WO2017086458A1 - Medical pump system, medical pump control method, medical pump control program, and medical pump - Google Patents
Medical pump system, medical pump control method, medical pump control program, and medical pump Download PDFInfo
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- WO2017086458A1 WO2017086458A1 PCT/JP2016/084314 JP2016084314W WO2017086458A1 WO 2017086458 A1 WO2017086458 A1 WO 2017086458A1 JP 2016084314 W JP2016084314 W JP 2016084314W WO 2017086458 A1 WO2017086458 A1 WO 2017086458A1
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- liquid
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- pipe
- blockage
- pump
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/142—Pressure infusion, e.g. using pumps
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
Definitions
- the present invention relates to a medical pump system, a medical pump control method, a medical pump control program, and a medical pump, for example, for sending a chemical solution to a patient or the like.
- a medical pump such as an infusion pump or a syringe pump has been used in order to accurately control the dose, administration rate, and the like.
- a medical pump administers a drug solution containing a drug or the like to a patient via a tube.
- the tube may be blocked when the tube is bent or twisted during the administration of the drug solution. If the medical pump continues to feed the drug solution even during the occlusion, the pressure increases in the tube, and therefore, the drug solution may be rapidly sent to the patient when the occlusion is released. Therefore, for example, in a syringe pump, when the blockage sensor detects blockage, a proposal has been made to alleviate the pressure increase by causing the motor to reversely rotate without continuously feeding liquid (for example, Patent Document 1). etc).
- a medical solution may be administered to a patient using a plurality of medical pumps.
- the tubes containing the chemicals sent by each medical pump are not sent separately to the patient via needles, catheters, etc., and finally through the co-infusion unit, into one tube, In many cases, each chemical is sent.
- each of the plurality of medical pumps has a separate occlusion sensor, a difference in pressure detection accuracy, a difference in occlusion determination setting, and the like are generated by each occlusion sensor.
- the present invention provides a medical pump system capable of accurately preventing the occurrence of a “suction phenomenon” in which a liquid such as a chemical solution is sucked from one medical pump to another medical pump, and the control of the medical pump It is an object to provide a method, a control program for a medical pump, and a medical pump.
- the above object is provided with a plurality of medical pumps that control the liquid to be provided to the subject, and the medical pump moves at least the liquid in the pipe portion that stores the liquid.
- a liquid moving part capable of detecting the in-pipe state information that is state information in the pipe part, and the pipe parts respectively disposed in the plurality of medical pumps. Is configured so that the liquids that are merged at the merging unit and the liquids contained therein are merged, and a blockage determination unit that generates blockage information of the tube unit based on the state information in the tube unit
- the liquid moving part is configured to be switchable between a liquid feeding mode for moving the liquid in the pipe part in the liquid feeding direction and a counter liquid feeding mode for moving in the counter liquid feeding direction.
- the liquid delivery module It is configured to change to the operation of the reaction liquid feeding mode based on the blockage information, and the blockage information is configured to be notified to the other medical pumps. This is achieved by the medical pump system that is characterized.
- the pipe part each arrange
- a merge part for example, "mixed injection part” etc.
- the liquid moving unit after the liquid moving unit operates in the liquid feeding mode, the liquid moving unit is configured to change to the operation in the counter liquid feeding mode based on the blockage information of the blockage determination unit. It is the structure notified to. Therefore, the other medical pumps that have received the occlusion information can stop the liquid feeding mode, so that one medical pump causes the liquid moving unit to execute in the operation of the counter liquid feeding mode. However, it is possible to prevent the occurrence of a “suction phenomenon” that sucks the liquid on the other side of the medical pump. Further, since the operation in the liquid feeding mode is executed, it is possible to prevent the occurrence of a situation in which the liquid is suddenly fed from the tube portion to the patient or the like when the blocked state is resolved.
- the liquid moving unit is configured to change to the operation in the counterfeed mode after the blockage information is notified to the other medical pump.
- the liquid moving unit is configured to change to the operation in the counter-feeding mode after the blockage information is notified to the other medical pumps. Even if the moving unit is executed in the operation of the liquid feeding mode, it is possible to more reliably prevent the occurrence of the “suction phenomenon” in which the liquid on the other medical pump side is sucked.
- a management device capable of communicating with the medical pump is provided, and the blockage information is notified from the management device to another medical pump.
- the blockage information since the blockage information is notified from the management device to another medical pump, the blockage information can be managed more reliably.
- the liquid feeding mode stop information generating unit is configured to generate counter liquid feeding mode stop information that is stop information of the counter liquid feeding mode based on the in-pipe state information.
- the said structure has the counter liquid feeding mode stop information generation part which produces
- the state information in the pipe part is pressure value information in the pipe part which is a pressure value in the pipe part, and when the pressure value information in the pipe part corresponds to information indicating a block state in the pipe part, And the expected liquid amount information corresponding to the pressure value in the pipe portion that stores the information on the expected staying liquid amount that is retained by the reaction liquid supply mode stop information generation unit based on the expected staying liquid amount information.
- the liquid mode stop information is generated.
- the reaction liquid supply mode stop information generation unit generates the reaction liquid supply mode stop information based on the expected liquid amount information (for example, the assumed chemical liquid amount).
- the counter liquid feeding mode is executed only for the amount of information on the expected staying liquid amount. Accordingly, when the occlusion state is resolved, it is possible to prevent the drug solution or the like from being rapidly sent from the pipe part to the patient, and to appropriately manage the amount of the drug solution flowing out.
- the above object is provided with a plurality of medical pumps that control the liquid to be provided to the subject, and the medical pump moves at least the liquid in the pipe portion that stores the liquid.
- a liquid moving part capable of detecting the in-pipe state information that is state information in the pipe part, and the pipe parts respectively disposed in the plurality of medical pumps. Is configured so that the liquids that are merged at the merging unit and the liquids contained therein are merged, and a blockage determination unit that generates blockage information of the tube unit based on the state information in the tube unit
- the liquid moving part is configured to be switchable between a liquid feeding mode for moving the liquid in the pipe part in the liquid feeding direction and a liquid feeding mode for moving in the counter liquid feeding direction.
- the above object is provided with a plurality of medical pumps that control the liquid to be provided to the subject, and the medical pump moves at least the liquid in the pipe portion that stores the liquid.
- a liquid moving part capable of detecting the in-pipe state information that is state information in the pipe part, and the pipe parts respectively disposed in the plurality of medical pumps.
- the liquid moving part is provided in a medical pump system configured to be switchable between a liquid feeding mode for moving the liquid in the pipe part in the liquid feeding direction and a counter liquid feeding mode for moving in the counter liquid feeding direction.
- the liquid transfer After the operation in the liquid delivery mode, based on the blockage information, the step of changing to the counter liquid delivery mode operation, and the step of notifying the blockage information to the other medical pump, This is achieved by a control program for a medical pump characterized by being executed.
- the above object is a medical pump for controlling a liquid to be provided to a subject, wherein the medical pump moves at least the liquid in a pipe portion that stores the liquid.
- a liquid moving part that can be formed, and an in-pipe state information detecting unit that detects state information in the pipe part that is state information in the pipe part, and the pipe part disposed in the medical pump is a confluence part.
- the pipe is configured to merge with the liquid, and includes a blockage determination unit that generates blockage information of the pipe unit based on the state information in the pipe unit, and the liquid moving unit includes the liquid moving unit in the pipe unit.
- the liquid feeding mode is This is achieved by a medical pump characterized in that the blockage information is notified to another medical pump in which the other pipe section is arranged. .
- a medical pump system that can accurately prevent the occurrence of a “suction phenomenon” in which a liquid such as a chemical solution is sucked from one medical pump to another medical pump.
- a medical pump control method, a medical pump control program, and a medical pump can be provided.
- FIG. 1 It is the schematic which shows the pump system which is the medical pump system of this invention, for example. It is the schematic which shows the main structures of the infusion pump of FIG. It is a schematic explanatory drawing which shows the main structures of the liquid feeding drive part of the infusion pump shown in FIG. It is the schematic which shows the main structures of the syringe pump of FIG. It is a schematic explanatory drawing which shows the example which forms the same infusion line using the infusion pump and syringe pump of FIG. It is a schematic block diagram shown with the main structures of the management server of FIG. It is a schematic block diagram which shows the main structures of the server side various information storage part. It is a schematic block diagram which shows the main structures of the infusion pump shown in FIG.
- FIG. 1 is a schematic view showing, for example, a pump system 1 which is a medical pump system of the present invention.
- the pump system 1 is a system in a hospital, and has a management server 300 composed of a computer or the like that is a management device, and is in a state where it can communicate with the management server 300.
- a plurality of medical pumps for example, infusion pumps 10, 110, 120, 130 and syringe pumps 500, 530, 540, 550 are connected.
- the infusion pump 10 and the like and the syringe pump 500 and the like are pump identification information such as “A-1” to “A-4” and “B-1” to “B-4” which are pump identification numbers, respectively. The number is given.
- FIG. 2 is a schematic diagram showing the main configuration of the infusion pump 10 of FIG. Since the infusion pump 110 and the like in FIG. 1 have the same configuration as the infusion pump 10, the description thereof is omitted.
- the infusion pump 10 includes a pump-side display 21 that is a display unit that displays various types of information, and includes various operation buttons 22.
- a pilot lamp 22a that includes an LED inside, emits and displays light through a light diffusing agent, and indicates the operating state of the infusion pump 10, and fast-forward for injecting a chemical at an injection rate faster than a set flow rate (mL / h)
- a switch button 22b, a start switch button 22c, a stop switch button 22d, a menu selection button 22e, and the like are arranged.
- the infusion pump 10 is a liquid moving unit for pressing the pump-side tube 11 a and feeding a chemical solution therein, for example, a pipe unit disposed therein.
- a liquid feeding drive unit 30 is arranged.
- in-pipe state information for detecting a blockage or the like in the pump side tube 11a upstream from the liquid feeding drive unit 30 For example, an upstream blockage sensor 16 that is a detection unit is disposed.
- the in-pipe state information for detecting the blockage in the pump side tube 11a downstream from the liquid feeding drive unit 30 A downstream block sensor 17 serving as a detection unit is disposed.
- the upstream blockage sensor 16 and the downstream blockage sensor 17 are pressure sensors, for example, and are configured to detect the pressure in the pump side tube 11a.
- FIG. 3 is a schematic explanatory view showing a main configuration of the liquid feeding drive unit 30 of the infusion pump 10 shown in FIG.
- the liquid feeding drive unit 30 includes a cam structure 32 and a finger structure 33, and has a structure for controlling the liquid feeding of the chemical solution in the pump side tube 11 a with these structures. . That is, the operation of the cam structure 32 is configured to accurately control the feeding of the chemical solution in the pump side tube 11a.
- the finger structure 33 has six fingers 33a to 33f corresponding to the six cams 32a to 32f. ing.
- the six cams 32 a to 32 f are arranged with a phase difference from each other, and the cam structure 32 is connected to the output shaft 18 a of the drive motor 18. That is, when the drive motor 18 of FIG. 3 is driven and rotated, the plurality of fingers 33a to 33f are individually driven in the Y direction of FIG. 3 via the cams 32a to 32f, and the outer peripheral surface of the pump side tube 11a is shown in FIG. Are sequentially pressed along the T direction to feed the chemical solution in the pump side tube 11a (an example of a liquid feeding mode).
- the liquid feeding drive unit 30 controls the peristaltic movements of the plurality of fingers 33a to 33f to sequentially move the fingers 33a to 33f back and forth so that the wave travels, so that the pump side
- the chemical solution is transferred by squeezing the pump side tube 11a by moving the blockage point in the tube 11a in the T direction. Therefore, by rotating the drive motor 18 in FIG. 3 in reverse (operation), the liquid feeding direction of the chemical solution in the pump side tube 11a can be changed in the reverse direction (the direction opposite to the T direction in FIG. 3). It has a configuration (an example of a reverse liquid feeding mode).
- FIG. 4 is a schematic diagram showing the main configuration of the syringe pump 500 of FIG. Since the syringe pump 530 and the like in FIG. 1 have the same configuration as the syringe pump 500, description thereof is omitted.
- the syringe pump 500 is configured to fix a syringe body 511 of a syringe 510 filled with a chemical solution using a clamp 512.
- the feed screw is rotated by the rotation of the drive motor of the syringe pusher drive unit 517, and the syringe pusher pressing member 513 can press the syringe pusher 514 of the syringe 510 in the F direction toward the syringe body 511 side.
- the syringe pusher pressing member 513 and the syringe pusher 514 are examples of the liquid moving unit.
- medical solution in the syringe main body 511 can be liquid-fed to the pump side tube 11a (an example of liquid feeding mode).
- the structure which can move a chemical
- the syringe pusher pressing member 513 is provided with a blockage sensor 519 (an example of an in-pipe state information detection unit) and can acquire a blockage detection value.
- the syringe pump 500 has a syringe-side display 516 that displays various information, and also includes various syringe operation buttons 518.
- a medical worker for example, a nurse or the like administers a plurality of, for example, two types of chemical liquids to a target person, for example, a patient P, for example, according to a doctor's prescription, (For example, a case where a plurality of drugs are combined and finally administered to the patient P through one tube) is performed.
- FIG. 5 is a schematic explanatory diagram illustrating an example in which the same infusion line is formed using the infusion pump 10 and the syringe pump 500 of FIG. 1.
- the infusion pump 10 has a pump-side tube 11a disposed therein, and presses the pump-side tube 11a to feed, for example, a liquid medicine in the pump-side tube 11a.
- the syringe pump 500 has a syringe 510 inside, and the syringe 510 pushes out a chemical solution.
- medical solution container (syringe) 510 which accommodate the chemical
- These chemical containers 12a and 510 are configured to supply a chemical solution via the pump side tubes 11a and 11b, respectively.
- the two pump side tubes 11a and 11b are connected to, for example, a co-injection unit 13 which is a junction.
- the mixed injection part 13 is connected to, for example, a patient side tube 14 that is a subject side tube part, and the patient side tube 14 is connected to a blood vessel such as an arm of the patient P via an indwelling needle 15 or the like.
- the chemical solutions in the two pump-side tubes 11a and 11b in FIG. 5 are combined at the co-injection unit 13 and are administered to the patient via the patient-side tube 14 and the indwelling needle 15 or the like.
- the infusion pump 10 and the like, the syringe pump 500 and the like, and the management server 300 shown in FIG. 1 have a computer.
- the computer is not shown, such as a CPU (Central Processing Unit), a RAM (Random Access Memory), a ROM (Read Only Memory), and the like. These are connected via a bus.
- CPU Central Processing Unit
- RAM Random Access Memory
- ROM Read Only Memory
- FIG. 6 is a schematic block diagram showing the main configuration of the management server 300 of FIG.
- the management server 300 includes a “server control unit 301”.
- the server control unit 301 includes a “server-side communication device 302” that allows the management server 300 to communicate with the infusion pump 10 and the like.
- a “server-side display 303” for displaying information and a “server-side various information input device 304” for inputting various information are controlled.
- the server control unit 301 also controls a “server-side various information storage unit 310” shown in FIG.
- FIG. 7 is a schematic block diagram showing the main configuration of the server-side various information storage unit 310. Specific contents thereof will be described later.
- FIG. 8 is a schematic block diagram showing the main configuration of the infusion pump 10 shown in FIG. Since the infusion pump 110 and the like have the same configuration as the infusion pump 10, only the infusion pump 10 will be described below.
- the infusion pump 10 includes a “pump control unit 41”, and the pump control unit 41 includes a “pump-side communication device 42” for the infusion pump 10 to communicate with the management server 300 and the like. 2 controls the pump-side display 21, the drive motor 18, the upstream block sensor 16, the downstream block sensor 17, and the like.
- the pump-side control unit 41 also controls a “first various information storage unit 50”, a “second various information storage unit 60”, and a “third various information storage unit 70” illustrated in FIG.
- FIGS 9 to 11 are schematic block diagrams showing main configurations of the “first various information storage unit 50”, the “second various information storage unit 60”, and the “third various information storage unit 70”, respectively. is there. Specific contents thereof will be described later.
- step (ST”) 1 in FIG. 12 the management server 300 in FIG. 1 includes the management server 300, the infusion pump 10 and the like shown in FIG.
- Pump identification numbers for example, “A-1” to “A-4” and “B-1” to “B-4” are stored in association with “communication addresses”. Specifically, it is stored in the “server-side pump information storage unit 311” in FIG.
- the management server 300 can identify and manage the infusion pump 10 and the syringe pump 500 in the hospital and can communicate with each other.
- a medical staff such as a nurse uses the infusion pump 10 (A-1) and the syringe pump 500 (B-1) to administer two different drugs to the patient P.
- Start administration preparation Specifically, as shown in FIG. 5, two chemical liquid containers 12 a and 510, pump-side tubes 11 a and 11 b connected to these, and a mixed injection part 13 and a pipe part connected to the mixed injection part 13.
- the infusion pump 10 (A-1) and the syringe pump 500 (B-1) are arranged in an “infusion line (infusion line identification number C-1)” composed of the patient-side tube 14 and the like.
- the “infusion line identification number (C-1)” is input to the infusion pump 10 (A-1) and the syringe pump 500 (B-1) by a nurse or the like.
- This infusion line identification number (C-1) is stored in the “pump-side pump information storage unit 57” of the infusion pump 10 (A-1) shown in FIG. 9 (the same applies to the syringe pump 500 (B-1)).
