as a whole.
  • the control unit 23 may be configured as a processor such as a CPU (Central Processing Unit), for example. Details of the function of the control unit 23 will be described later.
  • CPU Central Processing Unit
  • the operation input unit 31 is composed of an operation panel as an input interface on which various operation buttons are arranged, and receives an input operation by an operator.
  • the operation buttons arranged on the operation panel as the operation input unit 31 are a power button for switching on/off the operation power supply of the medical pump 1, a start button for starting liquid delivery, and a stop for stopping liquid delivery. Including buttons etc.
  • the operation input unit 31 may be configured to include an input interface such as a touch panel, a keyboard, or a mouse that is provided integrally with the display unit 32. The operation input unit 31 outputs the input information to the control unit 23.
  • the display unit 32 includes a display device such as a liquid crystal display or an organic EL display.
  • the display unit 32 displays the set value and the measured value of the flow rate of the liquid to be fed, the set value and the measured value of the dose of the liquid to be fed, and the like based on the signal from the control unit 23.
  • the alarm notification unit 33 notifies an alarm based on the signal from the control unit 23.
  • the alarm notification unit 33 may include a speaker, for example, and may notify various alarms by sound or voice.
  • the alarm notification unit 33 may include, for example, a display device, and may display various alarms by display. When notifying various warnings by display, the display unit 32 may perform the function as the warning notifying unit 33.
  • the pump drive unit 34 drives the pump function of the medical pump 1.
  • the pump drive unit 34 includes, for example, a motor, and moves the slider 12 shown in FIGS. 1 and 2 along the extending direction A (see FIG. 2) based on a signal from the control unit 23.
  • the external power acquisition unit 40 acquires AC power from an external power source such as a commercial power grid.
  • the external power acquisition unit 40 may acquire the AC power from a plug inserted into an outlet via a cable, for example.
  • the external power acquisition unit 40 includes an AC/DC converter 41.
  • the AC/DC converter 41 converts AC power acquired from an external power source into DC power.
  • the external power acquisition unit 40 can supply the DC power output from the AC/DC converter 41 to each component including the alarm notification unit 33 of the medical pump 1.
  • the medical pump 1 can operate with the power supplied from the external power acquisition unit 40 when the external power acquisition unit 40 is acquiring AC power from the external power source.
  • the external power acquisition unit 40 can charge the main battery 42 and the sub battery 43.
  • the main battery 42 is a battery capable of supplying electric power to each component of the medical pump 1.
  • the main battery 42 can independently supply power to each component of the medical pump 1 in a state where the main battery 42 is not supplied with power from the external power acquisition unit 40.
  • the main battery 42 is a medical pump instead of the external power acquisition unit 40 when the external power acquisition unit 40 is not acquiring power from the external power source, for example, when the plug is not inserted into the outlet. Electric power can be supplied to each component including one alarm notification unit 33.
  • the main battery 42 may be a rechargeable secondary battery.
  • the main battery 42 may be, for example, a lithium ion battery or a nickel hydrogen battery, but is not limited to these, and may be another secondary battery.
  • the main battery 42 can charge the sub battery 43.
  • the sub-battery 43 can supply power to at least the alarm notification unit 33 of the medical pump 1.
  • the sub-battery 43 can independently supply power to the alarm notification unit 33 while it is not supplied with power from the external power acquisition unit 40 and the main battery 42.
  • the sub-battery 43 may be set so that it can supply power only to the alarm notification unit 33 of the medical pump 1.
  • the sub-battery 43 supplies power to the alarm notification unit 33 and issues an alarm to the alarm notification unit 33. It is possible to be notified.
  • the sub-battery 43 supplies power to the alarm notification unit 33 for at least a first predetermined time when both the external power acquisition unit 40 and the main battery 42 cannot supply power to the medical pump 1. It is possible.
  • the first predetermined time is, for example, 3 minutes.
  • the sub-battery 43 may be a capacitor.
  • the sub-battery 43 may be, for example, an electric double layer capacitor (super capacitor), a lithium ion capacitor, an aluminum electrolytic capacitor, a ceramic capacitor, or the like, but is not limited to these, and may be another capacitor.
  • the sub-battery 43 is an electric double layer capacitor, the sub-battery 43 can be small and have a large capacity as compared with the case of being another capacitor.
  • FIG. 4 is a diagram showing a state of charging when the external power acquisition unit 40 is acquiring power from the external power source.
  • FIG. 5 is a figure which shows the mode of charge when the external electric power acquisition part 40 has not acquired electric power from the external electric power source.
  • the external power acquisition unit 40 is connected to both the main battery 42 and the sub battery 43. Further, the main battery 42 is connected to the sub battery 43.
  • the external power acquisition unit 40 when the external power acquisition unit 40 is acquiring power from the external power source, the external power acquisition unit 40 can charge the main battery 42 via the charging path P1. Further, when the external power acquisition unit 40 is acquiring power from the external power source, the external power acquisition unit 40 can charge the sub-battery 43 through the charging path P2.
  • the main battery 42 can charge the sub battery 43 through the charging path P3.
  • the main battery 42 can charge the sub-battery 43 so that the main battery 42 can be used independently for medical use. It is possible to prevent the charge amount of the sub-battery 43 from decreasing due to self-discharge while the pump 1 is operating.
  • the main battery 42 can charge the sub-battery 43 when the external power acquisition unit 40 is not acquiring power from the external power source, the sub-battery 43 can be self-discharged like a capacitor. It is possible to adopt a large device. For example, if a nickel-hydrogen battery with a small self-discharge is adopted as the sub-battery 43, the nickel-hydrogen battery needs to be replaced regularly every two to three years. However, if a capacitor is used as the sub-battery 43, it is not necessary to replace it regularly. Therefore, if a capacitor is used as the sub-battery 43, the sub-battery 43 can be mounted on the substrate inside the medical pump 1. Further, since the capacitor is cheaper than the nickel-hydrogen battery, if the capacitor is used as the sub-battery 43, the cost of the medical pump 1 can be reduced.
  • the external power monitoring unit 70 monitors whether or not the external power acquisition unit 40 can supply power to the medical pump 1.
  • the external power monitoring unit 70 transmits to the control unit 23 a signal indicating whether or not the external power acquisition unit 40 can supply power to the medical pump 1.
  • the external power monitoring unit 70 detects the voltage on the output side of the AC/DC converter 41, for example, and when a predetermined voltage is detected, the external power acquisition unit 40 can supply power to the medical pump 1. If the predetermined voltage is not detected, it is determined that the external power acquisition unit 40 is not in a state in which power can be supplied to the medical pump 1. Alternatively, the external power monitoring unit 70 detects, for example, the voltage on the input side of the AC/DC converter 41 and determines whether the external power acquisition unit 40 is in a state in which power can be supplied to the medical pump 1. You may.
  • the external power acquisition unit 40 does not acquire power from the external power source, the voltage on the input side and the output side of the AC/DC converter 41 is not a predetermined voltage, so the external power monitoring unit 70 sets the external power The acquisition unit 40 determines that power cannot be supplied to the medical pump 1.
  • the main battery monitoring unit 72 monitors whether or not the main battery 42 can supply electric power to the medical pump 1.
  • the main battery monitoring unit 72 sends to the control unit 23 a signal indicating whether or not the main battery 42 is in a state capable of supplying electric power to the medical pump 1.
  • the main battery monitoring unit 72 detects the charge amount of the main battery 42, and when the charge amount is equal to or more than a predetermined threshold value, determines that the main battery 42 is in a state capable of supplying electric power to the medical pump 1. Then, when the charge amount is less than the predetermined threshold value, it is determined that the main battery 42 is not in a state capable of supplying electric power to the medical pump 1.
  • the main battery monitoring unit 72 detects the output voltage of the main battery 42, and the main battery 42 supplies electric power to the medical pump 1 based on whether the output voltage is equal to or higher than a predetermined threshold value. You may judge whether it is a possible state.
  • the sub-battery monitoring unit 73 monitors whether or not the sub-battery 43 can supply power to the alarm notification unit 33 of the medical pump 1.
  • the sub-battery monitoring unit 73 transmits to the control unit 23 a signal indicating whether or not the sub-battery 43 can supply power to the alarm notification unit 33.
  • the sub-battery monitoring unit 73 detects the charge amount of the sub-battery 43, and when the charge amount is equal to or more than a predetermined threshold value, determines that the sub-battery 43 is in a state in which power can be supplied to the alarm notification unit 33. Then, if the charge amount is less than the predetermined threshold value, it is determined that the sub-battery 43 is not in a state in which power can be supplied to the alarm notification unit 33.
  • the sub-battery monitoring unit 73 may determine the charge amount of the sub-battery 43 based on the output voltage of the sub-battery 43, for example.
  • the control unit 23 receives from the external power monitoring unit 70 a signal indicating whether or not the external power acquisition unit 40 is in a state capable of supplying power to the medical pump 1.
  • the control unit 23 receives from the main battery monitoring unit 72 a signal indicating whether or not the main battery 42 is in a state capable of supplying electric power to the medical pump 1.
  • the control unit 23 receives from the sub-battery monitoring unit 73 a signal indicating whether or not the sub-battery 43 is in a state in which power can be supplied to the alarm notification unit 33.
  • the control unit 23 When the control unit 23 receives a signal indicating that power cannot be supplied from any two of the external power monitoring unit 70, the main battery monitoring unit 72, and the sub-battery monitoring unit 73, the control unit 23 waits for the first predetermined time. In the meantime, the alarm notification unit 33 is caused to notify the alarm. For example, when the control unit 23 receives a signal indicating that the power cannot be supplied from the external power monitoring unit 70 and the main battery monitoring unit 72, the control unit 23 issues an alarm to the alarm notification unit 33 based on the power supplied by the sub battery 43. Let me know.
  • the alarm notification unit 33 is based on the power supplied by the main battery 42. To alert you.
  • the control unit 23 receives a signal indicating that power cannot be supplied from the main battery monitoring unit 72 and the sub battery monitoring unit 73, based on the power supplied by the external power acquisition unit 40, the control unit 23 issues an alarm notification. The unit 33 is informed of the alarm. In these cases, the control unit 23 may stop the operation of the pump driving unit 34 and the like to stop the function of the medical pump 1 as a pump.
  • the control unit 23 causes the external power acquisition unit 40, the main battery 42, and the sub battery
  • the alarm notification unit 33 By causing the alarm notification unit 33 to issue an alarm based on the remaining one of the batteries 43 that can supply electric power, the alarm is not issued even though the medical pump 1 cannot operate. Can be prevented.
  • the control unit 23 is in a state in which any two of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 cannot supply power during the second predetermined time after the medical pump 1 is activated.
  • the alarm notification unit 33 may be set not to notify the alarm. By doing so, for example, when the medical pump 1 is started in a state where the insertion plug of the medical pump 1 is not inserted into the outlet and the charge amount of the sub-battery 43 is less than the predetermined threshold value, an alarm is issued. It is possible to prevent the notification unit 33 from immediately issuing an alarm. In this case, if the main battery 42 charges the sub-battery 43 to a predetermined threshold value or more during the second predetermined time, the alarm notification unit 33 does not need to notify the alarm, and the user uses the medical pump 1. Can start.
  • the control unit 23 acquires information from the external power monitoring unit 70 whether the external power acquisition unit 40 can supply power, and the main battery monitoring unit 72 can supply power to the main battery 42. Information is acquired, and information whether the sub battery 43 can supply power is acquired from the sub battery monitoring unit 73 (step S101).
  • the control unit 23 determines whether or not any two of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 cannot supply power (step S102).
  • step S102 If any two of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 are not in a state in which power cannot be supplied, that is, two or more of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 are When the power can be supplied (No in step S102), the control unit 23 returns to the process of step S101.
  • control unit 23 starts the medical pump 1 for a second predetermined time. It is determined whether or not it is within (step S103).
  • step S103 If it is within the second predetermined time from the activation of the medical pump 1 (Yes in step S103), the control unit 23 returns to the process of step S101.
  • control unit 23 causes the alarm notification unit 33 to notify the alarm (step S104).
  • the medical pump 1 includes the main battery 42 and the sub-battery 43 that can supply electric power when the electric power is not supplied from the external electric power acquisition unit 40.
  • the sub battery 42 can charge the sub battery 43.
  • the main battery 42 charges the sub-battery 43 when the main battery 42 operates the medical pump 1 independently while the external power acquisition unit 40 is not acquiring power from the external power source. It becomes possible to do. Therefore, when the main battery 42 is operating the medical pump 1 while the external power acquisition unit 40 is not acquiring power from the external power source, the charge amount of the sub-battery 43 is reduced by self-discharge. Can be suppressed. Thereby, the medical pump 1 of the present embodiment can improve the convenience of the configuration including the main battery 42 and the sub battery 43.
  • the sub-battery 43 is described as a capacitor, but the sub-battery 43 may be a secondary battery such as a lithium ion battery or a nickel hydride battery.
  • control unit 23 causes the external power acquisition unit 40, the main battery 42, and the sub-battery 43 to supply electric power when the medical pump 1 is activated.
  • the alarm notification unit 33 may be set to notify the alarm without the second predetermined time.
  • the present disclosure relates to a medical pump used for delivering a liquid into a living body.

