WO2011045906A1 - 薬液調製支援システムおよび薬液調製支援方法 - Google Patents

薬液調製支援システムおよび薬液調製支援方法 Download PDF

Info

Publication number
WO2011045906A1
WO2011045906A1 PCT/JP2010/005979 JP2010005979W WO2011045906A1 WO 2011045906 A1 WO2011045906 A1 WO 2011045906A1 JP 2010005979 W JP2010005979 W JP 2010005979W WO 2011045906 A1 WO2011045906 A1 WO 2011045906A1
Authority
WO
WIPO (PCT)
Prior art keywords
weight
information
unit
medicine bottle
drug solution
Prior art date
Application number
PCT/JP2010/005979
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
奥田晃庸
中村徹
藤岡総一郎
水野修
太田章博
Original Assignee
パナソニック株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by パナソニック株式会社 filed Critical パナソニック株式会社
Priority to EP10823174A priority Critical patent/EP2489343A1/en
Priority to CN2010800409085A priority patent/CN102665643A/zh
Priority to JP2011543932A priority patent/JP5490140B2/ja
Priority to US13/501,404 priority patent/US20120199239A1/en
Publication of WO2011045906A1 publication Critical patent/WO2011045906A1/ja

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J3/00—Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
    • A61J3/002—Compounding apparatus specially for enteral or parenteral nutritive solutions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J2200/00—General characteristics or adaptations
    • A61J2200/70—Device provided with specific sensor or indicating means
    • A61J2200/74—Device provided with specific sensor or indicating means for weight

Definitions

  • the present invention relates to a drug solution preparation support system and drug solution adjustment support method that are used in audits when injecting drug solutions such as injection drugs into an infusion bag in the field of medicine and the like.
  • the drug solution is sucked into the syringe from the drug solution container (drug bottle), and the drug solution is injected into the infusion bag from the syringe. In this operation, the suction amount of the drug solution is confirmed There is a need to. In particular, for chemicals that cause human health if the application rate is incorrect, it is necessary to sufficiently check the amount of chemical solution.
  • the work of mixing the drug solution is generally performed manually by a nurse or a pharmacist.
  • the nurse or pharmacist inserts an injection needle into the drug solution container.
  • the drug solution is being aspirated.
  • suctioning a high viscosity drug solution such as glucose
  • a large force is required to operate the syringe.
  • suctioning a drug solution from a vial container requiring internal pressure adjustment a complicated procedure is required. Therefore, the work of taking out the drug solution from the drug solution container is a heavy burden on nurses and pharmacists.
  • FIG. 23 shows a conventional medicine inspection device used in sorting medicines (see, for example, Patent Document 1).
  • the medicine inspection device 1 is used to support a comparison inspection of medicines when the medicines are stocked.
  • a method of audit using the medicine audit device 1 will be described.
  • a worker such as a nurse or a pharmacist first inputs dispensing information into the data input and display device 2.
  • the storage and analysis device 3 Based on the data input and the dispensing information input to the display device 2, the storage and analysis device 3 transmits the image data and weight data of the medicine necessary for the dispensing to the comparison and determination device 4.
  • the storage and analysis device 3 stores in advance image data and weight data of medicines used in hospitals, dispensing pharmacies and the like.
  • the image data and weight data of the medicine stored in the storage and analysis device 3 are created in advance by the image data recognition device 5 and the weight measurement device 6 of the medicine inspection device 1.
  • the medicine inspection apparatus 1 executes the following process for each medicine placed on the medicine setting stage 7. That is, first, the image data recognition device 5 creates image data of the medicine placed on the medicine setting stage 7, and transmits the created image data to the comparison / determination device 4. The comparison and determination device 4 compares and determines the image data of the medicine placed on the medicine setting stage 7 with the image data transmitted from the storage and analysis device 3. The determination result (OK ⁇ NG) is transmitted to the data input and display device 2. Furthermore, if the determination result is OK, the weight measuring device 6 creates weight data of the drug placed on the drug setting stage 7, and transmits the created weight data to the comparison and determination device 4. The comparison and determination device 4 compares the weight data of the drug placed on the drug setting stage 7 with the weight data transmitted from the storage and analysis device 3 to make a determination. The determination result (OK ⁇ NG) is also transmitted to the data input and display device 2.
  • the conventional drug inspection device automatically verifies the appearance and weight of the individual medicines provided to assist in the verification audit as to whether the medicines provided are correct. By this inspection, it is possible to prevent a drug stocking error.
  • the conventional medicine inspection device can be used for the inspection at the time of arranging medicine containers.
  • this conventional medicine inspection device can not be used for an audit when preparing a medicine by mixing medicines or the like.
  • an object of the present invention is to provide a chemical solution preparation support system and a chemical solution preparation support method that can support an audit such as the injection amount of a chemical solution when preparing a chemical solution.
  • the drug solution preparation support system comprises the total weight of a medicine bottle placement unit on which a medicine bottle is placed and all medicine bottles placed on the medicine bottle placement unit.
  • the weight of the medicine bottle weight measurement unit having the first weight measurement unit to be measured, the infusion bag placement unit on which the infusion bag is placed, and the infusion bag placed on the infusion bag placement unit An audit information is generated based on a change in weight respectively measured by an infusion bag weight measurement unit having a second weight measurement unit, a storage unit, the medicine bottle weight measurement unit, and the infusion bag weight measurement unit.
  • the control unit that stores the generated audit information in the storage unit
  • information on the chemical solution to be injected into the infusion bag stored in the storage unit in advance or the audit information stored in the storage unit by the control unit Display at least one of It includes an information presentation unit, the.
  • Audit based on the change in weight measured in the medicine bottle weight measurement step to measure, the infusion bag weight measurement step to measure the weight of the infusion bag placed on the infusion bag mounting portion, and the medicine bottle weight measurement step Generating audit information based on a first audit information generation step of generating information and storing the generated audit information in the storage unit, and a change in weight measured by the infusion bag weight measurement step; And D. second audit information generation step of storing the executed audit information in the storage unit.
  • the present invention it is possible to support audits such as the suction amount of the drug solution when preparing the drug solution, the mixing and preparation order of the drug solution, and the injection amount of the drug solution. Therefore, according to the present invention, it is possible to prevent an error in taking a medicine bottle or an error in the amount of a drug solution. Therefore, according to the present invention, safe and accurate preparation of a drug solution can be achieved.
  • the perspective view showing the outline of the composition of the medical fluid preparation support system concerning the embodiment of the present invention The figure which shows the principal part of the vial weight measurement part which concerns on embodiment of this invention, and an infusion bag weight measurement part.
  • the figure which shows an example of the change of the weight measured by the vial weight measurement part which concerns on embodiment of this invention The figure which shows an example of the change of the weight measured by the vial weight measurement part which concerns on embodiment of this invention.
  • the figure which shows an example of the change of the weight measured by the vial weight measurement part which concerns on embodiment of this invention The figure which shows an example of the change of the weight measured by the vial weight measurement part which concerns on embodiment of this invention.
  • FIG. 1 Flow chart of the drug solution preparation support method according to the embodiment of the present invention
  • the figure which shows an example of the image shown on the screen of the information presentation part which concerns on embodiment of this invention The figure which shows an example of the image shown on the screen of the information presentation part which concerns on embodiment of this invention.
  • FIG. 1 is a perspective view showing the outline of the configuration of a drug solution preparation support system according to an embodiment of the present invention.
  • a chemical solution preparation support system 10 according to this embodiment comprises a drug solution preparation support device 11 and a medical information database 12 connected to the drug solution preparation support device 11 via a network.
  • the chemical solution preparation supporting device 11 includes a base portion 13.
  • the base unit 13 includes a medicine bottle weight measurement unit 14, an infusion bag weight measurement unit 15, a cradle unit 16, and an information presentation unit 17. Further, the housing of the base unit 13 incorporates the control unit 18 and the storage unit 19 as indicated by a broken line.
  • FIG. 2 is a view showing the main parts of a vial weight measurement unit and an infusion bag weight measurement unit according to the embodiment of the present invention.
  • the vial weight measurement unit 14 includes a vial placement unit 14 a on which a plurality of vials 20 can be placed, and a total vial 20 placed on the vial placement unit 14 a. And a weight measurement unit 14b that measures the total weight.
  • the weight measurement unit 14 b is disposed vertically below the medicine bottle placement unit 14 a.
  • FIG. 2 exemplifies how two vial containers 20a having different shapes and four ampoule containers 20b having different shapes are placed on the vial mounting portion 14a.
  • FIG. 1 shows a configuration in which the medicine bottle mounting portion of the medicine bottle weight measurement unit 14 can mount up to six medicine bottles 20, it is needless to say that the medicine bottle mounting of the medicine bottle weight measurement unit 14
  • the number of medicine bottles that can be placed in the holder is not limited to six.
  • the infusion bag weight measurement unit 15 is placed on the infusion bag placement unit 15 a on which the infusion bag 21 into which the drug solution is injected is placed and the infusion bag placement unit 15 a. And a weight measurement unit 15 b that measures the weight of the infusion bag 21.
  • the weight measurement unit 15 b is disposed vertically below the infusion bag mounting unit 15 a. Physiological saline is put in advance in the infusion bag 21 placed on the infusion bag placement unit 15a.
  • the infusion bag mounting portion of the infusion bag weight measurement unit 15 includes a support portion 15 c that supports the vicinity of the spout 21 b of the infusion bag 21.
  • the infusion bag 21 is supported by the support portion 15 c such that the spout surface 21 b of the infusion bag 21 faces obliquely upward.