- the “infusion line identification number transmission processing unit (program) 58” of FIG. 9 operates and refers to the “pump-side pump information storage unit 57”, and when the “infusion line identification number” is stored,
- the “infusion line identification number”, for example, “C-1” is transmitted as the “infusion line identification number” to the management server 300 and the own “pump identification number (A-1, B-1, etc.)” Are also transmitted to the management server 300.
- the management server 300 receives the “infusion line identification number (C-1)” and “pump identification numbers (A-1, B) received from the infusion pump 10 (A-1) and the syringe pump 500 (B-1). -1), the “infusion line identification number (C-1)” is stored in the “infusion line identification number” corresponding to the pump in the “server-side pump information storage unit 311”.
- the “infusion line” shown in FIG. 5 is specified by the “infusion line identification number (C-1)” in the management server 300, and the infusion pump 10 and the syringe pump 500 included in the infusion line are also included. Identified and stored. Therefore, the management server 300 can accurately grasp and manage which infusion pump 10 or the like is located in which infusion line.
- the preparation for administration of the drug solution is thus completed, and the drug solution administration process and the like will be described below with reference to FIG.
- the same infusion line is formed using the infusion pump 10 and the syringe pump 500, and the drug solution of the two drug bags 12 a and 12 b is administered to the patient P.
- the following description is based on an example in which the downstream blockage sensor 17 of the infusion pump 10 detects the blockage of the pump side tube 11a before the blockage sensor 519 of the syringe pump.
- data of “scheduled liquid feeding amount information” that is a scheduled liquid feeding amount of each drug solution to be administered to the patient P is input to the infusion pump 10 and the syringe pump 500.
- the infusion pump 10 will be mainly described in the present embodiment, the same software configuration is also mounted on the syringe pump 500.
- the data of the “scheduled delivery amount information” is stored in the “infusion pump side scheduled delivery amount information storage unit 51” of the infusion pump 10 of FIG.
- the infusion pump 10 and the syringe pump 500 operate to start the liquid feeding mode, for example, liquid feeding, and proceed to ST2.
- the infusion pump 10 and the syringe pump 500 are operated to start feeding the liquid medicine at a predetermined speed, and the “downstream occlusion sensor 17” of the infusion pump 10 and the occlusion sensor 519 of the syringe pump 500 are pump side tubes.
- measurement of “occlusion detection pressure” that is state information in the pipe portion in 11a and the like is started.
- the process proceeds to ST13 and ST14.
- the “integrated liquid feeding amount information calculation processing unit (program) 52” in FIG. 9 operates and refers to the “liquid feeding amount reference information storage unit 53” in FIG.
- liquid supply amount reference information that is the relationship information between the rotational speed of the drive motor 18 and the liquid supply amount, that is, how many times the drive motor 18 rotates. Information about whether the amount of liquid to be fed is stored.
- the integrated liquid supply amount information calculation processing unit (program) 52 obtains the “integrated liquid supply amount information” of the infusion pump 10 from the predetermined “liquid supply amount reference information” and the “rotation amount” information of the drive motor 18. The calculated value is stored in the “integrated liquid feeding amount information storage unit 54” in FIG. 9 (the same applies to the syringe pump 500). As described above, the cumulative liquid supply amount information storage unit 54 stores information on the cumulative liquid supply amount of the chemical solution such as the infusion pump 10.
- the infusion pump 10 stores the occlusion detection value of the “downstream occlusion sensor 17” in the “downstream occlusion detection value storage unit 55” in FIG. 5 (in the syringe pump 500, the “occlusion detection of the occlusion sensor 519”. Value ").
- the process proceeds to ST15.
- the “infusion pump blockage determination processing unit (program) 59” which is the blockage determination unit in FIG. 9 operates, and the “infusion pump blockage reference value information storage unit 56” in FIG. 9 is referred to.
- different numerical values may be stored in the infusion pump 10 and the syringe pump 500 in FIG. 1, and this case corresponds to this case.
- the syringe pump 500 sets “60 kPa” as a “blocking reference value” for determining that it is blocked, but the infusion pump 10 sets “30 kPa” as a “blocking reference value”.
- the infusion pump 10 determines that the “downstream side occlusion detection value” exceeds the occlusion reference value based on the “downstream occlusion detection value storage unit 55” and the “infusion pump occlusion reference value information storage unit 56” in FIG. Determine whether or not. That is, the infusion pump 10 determines whether or not the “downstream blocking detection value” reaches “30 kPa”.
- the syringe pump 500 in FIG. 5 determines whether or not the detection value of the “occlusion sensor 519” has reached “60 kPa”.
- the process proceeds to ST16. If the infusion pump 10 determines in ST16 that the “downstream blocking detection value” has reached “30 kPa”, it determines that a “blocking state” has occurred, and proceeds to ST17. In ST17, the “blocking flag” is attached in association with the corresponding detection value in the “downstream blocking detection value storage unit 55”.
- the blockage information is, for example, “Blockage alarm information” is transmitted to “Management server 300” together with “Pump identification number (A-1)” of “Pump-side pump information storage unit 57” in FIG.
- the management server 300 refers to the “server-side pump information storage unit 311” in FIG. 7, and transmits “blocking alarm information” “pump identification number”, for example, “blocking alarm information” for “A-1”. The presence information is stored.
- the “server side blockage alarm information transmission processing unit (program) 312” of FIG. 7 operates and the pump identification number of the infusion pump 10 in which the “blockage alarm” of the “server side pump information storage unit 311” is stored. Identify the infusion line identification number of “A-1”, eg “pump identification number” of another pump associated with “C-1”, eg, syringe pump 500 (B-1), The alarm target pump storage unit 313 is stored.
- the management server 300 sets the “communication address” corresponding to the “pump identification number (B-1)” of the “blockage alarm target pump storage unit 313” and the “server side pump information storage unit 311” in FIG. Acquired and transmits a “blocking alarm” to the syringe pump 500 (B-1) to notify that fact.
- the syringe pump 500 (B-1) that has received the “blocking alarm information” from the management server 300 stops the drive motor and stops the liquid feeding operation.
- the infusion pump 10 of FIG. 5 proceeds to ST23.
- ST23 when the “infusion pump reverse rotation operation processing section (program) 62” of FIG. 10 is operated and the “downstream closing detection value storage section 55” is attached with the “closed flag”, the drive motor 18 of the infusion pump 10 In the reverse liquid feeding mode, for example, the reverse operation is performed.
- This is a process for preventing the drug solution from suddenly flowing from the patient side tube 14 to the patient P when the blockage of the pump side tube 11a and the like is resolved.
- the drive motor of the syringe pump 500 in FIG. 5 and the like is stopped by ST22 and the liquid feeding is stopped.
- the management server 300 not the infusion pump 10, performs management such as transmission of “blocking alarm information” and the like, so that another syringe pump 500 belonging to the same infusion line (C-1). It is possible to reliably transmit “blocking alarm information” or the like.
- the “suction phenomenon” in which the infusion pump 10 sucks the chemical solution of the syringe pump 500 in the same infusion line can be prevented in advance, but as described above, the pump side tube 11a and the like are blocked.
- the pump side tube 11a and the like are blocked.
- ST24 and ST25 are executed.
- the “reverse operation integrated liquid feed amount information calculation processing section (program) 63” in FIG. 10 operates, and “liquid feed amount reference information” in the “liquid feed amount reference information storage section 53” in FIG.
- the “reverse operation integrated liquid supply information” which is the amount of the chemical solution integrated by the reverse operation of the infusion pump 10 is calculated from the “rotation amount” of 18 and the like, and “reverse operation integrated liquid supply information storage” of FIG. Part 64 ".
- the infusion pump 10 continues to store the blockage detection value of the downstream blockage sensor 17 in the “downstream blockage detection value storage unit 55” of FIG.
- the “infusion pump blockage elimination determination processing unit (program) 65” of FIG. 10 operates and is based on the “downstream side blockage detection value storage unit 55” and the “infusion pump blockage relaxation reference value information storage unit 67”. Then, it is determined whether or not the “downstream blockage detection value” is equal to or less than the blockage relaxation reference value. That is, it is determined whether or not the closed state generated in FIG. 5, for example, the state in which the pressure in the pump side tube 11a or the like due to the bending of the patient side tube 14 has increased is eliminated.
- ST29 when the “infusion pump reverse rotation operation stop processing unit (program) 66” in FIG. 10 operates and the “downstream blockage detection value storage unit 55” in FIG. 9 is flagged, the infusion pump 10 is driven.
- the reverse rotation operation of the motor 18 is stopped. Accordingly, when the reverse operation of the drive motor 18 is stopped together with the removal of the blockage, and the blockage state of the pump side tube 11a and the like is resolved, the liquid medicine is prevented from being rapidly sent from the patient side tube 14 to the patient P.
- the amount of the chemical liquid flowing out can be made appropriate.
- the process proceeds to ST30.
- the “scheduled liquid delivery amount arrival determination processing unit (program) 71” in FIG. 11 operates to operate the “reverse operation integrated liquid feed amount information storage unit 63” in FIG. 10 and “infusion pump side scheduled liquid feed in FIG. With reference to the “volume information storage unit 51”, it is determined whether or not the “reverse operation integrated liquid supply amount” has reached the “infusion pump side planned liquid supply amount”.
- the “expected discharged chemical amount information generation processing unit (program) 72” of FIG. 11 operates to acquire the blockage detection value of the “downstream blockage detection value storage unit 55”. Then, the “blockage detection value corresponding chemical liquid amount information storage unit 73” in FIG. 11 is referred to.
- the blockage detection value corresponding chemical liquid amount information storage unit 73 releases the blockage state at the blockage detection value, which is an estimated amount of drug solution that is excessively accumulated in the pump side tube 11a and the like that is assumed by the blockage detection value. Information on the amount of the assumed chemical liquid that is sometimes discharged from the pump side tube 11a or the like is stored in advance for each blockage detection value.
- the occlusion detection value corresponding chemical liquid amount information stored in the occlusion detection value corresponding chemical liquid amount information storage unit 73 is an example of the expected liquid amount information corresponding to the in-pipe pressure value.
- the assumed chemical liquid amount corresponding to the detected occlusion value is acquired from the “occluded detection value corresponding chemical liquid amount information storage unit 73” and stored in the “assumed chemical liquid amount information storage unit 74” of FIG.
- the “anticipated liquid amount determination processing unit (program) 75” which is the counter liquid supply mode stop information generation unit of FIG. 11 operates, and the “reverse operation integrated liquid supply amount information storage unit 64” of FIG. It is determined whether or not the “reverse operation integrated liquid supply amount” has reached the “assumed chemical liquid amount” in the “assumed chemical liquid amount information storage unit 74” of FIG.
- the drive motor 18 is reversely operated by the amount of the chemical liquid actually retained in the pump side tube 11a or the like, so that it is effectively retained in the pump side tube 11a or the like.
- the chemical solution can be returned to the chemical solution container 12a side.
- the occluded state it is possible to prevent the drug solution from being rapidly sent from the patient side tube 14 to the patient P.
- the present invention is not limited to the above-described embodiment and the like.
- an example of the management server 300 is shown, but the present invention is not limited to this, and a plurality of infusion pumps 10 and the like, a syringe pump 500 and the like are arranged in the same rack, and this rack is the management server 300.
- the “management apparatus” in the present invention includes not only the management server 300 but also a rack.
- the present invention may be configured such that a plurality of infusion pumps 10 and the like, the syringe pump 500 and the like communicate directly without using the management server 300 or a rack.
- Infusion pump reverse rotation stop processing unit program
- 67 Infusion pump blockage relaxation reference value information storage unit, 70 ... No. 3.
- Various information storage units 71... Scheduled liquid delivery amount arrival determination processing unit (program), 72... Expected liquid discharge amount information generation processing unit (program), 73.
- Storage unit 74 ... Assumed chemical solution amount information storage unit, 75 ... Assumed chemical solution amount judgment processing unit (program), 300 ... Management device, 301 ... Server control unit, 302 ... Server side communication Device, 303 ... Server side display, 304 ... Server side various information input device, 310 ... Server side various information storage unit, 311 ... Server side pump information storage unit, 312 ...
- Server side block Warning information Information transmission processing unit program
- 313... Occlusion alarm target pump storage unit 500, 530, 540, 550 ... Syringe pump, 510 ... Syringe (chemical solution container), 511 ... Syringe body, 512 ... Clamp, 513 ... Syringe pusher pressing member, 514 ... Syringe pusher, 516 ... Syringe side display, 517 ... Syringe pusher drive unit, 518 ... Syringe operation button, 519 ... Occlusion sensor, P ... Patient
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Abstract
[Problem] To provide a medical pump system and the like capable of precisely preventing the occurrence of a suction phenomenon in which a liquid of a liquid medicine or the like is mistakenly suctioned from one medical pump to another medical pump. [Solution] This medical pump system 1 is provided with: a plurality of medical pumps 10 having a liquid moving unit 30 for moving a liquid within a tube section 11a and a tube section inner condition information detection unit 17 for detecting tube section inner condition information, wherein the tube section disposed in the plurality of medical pumps are configured to merge at a merging section 13 and the liquid inside merges; and is further provided with a blockage determination unit 59 for generating blockage information of the tube section on the basis of tube section inner condition information of the condition information detection unit. The liquid moving unit has a configuration capable of switching between a feed mode and a counterfeed mode. The liquid moving unit changes to the operation of the counterfeed mode on the basis of the blockage information of the blockage determination unit, after operating in the feed mode, and the blockage information is reported to another medical pump.
Description
本発明は、例えば、患者等へ薬液等を送液するための医療用ポンプシステム、医療用ポンプの制御方法、医療用ポンプの制御プログラム及び医療用ポンプに関するものである。
The present invention relates to a medical pump system, a medical pump control method, a medical pump control program, and a medical pump, for example, for sending a chemical solution to a patient or the like.
従来から例えば、患者に対し薬液を投与する際に、その投与量や投与速度等を精度良く制御等するために輸液ポンプやシリンジポンプ等の医療用ポンプが用いられている。
このような医療用ポンプはチューブを介して薬剤等を含む薬液を患者に投与している。
しかし、薬液の投与中にチューブが折れ曲がったり、捻れたりすることにより、チューブが閉塞することがある。
この閉塞中も医療用ポンプが薬液を送液し続けると、チューブ内で圧力が高まるため、閉塞を解除した際に、急激に薬液が患者に送液されるおそれがある。
そこで、例えば、シリンジポンプでは、閉塞センサが閉塞を検知したとき、ポンプが引き続き送液を行わず、モータを逆転作動させて、圧力の高まりを緩和する提案がなされている(例えば、特許文献1等)。 Conventionally, for example, when a drug solution is administered to a patient, a medical pump such as an infusion pump or a syringe pump has been used in order to accurately control the dose, administration rate, and the like.
Such a medical pump administers a drug solution containing a drug or the like to a patient via a tube.
However, the tube may be blocked when the tube is bent or twisted during the administration of the drug solution.
If the medical pump continues to feed the drug solution even during the occlusion, the pressure increases in the tube, and therefore, the drug solution may be rapidly sent to the patient when the occlusion is released.
Therefore, for example, in a syringe pump, when the blockage sensor detects blockage, a proposal has been made to alleviate the pressure increase by causing the motor to reversely rotate without continuously feeding liquid (for example, Patent Document 1). etc).
このような医療用ポンプはチューブを介して薬剤等を含む薬液を患者に投与している。
しかし、薬液の投与中にチューブが折れ曲がったり、捻れたりすることにより、チューブが閉塞することがある。
この閉塞中も医療用ポンプが薬液を送液し続けると、チューブ内で圧力が高まるため、閉塞を解除した際に、急激に薬液が患者に送液されるおそれがある。
そこで、例えば、シリンジポンプでは、閉塞センサが閉塞を検知したとき、ポンプが引き続き送液を行わず、モータを逆転作動させて、圧力の高まりを緩和する提案がなされている(例えば、特許文献1等)。 Conventionally, for example, when a drug solution is administered to a patient, a medical pump such as an infusion pump or a syringe pump has been used in order to accurately control the dose, administration rate, and the like.
Such a medical pump administers a drug solution containing a drug or the like to a patient via a tube.
However, the tube may be blocked when the tube is bent or twisted during the administration of the drug solution.
If the medical pump continues to feed the drug solution even during the occlusion, the pressure increases in the tube, and therefore, the drug solution may be rapidly sent to the patient when the occlusion is released.
Therefore, for example, in a syringe pump, when the blockage sensor detects blockage, a proposal has been made to alleviate the pressure increase by causing the motor to reversely rotate without continuously feeding liquid (for example, Patent Document 1). etc).
ところで、医療用ポンプを複数用いて薬液を患者に投与する場合がある。この場合、各医療用ポンプが送液する薬液を収容するチューブはそれぞれ別々に針やカテーテル等を介して患者に送液することなく、混注部を介して、最終的に1本のチューブに、それぞれの薬液を送液することが多い。
また、複数の医療用ポンプは、それぞれ別個の閉塞センサを有しているため、各閉塞センサによって圧力検知の精度の相違や閉塞判断の設定の相違等が発生する。 By the way, a medical solution may be administered to a patient using a plurality of medical pumps. In this case, the tubes containing the chemicals sent by each medical pump are not sent separately to the patient via needles, catheters, etc., and finally through the co-infusion unit, into one tube, In many cases, each chemical is sent.
In addition, since each of the plurality of medical pumps has a separate occlusion sensor, a difference in pressure detection accuracy, a difference in occlusion determination setting, and the like are generated by each occlusion sensor.
