Drug solution administration device and control method therefor, drug solution administration system, and program

Abstract

This drug solution administration device administers a drug solution filled in a reservoir into the body of a patient, and is provided with a pump body. The pump body is provided with: a pump that transfers the drug solution filled in the reservoir into the body of the patient; a rechargeable battery that supplies power for driving the pump; a connector unit to which a charging cable or an external power source for charging the rechargeable battery can be connected; a detection unit that detects whether or not the pump body is mounted on a cradle device attached to the skin of the patient; and a control unit. The control unit, while it is detected that the pump body is mounted on the cradle device, causes a notification unit to issue an alert in response to the charging cable or the external power source being connected to the connector unit.

Description

Chemical liquid administration device, its control method, chemical liquid administration system, and program

[0001] The present disclosure relates to a medicinal liquid administration device, a control method thereof, a medicinal liquid administration system, and a program.

[0002] A medical solution administration device for administering a medical solution such as insulin into a patient's body is known. Patent Document 1 describes a device in which a battery is provided in a disposable part and / or a reusable part and used as a power source.

[0003] JP 2014-039846 A

[0004] However, if the drug solution administration device is being charged or the charging terminal is plugged or unplugged while in use, these operations may cause a current leak, the pump body to come off the cradle device, or the charging terminal to short out. As such, the conventional configuration leaves room for improvement regarding charging of the drug solution administration device.

[0005] An object of the present disclosure is to improve charging of rechargeable battery-powered drug solution administration devices.

[0006] According to the present disclosure, the drug solution administration device is (1) a drug solution administration device comprising a pump body that administers a drug solution filled in a reservoir into the patient's body, wherein the pump body comprises: a pump that transfers the drug solution filled in the reservoir into the patient's body; a rechargeable battery that supplies power to drive the pump; a connector unit that can connect a charging cable or an external power source to charge the rechargeable battery; a detection unit that detects whether the pump body is attached to a cradle device that is attached to the patient's skin; and a control unit, wherein the control unit causes an alarm unit to issue an alert in response to the charging cable or the external power source being connected to the connector unit while it is detected that the pump body is attached to the cradle device.

[0007] (2) In the medicinal liquid administration device of (1), the control unit may, in response to the charging cable or the external power source being connected to the connector unit while it is detected that the pump body is attached to the cradle device, transmit an alert notification signal to a remote control for operating the medicinal liquid administration device via a communication unit, and cause an alert to be issued from an output unit provided in the remote control.

[0008] (3) In the drug solution administration device of (1) or (2), an alarm unit is further provided for notifying a user of information, and the control unit may cause the alarm unit to issue an alert in response to the charging cable or the external power source being connected to the connector unit while it is detected that the pump body is attached to the cradle device.

[0009] (4) In any of the drug solution administration devices (1) to (3), the device further includes a charging circuit unit having a switch capable of switching between electrical connection and disconnection between the connector unit and the rechargeable battery, and the control unit may switch the switch to disconnection in response to the charging cable or the external power source being connected to the connector unit while the pump is transporting the drug solution into the patient's body.

[0010] (5) In any of the drug solution administration devices (1) to (4), the control unit may stop driving the pump in response to the charging cable or the external power source being connected to the connector unit while the pump is transporting the drug solution into the patient's body.

[0011] (6) In any of the drug solution administration devices (1) to (5), the pump body may include: a plunger provided in the reservoir and movable in the longitudinal direction of the reservoir; a movable part that can move within a movable area to engage with the plunger and press the plunger toward the tip of the reservoir; and a drive part that moves the movable part within the movable area.

[0012] (7) The drug solution administration device according to any one of (1) to (6) may further include a cradle device to which the pump body can be attached.

[0013] According to the present disclosure, a medicinal liquid administration system includes: (8) a medicinal liquid administration device according to any one of (1) to (7); and a remote control for operating the medicinal liquid administration device.

[0014] According to the present disclosure, the control method for a medicinal liquid administration device is (9) a control method for a medicinal liquid administration device having a pump body that administers a medicinal liquid filled in a reservoir into the patient's body, wherein the pump body comprises: a pump that transfers the medicinal liquid filled in the reservoir into the patient's body; a rechargeable battery that supplies power to drive the pump; a connector unit that can connect a charging cable or an external power source to charge the rechargeable battery; a detection unit that detects whether the pump body is attached to a cradle device that is attached to the patient's skin; and a control unit, wherein the control unit causes an alarm unit to issue an alert in response to the charging cable or the external power source being connected to the connector unit while it is detected that the pump body is attached to the cradle device.

[0015] According to the present disclosure, the program is: (10) a program for controlling a drug solution administration device having a pump body that administers a drug solution filled in a reservoir into the patient's body, wherein the pump body comprises: a pump that transfers the drug solution filled in the reservoir into the patient's body; a rechargeable battery that supplies power to drive the pump; a connector unit that can connect a charging cable or an external power source to charge the rechargeable battery; a detection unit that detects whether the pump body is attached to a cradle device that is attached to the patient's skin; and a control unit; and the program causes the control unit to execute a procedure for causing an alarm unit to issue an alert in response to the charging cable or the external power source being connected to the connector unit while it is detected that the pump body is attached to the cradle device.

[0016] According to an embodiment of the present disclosure, charging of a drug solution administration device that operates on a rechargeable battery can be improved.

[0017] 1 is a diagram showing an example of a medicinal liquid administration system according to an embodiment. FIG. 1 is a perspective view showing an example of the medicinal liquid administration device of FIG. 1. FIG. 2 is a perspective view showing an example of the medicinal liquid administration device in a separated state. FIG. 3 is a perspective view showing an example of the pump body of FIG. 3. FIG. 4 is a perspective view showing an example of the pump body in a disassembled state. FIG. 5 is a diagram showing an example of a cartridge in a state where the nut portion is in a non-contact position. FIG. 6 is a diagram showing an example of a cartridge in a state where the nut portion is in a predetermined position. FIG. 7 is a block diagram showing an example of a configuration related to control of the medicinal liquid administration device of FIG. 1. FIG. 8 is a block diagram showing an example of a hardware configuration of the remote control of FIG. 1. FIG. 9 is a flowchart showing an example of the operation of the medicinal liquid administration device of FIG. 1. FIG. 10 is a flowchart showing an example of the operation of the medicinal liquid administration device of FIG. 1.

[0018] Hereinafter, an embodiment of the present disclosure will be described with reference to the drawings. In each drawing, parts having the same configuration or function are denoted by the same reference numerals. In the description of this embodiment, duplicated descriptions of the same parts may be omitted or simplified as appropriate.

