WO2015041088A1 - Infusion pump - Google Patents

Infusion pump Download PDF

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Publication number
WO2015041088A1
WO2015041088A1 PCT/JP2014/073664 JP2014073664W WO2015041088A1 WO 2015041088 A1 WO2015041088 A1 WO 2015041088A1 JP 2014073664 W JP2014073664 W JP 2014073664W WO 2015041088 A1 WO2015041088 A1 WO 2015041088A1
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WO
WIPO (PCT)
Prior art keywords
flow rate
infusion
liquid feeding
tube
finger
Prior art date
Application number
PCT/JP2014/073664
Other languages
French (fr)
Japanese (ja)
Inventor
良一 赤井
高橋 秀典
Original Assignee
ニプロ株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by ニプロ株式会社 filed Critical ニプロ株式会社
Priority to JP2015537867A priority Critical patent/JP6369469B2/en
Publication of WO2015041088A1 publication Critical patent/WO2015041088A1/en

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Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F04POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
    • F04BPOSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
    • F04B43/00Machines, pumps, or pumping installations having flexible working members
    • F04B43/12Machines, pumps, or pumping installations having flexible working members having peristaltic action
    • F04B43/1223Machines, pumps, or pumping installations having flexible working members having peristaltic action the actuating elements, e.g. rollers, moving in a straight line during squeezing
    • 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
    • A61M5/14212Pumping with an aspiration and an expulsion action
    • A61M5/14228Pumping with an aspiration and an expulsion action with linear peristaltic action, i.e. comprising at least three pressurising members or a helical member
    • 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
    • A61M5/168Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F04POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
    • F04BPOSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
    • F04B43/00Machines, pumps, or pumping installations having flexible working members
    • F04B43/08Machines, pumps, or pumping installations having flexible working members having tubular flexible members
    • F04B43/082Machines, pumps, or pumping installations having flexible working members having tubular flexible members the tubular flexible member being pressed against a wall by a number of elements, each having an alternating movement in a direction perpendicular to the axes of the tubular member and each having its own driving mechanism