  • the injection needle of the syringe can be easily pierced into the injection / delivery stopper 21a of the infusion solution bag 21 when injecting the drug solution sucked into the syringe into the infusion solution bag 21 Become.
  • the injection needle is inserted into the injection / discharge plug 21a of the infusion bag 21 and the syringe is inserted into the injection needle pierced by the injection / discharge plug 21a to inject the drug solution into the infusion bag 21.
  • the syringe is inserted into the injection needle pierced by the injection / discharge plug 21a to inject the drug solution into the infusion bag 21.
  • Coring is a phenomenon in which a rubber plug is scraped off by an injection needle.
  • the medical solution is injected from the syringe to the infusion bag in a state where the injection needle is inserted into the injection / discharge plug 21a of the infusion bag 21, if the injection / discharge surface 21b of the infusion bag 21 faces obliquely upward
  • the injection needle can be prevented from being contaminated by touching anything other than the syringe.
  • control unit 18 is connected to the vial weight measurement unit 14 and the infusion bag weight measurement unit 15 via the signal line 22a, and the vial weight measurement unit 14 and the infusion bag weight measurement unit The data of the weight respectively measured by 15 is transmitted to the control part 18 via the signal line 22a.
  • the control unit 18 generates, on the basis of the change in weight measured by the medicine bottle weight measurement unit 14 and the infusion bag weight measurement unit 15, audit information representing the inspection result of the preparation operation of the drug solution.
  • the storage unit 19 is connected to the control unit 18 via the signal line 22 b, and the control unit 18 stores audit information in the storage unit 19.
  • the weight of each placed vial 20 may be measured individually. However, by measuring the total weight of all vials 20, the number of sensors can be reduced compared to the case where the weight of each vial 20 is individually measured.
  • the drug solution preparation support system 10 performs the counting audit of the medicine bottle, the kind of medicine bottle, and the like based on the change in weight measured by the medicine bottle weight measurement unit 14 and the infusion bag weight measurement unit 15 respectively. It is possible to support type check of chemical solution, audit of mixed preparation order of chemical solution, measurement audit of chemical solution, etc. With these audits, errors in the selection of medicine bottles, medicine bottles for preparation of medicine, etc. Mistakes and errors in the amount of chemical solution can be prevented. Therefore, according to the drug solution preparation support system 10, safe and accurate preparation of drug solution can be achieved. The operation of the drug solution preparation support system 10 when performing various audit processes will be described later.
  • the cradle unit 16 holds a syringe drive device 23.
  • the syringe drive device 23 drives the piston of the syringe 23 a attached to the syringe drive device 23.
  • the syringe drive device 23 can assist the suction of the drug solution into the cylinder of the syringe 23a and the injection of the drug solution from the cylinder of the syringe 23a into the infusion bag 21.
  • the cradle unit 16 includes a holding unit 16a that holds the syringe drive device 23, and a weight measurement unit (not shown) that measures the weight of the syringe drive device 23 held by the holding unit 16a.
  • the cradle unit 16 corresponds to a syringe weight measurement unit.
  • the weight measurement unit of the cradle unit 16 is also controlled via the signal line, similarly to the weight measurement unit 14a of the vial weight measurement unit 14 and the weight measurement unit 15b of the infusion bag weight measurement unit 15 shown in FIG.
  • the data of the weight measured by the weight measurement unit of the cradle unit 16 is transmitted to the control unit 18. Therefore, based on the weight measured by the cradle unit 16, the control unit 18 can generate audit information representing an inspection result of the preparation operation of the drug solution, and store the generated audit information in the storage unit 19.
  • the holding unit 16 a of the cradle unit 16 has a charging unit (not shown) for charging the syringe drive device 23. Therefore, while the syringe drive device 23 is held by the cradle unit 16, the power supply (not shown) of the syringe drive device 23 is charged.
  • the drug solution preparation support system 10 can support an audit as to whether the drug solution remains in the syringe 23 a or an audit of the amount of drug solution drawn in the syringe 23 a. By these audits, it is possible to prevent the mistake of the medicine bottle when preparing the drug solution, the mistake of the amount of drug solution, and the like.
  • the operation of the drug solution preparation support system 10 when performing various audit processes based on the weight measured by the cradle unit 16 will be described later.
  • the cradle unit 16 may be provided with a needle removing unit (not shown) for removing the used needle from the syringe 23a.
  • the needle removing portion can be constituted by, for example, a flat plate provided with a V-groove.
  • the flange portion of the syringe 23a can be hooked to the V groove, and the needle can be pulled out.
  • the information presentation unit 17 includes a screen 17 a.
  • the control unit 18 controls the image displayed on the screen 17 a based on various types of information stored in the storage unit 19.
  • information on a drug solution to be injected into the infusion bag 21, audit information, information on a patient to which the prepared drug solution is applied, etc. is displayed on the screen 17a of the information presentation unit 17
  • the information on the drug solution includes information necessary for preparation of the drug solution, such as the type of drug solution, the dose of the drug solution, and the preparation procedure of the drug solution. Note that only one of the information related to the chemical solution and the audit information may be displayed on the information presentation unit 17.
  • the drug solution preparation support system 10 can visually present information to the operator such as the type of drug solution to be injected into the infusion bag 21 and the mixing preparation order of drug solutions. It becomes. Therefore, the operator can easily and accurately confirm the information necessary for the preparation of the drug solution. In addition, the operator can prepare the drug solution efficiently.
  • the base unit 13 As shown in FIG. 1, the base unit 13 is integrated with the medicine bottle weight measurement unit 14, the infusion bag weight measurement unit 15, and the cradle unit 16. Further, the base unit 13 includes a work table (mixing preparation area) 13 a disposed adjacent to the medicine bottle weight measurement unit 14 and the infusion bag weight measurement unit 15. On this workbench 13a, workers such as a nurse and a pharmacist can carry out a preparation operation of a drug solution. Further, as described above, the information presentation unit 17 is installed in the base unit 13, and the control unit 18 and the storage unit 19 are built in the housing of the base unit 13. Therefore, with this configuration, the chemical solution preparation supporting device 11 can be made compact.
  • the medical fluid preparation support system may be configured such that the medicine bottle weight measurement unit 14, the infusion bag weight measurement unit 15, the cradle unit 16, and the information presentation unit 17 are separated from the base unit 13.
  • the medical information database 12 will be described.
  • medical information such as information on medical fluid, audit information, patient information and the like is transmitted and received between the medical fluid preparation support device 11 and the medical information database 12.
  • various types of information can be fetched from the medical information database 12 and stored (stored) in the storage unit 19 as necessary.
  • audit information stored in the storage unit 19 can be accumulated in the medical information database 12 as medical information.
  • the control unit 18 displays a full-size photograph image (real-shot image) of each medicine bottle 20 containing the drug solution to be injected into the infusion bag 21 based on the information on the drug solution stored in the storage unit 19.
  • the mixed preparation order is displayed on the screen 17a of FIG. Therefore, the information on the drug solution includes data of a photographed image.
  • a worker such as a nurse or a pharmacist can arrange and arrange the medicine bottles 20 in the mixed preparation order while comparing with the photographed images. Therefore, the worker can visually check the type of medicine (the type of medicine bottle). Therefore, for example, even when it is necessary to stock medicine bottles containing medicines of similar names, it is possible to prevent mistakes in the selection of medicine bottles and an error in the arrangement order of the medicine bottles. Furthermore, since the medicine bottles can be arranged in the order of mixing and preparation, it is possible to prevent an error in the order of suctioning the medicine (order of mixing medicines).
  • the medical fluid preparation support system 10 includes a reading unit 24 that reads prescription identification information (prescription ID) in order to fetch information on a medical fluid from the medical information database 12.
  • the prescription ID read by the reading unit 24 is stored in the storage unit 19 by the control unit 18.
  • the prescription ID stored in the storage unit 19 is transmitted by the control unit 18 to the medical information database 12.
  • the medical information database 12 transmits information related to a drug solution corresponding to the received prescription ID, patient information, and the like.
  • the control unit 18 causes the storage unit 19 to store information on a drug solution, patient information, and the like transmitted from the medical information database 12. For example, a one-dimensional or two-dimensional barcode can be used as the prescription ID.
  • a reading unit 24 for reading a prescription ID is provided on the back of the information presentation unit 17.
  • the reading unit 24 has a shape of a folder for holding a sheet (hereinafter, referred to as “prescription”) 25 on which a prescription is printed. Therefore, the reading unit 24 reads the prescription ID printed on the prescription 25 inserted in the folder.
  • the reading unit 24 for reading out the prescription identification information as described above, the medical information can be easily read from the medical information database 12. Further, by providing the folder of the prescription 25 on the back of the information presentation unit 17, it is possible to reduce the risk that the prescription 25 becomes contaminated with the medical solution etc. and the characters can not be read when the medical solution is prepared.
  • a reading unit that reads information on the drug solution and information on the drug printed on the surface of the prescription 25 is provided, and the information read by the reading unit is stored in the storage unit 19
  • an input unit that can input information related to the prescription ID and the medical solution is provided, and the information input by the input unit is stored in the storage unit 19 It is good also as composition which makes it memorize.
  • the chemical solution preparation support system 10 also includes a camera 26.
  • the camera 26 is used to authenticate the worker. That is, the control unit 18 performs authentication by comparing the image of the worker taken by the camera 26 with the image of the worker stored in the storage unit 19. In this way, only persons registered in advance can be permitted to work.