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

This medical pump is equipped with an external power acquisition unit that acquires power from an external power source and a first power supply unit and a second power supply unit capable of supplying power in a state in which power is not being supplied from the external power acquisition unit, and the first power supply unit is capable of charging the second power supply unit.

Description

医療用ポンプMedical pump

 本開示は、液体を生体内に送液するために用いられる医療用ポンプに関する。 The present disclosure relates to a medical pump used for delivering a liquid into a living body.

 従来、患者等の生体内に薬液等の液体を送液する際に、液体の投与量及び投与速度を精度良く制御することが可能なシリンジポンプ及び輸液ポンプなどの医療用ポンプが知られている。 BACKGROUND ART Conventionally, medical pumps such as syringe pumps and infusion pumps are known that can accurately control the dose amount and administration speed of a liquid when delivering a liquid such as a drug solution into a living body of a patient or the like. ..

 医療用ポンプは電気機器であるため、電力を消費して動作する。医療用ポンプは、商用電力系統などの外部電力源から交流電力の供給を受けて動作すること、及び、内蔵バッテリから電力の供給を受けて動作することの双方が可能となっているものが多い。  Medical pumps are electric devices that consume electric power to operate. Many medical pumps are capable of both being operated by receiving AC power from an external power source such as a commercial power system and operating by being supplied with power from a built-in battery. ..

 何らかの異常などにより、医療用ポンプが外部電力源及び内蔵バッテリの双方から電力の供給を受けることができなくなると、医療用ポンプは動作できなくなる。その場合、医療従事者などに、医療用ポンプに電源の異常が発生したことを報知できることが望ましい。 If the medical pump cannot receive power from both the external power source and the built-in battery due to some abnormality, the medical pump cannot operate. In that case, it is desirable to be able to inform a medical staff or the like that an abnormality of the power source has occurred in the medical pump.

 例えば、医療用ポンプなどに対する規格であるIEC60601-2-24:2012では、医療用ポンプが外部電力源及び内蔵バッテリの双方から電力の供給を受けることができなくなった場合に、高優先度の警報を3分以上報知することが可能であることが要求されている。 For example, IEC60601-2-24:2012, which is a standard for medical pumps, etc., gives a high-priority alarm when a medical pump cannot be supplied with power from both an external power source and a built-in battery. Is required to be notified for 3 minutes or more.

 上述の規格による要求を満たすことが可能な医療用ポンプとして、例えば特許文献1には、メインバッテリに加えてサブバッテリを備え、サブバッテリが警報を報知可能な医療用ポンプが開示されている。 As a medical pump that can meet the requirements according to the above-mentioned standards, for example, Patent Document 1 discloses a medical pump that includes a main battery and a sub battery, and the sub battery can notify an alarm.

国際公開第2017/086459号International Publication No. 2017/086459

 メインバッテリ及びサブバッテリを備える医療用ポンプの利便性には改善の余地がある。 There is room for improvement in the convenience of medical pumps that have a main battery and a sub battery.

 本開示の目的は、メインバッテリ及びサブバッテリを備える構成の利便性を向上させることができる医療用ポンプを提供することにある。 An object of the present disclosure is to provide a medical pump that can improve the convenience of a configuration including a main battery and a sub battery.

 本開示の第1の態様としての医療用ポンプは、外部電力源から電力を取得する外部電力取得部と、前記外部電力取得部から電力の供給を受けていない状態で電力を供給することが可能な第1の電力供給部及び第2の電力供給部と、を備え、前記第1の電力供給部は、前記第2の電力供給部を充電することが可能である。 The medical pump according to the first aspect of the present disclosure can supply electric power in a state in which the external electric power acquisition unit that acquires electric power from the external electric power source and the electric power supply from the external electric power acquisition unit are not received. A first power supply unit and a second power supply unit, and the first power supply unit is capable of charging the second power supply unit.

 本開示の一実施形態としての医療用ポンプにおいて、前記第1の電力供給部は、前記外部電力取得部が外部電力源から電力を取得していないときに、前記第2の電力供給部を充電する。 In the medical pump as one embodiment of the present disclosure, the first power supply unit charges the second power supply unit when the external power acquisition unit is not acquiring power from an external power source. To do.