Definitions

  • the present invention relates to an infusion pump used for injecting medical chemicals into the body.
  • an infusion pump there is a finger type (peristaltic type) infusion pump.
  • the finger-type infusion pump for example, drives the finger forward and backward with respect to the infusion tube with the infusion tube connected to the infusion bag between the finger and the tube holding plate, and presses the infusion tube with the finger.
  • This is an infusion pump that delivers the infusion by doing so.
  • an infusion pump of a system full press system
  • an infusion pump of an intermediate pressure closing method in which an infusion tube is not completely closed with a finger
  • This semi-occluded infusion pump is, for example, a liquid feeding finger that delivers liquid without completely crushing the infusion tube, and an infusion tube arranged on the upstream side and the downstream side of the liquid feeding direction of the liquid feeding finger. It is equipped with a closing finger or the like that performs complete pressure closing and opening.
  • a drip tube connected to the infusion tube is disposed upstream of the infusion pump in the infusion feeding direction, and a drip sensor for detecting a drip in the drip tube is provided. Based on the output of the drip sensor, the actual number of infusions (mL / h) is calculated by measuring the number of drops dropped in the drip tube and the drop time interval (for example, Patent Document 3). reference). Then, the actual flow rate calculated in this way is compared with the set flow rate to determine a flow rate abnormality or the like.
  • the infusion pump may be set so that a plurality of droplets (for example, two droplets) are dropped in the drip cylinder by one cycle of liquid feeding.
  • the liquid droplets dropped in the drip tube may be connected in one cycle of the liquid feeding (for example, 2 drops are originally 1 drop). It may be a drop).
  • an error may occur in the flow rate calculated based on the output of the dropping sensor, so that it is impossible to guarantee the accuracy of the flow rate determination (flow rate abnormality determination) based on the output of the dropping sensor.
  • the upper limit is a flow rate at which there is no possibility that the droplets dropped in the drip tube are connected to each other.
  • the upper limit value is a flow rate at which there is no possibility that the droplets dropped in the drip tube are connected to each other.
  • the present invention has been made in view of such circumstances, and an object thereof is to provide an infusion pump capable of infusion at a high flow rate.
  • the present invention relates to a pump mechanism that presses an infusion tube to deliver the infusion in the infusion tube, and a drip that detects a drop that drops in a drip tube disposed upstream of the pump mechanism in the infusion feeding direction.
  • an infusion pump comprising a sensor and capable of performing flow rate control for controlling the driving of the pump mechanism according to a set flow rate and determining the flow rate of the liquid delivery based on the output of the dropping sensor. Yes.
  • a control mode of the pump mechanism it is possible to set a high flow rate mode in which liquid is dropped at a flow rate larger than the normal use flow rate range where there is no possibility that droplets dropping in the drip tube are connected to each other.
  • the normal use flow rate range it is set so that a plurality of droplets are dropped from the drip tube in one cycle of liquid feeding, and when the high flow rate mode is set, 1 of liquid feeding is set.
  • the inhalation period of the infusion solution during the cycle is shortened, and one droplet is dropped from the infusion tube in one cycle of the liquid feeding.
  • a plurality of droplets are set to be dropped from the drip tube in one cycle of liquid feeding.
  • the high flow rate mode is set, the inhalation period of the infusion in one cycle of the liquid feeding is shortened (droplet is intentionally connected), and the infusion tube is removed from the infusion cylinder in one cycle of the liquid feeding.
  • One drop is set to drop. In this way, in the high flow mode, the droplets dropped from the drip tube are intentionally connected so that one drop is always dropped from the drip tube in one cycle of liquid delivery. Even so, it is possible to ensure the accuracy of the flow rate determination (flow rate abnormality determination) based on the output of the dropping sensor.
  • the pump mechanism is arranged on the upstream side in the infusion feeding direction of the infusion feeding direction of the infusion feeding direction of the infusion feeding finger by the advancing / retreating movement, and is disposed on the upstream side of the infusion feeding direction of the infusion feeding finger.
  • the structure includes a finger, an upstream closing finger, and a cam and a cam shaft for individually driving the forward and backward driving fingers of the downstream closing finger.
  • the infusion period during one cycle of liquid feeding may be shortened by changing the rotational speed of the cam shaft of the pump mechanism during one cycle of liquid feeding.
  • the accuracy of the flow rate determination based on the output of the drip sensor can be ensured even in the high flow rate mode, so that the infusion at a high flow rate is possible.
  • the infusion pump 1 of this example is a semi-occluded infusion pump, and includes a pump body 11 and a door 12 that closes the front surface side (tube attachment position) of the pump body 11.
  • the door 12 is swingably (rotatably) supported by the pump body 11 via hinges 13 and 13, and is opened from the position at which the front side of the pump body 11 is completely closed (for example, 180 degrees). Oscillate until the position).
  • the pump main body 11 and the door 12 are provided with a door lock mechanism 14 for holding the closed state when the door 12 is closed.
  • the door lock mechanism 14 includes a door lock lever 14a disposed on the door 12 side, a hook 14b disposed on the pump main body 11 side, and the like, and the door lock lever 14a is rotated with the door 12 closed. Then, the door 12 can be locked in the closed state by being hooked on the hook 14b.
  • a tube mounting guide (guide groove) 111 is provided on the front wall 110 of the pump body 11.
  • the tube mounting guide 111 includes an upstream guide portion 111a, a pump finger portion 111b enlarged from the upstream guide portion 111a in a rectangular shape, and a downstream guide portion 111c in order from the upstream side in the infusion feeding direction.
  • the pump finger portion 111b faces the distal end portions of the liquid feeding fingers 21... 21 of the liquid feeding portion 20 of the pump mechanism 2 to be described later and the distal end portions of the closing fingers 31 and 31 of the valve portions 30A and 30B.
  • the upstream guide portion 111a of the tube mounting guide 111 is formed in a laterally curved shape (curved shape), and the tip portion thereof serves as an infusion tube inlet 1a. Further, the downstream guide portion 111c on the downstream side of the pump finger portion 111b is formed in a shape extending linearly in the vertical direction. A lower end portion of the downstream guide portion 111c serves as an infusion tube outlet 1b.
  • a bubble sensor (for example, an ultrasonic sensor) 71 that detects bubbles mixed in the infusion tube T attached to the pump main body 11 is disposed in the downstream guide portion 111c.
  • the groove width of the upstream guide portion 111a and the groove width of the downstream guide portion 111c are respectively large corresponding to the outer diameter (diameter) of an infusion tube (for example, made of polyvinyl chloride or polybutadiene) T connected to the chemical solution bag.
  • the infusion tube T can be attached to the infusion pump 1 by fitting the infusion tube T into the upstream guide portion 111a and the downstream guide portion 111c.
  • a tube clamp 112 is provided on the upstream guide portion 111a.
  • the tube clamp 112 is a member that temporarily holds the infusion tube T when the tube is attached to the infusion pump 1, and the clamp is automatically released when the door 12 is closed after the tube is attached.
  • a clamp lever (not shown) is provided in the vicinity of the tube clamp 112. When the infusion tube T is mounted, the tube clamp 112 can be opened by operating the clamp lever. it can.
  • a closing sensor 72 for detecting closing on the downstream side of the infusion tube T is provided on the inner surface side of the door 12.
  • a liquid feeding part pressing plate 24 is provided on the inner surface side of the door 12.
  • the liquid feeding part pressing plate 24 is provided at a position corresponding to the liquid feeding fingers 21... 21 of the liquid feeding part 20 described later.
  • the liquid feeding part presser plate 24 is spaced from the distal end surface 21a of the liquid feeding finger 21 in the last retracted position with the door 12 closed, corresponding to the outer diameter (diameter) of the infusion tube T. (Refer to FIG. 4, FIG. 7, etc.).
  • valve portion pressing plates 34 are provided on the inner surface side of the door 12.
  • the valve part pressing plates 34 and 34 are provided at positions corresponding to the respective closing fingers 31 and 31 of the upstream valve part 30A and the downstream valve part 30B, which will be described later.
  • These valve part holding plates 34 and 34 are in the state where the door 12 is closed, and the outer diameter (diameter) of the infusion tube T with respect to the tips of the projections 31a and 31a of the closing fingers 31 and 31 in the last retracted position. ) With an interval corresponding to (see FIG. 4, FIG. 7, etc.).
  • An elastic member such as a compression coil spring is disposed on the back side (door 12 side) of the liquid feeding part pressing plate 24 and the valve part pressing plates 34, 34, respectively, and the infusion tube T is The load that the infusion tube T receives from each finger 21, 31 when being pressed by the liquid feeding fingers 21, 21 of the liquid feeding part 20 and the closing fingers 31, 31 of the upstream and downstream valve parts 30 A, 30 B. If it is too large, it is retracted to the door 12 side. Thereby, the overload which the infusion tube T receives from each finger 21 and 31 can be reduced, and the lifetime of the infusion tube T can be extended.
  • a liquid crystal panel 3a of the liquid crystal display unit 3 for displaying various information and an operation unit 4 in which switches described later are arranged are arranged on the front surface of the door 12. Further, an indicator 5 that informs the operating state of the infusion pump 1 is arranged at the upper center of the door 12.
  • the door 12 When the infusion tube T is set in the infusion pump 1 having the above configuration, the door 12 is opened, and the infusion tube T connected to the chemical solution bag is connected to the [upstream guide portion 111a] ⁇ [pump finger portion 111b] ⁇ [ The infusion tube T is attached to the infusion pump 1 in the order of the downstream guide portion 111c]. After such tube mounting is completed, the door 12 is closed, and the door 12 is locked in the closed state by the door lock mechanism 14 to complete the setting of the infusion tube T. In this example, as described above, in a state where the door 12 is closed, the tube clamp 112 of the upstream guide portion 111a is opened. Further, when the door 12 is opened after completion of the infusion, the infusion tube T is closed by the tube clamp 112, and free flow that is a free fall of the infusion is prevented.
  • the infusion set applied to the infusion pump 1 of the present embodiment includes an infusion bag for storing a medicinal solution, an infusion tube 100 (see FIG. 3) for visually confirming the flow rate of the infusion solution, An upstream infusion tube T connecting the infusion tube 100, a downstream infusion tube T connected to the infusion tube 100, a roller clamp provided in the middle of the downstream infusion tube T, and an infusion tube T It is comprised by the injection needle (venous needle) etc. which are connected to the front-end
  • the infusion tube T between the infusion tube 100 and the roller clamp of such an infusion set is mounted on the pump body 11 in the manner described above, and the infusion tube 100 is disposed upstream of the infusion pump 1 in the infusion feeding direction. (See FIG. 3).
  • the infusion pump 1 of this embodiment is provided with the dripping sensor 8 which detects the droplet dripped inside the said infusion tube 100, as shown in FIG.
  • the dropping sensor 8 includes a light emitting unit 8a that outputs light such as infrared rays and a light receiving unit 8b that receives output light from the light emitting unit 8a.
  • the drip sensor 8 is detachably attached to the drip tube 100 by a clamp (not shown) or the like, and in the attached state, the optical axis of the light emitting unit 8a coincides with the droplet dropping position, and the light emitting unit 8a and the light receiving unit. 8b is opposed to the drip tube 100.
  • the light receiving unit 8b When the light receiving unit 8b receives the light from the light emitting unit 8a (when the light from the light emitting unit 8a passes through without being blocked by the droplet), the light receiving unit 8b outputs, for example, an OFF signal, When the light from the light emitting unit 8a is blocked by the droplet, the light receiving unit 8b is configured to output an ON signal.
  • An output signal of the dropping sensor 8 (light receiving unit 8b) is input to the control unit 300 described later.
  • the pump mechanism 2 includes an upstream valve unit 30A, a liquid feeding unit 20, a downstream valve unit 30B, a liquid feeding unit pressing plate 24, valve unit pressing plates 34 and 34, a driving unit 200, and the like.
  • the driving unit 200 individually includes the three liquid feeding fingers 21... 21 of the liquid feeding unit 20, the upstream valve unit 30A, and the closing fingers 31 and 31 of the downstream valve unit 30B. Move forward and backward (forward movement or backward movement).
  • the liquid feeding unit 20 includes three liquid feeding fingers 21. Of these three liquid feeding fingers 21... 21, the upstream one in the infusion feeding direction is the first liquid feeding finger 21, the middle one is the second liquid feeding finger 21, and the downstream one is the third liquid feeding finger. It may be called a finger 21. In the present embodiment, the first liquid feeding finger 21, the second liquid feeding finger 21, and the third liquid feeding finger 21 have the same configuration. Therefore, in the following description, one liquid feeding finger 21 (first Only the configuration of the single liquid delivery finger 21) will be described with reference to FIGS.
  • the liquid feeding finger 21 is a member having a rectangular cross section, and the front-rear direction of the pump main body 11 (the X direction perpendicular to the longitudinal direction of the infusion tube T attached to the pump main body 11 (perpendicular to the front wall 110 of the pump main body 11). Direction)).
  • the liquid feeding finger 21 is slidably supported by a guide member 50 (see FIG. 4), and can move forward and backward in the front-rear direction (X direction) of the pump body 11.
  • the guide member 50 is supported and fixed to the pump body 11.
  • the liquid feeding finger 21 is moved forward and backward (forward movement or backward movement) by a driving unit 200 described later, and when the liquid feeding finger 21 is in the last retracted position, as shown in FIGS. 4 and 7A, etc.
  • the distal end surface 21a of the liquid finger 21 is disposed at a position (a position corresponding to the outer peripheral surface of the infusion tube T) in contact with the outer peripheral surface of the infusion tube T (circular state) attached to the pump body 11. Further, when the liquid feeding finger 21 moves forward from this state (the state at the last retracted position), the infusion tube T is pressed during the forward movement process.
  • the infusion tube T is driven so as not to be completely occluded as shown in FIG. 8 when the infusion finger 21 is in the most advanced position.
  • the stroke of the forward / backward movement of the liquid feeding finger 21 by the part 200 is set.
  • the valve unit 30A (30B) includes a closing finger 31.
  • the closing finger 31 is a member having a rectangular cross section, and is similar to the liquid feeding finger 21 described above in the front-rear direction of the pump body 11 (the X direction (pump body perpendicular to the longitudinal direction of the infusion tube T attached to the pump body 11). 11 in the direction perpendicular to the front wall 110)). Further, a protruding portion 31 a is provided at the distal end portion of the closing finger 31.
  • the closing finger 31 is slidably supported by a guide member 50 (the same guide member 50 as the liquid feeding finger 21 of the liquid feeding section 20), and can move forward and backward in the front-rear direction (X direction) of the pump body 11. It has become.
  • the closing finger 31 is moved forward and backward (forward movement or backward movement) by the driving unit 200 described later, and when the closing finger 31 is in the last retracted position, as shown in FIG. 4 and FIG.
  • the tip of 31a is arrange
  • the infusion tube T is pressed during the forward movement process.
  • the stroke of the forward / backward movement of the closing finger 31 by the drive unit 200 is set so as to be closed.
  • the drive unit 200 includes cams 221a, 221b, and 221c for individually advancing and retracting the liquid feeding fingers 21 and 21 of the liquid feeding unit 20, and upstream and downstream valve units 30A and 30B.
  • cams 221a, 221b, 221c, 231a, 231b are cam shafts 201, respectively. Is attached to be integrally rotatable.
  • the cam shaft 201 is disposed along the vertical direction of the pump body 11 (the arrangement direction of the fingers 21... 21, 31, 31).
  • a timing pulley (driven pulley) 203 is attached to the upper end portion of the cam shaft 201 so as to be integrally rotatable. Further, a timing pulley (drive pulley) 204 is provided on the rotating shaft 202a of the stepping motor 202 so as to be integrally rotatable. A timing belt 205 is wound between the timing pulley 203 of the cam shaft 201 and the timing pulley 204 on the stepping motor 202 side, and the cam shaft 201 is rotated by driving of the stepping motor 202.
  • the above-described driving of the stepping motor 202 causes the liquid feeding fingers 21 and 21 of the liquid feeding section 20 and the closing fingers of the upstream and downstream valve sections 30A and 30B.
  • the cam shapes of the cams 221a, 221b, 221c, 231a, and 231b are set so that the fingers 31 and 31 are driven forward and backward by the operations shown in FIGS.
  • the stepping motor 202 since the stepping motor 202 is used as an electric motor that applies a rotational force to the camshaft 201, the rotational speed of the camshaft 201 is arbitrarily changed during one cycle of liquid feeding (see FIG. 10).
  • the stepping motor 202 can control the rotation speed of the rotating shaft 202a by controlling the driving pulse (for example, duty control) applied to the motor driver. Therefore, by changing the drive pulse given to the stepping motor 202 during one cycle of liquid feeding (changing the duty ratio of the drive pulse), the rotational speed of the camshaft 201 can be arbitrarily changed within that cycle. It is. Accordingly, for example, as shown in FIG. 10, even if the period (time) of one cycle is the same, the ratio between the discharge period of liquid feeding and the suction period can be variably set (for example, FIG. The suction period of FIG. 10 (B) can be shortened with respect to A).
  • the driving of the above stepping motor 202 is controlled by the control unit 300.
  • the stepping motor 202, the control unit 300, and the like are supplied with electric power from a battery built in the infusion pump 1 or a commercial power source.
  • a mechanism in which an electric motor and a rotation-translation mechanism (for example, rack and pinion) are combined may be applied, or a drive using a solenoid as a drive source may be applied.
  • the liquid crystal display unit 3 includes a liquid crystal panel 3 a and a drive driver (not shown), and the liquid crystal panel 3 a is disposed on the front surface of the door 12.
  • operation information such as integrated amount [mL], scheduled infusion volume [mL], flow rate [mL / h], alarm information (message, etc.), and various settings by the user
  • the user setting screen is displayed.
  • the operation unit 4 includes a start switch 41 for starting infusion, a stop switch 42 for stopping an infusion operation and an alarm, a fast-forward switch 43 used when preparing for infusion, a display changeover switch 44, and a numerical value setting.
  • An up switch 45, a numerical value setting down switch 46, an integrated amount reset switch 47, an infusion needle size selection switch 48, and the like are provided.
  • the display changeover switch 44 is a switch for switching the display to items (for example, flow rate, scheduled amount, scheduled time, high flow rate mode, etc.) for inputting numerical values and the like.
  • the numerical value setting up switch 45 and the numerical value setting down switch 46 are switches for increasing or decreasing numerical values such as a flow rate, a predetermined amount, and a scheduled time. It consists of a total of three switches: a numerical value setting switch for the eye and a numerical value setting switch for the third digit on the left side.
  • control unit 300 will be described.
  • the control unit 300 is composed mainly of a microcomputer or the like, and includes a CPU (Central Processing Unit), a ROM (Read Only Memory), a RAM (Random Access Memory), a nonvolatile RAM, an I / O interface, and the like.
  • a bus line for connecting the functional units to each other is provided.
  • control unit 300 is connected to the operation unit 4, the bubble sensor 71, the blockage sensor 72, the power switch 7 (for example, disposed on the back surface of the pump main body 11), and the like.
  • a sensor 8 is connected. Signals from switches and sensors of the operation unit 4 are input to the control unit 300.
  • the control unit 300 is connected to the liquid crystal display unit 3, the indicator 5, the sound generation unit 6, the stepping motor 202 for driving the pump mechanism 2, and the like.
  • the control unit 300 controls the rotational speed of the stepping motor 202 of the pump mechanism 2 according to the set value (set flow rate) of the infusion flow set by operating the switches of the operation unit 4. Adjust the variable.
  • the flow rate can be set in units of [1 mL / h] within the range of 1 mL / h to 1200 mL / h. This flow control will be described later.
  • the control unit 300 calculates the flow rate based on the output of the dropping sensor 8. This flow rate calculation process will also be described later.
  • FIG. 7A is a diagram showing a state (initial state) in which the infusion tube T is mounted on the pump body 11 and the door 12 is closed.
  • this initial state only the closing finger 31 of the downstream valve portion 30B is at the most advanced position, and the infusion tube T is completely closed by the protrusion 31a of the closing finger 31.
  • the first liquid delivery finger 21 of the liquid delivery section 20 moves forward and presses the infusion tube T (FIG. 8A).
  • the infusion tube T is pressed by the first infusion finger 21
  • the infusion in the infusion tube T is sent downstream.
  • the second liquid feeding finger 21 and the third liquid feeding finger 21 sequentially move forward (FIGS. 8B to 8C).
  • the infusion tube T is pressed by the infusion fingers 21 and 21, the infusion in the infusion tube T is further sent to the downstream side.
  • the infusion in the infusion tube T is fed by the peristaltic motion of the three liquid feeding fingers 21.
  • the infusion pump 1 of this example is a semi-occlusion type, even if each of the liquid feeding fingers 21 of the liquid feeding unit 20 reaches the most advanced position, it is shown in FIGS. 8 (A) to 8 (C). As such, the infusion tube T is not completely crushed.
  • the infusion in the infusion tube T can be continuously sent out downstream.
  • the liquid flow rate can be variably adjusted by controlling the cycle of the liquid supply cycle. Further, as described above, by changing the drive pulse applied to the stepping motor 202 within one cycle of liquid feeding, the liquid ejection period and the suction period can be variably set during that cycle (see FIG. (See FIG. 10).
  • the infusion tube 100 has 20 infusion tubes 100. A case where an infusion bag is used will be described.
  • the infusion pump 1 of this embodiment it is set so that 0.1 cc (0.1 mL) of liquid can be delivered in one cycle of the above-described liquid feeding, and 20 drops of the above-mentioned 20 drops in one cycle of liquid feeding. It is set so that two droplets are dropped from the drip tube 100 (0.05 cc / 1 droplet).
  • the infusion pump 1 (semi-enclosed infusion pump) having such a setting, when the flow rate of the liquid feed reaches a high flow rate exceeding 600 mL / h, for example, the inside of the drip tube 100 is dropped in one cycle of the liquid feed.
  • the droplets are connected to each other, and there is a high possibility that a drop of 2 drops will be a drop of 1 drop.
  • the flow rate is such that there is no possibility that a droplet dropped in the drip tube 100 is connected, and the flow rate can guarantee the accuracy of the flow rate calculation based on the output of the drop sensor 8 (for example, 600 mL).
  • the following flow range is defined as a normal use range (hereinafter also referred to as a normal use flow range).
  • a normal use flow range hereinafter also referred to as a normal use flow range.
  • a high flow rate mode in which liquid feeding is performed in a high flow rate region (a high flow rate region of 601 mL / h or more) exceeding the normal use flow rate region can be set.
  • a high flow rate region a high flow rate region of 601 mL / h or more
  • Control and processing in the high flow rate mode will be described later.
  • control and processing executed by the control unit 300 will be described below.
  • the flow rate from 1 mL / h to 600 mL / h can be set by operating the switches of the operation unit 4.
  • the control unit 300 supplies a drive pulse corresponding to the set flow rate set by the operation of the operation unit 4 (a drive pulse having a duty ratio corresponding to the set flow rate) to the stepping motor 202 of the pump mechanism 2, and the stepping motor By controlling the rotational speed of 202, the liquid feed flow rate of the pump mechanism 2 is controlled to the set flow rate.
  • the control unit 300 displays a message indicating the occurrence of free flow on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3, or drives the sound generation unit 6 to generate a buzzer sound. Informing a user such as a nurse that a free flow has occurred.
  • the control unit 300 determines the flow rate abnormality by calculating the flow rate based on the output of the dropping sensor 8. Specifically, the control unit 300 counts the number of droplets dropped per unit time (for example, per minute) of the droplets dropped in the drip tube 100 based on the output signal of the drop sensor 8 (counts ON signal). The liquid flow rate (mL / h) is calculated (converted) from the droplet count value.
  • the controller 300 sequentially executes a flow rate calculation process based on the output of the drip sensor 8 during the infusion in the normal use flow rate region, and calculates the calculated flow rate (actual flow rate) and the set flow rate (1 mL / The difference between the set flow rate and the calculated flow rate (flow rate difference) is calculated using the set flow rate from h to 600 mL / h.
  • a predetermined allowable range a range in which the flow rate can be regarded as normal
  • it is determined that the flow rate is normal.
  • the flow rate difference is out of the allowable range, it is determined that the flow rate is abnormal.
  • control unit 300 When it is determined that the flow rate is abnormal, the control unit 300 displays a message indicating the abnormal flow rate on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3 or drives the sound generation unit 6 to generate a buzzer sound. To inform a user such as a nurse that the flow rate is abnormal.
  • the control unit 300 displays a message indicating that the liquid is in the liquid state on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3, and also drives the sound generation unit 6 to generate a buzzer sound. The user such as a nurse is informed that this is the state.
  • required empirically by experiment, calculation, etc. is set.
  • the suction period and the discharge period in one cycle are controlled by changing the rotation speed of the camshaft 201 (rotation speed of the stepping motor 202) in the above-described one cycle.
  • the suction period is set to a length that can secure the time required for two droplets to drop from the drip tube 100 in one cycle.
  • the discharge period is set as long as possible after securing such a suction period.
  • the discharge period is set to be long in this way, the forward speed of the liquid feeding fingers 21... 21 and the closing fingers 31 and 31 during the discharge period can be slowed, and stable liquid feeding is performed while suppressing pulsation and the like. be able to.
  • liquid feeding is normally performed in the normal use flow rate range of 600 mL / h or less, but the high flow rate mode is set when infusion at a high flow rate is necessary. be able to.
  • the high flow rate mode is set by, for example, operating the display changeover switch 44 of the operation unit 4 to display the item “high flow rate mode setting” on the screen of the liquid crystal panel 3 a of the liquid crystal display unit 3. By pressing the start switch 41, the high flow rate mode can be set. When returning to the normal use flow rate liquid delivery mode, the display changeover switch 44 is operated to display the item “high flow rate mode release” on the liquid crystal panel 3a of the liquid crystal display unit 3 and start in this display state. By pressing the switch 41, it is possible to cancel the high flow rate mode and return to the liquid supply mode at the normal use flow rate.
  • control unit 300 performs the following control and processing.
  • the flow rate from 601 mL / h to 1200 mL / h can be set by operating the switches of the operation unit 4.
  • the control unit 300 supplies a drive pulse corresponding to the set flow rate set by the operation of the operation unit 4 (a drive pulse having a duty ratio corresponding to the set flow rate) to the stepping motor 202 of the pump mechanism 2, and the stepping motor 202.
  • the liquid feed flow rate of the pump mechanism 2 is controlled to the set flow rate.
  • the controller 300 receives an ON signal (droplet detection signal) from the drop sensor 8 when the drop of the droplet is detected when the pump mechanism 2 is in a stopped state when the high flow rate mode is set.
  • the control unit 300 displays a message indicating the occurrence of free flow on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3 or drives the sound generation unit 6 to generate a buzzer sound. To inform a user such as a nurse that a free flow has occurred.
  • the suction period in one cycle of liquid feeding is the period from FIG. 9 to FIG. 7A as described above. If this suction period is shortened, the upstream side valve unit 30A in the suction period is reduced. The retraction speeds of the closing finger 31 and the three liquid feeding fingers 21... 21 of the liquid feeding unit 20 are increased. That is, if the suction period is shortened, the suction speed is increased. The suction speed (suction force) increases as the suction period becomes shorter, and the droplet dropping interval becomes shorter. Therefore, by making the suction period as short as possible and increasing the suction speed (suction force), it is possible to intentionally connect the droplets dropped in the drip tube 100.
  • FIG. 10 (B) and FIG. 10 (C) As shown in FIG. 5, the change control of the rotation speed of the camshaft 201 (rotation speed of the stepping motor 202) during one cycle is executed so that the suction period during one cycle is the same period as when the flow rate is 1200 mL / h. This ensures that one drop is dropped in one cycle. In this manner, by making sure that one droplet (0.1 cc / 1 droplet) is dropped in one cycle of liquid feeding in the high flow rate mode, the drop sensor even in the high flow rate mode. The accuracy of the flow rate abnormality determination based on the output of 8 (accuracy equivalent to the normal use flow rate range) can be secured.
  • Such a process is set so that one drop is surely dropped in one cycle, and the flow rate is calculated based on the output of the drop sensor 8 to determine a flow rate abnormality.
  • the control unit 300 counts the number of drops per unit time (for example, per minute) of droplets dropped in the drip tube 100 from the output signal of the drop sensor 8 (counts the ON signal), and The flow rate (mL / h) of the liquid feeding is calculated (converted) from the droplet count value.
  • the volume of the drop per drop is 0.1 mL.
  • control unit 300 sequentially executes a flow rate calculation process based on the output of the drip sensor 8 during the infusion in the high flow rate mode, and calculates the calculated flow rate (actual flow rate) and the set flow rate (601 mL / The set flow rate from h to 1200 mL / h) is used to calculate the difference between the set flow rate and the calculated flow rate (flow rate difference).
  • a predetermined allowable range a range in which the flow rate can be regarded as normal
  • it is determined that the flow rate is normal.
  • the flow rate difference is out of the allowable range, it is determined that the flow rate is abnormal.
  • control unit 300 When it is determined that the flow rate is abnormal, the control unit 300 displays a message indicating the abnormal flow rate on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3 or drives the sound generation unit 6 to generate a buzzer sound. To inform a user such as a nurse that the flow rate is abnormal.
  • (B4) When the pump mechanism 2 is in the driving state when the high flow rate mode is set, when droplet dropping is not detected for a certain period (when the ON signal (droplet detection signal) is not output from the dropping sensor 8 for a certain period).
  • the control unit 300 displays a message indicating that the liquid is in the liquid state on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3, or drives the sound generation unit 6 to generate a buzzer sound. To inform the user such as a nurse that the liquid is empty.
  • required empirically by experiment, calculation, etc. is set.
  • the drip tube 100 in the high flow rate mode in which liquid droplets dropped in the drip tube 100 are not likely to be connected to each other and are supplied at a flow rate larger than the normal use flow rate region, the drip tube 100 is used. Are set so that one drop is surely dropped from the drip tube in one cycle of liquid feeding, so even in the high flow rate mode, the drop sensor 8 The accuracy of the flow rate abnormality determination based on the output of (the accuracy equivalent to the normal use flow rate range) can be ensured. This enables infusion at a high flow rate.
  • the normal use flow rate range and the high flow rate range are separated using 600 mL / h as a threshold value, but an appropriate value is set for the threshold value according to the setting state of the pump mechanism 2 and the like. May be.
  • the flow rate is calculated by counting the number of droplets dropped per unit time (per minute), but the present invention is not limited to this.
  • the flow rate may be calculated by measuring the time required for the count value of the droplets counted from the output of the drop sensor 8 to reach a predetermined value. Further, the flow rate may be calculated by obtaining the dropping time interval of the droplets dropped in the drip tube 100 from the output of the dropping sensor 8.
  • the present invention is not limited to this, and the drip per mL as the drip tube 100 is used.
  • the present invention can also be applied when using a drip tube having 60 drops.
  • the number of the liquid feeding fingers 21 provided in the liquid feeding unit 20 is three, but the present invention is not limited to this, and the number of the liquid feeding fingers 21 provided in the liquid feeding unit 20 is two. There may be one or four or more.
  • a plurality of (three) liquid feeding fingers 21... 21 of the liquid feeding unit 20 are arranged at intervals, but the liquid feeding fingers 21. May be. Further, the closing fingers 31, 31 of the upstream and downstream valve portions 30 ⁇ / b> A, 30 ⁇ / b> B may also be arranged in a state of being close to the liquid feeding finger 21 of the liquid feeding portion 20.
  • the present invention can be used for an infusion pump used for injecting a medical drug solution into the body.