  • this camera 26 can also be used for authentication of the medicine bottle 20 containing the chemical
  • a reflection type photo sensor may be embedded at each position where the medicine bottle of the medicine bottle weight measurement unit 14 is placed, and a signal generated by the reflection type photo sensor may be transmitted to the control unit 18.
  • a signal generated by the reflection type photo sensor may be transmitted to the control unit 18.
  • the liquid medicine preparation supporting device 11 displays an LED (Light Emitting Diode) display corresponding to each position where the medicine bottle weight measurement unit 14 is placed in the vicinity of the medicine bottle weight measurement unit 14.
  • a department is provided.
  • the light emission of the LED display unit is controlled by the control unit 18. That is, the control unit 18 causes the LED display unit corresponding to the medicine bottle 20 to be suctioned to emit light. By the light emission of the LED display unit, it is possible to explicitly instruct the operator about the medicine bottle 20 to be sucked.
  • a worker such as a nurse or a pharmacist inserts the prescription 25 into the reading unit 24 provided on the back of the information presentation unit 17.
  • information on the patient, information on a drug solution applied to the patient, a prescription ID and the like are printed.
  • the reading unit 24 reads the prescription ID printed on the prescription 25.
  • the read prescription ID is stored in the storage unit 19 by the control unit 18.
  • the prescription ID stored in the storage unit 19 is transmitted by the control unit 18 to the medical information database 12.
  • the medical information database 12 transmits information on a patient corresponding to the received prescription ID, information on a drug solution, and the like.
  • the transmitted information on the patient and the drug solution is stored in the storage unit 19 by the control unit 18.
  • control unit 18 causes the screen 17 a of the information presentation unit 17 to display an instruction corresponding to each step of the liquid preparation operation based on the patient information stored in the storage unit 19 and the information on the medical solution. Therefore, the worker can perform the preparation operation of the drug solution in accordance with the instruction displayed on the screen 17 a of the information presentation unit 17.
  • FIG. 3 is a diagram showing an example of an instruction displayed on the screen 17 a of the information presentation unit 17.
  • FIG. 3 shows an example of an image instructing the operator to place the medicine bottle 20 on the medicine bottle placement part 14a and place the infusion bag 21 on the infusion bag placement part 15a.
  • a status display 17b indicating the current status of the liquid preparation operation is displayed.
  • the status display 17b allows the operator to easily confirm which step of the liquid preparation operation is currently. Therefore, even if there is a work interruption, the worker can easily resume the work.
  • a work instruction display 17c and a completion button 17d are displayed below the status display 17b.
  • the content displayed on the work instruction display 17c changes in accordance with each step of the chemical liquid preparation operation.
  • a patient information display 17e showing the patient's name, a hospital room and the like is displayed below the work instruction display 17c and the completion button 17d.
  • a drug solution information display 17f is displayed, which shows information on a drug solution to be injected into the infusion bag 21.
  • names of drug solutions and doses of drug solutions are displayed side by side from the left in the order of mixing and preparation, together with the photographed images 20c of medicine bottles to be sorted.
  • the operator can display the photographed images 20c of the medicine bottles 20 containing the drug solution to be injected into the infusion bag 21 in order of the mixing preparation on the screen 17a of the information presenting unit 17.
  • the vials 20 can be arranged on the vial placement portion 14a in a manner that approximately overlaps the image 20c. Therefore, the worker can align and place the medicine bottles 20 containing the drug solution to be injected into the infusion bag 21 on the medicine bottle mounting portion 14a in the mixing and preparation order.
  • FIG. 3 exemplifies the case where the medical solutions that need to be injected into the infusion bag 21 are the medical solutions A, B, and C.
  • the medical solutions A, B and C are mixed and prepared in this order.
  • the medicine bottles 20 containing the medicines A, B and C are prepared on the medicine bottle mounting portion 14a, the medicines prepared on the basis of the change in weight measured by the medicine bottle weight measurement unit 14 It is possible to support verification inspection of bottle type (type of drug solution), audit of arrangement order of medicine bottles, and counting audit of medicine bottles that have been prepared.
  • FIG. 4 is a view showing an example of a change in weight measured by the vial weight measuring unit 14 when the medicine bottles 20 containing the drug solutions A, B, C are placed on the vial mounting portion 14a. is there.
  • the operator places the medicine bottle 20 (hereinafter referred to as medicine bottle A) containing the medicine A on the medicine bottle mounting portion 14a.
  • the weight W1 of the vial A is measured by the vial weight measurement unit 14.
  • the control unit 18 recognizes the measured amount of increase ⁇ W1 as the weight of the vial A and stores it in the storage unit 19.
  • the control unit 18 compares the recognized weight ⁇ W1 of the vial A with the data (predetermined value) of the initial weight of the vial A previously stored in the storage unit 19 and stores the comparison result.
  • the measured weight ⁇ W1 of the drug solution A and the comparison result are stored in the storage unit 19 as audit information.
  • the initial weight of the medicine bottle means the weight of the unopened medicine bottle when the medical solution is used up.
  • the initial weight of the medicine bottle means the weight of the medicine bottle after the previous use.
  • the weight of the vial after the previous use may be registered in the medical information database 12 in association with the identification information given to each vial.
  • the medicine bottle B When the medicine bottle 20 containing the drug solution B (hereinafter referred to as the medicine bottle B) is placed on the medicine bottle mounting portion 14a by the operator, as shown in FIG.
  • the total weight W2 of the medicine bottle B is measured by the medicine bottle weight measurement unit 14.
  • the measured weight ⁇ W2 of the medicine bottle B and the comparison result are stored in the storage unit 19 as audit information.
  • the medicine bottle 20 containing the medicine solution C (hereinafter referred to as the medicine bottle C) is placed on the medicine bottle mounting portion 14a by the operator, as shown in FIG.
  • the total weight W3 of the medicine bottle C is measured by the medicine bottle weight measurement unit 14.
  • the control unit 18 recognizes the measured amount of increase ⁇ W3 as the weight of the medicine bottle C and stores it in the storage unit 19.
  • the control unit 18 compares the recognized weight ⁇ W3 of the vial C with the data (predetermined value) of the initial weight of the vial C previously stored in the storage unit 19 and stores the comparison result. It is stored in the unit 19.
  • the measured weight ⁇ W3 of the medicine bottle C and the comparison result are stored in the storage unit 19 as audit information.
  • the medicines sorted out by measuring the weight of the vial 20 placed on the vial placement unit 14 a It is possible to support verification of the type of bottle (chemical solution).
  • the assortment error information may be displayed on the screen 17 a of the information presentation unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the sorting error information generated by the control unit 18.
  • the control unit 18 counts the number of changes in weight measured by the vial weight measuring unit 14 when the medicine bottles 20 are placed on the vial mounting unit 14a, and based on the counting result, The number of medicine bottles 20 placed on the medicine bottle placement unit 14a is measured.
  • the measured data is stored in the storage unit 19 by the control unit 18.
  • the control unit 18 compares the measured number of medicine bottles 20 with the data (predetermined value) of the number of medicine bottles previously stored in the storage unit 19 and stores the comparison result in the storage unit 19. Do.
  • the measured number of medicine bottles 20 and the comparison result are stored in the storage unit 19 as audit information.
  • the included data may be used.
  • the control unit 18 may analyze the number of medicine bottles from the information on the drug solution, and store the analyzed data on the number of medicine bottles in the storage unit 19. For example, the control unit 18 can analyze the number of medicine bottles based on the number of photographed images included in the information on the liquid medicine.
  • counting the number of changes in weight measured by the vial weight measuring unit 14 can support counting audits of the prepared vials.
  • the control unit 18 when the control unit 18 recognizes that the measured number of medicine bottles 20 does not match the data (predetermined value) of the number of medicine bottles previously stored in the storage unit 19, the medicine bottles arranged Generate counting error information indicating that the number of 20 is insufficient.
  • the counting error information may be displayed on the screen 17 a of the information presenting unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the counting error information generated by the control unit 18.
  • the drug solution preparation support system 10 can support an audit as to whether or not there is an error in the selection of medicine bottles (drug solution).
  • the weight of the medicine may be measured.
  • the control unit 18 recognizes the weight of the medicine bottle 20 based on the increase in weight measured by the medicine bottle weight measurement unit 14, and offsets the weight of the medicine bottle alone from the recognized weight. Measure the weight of the drug solution.
  • the measured data is stored in the storage unit 19 by the control unit 18.
  • the control unit 18 compares the measured weight of the drug solution with the data of the initial weight of the drug solution previously stored in the storage unit 19, and stores the comparison result in the storage unit 19. Even in this case, it is possible to support an audit as to whether or not there is an error in the selection of medicine bottles (chemical solutions).
  • the control unit 18 may analyze the initial weight of the chemical solution from the information on the chemical solution, and store in the storage unit 19 data of the analyzed initial weight of the chemical solution. Specifically, the control unit 18 may obtain the initial weight of the drug solution by calculating the difference between the initial weight of the medicine bottle and the weight of the single medicine bottle.
  • the initial weight of the drug solution means the weight of the drug solution contained in the unopened medicine bottle when the drug solution is used up. On the other hand, in the case where the medicine contained in the medicine bottle is divided and used plural times, it means the weight of the medicine contained in the medicine bottle after the previous use.
  • the operator After the medicine bottles 20 containing the medicines to be infused into the infusion bag 21 are arranged on the medicine bottle mounting portion 14a, the operator first picks up the medicine bottles 20 containing the medicine A and A prescribed amount of drug solution A is aspirated into the syringe 23a from the medicine bottle 20 taken. Then, the worker returns the medicine bottle 20 from which the liquid medicine A has been sucked back to the original position on the medicine bottle mounting portion 14a. Next, the operator picks up the medicine bottle 20 containing the medicine solution B, and sucks the medicine solution B from the medicine bottle 20 picked up by the hand into the syringe 23a by a predetermined dose.