また、複数の医療用ポンプは、それぞれ別個の閉塞センサを有しているため、各閉塞センサによって圧力検知の精度の相違や閉塞判断の設定の相違等が発生する。 By the way, a medical solution may be administered to a patient using a plurality of medical pumps. In this case, the tubes containing the chemicals sent by each medical pump are not sent separately to the patient via needles, catheters, etc., and finally through the co-infusion unit, into one tube, In many cases, each chemical is sent.
In addition, since each of the plurality of medical pumps has a separate occlusion sensor, a difference in pressure detection accuracy, a difference in occlusion determination setting, and the like are generated by each occlusion sensor.
このような医療用ポンプが、混注部を介して1本のチューブで薬液を患者等に投与する際に、当該チューブに閉塞が発生すると、医療用ポンプ毎に閉塞と判断する時期等が相違するおそれがある。すなわち、或る医療用ポンプは、閉塞を検知して,モータを逆転作動(動作)するが、他の医療用ポンプは、引き続き送液動作を実行するという事態が発生する。
この場合、各医療用ポンプが送液する薬液を収容する各チューブが接続されている「混注部」で以下のような問題が発生するおそれがある。
すなわち、引き続き送液を実行している医療用ポンプの薬液等が、「混在部」を介して、逆転動作を実行している医療用ポンプ側に吸引される「吸引現象」が発生するという問題がある。 When such a medical pump administers a drug solution to a patient or the like with a single tube via a co-infusion unit, when the tube is clogged, the timing for determining the clogging for each medical pump is different. There is a fear. That is, a certain medical pump detects a blockage and reversely operates (operates) the motor, while another medical pump continues to execute a liquid feeding operation.
In this case, there is a possibility that the following problems may occur in the “mixed injection portion” to which each tube that stores the chemical solution sent by each medical pump is connected.
In other words, there is a problem that a “suction phenomenon” occurs in which the chemical liquid or the like of the medical pump that is continuously performing liquid feeding is sucked through the “mixed part” to the medical pump that is performing the reverse rotation operation. There is.
この場合、各医療用ポンプが送液する薬液を収容する各チューブが接続されている「混注部」で以下のような問題が発生するおそれがある。
すなわち、引き続き送液を実行している医療用ポンプの薬液等が、「混在部」を介して、逆転動作を実行している医療用ポンプ側に吸引される「吸引現象」が発生するという問題がある。 When such a medical pump administers a drug solution to a patient or the like with a single tube via a co-infusion unit, when the tube is clogged, the timing for determining the clogging for each medical pump is different. There is a fear. That is, a certain medical pump detects a blockage and reversely operates (operates) the motor, while another medical pump continues to execute a liquid feeding operation.
In this case, there is a possibility that the following problems may occur in the “mixed injection portion” to which each tube that stores the chemical solution sent by each medical pump is connected.
In other words, there is a problem that a “suction phenomenon” occurs in which the chemical liquid or the like of the medical pump that is continuously performing liquid feeding is sucked through the “mixed part” to the medical pump that is performing the reverse rotation operation. There is.
そこで、本発明は、一の医療用ポンプから他の医療用ポンプへ薬液等の液体が吸引される「吸引現象」の発生を精度良く防止することができる医療用ポンプシステム、医療用ポンプの制御方法、医療用ポンプの制御プログラム及び医療用ポンプを提供することを目的とする。
Therefore, the present invention provides a medical pump system capable of accurately preventing the occurrence of a “suction phenomenon” in which a liquid such as a chemical solution is sucked from one medical pump to another medical pump, and the control of the medical pump It is an object to provide a method, a control program for a medical pump, and a medical pump.
上記目的は、本発明にあっては、対象者に提供する液体を制御する複数の医療用ポンプを備え、前記医療用ポンプは、少なくとも、前記液体を収容する管部内の前記液体を移動させることができる液体移動部と、前記管部内の状態情報である管部内状態情報を検知する管部内状態情報検知部と、を有し、複数の前記医療用ポンプに、それぞれ配置されている前記管部は、合流部で合流し、それぞれの内部に収容されている前記液体が合流する構成となっており、また、前記管部内状態情報に基づき、前記管部の閉塞情報を生成する閉塞判断部を備え、前記液体移動部は、前記管部内の前記液体を送液方向に移動させる送液モードと、反送液方向に移動させる反送液モードに切り替え可能な構成となっており、前記液体移動部は、前記送液モードで動作した後、前記閉塞情報に基づき、前記反送液モードの動作に変更する構成となっており、前記閉塞情報は、他の前記医療用ポンプに報知される構成となっていることを特徴とする医療用ポンプシステムにより達成される。
In the present invention, the above object is provided with a plurality of medical pumps that control the liquid to be provided to the subject, and the medical pump moves at least the liquid in the pipe portion that stores the liquid. And a liquid moving part capable of detecting the in-pipe state information that is state information in the pipe part, and the pipe parts respectively disposed in the plurality of medical pumps. Is configured so that the liquids that are merged at the merging unit and the liquids contained therein are merged, and a blockage determination unit that generates blockage information of the tube unit based on the state information in the tube unit And the liquid moving part is configured to be switchable between a liquid feeding mode for moving the liquid in the pipe part in the liquid feeding direction and a counter liquid feeding mode for moving in the counter liquid feeding direction. The liquid delivery module It is configured to change to the operation of the reaction liquid feeding mode based on the blockage information, and the blockage information is configured to be notified to the other medical pumps. This is achieved by the medical pump system that is characterized.
前記構成によれば、複数の医療用ポンプに、それぞれ配置されている管部は、合流部(例えば、「混注部」等)で合流し、それぞれの内部に収容されている液体が合流する構成となっている。
すなわち、一の医療用ポンプの液体移動部が、送液モードで動作した後、閉塞判断部の閉塞情報に基づき、反送液モードの動作に変更しても、他の医療用ポンプは送液モードの動作を依然として実行していると、合流部を介して他の医療用ポンプが送液する液体を、一の医療用ポンプが吸引する「吸引現象」が発生するおそれがある、
この点、前記構成では、液体移動部は、送液モードで動作した後、閉塞判断部の閉塞情報に基づき、反送液モードの動作に変更する構成となり、閉塞情報は、他の医療用ポンプに報知される構成となっている。
したがって、閉塞情報を受信した他の医療用ポンプは、その送液モードを停止することができ、これにより、一の医療用ポンプは、液体移動部を、反送液モードの動作で実行させても、他の医療用ポンプ側の液体を吸引する「吸引現象」の発生を未然に防止することができる。
また、前記反送液モードの動作を実行するので、閉塞状態が解消したとき、液体が管部から患者等の側に急激に送液されてしまうという事態の発生も防止することができる。 According to the said structure, the pipe part each arrange | positioned at several medical pumps merges by a merge part (for example, "mixed injection part" etc.), and the liquid accommodated in each inside merges It has become.
That is, even if the liquid moving part of one medical pump operates in the liquid feeding mode and then changes to the operation in the counter liquid feeding mode based on the blockage information of the blockage determination part, the other medical pumps do not feed liquid. If the operation of the mode is still executed, there may be a “suction phenomenon” in which one medical pump sucks the liquid sent by another medical pump through the junction.
In this regard, in the above configuration, after the liquid moving unit operates in the liquid feeding mode, the liquid moving unit is configured to change to the operation in the counter liquid feeding mode based on the blockage information of the blockage determination unit. It is the structure notified to.
Therefore, the other medical pumps that have received the occlusion information can stop the liquid feeding mode, so that one medical pump causes the liquid moving unit to execute in the operation of the counter liquid feeding mode. However, it is possible to prevent the occurrence of a “suction phenomenon” that sucks the liquid on the other side of the medical pump.
Further, since the operation in the liquid feeding mode is executed, it is possible to prevent the occurrence of a situation in which the liquid is suddenly fed from the tube portion to the patient or the like when the blocked state is resolved.
すなわち、一の医療用ポンプの液体移動部が、送液モードで動作した後、閉塞判断部の閉塞情報に基づき、反送液モードの動作に変更しても、他の医療用ポンプは送液モードの動作を依然として実行していると、合流部を介して他の医療用ポンプが送液する液体を、一の医療用ポンプが吸引する「吸引現象」が発生するおそれがある、
この点、前記構成では、液体移動部は、送液モードで動作した後、閉塞判断部の閉塞情報に基づき、反送液モードの動作に変更する構成となり、閉塞情報は、他の医療用ポンプに報知される構成となっている。
したがって、閉塞情報を受信した他の医療用ポンプは、その送液モードを停止することができ、これにより、一の医療用ポンプは、液体移動部を、反送液モードの動作で実行させても、他の医療用ポンプ側の液体を吸引する「吸引現象」の発生を未然に防止することができる。
また、前記反送液モードの動作を実行するので、閉塞状態が解消したとき、液体が管部から患者等の側に急激に送液されてしまうという事態の発生も防止することができる。 According to the said structure, the pipe part each arrange | positioned at several medical pumps merges by a merge part (for example, "mixed injection part" etc.), and the liquid accommodated in each inside merges It has become.
That is, even if the liquid moving part of one medical pump operates in the liquid feeding mode and then changes to the operation in the counter liquid feeding mode based on the blockage information of the blockage determination part, the other medical pumps do not feed liquid. If the operation of the mode is still executed, there may be a “suction phenomenon” in which one medical pump sucks the liquid sent by another medical pump through the junction.
In this regard, in the above configuration, after the liquid moving unit operates in the liquid feeding mode, the liquid moving unit is configured to change to the operation in the counter liquid feeding mode based on the blockage information of the blockage determination unit. It is the structure notified to.
Therefore, the other medical pumps that have received the occlusion information can stop the liquid feeding mode, so that one medical pump causes the liquid moving unit to execute in the operation of the counter liquid feeding mode. However, it is possible to prevent the occurrence of a “suction phenomenon” that sucks the liquid on the other side of the medical pump.
Further, since the operation in the liquid feeding mode is executed, it is possible to prevent the occurrence of a situation in which the liquid is suddenly fed from the tube portion to the patient or the like when the blocked state is resolved.
好ましくは、前記液体移動部は、前記閉塞情報が、他の前記医療用ポンプに報知された後、前記反送液モードの動作に変更する構成となっていることを特徴とする。
Preferably, the liquid moving unit is configured to change to the operation in the counterfeed mode after the blockage information is notified to the other medical pump.
前記構成によれば、液体移動部は、閉塞情報が、他の医療用ポンプに報知された後、反送液モードの動作に変更する構成となっているので、一の医療用ポンプが、液体移動部を、反送液モードの動作で実行させても、他の医療用ポンプ側の液体を吸引する「吸引現象」の発生をより確実に防止することができる。
According to the above configuration, the liquid moving unit is configured to change to the operation in the counter-feeding mode after the blockage information is notified to the other medical pumps. Even if the moving unit is executed in the operation of the liquid feeding mode, it is possible to more reliably prevent the occurrence of the “suction phenomenon” in which the liquid on the other medical pump side is sucked.
好ましくは、前記医療用ポンプと通信可能な管理装置を有し、前記閉塞情報は、前記管理装置から他の前記医療用ポンプへ報知される構成となっていることを特徴とする。
Preferably, a management device capable of communicating with the medical pump is provided, and the blockage information is notified from the management device to another medical pump.
前記構成によれば、閉塞情報は、管理装置から他の医療用ポンプへ報知される構成となっているので、閉塞情報の管理をより確実に行うことができる。
According to the above configuration, since the blockage information is notified from the management device to another medical pump, the blockage information can be managed more reliably.
好ましくは、前記管部内状態情報に基づいて前記反送液モードの停止情報である反送液モード停止情報を生成する反送液モード停止情報生成部を有することを特徴とする。
Preferably, the liquid feeding mode stop information generating unit is configured to generate counter liquid feeding mode stop information that is stop information of the counter liquid feeding mode based on the in-pipe state information.
前記構成によれば、管部内状態情報に基づいて反送液モードの停止情報である反送液モード停止情報を生成する反送液モード停止情報生成部を有する。
したがって、管部内状態情報に基づいて反送液モード停止情報が生成されるので、適切なタイミングで反送液モードを停止でき、閉塞状態が解消したとき、薬液等が管部から患者に急激に送液されてしまうことをより精度良く防止することができると共に、薬液の流れ出る量等を適切に管理することができる。 According to the said structure, it has the counter liquid feeding mode stop information generation part which produces | generates the counter liquid feeding mode stop information which is the stop information of counter liquid feeding mode based on the pipe state state information.
Therefore, since the liquid feeding mode stop information is generated based on the in-pipe state information, the reverse liquid feeding mode can be stopped at an appropriate timing. It is possible to prevent the liquid from being fed with higher accuracy and to appropriately manage the amount of the chemical liquid flowing out.
したがって、管部内状態情報に基づいて反送液モード停止情報が生成されるので、適切なタイミングで反送液モードを停止でき、閉塞状態が解消したとき、薬液等が管部から患者に急激に送液されてしまうことをより精度良く防止することができると共に、薬液の流れ出る量等を適切に管理することができる。 According to the said structure, it has the counter liquid feeding mode stop information generation part which produces | generates the counter liquid feeding mode stop information which is the stop information of counter liquid feeding mode based on the pipe state state information.
Therefore, since the liquid feeding mode stop information is generated based on the in-pipe state information, the reverse liquid feeding mode can be stopped at an appropriate timing. It is possible to prevent the liquid from being fed with higher accuracy and to appropriately manage the amount of the chemical liquid flowing out.
好ましくは、前記管部内状態情報が、前記管部内の圧力値である管部内圧力値情報であり、前記管部内圧力値情報が、前記管部内の閉塞状態を示す情報に相当するとき、その閉塞により滞留している予想滞留液体量情報を記憶する管部内圧力値対応予想液体量情報を有し、前記反送液モード停止情報生成部は、前記予想滞留液体量情報に基づいて、前記反送液モード停止情報を生成することを特徴とする。
Preferably, the state information in the pipe part is pressure value information in the pipe part which is a pressure value in the pipe part, and when the pressure value information in the pipe part corresponds to information indicating a block state in the pipe part, And the expected liquid amount information corresponding to the pressure value in the pipe portion that stores the information on the expected staying liquid amount that is retained by the reaction liquid supply mode stop information generation unit based on the expected staying liquid amount information. The liquid mode stop information is generated.
前記構成によれば、反送液モード停止情報生成部は、予想液体量情報(例えば、想定薬液量等)に基づいて、反送液モード停止情報を生成するので、閉塞状態で管部内に滞留している予想滞留液体量情報分のみ反送液モードを実行する。
したがって、閉塞状態が解消したとき、薬液等が管部から患者に急激に送液されてしまうことを極めて正確に防止することができると共に、薬液の流れ出る量等を適切に管理することができる。 According to the above-described configuration, the reaction liquid supply mode stop information generation unit generates the reaction liquid supply mode stop information based on the expected liquid amount information (for example, the assumed chemical liquid amount). The counter liquid feeding mode is executed only for the amount of information on the expected staying liquid amount.
Accordingly, when the occlusion state is resolved, it is possible to prevent the drug solution or the like from being rapidly sent from the pipe part to the patient, and to appropriately manage the amount of the drug solution flowing out.
したがって、閉塞状態が解消したとき、薬液等が管部から患者に急激に送液されてしまうことを極めて正確に防止することができると共に、薬液の流れ出る量等を適切に管理することができる。 According to the above-described configuration, the reaction liquid supply mode stop information generation unit generates the reaction liquid supply mode stop information based on the expected liquid amount information (for example, the assumed chemical liquid amount). The counter liquid feeding mode is executed only for the amount of information on the expected staying liquid amount.
Accordingly, when the occlusion state is resolved, it is possible to prevent the drug solution or the like from being rapidly sent from the pipe part to the patient, and to appropriately manage the amount of the drug solution flowing out.