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Abstract

 The device permits setting of a high flow rate mode in which a solution is fed at a higher flow rate than in a normal usage flow rate zone in which there is no possibility that drops dripping down within a drip tube (100) will coalesce. In the case that the normal usage flow rate zone is selected, the setting is such that multiple drops drip down from the drip tube (100) in a single cycle of solution feed, and in the case in which the high flow rate mode has been set, the setting is such that drops dripping down from the drip tube (100) are deliberately induced to coalesce, and a single drop drips down from the drip tube (100) in a single cycle of solution feed without fail. Even during the high speed mode produced by this setting, it is possible to ensure accurate flow rate determination on the basis of the output of a drip sensor (8), and transfusion at a high flow rate is possible.

Description

輸液ポンプInfusion pump
 本発明は、医療用の薬液を体内に注入する場合などに用いる輸液ポンプに関する。 The present invention relates to an infusion pump used for injecting medical chemicals into the body.
 輸液ポンプとしては、フィンガ式(ペリスタルティック式)の輸液ポンプがある。フィンガ式輸液ポンプは、例えば、フィンガとチューブ押え板との間に、輸液バッグに接続された輸液チューブを配置した状態で、フィンガを輸液チューブに対して進退駆動させ、フィンガにて輸液チューブを押圧することにより輸液を送り出す方式の輸液ポンプである。 As an infusion pump, there is a finger type (peristaltic type) infusion pump. The finger-type infusion pump, for example, drives the finger forward and backward with respect to the infusion tube with the infusion tube connected to the infusion bag between the finger and the tube holding plate, and presses the infusion tube with the finger. This is an infusion pump that delivers the infusion by doing so.
 フィンガ式輸液ポンプとしては、フィンガで輸液チューブを完全に圧閉する方式(フルプレス方式)の輸液ポンプがある。また、フィンガで輸液チューブを完全に圧閉しない中間圧閉方式(半閉塞方式)の輸液ポンプが提案されている(例えば、特許文献1及び2参照)。この半閉塞方式の輸液ポンプは、例えば、輸液チューブを完全につぶさずに送液を行う送液フィンガ、及び、この送液フィンガの輸液送り方向の上流側と下流側にそれぞれ配置され、輸液チューブの完全圧閉と開放とを行う閉塞フィンガなどを備えている。 As a finger type infusion pump, there is an infusion pump of a system (full press system) in which an infusion tube is completely closed with a finger. Further, an infusion pump of an intermediate pressure closing method (semi-occlusion method) in which an infusion tube is not completely closed with a finger has been proposed (see, for example, Patent Documents 1 and 2). This semi-occluded infusion pump is, for example, a liquid feeding finger that delivers liquid without completely crushing the infusion tube, and an infusion tube arranged on the upstream side and the downstream side of the liquid feeding direction of the liquid feeding finger. It is equipped with a closing finger or the like that performs complete pressure closing and opening.
 このような輸液ポンプにあっては、例えば、輸液チューブに接続された点滴筒を輸液ポンプの輸液送り方向の上流側に配置するとともに、点滴筒内を滴下する液滴を検出する滴下センサを設け、その滴下センサの出力に基づいて点滴筒内を滴下する液滴の滴下数や滴下時間間隔などを計測して実際の輸液の流量(mL/h)を算出している(例えば、特許文献3参照)。そして、このようにして算出した実際の流量と設定流量とを比較して流量異常などを判定している。 In such an infusion pump, for example, a drip tube connected to the infusion tube is disposed upstream of the infusion pump in the infusion feeding direction, and a drip sensor for detecting a drip in the drip tube is provided. Based on the output of the drip sensor, the actual number of infusions (mL / h) is calculated by measuring the number of drops dropped in the drip tube and the drop time interval (for example, Patent Document 3). reference). Then, the actual flow rate calculated in this way is compared with the set flow rate to determine a flow rate abnormality or the like.
特許第3595136号公報Japanese Patent No. 3595136 特開昭55-005485号公報JP-A-55-005485 特開2002-336350号公報JP 2002-336350 A
 ところで、輸液ポンプでは、1サイクルの送液で点滴筒内に複数滴(例えば2滴)の液滴が滴下するように設定される場合がある。このような設定の輸液ポンプでは、送液の流量が高流量になると、送液の1サイクルにおいて点滴筒内を滴下する液滴同士がつながってしまう場合がある(例えば本来2滴の滴下が1滴の滴下となる場合がある)。こうした状況になると、滴下センサの出力に基づいて算出される流量に誤差が生じる場合があるため、滴下センサの出力に基づく流量判定(流量異常判定)の精度を保証できなくなる。 By the way, the infusion pump may be set so that a plurality of droplets (for example, two droplets) are dropped in the drip cylinder by one cycle of liquid feeding. In the infusion pump having such a setting, when the flow rate of the liquid feeding becomes high, the liquid droplets dropped in the drip tube may be connected in one cycle of the liquid feeding (for example, 2 drops are originally 1 drop). It may be a drop). In such a situation, an error may occur in the flow rate calculated based on the output of the dropping sensor, so that it is impossible to guarantee the accuracy of the flow rate determination (flow rate abnormality determination) based on the output of the dropping sensor.
 このため、従来では、点滴筒内を滴下する液滴同士がつながる可能性がない流量を上限値としている。しかしながら、輸液ポンプの使用に際しては、そのような上限値を超える流量での送液が要求される場合もあり、こうした高流量での輸液が可能な輸液ポンプの提供が望まれている。 Therefore, conventionally, the upper limit is a flow rate at which there is no possibility that the droplets dropped in the drip tube are connected to each other. However, when using an infusion pump, there is a case where liquid feeding at a flow rate exceeding such an upper limit value is required, and it is desired to provide an infusion pump capable of infusion at such a high flow rate.
 本発明は、このような実情に鑑みてなされたものであり、その目的は、高流量での輸液が可能な輸液ポンプを提供することにある。 The present invention has been made in view of such circumstances, and an object thereof is to provide an infusion pump capable of infusion at a high flow rate.
 本発明は、輸液チューブを押圧して当該輸液チューブ内の輸液を送液するポンプ機構と、前記ポンプ機構の輸液送り方向の上流側に配置された点滴筒内を滴下する液滴を検出する滴下センサとを備え、設定流量に応じて前記ポンプ機構の駆動を制御する流量制御、及び、前記滴下センサの出力に基づいて送液の流量を判定する流量判定の実行が可能な輸液ポンプを前提としている。このような輸液ポンプにおいて、前記ポンプ機構の制御モードとして前記点滴筒内を滴下する液滴同士がつながる可能性がない通常使用流量域よりも大きな流量で送液を行う高流量モードの設定が可能であり、前記通常使用流量域である場合は送液の1サイクルで前記点滴筒から複数滴の液滴が滴下するように設定され、前記高流量モードが設定された場合には送液の1サイクル中の輸液の吸入期間を短くして当該送液の1サイクルで前記点滴筒から1滴の液滴が滴下するように構成されていることを特徴としている。 The present invention relates to a pump mechanism that presses an infusion tube to deliver the infusion in the infusion tube, and a drip that detects a drop that drops in a drip tube disposed upstream of the pump mechanism in the infusion feeding direction. Assuming an infusion pump comprising a sensor and capable of performing flow rate control for controlling the driving of the pump mechanism according to a set flow rate and determining the flow rate of the liquid delivery based on the output of the dropping sensor. Yes. In such an infusion pump, as a control mode of the pump mechanism, it is possible to set a high flow rate mode in which liquid is dropped at a flow rate larger than the normal use flow rate range where there is no possibility that droplets dropping in the drip tube are connected to each other. In the case of the normal use flow rate range, it is set so that a plurality of droplets are dropped from the drip tube in one cycle of liquid feeding, and when the high flow rate mode is set, 1 of liquid feeding is set. The inhalation period of the infusion solution during the cycle is shortened, and one droplet is dropped from the infusion tube in one cycle of the liquid feeding.
 本発明によれば、通常使用流量域(流量判定精度が保障できる流量域)である場合は、送液の1サイクルで点滴筒から複数滴(例えば2滴)の液滴が滴下するように設定する一方、高流量モードが設定された場合には、送液の1サイクル中の輸液の吸入期間を短くして(液滴を意図的につなげて)、当該送液の1サイクルで点滴筒から1滴の液滴が滴下するように設定している。このように高流量モード時には、点滴筒を滴下する液滴を意図的につなげて送液の1サイクルで点滴筒から必ず1滴の液滴が滴下するように設定することで、高流量モード時であっても、滴下センサの出力に基づく流量判定(流量異常判定)の精度を確保することが可能となる。 According to the present invention, when the flow rate is in the normal use flow rate range (the flow rate range in which the flow rate determination accuracy can be ensured), a plurality of droplets (for example, 2 droplets) are set to be dropped from the drip tube in one cycle of liquid feeding. On the other hand, when the high flow rate mode is set, the inhalation period of the infusion in one cycle of the liquid feeding is shortened (droplet is intentionally connected), and the infusion tube is removed from the infusion cylinder in one cycle of the liquid feeding. One drop is set to drop. In this way, in the high flow mode, the droplets dropped from the drip tube are intentionally connected so that one drop is always dropped from the drip tube in one cycle of liquid delivery. Even so, it is possible to ensure the accuracy of the flow rate determination (flow rate abnormality determination) based on the output of the dropping sensor.
 本発明において、前記ポンプ機構を、進退移動が可能でその前進移動過程で輸液チューブを押圧する送液フィンガと、前記送液フィンガの輸液送り方向の上流側に配置され、進退移動により輸液チューブの閉塞と開放とを行う上流側の閉塞フィンガと、前記送液フィンガの輸液送り方向の下流側に配置され、進退移動により輸液チューブの閉塞と開放とを行う下流側の閉塞フィンガと、前記送液フィンガ、前記上流側の閉塞フィンガ、及び、前記下流側の閉塞フィンガの各フィンガを個別に進退駆動するためのカム及びカム軸とを備えた構成とし、前記高流量モードが設定された場合には、送液の1サイクル中の前記ポンプ機構のカム軸の回転速度を変更して当該送液の1サイクル中の輸液の吸入期間を短くするようにしてもよい。 In the present invention, the pump mechanism is arranged on the upstream side in the infusion feeding direction of the infusion feeding direction of the infusion feeding direction of the infusion feeding finger by the advancing / retreating movement, and is disposed on the upstream side of the infusion feeding direction of the infusion feeding finger. An upstream closing finger for closing and opening, a downstream closing finger that is disposed downstream of the liquid feeding direction of the liquid feeding finger and that closes and opens the infusion tube by advancing and retreating, and the liquid feeding When the high flow rate mode is set, the structure includes a finger, an upstream closing finger, and a cam and a cam shaft for individually driving the forward and backward driving fingers of the downstream closing finger. The infusion period during one cycle of liquid feeding may be shortened by changing the rotational speed of the cam shaft of the pump mechanism during one cycle of liquid feeding.
 本発明の輸液ポンプによれば、高流量モード時であっても、滴下センサの出力に基づく流量判定の精度を確保することができるので、高流量での輸液が可能になる。 According to the infusion pump of the present invention, the accuracy of the flow rate determination based on the output of the drip sensor can be ensured even in the high flow rate mode, so that the infusion at a high flow rate is possible.
本発明を適用する輸液ポンプの一例を示す外観斜視図である。It is an external appearance perspective view which shows an example of the infusion pump to which this invention is applied. 図1の輸液ポンプの正面図である。It is a front view of the infusion pump of FIG. 図1の輸液ポンプを扉を開いた状態で示す概略構成図である。It is a schematic block diagram which shows the infusion pump of FIG. 1 in the state which opened the door. ポンプ機構の構成を示す部分断面側面図である。It is a fragmentary sectional side view which shows the structure of a pump mechanism. ポンプ機構の駆動部の構成を模式的に示す図である。It is a figure which shows typically the structure of the drive part of a pump mechanism. 輸液ポンプの制御系の構成を示すブロック図である。It is a block diagram which shows the structure of the control system of an infusion pump. 図4に示すポンプ機構の動作説明図である。It is operation | movement explanatory drawing of the pump mechanism shown in FIG. 図4に示すポンプ機構の動作説明図である。It is operation | movement explanatory drawing of the pump mechanism shown in FIG. 図4に示すポンプ機構の動作説明図である。It is operation | movement explanatory drawing of the pump mechanism shown in FIG. 送液の1サイクルにおける吐出期間と吸込期間とを示す図である。It is a figure which shows the discharge period and suction period in 1 cycle of liquid feeding.
 以下、本発明の実施形態を図面に基づいて説明する。 Hereinafter, embodiments of the present invention will be described with reference to the drawings.
 本発明の輸液ポンプの一例について図1~図6を参照して説明する。 An example of the infusion pump of the present invention will be described with reference to FIGS.
 この例の輸液ポンプ1は、半閉塞方式の輸液ポンプであって、ポンプ本体11と、このポンプ本体11の前面側(チューブ取付位置)を閉鎖する扉12とを備えている。扉12はヒンジ13,13を介してポンプ本体11に揺動自在(回転自在)に支持されており、ポンプ本体11の前面側を完全に閉鎖する位置から、完全開放位置(例えば、180°開く位置)までの間において揺動可能となっている。 The infusion pump 1 of this example is a semi-occluded infusion pump, and includes a pump body 11 and a door 12 that closes the front surface side (tube attachment position) of the pump body 11. The door 12 is swingably (rotatably) supported by the pump body 11 via hinges 13 and 13, and is opened from the position at which the front side of the pump body 11 is completely closed (for example, 180 degrees). Oscillate until the position).
 ポンプ本体11及び扉12には、扉12を閉めたときに、その閉塞状態を保持するための扉ロック機構14が設けられている。扉ロック機構14は、扉12側に配置のドアロックレバー14a、及び、ポンプ本体11側に配置のフック14bなどによって構成されており、扉12を閉鎖した状態でドアロックレバー14aを回動操作してフック14bに引っ掛けることによって扉12を閉鎖状態にロックすることができる。 The pump main body 11 and the door 12 are provided with a door lock mechanism 14 for holding the closed state when the door 12 is closed. The door lock mechanism 14 includes a door lock lever 14a disposed on the door 12 side, a hook 14b disposed on the pump main body 11 side, and the like, and the door lock lever 14a is rotated with the door 12 closed. Then, the door 12 can be locked in the closed state by being hooked on the hook 14b.
 ポンプ本体11の前面壁110にはチューブ装着ガイド(ガイド溝)111が設けられている。チューブ装着ガイド111は、輸液送り方向の上流側から順に、上流側ガイド部111a、この上流側ガイド部111aから矩形状に拡大したポンプフィンガ部111b、及び、下流側ガイド部111cを備えている。ポンプフィンガ部111bには、後述するポンプ機構2の送液部20の送液フィンガ21・・21の先端部、及び、バルブ部30A,30Bの閉塞フィンガ31,31の先端部が臨んでいる。 A tube mounting guide (guide groove) 111 is provided on the front wall 110 of the pump body 11. The tube mounting guide 111 includes an upstream guide portion 111a, a pump finger portion 111b enlarged from the upstream guide portion 111a in a rectangular shape, and a downstream guide portion 111c in order from the upstream side in the infusion feeding direction. The pump finger portion 111b faces the distal end portions of the liquid feeding fingers 21... 21 of the liquid feeding portion 20 of the pump mechanism 2 to be described later and the distal end portions of the closing fingers 31 and 31 of the valve portions 30A and 30B.
 チューブ装着ガイド111の上流側ガイド部111aは横方向に湾曲した形状(曲り形状)に形成されており、その先端部が輸液チューブ入口1aとなっている。また、ポンプフィンガ部111bの下流側の下流側ガイド部111cは上下方向に直線状に延びる形状に形成されている。この下流側ガイド部111cの下端部が輸液チューブ出口1bとなっている。下流側ガイド部111cには、ポンプ本体11に装着された輸液チューブT内に混入した気泡を検出する気泡センサ(例えば、超音波センサ)71が配置されている。 The upstream guide portion 111a of the tube mounting guide 111 is formed in a laterally curved shape (curved shape), and the tip portion thereof serves as an infusion tube inlet 1a. Further, the downstream guide portion 111c on the downstream side of the pump finger portion 111b is formed in a shape extending linearly in the vertical direction. A lower end portion of the downstream guide portion 111c serves as an infusion tube outlet 1b. A bubble sensor (for example, an ultrasonic sensor) 71 that detects bubbles mixed in the infusion tube T attached to the pump main body 11 is disposed in the downstream guide portion 111c.
 上流側ガイド部111aの溝幅及び下流側ガイド部111cの溝幅は、それぞれ、薬液バッグに接続される輸液チューブ(例えば、ポリ塩化ビニルやポリブタジエン製)Tの外径(直径)に対応する大きさとなっており、これら上流側ガイド部111a及び下流側ガイド部111cに輸液チューブTを嵌め込むことによって、輸液ポンプ1に輸液チューブTを装着することができる。 The groove width of the upstream guide portion 111a and the groove width of the downstream guide portion 111c are respectively large corresponding to the outer diameter (diameter) of an infusion tube (for example, made of polyvinyl chloride or polybutadiene) T connected to the chemical solution bag. The infusion tube T can be attached to the infusion pump 1 by fitting the infusion tube T into the upstream guide portion 111a and the downstream guide portion 111c.
 上流側ガイド部111aにはチューブクランプ112が設けられている。チューブクランプ112は、輸液ポンプ1へのチューブ装着時に、輸液チューブTを一時的に保持する部材であり、チューブ装着後に扉12を閉じた際に自動的にクランプが解除されるようになっている。なお、チューブクランプ112の近傍には、クランプレバー(図示せず)が設けられており、輸液チューブTの装着の際に、そのクランプレバーを操作することによりチューブクランプ112を開放状態にすることができる。 A tube clamp 112 is provided on the upstream guide portion 111a. The tube clamp 112 is a member that temporarily holds the infusion tube T when the tube is attached to the infusion pump 1, and the clamp is automatically released when the door 12 is closed after the tube is attached. . A clamp lever (not shown) is provided in the vicinity of the tube clamp 112. When the infusion tube T is mounted, the tube clamp 112 can be opened by operating the clamp lever. it can.
 一方、扉12の内面側には、輸液チューブTの下流側の閉鎖を検知する閉塞センサ72が設けられている。また、扉12の内面側には送液部押え板24が設けられている。送液部押え板24は、後述する送液部20の送液フィンガ21・・21に対応する位置に設けられている。送液部押え板24は、扉12を閉じた状態で、最後退位置にある状態の送液フィンガ21の先端面21aに対して、輸液チューブTの外径(直径)に対応する間隔をあけて対向するようになっている(図4、図7等参照)。 On the other hand, on the inner surface side of the door 12, a closing sensor 72 for detecting closing on the downstream side of the infusion tube T is provided. Further, a liquid feeding part pressing plate 24 is provided on the inner surface side of the door 12. The liquid feeding part pressing plate 24 is provided at a position corresponding to the liquid feeding fingers 21... 21 of the liquid feeding part 20 described later. The liquid feeding part presser plate 24 is spaced from the distal end surface 21a of the liquid feeding finger 21 in the last retracted position with the door 12 closed, corresponding to the outer diameter (diameter) of the infusion tube T. (Refer to FIG. 4, FIG. 7, etc.).
 また、扉12の内面側にはバルブ部押え板34,34が設けられている。バルブ部押え板34,34は、それぞれ、後述する上流側のバルブ部30A及び下流側のバルブ部30Bの各閉塞フィンガ31,31に対応する位置に設けられている。これらバルブ部押え板34,34は、扉12を閉じた状態で、最後退位置にある状態の閉塞フィンガ31,31の突部31a,31aの先端に対して、輸液チューブTの外径(直径)に対応する間隔をあけて対向するようになっている(図4、図7等参照)。 Further, valve portion pressing plates 34 are provided on the inner surface side of the door 12. The valve part pressing plates 34 and 34 are provided at positions corresponding to the respective closing fingers 31 and 31 of the upstream valve part 30A and the downstream valve part 30B, which will be described later. These valve part holding plates 34 and 34 are in the state where the door 12 is closed, and the outer diameter (diameter) of the infusion tube T with respect to the tips of the projections 31a and 31a of the closing fingers 31 and 31 in the last retracted position. ) With an interval corresponding to (see FIG. 4, FIG. 7, etc.).