[0019] (Configuration of medicinal liquid administration system) Fig. 1 is a diagram showing an example of a medicinal liquid administration system 100 according to one embodiment. The medicinal liquid administration system 100 administers a medicinal liquid such as insulin into the living body of a patient. The medicinal liquid administration system 100 includes a medicinal liquid administration device 1 and a remote control 90.

[0020] As will be described later with reference to Fig. 5 etc., the drug solution administration device 1 is a device that continuously or intermittently administers a drug solution filled in a reservoir (syringe) 18 into a living body by the pressing action of a plunger 20. The drug solution administration device 1 may be, for example, a portable device that can be attached to the abdomen or the like of a patient (patch type). However, the drug solution administration device 1 is not limited to the patch type and may also be a tube type or the like.

[0021] The remote control 90 is a device used by a user, such as a patient, to operate the drug solution administration device 1. The remote control 90 notifies the user of information received from the drug solution administration device 1 and accepts user operations on the drug solution administration device 1. In this embodiment, the remote control 90 is implemented by a dedicated device compatible with the drug solution administration device 1, but it may also be implemented by a general-purpose information processing device such as a smartphone or tablet. In this embodiment, an example is described in which the remote control 90 serves as a user interface for notifying the user of information and accepting information input from the user. However, instead, all or part of the user interface functions may be provided by the drug solution administration device 1. In this embodiment, the user of the drug solution administration system 100 is the patient himself / herself. However, the user may also be a person other than the patient, including the patient's family members and medical professionals such as doctors and nurses.

[0022] The drug solution administration device 1 and the remote control 90 are communicably connected to each other via a wireless communication line, a wired communication line, or a combination thereof. An example in which the drug solution administration device 1 and the remote control 90 are communicably connected to each other via Bluetooth (registered trademark) will be described below.

[0023] (Configuration of the drug solution administration device) Fig. 2 is an example of a perspective view of the drug solution administration device 1 of Fig. 1. Fig. 3 is an example of a perspective view of the drug solution administration device 1 of Fig. 1 when separated. The drug solution administration device 1 has a pump body 10, a cradle device 11 to which the pump body 10 is detachably attached, and a cannula port 106 attached to the cradle device 11. The pump body 10 and the cradle device 11 have a structure in which they engage with each other and can be repeatedly detached. Fig. 4 is a perspective view showing an example of the pump body 10 of Fig. 3.

[0024] The pump body 10 includes a housing 111 that houses each component of the medicinal solution administration device 1, such as the reservoir 18 and the plunger 20. As illustrated in Figures 2 and 3, the housing 111 may be formed in a flat, approximately rectangular parallelepiped shape with rounded corners. The top surface 121 of the housing 111 is one side of the pump body 10 that is located opposite the side that is attached to the cradle device 11. The top surface 121 may be formed in a generally rectangular shape with rounded corners when viewed from above. A front surface 123 and a back surface 124 that face each other are connected approximately vertically to an end of the top surface 121 in a first direction. A first side surface 125 and a second side surface 126 that face each other are connected approximately vertically to an end of the top surface 121 in a second direction.

[0025] As shown in FIGS. 2 and 3 , the pump body 10 includes a connector 75 on the top surface 121. The connector 75 is a connector that can be connected to an external power source. When the external power source is connected to the connector 75, the pump body 10 receives power from the power source via a charging cable and charges the rechargeable battery 42 (see FIG. 5 ) provided in the device main body 14. The connector 75 is, for example, a connector that complies with a general-purpose standard such as USB (Universal Serial Bus), but may be implemented using other methods that can receive power. In FIGS. 2 and 3 , the connector 75 is provided on the top surface 121, but it may also be provided at any position on the pump body 10 (e.g., on the side of the pump body 10, etc.). The connector 75 may include a cap to prevent dust and other contaminants from entering while the charging cable is not connected. In this embodiment, the connector 75 can be connected to a wired charging cable, but it may also be configured to receive power via a wireless power supply method.

[0026] As shown in FIGS. 3 and 4 , the pump body 10 may have an engagement structure at the first side surface portion 125 and the second side surface portion 126 that allows the pump body 10 and the cradle device 11 to be repeatedly detached from each other. The engagement structure may include, for example, a hook mechanism. Specifically, a first guide groove portion 135 and a first engagement hook portion 136 may be formed in the first side surface portion 125. A second guide groove portion 137 and a second engagement hook portion 138 may be formed in the second side surface portion 126. The first engagement hook portion 136 may be formed closer to the rear surface portion 124 than the first guide groove portion 135. The second engagement hook portion 138 may be formed closer to the rear surface portion 124 than the second guide groove portion 137. The first engagement hook portion 136 and the second engagement hook portion 138 may be detachably engaged with a pair of engagement receiving portions 162 provided on the cradle device 11, which will be described later.

[0027] The cradle device 11 is configured to be able to support the pump body 10. As shown in Figures 2 and 3, the cradle device 11 has a substantially flat mounting surface 141 and side walls 143, 144. The mounting surface 141 is formed in a substantially rectangular shape with curved corners when viewed from above. When the pump body 10 is attached to the cradle device 11, the bottom surface 122 (see Figure 4) of the housing 111 of the pump body 10 is placed on the mounting surface 141.

[0028] A detection rail 152, a sliding rail 153, and a mounting portion 155 may be provided on one surface of the mounting surface portion 141. The cannula port 106 may be mounted on the mounting portion 155. The mounting portion 155 may be provided with an insertion hole through which the cannula of the cannula port 106 is inserted.

[0029] The detection rail 152 is a protrusion that protrudes from one surface of the mounting surface 141. The detection rail 152 is used by the pump main body 10 to detect the attachment of the cradle device 11. The thickness of the detection rail 152 gradually increases from the mounting surface 141 toward the side wall 144. The detection rail 152 extends a predetermined length parallel to the side wall 143. When the pump main body 10 is attached to the cradle device 11, the detection rail 152 enters the detection groove 134 provided in the pump main body 10 and presses the attachment detection switch 133. The pump main body 10 detects the attachment of the cradle device 11 based on the pressing of the attachment detection switch 133. In other words, the attachment detection switch 133 functions as a detector that detects whether the pump main body 10 is attached to the cradle device 11.

[0030] The slide rail 153 extends parallel to the side wall 143 on one surface of the mounting surface 141. When the pump body 10 is attached to the cradle device 11, the slide groove 132 provided on the bottom surface 122 of the pump body 10 is slidably fitted into the slide rail 153.