上記目的は、本発明にあっては、対象者に提供する液体を制御する複数の医療用ポンプを備え、前記医療用ポンプは、少なくとも、前記液体を収容する管部内の前記液体を移動させることができる液体移動部と、前記管部内の状態情報である管部内状態情報を検知する管部内状態情報検知部と、を有し、複数の前記医療用ポンプに、それぞれ配置されている前記管部は、合流部で合流し、それぞれの内部に収容されている前記液体が合流する構成となっており、また、前記管部内状態情報に基づき、前記管部の閉塞情報を生成する閉塞判断部を備え、前記液体移動部は、前記管部内の液体を送液方向に移動させる送液モードと、反送液方向に移動させる反送液モードに切り替え可能な構成となっている医療用ポンプシステムの制御方法であって、前記液体移動部は、前記送液モードで動作した後、前記閉塞情報に基づき、前記反送液モードの動作に変更し、前記閉塞情報は、他の前記医療用ポンプに報知される構成となっていることを特徴とする医療用ポンプシステムの制御方法により達成される。
In the present invention, the above object is provided with a plurality of medical pumps that control the liquid to be provided to the subject, and the medical pump moves at least the liquid in the pipe portion that stores the liquid. And a liquid moving part capable of detecting the in-pipe state information that is state information in the pipe part, and the pipe parts respectively disposed in the plurality of medical pumps. Is configured so that the liquids that are merged at the merging unit and the liquids contained therein are merged, and a blockage determination unit that generates blockage information of the tube unit based on the state information in the tube unit The liquid moving part is configured to be switchable between a liquid feeding mode for moving the liquid in the pipe part in the liquid feeding direction and a liquid feeding mode for moving in the counter liquid feeding direction. Control method Then, after the liquid moving unit operates in the liquid feeding mode, the liquid moving unit is changed to the operation in the counter liquid feeding mode based on the blockage information, and the blockage information is notified to the other medical pumps. This is achieved by a method for controlling a medical pump system, characterized in that
上記目的は、本発明にあっては、対象者に提供する液体を制御する複数の医療用ポンプを備え、前記医療用ポンプは、少なくとも、前記液体を収容する管部内の前記液体を移動させることができる液体移動部と、前記管部内の状態情報である管部内状態情報を検知する管部内状態情報検知部と、を有し、複数の前記医療用ポンプに、それぞれ配置されている前記管部は、合流部で合流し、それぞれの内部に収容されている前記液体が合流する構成となっており、また、前記管部内状態情報に基づき、前記管部の閉塞情報を生成する閉塞判断部を備え、前記液体移動部は、前記管部内の液体を送液方向に移動させる送液モードと、反送液方向に移動させる反送液モードに切り替え可能な構成となっている医療用ポンプシステムに、前記液体移動部が、前記送液モードで動作した後、前記閉塞情報に基づき、前記反送液モードの動作に変更する工程と、前記閉塞情報が、他の前記医療用ポンプに報知される工程と、を実行させることを特徴とする医療用ポンプの制御プログラムにより達成される。
In the present invention, the above object is provided with a plurality of medical pumps that control the liquid to be provided to the subject, and the medical pump moves at least the liquid in the pipe portion that stores the liquid. And a liquid moving part capable of detecting the in-pipe state information that is state information in the pipe part, and the pipe parts respectively disposed in the plurality of medical pumps. Is configured so that the liquids that are merged at the merging unit and the liquids contained therein are merged, and a blockage determination unit that generates blockage information of the tube unit based on the state information in the tube unit The liquid moving part is provided in a medical pump system configured to be switchable between a liquid feeding mode for moving the liquid in the pipe part in the liquid feeding direction and a counter liquid feeding mode for moving in the counter liquid feeding direction. The liquid transfer After the operation in the liquid delivery mode, based on the blockage information, the step of changing to the counter liquid delivery mode operation, and the step of notifying the blockage information to the other medical pump, This is achieved by a control program for a medical pump characterized by being executed.
上記目的は、本発明にあっては、対象者に提供する液体を制御する医療用ポンプであって、前記医療用ポンプは、少なくとも、前記液体を収容する管部内の前記液体を移動させることができる液体移動部と、前記管部内の状態情報である管部内状態情報を検知する管部内状態情報検知部と、を有し、前記医療用ポンプに配置されている前記管部は、合流部で他の管部と前記液体が合流する構成となっており、前記管部内状態情報に基づき、前記管部の閉塞情報を生成する閉塞判断部を備え、前記液体移動部は、前記管部内の前記液体を送液方向に移動させる送液モードと、反送液方向に移動させる反送液モードに切り替え可能な構成となっており、前記液体移動部は、前記送液モードで動作した後、前記閉塞情報に基づき、前記反送液モードの動作に変更する構成となっており、前記閉塞情報を、他の前記管部が配置された他の医療用ポンプに報知する構成となっていることを特徴とする医療用ポンプにより達成される。
In the present invention, the above object is a medical pump for controlling a liquid to be provided to a subject, wherein the medical pump moves at least the liquid in a pipe portion that stores the liquid. A liquid moving part that can be formed, and an in-pipe state information detecting unit that detects state information in the pipe part that is state information in the pipe part, and the pipe part disposed in the medical pump is a confluence part. The pipe is configured to merge with the liquid, and includes a blockage determination unit that generates blockage information of the pipe unit based on the state information in the pipe unit, and the liquid moving unit includes the liquid moving unit in the pipe unit. It is configured to be switchable between a liquid feeding mode for moving the liquid in the liquid feeding direction and a counter liquid feeding mode for moving in the reverse liquid feeding direction, and the liquid moving unit operates in the liquid feeding mode, Based on the blockage information, the liquid feeding mode is This is achieved by a medical pump characterized in that the blockage information is notified to another medical pump in which the other pipe section is arranged. .
以上説明したように、本発明によれば、一の医療用ポンプから他の医療用ポンプへ薬液等の液体が吸引される「吸引現象」の発生を精度良く防止することができる医療用ポンプシステム、医療用ポンプの制御方法、医療用ポンプの制御プログラム及び医療用ポンプを提供することができる。
As described above, according to the present invention, a medical pump system that can accurately prevent the occurrence of a “suction phenomenon” in which a liquid such as a chemical solution is sucked from one medical pump to another medical pump. A medical pump control method, a medical pump control program, and a medical pump can be provided.
以下、この発明の好適な実施の形態を、添付図面等を参照しながら、詳細に説明する。
尚、以下に述べる実施の形態は、本発明の好適な具体例であるから、技術的に好ましい種々の限定が付されているが、本発明の範囲は、以下の説明において特に本発明を限定する旨の記載がない限り、これらの態様に限られるものではない。 DESCRIPTION OF EMBODIMENTS Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings.
The embodiments described below are preferred specific examples of the present invention, and thus various technically preferable limitations are given. However, the scope of the present invention is particularly limited in the following description. Unless otherwise stated, the present invention is not limited to these embodiments.
尚、以下に述べる実施の形態は、本発明の好適な具体例であるから、技術的に好ましい種々の限定が付されているが、本発明の範囲は、以下の説明において特に本発明を限定する旨の記載がない限り、これらの態様に限られるものではない。 DESCRIPTION OF EMBODIMENTS Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings.
The embodiments described below are preferred specific examples of the present invention, and thus various technically preferable limitations are given. However, the scope of the present invention is particularly limited in the following description. Unless otherwise stated, the present invention is not limited to these embodiments.
図1は、本発明の医療用ポンプシステムである例えば、ポンプシステム1を示す概略図である。
図1に示すように、本実施の形態では、ポンプシステム1は、病院内のシステムであり、管理装置であるコンピュータ等からなる管理サーバ300を有し、この管理サーバ300と通信可能な状態で、複数の医療用ポンプである例えば、輸液ポンプ10,110、120、130やシリンジポンプ500,530、540、550が接続されている。
また、輸液ポンプ10等やシリンジポンプ500等は、それぞれ、ポンプ識別情報である例えば、ポンプ識別番号である「A-1」乃至「A-4」や「B-1」乃至「B-4」の番号が付与されている。 FIG. 1 is a schematic view showing, for example, apump system 1 which is a medical pump system of the present invention.
As shown in FIG. 1, in the present embodiment, thepump system 1 is a system in a hospital, and has a management server 300 composed of a computer or the like that is a management device, and is in a state where it can communicate with the management server 300. A plurality of medical pumps, for example, infusion pumps 10, 110, 120, 130 and syringe pumps 500, 530, 540, 550 are connected.
Theinfusion pump 10 and the like and the syringe pump 500 and the like are pump identification information such as “A-1” to “A-4” and “B-1” to “B-4” which are pump identification numbers, respectively. The number is given.
図1に示すように、本実施の形態では、ポンプシステム1は、病院内のシステムであり、管理装置であるコンピュータ等からなる管理サーバ300を有し、この管理サーバ300と通信可能な状態で、複数の医療用ポンプである例えば、輸液ポンプ10,110、120、130やシリンジポンプ500,530、540、550が接続されている。
また、輸液ポンプ10等やシリンジポンプ500等は、それぞれ、ポンプ識別情報である例えば、ポンプ識別番号である「A-1」乃至「A-4」や「B-1」乃至「B-4」の番号が付与されている。 FIG. 1 is a schematic view showing, for example, a
As shown in FIG. 1, in the present embodiment, the
The
図2は、図1の輸液ポンプ10の主な構成を示す概略図である。図1の輸液ポンプ110等は、輸液ポンプ10と同様な構成であるため説明を省略する。
図2に示すように、輸液ポンプ10は、各種情報を表示する表示部であるポンプ側ディスプレイ21を有すると共に、各種操作ボタン22を備えている。
例えば、内部にLEDを含み、光拡散剤を介して発光・表示して輸液ポンプ10の動作状態を示すパイロットランプ22a、設定流量(mL/h)より早い注入速度で薬液を注入するための早送りスイッチボタン22b、開始スイッチボタン22c、停止スイッチボタン22d、メニュー選択ボタン22e等が配置されている。 FIG. 2 is a schematic diagram showing the main configuration of theinfusion pump 10 of FIG. Since the infusion pump 110 and the like in FIG. 1 have the same configuration as the infusion pump 10, the description thereof is omitted.
As shown in FIG. 2, theinfusion pump 10 includes a pump-side display 21 that is a display unit that displays various types of information, and includes various operation buttons 22.
For example, apilot lamp 22a that includes an LED inside, emits and displays light through a light diffusing agent, and indicates the operating state of the infusion pump 10, and fast-forward for injecting a chemical at an injection rate faster than a set flow rate (mL / h) A switch button 22b, a start switch button 22c, a stop switch button 22d, a menu selection button 22e, and the like are arranged.
図2に示すように、輸液ポンプ10は、各種情報を表示する表示部であるポンプ側ディスプレイ21を有すると共に、各種操作ボタン22を備えている。
例えば、内部にLEDを含み、光拡散剤を介して発光・表示して輸液ポンプ10の動作状態を示すパイロットランプ22a、設定流量(mL/h)より早い注入速度で薬液を注入するための早送りスイッチボタン22b、開始スイッチボタン22c、停止スイッチボタン22d、メニュー選択ボタン22e等が配置されている。 FIG. 2 is a schematic diagram showing the main configuration of the
As shown in FIG. 2, the
For example, a
図2に示すように、輸液ポンプ10は、その内部に配置される管部である例えば、ポンプ側チューブ11aを押圧等し、その内部の薬液を送液するための液体移動部である例えば、送液駆動部30が配置されている。
また、この送液駆動部30の上流側(後述する薬剤バッグ12a側で図において右側)には、送液駆動部30より上流側のポンプ側チューブ11a内の閉塞等を検知する管部内状態情報検知部である例えば、上流閉塞センサ16が配置されている。一方、送液駆動部30の下流側(後述する混注部13側で、図において左側)には、送液駆動部30より下流側のポンプ側チューブ11a内の閉塞等を検知する管部内状態情報検知部である下流閉塞センサ17が配置されている。
これら上流閉塞センサ16及び下流閉塞センサ17は、例えば、圧力センサであり、ポンプ側チューブ11a内の圧力を検知する構成となっている。 As shown in FIG. 2, theinfusion pump 10 is a liquid moving unit for pressing the pump-side tube 11 a and feeding a chemical solution therein, for example, a pipe unit disposed therein. A liquid feeding drive unit 30 is arranged.
In addition, on the upstream side of the liquid feeding drive unit 30 (on the right side in the figure on the side of themedicine bag 12a described later), in-pipe state information for detecting a blockage or the like in the pump side tube 11a upstream from the liquid feeding drive unit 30 For example, an upstream blockage sensor 16 that is a detection unit is disposed. On the other hand, on the downstream side of the liquid feeding drive unit 30 (on the side of the mixed injection unit 13 to be described later, the left side in the figure), the in-pipe state information for detecting the blockage in the pump side tube 11a downstream from the liquid feeding drive unit 30 A downstream block sensor 17 serving as a detection unit is disposed.
Theupstream blockage sensor 16 and the downstream blockage sensor 17 are pressure sensors, for example, and are configured to detect the pressure in the pump side tube 11a.
また、この送液駆動部30の上流側(後述する薬剤バッグ12a側で図において右側)には、送液駆動部30より上流側のポンプ側チューブ11a内の閉塞等を検知する管部内状態情報検知部である例えば、上流閉塞センサ16が配置されている。一方、送液駆動部30の下流側(後述する混注部13側で、図において左側)には、送液駆動部30より下流側のポンプ側チューブ11a内の閉塞等を検知する管部内状態情報検知部である下流閉塞センサ17が配置されている。
これら上流閉塞センサ16及び下流閉塞センサ17は、例えば、圧力センサであり、ポンプ側チューブ11a内の圧力を検知する構成となっている。 As shown in FIG. 2, the
In addition, on the upstream side of the liquid feeding drive unit 30 (on the right side in the figure on the side of the
The
図3は、図2に示す輸液ポンプ10の送液駆動部30の主な構成を示す概略説明図である。
送液駆動部30は、図3に示すように、カム構造体32とフィンガ構造体33を有し、これらの構造体でポンプ側チューブ11a内の薬液の送液を制御する構造となっている。
すなわち、このカム構造体32の動作によって、ポンプ側チューブ11a内の薬液の送液を精度良く制御する構成となっている。 FIG. 3 is a schematic explanatory view showing a main configuration of the liquidfeeding drive unit 30 of the infusion pump 10 shown in FIG.
As shown in FIG. 3, the liquidfeeding drive unit 30 includes a cam structure 32 and a finger structure 33, and has a structure for controlling the liquid feeding of the chemical solution in the pump side tube 11 a with these structures. .
That is, the operation of thecam structure 32 is configured to accurately control the feeding of the chemical solution in the pump side tube 11a.
送液駆動部30は、図3に示すように、カム構造体32とフィンガ構造体33を有し、これらの構造体でポンプ側チューブ11a内の薬液の送液を制御する構造となっている。
すなわち、このカム構造体32の動作によって、ポンプ側チューブ11a内の薬液の送液を精度良く制御する構成となっている。 FIG. 3 is a schematic explanatory view showing a main configuration of the liquid
As shown in FIG. 3, the liquid
That is, the operation of the
具体的には、複数のカム、例えば、6個のカム32a乃至32fを有し、フィンガ構造体33は、6個のカム32a乃至32fに対応して、6個のフィンガ33a乃至33fを有している。
6個のカム32a乃至32fは、互いに位相差を付けて配列されており、カム構造体32は、駆動モータ18の出力軸18aに連結されている。
すなわち、図3の駆動モータ18が駆動し、回転すると、カム32a乃至32fを介して、複数のフィンガ33a乃至33fが図3のY方向に個別駆動し、ポンプ側チューブ11aの外周面を図3のT方向に沿って順次押圧して、ポンプ側チューブ11a内の薬液の送液を行う構成となっている(送液モードの一例)。 Specifically, it has a plurality of cams, for example, sixcams 32a to 32f, and the finger structure 33 has six fingers 33a to 33f corresponding to the six cams 32a to 32f. ing.
The sixcams 32 a to 32 f are arranged with a phase difference from each other, and the cam structure 32 is connected to the output shaft 18 a of the drive motor 18.
That is, when thedrive motor 18 of FIG. 3 is driven and rotated, the plurality of fingers 33a to 33f are individually driven in the Y direction of FIG. 3 via the cams 32a to 32f, and the outer peripheral surface of the pump side tube 11a is shown in FIG. Are sequentially pressed along the T direction to feed the chemical solution in the pump side tube 11a (an example of a liquid feeding mode).
6個のカム32a乃至32fは、互いに位相差を付けて配列されており、カム構造体32は、駆動モータ18の出力軸18aに連結されている。
すなわち、図3の駆動モータ18が駆動し、回転すると、カム32a乃至32fを介して、複数のフィンガ33a乃至33fが図3のY方向に個別駆動し、ポンプ側チューブ11aの外周面を図3のT方向に沿って順次押圧して、ポンプ側チューブ11a内の薬液の送液を行う構成となっている(送液モードの一例)。 Specifically, it has a plurality of cams, for example, six
The six
That is, when the
送液駆動部30は、上述のように、複数のフィンガ33a乃至33fの蠕動様運動を制御することにより、フィンガ33a乃至33fを順次、前後進させ、あたかも波動が進行するようにして、ポンプ側チューブ11a内の閉塞点をT方向に移動させることでポンプ側チューブ11aをしごいて薬液を移送する構成となっている。
したがって、図3の駆動モータ18の回転を逆転作動(動作)させることで、ポンプ側チューブ11a内の薬液の送液方向を逆方向(図3のT方向と反対方向)に変更させることもできる構成となっている(反送液モードの一例)。 As described above, the liquidfeeding drive unit 30 controls the peristaltic movements of the plurality of fingers 33a to 33f to sequentially move the fingers 33a to 33f back and forth so that the wave travels, so that the pump side The chemical solution is transferred by squeezing the pump side tube 11a by moving the blockage point in the tube 11a in the T direction.
Therefore, by rotating thedrive motor 18 in FIG. 3 in reverse (operation), the liquid feeding direction of the chemical solution in the pump side tube 11a can be changed in the reverse direction (the direction opposite to the T direction in FIG. 3). It has a configuration (an example of a reverse liquid feeding mode).
したがって、図3の駆動モータ18の回転を逆転作動(動作)させることで、ポンプ側チューブ11a内の薬液の送液方向を逆方向(図3のT方向と反対方向)に変更させることもできる構成となっている(反送液モードの一例)。 As described above, the liquid
Therefore, by rotating the
図4は、図1のシリンジポンプ500の主な構成を示す概略図である。図1のシリンジポンプ530等は、シリンジポンプ500と同様な構成であるため説明を省略する。
図4に示すように、シリンジポンプ500は、薬液を充填したシリンジ510のシリンジ本体511を、クランプ512を用いて固定する構成となっている。
また、シリンジ押子駆動部517の駆動モータの回転によって、送りネジが回転し、シリンジ押子押圧部材513は、シリンジ510のシリンジ押子514を、シリンジ本体511側へF方向に押圧することができる構成ともなっている。すなわち、シリンジ押子押圧部材513やシリンジ押子514等が液体移動部の一例となっている。
これにより、シリンジ本体511内の薬液は、ポンプ側チューブ11aへ送液することができる(送液モードの一例)。 FIG. 4 is a schematic diagram showing the main configuration of thesyringe pump 500 of FIG. Since the syringe pump 530 and the like in FIG. 1 have the same configuration as the syringe pump 500, description thereof is omitted.