 なお、送液部押え板24及びバルブ部押え板34,34の裏面側(扉12側)にはそれぞれ圧縮コイルばね等の弾性部材(図示せず)が配置されており、輸液チューブTが、送液部20の送液フィンガ21・・21、上流側及び下流側のバルブ部30A,30Bの閉塞フィンガ31,31によって押圧される際に、輸液チューブTが各フィンガ21,31から受ける負荷が大きすぎる場合は、扉12側へ後退するようなっている。これにより輸液チューブTが各フィンガ21,31から受ける過負荷を軽減することができ、輸液チューブTの寿命を延ばすことができる。 An elastic member (not shown) such as a compression coil spring is disposed on the back side (door 12 side) of the liquid feeding part pressing plate 24 and the valve part pressing plates 34, 34, respectively, and the infusion tube T is The load that the infusion tube T receives from each finger 21, 31 when being pressed by the liquid feeding fingers 21, 21 of the liquid feeding part 20 and the closing fingers 31, 31 of the upstream and downstream valve parts 30 A, 30 B. If it is too large, it is retracted to the door 12 side. Thereby, the overload which the infusion tube T receives from each finger 21 and 31 can be reduced, and the lifetime of the infusion tube T can be extended.
 そして、扉12の前面には、各種情報を表示する液晶表示部3の液晶パネル3a、及び、後述するスイッチ類が配列された操作部4が配置されている。さらに、扉12の上部中央に当該輸液ポンプ1の動作状態を知らせるインジケータ5が配置されている。 Further, on the front surface of the door 12, a liquid crystal panel 3a of the liquid crystal display unit 3 for displaying various information and an operation unit 4 in which switches described later are arranged are arranged. Further, an indicator 5 that informs the operating state of the infusion pump 1 is arranged at the upper center of the door 12.
 以上の構成の輸液ポンプ1に輸液チューブTをセットする際には、扉12を開き、薬液バッグに接続された輸液チューブTを、[上流側ガイド部111a]→[ポンプフィンガ部111b]→[下流側ガイド部111c]の順に配置して当該輸液ポンプ1に輸液チューブTを装着する。このようなチューブ装着が終了した後に、扉12を閉め、扉ロック機構14によって扉12を閉鎖状態にロックすることにより、輸液チューブTのセッティングを完了する。なお、この例では、上述したように、扉12を閉塞した状態では、上流側ガイド部111aのチューブクランプ112は開放される。また、輸液完了後などにおいて、扉12を開いたときには、チューブクランプ112によって輸液チューブTが閉塞され、輸液の自由落下であるフリーフローが防止される。 When the infusion tube T is set in the infusion pump 1 having the above configuration, the door 12 is opened, and the infusion tube T connected to the chemical solution bag is connected to the [upstream guide portion 111a] → [pump finger portion 111b] → [ The infusion tube T is attached to the infusion pump 1 in the order of the downstream guide portion 111c]. After such tube mounting is completed, the door 12 is closed, and the door 12 is locked in the closed state by the door lock mechanism 14 to complete the setting of the infusion tube T. In this example, as described above, in a state where the door 12 is closed, the tube clamp 112 of the upstream guide portion 111a is opened. Further, when the door 12 is opened after completion of the infusion, the infusion tube T is closed by the tube clamp 112, and free flow that is a free fall of the infusion is prevented.
 ここで、本実施形態の輸液ポンプ1に適用される輸液セットは、薬液を収容する輸液バッグ、点滴液の流量を目視にて確認するための点滴筒100(図3参照)、これら輸液バッグと点滴筒100とをつなぐ上流側の輸液チューブT、上記点滴筒100に接続される下流側の輸液チューブT、この下流側の輸液チューブTの途中に設けられたローラクランプ、及び、輸液チューブTの先端部に接続される注射針(静脈針)などによって構成されている。このような輸液セットの上記点滴筒100とローラクランプとの間の輸液チューブTがポンプ本体11に上記した要領で装着され、点滴筒100が輸液ポンプ1の輸液送り方向の上流側に配置される(図3参照)。 Here, the infusion set applied to the infusion pump 1 of the present embodiment includes an infusion bag for storing a medicinal solution, an infusion tube 100 (see FIG. 3) for visually confirming the flow rate of the infusion solution, An upstream infusion tube T connecting the infusion tube 100, a downstream infusion tube T connected to the infusion tube 100, a roller clamp provided in the middle of the downstream infusion tube T, and an infusion tube T It is comprised by the injection needle (venous needle) etc. which are connected to the front-end | tip part. The infusion tube T between the infusion tube 100 and the roller clamp of such an infusion set is mounted on the pump body 11 in the manner described above, and the infusion tube 100 is disposed upstream of the infusion pump 1 in the infusion feeding direction. (See FIG. 3).
 そして、本実施形態の輸液ポンプ1は、図3に示すように、上記点滴筒100内を滴下する液滴を検出する滴下センサ8を備えている。滴下センサ8は、赤外線等の光を出力する発光部8aと、その発光部8aの出力光を受光する受光部8bとを備えている。滴下センサ8は、クランプ(図示せず)等によって点滴筒100に着脱自在に装着され、その装着状態で発光部8aの光軸が液滴の滴下位置に一致するとともに、発光部8aと受光部8bとが点滴筒100を挟んで対向するようになっている。そして、その発光部8aからの光を受光部8bが受光した場合(発光部8aからの光が液滴により遮られずに通過した場合)は、受光部8bは例えばOFF信号を出力し、一方、発光部8aからの光が液滴で遮られた場合は受光部8bはON信号を出力するように構成されている。この滴下センサ8(受光部8b)の出力信号は後述する制御部300に入力される。 And the infusion pump 1 of this embodiment is provided with the dripping sensor 8 which detects the droplet dripped inside the said infusion tube 100, as shown in FIG. The dropping sensor 8 includes a light emitting unit 8a that outputs light such as infrared rays and a light receiving unit 8b that receives output light from the light emitting unit 8a. The drip sensor 8 is detachably attached to the drip tube 100 by a clamp (not shown) or the like, and in the attached state, the optical axis of the light emitting unit 8a coincides with the droplet dropping position, and the light emitting unit 8a and the light receiving unit. 8b is opposed to the drip tube 100. When the light receiving unit 8b receives the light from the light emitting unit 8a (when the light from the light emitting unit 8a passes through without being blocked by the droplet), the light receiving unit 8b outputs, for example, an OFF signal, When the light from the light emitting unit 8a is blocked by the droplet, the light receiving unit 8b is configured to output an ON signal. An output signal of the dropping sensor 8 (light receiving unit 8b) is input to the control unit 300 described later.
 -ポンプ機構-
 次に、ポンプ機構2の具体的な構成例について図3~図5を参照して説明する。図4において、各フィンガについては切断しないで表記している。
-Pump mechanism-
Next, a specific configuration example of the pump mechanism 2 will be described with reference to FIGS. In FIG. 4, each finger is shown without being cut.
 ポンプ機構2は、上流側のバルブ部30A、送液部20、下流側のバルブ部30B、送液部押え板24、バルブ部押え板34,34、及び、駆動部200などを備えている。駆動部200は、後述するように、送液部20の3つの送液フィンガ21・・21、上流側のバルブ部30A及び下流側のバルブ部30Bの閉塞フィンガ31,31の各フィンガをそれぞれ個別に進退移動(前進移動または後退移動)する。 The pump mechanism 2 includes an upstream valve unit 30A, a liquid feeding unit 20, a downstream valve unit 30B, a liquid feeding unit pressing plate 24, valve unit pressing plates 34 and 34, a driving unit 200, and the like. As will be described later, the driving unit 200 individually includes the three liquid feeding fingers 21... 21 of the liquid feeding unit 20, the upstream valve unit 30A, and the closing fingers 31 and 31 of the downstream valve unit 30B. Move forward and backward (forward movement or backward movement).
 <送液部>
 送液部20は、3つの送液フィンガ21・・21を備えている。これら3つの送液フィンガ21・・21のうち、輸液送り方向の上流側のものを第1送液フィンガ21、中流部のものを第2送液フィンガ21、下流側のものを第3送液フィンガ21と言う場合もある。なお、本実施形態において、第1送液フィンガ21と、第2送液フィンガ21と、第3送液フィンガ21とは同じ構成であるので、以下の説明では、1つの送液フィンガ21(第1送液フィンガ21)の構成についてのみ、図3~図5を参照して説明する。
<Liquid feeding part>
The liquid feeding unit 20 includes three liquid feeding fingers 21. Of these three liquid feeding fingers 21... 21, the upstream one in the infusion feeding direction is the first liquid feeding finger 21, the middle one is the second liquid feeding finger 21, and the downstream one is the third liquid feeding finger. It may be called a finger 21. In the present embodiment, the first liquid feeding finger 21, the second liquid feeding finger 21, and the third liquid feeding finger 21 have the same configuration. Therefore, in the following description, one liquid feeding finger 21 (first Only the configuration of the single liquid delivery finger 21) will be described with reference to FIGS.
 送液フィンガ21は、断面矩形の部材であって、上記ポンプ本体11の前後方向(ポンプ本体11に装着した輸液チューブTの長手方向と直交するX方向(ポンプ本体11の前面壁110と直交する方向))に沿って配置されている。送液フィンガ21は、ガイド部材50(図4参照)にスライド自在に支持されており、上記ポンプ本体11の前後方向(X方向)に進退移動が可能となっている。ガイド部材50はポンプ本体11に支持固定されている。 The liquid feeding finger 21 is a member having a rectangular cross section, and the front-rear direction of the pump main body 11 (the X direction perpendicular to the longitudinal direction of the infusion tube T attached to the pump main body 11 (perpendicular to the front wall 110 of the pump main body 11). Direction)). The liquid feeding finger 21 is slidably supported by a guide member 50 (see FIG. 4), and can move forward and backward in the front-rear direction (X direction) of the pump body 11. The guide member 50 is supported and fixed to the pump body 11.
 送液フィンガ21は、後述する駆動部200によって進退移動(前進移動または後退移動)され、送液フィンガ21が最後退位置にあるときには、図4及び図7(A)等に示すように、送液フィンガ21の先端面21aが上記ポンプ本体11に装着された輸液チューブT(真円状態)の外周面に接触する位置(輸液チューブTの外周面に対応する位置)に配置される。また、この状態(最後退位置にある状態)から、送液フィンガ21が前進移動すると、その前進移動過程で輸液チューブTが押圧される。ここで、この例の輸液ポンプ1は半閉塞方式であるので、送液フィンガ21が最前進位置にある状態のときに、図8に示すように、輸液チューブTが完全に閉塞されないように駆動部200による送液フィンガ21の進退移動のストロークが設定されている。 The liquid feeding finger 21 is moved forward and backward (forward movement or backward movement) by a driving unit 200 described later, and when the liquid feeding finger 21 is in the last retracted position, as shown in FIGS. 4 and 7A, etc. The distal end surface 21a of the liquid finger 21 is disposed at a position (a position corresponding to the outer peripheral surface of the infusion tube T) in contact with the outer peripheral surface of the infusion tube T (circular state) attached to the pump body 11. Further, when the liquid feeding finger 21 moves forward from this state (the state at the last retracted position), the infusion tube T is pressed during the forward movement process. Here, since the infusion pump 1 of this example is a semi-occlusion type, the infusion tube T is driven so as not to be completely occluded as shown in FIG. 8 when the infusion finger 21 is in the most advanced position. The stroke of the forward / backward movement of the liquid feeding finger 21 by the part 200 is set.
 <バルブ部>
 次に、上流側のバルブ部30A及び下流側のバルブ部30Bについて図3~図5を参照して説明する。これら上流側のバルブ部30Aと下流側バルブ部30Bとは同じ構成であるので、以下の説明では、一方のバルブ部(上流側のバルブ部30A)についてのみ説明する。
<Valve part>
Next, the upstream valve portion 30A and the downstream valve portion 30B will be described with reference to FIGS. Since the upstream side valve unit 30A and the downstream side valve unit 30B have the same configuration, only one valve unit (upstream side valve unit 30A) will be described in the following description.
 バルブ部30A(30B)は、閉塞フィンガ31を備えている。閉塞フィンガ31は、断面矩形の部材であって、上記した送液フィンガ21と同様に、ポンプ本体11の前後方向(ポンプ本体11に装着した輸液チューブTの長手方向と直交するX方向(ポンプ本体11の前面壁110と直交する方向))に沿って配置されている。また、閉塞フィンガ31の先端部分には突部31aが設けられている。閉塞フィンガ31は、ガイド部材50(送液部20の送液フィンガ21と同じガイド部材50)にスライド自在に支持されており、上記ポンプ本体11の前後方向(X方向)に進退移動が可能となっている。 The valve unit 30A (30B) includes a closing finger 31. The closing finger 31 is a member having a rectangular cross section, and is similar to the liquid feeding finger 21 described above in the front-rear direction of the pump body 11 (the X direction (pump body perpendicular to the longitudinal direction of the infusion tube T attached to the pump body 11). 11 in the direction perpendicular to the front wall 110)). Further, a protruding portion 31 a is provided at the distal end portion of the closing finger 31. The closing finger 31 is slidably supported by a guide member 50 (the same guide member 50 as the liquid feeding finger 21 of the liquid feeding section 20), and can move forward and backward in the front-rear direction (X direction) of the pump body 11. It has become.
 閉塞フィンガ31は、後述する駆動部200によって進退移動(前進移動または後退移動)され、閉塞フィンガ31が最後退位置にあるときには、図4及び図7等に示すように、閉塞フィンガ31の突部31aの先端が上記ポンプ本体11に装着された輸液チューブT(真円状態)の外周面に接触する位置(輸液チューブTの外周面に対応する位置)に配置される。また、この状態(最後退位置にある状態)から、閉塞フィンガ31が前進移動すると、その前進移動過程で輸液チューブTが押圧される。ここで、バルブ部30A(30B)においては輸液チューブTを完全圧閉するので、閉塞フィンガ31が最前進位置にある状態のときに、図7(B)等に示すように輸液チューブTが完全に閉塞されるように駆動部200による閉塞フィンガ31の進退移動のストロークが設定されている。 The closing finger 31 is moved forward and backward (forward movement or backward movement) by the driving unit 200 described later, and when the closing finger 31 is in the last retracted position, as shown in FIG. 4 and FIG. The tip of 31a is arrange | positioned in the position (position corresponding to the outer peripheral surface of the infusion tube T) which contacts the outer peripheral surface of the infusion tube T (perfect circle state) with which the said pump main body 11 was mounted | worn. Further, when the closing finger 31 moves forward from this state (the state at the last retracted position), the infusion tube T is pressed during the forward movement process. Here, since the infusion tube T is completely closed in the valve portion 30A (30B), when the closing finger 31 is in the most advanced position, the infusion tube T is completely as shown in FIG. The stroke of the forward / backward movement of the closing finger 31 by the drive unit 200 is set so as to be closed.
 <駆動部>
 駆動部200は、図5に示すように、送液部20の送液フィンガ21・・21を個別に進退駆動するためのカム221a,221b,221c、上流側及び下流側のバルブ部30A,30Bの閉塞フィンガ31,31をそれぞれ個別に進退駆動するためのカム231a,231b、カム軸201、及び、ステッピングモータ202などを備えており、各カム221a,221b,221c,231a,231bはカム軸201に一体回転可能に取り付けられている。カム軸201は、ポンプ本体11の上下方向(フィンガ21・・21,31,31の配列方向)に沿って配置されている。
<Driver>
As shown in FIG. 5, the drive unit 200 includes cams 221a, 221b, and 221c for individually advancing and retracting the liquid feeding fingers 21 and 21 of the liquid feeding unit 20, and upstream and downstream valve units 30A and 30B. Are provided with cams 231a, 231b, a cam shaft 201, a stepping motor 202, and the like for individually driving the closing fingers 31, 31 respectively, and the cams 221a, 221b, 221c, 231a, 231b are cam shafts 201, respectively. Is attached to be integrally rotatable. The cam shaft 201 is disposed along the vertical direction of the pump body 11 (the arrangement direction of the fingers 21... 21, 31, 31).
 カム軸201の上端部にはタイミングプーリ(従動プーリ)203が一体回転可能に取り付けられている。また、ステッピングモータ202の回転軸202aにはタイミングプーリ(駆動プーリ)204が一体回転可能に設けられている。これらカム軸201のタイミングプーリ203とステッピングモータ202側のタイミングプーリ204との間にタイミングベルト205が巻き掛けられており、ステッピングモータ202の駆動によりカム軸201が回転するようになっている。 A timing pulley (driven pulley) 203 is attached to the upper end portion of the cam shaft 201 so as to be integrally rotatable. Further, a timing pulley (drive pulley) 204 is provided on the rotating shaft 202a of the stepping motor 202 so as to be integrally rotatable. A timing belt 205 is wound between the timing pulley 203 of the cam shaft 201 and the timing pulley 204 on the stepping motor 202 side, and the cam shaft 201 is rotated by driving of the stepping motor 202.
 そして、本実施形態では、上記したステッピングモータ202の駆動(カム軸201の回転)により、送液部20の送液フィンガ21・・21、上流側及び下流側のバルブ部30A,30Bの閉塞フィンガ31,31の各フィンガが、それぞれ、図7~図9に示すような動作で進退駆動するように、カム221a,221b,221c,231a,231bのカム形状が設定されている。 In the present embodiment, the above-described driving of the stepping motor 202 (rotation of the cam shaft 201) causes the liquid feeding fingers 21 and 21 of the liquid feeding section 20 and the closing fingers of the upstream and downstream valve sections 30A and 30B. The cam shapes of the cams 221a, 221b, 221c, 231a, and 231b are set so that the fingers 31 and 31 are driven forward and backward by the operations shown in FIGS.
 ここで、本実施形態では、カム軸201に回転力を与える電動モータとしてステッピングモータ202を用いているので、送液の1サイクル(図10参照)中にカム軸201の回転速度を任意に変更することが可能である。すなわち、ステッピングモータ202は、周知のように、モータドライバに与える駆動パルスを制御(例えばデューティ制御)することにより、回転軸202aの回転速度を制御できるようになっている。したがって、ステッピングモータ202に与える駆動パルスを送液の1サイクル中に変更(駆動パルスのデューティ比を変更)することにより、その1サイクル内においてカム軸201の回転速度を任意に変更することが可能である。これによって、例えば図10に示すように、1サイクルの期間(時間)は同じであっても、送液の吐出期間と吸込期間との比率を可変に設定することができる(例えば、図10(A)に対して図10(B)の吸込期間を短くすることができる)。 Here, in this embodiment, since the stepping motor 202 is used as an electric motor that applies a rotational force to the camshaft 201, the rotational speed of the camshaft 201 is arbitrarily changed during one cycle of liquid feeding (see FIG. 10). Is possible. That is, as is well known, the stepping motor 202 can control the rotation speed of the rotating shaft 202a by controlling the driving pulse (for example, duty control) applied to the motor driver. Therefore, by changing the drive pulse given to the stepping motor 202 during one cycle of liquid feeding (changing the duty ratio of the drive pulse), the rotational speed of the camshaft 201 can be arbitrarily changed within that cycle. It is. Accordingly, for example, as shown in FIG. 10, even if the period (time) of one cycle is the same, the ratio between the discharge period of liquid feeding and the suction period can be variably set (for example, FIG. The suction period of FIG. 10 (B) can be shortened with respect to A).
 以上のステッピングモータ202の駆動は制御部300によって制御される。これらステッピングモータ202及び制御部300等には、輸液ポンプ1に内蔵の電池または商用電源からの電力が供給されるようになっている。 The driving of the above stepping motor 202 is controlled by the control unit 300. The stepping motor 202, the control unit 300, and the like are supplied with electric power from a battery built in the infusion pump 1 or a commercial power source.
 なお、駆動部200としては、電動モータと回転-並進機構(例えばラックアンドピニオン)とを組み合わせた機構を適用してもよいし、ソレノイドを駆動源とするものを適用してもよい。 As the drive unit 200, a mechanism in which an electric motor and a rotation-translation mechanism (for example, rack and pinion) are combined may be applied, or a drive using a solenoid as a drive source may be applied.
 -液晶表示部・操作部-
 液晶表示部3は、液晶パネル3a及びその駆動ドライバ(図示せず)などによって構成されており、その液晶パネル3aが扉12の前面に配置されている。液晶パネル3aの画面上には、積算量[mL]、輸液の予定量[mL]、流量[mL/h]などの動作情報、警報情報(メッセージ等)、及び、ユーザが各種設定を行うためのユーザ設定画面などが表示される。