[0031] A side wall 144 extends substantially perpendicularly from the end of the mounting surface 141 in the first direction. Opposing side wall 143 extend substantially perpendicularly from the end of the mounting surface 141 in the second direction. When the pump body 10 is attached to the cradle device 11, the side wall 143 faces the first side surface 125 and the second side surface 126 of the housing 111 of the pump body 10. The side wall 144 faces the front surface 123 of the housing 111.

[0032] As shown in Figure 3, cradle device 11 may have a fitting hole 154, which is an opening, in side wall portion 144. When pump body 10 is attached to cradle device 11, fitting protrusion 131 (see Figure 4) provided on front surface portion 123 of pump body 10 may fit into fitting hole 154.

[0033] The side wall portion 143 may be formed with a guide rail 151, a posture correction portion 156, and an engagement receiving portion 162. The engagement receiving portion 162 may be an opening formed by cutting out a substantially rectangular shape from the side wall portion 143. The engagement receiving portions 162 may be provided on the side wall portion 143 facing each other depending on the arrangement of the first engagement hook portion 136 and the second engagement hook portion 138. When the pump body 10 is attached to the cradle device 11, the first engagement hook portion 136 and the second engagement hook portion 138 may detachably engage with the pair of engagement receiving portions 162.

[0034] As shown in FIG. 3 , the guide rail 151 is a protrusion formed on the side wall portion 143. The guide rail 151 does not necessarily have to be a continuous protrusion. For example, as shown in FIG. 3 , a notch 158 may be appropriately provided midway along the guide rail 151. A guide rail 151 may be provided on each of the opposing side wall portions 143. When the pump body 10 is attached to the cradle device 11, the guide rail 151 engages with a first guide groove 135 provided on the first side surface portion 125 and a second guide groove 137 provided on the second side surface portion 126 of the pump body 10. This guides the attachment direction of the pump body 10.

[0035] 2 and 3 , posture correcting portion 156 is a plate-shaped protrusion extending upward from side wall portion 143. Posture correcting portion 156 may have a curved shape corresponding to the shape of the connection portion (corner) between top surface portion 121 of housing 111 of pump body 10 and first side surface portion 125 and second side surface portion 126.

[0036] The cradle device 11 may be provided with an adhesive sheet to be attached to the patient's skin. The adhesive sheet may be attached to the other surface opposite to one surface of the mounting surface portion 141 of the cradle device 11. The adhesive sheet may have an opening formed therein through which a cannula of the cannula port 106 described below passes. The adhesive sheet may be made of a flexible material. The adhesive sheet may form an adhesive layer to be attached to the patient's skin on the surface opposite to the mounting surface portion 141. Before being attached to the patient's skin, the adhesive layer of the adhesive sheet may be covered with release paper.

[0037] The cannula port 106 may have a port body 181 capable of holding a cannula therein. The port body 181 may have a cylindrical connection portion. When a cannula is connected, the interior of the connection portion (cylindrical bore), the port body 181, and the cannula are in communication. A cap 182 is attached to the tip of the connection portion, and the other end of the connection portion is connected to the port body 181. The cap 182 seals the tip opening of the connection portion. This isolates the interior of the cannula port 106 from the external environment.

[0038] When the cannula port 106 is attached to the attachment portion 155 of the cradle device 11 using a puncture mechanism (not shown), the cannula penetrates the mounting surface 141 together with the puncture needle and protrudes to the other surface of the mounting surface 141 (the surface that is attached to the skin). The cannula is then inserted into the living body together with the puncture needle. The puncture needle is then removed, leaving the cannula in the living body.

[0039] The connection portion of the port body 181 may face upstream in the installation direction. The connecting needle 112 (see FIG. 4 ) exposed to the outside of the pump body 10 is fluidly connected to the outlet tube 29. The connecting needle 112 punctures the septum surface of the cap 182 and enters the bore. This connects the port body 181 to the outlet tube 29 (see FIG. 6 , etc.) of the pump body 10, and fluidly connects the outlet tube 29 to the cannula. When the drive unit 40 (see FIG. 6 , etc.) is driven, the medicinal liquid stored in the reservoir 18 of the pump body 10 is sent to the cannula port 106 via the outlet tube 29 and administered to the patient from the cannula. In other words, the outlet tube 29 connects to the reservoir 18 and functions as a flow path for delivering the medicinal liquid to the outside of the reservoir 18. When the connecting needle tube 112 is connected to the outlet tube 29 , the flow path of the drug solution administration device 1 may include the outlet tube 29 and the connecting needle tube 112 .

[0040] 4 shows a perspective view of an example of pump body 10, viewed from a direction that allows bottom surface portion 122, front surface portion 123, and first side surface portion 125 to be seen. Bottom surface storage portion 127 is formed at the corners of bottom surface portion 122, first side surface portion 125, and front surface portion 123 of housing 111. Bottom surface storage portion 127 is a recessed space that extends from bottom surface portion 122 toward top surface portion 121 with a predetermined length (thickness) and a predetermined area (width).

[0041] A cylindrical connection port 128 is formed in a wall surface 127a of the bottom storage portion 127 on the side of the rear surface 124 in the first direction. The connection port 128 has a tubular hole 128a that protrudes from the wall surface 127a toward the front surface 123 in the first direction (i.e., in the installation direction). The connection needle tube 112 is disposed in the tubular hole 128a of the connection port 128. The tubular hole 128a protrudes from the wall surface 127a so as to surround the periphery of the connection needle tube 112, thereby protecting the connection needle tube 112. Furthermore, the connection needle tube 112 protrudes from the wall surface 127a within the tubular hole 128a toward the front surface 123 in the first direction (in the installation direction). In other words, the direction in which the connection port 128 protrudes from the wall surface 127a is parallel to the first direction.

[0042] When the pump body 10 is attached to the cradle device 11, the cannula port 106 attached to the cradle device 11 is housed in the bottom storage compartment 127. Furthermore, the port body 181 and cap 182 of the cannula port 106 are inserted into the cylindrical bore 128a of the connection port 128. Furthermore, the connecting needle tube 112 protrudes from the wall surface 127a within the cylindrical bore 128a toward the front surface 123 in the first direction (i.e., in the attachment direction). In other words, the direction in which the connecting needle tube 112 protrudes from the wall surface 127a is parallel to the first direction.

[0043] (Configuration of Pump Main Body) Fig. 5 is an example of an exploded perspective view of the pump main body 10 of Fig. 3. Fig. 6 is a diagram showing an example of the cartridge 12 in a state where the nut portion 24 is in a non-contact position. Fig. 7 is a diagram showing an example of the cartridge 12 in a state where the nut portion 24 is in a predetermined position.