  • the worker returns the medicine bottle 20 from which the liquid medicine B has been sucked back to the original position on the medicine bottle mounting portion 14a.
  • the operator picks up the medicine bottle 20 containing the medicine C, and sucks the medicine C from the medicine bottle 20 picked up by the hand into the syringe 23a by a predetermined dose. Then, the worker returns the medicine bottle 20 from which the drug solution C has been sucked back to the original position on the medicine bottle placement portion 14a.
  • the injection of the drug solution from the syringe 23a into the infusion bag 21 may be performed after suctioning the drug solution from one vial 20 into the syringe 23a, or the drug solution is sucked from the plurality of drug bottles 20 into the syringe 23a. You may go after you
  • a comparison audit of the kind of medicine bottle taken (the kind of liquid medicine) based on the weight measured by the medicine bottle weight measurement unit 14 It can support the order of picking up vials and the number of times the vials have been taken up. Also, when the medicine bottle 20 is returned onto the medicine bottle placement unit 14a, based on the weight measured by the medicine bottle weight measurement unit 14, the measurement audit of the drug solution sucked into the syringe 23a, the suctioned, It is possible to support a checkup on the type of drug solution, an audit on the mixed preparation order of drug solutions, and an audit on the number of times the medicine bottle is returned.
  • FIG. 5 is a view showing an example of a change in weight measured by the vial weight measuring unit 14 when each of the vials 20 containing the drug solutions A, B and C is taken from the vial mounting portion 14a. .
  • the total weight W3 of the medicine bottle A to the medicine bottle C is measured by the medicine bottle weight measurement unit 14 as shown in FIG. There is.
  • the operator picks up the medicine bottle A from the medicine bottle mounting portion 14a in order to suction the liquid medicine A.
  • the weight W4 of the vial B and the vial C is measured by the vial weight measurement unit 14.
  • control unit 18 compares the recognized weight ⁇ W4 of the vial A with the data (predetermined value) of the initial weight of the vial A previously stored in the storage unit 19 and stores the comparison result.
  • the measured weight ⁇ W4 of the medicine bottle A and the comparison result are stored in the storage unit 19 as audit information.
  • the data of the initial weight contained in the information on the drug solution may be used as the data of the initial weight of each drug vial containing the drug solutions A, B, and C, or the drug vials on the drug vial mounting portion 14a
  • the data of the initial weight measured when sorting 20 may be used.
  • control unit 18 recognizes the measured amount of decrease ⁇ W5 as the weight of the medicine bottle B and stores it in the storage unit 19. Further, the control unit 18 compares the recognized weight ⁇ W5 of the vial B with the data (predetermined value) of the initial weight of the vial B previously stored in the storage unit 19 and stores the comparison result.
  • the measured weight ⁇ W5 of the medicine bottle B and the comparison result are stored in the storage unit 19 as audit information.
  • control unit 18 recognizes the measured amount of decrease ⁇ W6 as the weight of the medicine bottle C and stores it in the storage unit 19. Furthermore, the control unit 18 compares the recognized weight ⁇ W6 of the medicine bottle C with the data (predetermined value) of the initial weight of the medicine bottle C previously stored in the storage unit 19 and stores the comparison result Remember to 19. Thus, the measured weight ⁇ W6 of the medicine bottle C and the comparison result are stored in the storage unit 19 as audit information.
  • the vial placement unit 14a is measured by measuring the weight of the vial 20 taken from the vial placement unit 14a. It can support the matching audit of the type of medicine bottle (medical solution) taken from
  • the picking error information when the control unit 18 recognizes that the measured weight of the medicine bottle 20 does not match the data (predetermined value) of the initial weight of the medicine bottle previously stored in the storage unit 19, the picking error information Generate Here, “do not match” means that they do not match within the error range.
  • the picking error information may be displayed on the screen 17 a of the information presenting unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the picking error information generated by the control unit 18.
  • control unit 18 counts the number of times of change in weight measured by the medicine bottle weight measurement unit 14 when the medicine solution is aspirated from each medicine bottle 20 containing the medicine solutions A, B, C. Based on the counting result, the number of medicine bottles 20 picked up from the medicine bottle placement unit 14a is measured. The measured data is stored in the storage unit 19 by the control unit 18. Then, the control unit 18 compares the measured number of vials 20 with the data (predetermined value) of the number of vials previously stored in the storage unit 19 and places the information on the vial placement unit 14a. It is determined whether the placed whole medicine bottle 20 has been taken up.
  • the data on the number of vials may use the data on the number of vials contained in the information on the drug solution, or the data of the number of vials analyzed by the control unit 18 from the information on the drug solution may be used Alternatively, data on the number of vials measured when the vials 20 are placed on the vial placement unit 14a may be used.
  • the drug solution preparation support system 10 can support an audit as to whether or not there is an error in picking up a medicine bottle (drug solution).
  • the weight of the medicine solution may be measured if the data of the weight of the medicine bottle can be confirmed from the information on the medicine solution.
  • the control unit 18 recognizes the weight of the vial 20 based on the decrease in weight measured by the vial weight measurement unit 14 and offsets the weight of the single vial from the recognized weight. Measure the weight of the drug solution.
  • the measured data is stored in the storage unit 19 by the control unit 18.
  • the control unit 18 compares the measured weight of the drug solution with the data of the initial weight of the drug solution previously stored in the storage unit 19, and stores the comparison result in the storage unit 19. Even in this case, it is possible to support an audit as to whether or not there is an error in picking up the medicine bottle (medical solution).
  • FIG. 6 is a view showing an example of a change in weight measured by the vial weight measuring unit 14 when each medicine bottle 20 from which the medicines A, B and C are sucked is returned to the medicine bottle placement unit 14a. .
  • the total weight W3 of the medicine bottle A to the medicine bottle C is measured by the medicine bottle weight measurement unit 14 as shown in FIG. There is.
  • the operator picks up the medicine bottle A from the medicine bottle mounting portion 14a in order to suction the liquid medicine A.
  • the operator returns the medicine bottle 20 from which the drug solution A is sucked to the original position on the medicine bottle mounting portion 14a.
  • the weight W5 is measured by the medicine bottle weight measurement unit 14.
  • control unit 18 recognizes the measured amount of decrease ⁇ W7 as the suctioned weight of the liquid medicine A and stores it in the storage unit 19. Furthermore, the control unit 18 compares the suctioned weight ⁇ W7 of the recognized drug solution A with the data (predetermined value) of the suctioned weight of the drug solution A previously stored in the storage unit 19 and stores the comparison result.
  • the suctioned weight ⁇ W7 of the measured drug solution A and the comparison result are stored in the storage unit 19 as audit information.
  • the included data may be used.
  • the control unit 18 may calculate the suction weight of the chemical solution from the data of the dose of the chemical solution contained in the information on the chemical solution, and store the data of the suction weight of the calculated chemical solution in the storage unit 19.
  • the control unit 18 may calculate the suction amount of the chemical solution from the suction weight of the measured chemical solution, and compare the calculated suction amount with the data of the dose of the chemical solution contained in the information on the chemical solution.
  • the operator picks up the medicine bottle B from the medicine bottle mounting portion 14a in order to suction the liquid medicine B. Then, after suctioning the drug solution B, the operator returns the medicine bottle 20 from which the drug solution B has been sucked back to the original position on the medicine bottle mounting portion 14a.
  • the weight W7 is measured by the medicine bottle weight measurement unit 14.
  • control unit 18 compares the suctioned weight ⁇ W 8 of the recognized chemical solution B with the data (predetermined value) of the suctioned weight of the chemical solution B previously stored in the storage unit 19 and stores the comparison result.
  • the suctioned weight ⁇ W8 of the measured drug solution B and the comparison result are stored in the storage unit 19 as audit information.
  • the operator picks up the medicine bottle C from the medicine bottle mounting portion 14a in order to suction the medicine C. Then, after suctioning the drug solution C, the operator returns the medicine bottle 20 from which the drug solution C has been sucked back to the original position on the medicine bottle mounting portion 14a.
  • the weight W9 is measured by the medicine bottle weight measurement unit 14.
  • control unit 18 compares the suctioned weight ⁇ W 9 of the recognized drug solution C with the data (predetermined value) of the suctioned weight of the drug solution C previously stored in the storage unit 19 and stores the comparison result.
  • the suctioned weight ⁇ W9 of the measured drug solution C and the comparison result are stored in the storage unit 19 as audit information.
  • the control unit 18 recognizes that the measured suction weight of the chemical solution or the suction amount of the chemical solution does not match the suction weight of the chemical solution or the data (predetermined value) of the dose of the chemical solution previously stored in the storage unit 19. If it does, generate suction error information.
  • "do not match” means that they do not match within the error range.
  • the suction error information indicates at least one of the fact that there is an error in the suction amount, that there is an error in the type of the suctioned drug solution, and that the drug solution has been spilled.
  • the suction error information may be displayed on the screen 17 a of the information presentation unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the suction error information generated by the control unit 18.
  • the weight W4 is measured by the medicine bottle weight measurement unit 14, and the medicine bottle 20 from which the medicine solution A is sucked is
  • the weight W5 is measured by the medicine bottle weight measurement unit 14.