-Liquid crystal display and operation unit-
The liquid crystal display unit 3 includes a liquid crystal panel 3 a and a drive driver (not shown), and the liquid crystal panel 3 a is disposed on the front surface of the door 12. On the screen of the liquid crystal panel 3a, operation information such as integrated amount [mL], scheduled infusion volume [mL], flow rate [mL / h], alarm information (message, etc.), and various settings by the user The user setting screen is displayed.
 操作部4は、図2に示すように、輸液を開始する開始スイッチ41、輸液動作や警報の停止を行う停止スイッチ42、輸液準備の際に使用する早送りスイッチ43、表示切替スイッチ44、数値設定アップスイッチ45、数値設定ダウンスイッチ46、積算量リセットスイッチ47、及び、点滴針サイズ選択スイッチ48などを備えている。 As shown in FIG. 2, the operation unit 4 includes a start switch 41 for starting infusion, a stop switch 42 for stopping an infusion operation and an alarm, a fast-forward switch 43 used when preparing for infusion, a display changeover switch 44, and a numerical value setting. An up switch 45, a numerical value setting down switch 46, an integrated amount reset switch 47, an infusion needle size selection switch 48, and the like are provided.
 表示切替スイッチ44は、数値等を入力する項目(例えば、流量、予定量、予定時間、高流量モードなど)への表示の切り替えを行うためのスイッチである。 The display changeover switch 44 is a switch for switching the display to items (for example, flow rate, scheduled amount, scheduled time, high flow rate mode, etc.) for inputting numerical values and the like.
 数値設定アップスイッチ45、数値設定ダウンスイッチ46は、流量、予定量、予定時間などの数値を増加または減少させるスイッチであって、それぞれ、右側の1桁目の数値設定用スイッチ、中央の2桁目の数値設定用スイッチ、及び、左側の3桁目の数値設定用スイッチの合計3つのスイッチで構成されている。 The numerical value setting up switch 45 and the numerical value setting down switch 46 are switches for increasing or decreasing numerical values such as a flow rate, a predetermined amount, and a scheduled time. It consists of a total of three switches: a numerical value setting switch for the eye and a numerical value setting switch for the third digit on the left side.
 -制御部-
 次に、制御部300について説明する。
-Control unit-
Next, the control unit 300 will be described.
 制御部300は、マイクロコンピュータ等を主体として構成されており、CPU(Central Processing Unit)、ROM(Read Only Memory)、RAM(Random Access Memory)、不揮発性RAM、I/Oインターフェース、及び、これらの機能部を互いに接続するバスラインなど備えている。 The control unit 300 is composed mainly of a microcomputer or the like, and includes a CPU (Central Processing Unit), a ROM (Read Only Memory), a RAM (Random Access Memory), a nonvolatile RAM, an I / O interface, and the like. A bus line for connecting the functional units to each other is provided.
 制御部300には、図6に示すように、操作部4、気泡センサ71、閉塞センサ72、電源スイッチ7(例えばポンプ本体11の裏面に配置)などが接続されており、また、上記した滴下センサ8が接続される。それら操作部4のスイッチ類やセンサからの信号が制御部300に入力される。また、制御部300には、液晶表示部3、インジケータ5、音発生部6、及び、上記ポンプ機構2の駆動用のステッピングモータ202などが接続されている。 As shown in FIG. 6, the control unit 300 is connected to the operation unit 4, the bubble sensor 71, the blockage sensor 72, the power switch 7 (for example, disposed on the back surface of the pump main body 11), and the like. A sensor 8 is connected. Signals from switches and sensors of the operation unit 4 are input to the control unit 300. The control unit 300 is connected to the liquid crystal display unit 3, the indicator 5, the sound generation unit 6, the stepping motor 202 for driving the pump mechanism 2, and the like.
 そして、制御部300は、操作部4のスイッチ類の操作にて設定された輸液の流量の設定値(設定流量)に応じて、ポンプ機構2のステッピングモータ202の回転速度を制御することにより流量を可変に調整する。この例では、流量を1mL/h~1200mL/hの範囲内において、[1mL/h]単位で設定することができる。この流量制御については後述する。また、制御部300は、滴下センサ8の出力に基づいて流量を算出する。この流量算出処理についても後述する。 Then, the control unit 300 controls the rotational speed of the stepping motor 202 of the pump mechanism 2 according to the set value (set flow rate) of the infusion flow set by operating the switches of the operation unit 4. Adjust the variable. In this example, the flow rate can be set in units of [1 mL / h] within the range of 1 mL / h to 1200 mL / h. This flow control will be described later. Further, the control unit 300 calculates the flow rate based on the output of the dropping sensor 8. This flow rate calculation process will also be described later.
 -ポンプ機構の動作説明-
 次に、ポンプ機構2の動作について図7~図9を参照して説明する。なお、図7~図9において、各フィンガについては切断しないで表記している。
-Explanation of operation of pump mechanism-
Next, the operation of the pump mechanism 2 will be described with reference to FIGS. 7 to 9, each finger is shown without being cut.
 [S1]まず、図7(A)は、輸液チューブTをポンプ本体11に装着し、扉12を閉じた状態(初期状態)を示す図である。この初期状態では、下流側のバルブ部30Bの閉塞フィンガ31のみが最前進位置にあり、その閉塞フィンガ31の突部31aにて輸液チューブTが完全に閉塞されている。 [S1] First, FIG. 7A is a diagram showing a state (initial state) in which the infusion tube T is mounted on the pump body 11 and the door 12 is closed. In this initial state, only the closing finger 31 of the downstream valve portion 30B is at the most advanced position, and the infusion tube T is completely closed by the protrusion 31a of the closing finger 31.
 [S2]図7(A)の状態から、上流側のバルブ部30Aの閉塞フィンガ31が前進移動し、その閉塞フィンガ31が最前進位置にまで移動した状態で、送液部20の上流側の輸液チューブTが完全に閉塞される(図7(B))。 [S2] From the state of FIG. 7A, the closing finger 31 of the upstream valve portion 30A moves forward, and the closing finger 31 moves to the most advanced position. The infusion tube T is completely occluded (FIG. 7B).
 [S3]図7(B)の状態から、下流側のバルブ部30Bの閉塞フィンガ31が最前進位置から後退移動し、その閉塞フィンガ31が最後退位置にまで移動した状態で、送液部20の上流側の輸液チューブTが完全に開放される(図7(C))。 [S3] From the state of FIG. 7B, the closing finger 31 of the downstream valve portion 30B moves backward from the most advanced position, and the closing finger 31 moves to the last retracted position. The infusion tube T on the upstream side is completely opened (FIG. 7C).
 [S4]図7(C)に示す状態から、送液部20の第1送液フィンガ21が前進して輸液チューブTを押圧する(図8(A))。この第1送液フィンガ21による輸液チューブTの押圧によって、輸液チューブT内の輸液が下流側に送り出される。このような第1送液フィンガ21の前進移動に続いて第2送液フィンガ21と第3送液フィンガ21とが順次前進移動し(図8(B)~図8(C))、その各送液フィンガ21,21による輸液チューブTの押圧によって輸液チューブT内の輸液が更に下流側に送り出される。このように、この例では、3つの送液フィンガ21・・21の蠕動運動によって輸液チューブT内の輸液が送液される。ここで、この例の輸液ポンプ1は半閉塞方式であるので、送液部20の各送液フィンガ21が最前進位置に到達しても、図8(A)~図8(C)に示すように、輸液チューブTは完全におしつぶされない。 [S4] From the state shown in FIG. 7C, the first liquid delivery finger 21 of the liquid delivery section 20 moves forward and presses the infusion tube T (FIG. 8A). When the infusion tube T is pressed by the first infusion finger 21, the infusion in the infusion tube T is sent downstream. Following the forward movement of the first liquid feeding finger 21 as described above, the second liquid feeding finger 21 and the third liquid feeding finger 21 sequentially move forward (FIGS. 8B to 8C). When the infusion tube T is pressed by the infusion fingers 21 and 21, the infusion in the infusion tube T is further sent to the downstream side. Thus, in this example, the infusion in the infusion tube T is fed by the peristaltic motion of the three liquid feeding fingers 21. Here, since the infusion pump 1 of this example is a semi-occlusion type, even if each of the liquid feeding fingers 21 of the liquid feeding unit 20 reaches the most advanced position, it is shown in FIGS. 8 (A) to 8 (C). As such, the infusion tube T is not completely crushed.
 [S5]図8(C)の状態から、下流側のバルブ部30Bの閉塞フィンガ31が前進移動し、その閉塞フィンガ31が最前進位置に移動した状態で送液部20の下流側の輸液チューブTが完全に閉塞される(図9)。 [S5] From the state of FIG. 8C, the closing finger 31 of the downstream valve portion 30B moves forward and the closing finger 31 moves to the most advanced position. T is completely occluded (FIG. 9).
 [S6]図9の状態から、上流側のバルブ部30Aの閉塞フィンガ31、及び、送液部20の3つの送液フィンガ21・・21が最後退位置に移動し、これら閉塞フィンガ31及び送液フィンガ21・・21の最後退位置への移動過程で輸液が吸引されて、図7(A)に示す初期状態に戻る。この図9の状態(吸込開始)から図7(B)の状態(吸込停止)までの期間が送液の吸込期間であり、図7(C)の状態(吐出開始)から図8(A)~図8(C)の動作を経て図9の状態(吐出停止)に至るまでの期間が送液の吐出期間である。 [S6] From the state shown in FIG. 9, the closing finger 31 of the upstream valve section 30A and the three liquid feeding fingers 21... 21 of the liquid feeding section 20 are moved to the last retracted position. The infusion solution is sucked in the process of moving the liquid fingers 21... 21 to the last retracted position, and the initial state shown in FIG. The period from the state of FIG. 9 (suction start) to the state of FIG. 7B (suction stop) is the liquid feeding suction period, and from the state of FIG. 7C (discharge start) to FIG. 8A. The period from the operation of FIG. 8C to the state of FIG. 9 (discharge stop) is the liquid discharge period.
 以上の動作で送液の1サイクルが完了し、このようなサイクルを順次繰り返していくことにより、輸液チューブT内の輸液を下流側に連続して送り出すことができる。そして、その送液流量は、上記送液サイクルの周期を制御することによって可変に調整することができる。また、上述したように、ステッピングモータ202に与える駆動パルスを送液の1サイクル内で変更することにより、その1サイクル中において送液の吐出期間と吸込期間とを可変に設定することができる(図10参照)。 With the above operation, one cycle of liquid feeding is completed, and by sequentially repeating such a cycle, the infusion in the infusion tube T can be continuously sent out downstream. The liquid flow rate can be variably adjusted by controlling the cycle of the liquid supply cycle. Further, as described above, by changing the drive pulse applied to the stepping motor 202 within one cycle of liquid feeding, the liquid ejection period and the suction period can be variably set during that cycle (see FIG. (See FIG. 10).
 -特徴部分-
 次に、本実施形態の特徴部分について説明する。
-Features-
Next, the characteristic part of this embodiment is demonstrated.
 まず、輸液セットの点滴筒としては、1mL当たりの滴下数が20滴の点滴筒と、1mL当たりの滴下数が60滴の点滴筒とがあり、本実施形態では20滴の点滴筒100を有する輸液バッグを用いる場合について説明する。 First, as an infusion tube of an infusion set, there are an infusion tube with 20 drops per mL and an infusion tube with 60 drops per mL. In this embodiment, the infusion tube 100 has 20 infusion tubes 100. A case where an infusion bag is used will be described.
 また、本実施形態の輸液ポンプ1では、上記した送液の1サイクルで0.1cc(0.1mL)の送液を行えるように設定されており、その1サイクルの送液で上記20滴の点滴筒100から2滴の液滴が滴下するように設定されている(0.05cc/1滴)。 Moreover, in the infusion pump 1 of this embodiment, it is set so that 0.1 cc (0.1 mL) of liquid can be delivered in one cycle of the above-described liquid feeding, and 20 drops of the above-mentioned 20 drops in one cycle of liquid feeding. It is set so that two droplets are dropped from the drip tube 100 (0.05 cc / 1 droplet).
 このような設定の輸液ポンプ1(半閉塞方式の輸液ポンプ)にあっては、送液の流量が例えば600mL/hを超える高流量になると、送液の1サイクルにおいて点滴筒100内を滴下する液滴同士がつながってしまい、本来2滴の滴下が1滴の滴下となる可能性が高くなる。また、流量によっては液滴がつながる状態と液滴がつながらない状態とが混在する可能性もある。そして、このような液滴のつながりが発生すると、滴下センサ8の出力に基づいて算出される流量に誤差が生じる場合がある。すなわち、送液の1サイクルにおいて点滴筒100内を滴下する液滴がつながってしまうと、上記した点滴筒100内を滴下する液滴の滴下数の計数値や、液滴の滴下時間間隔に誤差が含まれるため、流量を正確に算出することができない。また、看護師等のユーザは点滴筒内を滴下する液滴を見て流量を確認しているが、上述の如く液滴のつながりが発生すると、流量を目視にて確認することが難しくなる。 In the infusion pump 1 (semi-enclosed infusion pump) having such a setting, when the flow rate of the liquid feed reaches a high flow rate exceeding 600 mL / h, for example, the inside of the drip tube 100 is dropped in one cycle of the liquid feed. The droplets are connected to each other, and there is a high possibility that a drop of 2 drops will be a drop of 1 drop. Also, depending on the flow rate, there may be a mixture of a state in which droplets are connected and a state in which droplets are not connected. When such a connection of droplets occurs, an error may occur in the flow rate calculated based on the output of the dropping sensor 8. That is, if droplets dropping in the drip tube 100 are connected in one cycle of liquid feeding, there is an error in the count value of the number of droplets dropped in the drip tube 100 and the droplet dropping time interval. Therefore, the flow rate cannot be calculated accurately. In addition, a user such as a nurse checks the flow rate by looking at the liquid droplets dropping in the drip tube. However, when the liquid droplets are connected as described above, it is difficult to visually confirm the flow rate.
 このような点を考慮して、従来では、点滴筒100内を滴下する液滴がつながる可能性がない流量であって、滴下センサ8の出力に基づく流量算出の精度を保証できる流量(例えば600mL/h)以下の流量域を通常の使用範囲(以下、通常使用流量域ともいう)としている。しかしながら、輸液ポンプの使用に際しては、そのような通常使用流量域を超える流量での送液が要求される場合もある。 Considering such points, conventionally, the flow rate is such that there is no possibility that a droplet dropped in the drip tube 100 is connected, and the flow rate can guarantee the accuracy of the flow rate calculation based on the output of the drop sensor 8 (for example, 600 mL). / H) The following flow range is defined as a normal use range (hereinafter also referred to as a normal use flow range). However, when using an infusion pump, there are cases where liquid feeding at a flow rate exceeding such a normal use flow rate range is required.
 そこで、本実施形態では、ポンプ機構2の駆動モードとして、通常使用流量域を超える高流量域(601mL/h以上の高流量域)において送液を行う高流量モードの設定が可能な構成とするとともに、その高流量での輸液を実現するにあたり妨げとなるような問題点を解消することで、高流量での輸液が必要である場合には、それに対応できるようにしている。その高流量モードでの制御・処理については後述する。 Therefore, in the present embodiment, as a drive mode of the pump mechanism 2, a high flow rate mode in which liquid feeding is performed in a high flow rate region (a high flow rate region of 601 mL / h or more) exceeding the normal use flow rate region can be set. At the same time, by solving the problems that hinder the realization of the infusion at the high flow rate, it is possible to cope with the case where the infusion at the high flow rate is necessary. Control and processing in the high flow rate mode will be described later.
 以下、制御部300が実行する制御・処理などについて以下に説明する。 Hereinafter, control and processing executed by the control unit 300 will be described below.
 <通常使用流量域での制御・処理>
 まず、600mL/h以下の通常使用流量域での制御・処理について説明する。
<Control and processing in the normal flow rate range>
First, control and processing in a normal use flow rate range of 600 mL / h or less will be described.
 (a1)通常使用流量域では、操作部4のスイッチ類の操作により1mL/hから600mL/hまでの流量を設定することができる。制御部300は、その操作部4の操作にて設定された設定流量に応じた駆動パルス(設定流量に応じたデューティ比の駆動パルス)をポンプ機構2のステッピングモータ202に供給して、ステッピングモータ202の回転速度を制御することにより、ポンプ機構2の送液流量を上記設定流量に制御する。 (A1) In the normal use flow rate range, the flow rate from 1 mL / h to 600 mL / h can be set by operating the switches of the operation unit 4. The control unit 300 supplies a drive pulse corresponding to the set flow rate set by the operation of the operation unit 4 (a drive pulse having a duty ratio corresponding to the set flow rate) to the stepping motor 202 of the pump mechanism 2, and the stepping motor By controlling the rotational speed of 202, the liquid feed flow rate of the pump mechanism 2 is controlled to the set flow rate.
 (a2)通常使用流量域でポンプ機構2が停止状態であるときに、液滴の滴下を検出した場合(滴下センサ8のからのON信号(液滴検出信号)を制御部300が受信した場合)、制御部300は、フリーフローの発生を示すメッセージ等を液晶表示部3の液晶パネル3aの画面上に表示したり、また、音発生部6を駆動してブザー音を発生したりして、フリーフローが発生していることを看護師等のユーザに知らせる。 (A2) When the drop of droplets is detected when the pump mechanism 2 is stopped in the normal use flow rate range (when the control unit 300 receives an ON signal (droplet detection signal) from the drop sensor 8) ), The control unit 300 displays a message indicating the occurrence of free flow on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3, or drives the sound generation unit 6 to generate a buzzer sound. Informing a user such as a nurse that a free flow has occurred.
 (a3)通常使用流量域である場合には、制御部300は滴下センサ8の出力に基づいて流量を算出して流量異常を判定する。具体的には、制御部300は、滴下センサ8の出力信号に基づいて、点滴筒100内を滴下する液滴の単位時間当たり(例えば1分当たり)の滴下数を計数(ON信号をカウント)し、その滴数計数値から送液の流量(mL/h)を算出(換算)する。例えば、点滴筒100として1mL当たりの滴下数が20滴の点滴筒を使用する場合、1滴当たりの液滴の容積は0.05mLであるので、1分当たりの滴下数(滴数計数値)がna滴である場合、その滴数計数値naを用いて流量(mL/h)を、演算式[流量=0.05(mL/1滴)×na(滴/min)×60]から算出する。 (A3) When the flow rate is in the normal use flow rate range, the control unit 300 determines the flow rate abnormality by calculating the flow rate based on the output of the dropping sensor 8. Specifically, the control unit 300 counts the number of droplets dropped per unit time (for example, per minute) of the droplets dropped in the drip tube 100 based on the output signal of the drop sensor 8 (counts ON signal). The liquid flow rate (mL / h) is calculated (converted) from the droplet count value. For example, when a drip tube with 20 drops per mL is used as the drip tube 100, the volume of the droplet per drop is 0.05 mL, so the number of drops per minute (drop count value) Is a na drop, the flow rate (mL / h) is calculated from the drop count value na from the arithmetic expression [flow rate = 0.05 (mL / 1 drop) × na (drop / min) × 60]. To do.
 そして、制御部300は、通常使用流量域での輸液中において、上記した滴下センサ8の出力に基づく流量の算出処理を逐次実行し、その算出流量(実際の流量)と上記設定流量(1mL/hから600mL/hまでの設定流量)とを用い、設定流量と算出流量との差(流量差)を算出する。その算出した流量差が所定の許容範囲(流量が正常とみなせる範囲)内である場合は流量が正常であると判定する。一方、上記流量差が許容範囲から外れている場合は流量異常であると判定する。流量異常と判定した場合には、制御部300は、その流量異常を示すメッセージ等を液晶表示部3の液晶パネル3aの画面上に表示したり、また、音発生部6を駆動してブザー音を発生したりして、流量異常であることを看護師等のユーザに知らせる。 Then, the controller 300 sequentially executes a flow rate calculation process based on the output of the drip sensor 8 during the infusion in the normal use flow rate region, and calculates the calculated flow rate (actual flow rate) and the set flow rate (1 mL / The difference between the set flow rate and the calculated flow rate (flow rate difference) is calculated using the set flow rate from h to 600 mL / h. When the calculated flow rate difference is within a predetermined allowable range (a range in which the flow rate can be regarded as normal), it is determined that the flow rate is normal. On the other hand, when the flow rate difference is out of the allowable range, it is determined that the flow rate is abnormal. When it is determined that the flow rate is abnormal, the control unit 300 displays a message indicating the abnormal flow rate on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3 or drives the sound generation unit 6 to generate a buzzer sound. To inform a user such as a nurse that the flow rate is abnormal.