[0044] As shown in Figure 5, the pump body 10 includes a disposable cartridge 12 and a reusable device body 14. The cartridge 12 includes a base portion 16 that is shaped like a flat box and has an opening on one side. The base portion 16 has a generally rectangular shape in plan view. The base portion 16 may be detachably attached to a cradle device 11 that can be attached to the patient's skin.

[0045] 5, the base portion 16 is provided with a reservoir 18 filled with a medicinal solution, a plunger 20 provided to extend from the inside of the reservoir 18, a feed screw shaft 22 disposed coaxially with the plunger 20, and a nut portion (movable portion) 24 threaded onto the feed screw shaft 22. The base portion 16 is configured as a disposable member.

[0046] The reservoir 18 extends cylindrically in the longitudinal direction of the base portion 16. The outer and inner diameters of the distal end of the reservoir 18 taper toward the distal end. The distal end of the reservoir 18 is formed with an introduction port 26 for introducing the medicinal liquid into the reservoir 18 and an outlet port 28 (see FIG. 6 ) for discharging the medicinal liquid from the reservoir 18. The outlet port 28 is connected to an outlet tube 29 that guides the medicinal liquid from the reservoir 18 to the cannula.

[0047] As shown in FIG. 6 , the plunger 20 is integrally molded from a resin material or the like and is disposed within the reservoir 18 so as to be slidable liquid-tightly along the axial direction of the reservoir 18. The plunger 20 includes a plunger body 30 constituting the tip side and a pusher 32 disposed on the plunger body 30 and constituting the rear end side. A seal member (sealing member) 34 is attached to the cylindrical rear end side of the plunger body 30. The seal member 34 is attached to the outer surface of the plunger body 30. The seal member 34 presses against the inner wall surface of the reservoir 18 to prevent leakage of the medicinal solution filled in the reservoir 18. The seal member 34 moves back and forth along the inner wall surface of the reservoir 18 in the left-right direction in FIGS. 6 and 7 while engaging with the cylindrical inner wall surface to prevent leakage of the medicinal solution from the boundary between the plunger body 30 and the inner wall surface of the reservoir 18. The size of the internal space of reservoir 18 that contains the medicinal liquid varies depending on the position of plunger body 30 in reservoir 18. In this embodiment, seal member 34 is configured by an O-ring, but is not limited to this as long as it can prevent the medicinal liquid in reservoir 18 from leaking from plunger body 30. Seal member 34 may be configured by an elastic material, such as silicone rubber.

[0048] The pusher 32 has a pair of extensions 36 that extend rearward from the plunger body 30 to the outside of the reservoir 18, and a pair of claws 38 provided at the rear ends of the extensions 36. One end of the feed screw shaft 22 is journaled by a bearing 39, and constitutes a drive unit 40 that moves the nut portion 24 within the movable range.

[0049] The drive unit 40 further includes a rechargeable battery 42 as a power source, a motor 44 driven by the rechargeable battery 42, a gearbox (power transmission mechanism) 46 that reduces the rotational driving force of the motor 44 and transmits it, and a transmission shaft 52 to which a spur gear 50 that meshes with an output gear 48 of the gearbox 46 is fixed and which is engaged with the feed screw shaft 22 so as to be able to rotate integrally with the feed screw shaft 22.

[0050] In this embodiment, the transmission shaft 52 is provided in the cartridge 12, and the rechargeable battery 42, motor 44, and gear box 46 are provided in the device main body 14. By providing the rechargeable battery 42, motor 44, and gear box 46 in the device main body 14 in this way, the cost of the cartridge 12 can be reduced.

[0051] The rechargeable battery 42 is a secondary battery that can be repeatedly charged and discharged. The rechargeable battery 42 is provided with terminals 54 that are electrically connected to the motor 44 of the device body 14 when the device body 14 is connected to the cartridge 12. The transmission shaft 52 is supported by a pair of bearings 56 provided in the base portion 16 and is disposed coaxially with the feed screw shaft 22.

[0052] When the motor 44 rotates, its rotational force is transmitted to the feed screw shaft 22, and the rotation of the feed screw shaft 22 moves the nut portion 24 toward or away from the reservoir 18. Hereinafter, rotation of the motor 44 to move the nut portion 24 toward the reservoir 18 is referred to as forward rotation (forward rotation). Rotation in the direction opposite to the forward direction is referred to as reverse rotation (reverse rotation). The motor 44 is configured to be capable of rotating in both the forward and reverse directions. The motor 44 is configured so that if a force greater than a certain level is applied to the forward or reverse rotation, the rotational drive force is not transmitted to the gear box 46 and subsequent components. For example, a stepping motor may be used as the motor 44. If a stepping motor is used, when a force greater than a certain level is applied to the forward or reverse rotation, the motor 44 loses synchronization with the input pulses and no longer transmits the rotational drive force (out of step). Even if the motor 44 rotates in the reverse direction while the nut portion 24 is in contact with the bearing 56 due to step-out, it is possible to prevent damage due to excessive force being applied to mechanisms such as the motor 44, gear box 46, and transmission shaft 52. A rotary encoder (not shown) is provided on the output shaft of the motor 44, and it is possible to determine whether the motor 44 has become out of synchronization with the input pulse (step-out) by detecting the rotation of the motor 44 with the rotary encoder. The operating state of the motor 44 is transmitted to the control unit 71 as a rotary encoder output.

[0053] The nut portion 24 is integrally molded from a resin material and has a nut portion main body 58 formed in a substantially rectangular parallelepiped shape, and a slide portion 60 provided on the nut portion main body 58. The nut portion main body 58 is formed with a threaded hole 62 into which the feed screw shaft 22 screws, and a pair of through holes 64 formed on either side of the threaded hole 62 and through which the claw portions 38 pass. A reinforcing cover 66 made of, for example, a metal material or the like is attached to the outer surface of the nut portion main body 58.

[0054] The slide portion 60 slides relative to a guide wall 68 that is provided on the base portion 16 and extends along the axial direction of the plunger 20. That is, before use, the nut portion 24 is in a non-contact position where it does not contact the plunger 20 (see FIG. 6), and the rotation of the feed screw shaft 22 moves it from the non-contact position to a contact position where the nut portion 24 and plunger 20 are engaged. After contacting the plunger 20, further rotation of the feed screw shaft 22 causes the nut portion 24 to press the plunger 20 toward the distal end (see FIG. 7). The guide wall 68 may be provided with a restricting portion that functions as a stopper to prevent the slide portion 60 from moving further backward.