As shown in FIG. 4, thesyringe pump 500 is configured to fix a syringe body 511 of a syringe 510 filled with a chemical solution using a clamp 512.
Also, the feed screw is rotated by the rotation of the drive motor of the syringepusher drive unit 517, and the syringe pusher pressing member 513 can press the syringe pusher 514 of the syringe 510 in the F direction toward the syringe body 511 side. It can also be configured. That is, the syringe pusher pressing member 513 and the syringe pusher 514 are examples of the liquid moving unit.
Thereby, the chemical | medical solution in the syringemain body 511 can be liquid-fed to the pump side tube 11a (an example of liquid feeding mode).
図4に示すように、シリンジポンプ500は、薬液を充填したシリンジ510のシリンジ本体511を、クランプ512を用いて固定する構成となっている。
また、シリンジ押子駆動部517の駆動モータの回転によって、送りネジが回転し、シリンジ押子押圧部材513は、シリンジ510のシリンジ押子514を、シリンジ本体511側へF方向に押圧することができる構成ともなっている。すなわち、シリンジ押子押圧部材513やシリンジ押子514等が液体移動部の一例となっている。
これにより、シリンジ本体511内の薬液は、ポンプ側チューブ11aへ送液することができる(送液モードの一例)。 FIG. 4 is a schematic diagram showing the main configuration of the
As shown in FIG. 4, the
Also, the feed screw is rotated by the rotation of the drive motor of the syringe
Thereby, the chemical | medical solution in the syringe
また、シリンジ510のシリンジ押子514をF方向と逆方向に移動することで反送液方向(反送液モード)に薬液を移動させることができる構成となっている。
シリンジ押子押圧部材513には、閉塞センサ519(管部内状態情報検知部の一例)が配置され、閉塞検出値を取得することができる。
なお、図4に示すように、シリンジポンプ500は、各種情報を表示するシリンジ側ディスプレイ516を有し、各種のシリンジ操作ボタン518も備えている。 Moreover, it is the structure which can move a chemical | medical solution to a reverse liquid feeding direction (reverse liquid feeding mode) by moving thesyringe presser 514 of the syringe 510 to a reverse direction to F direction.
The syringepusher pressing member 513 is provided with a blockage sensor 519 (an example of an in-pipe state information detection unit) and can acquire a blockage detection value.
As shown in FIG. 4, thesyringe pump 500 has a syringe-side display 516 that displays various information, and also includes various syringe operation buttons 518.
シリンジ押子押圧部材513には、閉塞センサ519(管部内状態情報検知部の一例)が配置され、閉塞検出値を取得することができる。
なお、図4に示すように、シリンジポンプ500は、各種情報を表示するシリンジ側ディスプレイ516を有し、各種のシリンジ操作ボタン518も備えている。 Moreover, it is the structure which can move a chemical | medical solution to a reverse liquid feeding direction (reverse liquid feeding mode) by moving the
The syringe
As shown in FIG. 4, the
ところで、本実施の形態では、医療従事者である例えば、看護師等が、医師の処方に従い複数、例えば、2種類の薬液を対象者である例えば、患者Pに投与する場合、同一の輸液ライン(例えば、複数の薬剤を合流させ、最終的に1本のチューブで患者Pに投与する場合等)を用いて行う。
By the way, in this embodiment, when a medical worker, for example, a nurse or the like administers a plurality of, for example, two types of chemical liquids to a target person, for example, a patient P, for example, according to a doctor's prescription, (For example, a case where a plurality of drugs are combined and finally administered to the patient P through one tube) is performed.
図5は、図1の輸液ポンプ10とシリンジポンプ500を用いて同一の輸液ラインを形成し例を示す概略説明図である。
輸液ポンプ10は、図5に示すように、内部にポンプ側チューブ11aを配置し、このポンプ側チューブ11aを押圧等することで、ポンプ側チューブ11a内の液体である例えば、薬液を送液させる構成となっており、シリンジポンプ500は、内部にシリンジ510を有し、このシリンジ510で薬液を押し出す構成となっている。 FIG. 5 is a schematic explanatory diagram illustrating an example in which the same infusion line is formed using theinfusion pump 10 and the syringe pump 500 of FIG. 1.
As shown in FIG. 5, theinfusion pump 10 has a pump-side tube 11a disposed therein, and presses the pump-side tube 11a to feed, for example, a liquid medicine in the pump-side tube 11a. The syringe pump 500 has a syringe 510 inside, and the syringe 510 pushes out a chemical solution.
輸液ポンプ10は、図5に示すように、内部にポンプ側チューブ11aを配置し、このポンプ側チューブ11aを押圧等することで、ポンプ側チューブ11a内の液体である例えば、薬液を送液させる構成となっており、シリンジポンプ500は、内部にシリンジ510を有し、このシリンジ510で薬液を押し出す構成となっている。 FIG. 5 is a schematic explanatory diagram illustrating an example in which the same infusion line is formed using the
As shown in FIG. 5, the
また、本実施の形態では、輸液ポンプ10とシリンジポンプ500が送液する薬液を内部に収容している薬液容器(薬液バッグ)12a、薬液容器(シリンジ)510が配置されている。
これら薬剤容器12a、510は、それぞれポンプ側チューブ11a、11bを介して薬液を供給する構成となっている。 Moreover, in this Embodiment, the chemical | medical solution container (chemical | medical solution bag) 12a and the chemical | medical solution container (syringe) 510 which accommodate the chemical | medical solution which theinfusion pump 10 and the syringe pump 500 send inside are arrange | positioned.
These chemical containers 12a and 510 are configured to supply a chemical solution via the pump side tubes 11a and 11b, respectively.
これら薬剤容器12a、510は、それぞれポンプ側チューブ11a、11bを介して薬液を供給する構成となっている。 Moreover, in this Embodiment, the chemical | medical solution container (chemical | medical solution bag) 12a and the chemical | medical solution container (syringe) 510 which accommodate the chemical | medical solution which the
These
また、2つのポンプ側チューブ11a、11bは、図5に示すように、それぞれ合流部である例えば、混注部13に接続されている。
この混注部13は、対象者側管部である例えば、患者側チューブ14に接続され、この患者側チューブ14は、留置針15等を介して、患者Pの腕等の血管と接続されている。
したがって、図5の2つのポンプ側チューブ11a、11b内の薬液は、混注部13で合流し、患者側チューブ14と留置針15等を介して、患者に投与される構成となっている。 Moreover, as shown in FIG. 5, the two pump side tubes 11a and 11b are connected to, for example, a co-injection unit 13 which is a junction.
Themixed injection part 13 is connected to, for example, a patient side tube 14 that is a subject side tube part, and the patient side tube 14 is connected to a blood vessel such as an arm of the patient P via an indwelling needle 15 or the like. .
Therefore, the chemical solutions in the two pump- side tubes 11a and 11b in FIG. 5 are combined at the co-injection unit 13 and are administered to the patient via the patient-side tube 14 and the indwelling needle 15 or the like.
この混注部13は、対象者側管部である例えば、患者側チューブ14に接続され、この患者側チューブ14は、留置針15等を介して、患者Pの腕等の血管と接続されている。
したがって、図5の2つのポンプ側チューブ11a、11b内の薬液は、混注部13で合流し、患者側チューブ14と留置針15等を介して、患者に投与される構成となっている。 Moreover, as shown in FIG. 5, the two
The
Therefore, the chemical solutions in the two pump-
図1に示す輸液ポンプ10等、シリンジポンプ500等及び管理サーバ300は、コンピュータを有し、コンピュータは、図示しないCPU(Central Processing Unit)、RAM(Random Access Memory)、ROM(Read Only Memory)等を有し、これらは、バスを介して接続されている。
The infusion pump 10 and the like, the syringe pump 500 and the like, and the management server 300 shown in FIG. 1 have a computer. The computer is not shown, such as a CPU (Central Processing Unit), a RAM (Random Access Memory), a ROM (Read Only Memory), and the like. These are connected via a bus.
図6は、図1の管理サーバ300の主な構成と示す概略ブロック図である。図6に示すように、管理サーバ300は、「サーバ制御部301」を有し、サーバ制御部301は、管理サーバ300が輸液ポンプ10等と通信するための「サーバ側通信装置302」、各種情報を表示する「サーバ側ディスプレイ303」及び各種情報を入力する「サーバ側各種情報入力装置304」を制御する。
また、サーバ制御部301は、図6に示す「サーバ側各種情報記憶部310」も制御する。 FIG. 6 is a schematic block diagram showing the main configuration of themanagement server 300 of FIG. As shown in FIG. 6, the management server 300 includes a “server control unit 301”. The server control unit 301 includes a “server-side communication device 302” that allows the management server 300 to communicate with the infusion pump 10 and the like. A “server-side display 303” for displaying information and a “server-side various information input device 304” for inputting various information are controlled.
Theserver control unit 301 also controls a “server-side various information storage unit 310” shown in FIG.
また、サーバ制御部301は、図6に示す「サーバ側各種情報記憶部310」も制御する。 FIG. 6 is a schematic block diagram showing the main configuration of the
The
図7は、サーバ側各種情報記憶部310の主な構成を示す概略ブロック図である。これらの具体的な内容は後述する。
FIG. 7 is a schematic block diagram showing the main configuration of the server-side various information storage unit 310. Specific contents thereof will be described later.
図8は、図1等に示す輸液ポンプ10の主な構成を示す概略ブロック図である。輸液ポンプ110等は、輸液ポンプ10と同様の構成のため、以下、輸液ポンプ10についてのみ説明する。
図8に示すように、輸液ポンプ10は、「ポンプ制御部41」を有し、ポンプ制御部41は、輸液ポンプ10が管理サーバ300等と通信するための「ポンプ側通信装置42」や図2等で示すポンプ側ディスプレイ21、駆動モータ18、上流側閉塞センサ16及び下流側閉塞センサ17等を制御する。
また、ポンプ側制御部41は、図4に示す「第1の各種情報記憶部50」、「第2の各種情報記憶部60」及び「第3の各種情報記憶部70」も制御する。 FIG. 8 is a schematic block diagram showing the main configuration of theinfusion pump 10 shown in FIG. Since the infusion pump 110 and the like have the same configuration as the infusion pump 10, only the infusion pump 10 will be described below.
As shown in FIG. 8, theinfusion pump 10 includes a “pump control unit 41”, and the pump control unit 41 includes a “pump-side communication device 42” for the infusion pump 10 to communicate with the management server 300 and the like. 2 controls the pump-side display 21, the drive motor 18, the upstream block sensor 16, the downstream block sensor 17, and the like.
The pump-side control unit 41 also controls a “first various information storage unit 50”, a “second various information storage unit 60”, and a “third various information storage unit 70” illustrated in FIG.
図8に示すように、輸液ポンプ10は、「ポンプ制御部41」を有し、ポンプ制御部41は、輸液ポンプ10が管理サーバ300等と通信するための「ポンプ側通信装置42」や図2等で示すポンプ側ディスプレイ21、駆動モータ18、上流側閉塞センサ16及び下流側閉塞センサ17等を制御する。
また、ポンプ側制御部41は、図4に示す「第1の各種情報記憶部50」、「第2の各種情報記憶部60」及び「第3の各種情報記憶部70」も制御する。 FIG. 8 is a schematic block diagram showing the main configuration of the
As shown in FIG. 8, the
The pump-
図9乃至図11は、それぞれ「第1の各種情報記憶部50」、「第2の各種情報記憶部60」及び「第3の各種情報記憶部70」の主な構成を示す概略ブロック図である。これらの具体的な内容は後述する。
9 to 11 are schematic block diagrams showing main configurations of the “first various information storage unit 50”, the “second various information storage unit 60”, and the “third various information storage unit 70”, respectively. is there. Specific contents thereof will be described later.
図12乃至図16は、本実施の形態に係るポンプシステム1の主な動作例等を示す概略フローチャートである。
先ず、図12のステップ(以下「ST」とする。)1では、図1の管理サーバ300に、管理サーバ300と通信対象の図1に示す輸液ポンプ10等とシリンジポンプ500等について、それぞれのポンプ識別番号(例えば、「A-1」~「A-4」や「B-1」~「B-4」を「通信用アドレス」を関連付けて記憶する。
具体的には、図7の「サーバ側ポンプ情報記憶部311」に記憶する。 12 to 16 are schematic flowcharts showing main operation examples and the like of thepump system 1 according to the present embodiment.
First, in step (hereinafter referred to as “ST”) 1 in FIG. 12, themanagement server 300 in FIG. 1 includes the management server 300, the infusion pump 10 and the like shown in FIG. Pump identification numbers (for example, “A-1” to “A-4” and “B-1” to “B-4” are stored in association with “communication addresses”.
Specifically, it is stored in the “server-side pumpinformation storage unit 311” in FIG.
先ず、図12のステップ(以下「ST」とする。)1では、図1の管理サーバ300に、管理サーバ300と通信対象の図1に示す輸液ポンプ10等とシリンジポンプ500等について、それぞれのポンプ識別番号(例えば、「A-1」~「A-4」や「B-1」~「B-4」を「通信用アドレス」を関連付けて記憶する。
具体的には、図7の「サーバ側ポンプ情報記憶部311」に記憶する。 12 to 16 are schematic flowcharts showing main operation examples and the like of the
First, in step (hereinafter referred to as “ST”) 1 in FIG. 12, the
Specifically, it is stored in the “server-side pump
これにより、管理サーバ300は、病院内の輸液ポンプ10等やシリンジポンプ500等を識別管理可能となると共に、通信可能となる。
Thereby, the management server 300 can identify and manage the infusion pump 10 and the syringe pump 500 in the hospital and can communicate with each other.
この状態で、例えば、医療従事者である例えば、看護師等が、患者Pに2つの異なる薬剤を投与するため輸液ポンプ10(A-1)とシリンジポンプ500(B-1)を使用して、投与準備を開始する。
具体的には、図5に示すように、2つの薬液容器12a、510と、これらに接続されるポンプ側チューブ11a、11b、そして、混注部13、混注部13に接続される管部である例えば、患者側チューブ14等から構成される「輸液ライン(輸液ライン識別番号C-1)」に、輸液ポンプ10(A-1)とシリンジポンプ500(B-1)を配置する。 In this state, for example, a medical staff such as a nurse uses the infusion pump 10 (A-1) and the syringe pump 500 (B-1) to administer two different drugs to the patient P. Start administration preparation.
Specifically, as shown in FIG. 5, two chemical liquid containers 12 a and 510, pump- side tubes 11 a and 11 b connected to these, and a mixed injection part 13 and a pipe part connected to the mixed injection part 13. For example, the infusion pump 10 (A-1) and the syringe pump 500 (B-1) are arranged in an “infusion line (infusion line identification number C-1)” composed of the patient-side tube 14 and the like.
具体的には、図5に示すように、2つの薬液容器12a、510と、これらに接続されるポンプ側チューブ11a、11b、そして、混注部13、混注部13に接続される管部である例えば、患者側チューブ14等から構成される「輸液ライン(輸液ライン識別番号C-1)」に、輸液ポンプ10(A-1)とシリンジポンプ500(B-1)を配置する。 In this state, for example, a medical staff such as a nurse uses the infusion pump 10 (A-1) and the syringe pump 500 (B-1) to administer two different drugs to the patient P. Start administration preparation.
Specifically, as shown in FIG. 5, two chemical
次いで、ST2へ進む。ST2では、看護師等により輸液ポンプ10(A-1)とシリンジポンプ500(B-1)に「輸液ライン識別番号(C-1)」が入力される。この輸液ライン識別番号(C-1)は図9に示す輸液ポンプ10(A-1)(シリンジポンプ500(B-1)も同様)の「ポンプ側ポンプ情報記憶部57」に記憶される。
Next, proceed to ST2. In ST2, the “infusion line identification number (C-1)” is input to the infusion pump 10 (A-1) and the syringe pump 500 (B-1) by a nurse or the like. This infusion line identification number (C-1) is stored in the “pump-side pump information storage unit 57” of the infusion pump 10 (A-1) shown in FIG. 9 (the same applies to the syringe pump 500 (B-1)).
次いで、ST3へ進む。ST3では、図9の「輸液ライン識別番号送信処理部(プログラム)58」が動作し、「ポンプ側ポンプ情報記憶部57」を参照し、「輸液ライン識別番号」が記憶されているときは、当該「輸液ライン識別番号」である例えば、「C-1」を「輸液ライン識別番号」として、管理サーバ300に送信すると共に、自己の「ポンプ識別番号(A-1、B-1等)」を併せて管理サーバ300に送信する。
Next, proceed to ST3. In ST3, the “infusion line identification number transmission processing unit (program) 58” of FIG. 9 operates and refers to the “pump-side pump information storage unit 57”, and when the “infusion line identification number” is stored, The “infusion line identification number”, for example, “C-1” is transmitted as the “infusion line identification number” to the management server 300 and the own “pump identification number (A-1, B-1, etc.)” Are also transmitted to the management server 300.