 本開示の一実施形態としての医療用ポンプは、警報を報知する警報報知部をさらに備え、前記第2の電力供給部は、前記外部電力取得部及び前記第1の電力供給部の双方が電力を供給することができないときに、第1の所定時間の間、前記警報報知部に電力を供給することが可能である。 A medical pump according to an embodiment of the present disclosure further includes an alarm notification unit that notifies an alarm, and the second power supply unit is configured such that both the external power acquisition unit and the first power supply unit supply power. When it is not possible to supply the power, it is possible to supply power to the alarm notification unit for the first predetermined time.

 本開示の一実施形態としての医療用ポンプは、制御部をさらに備え、前記制御部は、前記外部電力取得部、前記第1の電力供給部及び前記第2の電力供給部のいずれか2つが電力を供給することができないときに、前記警報報知部に警報を報知させる。 The medical pump as one embodiment of the present disclosure further includes a control unit, and the control unit has any two of the external power acquisition unit, the first power supply unit, and the second power supply unit. When the electric power cannot be supplied, the alarm informing unit is informed of the alarm.

 本開示の一実施形態としての医療用ポンプにおいて、前記制御部は、前記医療用ポンプが起動してから第2の所定時間の間は、前記外部電力取得部、前記第1の電力供給部及び前記第2の電力供給部のいずれか2つが前記医療用ポンプに電力を供給することができなくても、前記警報報知部に警報を報知させない。 In the medical pump as one embodiment of the present disclosure, the control unit controls the external power acquisition unit, the first power supply unit, and the external power acquisition unit for a second predetermined time after the medical pump is activated. Even if any two of the second power supply units cannot supply power to the medical pump, the alarm notification unit is not notified of an alarm.

 本開示の一実施形態としての医療用ポンプにおいて、前記第1の電力供給部は、前記外部電力取得部から供給される電力で充電可能な電池である。 In the medical pump according to an embodiment of the present disclosure, the first power supply unit is a battery that can be charged with the power supplied from the external power acquisition unit.

 本開示の一実施形態としての医療用ポンプにおいて、前記第2の電力供給部は、コンデンサである。 In the medical pump as one embodiment of the present disclosure, the second power supply unit is a capacitor.

 本開示の医療用ポンプによると、メインバッテリ及びサブバッテリを備える構成の利便性を向上させることができる。 According to the medical pump of the present disclosure, the convenience of the configuration including the main battery and the sub battery can be improved.

本開示の一実施形態に係る医療用ポンプの正面図である。1 is a front view of a medical pump according to an embodiment of the present disclosure. シリンジを載置した状態の図1に示す医療用ポンプの正面図である。It is a front view of the medical pump shown in FIG. 1 in which the syringe is mounted. 図1に示す医療用ポンプの機能ブロック図である。It is a functional block diagram of the medical pump shown in FIG. 外部電力取得部が外部電力源から電力を取得しているときに、外部電力取得部によってメインバッテリ及びサブバッテリを充電する様子を示す図である。It is a figure which shows a mode that an external power acquisition part charges a main battery and a sub-battery, when the external power acquisition part is acquiring power from an external power source. 外部電力取得部が外部電力源から電力を取得していないときに、メインバッテリによってサブバッテリを充電する様子を示す図である。It is a figure which shows a mode that a sub battery is charged with a main battery, when the external electric power acquisition part has not acquired electric power from an external electric power source. 本開示の一実施形態に係る医療用ポンプの動作の一例を示すフローチャートである。5 is a flowchart showing an example of operation of the medical pump according to the embodiment of the present disclosure.

 以下、本開示の一実施形態について、図面を参照して説明する。各図において共通の構成部には、同一の符号を付している。 Hereinafter, an embodiment of the present disclosure will be described with reference to the drawings. In each figure, common components are given the same reference numerals.

 図1は、本開示の一実施形態に係る医療用ポンプ1の正面図である。本実施形態においては、医療用ポンプ1はシリンジポンプであるものとして説明するが、医療用ポンプ1はシリンジポンプに限定されない。医療用ポンプ1は、輸液ポンプ、栄養ポンプ、又は血液ポンプであってもよい。 FIG. 1 is a front view of a medical pump 1 according to an embodiment of the present disclosure. In this embodiment, the medical pump 1 is described as a syringe pump, but the medical pump 1 is not limited to a syringe pump. The medical pump 1 may be an infusion pump, a nutrition pump, or a blood pump.

 図2は、シリンジ50を載置した状態の医療用ポンプ1の正面図である。図2に示すように、医療用ポンプ1は、シリンジ50の中空部52に収容された液体を送液するポンプとして構成されている。 FIG. 2 is a front view of the medical pump 1 with the syringe 50 placed thereon. As shown in FIG. 2, the medical pump 1 is configured as a pump that feeds the liquid contained in the hollow portion 52 of the syringe 50.

 図1及び図2に示すように、医療用ポンプ1は、本体カバー2を備えている。本体カバー2は、耐薬品性を有する成型樹脂材料により一体成型されている。これにより、本体カバー2は防沫処理構造を有する。防沫処理構造は、仮に医療用ポンプ1に薬剤等がかかっても、医療用ポンプ1の内部に薬剤等が侵入することを抑制することができる。 As shown in FIGS. 1 and 2, the medical pump 1 includes a body cover 2. The body cover 2 is integrally molded with a molding resin material having chemical resistance. As a result, the main body cover 2 has a splash-proof treatment structure. Even if the medical pump 1 is exposed to a drug or the like, the splash-proof treatment structure can prevent the drug or the like from entering the inside of the medical pump 1.

 図1及び図2に示すように、医療用ポンプ1は、シリンジ50を載置可能な載置部11を備えている。図2に示すように、載置部11に載置可能なシリンジ50は、内部に中空部52を区画する円筒状の外筒51と、外筒51の基端側から中空部52内に挿入され、外筒51の内周面の周方向に隙間なく密着しながら外筒51の延在方向A(以下、単に「延在方向A」と記載する。)に沿って中空部52を移動可能な押子55と、を有する。外筒51は、基端に外筒フランジ53を有し、先端に中空部52と外部とを連通する出口孔54を区画している。出口孔54には、可撓性を有するチューブ60が装着される。押子55は、基端に押子フランジ56を有する。シリンジ50の中空部52には、薬液等の液体が収容されている。 As shown in FIGS. 1 and 2, the medical pump 1 includes a mounting portion 11 on which a syringe 50 can be mounted. As shown in FIG. 2, the syringe 50 that can be mounted on the mounting portion 11 has a cylindrical outer cylinder 51 that defines a hollow portion 52 therein, and a syringe 50 that is inserted into the hollow portion 52 from the proximal end side of the outer cylinder 51. The hollow portion 52 can be moved along the extending direction A of the outer cylinder 51 (hereinafter, simply referred to as “extending direction A”) while closely contacting the inner peripheral surface of the outer cylinder 51 without a gap. And a pusher 55. The outer cylinder 51 has an outer cylinder flange 53 at the base end, and defines an outlet hole 54 that communicates the hollow portion 52 with the outside at the tip. A flexible tube 60 is attached to the outlet hole 54. The pusher 55 has a pusher flange 56 at the base end. A liquid such as a drug solution is stored in the hollow portion 52 of the syringe 50.

 図2に示すように、載置部11は、シリンジ50の外筒51を載置可能である。また、図1及び図2に示すように、医療用ポンプ1は、シリンジ50の外筒51が載置部11に載置されると、外筒フランジ53の一部を収納して外筒51を医療用ポンプ1に対して延在方向Aに固定するスリット15を備えている。 As shown in FIG. 2, the mounting portion 11 can mount the outer cylinder 51 of the syringe 50. In addition, as shown in FIGS. 1 and 2, when the outer cylinder 51 of the syringe 50 is mounted on the mounting portion 11, the medical pump 1 accommodates a part of the outer cylinder flange 53 to accommodate the outer cylinder 51. Is provided in the extending direction A with respect to the medical pump 1.

 図1及び図2に示すように、医療用ポンプ1は、スライダ12を備えている。スライダ12は、載置部11に載置されるシリンジ50の押子55と共に延在方向Aに沿って移動可能である。スライダ12は押子固定部13を備える。押子固定部13は、載置部11に載置されたシリンジ50の押子55をスライダ12に固定する。押子固定部13は、載置されたシリンジ50の押子フランジ56を挟み込むようにして、押子フランジ56をスライダ12に対して固定することが可能である。押子55は、押子固定部13により押子フランジ56がスライダ12に対して固定された状態では、スライダ12の延在方向Aに沿う移動に伴ってスライダ12と一体的に移動する。このとき、載置部11に載置された外筒51は、外筒フランジ53の一部がスリット15に収納されているため、医療用ポンプ1に対して延在方向Aにおいて固定されている。従って、スライダ12がシリンジ50の先端側に移動すると、押子55が外筒51に対して先端側に移動し、中空部52に収容された液体が出口孔54から排出される。そのため、中空部52に収容された液体を、チューブ60を通じて生体内に向かって送液することができる。 As shown in FIGS. 1 and 2, the medical pump 1 includes a slider 12. The slider 12 is movable along the extension direction A together with the pusher 55 of the syringe 50 mounted on the mounting unit 11. The slider 12 includes a pusher fixing portion 13. The pusher fixing section 13 fixes the pusher 55 of the syringe 50 placed on the placing section 11 to the slider 12. The pusher fixing portion 13 can fix the pusher flange 56 to the slider 12 by sandwiching the pusher flange 56 of the mounted syringe 50. When the pusher flange 56 is fixed to the slider 12 by the pusher fixing portion 13, the pusher 55 moves integrally with the slider 12 as the slider 12 moves in the extending direction A. At this time, the outer cylinder 51 mounted on the mounting portion 11 is fixed to the medical pump 1 in the extending direction A because a part of the outer cylinder flange 53 is housed in the slit 15. .. Therefore, when the slider 12 moves to the tip side of the syringe 50, the pusher 55 moves to the tip side with respect to the outer cylinder 51, and the liquid contained in the hollow portion 52 is discharged from the outlet hole 54. Therefore, the liquid contained in the hollow portion 52 can be sent to the inside of the living body through the tube 60.