[0055] As shown in FIGS. 5 to 7 , the device main body 14 includes a lid that is detachably attached to the base 16 so as to close the opening of the base 16, as well as a control unit 71, a storage unit 72, and a communication unit 73. The lid may be provided on the top surface 121 of the housing 111. The control unit 71 is electrically connected to the rechargeable battery 42, the motor 44, the storage unit 72, the communication unit 73, the charging circuit unit 74, the connector unit 75, and the notification unit 77 via a bus 79 (see FIG. 8 ). The control unit 71 controls each unit of the medicinal solution administration device 1 to perform processing related to the operation of the medicinal solution administration device 1. For example, the control unit 71 controls the drive of the motor 44 based on information related to medicinal solution administration transmitted from the remote control 90.

[0056] Fig. 8 is a block diagram showing an example of a configuration related to control of the drug solution administration device 1 of Fig. 1. As described above, the rechargeable battery 42, the motor 44, the storage unit 72, the communication unit 73, the charging circuit unit 74, the connector unit 75, and the notification unit 77 are electrically connected to the control unit 71 via the bus 79.

[0057] The control unit 71 is one or more processors. The control unit 71 is communicably connected to each component of the medicinal solution administration device 1 and controls the operation of the entire medicinal solution administration device 1. The processor is a general-purpose processor such as a CPU (Central Processing Unit), or a dedicated processor specialized for specific processing. The control unit 71 may include one or more dedicated circuits, or one or more processors in the control unit 71 may be replaced with one or more dedicated circuits. The dedicated circuit is, for example, an FPGA (Field Programmable Gate Array).

[0058] The storage unit 72 is one or more semiconductor memories, one or more magnetic memories, one or more optical memories, or a combination of at least two of these. The semiconductor memory is, for example, a random access memory (RAM) or a read-only memory (ROM). The storage unit 72 functions as, for example, a main storage device, an auxiliary storage device, or a cache memory. For example, the storage unit 72 may store information from the control unit 71. Furthermore, the information stored in the storage unit 72 may be transmitted to the remote control 90 via the communication unit 73 under the control of the control unit 71.

[0059] The communication unit 73 is a communication interface for communicating with the remote control 90. In this embodiment, the communication unit 73 communicates with the remote control 90 via Bluetooth (registered trademark), but this is not limiting, and communication may be via, for example, another wireless communication path such as a wireless LAN (Local Area Network) or a wired cable.

[0060] The charging circuit unit 74 is an electric circuit for transferring power supplied from a power source connected to the connector unit 75 to the rechargeable battery 42. The charging circuit unit 74 includes a switch that can electrically connect and disconnect the connector unit 75 and the rechargeable battery 42.

[0061] The notification unit 77 notifies the user of information. The notification unit 77 is, for example, but not limited to, a speaker that outputs sound, a display that outputs images (e.g., a liquid crystal display), an LED lamp, a vibrator, or a combination thereof.

[0062] The control of the chemical solution administration device 1 may be performed by executing a program on a processor included in the control unit 71. That is, the control of the chemical solution administration device 1 may be realized by software. In this case, the program causes a computer to execute processing of steps included in the operation of the chemical solution administration device 1, thereby causing the computer to realize functions corresponding to the processing of those steps. Alternatively, some or all of the functions of the chemical solution administration device 1 may be realized by a dedicated circuit included in the control unit 71. That is, some or all of the functions of the chemical solution administration device 1 may be realized by hardware.

[0063] (Configuration of Remote Control) Fig. 9 is a block diagram showing an example of the hardware configuration of the remote control 90 in Fig. 1. The remote control 90 includes a control unit 91, a storage unit 92, a communication unit 93, an input unit 94, an output unit 95, and a bus 99.

[0064] The control unit 91 is one or more processors. The control unit 91 is communicably connected to each component of the remote control 90 via a bus 99 and controls the operation of the entire remote control 90. The processor is a general-purpose processor such as a CPU or a GPU (Graphics Processing Unit), or a dedicated processor specialized for a specific process. The control unit 91 may include one or more dedicated circuits, or the one or more processors in the control unit 91 may be replaced with one or more dedicated circuits. The dedicated circuit is, for example, an FPGA.

[0065] The storage unit 92 is one or more semiconductor memories, one or more magnetic memories, one or more optical memories, or a combination of at least two of these. The semiconductor memories are, for example, RAM or ROM. The RAM is, for example, SRAM (Static RAM) or DRAM (Dynamic RAM). The ROM is, for example, EEPROM (Electrically Erasable Programmable ROM). The storage unit 92 functions, for example, as a main storage device, an auxiliary storage device, or a cache memory.

[0066] The communication unit 93 is a communication interface for communicating with the medicinal solution administration device 1. The communication unit 93 communicates with the medicinal solution administration device 1 to transmit information input by a user to the medicinal solution administration device 1 and to receive information from the medicinal solution administration device 1. The communication unit 93 communicates with the medicinal solution administration device 1 via Bluetooth (registered trademark), for example, but is not limited to this, and communication may also be via another wireless communication path such as a wireless LAN or a wired cable, for example.

[0067] The input unit 94 includes one or more input interfaces that accept input operations from a user and acquire input information based on the user operations. The input unit 94 is, for example, a touch screen that is integrated with the display (display device) of the output unit 95, but is not limited to this and may also be physical keys (for example, an external numeric keypad), capacitance keys, a pointing device, a microphone that accepts voice input, or the like.

[0068] The output unit 95 as a display unit includes one or more output interfaces that output information to the user and notify the user. For example, the output unit 95 may be, but is not limited to, a display that outputs information by image display, an LED (Light Emitting Diode), a speaker, or a vibrator. The input unit 94 and the output unit 95 act as an input / output unit that is an interface between the user and the medicinal solution administration device 1. In this embodiment, an example in which such an input / output unit is provided in the remote control 90 will be described, but it may also be provided in the medicinal solution administration device 1 or another device.

[0069] The functions of the remote control 90 may be realized by executing a program according to this embodiment on a processor included in the control unit 91. That is, the functions of the remote control 90 may be realized by software. In this case, the program causes a computer to execute processing of steps included in the operation of the remote control 90, thereby causing the computer to realize functions corresponding to the processing of those steps. Alternatively, some or all of the functions of the remote control 90 may be realized by a dedicated circuit included in the control unit 91. That is, some or all of the functions of the remote control 90 may be realized by hardware.

[0070] (Operation of the drug solution administration device) When operating the drug solution administration device 1 according to this embodiment, the user first removes the cartridge 12 from the packaging container. In this state, the reservoir 18 of the cartridge 12 is not filled with drug solution, and the nut portion 24 is in a non-contact position where it does not contact the plunger 20 (see FIG. 6 ).