次いで、ST4へ進む。ST4では、管理サーバ300は、輸液ポンプ10(A-1)やシリンジポンプ500(B-1)から受信した「輸液ライン識別番号(C-1)」と「ポンプ識別番号(A-1、B-1)に基づき、「サーバ側ポンプ情報記憶部311」の当該ポンプに対応する「輸液ライン識別番号」に「輸液ライン識別番号(C-1)」を記憶する。
Next, proceed to ST4. In ST4, the management server 300 receives the “infusion line identification number (C-1)” and “pump identification numbers (A-1, B) received from the infusion pump 10 (A-1) and the syringe pump 500 (B-1). -1), the “infusion line identification number (C-1)” is stored in the “infusion line identification number” corresponding to the pump in the “server-side pump information storage unit 311”.
以上により、図5に示す「輸液ライン」は、管理サーバ300において、その「輸液ライン識別番号(C-1)」で特定されると共に、その輸液ラインに含まれる輸液ポンプ10、シリンジポンプ500も特定されて記憶される。
したがって、どの輸液ポンプ10等が、どの輸液ラインに配置されているかを管理サーバ300は正確に把握、管理をすることができる。 As described above, the “infusion line” shown in FIG. 5 is specified by the “infusion line identification number (C-1)” in themanagement server 300, and the infusion pump 10 and the syringe pump 500 included in the infusion line are also included. Identified and stored.
Therefore, themanagement server 300 can accurately grasp and manage which infusion pump 10 or the like is located in which infusion line.
したがって、どの輸液ポンプ10等が、どの輸液ラインに配置されているかを管理サーバ300は正確に把握、管理をすることができる。 As described above, the “infusion line” shown in FIG. 5 is specified by the “infusion line identification number (C-1)” in the
Therefore, the
以上で、薬液の投与準備が終了するので、以下、図13等を用いて、薬液の投与工程等を説明する。
本実施の形態では、図5に示すように、輸液ポンプ10とシリンジポンプ500を使用同じ輸液ラインを形成し、患者Pに2つの薬剤バッグ12a、12bの薬液を投与する場合で、図5の輸液ポンプ10の下流閉塞センサ17がシリンジポンプの閉塞センサ519より先にポンプ側チューブ11aの閉塞を検知した例に基づき、以下説明する。 The preparation for administration of the drug solution is thus completed, and the drug solution administration process and the like will be described below with reference to FIG.
In the present embodiment, as shown in FIG. 5, the same infusion line is formed using theinfusion pump 10 and the syringe pump 500, and the drug solution of the two drug bags 12 a and 12 b is administered to the patient P. The following description is based on an example in which the downstream blockage sensor 17 of the infusion pump 10 detects the blockage of the pump side tube 11a before the blockage sensor 519 of the syringe pump.
本実施の形態では、図5に示すように、輸液ポンプ10とシリンジポンプ500を使用同じ輸液ラインを形成し、患者Pに2つの薬剤バッグ12a、12bの薬液を投与する場合で、図5の輸液ポンプ10の下流閉塞センサ17がシリンジポンプの閉塞センサ519より先にポンプ側チューブ11aの閉塞を検知した例に基づき、以下説明する。 The preparation for administration of the drug solution is thus completed, and the drug solution administration process and the like will be described below with reference to FIG.
In the present embodiment, as shown in FIG. 5, the same infusion line is formed using the
先ず、図5に示すように、患者Pに投与する例えば、異なる種類の薬液を2つの薬液容器12a、510に収容し、それぞれの薬液容器12a、510にポンプ側チューブ11a、11bが接続され、これらポンプ側チューブ11a、11bが混注部13に接続されている。
これにより、2つのポンプ側チューブ11a、11bは、混在部13を介して、1本の患者側チューブ14と接続される。
また、この患者チューブ14は、留置針15を介して患者Pと接続されることになる。 First, as shown in FIG. 5, for example, different types of chemical liquids to be administered to a patient P are accommodated in two chemical liquid containers 12 a and 510, and pump side tubes 11 a and 11 b are connected to the respective chemical liquid containers 12 a and 510. These pump side tubes 11 a and 11 b are connected to the mixed injection part 13.
As a result, the two pump- side tubes 11 a and 11 b are connected to one patient-side tube 14 via the mixed portion 13.
Further, thepatient tube 14 is connected to the patient P through the indwelling needle 15.
これにより、2つのポンプ側チューブ11a、11bは、混在部13を介して、1本の患者側チューブ14と接続される。
また、この患者チューブ14は、留置針15を介して患者Pと接続されることになる。 First, as shown in FIG. 5, for example, different types of chemical liquids to be administered to a patient P are accommodated in two chemical
As a result, the two pump-
Further, the
この状態で、図13のST11では、患者Pに投与する各薬液の予定送液量である「予定送液量情報」のデータを、輸液ポンプ10及びシリンジポンプ500に入力する。
以下、本実施の形態では、主に輸液ポンプ10について説明するが、同様のソフト構成は、シリンジポンプ500についても搭載されている。
この「予定送液量情報」のデータは、具体的には、図9の輸液ポンプ10の「輸液ポンプ側予定送液量情報記憶部51」に記憶される。 In this state, in ST11 of FIG. 13, data of “scheduled liquid feeding amount information” that is a scheduled liquid feeding amount of each drug solution to be administered to the patient P is input to theinfusion pump 10 and the syringe pump 500.
Hereinafter, although theinfusion pump 10 will be mainly described in the present embodiment, the same software configuration is also mounted on the syringe pump 500.
Specifically, the data of the “scheduled delivery amount information” is stored in the “infusion pump side scheduled delivery amountinformation storage unit 51” of the infusion pump 10 of FIG.
以下、本実施の形態では、主に輸液ポンプ10について説明するが、同様のソフト構成は、シリンジポンプ500についても搭載されている。
この「予定送液量情報」のデータは、具体的には、図9の輸液ポンプ10の「輸液ポンプ側予定送液量情報記憶部51」に記憶される。 In this state, in ST11 of FIG. 13, data of “scheduled liquid feeding amount information” that is a scheduled liquid feeding amount of each drug solution to be administered to the patient P is input to the
Hereinafter, although the
Specifically, the data of the “scheduled delivery amount information” is stored in the “infusion pump side scheduled delivery amount
次いで、ST12で、輸液ポンプ10とシリンジポンプ500が動作し、送液モードである例えば、送液を開始し、ST2に進む。ST2では、輸液ポンプ10とシリンジポンプ500が動作して、所定の速度で当該薬液の送液を開始すると共に輸液ポンプ10の「下流閉塞センサ17」及びシリンジポンプ500の閉塞センサ519がポンプ側チューブ11a等内の管部内状態情報である例えば、「閉塞検出圧」の測定を開始する。
Next, in ST12, the infusion pump 10 and the syringe pump 500 operate to start the liquid feeding mode, for example, liquid feeding, and proceed to ST2. In ST2, the infusion pump 10 and the syringe pump 500 are operated to start feeding the liquid medicine at a predetermined speed, and the “downstream occlusion sensor 17” of the infusion pump 10 and the occlusion sensor 519 of the syringe pump 500 are pump side tubes. For example, measurement of “occlusion detection pressure” that is state information in the pipe portion in 11a and the like is started.
次いで、ST13及びST14へ進む。ST13では、図9の「積算送液量情報演算処理部(プログラム)52」が動作し、図9の「送液量基準情報記憶部53」を参照する。この送液量基準情報記憶部53には、駆動モータ18の回転数と送液量の関係情報である「送液量基準情報」、すなわち、駆動モータ18が何回、回転すれば、どの程度の送液量となるかについての情報が記憶されている。
Next, the process proceeds to ST13 and ST14. In ST13, the “integrated liquid feeding amount information calculation processing unit (program) 52” in FIG. 9 operates and refers to the “liquid feeding amount reference information storage unit 53” in FIG. In the liquid supply amount reference information storage unit 53, “liquid supply amount reference information” that is the relationship information between the rotational speed of the drive motor 18 and the liquid supply amount, that is, how many times the drive motor 18 rotates. Information about whether the amount of liquid to be fed is stored.
したがって、積算送液量情報演算処理部(プログラム)52は、この既定の「送液量基準情報」と駆動モータ18の「回転量」情報等から輸液ポンプ10の「積算送液量情報」を演算し、図9の「積算送液量情報記憶部54」に記憶させる(シリンジポンプ500のも同様)。
このように、積算送液量情報記憶部54には、輸液ポンプ10等の累積の薬液の送液量の情報が記憶されることになる。 Therefore, the integrated liquid supply amount information calculation processing unit (program) 52 obtains the “integrated liquid supply amount information” of the infusion pump 10 from the predetermined “liquid supply amount reference information” and the “rotation amount” information of thedrive motor 18. The calculated value is stored in the “integrated liquid feeding amount information storage unit 54” in FIG. 9 (the same applies to the syringe pump 500).
As described above, the cumulative liquid supply amountinformation storage unit 54 stores information on the cumulative liquid supply amount of the chemical solution such as the infusion pump 10.
このように、積算送液量情報記憶部54には、輸液ポンプ10等の累積の薬液の送液量の情報が記憶されることになる。 Therefore, the integrated liquid supply amount information calculation processing unit (program) 52 obtains the “integrated liquid supply amount information” of the infusion pump 10 from the predetermined “liquid supply amount reference information” and the “rotation amount” information of the
As described above, the cumulative liquid supply amount
一方、ST14では、輸液ポンプ10が「下流側閉塞センサ17」の閉塞検出値を図5の「下流側閉塞検出値記憶部55」に記憶する(シリンジポンプ500では、閉塞センサ519の「閉塞検出値」を記憶)。
次いで、ST15へ進む。ST15では、図9の閉塞判断部である例えば、「輸液ポンプ閉塞判断処理部(プログラム)59」が動作し、図9の「輸液ポンプ閉塞基準値情報記憶部56」を参照する。
このとき、図1の輸液ポンプ10とシリンジポンプ500とでは、異なる数値が記憶されている場合があり、本実施の形態では、この場合に該当する。 On the other hand, in ST14, the infusion pump 10 stores the occlusion detection value of the “downstream occlusion sensor 17” in the “downstream occlusion detection value storage unit 55” in FIG. 5 (in the syringe pump 500, the “occlusion detection of the occlusion sensor 519”. Value ").
Next, the process proceeds to ST15. In ST15, for example, the “infusion pump blockage determination processing unit (program) 59” which is the blockage determination unit in FIG. 9 operates, and the “infusion pump blockage reference valueinformation storage unit 56” in FIG. 9 is referred to.
At this time, different numerical values may be stored in theinfusion pump 10 and the syringe pump 500 in FIG. 1, and this case corresponds to this case.
次いで、ST15へ進む。ST15では、図9の閉塞判断部である例えば、「輸液ポンプ閉塞判断処理部(プログラム)59」が動作し、図9の「輸液ポンプ閉塞基準値情報記憶部56」を参照する。
このとき、図1の輸液ポンプ10とシリンジポンプ500とでは、異なる数値が記憶されている場合があり、本実施の形態では、この場合に該当する。 On the other hand, in ST14, the infusion pump 10 stores the occlusion detection value of the “
Next, the process proceeds to ST15. In ST15, for example, the “infusion pump blockage determination processing unit (program) 59” which is the blockage determination unit in FIG. 9 operates, and the “infusion pump blockage reference value
At this time, different numerical values may be stored in the
すなわち、シリンジポンプ500は、例えば、「60kPa」を閉塞と判断する「閉塞基準値」としているが、輸液ポンプ10は、「30kPa」を「閉塞基準値」と設定している。
That is, for example, the syringe pump 500 sets “60 kPa” as a “blocking reference value” for determining that it is blocked, but the infusion pump 10 sets “30 kPa” as a “blocking reference value”.
したがって、輸液ポンプ10は、図9の「下流側閉塞検出値記憶部55」及び「輸液ポンプ閉塞基準値情報記憶部56」に基づいて、「下流側閉塞検出値」が閉塞基準値を超えているか否かを判断する。
すなわち、輸液ポンプ10は、「下流側閉塞検出値」が「30kPa」に達しているか否かを判断する。 Therefore, theinfusion pump 10 determines that the “downstream side occlusion detection value” exceeds the occlusion reference value based on the “downstream occlusion detection value storage unit 55” and the “infusion pump occlusion reference value information storage unit 56” in FIG. Determine whether or not.
That is, theinfusion pump 10 determines whether or not the “downstream blocking detection value” reaches “30 kPa”.
すなわち、輸液ポンプ10は、「下流側閉塞検出値」が「30kPa」に達しているか否かを判断する。 Therefore, the
That is, the
一方、図5のシリンジポンプ500は、「閉塞センサ519」の検出値が「60kPa」に達しているか否かを判断する。
On the other hand, the syringe pump 500 in FIG. 5 determines whether or not the detection value of the “occlusion sensor 519” has reached “60 kPa”.
次いで、ST16へ進む。ST16で、輸液ポンプ10は「下流側閉塞検出値」が「30kPa」に達していると判断したときは、「閉塞状態」が生じていると判断し、ST17へ進む。
ST17では、「下流側閉塞検出値記憶部55」の該当する検出値に関連付けて「閉塞フラグ」を付する。 Next, the process proceeds to ST16. If theinfusion pump 10 determines in ST16 that the “downstream blocking detection value” has reached “30 kPa”, it determines that a “blocking state” has occurred, and proceeds to ST17.
In ST17, the “blocking flag” is attached in association with the corresponding detection value in the “downstream blocking detectionvalue storage unit 55”.
ST17では、「下流側閉塞検出値記憶部55」の該当する検出値に関連付けて「閉塞フラグ」を付する。 Next, the process proceeds to ST16. If the
In ST17, the “blocking flag” is attached in association with the corresponding detection value in the “downstream blocking detection
このとき、図5のシリンジポンプ500は、「閉塞センサ519」の検出値が「60kPa」に達していないので、未だ、閉塞とは判断せず、「閉塞フラグ」が付されない。
At this time, since the detection value of the “occlusion sensor 519” has not reached “60 kPa”, the syringe pump 500 of FIG. 5 is not yet judged to be obstructed, and the “occlusion flag” is not attached.
次いで、ST18へ進む。ST18では、図10の「ポンプ側閉塞警報情報送信処理部(プログラム)61」が動作し、「下流側閉塞検出値記憶部55」に「閉塞フラグ」付されたとき、閉塞情報である例えば、「閉塞警報情報」を図9の「ポンプ側ポンプ情報記憶部57」の「ポンプ識別番号(A-1)」と共に「管理サーバ300」へ送信する。
Next, proceed to ST18. In ST18, when the “pump blockage alarm information transmission processing unit (program) 61” of FIG. 10 is operated and the “blockage flag” is added to the “downstream blockage detection value storage unit 55”, the blockage information is, for example, “Blockage alarm information” is transmitted to “Management server 300” together with “Pump identification number (A-1)” of “Pump-side pump information storage unit 57” in FIG.
次いで、ST19へ進む。ST19では、管理サーバ300は、図7の「サーバ側ポンプ情報記憶部311」を参照し、「閉塞警報情報」を送信した「ポンプ識別番号」例えば、「A-1」について「閉塞警報情報」の存在情報を記憶する。
Next, proceed to ST19. In ST19, the management server 300 refers to the “server-side pump information storage unit 311” in FIG. 7, and transmits “blocking alarm information” “pump identification number”, for example, “blocking alarm information” for “A-1”. The presence information is stored.
次いで、ST20へ進む。ST20では、図7の「サーバ側閉塞警報情報送信処理部(プログラム)312」が動作し、「サーバ側ポンプ情報記憶部311」の「閉塞警報」が記憶されている輸液ポンプ10のポンプ識別番号「A-1」の輸液ライン識別番号、例えば、「C-1」と関連付けられている他のポンプ、例えば、シリンジポンプ500(B-1」)の「ポンプ識別番号」を特定し、「閉塞警報対象ポンプ記憶部313」に記憶する。
Next, proceed to ST20. In ST20, the “server side blockage alarm information transmission processing unit (program) 312” of FIG. 7 operates and the pump identification number of the infusion pump 10 in which the “blockage alarm” of the “server side pump information storage unit 311” is stored. Identify the infusion line identification number of “A-1”, eg “pump identification number” of another pump associated with “C-1”, eg, syringe pump 500 (B-1), The alarm target pump storage unit 313 is stored.
次いで、ST21へ進む。ST21では、管理サーバ300は、図7の「閉塞警報対象ポンプ記憶部313」の「ポンプ識別番号(B-1)」と「サーバ側ポンプ情報記憶部311」の対応する「通信用アドレス」を取得して、シリンジポンプ500(B-1)に「閉塞警報」を送信し、その旨を報知する。
Next, proceed to ST21. In ST21, the management server 300 sets the “communication address” corresponding to the “pump identification number (B-1)” of the “blockage alarm target pump storage unit 313” and the “server side pump information storage unit 311” in FIG. Acquired and transmits a “blocking alarm” to the syringe pump 500 (B-1) to notify that fact.
次いで、ST22へ進む。ST22では、管理サーバ300から「閉塞警報情報」を受信したシリンジポンプ500(B-1)は、駆動モータを停止し、送液動作を停止する。
Next, proceed to ST22. In ST22, the syringe pump 500 (B-1) that has received the “blocking alarm information” from the management server 300 stops the drive motor and stops the liquid feeding operation.