  • control unit 18 recognizes the weight ⁇ W10 of the recognized medicine bottle A after suction and the data (predetermined value) of the weight of the medicine bottle in which the medicine solution A has been suctioned by a predetermined dose previously stored in the storage unit 19. And the comparison result is stored in the storage unit 19. Thus, the measured weight ⁇ W10 of the medicine bottle A after suction and the comparison result are stored in the storage unit 19 as audit information.
  • the data included in the information may be used.
  • the control unit 18 may analyze the weight of the medicine bottle from which the medicine solution has been sucked by a predetermined dose from the information on the medicine solution, and store the analyzed data in the storage unit 19.
  • the weight of the medicine bottle from which the drug solution has been sucked by a predetermined dose can be obtained, for example, by taking the difference between the initial weight of the drug bottle and the suction weight of the drug solution.
  • the weight of the medicine bottle 20 from which the medicine was aspirated is measured, thereby supporting the comparison audit of the type of medicine aspirated. can do.
  • the control unit 18 recognizes that the measured weight of the medicine bottle 20 after the suction of the drug solution does not match the data of the weight of the medicine bottle after the drug solution suction, which is previously stored in the storage unit 19.
  • Generate suction error information means not agreeing within the error range.
  • the suction error information indicates at least one of the fact that there is an error in the suction amount, that there is an error in the type of the suctioned drug solution, and that the drug solution has been spilled.
  • the suction error information may be displayed on the screen 17 a of the information presentation unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the suction error information generated by the control unit 18.
  • control unit 18 counts the number of times of change in weight measured by the medicine bottle weight measurement unit 14 when the medicine solution is aspirated from each medicine bottle 20 containing the medicine solutions A, B, C. Based on the counting result, the number of vials 20 returned onto the vial placement unit 14a is measured. The measured data is stored in the storage unit 19 by the control unit 18. Then, the control unit 18 compares the measured number of medicine bottles 20 with the data (predetermined value) of the number of medicine bottles previously stored in the storage unit 19 to obtain all the medicines on the medicine bottle placement unit 14a. It is determined whether the medicine bottle 20 has been returned.
  • the drug solution preparation support system 10 can support an audit as to whether or not there is an error in the suction amount of the drug solution or the like.
  • the control unit 18 measures the injection weight of the drug solution injected into the infusion bag 21 based on the increase in weight measured by the infusion bag weight measurement unit 15.
  • the measured injection weight of the drug solution is stored in the storage unit 19 by the control unit 18.
  • the control unit 18 compares the measured injection weight of the chemical solution with the data (predetermined value) of the injection weight of the chemical solution previously stored in the storage unit 19 and stores the comparison result in the storage unit 19. .
  • the measured injection weight of the drug solution and the comparison result are stored in the storage unit 19 as audit information.
  • the control unit 18 may calculate the injection weight of the chemical solution from the data of the dose of the chemical solution contained in the information on the chemical solution, and store the calculated data of the injection weight of the chemical solution in the storage unit 19 .
  • the control unit 18 may calculate the injection amount of the chemical solution from the measured injection weight of the chemical solution, and compare the calculated injection amount with the data of the dose of the chemical solution contained in the information on the chemical solution.
  • control unit 18 recognizes that the measured injection weight of the drug solution or the injection amount of the drug solution does not match the injection weight of the drug solution or the dose data (predetermined value) of the drug solution previously stored in the storage unit 19. If it does, it will generate injection error information.
  • injection error information indicates at least one of the fact that there is an error in the injection amount, that there is an error in the type of the injected liquid drug, that the liquid drug remains in the syringe 23a, and that the liquid drug has been spilled.
  • the injection error information may be displayed on the screen 17 a of the information presentation unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the injection error information generated by the control unit 18.
  • control unit 18 counts the number of changes in weight measured by the infusion bag weight measurement unit 15, and measures the number of times the drug solution is injected into the infusion bag 21 based on the counting result.
  • the measured data is stored in the storage unit 19 by the control unit 18.
  • the control unit 18 compares the measured number of injections of the drug solution with the data (predetermined value) of the number of medicine bottles previously stored in the storage unit 19 and stores the comparison result in the storage unit 19. .
  • the measured number of times of injection of the drug solution and the comparison result are stored in the storage unit 19 as audit information.
  • the data on the number of medicine bottles may use the data on the number of medicines contained in the information on medicines, or the control unit 18 may use the data on the number of medicines analyzed from the information on medicines Alternatively, data on the number of medicines measured when the medicine bottles 20 are placed on the medicine bottle placement unit 14a may be used, or the medicine solution is sucked from the medicine bottles 20 prepared on the medicine bottle placement unit 14a. Data on the number of chemical solutions measured at that time may be used.
  • the control unit 18 recognizes that the measured number of times of injection of the chemical solution does not match the data of the number of medicine bottles previously stored in the storage unit 19, the number of times of injection of the chemical solution is insufficient. Generate counting error information indicating that.
  • the counting error information may be displayed on the screen 17 a of the information presenting unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the counting error information generated by the control unit 18.
  • the chemical solution preparation support system 10 can support an audit as to whether or not there is an error in the injection amount of the chemical solution or the like.
  • the control unit 18 may analyze the number of times of injection of the chemical solution from the information on the chemical solution, and store the data of the number of times of injection of the analyzed chemical solution in the storage unit 19. For example, the control unit 18 can analyze the number of times of injection of the chemical solution from the data of the mixing and preparation procedure of the chemical solution included in the information on the chemical solution.
  • the syringe drive device 23 is held by the operator's hand when suctioning a drug solution from the medicine bottle 20 or when injecting a drug solution into the infusion bag 21, and is not held by the cradle unit 16.
  • the weight of the syringe drive 23 increases from the initial weight.
  • the initial weight of the syringe drive device 23 is the weight when the inside of the syringe 23a is empty.
  • the control unit 18 measures the suctioned weight of the drug solution sucked into the syringe 23a based on the weight measured by the cradle unit 16. The measured suction weight is stored in the storage unit 19 by the control unit 18.
  • control unit 18 compares the measured suctioned weight of the drug solution with the data of the suctioned weight of the drug solution previously stored in the storage unit 19, and stores the comparison result in the storage unit 19.
  • the suctioned weight of the measured drug solution and the comparison result are stored in the storage unit 19 as audit information.
  • the included data may be used.
  • the control unit 18 may calculate the suction weight of the chemical solution from the data of the dose of the chemical solution contained in the information on the chemical solution, and store the calculated data of the suction weight of the chemical solution in the storage unit 19 .
  • the control unit 18 may calculate the suction amount of the chemical solution from the suction weight of the measured chemical solution, and compare the calculated suction amount with the data of the dose of the chemical solution contained in the information on the chemical solution.
  • the data of the suction amount of the drug solution or the data of the suction weight of the drug solution the data of the suction amount of the drug solution or the data of the suction weight of the drug solution measured based on the change in weight measured by the medicine bottle weight measurement unit 14 You may use.
  • the measurement audit of the drug solution sucked in the syringe 23a, or suction in the syringe 23a It is possible to support the verification audit of the type of chemical solution.
  • control unit 18 does not match the measured suctioned weight of the chemical solution or the suctioned amount of the chemical solution with the data of the suctioned weight of the chemical solution or the dose data (predetermined value) of the chemical solution previously stored in the storage unit 19. Generates suction error information when it recognizes Here, "does not match” means that they do not match within the tolerance.
  • the suction error information indicates at least one of the fact that there is an error in the suction amount, that there is an error in the type of the suctioned drug solution, and that the drug solution has been spilled.
  • the suction error information may be displayed on the screen 17 a of the information presentation unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the suction error information generated by the control unit 18.
  • control unit 18 counts the number of times of measurement of the weight by the cradle unit 16, and measures the number of times of injecting the medical fluid from the syringe 23a into the infusion bag based on the counting result.
  • the measured data is stored in the storage unit 19 by the control unit 18.
  • the control unit 18 compares the measured number of injections of the drug solution with the data (predetermined value) of the number of medicine bottles previously stored in the storage unit 19 and stores the comparison result in the storage unit 19. .
  • the measured number of times of injection of the drug solution and the comparison result are stored in the storage unit 19 as audit information.
  • the control unit 18 recognizes that the measured number of times of injection of the chemical solution does not match the data of the number of medicine bottles previously stored in the storage unit 19, the number of times of injection of the chemical solution is insufficient. Generate counting error information indicating that.
  • the counting error information may be displayed on the screen 17 a of the information presenting unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the counting error information generated by the control unit 18.
  • the drug solution preparation support system 10 can support an audit as to whether or not there is an error in the suction amount of the drug solution or the like.
  • the control unit 18 controls the weight measured by the cradle unit 16 to be the initial weight of the syringe drive unit 23. It is determined whether or not they match. Then, the control unit 18 generates the determination result as audit information.
  • the control unit 18 also generates remaining error information when recognizing that the drug solution remains in the syringe 23a.
  • the remaining error information may be displayed on the screen 17 a of the information presentation unit 17.
  • the chemical solution preparation support system 10 may be provided with a device (not shown) that sounds an alarm sound corresponding to the remaining error information generated by the control unit 18.
  • the drug solution preparation support system 10 As described above, according to the drug solution preparation support system 10 according to the present embodiment, it is possible to reliably prevent an error in taking a medicine bottle, an error in suction amount of drug solution, and the like. Therefore, according to the drug solution preparation support system 10, it is possible to effectively prevent operation errors (dispensing errors) such as mixing procedure order of drug solution and measurement error of drug solution, and to realize safe and accurate preparation of drug solution.