[0071] Next, the user adjusts the position of plunger 20 relative to reservoir 18, and fills a desired amount of medicinal liquid into reservoir 18 through introduction port 26 from a medicinal liquid container, such as a vial in which the medicinal liquid is sealed. Thereafter, the user connects device main body 14 to cartridge 12. As a result, power from rechargeable battery 42 of cartridge 12 is supplied to the components of device main body 14, and output gear 48 of gear box 46 of device main body 14 meshes with spur gear 50 of cartridge 12. Control unit 71, memory unit 72, etc. are started up by receiving power from this rechargeable battery 42.

[0072] Next, the user fills the cartridge 12 removed from the packaging container with the medicinal liquid, connects the cartridge 12 to the device main body 14, and then primes the medicinal liquid administration device 1. Priming refers to an operation of engaging the nut portion 24 of the medicinal liquid administration device 1 with the plunger 20 and filling the flow path of the medicinal liquid administration device 1, including the outlet tube 29, with the medicinal liquid. Specifically, the user operates the remote control 90 to rotate the motor 44 in the forward direction. As a result, the rotational driving force of the motor 44 is transmitted to the feed screw shaft 22 via the gear box 46, the spur gear 50, and the transmission shaft 52, causing the feed screw shaft 22 to rotate and the nut portion 24 to slide along the guide wall 68 and advance toward the plunger 20.

[0073] As the nut portion 24 advances toward the distal end of the reservoir 18, the pair of claws 38 abut against the wall surfaces defining the through-hole 64 of the nut portion 24, causing the pair of extensions 36 to bend toward each other. Then, as the claws 38 pass through the through-hole 64, the extensions 36 return from their bent state to their original state, and the nut portion 24 engages with the rear end of the plunger 20. This enables the nut portion 24 to press the plunger 20 toward the distal end. Subsequently, by further advancing the nut portion 24, the medicinal liquid in the reservoir 18 is pressed against the plunger 20, filling the inner bore of the outlet tube 29 with the medicinal liquid, thereby completing priming. This priming is completed when the user visually confirms that the medicinal liquid has been discharged from the connecting needle tube 112, which is fluidly connected to the outlet tube 29 and exposed to the outside of the medicinal liquid administration device 1. When the user visually confirms that the medicinal solution has been discharged from the connecting needle tube 112, the user instructs the medicinal solution administration device 1 to stop priming. For example, the remote control 90 may display an image of a priming stop button on the display of the output unit 95, and notify the medicinal solution administration device 1 to stop the motor 44 in response to the user selecting the priming stop button.

[0074] Next, the user attaches the cradle device 11 to a predetermined location on the skin (e.g., the patient's abdomen), uses the puncture mechanism to place the cannula of the cannula port 106 inside the body, and engages the cannula port 106 with the cradle device 11. Next, the user attaches the pump body 10, to which the cartridge 12 and device body 14 are connected, to the cradle device 11, thereby connecting the outlet tube 29 to the cannula. In this state, the control unit 71 controls the rotation of the motor 44, thereby continuously or intermittently administering the medicinal solution from the reservoir 18 into the body. The control unit 71 controls the rotation of the motor 44 according to a medicinal solution administration schedule instructed via the remote control 90, and administers the medicinal solution at various rates, such as a basal rate or a bolus, depending on the patient's condition. The basal rate is the amount of medicinal solution per unit time that corresponds to the basal secretion of insulin. The bolus is the amount of medicinal solution that corresponds to the additional secretion of insulin in response to a meal or an increase in blood glucose level.

[0075] The reservoir 18 of the cartridge 12 is filled with an amount of medicinal liquid to be administered in an administration cycle of a certain number of days. After the medicinal liquid filled in the reservoir 18 is administered into the body over, for example, three days to one week, the cartridge 12 is replaced and discarded. The cartridge 12 is replaced with a new cartridge after each administration cycle. Each time the cartridge 12 is replaced, the reservoir 18 of the cartridge 12 is filled with medicinal liquid, the cartridge 12 is connected to the device main body 14, and a priming operation is performed. After these operations, while the medicinal liquid is being administered, the medicinal liquid administration device 1 can estimate the amount of medicinal liquid to be administered based on, for example, the number of rotations of the motor 44 performed during priming and liquid delivery. The medicinal liquid administration device 1 according to this embodiment includes a disposable cartridge 12 and a reusable device main body 14, thereby reducing running costs.

[0076] The amount of medicinal solution filled into the reservoir 18 of the cartridge 12 varies depending on the age and condition of the patient, even if the length of the administration cycle is the same. For example, if the reservoir 18 is filled with a three-day amount of medicinal solution, the cartridge 12 for adults will be filled with more medicinal solution than the cartridge 12 for children.

[0077] As described above, the medicinal solution administration device 1 according to this embodiment includes a rechargeable battery 42 as a power source, which can be repeatedly charged and discharged. The rechargeable battery 42 is charged by connecting an external power source to the connector 75 of the device body 14. In this configuration, if charging or disconnecting the charging cable during medicinal solution administration is performed, these actions may result in a short circuit, the pump body 10 becoming detached from the cradle device 11, or a short circuit of the charging terminals. Alternatively, a malfunction of the charging adapter may result in excessive power being supplied to the medicinal solution administration device 1 while it is attached to the patient's abdomen. Therefore, it is necessary to reduce the possibility of such problems occurring.

[0078] Therefore, while attachment detection switch 133 detects that pump body 10 is attached to cradle device 11, medicinal solution administration device 1 causes remote control 90 or notification unit 77 to issue an alert in response to connection of an external power source to connector unit 75. Therefore, in response to the alert, the user can stop continuing charging while medicinal solution administration device 1 is attached to the patient's abdomen by unplugging the charging cable from connector unit 75 or removing pump body 10 from cradle device 11.

[0079] Furthermore, when an external power source is connected to the connector unit 75 while the pump body 10 is attached to the cradle device 11, the medicinal solution administration device 1 may issue an alert and also turn off the switch of the charging circuit unit 74. Alternatively, when an external power source is connected to the connector unit 75 while the medicinal solution administration device 1 is driving the motor 44 to perform a liquid delivery operation, the medicinal solution administration device 1 may issue an alert and also stop driving the motor 44. With this configuration, it is possible to prevent malfunctions such as electric leakage, terminal shorts, and excessive power supply without the user having to take any special action.