 図1及び図2に示すように、医療用ポンプ1は、載置部11に載置されたシリンジ50の外筒51を固定するシリンジ用クランプ14を備えている。シリンジ用クランプ14は、本実施形態では、延在方向Aに直交する方向Bに沿って移動可能であり、載置部11に載置されたシリンジ50の外筒51を、載置部11との間で挟み込むようにして固定することが可能である。また、シリンジ用クランプ14で外筒51を固定することで、外筒フランジ53の一部がスリット15から外れにくくなるため、外筒51は医療用ポンプ1に対して強固に固定される。 As shown in FIGS. 1 and 2, the medical pump 1 includes a syringe clamp 14 that fixes an outer cylinder 51 of the syringe 50 mounted on the mounting portion 11. In the present embodiment, the syringe clamp 14 is movable along the direction B orthogonal to the extending direction A, and the outer cylinder 51 of the syringe 50 mounted on the mounting unit 11 is replaced with the mounting unit 11. It is possible to fix it by sandwiching it between them. Further, fixing the outer cylinder 51 with the syringe clamp 14 makes it difficult for a part of the outer cylinder flange 53 to come off the slit 15, so that the outer cylinder 51 is firmly fixed to the medical pump 1.

 図1及び図2に示すように、医療用ポンプ1は、載置部11にシリンジ50が載置された場合にシリンジ50よりも先端側となる位置に、切欠き状のチューブガイド部16を備えている。チューブガイド部16は、シリンジ50が載置部11に載置された状態で、シリンジ50の先端に装着されたチューブ60を通過させて位置決めするために利用される。 As shown in FIGS. 1 and 2, the medical pump 1 includes a notched tube guide portion 16 at a position closer to the tip side than the syringe 50 when the syringe 50 is placed on the placing portion 11. I have it. The tube guide portion 16 is used for allowing the tube 60 attached to the tip of the syringe 50 to pass therethrough while positioning the syringe 50 placed on the placing portion 11.

 図3は、医療用ポンプ1の機能ブロック図である。図3に示すように、医療用ポンプ1は、機能ブロックとして、回路部20と、操作入力部31と、表示部32と、警報報知部33と、ポンプ駆動部34と、外部電力監視部70と、メインバッテリ監視部72と、サブバッテリ監視部73と、を備える。また、医療用ポンプ1は、医療用ポンプ1に電力を供給可能な電力供給部として、外部電力取得部40と、第1の電力供給部としてのメインバッテリ42と、第2の電力供給部としてのサブバッテリ43と、を備える。 FIG. 3 is a functional block diagram of the medical pump 1. As shown in FIG. 3, the medical pump 1 includes, as functional blocks, a circuit unit 20, an operation input unit 31, a display unit 32, an alarm notification unit 33, a pump drive unit 34, and an external power monitoring unit 70. And a main battery monitoring unit 72 and a sub battery monitoring unit 73. Further, the medical pump 1 serves as an electric power supply unit capable of supplying electric power to the medical pump 1, an external electric power acquisition unit 40, a main battery 42 as a first electric power supply unit, and a second electric power supply unit. Sub battery 43 of.

 回路部20は、計時部21と、記憶部22と、制御部23と、を備える。 The circuit unit 20 includes a clock unit 21, a storage unit 22, and a control unit 23.

 計時部21は、時間を測定し、時刻を刻み、例えば、RTC(Real Time Clock:リアルタイムクロック)により実現され得る。計時部21は、制御部23の一機能として実現されてもよい。 The clock unit 21 measures time, ticks the time, and can be realized by, for example, RTC (Real Time Clock: real time clock). The clock unit 21 may be realized as a function of the control unit 23.

 記憶部22は、種々の情報及びプログラムを記憶する。記憶部22は、例えば、HDD(Hard Disk Drive)、SSD(Solid State Drive)、EEPROM(Electrically Erasable Programmable Read-Only Memory)、ROM(Read-Only Memory)、及びRAM(Random Access Memory)等の任意の記憶装置を有する。 The storage unit 22 stores various information and programs. The storage unit 22 is, for example, a HDD (Hard Disk Drive), SSD (Solid State Drive), EEPROM (Electrically Erasable Programmable Read-Only AnyMemory), ROM (Read-Only Any), ROM (Read-Only Any), and ROM (Read-Only Any). It has a storage device.

 制御部23は、例えば記憶部22に記憶された特定の情報及びプログラムを読み込むことにより特定の機能を実現し、医療用ポンプ1全体の動作を制御する。制御部23は、例えばCPU(Central Processing Unit)などのプロセッサとして構成されてよい。制御部23の機能の詳細については後述する。 The control unit 23 realizes a specific function by reading, for example, specific information and a program stored in the storage unit 22, and controls the operation of the medical pump 1 as a whole. The control unit 23 may be configured as a processor such as a CPU (Central Processing Unit), for example. Details of the function of the control unit 23 will be described later.

 操作入力部31は、図1及び図2に示すように、各種の操作ボタンが配置された入力インターフェースとしての操作パネルで構成され、操作者による入力操作を受け付ける。操作入力部31としての操作パネルに配置される操作ボタンは、医療用ポンプ1の動作電源のオンオフを切り替えるための電源ボタン、送液を開始するための開始ボタン、送液を停止するための停止ボタン等を含む。操作入力部31は、表示部32と一体的に設けられるタッチパネル、キーボード、又はマウス等の入力インターフェースを含んで構成されていてもよい。操作入力部31は、入力された情報を、制御部23に出力する。 As shown in FIGS. 1 and 2, the operation input unit 31 is composed of an operation panel as an input interface on which various operation buttons are arranged, and receives an input operation by an operator. The operation buttons arranged on the operation panel as the operation input unit 31 are a power button for switching on/off the operation power supply of the medical pump 1, a start button for starting liquid delivery, and a stop for stopping liquid delivery. Including buttons etc. The operation input unit 31 may be configured to include an input interface such as a touch panel, a keyboard, or a mouse that is provided integrally with the display unit 32. The operation input unit 31 outputs the input information to the control unit 23.

 表示部32は、図1及び図2に示すように、例えば液晶ディスプレイ又は有機ELディスプレイなどの表示デバイスを含む。表示部32は、制御部23からの信号に基づいて、送液される液体の流量の設定値や実測値、及び、送液される液体の投与量の設定値や実測値等を表示する。 As shown in FIGS. 1 and 2, the display unit 32 includes a display device such as a liquid crystal display or an organic EL display. The display unit 32 displays the set value and the measured value of the flow rate of the liquid to be fed, the set value and the measured value of the dose of the liquid to be fed, and the like based on the signal from the control unit 23.

 警報報知部33は、制御部23からの信号に基づいて、警報を報知する。警報報知部33は、例えばスピーカを含み、音又は音声などにより、各種の警報を報知してよい。警報報知部33は、例えば表示デバイスを含み、表示により各種の警報を報知してよい。表示により各種の警報を報知する場合、表示部32が、警報報知部33としての機能を実行してもよい。 The alarm notification unit 33 notifies an alarm based on the signal from the control unit 23. The alarm notification unit 33 may include a speaker, for example, and may notify various alarms by sound or voice. The alarm notification unit 33 may include, for example, a display device, and may display various alarms by display. When notifying various warnings by display, the display unit 32 may perform the function as the warning notifying unit 33.

 ポンプ駆動部34は、医療用ポンプ1のポンプ機能を駆動する。ポンプ駆動部34は、例えばモータを含み、制御部23からの信号に基づいて、図1及び図2に示すスライダ12を、延在方向A(図2参照)に沿って移動させる。 The pump drive unit 34 drives the pump function of the medical pump 1. The pump drive unit 34 includes, for example, a motor, and moves the slider 12 shown in FIGS. 1 and 2 along the extending direction A (see FIG. 2) based on a signal from the control unit 23.