  • operation errors disensing errors
  • the chemical solution preparation support system 10 automatically and reliably generates audit information. Therefore, according to the drug solution preparation support system 10, the drug solution preparation work can be made more efficient.
  • the drug solution preparation support system 10 it is possible to immediately notify the operator when an operation error such as an error in taking a medicine bottle or a measurement error of a drug solution occurs. Therefore, according to the drug solution preparation support system 10, it is not necessary to waste the drug solution (medicine bottle) and the infusion bag, and the cost for preparing the drug solution can be reduced. For example, if a measurement error of the drug solution first sucked into the syringe is detected before injecting the drug solution into the infusion bag, the medicine bottle intended for suction of the drug solution thereafter and the infusion bag are not discarded. It is
  • the drug solution preparation support system 10 performs not only the weight measured by the vial weight measuring unit 14 but also the weight measured by the infusion bag weight measuring unit 15 and the cradle unit 16, the medicine is inspected. It is possible to prevent double or triple operation errors such as mistaking of a bottle or an error in the amount of chemical solution. Therefore, according to the chemical solution preparation support system 10, it is possible to prepare a safer and more accurate chemical solution.
  • the medicine solution preparation support system 10 returns the medicine bottle 20 from which the medicine is sucked to the medicine bottle mounting unit 14a. Since the amount of increase in weight at the time of being taken is also measured, it is possible to grasp quantitatively from which medicine bottle a drug solution is currently being suctioned. That is, the chemical solution preparation support system 10 can automatically determine which step of the preparation process of the chemical solution is currently. Therefore, the control unit 18 can display the information of the current step on the screen 17 a of the information presentation unit 17. Therefore, even when the work interruption occurs, the worker can easily resume the preparation operation of the drug solution by confirming the screen 17a. That is, dispensing errors due to work interruption can be effectively prevented.
  • FIG. 7 shows a flowchart of a drug solution preparation support method according to this embodiment.
  • the step S1 for reading a prescription ID the first display step S2, the step S3 for collecting medicine bottles, and the step S4 for sucking a drug solution , And step S5 of injecting a drug solution and second display step S6.
  • step S1 the reading unit 24 reads the prescription ID printed on the prescription 25, the control unit 18 transmits the prescription ID to the medical information database 12, and the medical information database 12 receives the patient information according to the received prescription ID.
  • the control unit 18 causes the storage unit 19 to store the received information on the patient, the information on the medical solution, and the like.
  • step S2 the control unit 18 reads out data such as the type of the drug solution, the dose of the drug solution, and the photographed image of the medicine bottle included in the information on the drug solution from the storage unit 19 and displays it on the screen 17a of the information presentation unit 17. .
  • step S3 a worker such as a nurse or a pharmacist stocks the medicine bottle 20 containing the drug solution to be injected into the infusion bag 21 on the medicine bottle placement unit 14a.
  • the vial weight measurement unit 14 measures the total weight of all the vials placed on the vial placement unit 14a (a vial weight measurement step).
  • the control unit 18 generates audit information representing the inspection result of the medicine bottle sorting operation based on the change in weight measured by the medicine bottle weight measurement unit 14, and stores the generated audit information in the storage unit 19.
  • Store first audit information generation step
  • step S4 the worker picks up the medicine bottle 20 from the medicine bottle placement unit 14a. Then, the operator operates the syringe drive device 23 to suck the drug solution from the taken drug bottle 20 into the syringe 23a mounted on the syringe drive device 23, and the drug bottle 20 after the drug solution suction is drug bottle It returns on the mounting part 14a. At this time, the vial weight measurement unit 14 measures the total weight of all the vials placed on the vial placement unit 14a (a vial weight measurement step).
  • control unit 18 generates, based on the change in weight measured by the medicine bottle weight measurement unit 14, audit information representing an inspection result of the picking operation of the medicine bottle and the suction operation of the drug solution, and the generated audit information Are stored in the storage unit 19 (first audit information generation step).
  • step S4 the medicine bottles are taken in a predetermined mixing and preparation order based on the change in weight measured by the medicine bottle weight measurement unit 14 due to the medicine bottle 20 being picked up from the drug solution placement unit 14a. It will be audited whether it is taken up without a doubt.
  • a predetermined dose from the medicine bottle 20 picked up based on a change in weight measured by the medicine bottle weight measurement unit 14 due to the medicine bottle 20 after the liquid medicine suctioning being returned to the medicine bottle placement unit 14a. It is audited whether or not the drug solution is definitely aspirated.
  • step S5 the operator operates the syringe drive device 23 to inject a drug solution from the syringe 23a into the infusion bag 21.
  • the infusion bag weight measurement unit 15 measures the weight of the infusion bag 21 placed on the infusion bag placement unit 15a (infusion bag weight measurement step).
  • the control unit 18 Based on the change in weight measured by the infusion bag weight measurement unit 15, the control unit 18 generates audit information representing the audit result of the liquid injection operation, and stores the generated audit information in the storage unit 19. (2nd audit information generation step).
  • step S6 the control unit 18 reads out the audit information from the storage unit 19 and causes the screen 17a of the information presentation unit 17 to display it.
  • the medical fluid preparation support device 11 may be provided with an input unit that can input a prescription ID instead of the reading unit 24 so that the input prescription ID may be transmitted to the medical information database 12 in step S1.
  • FIG. 8 shows the first half of a flowchart of a specific example of the chemical solution preparation support method according to this embodiment
  • FIG. 9 shows the second half of the flowchart.
  • FIGS. 10 to 22 show an example of an image displayed on the screen 17 a of the information presentation unit 17 along the flowcharts shown in FIGS. 8 and 9.
  • the image displayed on the screen 17 a of the information presentation unit 17 is controlled by the control unit 18.
  • the case where all the medical fluid to be injected into the infusion bag 21 is injected into the infusion bag 21 at one time will be described.
  • the cases where the medicines A, B and C need to be injected into the infusion bag 21 and the medicines A, B and C are mixed and prepared in this order will be described. .
  • step S10 an image instructing the worker to insert the prescription 25 into the reading unit 24 is displayed on the screen 17a of the information presenting unit 17.
  • the reading unit 24 reads the prescription ID printed on the prescription 25 (step S11). Move to step S12.
  • step S12 the control unit 18 transmits the prescription ID read by the reading unit 24 to the medical information database 12.
  • the medical information database 12 transmits information on a drug solution according to the received prescription ID, patient information, and the like.
  • the control unit 18 causes the storage unit 19 to store the information transmitted from the medical information database 12.
  • an image is displayed on the screen 17a of the information presentation unit 17 indicating that information on a drug solution, information on a patient, and the like are currently being acquired from the medical information database 12.
  • the process moves to step S13.
  • step S13 the medicine bottle 20 is placed on the medicine bottle placement unit 14a on the screen 17a of the information presentation unit 17 as shown in FIG. 12 based on the information on the drug solution and the patient information stored in the storage unit 19.
  • An image is displayed that instructs the operator to place the infusion bag 21 on the infusion bag placement unit 15a.
  • the operator places the medicine bottle 20 on the medicine bottle placement unit 14a and places the infusion bag 21 on the infusion bag placement unit 15a according to the instruction displayed on the screen 17a.
  • control unit 18 counts the number of changes in weight measured by the medicine bottle weight measurement unit 14, and based on the counting result, the number of collected medicine bottles 20 is calculated. It may be measured.
  • control unit 18 recognizes the weight measured by the infusion bag weight measurement unit 15 when the infusion bag 21 is placed on the infusion bag placement unit 15a as the initial weight of the infusion bag 21, and stores the storage unit.
  • the control unit 18 recognizes the weight measured by the infusion bag weight measurement unit 15 when the infusion bag 21 is placed on the infusion bag placement unit 15a as the initial weight of the infusion bag 21, and stores the storage unit.
  • the operator arranges the entire medicine bottle 20 on the medicine bottle placement unit 14a, places the infusion solution bag 21 on the infusion solution bag placement unit 15a, and then operates the completion button 17d on the screen 17a (step S14). Thereby, it moves to step S15.
  • control unit 18 automatically recognizes that the entire medicine bottle 20 is placed on the medicine bottle placement unit 14a and the infusion bag 21 is placed on the infusion bag placement unit 15a. You may move to S15.
  • the completion of the assortment of medicine bottles 20 can be determined, for example, from the result of the matching audit of the kind of medicine bottles 20 (kind of liquid medicine) prepared. Also, for example, does the completion of the assortment of vials 20 coincide with the data of the total value of the initial weights of all the vials previously stored in the storage unit 19 as measured by the vial weight measuring unit 14? It can be determined by whether or not.
  • to match means to match within an error range.
  • the included data may be used.
  • the control unit 18 calculates the total value of the initial weights of all vials using the data of the initial weights of all vials included in the information on the drug solution, and stores the calculation result in the storage unit 19 It is also good.
  • control unit 18 may perform count inspection of the prepared medicine bottles, as described above. Further, as described above, when the error state is recognized from the counting audit of the medicine bottle (medical solution), an image indicating the occurrence of the error state may be displayed on the screen 17a (error information generation step). Alternatively, a buzzer sound (alarm sound) or the like may be sounded to notify occurrence of an error state.
  • step S15 as shown in FIG. 13, the syringe drive unit 23 is taken out from the cradle unit 16 on the screen 17a of the information presentation unit 17, and the syringe drive unit 23 taken out is attached to the syringe drive unit 23.
  • An image is displayed that instructs the operator to attach the injection needle 23b to the syringe 23a attached to the.