一方、図5の輸液ポンプ10は、ST23へ進む。ST23では、図10の「輸液ポンプ逆転動作処理部(プログラム)62」が動作し、「下流側閉塞検出値記憶部55」に「閉鎖フラグ」が付されたとき、輸液ポンプ10の駆動モータ18を反送液モードである例えば、逆転動作させる。
これは、ポンプ側チューブ11a等の閉塞が解消したとき、薬液が患者側チューブ14から患者Pへ急激に流れ出すことを防ぐための工程である。
本実施の形態では、この逆転動作を実行しても、図5等のシリンジポンプ500の駆動モータは、ST22により、停止され送液が停止されている。 On the other hand, theinfusion pump 10 of FIG. 5 proceeds to ST23. In ST23, when the “infusion pump reverse rotation operation processing section (program) 62” of FIG. 10 is operated and the “downstream closing detection value storage section 55” is attached with the “closed flag”, the drive motor 18 of the infusion pump 10 In the reverse liquid feeding mode, for example, the reverse operation is performed.
This is a process for preventing the drug solution from suddenly flowing from thepatient side tube 14 to the patient P when the blockage of the pump side tube 11a and the like is resolved.
In the present embodiment, even if this reverse rotation operation is executed, the drive motor of thesyringe pump 500 in FIG. 5 and the like is stopped by ST22 and the liquid feeding is stopped.
これは、ポンプ側チューブ11a等の閉塞が解消したとき、薬液が患者側チューブ14から患者Pへ急激に流れ出すことを防ぐための工程である。
本実施の形態では、この逆転動作を実行しても、図5等のシリンジポンプ500の駆動モータは、ST22により、停止され送液が停止されている。 On the other hand, the
This is a process for preventing the drug solution from suddenly flowing from the
In the present embodiment, even if this reverse rotation operation is executed, the drive motor of the
このため、輸液ポンプ10(A-1)が逆転動作を実行しても、同じ輸液ライン(C-1)に配置されているシリンジポンプ500(B-1)の薬液が混注部13を介して、輸液ポンプ10(A-1)により吸引されるという「吸引現象」の発生を確実に防止することができる。
特に、本実施の形態によれば、「閉塞警報情報」等の送信等の管理を輸液ポンプ10ではなく、管理サーバ300が行うので、同一輸液ライン(C-1)に属する他のシリンジポンプ500等への「閉塞警報情報」の送信等を確実に行うことができる。 For this reason, even if the infusion pump 10 (A-1) performs the reverse rotation operation, the medicinal solution of the syringe pump 500 (B-1) arranged in the same infusion line (C-1) passes through theco-injection unit 13. Thus, it is possible to reliably prevent the “suction phenomenon” from being sucked by the infusion pump 10 (A-1).
In particular, according to the present embodiment, themanagement server 300, not the infusion pump 10, performs management such as transmission of “blocking alarm information” and the like, so that another syringe pump 500 belonging to the same infusion line (C-1). It is possible to reliably transmit “blocking alarm information” or the like.
特に、本実施の形態によれば、「閉塞警報情報」等の送信等の管理を輸液ポンプ10ではなく、管理サーバ300が行うので、同一輸液ライン(C-1)に属する他のシリンジポンプ500等への「閉塞警報情報」の送信等を確実に行うことができる。 For this reason, even if the infusion pump 10 (A-1) performs the reverse rotation operation, the medicinal solution of the syringe pump 500 (B-1) arranged in the same infusion line (C-1) passes through the
In particular, according to the present embodiment, the
以上のように、本実施の形態では、同一輸液ラインのシリンジポンプ500の薬液を輸液ポンプ10が吸引する「吸引現象」は未然に防止できるが、上述のように、ポンプ側チューブ11a等の閉塞が解消したとき、薬液が患者側チューブ14から患者Pへ急激に流れ出すことを防ぐと共に、薬液の流れ出る量等を適切に管理する必要がある。
そこで、本実施の形態では、以下のような工程を実行する。 As described above, in the present embodiment, the “suction phenomenon” in which theinfusion pump 10 sucks the chemical solution of the syringe pump 500 in the same infusion line can be prevented in advance, but as described above, the pump side tube 11a and the like are blocked. When the problem is solved, it is necessary to prevent the drug solution from flowing out from the patient side tube 14 to the patient P and to appropriately manage the amount of the drug solution flowing out.
Therefore, in the present embodiment, the following steps are executed.
そこで、本実施の形態では、以下のような工程を実行する。 As described above, in the present embodiment, the “suction phenomenon” in which the
Therefore, in the present embodiment, the following steps are executed.
先ず、ST24及びST25が実行される。ST24では、図10の「逆転動作積算送液量情報演算処理部(プログラム)63」が動作し、図9の「送液量基準情報記憶部53」の「送液量基準情報」と駆動モータ18の「回転量」等から輸液ポンプ10の逆転動作により積算された薬液の送液量である「逆転動作積算送液量情報」を演算し、図10の「逆転動作積算送液量情報記憶部64」に記憶する。
First, ST24 and ST25 are executed. In ST24, the “reverse operation integrated liquid feed amount information calculation processing section (program) 63” in FIG. 10 operates, and “liquid feed amount reference information” in the “liquid feed amount reference information storage section 53” in FIG. The “reverse operation integrated liquid supply information” which is the amount of the chemical solution integrated by the reverse operation of the infusion pump 10 is calculated from the “rotation amount” of 18 and the like, and “reverse operation integrated liquid supply information storage” of FIG. Part 64 ".
ST25では、輸液ポンプ10が、下流側閉塞センサ17の閉塞検出値を図9の「下流側閉塞検出値記憶部55」に記憶し続ける。
次いで、ST26では、図10の「輸液ポンプ閉塞解消判断処理部(プログラム)65」が動作し、「下流側閉塞検出値記憶部55」及び「輸液ポンプ閉塞緩和基準値情報記憶部67」に基づいて「下流側閉塞検出値」が閉塞緩和基準値以下であるか否かを判断する。
すなわち、図5に発生した閉塞状態、例えば、患者側チューブ14の折れ曲がりによるポンプ側チューブ11a等内の圧力が高まった状態が解消したか否かを判断する。 In ST25, theinfusion pump 10 continues to store the blockage detection value of the downstream blockage sensor 17 in the “downstream blockage detection value storage unit 55” of FIG.
Next, in ST26, the “infusion pump blockage elimination determination processing unit (program) 65” of FIG. 10 operates and is based on the “downstream side blockage detectionvalue storage unit 55” and the “infusion pump blockage relaxation reference value information storage unit 67”. Then, it is determined whether or not the “downstream blockage detection value” is equal to or less than the blockage relaxation reference value.
That is, it is determined whether or not the closed state generated in FIG. 5, for example, the state in which the pressure in thepump side tube 11a or the like due to the bending of the patient side tube 14 has increased is eliminated.
次いで、ST26では、図10の「輸液ポンプ閉塞解消判断処理部(プログラム)65」が動作し、「下流側閉塞検出値記憶部55」及び「輸液ポンプ閉塞緩和基準値情報記憶部67」に基づいて「下流側閉塞検出値」が閉塞緩和基準値以下であるか否かを判断する。
すなわち、図5に発生した閉塞状態、例えば、患者側チューブ14の折れ曲がりによるポンプ側チューブ11a等内の圧力が高まった状態が解消したか否かを判断する。 In ST25, the
Next, in ST26, the “infusion pump blockage elimination determination processing unit (program) 65” of FIG. 10 operates and is based on the “downstream side blockage detection
That is, it is determined whether or not the closed state generated in FIG. 5, for example, the state in which the pressure in the
次いで、ST27で、下流側閉塞検出値が閉塞緩和基準値以下であると判断されると、ST28へ進む。
ST28では、図9の「下流側閉塞検出値記憶部55」の該当する検出値に関連付けて解消フラグを付する。 Next, when it is determined in ST27 that the downstream blockage detection value is equal to or less than the blockage relaxation reference value, the process proceeds to ST28.
In ST28, a cancellation flag is attached in association with the corresponding detection value in the “downstream blockage detectionvalue storage unit 55” in FIG.
ST28では、図9の「下流側閉塞検出値記憶部55」の該当する検出値に関連付けて解消フラグを付する。 Next, when it is determined in ST27 that the downstream blockage detection value is equal to or less than the blockage relaxation reference value, the process proceeds to ST28.
In ST28, a cancellation flag is attached in association with the corresponding detection value in the “downstream blockage detection
次いで、ST29へ進む。ST29では、図10の「輸液ポンプ逆転動作停止処理部(プログラム)66」が動作し、図9の「下流側閉塞検出値記憶部55」に解消フラグが付されたとき、輸液ポンプ10の駆動モータ18の逆転動作を停止させる。
したがって、閉塞解消と共に駆動モータ18の逆転動作が停止され、ポンプ側チューブ11a等の閉塞状態が解消したときに、薬液が患者側チューブ14から患者Pに急激に送液されてしまうことを防止することもできると共に、薬液の流れ出る量等を適切にすることができる。 Next, the process proceeds to ST29. In ST29, when the “infusion pump reverse rotation operation stop processing unit (program) 66” in FIG. 10 operates and the “downstream blockage detectionvalue storage unit 55” in FIG. 9 is flagged, the infusion pump 10 is driven. The reverse rotation operation of the motor 18 is stopped.
Accordingly, when the reverse operation of thedrive motor 18 is stopped together with the removal of the blockage, and the blockage state of the pump side tube 11a and the like is resolved, the liquid medicine is prevented from being rapidly sent from the patient side tube 14 to the patient P. In addition, the amount of the chemical liquid flowing out can be made appropriate.
したがって、閉塞解消と共に駆動モータ18の逆転動作が停止され、ポンプ側チューブ11a等の閉塞状態が解消したときに、薬液が患者側チューブ14から患者Pに急激に送液されてしまうことを防止することもできると共に、薬液の流れ出る量等を適切にすることができる。 Next, the process proceeds to ST29. In ST29, when the “infusion pump reverse rotation operation stop processing unit (program) 66” in FIG. 10 operates and the “downstream blockage detection
Accordingly, when the reverse operation of the
しかし、ST27で、ポンプ側チューブ11a等内の圧力が高まった状態が解消していないと判断されたときは、ST30へ進む。ST30では、図11の「予定送液量到達判断処理部(プログラム)71」が動作し、図10の「逆転動作積算送液量情報記憶部63」と図9の「輸液ポンプ側予定送液量情報記憶部51」を参照し、「逆転動作積算送液量」が「輸液ポンプ側予定送液量」に達しているか否かを判断する。
However, if it is determined in ST27 that the pressure in the pump side tube 11a or the like has not increased, the process proceeds to ST30. In ST30, the “scheduled liquid delivery amount arrival determination processing unit (program) 71” in FIG. 11 operates to operate the “reverse operation integrated liquid feed amount information storage unit 63” in FIG. 10 and “infusion pump side scheduled liquid feed in FIG. With reference to the “volume information storage unit 51”, it is determined whether or not the “reverse operation integrated liquid supply amount” has reached the “infusion pump side planned liquid supply amount”.
すなわち、薬液の送液方向と反対方向への移動が輸液ポンプ10の予定の送液量を超える場合は、逆転動作を継続する必要がないので、かかる事態となっているか否かを判断する。
That is, when the movement of the chemical liquid in the direction opposite to the liquid feeding direction exceeds the planned liquid feeding amount of the infusion pump 10, it is not necessary to continue the reverse rotation operation, so it is determined whether or not this situation occurs.
そこで、ST31で、「逆転動作積算送液量」が「輸液ポンプ側予定送液量」に達していると判断したときは、ST32へ進み、輸液ポンプ10の駆動モータ18の逆転動作を停止させる。
これにより、閉塞状態が解消したとき、薬液が患者側チューブ14から患者Pに急激に送液されてしまうことを防止することもできると共に、薬液の流れ出る量等を適切にすることができる。 Therefore, when it is determined in ST31 that the “reverse operation integrated liquid supply amount” has reached the “infusion pump side planned liquid supply amount”, the process proceeds to ST32 and the reverse operation of thedrive motor 18 of the infusion pump 10 is stopped. .
Thereby, when the obstruction | occlusion state is eliminated, it is possible to prevent the drug solution from being rapidly sent from the patient-side tube 14 to the patient P, and to make the amount of the drug solution flowing out appropriate.
これにより、閉塞状態が解消したとき、薬液が患者側チューブ14から患者Pに急激に送液されてしまうことを防止することもできると共に、薬液の流れ出る量等を適切にすることができる。 Therefore, when it is determined in ST31 that the “reverse operation integrated liquid supply amount” has reached the “infusion pump side planned liquid supply amount”, the process proceeds to ST32 and the reverse operation of the
Thereby, when the obstruction | occlusion state is eliminated, it is possible to prevent the drug solution from being rapidly sent from the patient-
一方、ST31で「逆転動作積算送液量」が「輸液ポンプ側予定送液量」に達していない場合、ST33へ進む、
On the other hand, if the “reverse operation integrated liquid supply amount” does not reach the “infusion pump side planned liquid supply amount” in ST31, the process proceeds to ST33.
ST33では、図11の「予想排出薬液量情報生成処理部(プログラム)72」が動作し、「下流側閉塞検出値記憶部55」の閉塞検出値を取得する。そして、図11の「閉塞検出値対応薬液量情報記憶部73」を参照する。
この閉塞検出値対応薬液量情報記憶部73には、当該閉塞検出値で想定されるポンプ側チューブ11a等内に過剰に溜まっている想定薬液量、すなわち、当該閉塞検出値において閉塞状態を解除したときにポンプ側チューブ11a等から排出される想定薬液量の情報が、閉塞検出値毎に予め記憶されている。 In ST33, the “expected discharged chemical amount information generation processing unit (program) 72” of FIG. 11 operates to acquire the blockage detection value of the “downstream blockage detectionvalue storage unit 55”. Then, the “blockage detection value corresponding chemical liquid amount information storage unit 73” in FIG. 11 is referred to.
The blockage detection value corresponding chemical liquid amount information storage unit 73 releases the blockage state at the blockage detection value, which is an estimated amount of drug solution that is excessively accumulated in thepump side tube 11a and the like that is assumed by the blockage detection value. Information on the amount of the assumed chemical liquid that is sometimes discharged from the pump side tube 11a or the like is stored in advance for each blockage detection value.
この閉塞検出値対応薬液量情報記憶部73には、当該閉塞検出値で想定されるポンプ側チューブ11a等内に過剰に溜まっている想定薬液量、すなわち、当該閉塞検出値において閉塞状態を解除したときにポンプ側チューブ11a等から排出される想定薬液量の情報が、閉塞検出値毎に予め記憶されている。 In ST33, the “expected discharged chemical amount information generation processing unit (program) 72” of FIG. 11 operates to acquire the blockage detection value of the “downstream blockage detection
The blockage detection value corresponding chemical liquid amount information storage unit 73 releases the blockage state at the blockage detection value, which is an estimated amount of drug solution that is excessively accumulated in the
具体的には、予め実験等で計測した想定薬液量の情報となっている。なお、この想定薬液量が予想滞留液体量情報の一例となっている。また、閉塞検出値対応薬液量情報記憶部73に記憶されている閉塞検出値対応薬液量情報が管部内圧力値対応予想液体量情報の一例となっている。
Specifically, it is information on the estimated amount of the chemical solution measured in advance through experiments or the like. In addition, this estimated chemical | medical solution amount is an example of anticipated staying liquid amount information. Further, the occlusion detection value corresponding chemical liquid amount information stored in the occlusion detection value corresponding chemical liquid amount information storage unit 73 is an example of the expected liquid amount information corresponding to the in-pipe pressure value.
したがって、ST33では、当該閉塞検出値に対応する想定薬液量を「閉塞検出値対応薬液量情報記憶部73」から取得し、図11の「想定薬液量情報記憶部74」に記憶する。
Therefore, in ST33, the assumed chemical liquid amount corresponding to the detected occlusion value is acquired from the “occluded detection value corresponding chemical liquid amount information storage unit 73” and stored in the “assumed chemical liquid amount information storage unit 74” of FIG.
次いで、ST34へ進む。ST34では、図11の反送液モード停止情報生成部である例えば、「想定薬液量判断処理部(プログラム)75」が動作し、図10の「逆転動作積算送液量情報記憶部64」の「逆転動作積算送液量」が、図11の「想定薬液量情報記憶部74」の「想定薬液量」に達したか否かを判断する。
Next, proceed to ST34. In ST34, for example, the “anticipated liquid amount determination processing unit (program) 75” which is the counter liquid supply mode stop information generation unit of FIG. 11 operates, and the “reverse operation integrated liquid supply amount information storage unit 64” of FIG. It is determined whether or not the “reverse operation integrated liquid supply amount” has reached the “assumed chemical liquid amount” in the “assumed chemical liquid amount information storage unit 74” of FIG.
すなわち、当該閉塞検出値において、実際にポンプ側チューブ11a等において滞留等している薬液量の分だけ、駆動モータ18を逆転動作させるので、効果的にポンプ側チューブ11a等内に滞留している薬液を薬液容器12a側に戻すことができる。
また、閉塞状態が解消したとき、薬液が患者側チューブ14から患者Pに急激に送液されてしまうことを防止することもできる。 That is, in the blockage detection value, thedrive motor 18 is reversely operated by the amount of the chemical liquid actually retained in the pump side tube 11a or the like, so that it is effectively retained in the pump side tube 11a or the like. The chemical solution can be returned to the chemical solution container 12a side.
In addition, when the occluded state is resolved, it is possible to prevent the drug solution from being rapidly sent from thepatient side tube 14 to the patient P.