 外部電力取得部40は、商用電力系統などの外部電力源から交流電力を取得する。外部電力取得部40は、例えば、コンセントに差し込まれた差し込みプラグから、ケーブルを介して交流電力を取得してよい。外部電力取得部40は、AC/DCコンバータ41を備える。AC/DCコンバータ41は、外部電力源から取得した交流電力を直流電力に変換する。外部電力取得部40は、AC/DCコンバータ41が出力する直流電力を、医療用ポンプ1の警報報知部33も含めた各構成要素に供給可能である。医療用ポンプ1は、外部電力取得部40が外部電力源から交流電力を取得しているとき、外部電力取得部40から供給される電力によって動作可能である。 The external power acquisition unit 40 acquires AC power from an external power source such as a commercial power grid. The external power acquisition unit 40 may acquire the AC power from a plug inserted into an outlet via a cable, for example. The external power acquisition unit 40 includes an AC/DC converter 41. The AC/DC converter 41 converts AC power acquired from an external power source into DC power. The external power acquisition unit 40 can supply the DC power output from the AC/DC converter 41 to each component including the alarm notification unit 33 of the medical pump 1. The medical pump 1 can operate with the power supplied from the external power acquisition unit 40 when the external power acquisition unit 40 is acquiring AC power from the external power source.

 外部電力取得部40は、メインバッテリ42及びサブバッテリ43を充電することが可能である。 The external power acquisition unit 40 can charge the main battery 42 and the sub battery 43.

 メインバッテリ42は、医療用ポンプ1の各構成要素に電力を供給可能な電池である。メインバッテリ42は、外部電力取得部40から電力の供給を受けていない状態で、独立して、医療用ポンプ1の各構成要素に電力を供給することが可能である。 The main battery 42 is a battery capable of supplying electric power to each component of the medical pump 1. The main battery 42 can independently supply power to each component of the medical pump 1 in a state where the main battery 42 is not supplied with power from the external power acquisition unit 40.

 メインバッテリ42は、例えば、差し込みプラグがコンセントに差し込まれていないときなど、外部電力取得部40が外部電力源から電力を取得していないときに、外部電力取得部40の代わりに、医療用ポンプ1の警報報知部33も含めた各構成要素に電力を供給することができる。 The main battery 42 is a medical pump instead of the external power acquisition unit 40 when the external power acquisition unit 40 is not acquiring power from the external power source, for example, when the plug is not inserted into the outlet. Electric power can be supplied to each component including one alarm notification unit 33.

 メインバッテリ42は、充電可能な二次電池であってよい。メインバッテリ42は、例えば、リチウムイオン電池又はニッケル水素電池などであってよいが、これらに限られず、他の二次電池であってもよい。 The main battery 42 may be a rechargeable secondary battery. The main battery 42 may be, for example, a lithium ion battery or a nickel hydrogen battery, but is not limited to these, and may be another secondary battery.

 メインバッテリ42は、サブバッテリ43を充電することが可能である。 The main battery 42 can charge the sub battery 43.

 サブバッテリ43は、少なくとも医療用ポンプ1の警報報知部33に電力を供給することが可能である。サブバッテリ43は、外部電力取得部40及びメインバッテリ42から電力の供給を受けていない状態で、独立して、警報報知部33に電力を供給することが可能である。なお、サブバッテリ43は、医療用ポンプ1の警報報知部33のみに電力を供給することが可能である設定であってもよい。 The sub-battery 43 can supply power to at least the alarm notification unit 33 of the medical pump 1. The sub-battery 43 can independently supply power to the alarm notification unit 33 while it is not supplied with power from the external power acquisition unit 40 and the main battery 42. The sub-battery 43 may be set so that it can supply power only to the alarm notification unit 33 of the medical pump 1.

 サブバッテリ43は、外部電力取得部40及びメインバッテリ42の双方が医療用ポンプ1に電力を供給することができないときに、警報報知部33に電力を供給して、警報報知部33に警報を報知させることが可能である。サブバッテリ43は、外部電力取得部40及びメインバッテリ42の双方が医療用ポンプ1に電力を供給することができないときに、少なくとも第1の所定時間の間、警報報知部33に電力を供給することが可能である。第1の所定時間は、例えば3分間である。 When both the external power acquisition unit 40 and the main battery 42 cannot supply power to the medical pump 1, the sub-battery 43 supplies power to the alarm notification unit 33 and issues an alarm to the alarm notification unit 33. It is possible to be notified. The sub-battery 43 supplies power to the alarm notification unit 33 for at least a first predetermined time when both the external power acquisition unit 40 and the main battery 42 cannot supply power to the medical pump 1. It is possible. The first predetermined time is, for example, 3 minutes.

 サブバッテリ43は、コンデンサであってよい。サブバッテリ43は、例えば、電気二重層コンデンサ(スーパーキャパシタ)、リチウムイオンコンデンサ、アルミ電解コンデンサ、又はセラミックコンデンサなどであってよいが、これらに限られず、他のコンデンサであってもよい。サブバッテリ43は、電気二重層コンデンサである場合、他のコンデンサである場合と比べて、小型で大容量を有することができる。 The sub-battery 43 may be a capacitor. The sub-battery 43 may be, for example, an electric double layer capacitor (super capacitor), a lithium ion capacitor, an aluminum electrolytic capacitor, a ceramic capacitor, or the like, but is not limited to these, and may be another capacitor. When the sub-battery 43 is an electric double layer capacitor, the sub-battery 43 can be small and have a large capacity as compared with the case of being another capacitor.

 図4及び図5を参照して、メインバッテリ42及びサブバッテリ43の充電について説明する。図4は、外部電力取得部40が外部電力源から電力を取得しているときの充電の様子を示す図である。図5は、外部電力取得部40が外部電力源から電力を取得していないときの充電の様子を示す図である。 The charging of the main battery 42 and the sub-battery 43 will be described with reference to FIGS. 4 and 5. FIG. 4 is a diagram showing a state of charging when the external power acquisition unit 40 is acquiring power from the external power source. FIG. 5: is a figure which shows the mode of charge when the external electric power acquisition part 40 has not acquired electric power from the external electric power source.

 図4及び図5に示すように、外部電力取得部40は、メインバッテリ42及びサブバッテリ43の双方と接続している。また、メインバッテリ42は、サブバッテリ43と接続している。 As shown in FIGS. 4 and 5, the external power acquisition unit 40 is connected to both the main battery 42 and the sub battery 43. Further, the main battery 42 is connected to the sub battery 43.

 図4に示すように、外部電力取得部40が外部電力源から電力を取得しているとき、外部電力取得部40は、充電経路P1によって、メインバッテリ42を充電することが可能である。また、外部電力取得部40が外部電力源から電力を取得しているとき、外部電力取得部40は、充電経路P2によって、サブバッテリ43を充電することが可能である。 As shown in FIG. 4, when the external power acquisition unit 40 is acquiring power from the external power source, the external power acquisition unit 40 can charge the main battery 42 via the charging path P1. Further, when the external power acquisition unit 40 is acquiring power from the external power source, the external power acquisition unit 40 can charge the sub-battery 43 through the charging path P2.

 図5に示すように、外部電力取得部40が外部電力源から電力を取得していなとき、メインバッテリ42は、充電経路P3によって、サブバッテリ43を充電することが可能である。 As shown in FIG. 5, when the external power acquisition unit 40 is not acquiring power from the external power source, the main battery 42 can charge the sub battery 43 through the charging path P3.

 このように、外部電力取得部40が外部電力源から電力を取得していないときに、メインバッテリ42がサブバッテリ43を充電することが可能であることにより、メインバッテリ42が独立して医療用ポンプ1を動作させているときに、サブバッテリ43の充電量が自己放電によって低下することを抑制することができる。 In this way, when the external power acquisition unit 40 is not acquiring power from the external power source, the main battery 42 can charge the sub-battery 43 so that the main battery 42 can be used independently for medical use. It is possible to prevent the charge amount of the sub-battery 43 from decreasing due to self-discharge while the pump 1 is operating.

 また、外部電力取得部40が外部電力源から電力を取得していないときに、メインバッテリ42がサブバッテリ43を充電することが可能であることにより、サブバッテリ43にコンデンサのような自己放電の大きいデバイスを採用することが可能となる。例えばサブバッテリ43として自己放電の小さいニッケル水素電池を採用すると、ニッケル水素電池は2~3年毎程度に定期的に交換することが必要でなる。しかしながら、サブバッテリ43としてコンデンサを採用すると、定期的な交換の必要がなくなる。そのため、サブバッテリ43としてコンデンサを採用すると、医療用ポンプ1の内部の基板にサブバッテリ43を実装することが可能となる。また、コンデンサはニッケル水素電池より低価格であるため、サブバッテリ43としてコンデンサを採用すると、医療用ポンプ1を低コスト化することができる。 Further, since the main battery 42 can charge the sub-battery 43 when the external power acquisition unit 40 is not acquiring power from the external power source, the sub-battery 43 can be self-discharged like a capacitor. It is possible to adopt a large device. For example, if a nickel-hydrogen battery with a small self-discharge is adopted as the sub-battery 43, the nickel-hydrogen battery needs to be replaced regularly every two to three years. However, if a capacitor is used as the sub-battery 43, it is not necessary to replace it regularly. Therefore, if a capacitor is used as the sub-battery 43, the sub-battery 43 can be mounted on the substrate inside the medical pump 1. Further, since the capacitor is cheaper than the nickel-hydrogen battery, if the capacitor is used as the sub-battery 43, the cost of the medical pump 1 can be reduced.