 (a4)通常使用流量域でポンプ機構2が駆動状態であるときに、液滴の滴下を一定期間検出しない場合(滴下センサ8からON信号(液滴検出信号)が一定期間出力されない場合)、制御部300は、空液状態であることを示すメッセージ等を液晶表示部3の液晶パネル3aの画面上に表示し、また、音発生部6を駆動してブザー音を発生して、空液の状態であることを看護師等のユーザに知らせる。なお、上記空液を判定する一定期間(時間)については、実験・計算などにより経験的に求めた値を設定する。 (A4) When the pump mechanism 2 is in a driving state in the normal use flow rate range, when droplet dropping is not detected for a certain period (when the ON signal (droplet detection signal) is not output from the dropping sensor 8 for a certain period), The control unit 300 displays a message indicating that the liquid is in the liquid state on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3, and also drives the sound generation unit 6 to generate a buzzer sound. The user such as a nurse is informed that this is the state. In addition, about the fixed period (time) which determines the said air liquid, the value calculated | required empirically by experiment, calculation, etc. is set.
 ここで、通常使用流量域において送液を行う場合、上記した1サイクル中のカム軸201の回転速度(ステッピングモータ202の回転速度)の変更制御により、1サイクル中の吸込期間と吐出期間との比率を設定する。具体的に、吸込期間については、1サイクルで点滴筒100から2滴の液滴が滴下するのに必要な時間を確保できるような長さの期間を設定する。また、吐出期間については、そのような吸込期間を確保したうえで可能な限り長い期間を設定する。このようにして吐出期間を長く設定すると、吐出期間における送液フィンガ21・・21及び閉塞フィンガ31,31の前進速度を遅くすることが可能となり、脈動等を抑制して安定した送液を行うことができる。 Here, when liquid feeding is performed in the normal use flow rate range, the suction period and the discharge period in one cycle are controlled by changing the rotation speed of the camshaft 201 (rotation speed of the stepping motor 202) in the above-described one cycle. Set the ratio. Specifically, the suction period is set to a length that can secure the time required for two droplets to drop from the drip tube 100 in one cycle. The discharge period is set as long as possible after securing such a suction period. When the discharge period is set to be long in this way, the forward speed of the liquid feeding fingers 21... 21 and the closing fingers 31 and 31 during the discharge period can be slowed, and stable liquid feeding is performed while suppressing pulsation and the like. be able to.
 <高流量モード設定処理>
 本実施形態では、上記したように、通常は600mL/h以下の通常使用流量域において送液を行うようになっているが、高流量での輸液が必要である場合に高流量モードを設定することができる。
<High flow mode setting process>
In this embodiment, as described above, liquid feeding is normally performed in the normal use flow rate range of 600 mL / h or less, but the high flow rate mode is set when infusion at a high flow rate is necessary. be able to.
 その高流量モードの設定は、例えば、操作部4の表示切替スイッチ44を操作して、液晶表示部3の液晶パネル3aの画面上に“高流量モード設定”の項を表示し、この表示状態で開始スイッチ41を押すという操作により、高流量モードを設定することができる。なお、通常使用流量の送液モードに戻す場合、表示切替スイッチ44の操作により、液晶表示部3の液晶パネル3aの画面上に“高流量モード解除”の項を表示し、この表示状態で開始スイッチ41を押すことにより、高流量モードを解除して通常使用流量の送液モードに戻すことができる。 The high flow rate mode is set by, for example, operating the display changeover switch 44 of the operation unit 4 to display the item “high flow rate mode setting” on the screen of the liquid crystal panel 3 a of the liquid crystal display unit 3. By pressing the start switch 41, the high flow rate mode can be set. When returning to the normal use flow rate liquid delivery mode, the display changeover switch 44 is operated to display the item “high flow rate mode release” on the liquid crystal panel 3a of the liquid crystal display unit 3 and start in this display state. By pressing the switch 41, it is possible to cancel the high flow rate mode and return to the liquid supply mode at the normal use flow rate.
 <高流量モードでの制御・処理>
 上記した操作により、高流量モードが設定されている場合、制御部300は以下の制御・処理を行う。
<Control and processing in high flow mode>
When the high flow rate mode is set by the above operation, the control unit 300 performs the following control and processing.
 (b1)高流量モードが設定されている場合、操作部4のスイッチ類の操作により、601mL/hから1200mL/hまでの流量を設定することが可能である。制御部300は、その操作部4の操作により設定された設定流量に応じた駆動パルス(設定流量に応じたデューティ比の駆動パルス)をポンプ機構2のステッピングモータ202に供給して、ステッピングモータ202の回転速度を制御することによりポンプ機構2の送液流量を設定流量に制御する。 (B1) When the high flow rate mode is set, the flow rate from 601 mL / h to 1200 mL / h can be set by operating the switches of the operation unit 4. The control unit 300 supplies a drive pulse corresponding to the set flow rate set by the operation of the operation unit 4 (a drive pulse having a duty ratio corresponding to the set flow rate) to the stepping motor 202 of the pump mechanism 2, and the stepping motor 202. By controlling the rotation speed of the pump mechanism 2, the liquid feed flow rate of the pump mechanism 2 is controlled to the set flow rate.
 (b2)高流量モード設定時でポンプ機構2が停止状態であるときに、液滴の滴下を検出した場合(滴下センサ8のからのON信号(液滴検出信号)を制御部300が受信した場合)、制御部300は、フリーフローの発生を示すメッセージ等を液晶表示部3の液晶パネル3aの画面上に表示したり、また、音発生部6を駆動してブザー音を発生したりして、フリーフローが発生していることを看護師等のユーザに知らせる。 (B2) The controller 300 receives an ON signal (droplet detection signal) from the drop sensor 8 when the drop of the droplet is detected when the pump mechanism 2 is in a stopped state when the high flow rate mode is set. The control unit 300 displays a message indicating the occurrence of free flow on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3 or drives the sound generation unit 6 to generate a buzzer sound. To inform a user such as a nurse that a free flow has occurred.
 (b3)高流量モードが設定されている場合、送液の1サイクル中の吸込期間を短くして1サイクルで点滴筒100から1滴の液滴が滴下するように制御する。この制御について説明する。 (B3) When the high flow rate mode is set, the suction period during one cycle of liquid feeding is shortened, and control is performed so that one droplet is dropped from the drip tube 100 in one cycle. This control will be described.
 まず、送液の1サイクル中の吸込期間は、上述したように、図9から図7(A)までの期間であり、この吸込期間を短くすると、当該吸込期間における上流側のバルブ部30Aの閉塞フィンガ31、及び、送液部20の3つの送液フィンガ21・・21の後退速度が速くなる。つまり、吸込期間を短くすると吸込速度が速くなる。その吸込速度(吸引力)は吸込期間が短いほど大きくなって液滴の滴下間隔が短くなる。したがって、吸込期間を可能な限り短くして吸込速度(吸引力)を大きくすることによって、点滴筒100内を滴下する液滴を意図的につなげることが可能になる。ここで、1200mL/hの高流量で薬液を送液する場合、送液のサイクル周期(時間)が非常に短いので、1サイクルにおける吐出期間と吸込期間との比率をどのように設定しても、点滴筒100内を滴下する液滴が必ずつながるようになる(1サイクルで必ず1滴の液滴が滴下する)。 First, the suction period in one cycle of liquid feeding is the period from FIG. 9 to FIG. 7A as described above. If this suction period is shortened, the upstream side valve unit 30A in the suction period is reduced. The retraction speeds of the closing finger 31 and the three liquid feeding fingers 21... 21 of the liquid feeding unit 20 are increased. That is, if the suction period is shortened, the suction speed is increased. The suction speed (suction force) increases as the suction period becomes shorter, and the droplet dropping interval becomes shorter. Therefore, by making the suction period as short as possible and increasing the suction speed (suction force), it is possible to intentionally connect the droplets dropped in the drip tube 100. Here, when a chemical solution is fed at a high flow rate of 1200 mL / h, since the cycle cycle (time) of the feeding is very short, no matter how the ratio between the discharge period and the suction period in one cycle is set. The droplets that drop in the drip tube 100 are always connected (one droplet is always dropped in one cycle).
 このような点を考慮し、本実施形態では、高流量モード時において設定される設定流量(601mL/h~1200mL/h)の大きさに関係なく、図10(B)及び図10(C)に示すように、1サイクル中の吸込期間を流量1200mL/hの場合と同じ期間となるように、1サイクル中のカム軸201の回転速度(ステッピングモータ202の回転速度)の変更制御を実行することで、1サイクルで確実に1滴の液滴が滴下するようにする。このようにして、高流量モード時において送液の1サイクルで必ず1滴の液滴(0.1cc/1滴)が滴下するようにすることで、高流量モード時であっても、滴下センサ8の出力に基づく流量異常判定の精度(通常使用流量域と同等の精度)を確保することができる。 In consideration of such points, in this embodiment, regardless of the magnitude of the set flow rate (601 mL / h to 1200 mL / h) set in the high flow rate mode, FIG. 10 (B) and FIG. 10 (C) As shown in FIG. 5, the change control of the rotation speed of the camshaft 201 (rotation speed of the stepping motor 202) during one cycle is executed so that the suction period during one cycle is the same period as when the flow rate is 1200 mL / h. This ensures that one drop is dropped in one cycle. In this manner, by making sure that one droplet (0.1 cc / 1 droplet) is dropped in one cycle of liquid feeding in the high flow rate mode, the drop sensor even in the high flow rate mode. The accuracy of the flow rate abnormality determination based on the output of 8 (accuracy equivalent to the normal use flow rate range) can be secured.
 このような処理により1サイクルで確実に1滴の液滴が滴下するように設定して、滴下センサ8の出力に基づいて流量を算出して流量異常を判定する。具体的には、制御部300は、滴下センサ8の出力信号から点滴筒100内を滴下する液滴の単位時間当たり(例えば1分当たり)の滴下数を計数(ON信号をカウント)し、その滴数計数値から送液の流量(mL/h)を算出(換算)する。ここで、高流量モードにあっては、上記したように、1サイクルで確実に1滴の液滴が滴下するように設定しているので、1滴当たりの液滴の容積は0.1mLとなり、1分当たりの滴下数(滴数計数値)がnb滴(nbはna/2に相当)である場合、その滴数計数値nbを用いて流量(mL/h)を、演算式[流量=0.1(mL/1滴)×nb(滴/min)×60]から算出する。 Such a process is set so that one drop is surely dropped in one cycle, and the flow rate is calculated based on the output of the drop sensor 8 to determine a flow rate abnormality. Specifically, the control unit 300 counts the number of drops per unit time (for example, per minute) of droplets dropped in the drip tube 100 from the output signal of the drop sensor 8 (counts the ON signal), and The flow rate (mL / h) of the liquid feeding is calculated (converted) from the droplet count value. Here, in the high flow rate mode, as described above, since one drop is surely dropped in one cycle, the volume of the drop per drop is 0.1 mL. When the number of drops per minute (drop count value) is nb drops (nb is equivalent to na / 2), the flow rate (mL / h) is calculated using the drop count value nb using the formula [flow rate = 0.1 (mL / 1 drop) × nb (drops / min) × 60].
 そして、制御部300は、高流量モード時での輸液中において、上記した滴下センサ8の出力に基づく流量の算出処理を逐次実行し、その算出流量(実際の流量)と上記設定流量(601mL/hから1200mL/hまでの設定流量)とを用い、設定流量と算出流量との差(流量差)を算出する。その算出した流量差が所定の許容範囲(流量が正常とみなせる範囲)内である場合は流量が正常であると判定する。一方、上記流量差が許容範囲から外れている場合は流量異常であると判定する。流量異常と判定した場合には、制御部300は、その流量異常を示すメッセージ等を液晶表示部3の液晶パネル3aの画面上に表示したり、また、音発生部6を駆動してブザー音を発生したりして、流量異常であることを看護師等のユーザに知らせる。 Then, the control unit 300 sequentially executes a flow rate calculation process based on the output of the drip sensor 8 during the infusion in the high flow rate mode, and calculates the calculated flow rate (actual flow rate) and the set flow rate (601 mL / The set flow rate from h to 1200 mL / h) is used to calculate the difference between the set flow rate and the calculated flow rate (flow rate difference). When the calculated flow rate difference is within a predetermined allowable range (a range in which the flow rate can be regarded as normal), it is determined that the flow rate is normal. On the other hand, when the flow rate difference is out of the allowable range, it is determined that the flow rate is abnormal. When it is determined that the flow rate is abnormal, the control unit 300 displays a message indicating the abnormal flow rate on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3 or drives the sound generation unit 6 to generate a buzzer sound. To inform a user such as a nurse that the flow rate is abnormal.
 (b4)高流量モード設定時でポンプ機構2が駆動状態であるときに、液滴の滴下を一定期間検出しない場合(滴下センサ8からON信号(液滴検出信号)が一定期間出力されない場合)、制御部300は、空液状態であることを示すメッセージ等を液晶表示部3の液晶パネル3aの画面上に表示したり、また、音発生部6を駆動してブザー音を発生したりして、空液の状態であることを看護師等のユーザに知らせる。なお、上記空液を判定する一定期間(時間)については、実験・計算などにより経験的に求めた値を設定する。 (B4) When the pump mechanism 2 is in the driving state when the high flow rate mode is set, when droplet dropping is not detected for a certain period (when the ON signal (droplet detection signal) is not output from the dropping sensor 8 for a certain period). The control unit 300 displays a message indicating that the liquid is in the liquid state on the screen of the liquid crystal panel 3a of the liquid crystal display unit 3, or drives the sound generation unit 6 to generate a buzzer sound. To inform the user such as a nurse that the liquid is empty. In addition, about the fixed period (time) which determines the said air liquid, the value calculated | required empirically by experiment, calculation, etc. is set.
 <効果>
 以上説明したように、本実施形態によれば、点滴筒100内を滴下する液滴同士がつながる可能性がない通常使用流量域よりも大きな流量で送液を行う高流量モード時には、点滴筒100を滴下する液滴を意図的につなげて、送液の1サイクルで点滴筒から必ず1滴の液滴が滴下するように設定しているので、高流量モード時であっても、滴下センサ8の出力に基づく流量異常判定の精度(通常使用流量域と同等の精度)を確保することができる。これにより高流量での輸液が可能になる。
<Effect>
As described above, according to the present embodiment, in the high flow rate mode in which liquid droplets dropped in the drip tube 100 are not likely to be connected to each other and are supplied at a flow rate larger than the normal use flow rate region, the drip tube 100 is used. Are set so that one drop is surely dropped from the drip tube in one cycle of liquid feeding, so even in the high flow rate mode, the drop sensor 8 The accuracy of the flow rate abnormality determination based on the output of (the accuracy equivalent to the normal use flow rate range) can be ensured. This enables infusion at a high flow rate.
 また、高流量モード時において送液の1サイクルで必ず1滴の液滴が滴下するように設定することで、高流量モード時であっても、看護師等のユーザは、点滴筒100内を滴下する液滴の滴数や滴下時間間隔から流量を容易に換算することが可能になるので、流量の目視確認が可能となる。 In addition, by setting so that one droplet is surely dropped in one cycle of liquid feeding in the high flow rate mode, a user such as a nurse can move the inside of the infusion tube 100 even in the high flow rate mode. Since the flow rate can be easily converted from the number of dropped droplets and the dropping time interval, the flow rate can be visually confirmed.
 -他の実施形態-
 以上の実施形態では、600mL/hを閾値として通常使用流量域と高流量域とを切り分けているが、その閾値については、ポンプ機構2の設定状態などに応じて適宜の値を設定するようにしてもよい。
-Other embodiments-
In the above embodiment, the normal use flow rate range and the high flow rate range are separated using 600 mL / h as a threshold value, but an appropriate value is set for the threshold value according to the setting state of the pump mechanism 2 and the like. May be.
 以上の実施形態では、単位時間当たり(1分当たり)の液滴の滴下数を計数して流量を算出しているが、本発明はこれに限定されない。例えば、滴下センサ8の出力から計数される液滴の計数値が所定値に達するのに要する時間を計測して流量を算出するようにしてもよい。また、滴下センサ8の出力から点滴筒100内を滴下する液滴の滴下時間間隔を求めて流量を算出するようにしてもよい。 In the above embodiment, the flow rate is calculated by counting the number of droplets dropped per unit time (per minute), but the present invention is not limited to this. For example, the flow rate may be calculated by measuring the time required for the count value of the droplets counted from the output of the drop sensor 8 to reach a predetermined value. Further, the flow rate may be calculated by obtaining the dropping time interval of the droplets dropped in the drip tube 100 from the output of the dropping sensor 8.
 以上の実施形態では、点滴筒100として1mL当たりの滴下数が20滴の点滴筒を使用する場合の例について説明したが、本発明はこれに限られることなく、点滴筒100として1mL当たりの滴下数が60滴の点滴筒を使用する場合にも適用することができる。 In the above embodiment, the example in the case of using a drip tube having 20 drops per mL as the drip tube 100 has been described, but the present invention is not limited to this, and the drip per mL as the drip tube 100 is used. The present invention can also be applied when using a drip tube having 60 drops.
 以上の実施形態では、通常使用流量域である場合、1サイクルの送液で点滴筒100から2滴の液滴が滴下するようにしているが、その1サイクルでの滴下数は3滴以上であってもよい。 In the above embodiment, in the normal use flow rate range, two droplets are dropped from the drip tube 100 in one cycle of liquid feeding, but the number of drops in one cycle is three or more. There may be.
 以上の実施形態では、送液部20に設ける送液フィンガ21の数を3つとしているが、本発明はこれに限られることなく、送液部20に設ける送液フィンガ21の数は、2つまたは4つ以上であってもよい。 In the above embodiment, the number of the liquid feeding fingers 21 provided in the liquid feeding unit 20 is three, but the present invention is not limited to this, and the number of the liquid feeding fingers 21 provided in the liquid feeding unit 20 is two. There may be one or four or more.
 以上の実施形態では、送液部20の複数(3つ)の送液フィンガ21・・21を間隔をあけて配置しているが、送液フィンガ21・・21を互いに近接した状態で配置してもよい。また、上流側及び下流側のバルブ部30A,30Bの閉塞フィンガ31,31についても、送液部20の送液フィンガ21に近接した状態で配置してもよい。 In the above embodiment, a plurality of (three) liquid feeding fingers 21... 21 of the liquid feeding unit 20 are arranged at intervals, but the liquid feeding fingers 21. May be. Further, the closing fingers 31, 31 of the upstream and downstream valve portions 30 </ b> A, 30 </ b> B may also be arranged in a state of being close to the liquid feeding finger 21 of the liquid feeding portion 20.
 以上の実施形態では、半閉塞方式の輸液ポンプ1に、本発明を適用した例を示しているが、本発明はこれに限られることなく、送液部20の送液フィンガ21によって輸液チューブTを完全に閉塞するフルプレス方式の輸液ポンプにも適用可能である。 Although the example which applied this invention to the semi-occlusion type infusion pump 1 is shown in the above embodiment, this invention is not limited to this, The infusion tube T by the liquid feeding finger 21 of the liquid feeding part 20 It is also applicable to a full press infusion pump that completely closes the fluid.
 本発明は、医療用の薬液を体内に注入する場合などに用いる輸液ポンプに利用することができる。 The present invention can be used for an infusion pump used for injecting a medical drug solution into the body.
 1 輸液ポンプ
 11 ポンプ本体
 12 扉
 2 ポンプ機構
 20 送液部
 21 送液フィンガ
 30A 上流側のバルブ部
 30B 下流側のバルブ部
 31 閉塞フィンガ
 3 液晶表示部
 3a 液晶パネル
 4 操作部
 8 滴下センサ
 100 点滴筒
 200 駆動部
 202 ステッピングモータ
 300 制御部
DESCRIPTION OF SYMBOLS 1 Infusion pump 11 Pump main body 12 Door 2 Pump mechanism 20 Liquid feeding part 21 Liquid feeding finger 30A Upstream valve part 30B Downstream valve part 31 Blocking finger 3 Liquid crystal display part 3a Liquid crystal panel 4 Operation part 8 Drop sensor 100 Drip cylinder 200 Drive unit 202 Stepping motor 300 Control unit