また、閉塞状態が解消したとき、薬液が患者側チューブ14から患者Pに急激に送液されてしまうことを防止することもできる。 That is, in the blockage detection value, the
In addition, when the occluded state is resolved, it is possible to prevent the drug solution from being rapidly sent from the
したがって、ST35で、「逆転動作積算送液量」が「想定薬液量」に達したと判断されたときは、ST36へ進み、輸液ポンプ10の駆動モータ18の逆転動作が停止される。
Therefore, when it is determined in ST35 that the “reverse operation integrated liquid supply amount” has reached the “assumed drug solution amount”, the process proceeds to ST36 and the reverse operation of the drive motor 18 of the infusion pump 10 is stopped.
本発明は、上述の実施の形態等に限定されない。本実施の形態では、管理サーバ300の例を示したが、本発明はこれに限らず、複数の輸液ポンプ10等やシリンジポンプ500等を同一のラックに配置し、このラックが、管理サーバ300の役割を発揮する場合も含まれる。すなわち、本発明における「管理装置」には、管理サーバ300のみならずラックも含まれる。
また、本発明は、複数の輸液ポンプ10等やシリンジポンプ500等が、管理サーバ300やラック等を介せずに直接、通信する構成としても構わない。 The present invention is not limited to the above-described embodiment and the like. In the present embodiment, an example of themanagement server 300 is shown, but the present invention is not limited to this, and a plurality of infusion pumps 10 and the like, a syringe pump 500 and the like are arranged in the same rack, and this rack is the management server 300. It also includes the case where the role of That is, the “management apparatus” in the present invention includes not only the management server 300 but also a rack.
In addition, the present invention may be configured such that a plurality of infusion pumps 10 and the like, thesyringe pump 500 and the like communicate directly without using the management server 300 or a rack.
また、本発明は、複数の輸液ポンプ10等やシリンジポンプ500等が、管理サーバ300やラック等を介せずに直接、通信する構成としても構わない。 The present invention is not limited to the above-described embodiment and the like. In the present embodiment, an example of the
In addition, the present invention may be configured such that a plurality of infusion pumps 10 and the like, the
1・・・ポンプシステム、10、110、120、130・・・輸液ポンプ、11a、11b・・・ポンプ側チューブ、12a・・・薬剤容器、13・・・混注部、14・・・患者側チューブ、15・・・留置針、16・・・上流閉塞センサ、17・・・下流側閉塞センサ、18・・・駆動モータ、18a・・・出力軸18a、21・・・ポンプ側ディスプレイ、22・・・各種操作ボタン、22a・・・パイロットランプ、22b・・・早送りスイッチボタン、22c・・・開始スイッチボタン、22d・・・停止スイッチボタン、22e・・・メニュー選択ボタン、30・・・送液駆動部、32・・・カム構造体、32a乃至32f・・・カム、33・・・フィンガ構造体、33a乃至33f・・・フィンガ、41・・・ポンプ制御部、42・・・ポンプ側通信装置、50・・・第1の各種情報記憶部、51・・・輸液ポンプ側予定送液量情報記憶部、52・・・積算送液量情報演算処理部(プログラム)、53・・・送液量基準情報記憶部、54・・・積算送液量情報記憶部、55・・・下流側閉塞検出値記憶部、56・・・輸液ポンプ閉塞基準値情報記憶部、57・・・ポンプ側ポンプ情報記憶部、58・・・輸液ライン識別番号送信処理部(プログラム)59・・・輸液ポンプ閉塞判断処理部(プログラム)、60・・・第2の各種情報記憶部、61・・・ポンプ側閉塞警報情報送信処理部(プログラム)、62・・・輸液ポンプ逆転動作処理部(プログラム)、63・・・逆転動作積算送液量情報演算処理部(プログラム)、64・・・逆転動作積算送液量情報記憶部、65・・・輸液ポンプ閉塞解消判断処理部(プログラム)、66・・・輸液ポンプ逆転動作停止処理部(プログラム)、67・・・輸液ポンプ閉塞緩和基準値情報記憶部、70・・・第3の各種情報記憶部、71・・・予定送液量到達判断処理部(プログラム)、72・・・予想排出薬液量情報生成処理部(プログラム)、73・・・閉塞検出値対応薬液量情報記憶部、74・・・想定薬液量情報記憶部、75・・・想定薬液量判断処理部(プログラム)、300・・・管理装置、301・・・サーバ制御部、302・・・サーバ側通信装置、303・・・サーバ側ディスプレイ、304・・・サーバ側各種情報入力装置、310・・・サーバ側各種情報記憶部、311・・・サーバ側ポンプ情報記憶部、312・・・サーバ側閉塞警報情報送信処理部(プログラム)、313・・・閉塞警報対象ポンプ記憶部、500、530,540、550・・・シリンジポンプ、510・・・シリンジ(薬液容器)、511・・・シリンジ本体、512・・・クランプ、513・・・シリンジ押子押圧部材、514・・・シリンジ押子、516・・・シリンジ側ディスプレイ、517・・・シリンジ押子駆動部、518・・・シリンジ操作ボタン、519・・・閉塞センサ、P・・・患者
DESCRIPTION OF SYMBOLS 1 ... Pump system 10, 110, 120, 130 ... Infusion pump, 11a, 11b ... Pump side tube, 12a ... Drug container, 13 ... Mixed injection part, 14 ... Patient side Tube, 15 ... Indwelling needle, 16 ... Upstream clogging sensor, 17 ... Downstream clogging sensor, 18 ... Drive motor, 18a ... Output shaft 18a, 21 ... Pump side display, 22 ... various operation buttons, 22a ... pilot lamp, 22b ... fast forward switch button, 22c ... start switch button, 22d ... stop switch button, 22e ... menu selection button, 30 ... Liquid feed drive unit, 32... Cam structure, 32 a to 32 f... Cam, 33... Finger structure, 33 a to 33 f. 42... Pump side communication device, 50... First various information storage unit, 51... Infusion pump side scheduled liquid supply information storage unit, 52. ), 53... Liquid feed amount reference information storage unit, 54... Integrated liquid feed amount information storage unit, 55... Downstream blockage detection value storage unit, 56. , 57... Pump side pump information storage unit, 58... Infusion line identification number transmission processing unit (program) 59... Infusion pump blockage judgment processing unit (program), 60. , 61... Pump side blockage alarm information transmission processing unit (program), 62... Infusion pump reverse rotation operation processing unit (program), 63. 64... Reverse operation integrated liquid feed amount information storage 65 ... Infusion pump blockage elimination judgment processing unit (program), 66 ... Infusion pump reverse rotation stop processing unit (program), 67 ... Infusion pump blockage relaxation reference value information storage unit, 70 ... No. 3. Various information storage units, 71... Scheduled liquid delivery amount arrival determination processing unit (program), 72... Expected liquid discharge amount information generation processing unit (program), 73. Storage unit, 74 ... Assumed chemical solution amount information storage unit, 75 ... Assumed chemical solution amount judgment processing unit (program), 300 ... Management device, 301 ... Server control unit, 302 ... Server side communication Device, 303 ... Server side display, 304 ... Server side various information input device, 310 ... Server side various information storage unit, 311 ... Server side pump information storage unit, 312 ... Server side block Warning information Information transmission processing unit (program), 313... Occlusion alarm target pump storage unit, 500, 530, 540, 550 ... Syringe pump, 510 ... Syringe (chemical solution container), 511 ... Syringe body, 512 ... Clamp, 513 ... Syringe pusher pressing member, 514 ... Syringe pusher, 516 ... Syringe side display, 517 ... Syringe pusher drive unit, 518 ... Syringe operation button, 519 ... Occlusion sensor, P ... Patient
Claims (8)
- 対象者に提供する液体を制御する複数の医療用ポンプを備え、
前記医療用ポンプは、少なくとも、前記液体を収容する管部内の前記液体を移動させることができる液体移動部と、
前記管部内の状態情報である管部内状態情報を検知する管部内状態情報検知部と、を有し、
複数の前記医療用ポンプに、それぞれ配置されている前記管部は、合流部で合流し、それぞれの内部に収容されている前記液体が合流する構成となっており、
また、前記管部内状態情報に基づき、前記管部の閉塞情報を生成する閉塞判断部を備え、
前記液体移動部は、前記管部内の前記液体を送液方向に移動させる送液モードと、反送液方向に移動させる反送液モードに切り替え可能な構成となっており、
前記液体移動部は、前記送液モードで動作した後、前記閉塞情報に基づき、前記反送液モードの動作に変更する構成となっており、
前記閉塞情報は、他の前記医療用ポンプに報知される構成となっていることを特徴とする医療用ポンプシステム。 A plurality of medical pumps for controlling the liquid provided to the subject;
The medical pump has at least a liquid moving part capable of moving the liquid in a pipe part containing the liquid;
An in-pipe state information detection unit that detects in-pipe state information, which is state information in the pipe, and
The tube portions respectively disposed in the plurality of medical pumps are joined at a joining portion, and the liquids accommodated in the insides are joined together,
Further, based on the in-pipe state information, a blockage determination unit that generates blockage information of the pipe unit,
The liquid moving part is configured to be switchable between a liquid feeding mode for moving the liquid in the tube part in the liquid feeding direction and a counter liquid feeding mode for moving in the counter liquid feeding direction.
The liquid moving unit is configured to change to the operation of the counter liquid feeding mode based on the blockage information after operating in the liquid feeding mode.
The occlusion information is configured to be notified to other medical pumps. - 前記液体移動部は、前記閉塞情報が、他の前記医療用ポンプに報知された後、前記反送液モードの動作に変更する構成となっていることを特徴とする請求項1に記載の医療用ポンプシステム。 2. The medical device according to claim 1, wherein the liquid moving unit is configured to change the operation to the reaction liquid feeding mode after the blockage information is notified to another medical pump. Pump system.
- 前記医療用ポンプと通信可能な管理装置を有し、
前記閉塞情報は、前記管理装置から他の前記医療用ポンプへ報知される構成となっていることを特徴とする請求項1又は請求項2に記載の医療用ポンプシステム。 A management device capable of communicating with the medical pump;
The medical pump system according to claim 1 or 2, wherein the blockage information is configured to be notified from the management device to another medical pump. - 前記管部内状態情報に基づいて前記反送液モードの停止情報である反送液モード停止情報を生成する反送液モード停止情報生成部を有することを特徴とする請求項1乃至請求項3のいずれか1項に記載の医療用ポンプシステム。 The liquid feeding mode stop information generation part which produces | generates the liquid feeding mode stop information which is the stop information of the said liquid feeding mode based on the in-pipe state information is provided. The medical pump system according to any one of the above.
- 前記管部内状態情報が、前記管部内の圧力値である管部内圧力値情報であり、前記管部内圧力値情報が、前記管部内の閉塞状態を示す情報に相当するとき、その閉塞により滞留している予想滞留液体量情報を記憶する管部内圧力値対応予想液体量情報を有し、前記反送液モード停止情報生成部は、前記予想滞留液体量情報に基づいて、前記反送液モード停止情報を生成することを特徴とする請求項4に記載の医療用ポンプシステム。 When the in-pipe state information is in-pipe pressure value information, which is a pressure value in the pipe, and the in-pipe pressure value information corresponds to information indicating a closed state in the pipe, the pipe is retained due to the blockage. The expected liquid amount information corresponding to the in-pipe pressure value stored therein, and the reaction liquid mode stop information generation unit stops the reaction liquid mode stop based on the expected residence liquid amount information. The medical pump system according to claim 4, wherein information is generated.
- 対象者に提供する液体を制御する複数の医療用ポンプを備え、
前記医療用ポンプは、少なくとも、前記液体を収容する管部内の前記液体を移動させることができる液体移動部と、
前記管部内の状態情報である管部内状態情報を検知する管部内状態情報検知部と、を有し、
複数の前記医療用ポンプに、それぞれ配置されている前記管部は、合流部で合流し、それぞれの内部に収容されている前記液体が合流する構成となっており、
また、前記管部内状態情報に基づき、前記管部の閉塞情報を生成する閉塞判断部を備え、
前記液体移動部は、前記管部内の液体を送液方向に移動させる送液モードと、反送液方向に移動させる反送液モードに切り替え可能な構成となっている医療用ポンプシステムの制御方法であって、
前記液体移動部は、前記送液モードで動作した後、前記閉塞情報に基づき、前記反送液モードの動作に変更し、
前記閉塞情報は、他の前記医療用ポンプに報知される構成となっていることを特徴とする医療用ポンプシステムの制御方法。 A plurality of medical pumps for controlling the liquid provided to the subject;
The medical pump has at least a liquid moving part capable of moving the liquid in a pipe part containing the liquid;
An in-pipe state information detection unit that detects in-pipe state information, which is state information in the pipe, and
The tube portions respectively disposed in the plurality of medical pumps are joined at a joining portion, and the liquids accommodated in the insides are joined together,
Further, based on the in-pipe state information, a blockage determination unit that generates blockage information of the pipe unit,
The method for controlling a medical pump system, wherein the liquid moving section is configured to be switchable between a liquid feeding mode for moving the liquid in the tube section in the liquid feeding direction and a counter liquid feeding mode for moving in the counter liquid feeding direction. Because
After the liquid moving unit operates in the liquid feeding mode, based on the blockage information, change to the operation of the counter liquid feeding mode,
The control method of the medical pump system, wherein the blockage information is notified to the other medical pumps. - 対象者に提供する液体を制御する複数の医療用ポンプを備え、
前記医療用ポンプは、少なくとも、前記液体を収容する管部内の前記液体を移動させることができる液体移動部と、
前記管部内の状態情報である管部内状態情報を検知する管部内状態情報検知部と、を有し、
複数の前記医療用ポンプに、それぞれ配置されている前記管部は、合流部で合流し、それぞれの内部に収容されている前記液体が合流する構成となっており、
また、前記管部内状態情報に基づき、前記管部の閉塞情報を生成する閉塞判断部を備え、
前記液体移動部は、前記管部内の液体を送液方向に移動させる送液モードと、反送液方向に移動させる反送液モードに切り替え可能な構成となっている医療用ポンプシステムに、前記液体移動部が、前記送液モードで動作した後、前記閉塞情報に基づき、前記反送液モードの動作に変更する工程と、
前記閉塞情報が、他の前記医療用ポンプに報知される工程と、を実行させることを特徴とする医療用ポンプの制御プログラム。 A plurality of medical pumps for controlling the liquid provided to the subject;
The medical pump has at least a liquid moving part capable of moving the liquid in a pipe part containing the liquid;
An in-pipe state information detection unit that detects in-pipe state information, which is state information in the pipe, and
The tube portions respectively disposed in the plurality of medical pumps are joined at a joining portion, and the liquids accommodated in the insides are joined together,
Further, based on the in-pipe state information, a blockage determination unit that generates blockage information of the pipe unit,
In the medical pump system configured to be switchable between a liquid feeding mode for moving the liquid in the tube part in the liquid feeding direction and a liquid feeding mode for moving in the counter liquid feeding direction. After the liquid moving unit operates in the liquid feeding mode, based on the blockage information, the step of changing to the operation of the counter liquid feeding mode,
A control program for the medical pump, wherein the blockage information is notified to the other medical pump. - 対象者に提供する液体を制御する医療用ポンプであって、
前記医療用ポンプは、少なくとも、前記液体を収容する管部内の前記液体を移動させることができる液体移動部と、
前記管部内の状態情報である管部内状態情報を検知する管部内状態情報検知部と、を有し、
前記医療用ポンプに配置されている前記管部は、合流部で他の管部と前記液体が合流する構成となっており、
前記管部内状態情報に基づき、前記管部の閉塞情報を生成する閉塞判断部を備え、
前記液体移動部は、前記管部内の前記液体を送液方向に移動させる送液モードと、反送液方向に移動させる反送液モードに切り替え可能な構成となっており、
前記液体移動部は、前記送液モードで動作した後、前記閉塞情報に基づき、前記反送液モードの動作に変更する構成となっており、
前記閉塞情報を、他の前記管部が配置された他の医療用ポンプに報知する構成となっていることを特徴とする医療用ポンプ。 A medical pump for controlling a liquid provided to a subject,
The medical pump has at least a liquid moving part capable of moving the liquid in a pipe part containing the liquid;
An in-pipe state information detection unit that detects in-pipe state information, which is state information in the pipe, and
The pipe part arranged in the medical pump has a configuration in which the liquid joins with another pipe part at the junction part,
Based on the in-pipe state information, a blockage determination unit that generates blockage information of the tube unit,
The liquid moving part is configured to be switchable between a liquid feeding mode for moving the liquid in the tube part in the liquid feeding direction and a counter liquid feeding mode for moving in the counter liquid feeding direction.
The liquid moving unit is configured to change to the operation of the counter liquid feeding mode based on the blockage information after operating in the liquid feeding mode.
A medical pump characterized in that the blockage information is notified to another medical pump in which the other pipe section is arranged.
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WO2014049647A1 (en) * | 2012-09-26 | 2014-04-03 | テルモ株式会社 | Syringe pump |
WO2014100658A1 (en) * | 2012-12-21 | 2014-06-26 | Deka Products Limited Partnership | Syringe pump system |
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WO2014049647A1 (en) * | 2012-09-26 | 2014-04-03 | テルモ株式会社 | Syringe pump |
WO2014100658A1 (en) * | 2012-12-21 | 2014-06-26 | Deka Products Limited Partnership | Syringe pump system |
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