 再び図3を参照して、外部電力監視部70、メインバッテリ監視部72、及びサブバッテリ監視部73について説明する。 With reference to FIG. 3 again, the external power monitoring unit 70, the main battery monitoring unit 72, and the sub battery monitoring unit 73 will be described.

 外部電力監視部70は、外部電力取得部40が医療用ポンプ1に電力を供給可能な状態であるか否かを監視する。外部電力監視部70は、外部電力取得部40が医療用ポンプ1に電力を供給可能な状態であるか否かを示す信号を制御部23に送信する。 The external power monitoring unit 70 monitors whether or not the external power acquisition unit 40 can supply power to the medical pump 1. The external power monitoring unit 70 transmits to the control unit 23 a signal indicating whether or not the external power acquisition unit 40 can supply power to the medical pump 1.

 外部電力監視部70は、例えば、AC/DCコンバータ41の出力側の電圧を検出して、所定の電圧が検出された場合、外部電力取得部40が医療用ポンプ1に電力を供給可能な状態であると判定し、所定の電圧が検出されない場合、外部電力取得部40が医療用ポンプ1に電力を供給可能な状態でないと判定する。または、外部電力監視部70は、例えば、AC/DCコンバータ41の入力側の電圧を検出して、外部電力取得部40が医療用ポンプ1に電力を供給可能な状態であるか否かを判定してもよい。 The external power monitoring unit 70 detects the voltage on the output side of the AC/DC converter 41, for example, and when a predetermined voltage is detected, the external power acquisition unit 40 can supply power to the medical pump 1. If the predetermined voltage is not detected, it is determined that the external power acquisition unit 40 is not in a state in which power can be supplied to the medical pump 1. Alternatively, the external power monitoring unit 70 detects, for example, the voltage on the input side of the AC/DC converter 41 and determines whether the external power acquisition unit 40 is in a state in which power can be supplied to the medical pump 1. You may.

 例えば、外部電力取得部40が外部電力源から電力を取得していない場合、AC/DCコンバータ41の入力側及び出力側の電圧は所定の電圧ではないため、外部電力監視部70は、外部電力取得部40が医療用ポンプ1に電力を供給可能な状態でないと判定する。 For example, when the external power acquisition unit 40 does not acquire power from the external power source, the voltage on the input side and the output side of the AC/DC converter 41 is not a predetermined voltage, so the external power monitoring unit 70 sets the external power The acquisition unit 40 determines that power cannot be supplied to the medical pump 1.

 メインバッテリ監視部72は、メインバッテリ42が医療用ポンプ1に電力を供給可能な状態であるか否かを監視する。メインバッテリ監視部72は、メインバッテリ42が医療用ポンプ1に電力を供給可能な状態であるか否かを示す信号を制御部23に送信する。 The main battery monitoring unit 72 monitors whether or not the main battery 42 can supply electric power to the medical pump 1. The main battery monitoring unit 72 sends to the control unit 23 a signal indicating whether or not the main battery 42 is in a state capable of supplying electric power to the medical pump 1.

 メインバッテリ監視部72は、例えば、メインバッテリ42の充電量を検出して、充電量が所定の閾値以上である場合、メインバッテリ42が医療用ポンプ1に電力を供給可能な状態であると判定し、充電量が所定の閾値未満である場合、メインバッテリ42が医療用ポンプ1に電力を供給可能な状態でないと判定する。または、メインバッテリ監視部72は、例えば、メインバッテリ42の出力電圧を検出して、出力電圧が所定の閾値以上であるか否かに基づいて、メインバッテリ42が医療用ポンプ1に電力を供給可能な状態であるか否かを判定してもよい。 For example, the main battery monitoring unit 72 detects the charge amount of the main battery 42, and when the charge amount is equal to or more than a predetermined threshold value, determines that the main battery 42 is in a state capable of supplying electric power to the medical pump 1. Then, when the charge amount is less than the predetermined threshold value, it is determined that the main battery 42 is not in a state capable of supplying electric power to the medical pump 1. Alternatively, the main battery monitoring unit 72 detects the output voltage of the main battery 42, and the main battery 42 supplies electric power to the medical pump 1 based on whether the output voltage is equal to or higher than a predetermined threshold value. You may judge whether it is a possible state.

 サブバッテリ監視部73は、サブバッテリ43が医療用ポンプ1の警報報知部33に電力を供給可能な状態であるか否かを監視する。サブバッテリ監視部73は、サブバッテリ43が警報報知部33に電力を供給可能な状態であるか否かを示す信号を制御部23に送信する。 The sub-battery monitoring unit 73 monitors whether or not the sub-battery 43 can supply power to the alarm notification unit 33 of the medical pump 1. The sub-battery monitoring unit 73 transmits to the control unit 23 a signal indicating whether or not the sub-battery 43 can supply power to the alarm notification unit 33.

 サブバッテリ監視部73は、例えば、サブバッテリ43の充電量を検出して、充電量が所定の閾値以上である場合、サブバッテリ43が警報報知部33に電力を供給可能な状態であると判定し、充電量が所定の閾値未満である場合、サブバッテリ43が警報報知部33に電力を供給可能な状態でないと判定する。サブバッテリ監視部73は、例えば、サブバッテリ43の出力電圧に基づいて、サブバッテリ43の充電量を判定してよい。 For example, the sub-battery monitoring unit 73 detects the charge amount of the sub-battery 43, and when the charge amount is equal to or more than a predetermined threshold value, determines that the sub-battery 43 is in a state in which power can be supplied to the alarm notification unit 33. Then, if the charge amount is less than the predetermined threshold value, it is determined that the sub-battery 43 is not in a state in which power can be supplied to the alarm notification unit 33. The sub-battery monitoring unit 73 may determine the charge amount of the sub-battery 43 based on the output voltage of the sub-battery 43, for example.

 制御部23は、外部電力監視部70から、外部電力取得部40が医療用ポンプ1に電力を供給可能な状態であるか否かを示す信号を受信する。制御部23は、メインバッテリ監視部72から、メインバッテリ42が医療用ポンプ1に電力を供給可能な状態であるか否かを示す信号を受信する。制御部23は、サブバッテリ監視部73から、サブバッテリ43が警報報知部33に電力を供給可能な状態であるか否かを示す信号を受信する。 The control unit 23 receives from the external power monitoring unit 70 a signal indicating whether or not the external power acquisition unit 40 is in a state capable of supplying power to the medical pump 1. The control unit 23 receives from the main battery monitoring unit 72 a signal indicating whether or not the main battery 42 is in a state capable of supplying electric power to the medical pump 1. The control unit 23 receives from the sub-battery monitoring unit 73 a signal indicating whether or not the sub-battery 43 is in a state in which power can be supplied to the alarm notification unit 33.

 制御部23は、外部電力監視部70、メインバッテリ監視部72、及びサブバッテリ監視部73のいずれか2つから、電力を供給可能な状態でない旨の信号を受信すると、第1の所定時間の間、警報報知部33に警報を報知させる。制御部23は、例えば、外部電力監視部70及びメインバッテリ監視部72から電力を供給可能な状態でない旨の信号を受信すると、サブバッテリ43が供給する電力に基づいて、警報報知部33に警報を報知させる。また、制御部23は、例えば、外部電力監視部70及びサブバッテリ監視部73から電力を供給可能な状態でない旨の信号を受信すると、メインバッテリ42が供給する電力に基づいて、警報報知部33に警報を報知させる。また、制御部23は、例えば、メインバッテリ監視部72及びサブバッテリ監視部73から電力を供給可能な状態でない旨の信号を受信すると、外部電力取得部40が供給する電力に基づいて、警報報知部33に警報を報知させる。制御部23は、これらの際、ポンプ駆動部34などの動作を停止させて、医療用ポンプ1のポンプとしての機能を停止させてもよい。 When the control unit 23 receives a signal indicating that power cannot be supplied from any two of the external power monitoring unit 70, the main battery monitoring unit 72, and the sub-battery monitoring unit 73, the control unit 23 waits for the first predetermined time. In the meantime, the alarm notification unit 33 is caused to notify the alarm. For example, when the control unit 23 receives a signal indicating that the power cannot be supplied from the external power monitoring unit 70 and the main battery monitoring unit 72, the control unit 23 issues an alarm to the alarm notification unit 33 based on the power supplied by the sub battery 43. Let me know. Further, for example, when the control unit 23 receives a signal indicating that the power cannot be supplied from the external power monitoring unit 70 and the sub-battery monitoring unit 73, the alarm notification unit 33 is based on the power supplied by the main battery 42. To alert you. In addition, for example, when the control unit 23 receives a signal indicating that power cannot be supplied from the main battery monitoring unit 72 and the sub battery monitoring unit 73, based on the power supplied by the external power acquisition unit 40, the control unit 23 issues an alarm notification. The unit 33 is informed of the alarm. In these cases, the control unit 23 may stop the operation of the pump driving unit 34 and the like to stop the function of the medical pump 1 as a pump.