Claims (2)

  1.  輸液チューブを押圧して当該輸液チューブ内の輸液を送液するポンプ機構と、前記ポンプ機構の輸液送り方向の上流側に配置された点滴筒内を滴下する液滴を検出する滴下センサとを備え、設定流量に応じて前記ポンプ機構の駆動を制御する流量制御、及び、前記滴下センサの出力に基づいて送液の流量を判定する流量判定の実行が可能な輸液ポンプにおいて、
     前記ポンプ機構の制御モードとして前記点滴筒内を滴下する液滴同士がつながる可能性がない通常使用流量域よりも大きな流量で送液を行う高流量モードの設定が可能であり、
     前記通常使用流量域である場合は送液の1サイクルで前記点滴筒から複数滴の液滴が滴下するように設定され、前記高流量モードが設定された場合には送液の1サイクル中の輸液の吸入期間を短くして当該送液の1サイクルで前記点滴筒から1滴の液滴が滴下するように構成されていることを特徴とする輸液ポンプ。
    A pump mechanism that presses the infusion tube to deliver the infusion in the infusion tube, and a drip sensor that detects a drop that drops in the drip tube disposed upstream of the pump mechanism in the infusion feeding direction. In an infusion pump capable of performing flow rate control for controlling the driving of the pump mechanism according to a set flow rate, and performing flow rate determination for determining the flow rate of liquid feeding based on the output of the dropping sensor,
    As a control mode of the pump mechanism, it is possible to set a high flow rate mode in which liquid is fed at a flow rate larger than a normal use flow rate range where there is no possibility that droplets dripping in the drip tube are connected,
    When it is in the normal use flow rate range, it is set so that a plurality of droplets are dropped from the drip tube in one cycle of liquid feeding, and when the high flow rate mode is set, it is set in one cycle of liquid feeding. An infusion pump, wherein the inhalation period of the infusion is shortened and one drop is dropped from the drip tube in one cycle of the liquid feeding.
  2.  請求項1に記載の輸液ポンプにおいて、
     前記ポンプ機構は、進退移動が可能でその前進移動過程で輸液チューブを押圧する送液フィンガと、前記送液フィンガの輸液送り方向の上流側に配置され、進退移動により輸液チューブの閉塞と開放とを行う上流側の閉塞フィンガと、前記送液フィンガの輸液送り方向の下流側に配置され、進退移動により輸液チューブの閉塞と開放とを行う下流側の閉塞フィンガと、前記送液フィンガ、前記上流側の閉塞フィンガ、及び、前記下流側の閉塞フィンガの各フィンガを個別に進退駆動するためのカム及びカム軸とを備え、
     前記高流量モードが設定された場合には、送液の1サイクル中の前記ポンプ機構のカム軸の回転速度を変更して当該送液の1サイクル中の輸液の吸入期間を短くすることを特徴とする輸液ポンプ。
    The infusion pump according to claim 1,
    The pump mechanism is arranged on the upstream side of the liquid feeding direction of the liquid feeding finger, which is capable of moving forward and backward and presses the liquid feeding tube in the forward movement process, and is closed and opened by the forward and backward movement. An upstream closing finger that is disposed downstream of the liquid feeding direction of the liquid feeding finger and that closes and opens the infusion tube by advancing and retreating, the liquid feeding finger, the upstream A closed closing finger on the side, and a cam and a camshaft for individually moving forward and backward for each finger of the closed closing finger on the downstream side,
    When the high flow rate mode is set, the rotational speed of the cam shaft of the pump mechanism during one cycle of liquid feeding is changed to shorten the infusion period of the infusion during one cycle of the liquid feeding. Infusion pump.
PCT/JP2014/073664 2013-09-17 2014-09-08 Infusion pump WO2015041088A1 (en)