  • the operator takes out the syringe drive device 23 from the cradle unit 16 according to the instruction displayed on the screen 17 a, mounts the syringe 23 a on the taken-out syringe drive device 23, and on the syringe 23 a attached to the syringe drive device 23. After the injection needle 23 b is attached, the syringe drive device 23 is returned to the cradle unit 16.
  • control unit 18 recognizes the weight measured by the cradle unit 16 when the syringe drive unit 23 is returned to the cradle unit 16 as the initial weight of the syringe drive unit 23 and stores the weight in the storage unit 19. .
  • step S16 After returning the syringe drive device 23 to the cradle unit 16, the operator operates the completion button 17d on the screen 17a. Thereby, it moves to step S16.
  • the control unit 18 may move to step S16 by automatically recognizing that the syringe drive device 23 has been returned to the cradle unit 16. Whether or not the syringe drive device 23 is returned can be determined, for example, based on whether or not the weight measured by the cradle unit 16 has changed from zero.
  • step S16 on the screen 17a of the information presentation unit 17, based on the information on the chemical solution stored in the storage unit 19, an image for instructing the operator of the medicine bottle to be aspirated is displayed.
  • FIG. 14 illustrates the case where the medicine bottle to be sucked is the medicine bottle A.
  • the drug solution information display 17f on which the shot image 20c of the drug bottle is displayed the shot image 20c of the drug bottle to be sucked and the name and the dose of the drug solution contained in the drug bottle to be sucked are Zoom in. By doing this, the operator can visually confirm the medicine bottle to be picked up, and it is possible to prevent the occurrence of a mistake in the medicine bottle.
  • step S16 when information on precautions when suctioning a chemical solution, such as the driving speed of the syringe drive device 23, is included in the information on the chemical solution, in step S16, the caution item 17g included in the information on the chemical solution is displayed on the screen 17a. Be done. By presenting a warning to the operator in this manner, safer and more accurate preparation of the drug solution can be achieved.
  • FIG. 14 shows, as an example, a caution item 17 g indicating that the syringe drive device 23 needs to be operated in the low speed mode because the chemical solution A easily foams. When the operator operates the syringe drive device 23 according to this caution item 17 g, it is possible to prevent the foaming and efficiently suction the chemical solution.
  • step S16 the light emission of the LED display unit corresponding to the medicine bottle 20 to be sucked is started.
  • the work instruction display 17c an instruction to suction the chemical solution from the medicine bottle 20 corresponding to the position where the LED display unit emits light (the LED display position) is displayed.
  • the light emission of the LED display unit continues until the taken medicine bottle 20 is returned onto the medicine bottle mounting portion 14a.
  • the operator picks up the medicine bottle 20 in accordance with the instructions displayed on the screen 17a.
  • the control unit 18 measures the weight of the picked-up vial 20 based on the change in weight measured by the vial weight measuring unit 14.
  • a comparison audit of the type of medicine bottle 20 (type of liquid medicine) taken up and an audit of the order of picking up the medicine bottle 20 are performed (step S16A).
  • the control unit 18 counts the number of changes in weight measured by the vial weight measuring unit 14, and based on the counting result, the medicine bottle loading unit 14 a The number of times 20 is picked up (the number of medicine bottles 20 picked up) may be measured.
  • step S17 After picking up the medicine bottle 20, the operator operates the completion button 17d on the screen 17a when not receiving a warning about occurrence of an error state from the liquid medicine preparation support system 10. Thereby, it moves to step S17. If the correct state is recognized from the result of the audit in step S16A, the process may automatically move to step S17. Alternatively, the control unit 18 may move to step S17 by automatically recognizing that the medicine bottle 20 has been picked up from the medicine bottle placement unit 14a. Whether or not the medicine bottle 20 has been picked up can be determined, for example, by whether or not the weight measured by the medicine bottle weight measurement unit 14 has decreased.
  • an image indicating the occurrence of an error state is displayed on the screen 17a (error information generation step).
  • a buzzer sound (alarm sound) or the like notifying the occurrence of an error state is sounded.
  • step S16 When returning from the error state, that is, when the operator returns the misplaced medicine bottle 20 onto the medicine bottle mounting portion 14a, the process returns to step S16. Whether or not the error state is recovered can be automatically determined, for example, by whether or not the weight measured by the vial weight measurement unit 14 has increased.
  • step S17 it is determined whether the picked up vial 20 is a vial container. This determination is made by the control unit 18 based on the information on the chemical solution stored in the storage unit 19. If the medicine bottle 20 is a vial container, the process moves to step S18. On the other hand, if the medicine bottle 20 is not a vial container, the process moves to step S19.
  • step S18 an image is displayed on the screen 17a of the information presentation unit 17 based on the information on the chemical solution stored in the storage unit 19 to instruct the operator to use the empty amount of the syringe and the pumping suction of the chemical solution.
  • FIG. 15 exemplifies a work instruction display 17c for displaying an instruction to pump and aspirate a medical solution after suctioning 10 ml of air to the syringe 23a.
  • the information on the operation procedure of the syringe drive device 23 is included in the information on the drug solution.
  • the medicine bottle 20 When the medicine bottle 20 is a vial container, in order to keep the internal pressure of the vial container as constant as possible at the time of suction of the drug solution, the replacement air of an amount corresponding to the amount of drug solution to be sucked (dose of the drug solution) There is a need. Also, it is necessary to perform pumping suction. Therefore, when the medicine bottle 20 is a vial container, the operator operates the syringe drive device 23 according to the instruction displayed on the screen 17a by presenting the operation procedure of the syringe drive device 23 to the worker. The drug solution can be suctioned efficiently.
  • the information on the operation procedure of the syringe drive device 23 is not limited to the instruction displayed on the work instruction display 17 c in FIG.
  • the operator sucks the drug solution from the taken medicine bottle 20, and then operates the completion button 17d on the screen 17a. Thereby, it moves to step S19.
  • the empty amount of the syringe is set to a slightly smaller amount than the dose of the drug solution.
  • step S19 based on the information on the drug solution stored in the storage unit 19, an image for instructing the operator to return the medicine bottle is displayed on the screen 17a of the information presentation unit 17.
  • FIG. 16 illustrates the case where the medicine bottle to be returned is the medicine bottle A.
  • the photographed image 20c or the like of the medicine bottle to be returned is enlarged and displayed.
  • the LED display unit corresponding to the medicine bottle to be returned emits light
  • the work instruction display 17c shows the medicine bottle at the position where the LED display unit emits light (the LED display position). An instruction to return is displayed. By so doing, the worker can more reliably return the medicine bottle 20 to the original position.
  • the control unit 18 measures the weight of the aspirated drug solution or the amount of the aspirated drug solution based on the change in the weight measured by the vial weight measurement unit 14. As a result, measurement audit of the aspirated drug solution, verification audit of the type of the drug solution aspirated, and audit of the mixed preparation order of the drug solution are performed (step S19A).
  • control unit 18 counts the number of changes in weight measured by the medicine bottle weight measurement unit 14 and, based on the counting result, the medicine bottle placement unit 14a The number of times 20 is returned (the number of returned medicine bottles 20) may be measured.
  • step S20 After returning the medicine bottle 20 to the medicine bottle placement unit 14a, the operator operates the completion button 17d on the screen 17a when not receiving a warning about occurrence of an error from the medicine preparation support system 10 (step S20). ). Thereby, it moves to step S21. If the correct state is recognized from the result of the audit in step S19A, the process may automatically move to step S21. Alternatively, the control unit 18 may move to step S21 by automatically recognizing that the medicine bottle 20 has been returned. Whether or not the medicine bottle 20 has been returned can be determined, for example, by whether or not the weight measured by the medicine bottle weight measurement unit 14 has increased.
  • step S21 the number of medicine bottles measured in step S16A or step S19A is compared with the data (predetermined value) of the number of medicine bottles previously stored in the storage unit 19, and the medicine bottle placement unit It is determined whether the drug solution is aspirated from the whole medicine bottle 20 placed on 14a. If the number of medicine bottles from which the drug solution has been suctioned matches the number of all medicine bottles 20 placed on the medicine bottle placement unit 14a, the process moves to step S22. If they do not match, the process returns to step S16. The processes from step S16 to step S21 are repeated until the number of medicine bottles from which the drug solution has been sucked matches the number of whole medicine bottles 20 placed on the medicine bottle placement unit 14a.
  • an error such as the suction amount of the chemical solution is found in the audit in step S19A, as described above, an image indicating the occurrence of an error state is displayed on the screen 17a (error information generation step). Alternatively, a buzzer sound (alarm sound) or the like notifying the occurrence of an error state is sounded.
  • the control unit 18 reads out from the storage unit 19 the prescription ID and audit information indicating an error such as the suction amount of the drug solution, and is transmitted to the medical information database 12.
  • the medical information database 12 records the received audit information in association with the prescription ID. Further, the control unit 18 causes the screen 17 a to display an image instructing the operator to remove the prescription 25 from the reading unit 24.
  • step S19A when an error such as the suction amount of the chemical solution is found in the audit in step S19A, the current preparation operation of the chemical solution is stopped. In response to the cancellation, the operator restarts preparation of the drug solution from the beginning (start of FIG. 8).
  • step S22 as shown in FIG. 17, the injection needle 23b is inserted into the outlet / outlet plug 21a of the infusion bag 21 on the screen 17a of the information presentation unit 17, and the drug solution in the syringe 23a is injected into the infusion bag 21.
  • the image for instructing the worker is displayed.
  • FIG. 17 exemplifies an infusion bag 21 in which 500 ml of physiological saline is put in advance.