[0080] Figures 10 and 11 are flowcharts showing an example of the operation of the chemical liquid administration device 1 of Figure 1. The operation of the chemical liquid administration device 1 described with reference to Figures 10 and 11 may correspond to one of the control methods for the chemical liquid administration device 1. The operation of each step in Figures 10 and 11 may be executed based on the control by the control unit 71 of the chemical liquid administration device 1.

[0081] 10, the control unit 71 determines whether the motor 44 is being driven and liquid is being delivered. If liquid is being delivered (YES in step S1), the control unit 71 proceeds to step S11 in FIG. 11, and if not (NO in step S1), the control unit 71 proceeds to step S2.

[0082] In step S2, control unit 71 determines whether a charging cable or an external power source is connected to connector unit 75. For example, control unit 71 may determine whether a charging cable or an external power source is connected to connector unit 75 based on the potential or current observed in charging circuit unit 74. Alternatively, connector unit 75 may be provided with an attachment detection switch or sensor for detecting physical contact when a charging cable is connected to connector unit 75. If a charging cable is connected (YES in step S2), control unit 71 proceeds to step S3, and if not (NO in step S2), control unit 71 returns to step S1.

[0083] In step S3, the control unit 71 determines whether or not the pump main body 10 is attached to the cradle device 11. Specifically, the control unit 71 may determine whether or not the pump main body 10 is attached to the cradle device 11 using the attachment detection switch 133. If the pump main body 10 is attached to the cradle device 11 (YES in step S3), the control unit 71 proceeds to step S4, and if not (NO in step S3), the control unit 71 proceeds to step S6.

[0084] In step S4, the control unit 71 performs a non-charging operation, which is an operation of stopping the supply of power to the rechargeable battery 42. Specifically, the control unit 71 may switch a switch provided in the charging circuit unit 74 to the disconnection state, thereby electrically disconnecting the connector unit 75 and the rechargeable battery 42.

[0085] In step S5, the control unit 71 notifies the user of an alert. Specifically, for example, the control unit 71 may transmit an alert notification signal via the communication unit 73 to the remote control 90 for operating the drug solution administration device 1, and cause the output unit 95 of the remote control 90 to notify the alert. For example, the remote control 90 may display an image indicating that the charging cable should be unplugged on the display of the output unit 95, light an LED in red or the like, output an alarm sound from the speaker of the output unit 95, or vibrate using a vibrator. The pump main body 10 may also output an alarm sound or vibrate using a vibrator, similar to the remote control 90. Alternatively, the control unit 71 may notify the alert by causing the notification unit 77 of the pump main body 10 to perform at least one of image display, audio output, LED lighting, and vibration. After completing the processing of step S5, the control unit 71 returns to step S1.

[0086] In step S6, the control unit 71 performs a charging operation, which is an operation of supplying power to the rechargeable battery 42. Specifically, the control unit 71 may connect a switch provided in the charging circuit unit 74 to electrically connect the connector unit 75 and the rechargeable battery 42. After completing the process of step S6, the control unit 71 returns to step S1.

[0087] In step S11 of Fig. 11, control unit 71 determines whether a charging cable or an external power source is connected to connector unit 75. This connection determination can be performed, for example, in the same manner as in step S2 of Fig. 10. If a charging cable or an external power source is connected (YES in step S11), control unit 71 proceeds to step S12, and if not (NO in step S11), control unit 71 returns to step S1 of Fig. 10.

[0088] In step S12, the control unit 71 stops the liquid delivery. Specifically, the control unit 71 stops driving the motor 44. When the predetermined schedule for administering the medicinal liquid is interrupted due to the stop of the liquid delivery, the control unit 71 may store the status of the interrupted liquid delivery in the memory unit 72. The status of the liquid delivery can be used when resuming the administration of the medicinal liquid.

[0089] In step S13, the control unit 71 determines whether the pump main body 10 is attached to the cradle device 11. The determination of attachment to the cradle device 11 can be performed, for example, in the same manner as in step S3 of Fig. 10. If the pump main body 10 is attached to the cradle device 11 (YES in step S13), the control unit 71 proceeds to step S4 of Fig. 10, and if not (NO in step S13), the control unit 71 proceeds to step S14.

[0090] In step S14, the control unit 71 performs a charging operation, which is an operation of supplying power to the rechargeable battery 42. The charging operation can be performed, for example, in the same manner as in step S6 of Fig. 10. After completing the process of step S14, the control unit 71 proceeds to step S15.

[0091] In step S15, control unit 71 determines whether a charging cable or an external power source is connected to connector unit 75. This connection determination can be performed, for example, in the same manner as in step S2 of Fig. 10. If a charging cable or an external power source is connected (YES in step S15), control unit 71 returns to step S13, and if not (NO in step S15), control unit 71 proceeds to step S16.

[0092] In step S16, the control unit 71 resumes the liquid delivery operation. Specifically, the control unit 71 resumes driving the motor 44. For example, if the state of the interrupted liquid delivery is stored in the memory unit 72, the control unit 71 may control the driving of the motor 44 to resume the schedule for administering the medicinal liquid from the state of the interrupted liquid delivery.

[0093] After it is confirmed that the charging cable has been removed (NO in step S15), the control unit 71 may not automatically resume the liquid delivery operation, but may resume the liquid delivery operation in response to a command to resume the liquid delivery operation from the user via the remote control 90. Vibrations, etc., associated with inserting and removing the charging cable at the connector unit 75 may cause the pump body 10 and the cradle device 11 to be incompletely attached. Therefore, by resuming the liquid delivery in response to a command from the user rather than automatically after the charging cable is removed, it is possible to prevent liquid leakage, etc., from occurring when the pump body 10 and the cradle device 11 are incompletely attached to each other.

[0094] Furthermore, the chemical solution administration device 1 may drive the motor 44 for the purpose of priming even when the pump body 10 is not attached to the cradle device 11. Priming refers to an operation of engaging the nut portion 24 of the chemical solution administration device 1 with the plunger 20 and filling the flow path of the chemical solution administration device 1, including the outlet tube 29, with the chemical solution. Regarding the driving of the motor 44 for such priming, the control unit 71 may be configured to automatically resume the delivery of the chemical solution after the charging cable or external power source is removed.

[0095] Furthermore, in order to prevent the sealing member 34 from adhering to the inner wall surface of the reservoir 18 when the liquid supply stop state continues for a predetermined time or longer, the liquid supply device 1 may automatically drive the motor 44 even when the pump body 10 is not attached to the cradle device 11 or during the charging operation of step S14. Specifically, the liquid supply device 1 may repeatedly rotate the motor 44 forward and backward at regular intervals. The control unit 71 may continue driving the motor 44 to prevent the sealing member 34 from adhering until the charging cable is unplugged. The control unit 71 may automatically resume the delivery of liquid for treatment after a certain time has elapsed since the charging cable was unplugged.