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JPH0277267A (en) * 1988-09-14 1990-03-16 Nikkiso Co Ltd Liquid transfusing pump
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JPH06317257A (en) * 1993-04-30 1994-11-15 Sharp Corp Transfusion pump device
JPH0759853A (en) * 1993-08-30 1995-03-07 Terumo Corp Transfusion pump
US20100256562A1 (en) * 1999-09-29 2010-10-07 Smisson-Cartledge Biomedical L.L.C. Rapid Infusion System
US20110196304A1 (en) * 2009-12-26 2011-08-11 The Board Of Regents Of The University Of Texas System Fluid Balance Monitoring System with Fluid Infusion Pump for Medical Treatment
JP2011160868A (en) * 2010-02-05 2011-08-25 Ricoh Co Ltd Flow rate control apparatus and pump apparatus
JP2012107555A (en) * 2010-11-16 2012-06-07 Nipro Corp Infusion pump

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Publication number Priority date Publication date Assignee Title
JPH0277267A (en) * 1988-09-14 1990-03-16 Nikkiso Co Ltd Liquid transfusing pump
JPH05277181A (en) * 1992-04-03 1993-10-26 Sharp Corp Infusion device
JPH06317257A (en) * 1993-04-30 1994-11-15 Sharp Corp Transfusion pump device
JPH0759853A (en) * 1993-08-30 1995-03-07 Terumo Corp Transfusion pump
US20100256562A1 (en) * 1999-09-29 2010-10-07 Smisson-Cartledge Biomedical L.L.C. Rapid Infusion System
US20110196304A1 (en) * 2009-12-26 2011-08-11 The Board Of Regents Of The University Of Texas System Fluid Balance Monitoring System with Fluid Infusion Pump for Medical Treatment
JP2011160868A (en) * 2010-02-05 2011-08-25 Ricoh Co Ltd Flow rate control apparatus and pump apparatus
JP2012107555A (en) * 2010-11-16 2012-06-07 Nipro Corp Infusion pump

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Publication number Priority date Publication date Assignee Title
WO2022164914A1 (en) * 2021-01-28 2022-08-04 Carefusion 303, Inc. Peristaltic pump with constant biasing force

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