 このように、外部電力取得部40、メインバッテリ42、及びサブバッテリ43のいずれか2つが電力を供給することができないときに、制御部23が、外部電力取得部40、メインバッテリ42、及びサブバッテリ43のうちの電力を供給可能な残りの1つに基づいて、警報報知部33に警報を報知させることにより、医療用ポンプ1が動作できなくなったにも関わらず警報が報知されないという事態になることを防ぐことができる。 Thus, when any two of the external power acquisition unit 40, the main battery 42, and the sub battery 43 cannot supply power, the control unit 23 causes the external power acquisition unit 40, the main battery 42, and the sub battery By causing the alarm notification unit 33 to issue an alarm based on the remaining one of the batteries 43 that can supply electric power, the alarm is not issued even though the medical pump 1 cannot operate. Can be prevented.

 制御部23は、医療用ポンプ1が起動してから第2の所定時間の間は、外部電力取得部40、メインバッテリ42、及びサブバッテリ43のいずれか2つが電力を供給することができない状態であっても、警報報知部33に警報を報知させない設定であってもよい。こうすることで、例えば、医療用ポンプ1の差し込みプラグがコンセントに差し込まれておらず、且つ、サブバッテリ43の充電量が所定の閾値未満の状態で医療用ポンプ1を起動したときに、警報報知部33が即座に警報を報知することを抑制することができる。この場合、第2の所定時間の間に、メインバッテリ42がサブバッテリ43を所定の閾値以上まで充電すれば、警報報知部33が警報を報知する必要がなくなり、ユーザは医療用ポンプ1の使用を開始することができる。 The control unit 23 is in a state in which any two of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 cannot supply power during the second predetermined time after the medical pump 1 is activated. Alternatively, the alarm notification unit 33 may be set not to notify the alarm. By doing so, for example, when the medical pump 1 is started in a state where the insertion plug of the medical pump 1 is not inserted into the outlet and the charge amount of the sub-battery 43 is less than the predetermined threshold value, an alarm is issued. It is possible to prevent the notification unit 33 from immediately issuing an alarm. In this case, if the main battery 42 charges the sub-battery 43 to a predetermined threshold value or more during the second predetermined time, the alarm notification unit 33 does not need to notify the alarm, and the user uses the medical pump 1. Can start.

 医療用ポンプ1が起動してから第2の所定時間の間は、外部電力取得部40、メインバッテリ42、及びサブバッテリ43のいずれか2つが電力を供給することができない状態であっても、警報報知部33に警報を報知させない設定である場合の医療用ポンプ1の動作を、図6に示すフローチャートを参照して説明する。 Even if any two of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 cannot supply power during the second predetermined time after the medical pump 1 is activated, The operation of the medical pump 1 when the alarm notification unit 33 is set not to notify an alarm will be described with reference to the flowchart shown in FIG.

 医療用ポンプ1が起動すると、制御部23は、外部電力監視部70から外部電力取得部40が電力供給可能であるかの情報を取得し、メインバッテリ監視部72からメインバッテリ42が電力供給可能であるかの情報を取得し、サブバッテリ監視部73からサブバッテリ43が電力供給可能であるかの情報を取得する(ステップS101)。 When the medical pump 1 is activated, the control unit 23 acquires information from the external power monitoring unit 70 whether the external power acquisition unit 40 can supply power, and the main battery monitoring unit 72 can supply power to the main battery 42. Information is acquired, and information whether the sub battery 43 can supply power is acquired from the sub battery monitoring unit 73 (step S101).

 制御部23は、外部電力取得部40、メインバッテリ42、及びサブバッテリ43のいずれか2つが電力供給できない状態であるか否かを判定する(ステップS102)。 The control unit 23 determines whether or not any two of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 cannot supply power (step S102).

 外部電力取得部40、メインバッテリ42、及びサブバッテリ43のいずれか2つが電力供給できない状態ではない場合、すわわち、外部電力取得部40、メインバッテリ42、及びサブバッテリ43の2つ以上が電力供給できる状態である場合(ステップS102のNo)、制御部23は、ステップS101の処理に戻る。 If any two of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 are not in a state in which power cannot be supplied, that is, two or more of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 are When the power can be supplied (No in step S102), the control unit 23 returns to the process of step S101.

 外部電力取得部40、メインバッテリ42、及びサブバッテリ43のいずれか2つが電力供給できない状態である場合(ステップS102のYes)、制御部23は、医療用ポンプ1の起動から第2の所定時間以内であるか否かを判定する(ステップS103)。 When any two of the external power acquisition unit 40, the main battery 42, and the sub-battery 43 cannot supply power (Yes in step S102), the control unit 23 starts the medical pump 1 for a second predetermined time. It is determined whether or not it is within (step S103).

 医療用ポンプ1の起動から第2の所定時間以内である場合(ステップS103のYes)、制御部23は、ステップS101の処理に戻る。 If it is within the second predetermined time from the activation of the medical pump 1 (Yes in step S103), the control unit 23 returns to the process of step S101.

 医療用ポンプ1の起動から第2の所定時間を経過している場合(ステップS103のNo)、制御部23は、警報報知部33に警報を報知させる(ステップS104)。 When the second predetermined time has elapsed from the activation of the medical pump 1 (No in step S103), the control unit 23 causes the alarm notification unit 33 to notify the alarm (step S104).

 以上のように、本実施形態の医療用ポンプ1は、外部電力取得部40から電力の供給を受けていない状態で電力を供給することが可能なメインバッテリ42及びサブバッテリ43を備え、メインバッテリ42は、サブバッテリ43を充電することが可能である。これにより、外部電力取得部40が外部電力源から電力を取得していない状態で、メインバッテリ42が独立して医療用ポンプ1を動作させているときに、メインバッテリ42がサブバッテリ43を充電することが可能となる。したがって、外部電力取得部40が外部電力源から電力を取得していない状態で、メインバッテリ42が医療用ポンプ1を動作させているときに、サブバッテリ43の充電量が自己放電によって低下することを抑制することができる。これにより、本実施形態の医療用ポンプ1は、メインバッテリ42及びサブバッテリ43を備える構成の利便性を向上させることができる。 As described above, the medical pump 1 according to the present embodiment includes the main battery 42 and the sub-battery 43 that can supply electric power when the electric power is not supplied from the external electric power acquisition unit 40. The sub battery 42 can charge the sub battery 43. As a result, the main battery 42 charges the sub-battery 43 when the main battery 42 operates the medical pump 1 independently while the external power acquisition unit 40 is not acquiring power from the external power source. It becomes possible to do. Therefore, when the main battery 42 is operating the medical pump 1 while the external power acquisition unit 40 is not acquiring power from the external power source, the charge amount of the sub-battery 43 is reduced by self-discharge. Can be suppressed. Thereby, the medical pump 1 of the present embodiment can improve the convenience of the configuration including the main battery 42 and the sub battery 43.

 本発明は、上述した各実施形態で特定された構成に限定されず、特許請求の範囲に記載した発明の要旨を逸脱しない範囲内で種々の変形が可能である。例えば、各構成部、各ステップなどに含まれる機能などは論理的に矛盾しないように再配置可能であり、複数の構成部やステップなどを1つに組み合わせたり、或いは分割したりすることが可能である。 The present invention is not limited to the configurations specified in the above-described embodiments, and various modifications can be made without departing from the scope of the invention described in the claims. For example, the functions included in each component, each step, etc. can be rearranged so as not to logically contradict, and a plurality of components, steps, etc. can be combined into one or divided. Is.

 また、本実施形態の医療用ポンプ1では、サブバッテリ43はコンデンサであるとして説明したが、サブバッテリ43は、リチウムイオン電池又はニッケル水素電池などの二次電池であってもよい。 Further, in the medical pump 1 of the present embodiment, the sub-battery 43 is described as a capacitor, but the sub-battery 43 may be a secondary battery such as a lithium ion battery or a nickel hydride battery.