[0096] After completing the process of step S16, the control unit 71 returns to step S1 in FIG.

[0097] As described above, when a charging cable or an external power source is connected to connector 75 while pump body 10 is attached to cradle device 11, medicinal solution administration device 1 issues an alert, stops charging, or stops driving motor 44. Therefore, medicinal solution administration device 1 can prevent problems such as electric leakage, terminal shorts, and excessive power supply.

[0098] In this embodiment, the pump body 10 that delivers a medicinal solution into the patient's body is configured as a syringe pump, but the principle of medicinal solution administration is not limited to a syringe. For example, the pump body 10 may be a roller pump, a PCA (Patient Controlled Analgesia) pump, or other pumps.

[0099] The present disclosure is not limited to the above-described embodiments. For example, multiple blocks shown in the block diagrams may be integrated, or one block may be divided. Multiple steps shown in the flowcharts may be executed in parallel or in a different order depending on the processing capabilities of the device executing each step, or as needed, instead of being executed in chronological order as described. Other modifications are possible without departing from the spirit of the present disclosure.

[0100] Furthermore, for example, the configuration and operation of the drug solution administration device 1 may be distributed among multiple computers that can communicate with each other. Furthermore, for example, some or all of the components of the drug solution administration device 1 may be provided in another device such as a remote control 90.

[0101] DESCRIPTION OF SYMBOLS 1 Drug solution administration device 10 Pump body 11 Cradle device 12 Cartridge 14 Device body 16 Base portion 18 Reservoir 20 Plunger 22 Feed screw shaft 24 Nut portion 26 Inlet port 28 Outlet port 29 Outlet pipe 30 Plunger body 32 Pusher 34 Seal member 36 Extension portion 38 Claw portion 39 Bearing 40 Drive portion 42 Rechargeable battery 44 Motor 46 Gear box 48 Output gear 50 Spur gear 52 Transmission shaft 54 ​​Terminal 56 Bearing 58 Nut portion body 60 Slide portion 62 Threaded hole 64 Through hole 66 Reinforcement cover 68 Guide wall 71 Control unit 72 Memory unit 73 Communication unit 74 Charging circuit unit 75 Connector unit 79 Bus 106 Cannula port 111 Housing 112 Connecting needle tube 121 Top surface 122 Bottom surface 123 Front surface 124 Back surface 125 First side surface 126 Second side surface 127 Bottom storage section 127a Wall surface 128 Connection port 128a Cylinder hole 131 Fitting protrusion 132 Slide groove 133 Mounting detection switch 134 Detection groove 135 First guide groove 136 First engaging hook 137 Second guide groove 138 Second engaging hook 141 Placement surface 143 Side wall 144 Side wall 151 Guide rail 152 Detection rail 153 Slide rail 154 Fitting hole 155 Mounting section 156 Posture correction section 158 Notch 162 Engagement receiving portion 181 Port body 182 Cap 90 Remote control 91 Control unit 92 Storage unit 93 Communication unit 94 Input unit 95 Output unit 99 Bus 100 Drug solution administration system

Claims

1. A drug solution administration device comprising a pump body for administering a drug solution filled in a reservoir into the body of a patient, the pump body comprising: a pump for transporting the drug solution filled in the reservoir into the body of the patient; a rechargeable battery for supplying power to drive the pump; a connector section to which a charging cable or an external power source for charging the rechargeable battery can be connected; a detection section for detecting whether the pump body is attached to a cradle device attached to the skin of the patient; and a control section, wherein the control section causes an alarm section to issue an alert in response to the charging cable or the external power source being connected to the connector section while it is detected that the pump body is attached to the cradle device.

2. The drug solution administration device of claim 1, wherein the control unit, in response to the charging cable or the external power source being connected to the connector unit while it is detected that the pump body is attached to the cradle device, transmits an alert notification signal via a communication unit to a remote control for operating the drug solution administration device, and causes an alert to be issued from an output unit provided in the remote control.

3. A drug solution administration device as described in claim 1, further comprising an alarm unit for notifying a user of information, wherein the control unit causes the alarm unit to issue an alert in response to the charging cable or the external power source being connected to the connector unit while it is detected that the pump body is attached to the cradle device.

4. The drug solution administration device of claim 1, further comprising a charging circuit section having a switch capable of switching between electrical connection and disconnection between the connector section and the rechargeable battery, wherein the control section switches the switch to disconnection in response to the charging cable or the external power source being connected to the connector section while the pump is transporting the drug solution into the patient's body.

5. The medicinal liquid administration device of claim 1, wherein the control unit stops the operation of the pump in response to the charging cable or the external power source being connected to the connector unit while the pump is transporting the medicinal liquid into the patient's body.

6. The drug solution administration device of claim 1, wherein the pump body comprises: a plunger provided within the reservoir and movable in the longitudinal direction of the reservoir; a movable part that moves within a movable range to engage with the plunger and press the plunger against the tip side of the reservoir; and a drive part that moves the movable part within the movable range.

7. The drug solution administration device according to claim 1, further comprising a cradle device to which the pump body can be attached.

8. A medicinal liquid administration system comprising: a medicinal liquid administration device according to any one of claims 1 to 7; and a remote control for operating the medicinal liquid administration device.

9. A control method for a drug solution administration device comprising a pump body for administering a drug solution filled in a reservoir into the patient's body, the pump body comprising: a pump for transporting the drug solution filled in the reservoir into the patient's body; a rechargeable battery for supplying power to drive the pump; a connector section to which a charging cable or an external power source for charging the rechargeable battery can be connected; a detection section for detecting whether the pump body is attached to a cradle device attached to the patient's skin; and a control section, the control section including a step of causing an alarm section to issue an alert in response to the charging cable or the external power source being connected to the connector section while it is detected that the pump body is attached to the cradle device.

10. A program for controlling a drug solution administration device having a pump body for administering a drug solution filled in a reservoir into the patient's body, the pump body comprising: a pump for transporting the drug solution filled in the reservoir into the patient's body; a rechargeable battery for supplying power to drive the pump; a connector section to which a charging cable or an external power source for charging the rechargeable battery can be connected; a detection section for detecting whether the pump body is attached to a cradle device that is attached to the patient's skin; and a control section; and the program causes the control section to execute a procedure for causing an alarm section to issue an alert in response to the charging cable or the external power source being connected to the connector section while it is detected that the pump body is attached to the cradle device.