 また、本実施形態の医療用ポンプ1では、制御部23は、医療用ポンプ1が起動した際に外部電力取得部40、メインバッテリ42、及びサブバッテリ43のいずれか2つが電力を供給することができない状態であった場合、第2の所定時間を置かずに警報報知部33に警報を報知させる設定であってもよい。 Further, in the medical pump 1 of the present embodiment, the control unit 23 causes the external power acquisition unit 40, the main battery 42, and the sub-battery 43 to supply electric power when the medical pump 1 is activated. When it is in a state in which the alarm cannot be performed, the alarm notification unit 33 may be set to notify the alarm without the second predetermined time.

 本開示は、液体を生体内に送液するために用いられる医療用ポンプに関する。 The present disclosure relates to a medical pump used for delivering a liquid into a living body.

 1:医療用ポンプ
 2:本体カバー
11:載置部
12:スライダ
13:押子固定部
14:シリンジ用クランプ
15:スリット
16:チューブガイド部
20:回路部
21:計時部
22:記憶部
23:制御部
31:操作入力部
32:表示部
33:警報報知部
34:ポンプ駆動部
40:外部電力取得部
41:AC/DCコンバータ
42:メインバッテリ(第1の電力供給部)
43:サブバッテリ(第2の電力供給部)
50:シリンジ
51:外筒
52:中空部
53:外筒フランジ
54:出口孔
55:押子
56:押子フランジ
60:チューブ
70:外部電力監視部
72:メインバッテリ監視部
73:サブバッテリ監視部
A:載置されたシリンジの外筒の延在方向
B:シリンジ用クランプの移動可能方向
P1~P3:充電経路
 
1: Medical pump 2: Body cover 11: Mounting part 12: Slider 13: Pusher fixing part 14: Syringe clamp 15: Slit 16: Tube guide part 20: Circuit part 21: Clock part 22: Storage part 23: Control unit 31: Operation input unit 32: Display unit 33: Warning notification unit 34: Pump drive unit 40: External power acquisition unit 41: AC/DC converter 42: Main battery (first power supply unit)
43: Sub battery (second power supply unit)
50: Syringe 51: Outer cylinder 52: Hollow part 53: Outer cylinder flange 54: Outlet hole 55: Presser 56: Presser flange 60: Tube 70: External power monitor 72: Main battery monitor 73: Sub battery monitor A: Extension direction of outer cylinder of mounted syringe B: Movable direction of syringe clamp P1 to P3: Charging path

Claims (7)

 外部電力源から電力を取得する外部電力取得部と、
 前記外部電力取得部から電力の供給を受けていない状態で電力を供給することが可能な第1の電力供給部及び第2の電力供給部と、を備え、
 前記第1の電力供給部は、前記第2の電力供給部を充電することが可能である、医療用ポンプ。
An external power acquisition unit that acquires power from an external power source,
A first power supply unit and a second power supply unit capable of supplying power in a state where power is not supplied from the external power acquisition unit,
The said 1st electric power supply part is a medical pump which can charge the said 2nd electric power supply part.
 請求項1に記載の医療用ポンプにおいて、
 前記第1の電力供給部は、前記外部電力取得部が外部電力源から電力を取得していないときに、前記第2の電力供給部を充電する、医療用ポンプ。
The medical pump according to claim 1,
The said 1st electric power supply part is a medical pump which charges the said 2nd electric power supply part, when the said external electric power acquisition part is not acquiring electric power from an external electric power source.
 請求項1又は2に記載の医療用ポンプにおいて、
 警報を報知する警報報知部をさらに備え、
 前記第2の電力供給部は、前記外部電力取得部及び前記第1の電力供給部の双方が電力を供給することができないときに、第1の所定時間の間、前記警報報知部に電力を供給することが可能である、医療用ポンプ。
The medical pump according to claim 1 or 2,
An alarm notification unit for alarming is further provided,
The second power supply unit supplies power to the alarm notification unit for a first predetermined time when both the external power acquisition unit and the first power supply unit cannot supply power. A medical pump that can be supplied.
 請求項3に記載の医療用ポンプにおいて、
 制御部をさらに備え、
 前記制御部は、前記外部電力取得部、前記第1の電力供給部及び前記第2の電力供給部のいずれか2つが電力を供給することができないときに、前記警報報知部に警報を報知させる、医療用ポンプ。
The medical pump according to claim 3,
Further provided with a control unit,
The control unit causes the alarm notification unit to notify an alarm when any two of the external power acquisition unit, the first power supply unit, and the second power supply unit cannot supply power. , Medical pumps.
 請求項4に記載の医療用ポンプにおいて、
 前記制御部は、前記医療用ポンプが起動してから第2の所定時間の間は、前記外部電力取得部、前記第1の電力供給部及び前記第2の電力供給部のいずれか2つが前記医療用ポンプに電力を供給することができなくても、前記警報報知部に警報を報知させない、医療用ポンプ。
The medical pump according to claim 4,
The control unit is configured such that any two of the external power acquisition unit, the first power supply unit, and the second power supply unit are in the second predetermined time after the medical pump is activated. A medical pump in which the alarm is not notified even if the medical pump cannot be supplied with electric power.
 請求項1から5のいずれか一項に記載の医療用ポンプにおいて、
 前記第1の電力供給部は、前記外部電力取得部から供給される電力で充電可能な電池である、医療用ポンプ。
The medical pump according to any one of claims 1 to 5,
The said 1st electric power supply part is a medical pump which is a battery rechargeable with the electric power supplied from the said external electric power acquisition part.
 請求項1から6のいずれか一項に記載の医療用ポンプにおいて、
 前記第2の電力供給部は、コンデンサである、医療用ポンプ。
 
The medical pump according to any one of claims 1 to 6,
The medical pump in which the second power supply unit is a capacitor.
PCT/JP2019/047700 2019-01-18 2019-12-05 Medical pump Ceased WO2020149045A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2020566142A JPWO2020149045A1 (en) 2019-01-18 2019-12-05 Medical pump

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2019006985 2019-01-18
JP2019-006985 2019-01-18

Publications (1)

Publication Number Publication Date
WO2020149045A1 true WO2020149045A1 (en) 2020-07-23

Family

ID=71613753

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2019/047700 Ceased WO2020149045A1 (en) 2019-01-18 2019-12-05 Medical pump

Country Status (2)

Country Link
JP (1) JPWO2020149045A1 (en)
WO (1) WO2020149045A1 (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH069764U (en) * 1992-07-07 1994-02-08 株式会社ダイヘン Welding wire feeding abnormality detection device
JP2004532664A (en) * 2000-12-21 2004-10-28 インシュレット コーポレイション Medical device remote control device and method
WO2017086459A1 (en) * 2015-11-20 2017-05-26 テルモ株式会社 Medical pump, method for controlling medical pump, and program for controlling medical pump
JP2018000753A (en) * 2016-07-06 2018-01-11 ソニー・オリンパスメディカルソリューションズ株式会社 Medical tool

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH069764U (en) * 1992-07-07 1994-02-08 株式会社ダイヘン Welding wire feeding abnormality detection device
JP2004532664A (en) * 2000-12-21 2004-10-28 インシュレット コーポレイション Medical device remote control device and method
WO2017086459A1 (en) * 2015-11-20 2017-05-26 テルモ株式会社 Medical pump, method for controlling medical pump, and program for controlling medical pump
JP2018000753A (en) * 2016-07-06 2018-01-11 ソニー・オリンパスメディカルソリューションズ株式会社 Medical tool

Also Published As

Publication number Publication date
JPWO2020149045A1 (en) 2021-11-25

Similar Documents

Publication Publication Date Title
EP2921190B1 (en) Liquid delivering pump
JP5898098B2 (en) Portable controller with integrated power supply for mechanical circulation assist system
US11241534B2 (en) Power management techniques for an infusion pump system
US11241531B2 (en) Medical liquid administration device
CA2934719C (en) Infusion pump battery capacity management and battery charge alert system and method
US8564447B2 (en) Battery life indication techniques for an electronic device
US20220088295A1 (en) Infusion pump system and method
US9018893B2 (en) Power control techniques for an electronic device
JPWO2002066102A1 (en) Syringe pump and liquid sending method
JP2010534084A (en) Energy supply for fluid delivery devices
JP2010508006A (en) Uninterruptible power supply for medical electrical equipment
US11992603B2 (en) Controller for an aerosol generator
CN108899955B (en) Power-off control device and active medical equipment
CN110787337A (en) Liquid medicine infusion device, monitoring system and monitoring method
WO2020149045A1 (en) Medical pump
JP4034491B2 (en) Syringe pump and drive control method when occlusion is detected
JP4754078B2 (en) Syringe pump and liquid feeding method
EP3120885A1 (en) Liquid delivery pump
JP2004000498A (en) Transfusion device
JP2001037875A (en) Medicine injector
KR101631010B1 (en) Low-power operating system of AED
JP2001224681A (en) Syringe pump and injection method
JP2012148008A (en) Infusion pump

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: 19910548

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2020566142

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: 19910548

Country of ref document: EP

Kind code of ref document: A1