  • step S22 The operator injects the drug solution into the infusion bag 21 according to the instruction displayed on the screen 17a. Also in step S22, the information on the operating procedure and driving speed of the syringe drive device 23 may be displayed on the screen 17a based on the information on the chemical solution stored in the storage unit 19.
  • the measurement audit of the injected medical fluid is performed. Further, as described above, when there is an error in the injection amount or the injection weight of the chemical solution, an image indicating the occurrence of an error state is displayed on the screen 17a (error information generation step). Alternatively, a buzzer sound (alarm sound) or the like notifying the occurrence of an error state is sounded. As a result, the operator can confirm that the drug solution remains in the syringe 23a. In this case, the worker injects the drug solution remaining in the syringe 23a into the infusion bag 21. By this inspection, the operator can easily confirm whether or not all the drug solution sucked into the syringe 23a has been injected into the infusion bag 21.
  • the operator operates the completion button 17 d on the screen 17 a after injecting the drug solution into the infusion bag 21. Thereby, it moves to step S23.
  • the control unit 18 may move to step S23 by automatically recognizing that the medical solution has been injected into the infusion bag 21. Whether or not the drug solution is injected can be determined, for example, by whether or not the weight measured by the infusion bag weight measurement unit 15 has increased.
  • step S23 as shown in FIG. 18, after removing the injection needle 23b from the syringe 23a attached to the syringe drive device 23 on the screen 17a of the information presentation unit 17, the syringe drive device 23 is returned to the cradle unit 16 An image for instructing the operator is displayed.
  • the operator returns the syringe drive device 23 to the cradle unit 16 in accordance with the instruction displayed on the screen 17 a.
  • the cradle unit 16 measures the weight of the syringe drive device 23 (syringe weight measurement step), and the controller 18 controls the medical fluid in the syringe 23a based on the weight measured by the cradle unit 16. It is determined whether or not there remains, and the result of the determination is stored in the storage unit 19 as audit information (third audit information generation step).
  • This inspection is performed because it is not possible to determine whether or not there is a mistake in spillage of the drug solution when the drug solution is injected into the infusion solution bag 21 only by the measurement audit of the drug solution injected into the infusion solution bag 21. Based on the weight measured by the cradle unit 16, it is possible to reliably determine whether or not the drug solution remains in the syringe 23 a by performing an audit as to whether the drug solution remains in the syringe 23 a.
  • an image indicating the occurrence of an error state is displayed on the screen 17a (error information generation step). Alternatively, a buzzer sound (alarm sound) or the like notifying the occurrence of an error state is sounded. In this case, the worker injects the drug solution remaining in the syringe 23a into the infusion bag 21.
  • step S24 After returning the syringe drive device 23 to the cradle unit 16, the operator operates the completion button 17d on the screen 17a. Thereby, it moves to step S24.
  • the control unit 18 may move to step S24 by automatically recognizing that the syringe drive device 23 has been returned to the cradle unit 16. Whether or not the syringe drive device 23 is returned can be determined, for example, by whether or not the weight measured by the cradle unit 16 has increased.
  • step S24 based on the patient information and the audit information stored in the storage unit 19, as shown in FIG. 19, the patient information and the audit information are displayed on the screen 17a of the information presentation unit 17.
  • the worker After confirming the patient information and the audit information displayed on the screen 17a, the worker operates the completion button 17d on the screen 17a.
  • the completion button 17d By the operation of the completion button 17d, a geometric pattern having a high contrast ratio as shown in FIG. 20 is projected on the screen 17a of the information presentation unit 17. Therefore, by using the screen 17 a as a background of the infusion bag 21, the worker can easily visually check foreign matters in the drug solution in the infusion bag 21 and white turbidity of the drug solution in the infusion bag 21.
  • the nurse or pharmacist who is the auditor confirms the audit information and the patient information displayed on the screen 17a, and after visually confirming the mixing state of the drug solution in the infusion bag 21, the completion button on the screen 17a Manipulate Thereby, it moves to step S25.
  • step S25 although not shown, an image is displayed on the screen 17a of the information presentation unit 17 asking the operator if the inspection result is normal.
  • the operator follows the instruction displayed on the screen 17a to designate whether the inspection result is OK or NG. This designation may be realized, for example, by the operator operating the OK button or the NG button on the screen 17a.
  • step S26 the prescription ID and the audit information stored in the storage unit 19 are transmitted by the control unit 18 to the medical information database 12.
  • the medical information database 12 records the received audit information in association with the prescription ID. During this time, as shown in FIG. 21, an image indicating that the audit information is being registered in the medical information database 12 is displayed on the screen 17a of the information presentation unit 17.
  • step S27 As shown in FIG. 22, an image for instructing the worker to seal the prescription 25 is displayed on the screen 17a of the information presentation unit 17.
  • the operator takes out the prescription 25 from the reading unit 24 in accordance with the instruction displayed on the screen 17 a and seals the prescription 25 taken out.
  • the operator operates the completion button 17d on the screen 17a (step S28). Thereby, it moves to step S29.
  • the control unit 18 may automatically determine.
  • step S29 although not shown, an image instructing the operator to discard the syringe 23a and the medicine bottle 20 is displayed on the screen 17a of the information presentation unit 17.
  • the operator discards the used medicine bottle 20 on the medicine bottle placement unit 14a according to the instruction displayed on the screen 17a. Further, the operator removes the syringe 23 a from the syringe drive device 23 held by the cradle unit 16 and discards it.
  • step S30 After discarding the syringe 23a and the medicine bottle 20, the operator operates the completion button 17d on the screen 17a (step S30). Thus, a series of drug solution preparation operations are completed.
  • the processing is ended by the control unit 18 automatically recognizing that the medicine bottle 20 has been picked up from the medicine bottle mounting part 14a and that the syringe drive unit 23 has been picked up from the cradle part 16. You may Whether or not the medicine bottle 20 is picked up can be determined, for example, by whether or not weight zero has been measured by the medicine bottle weight measurement unit 14. Further, whether or not the syringe drive device 23 is picked up from the cradle unit 16 can be determined, for example, based on whether or not zero weight has been measured by the cradle unit 16.
  • step S31 although not shown, an image for inputting the content of the error is displayed on the screen 17a of the information presentation unit 17.
  • the operator inputs the content of the error according to the instruction displayed on the screen 17a.
  • the information on the error is stored in the storage unit 19 by the control unit 18.
  • the operator After inputting the content of the error, the operator operates the completion button 17d on the screen 17a (step S32). Thereby, it moves to step S33.
  • step S33 the prescription ID and the error information stored in the storage unit 19 are transmitted by the control unit 18 to the medical information database 12.
  • the medical information database 12 records the received error information in association with the prescription ID.
  • an image indicating that error information is currently being registered in the medical information database 12 is displayed on the screen 17 a of the information presentation unit 17.
  • step S34 an image for instructing the operator to remove the prescription 25 is displayed on the screen 17a of the information presentation unit 17.
  • the worker removes the prescription 25 from the reading unit 24 in accordance with the instruction displayed on the screen 17a.
  • the operator operates the completion button 17d on the screen 17a (step S35). Thereby, it moves to step S29.
  • the control unit 18 may automatically determine.
  • step S29 and step S30 described above.
  • the worker again performs the preparation operation of the chemical solution from the beginning (start of FIG. 8).
  • the cradle unit 16 measures the weight of the syringe drive device 23 (syringe weight measurement step), and the controller 18 controls the suction weight of the chemical solution or the chemical solution based on the weight measured by the cradle unit 16.
  • the measurement audit of the drug solution sucked into the syringe 23a or the comparison audit of the type of drug solution sucked in the syringe 23a may be performed by measuring the suction amount (third audit information generation step).
  • the chemical solution preparation support method can be realized by the same method as the specific example shown in FIGS. 8 and 9.
  • the number of changes in weight measured by the infusion bag weight measurement unit 15 the number of times of injection of the drug solution may be audited.
  • the number of times of measurement of the weight by the cradle unit 16 the number of times of injection of the drug solution may be audited.
  • the above explanation can be made by dividing the medicines to be mixed into a plurality of groups in the mixing preparation order. Similar to the above embodiment, various audits can be supported.
  • the drug solution preparation support system 10 and the drug solution preparation support method according to this embodiment are applied also when injecting one drug solution into an infusion bag. Can.
  • the drug solution preparation support system and drug solution preparation support method of the present invention counting audit of medicine bottles, check audit of kind of medicine bottle (kind of medicine drug), audit of mixing preparation order of medicines, weighing audit of medicines, etc. Can help. Therefore, according to the drug solution preparation support system and drug solution preparation support method according to the present invention, it is possible to prevent erroneous selection of medicine bottle, mistake of medicine bottle when preparing drug solution, mistake of quantity of drug solution, etc. Safe and accurate preparation of the drug solution can be achieved. Further, according to the drug solution preparation support system and drug solution preparation support method of the present invention, a nurse or a pharmacist can handle the drug solution safely and accurately. Therefore, the drug solution preparation support system and drug solution preparation support method according to the present invention can greatly reduce the work load of a nurse or a pharmacist, and is useful for preparation of drug solution in the field of medical care and the like.
PCT/JP2010/005979 2009-10-14 2010-10-06 薬液調製支援システムおよび薬液調製支援方法 WO2011045906A1 (ja)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP10823174A EP2489343A1 (en) 2009-10-14 2010-10-06 System for assisting medicinal liquid preparation and method for assisting medicinal liquid preparation
CN2010800409085A CN102665643A (zh) 2009-10-14 2010-10-06 药液调配支援系统及药液调配支援方法
JP2011543932A JP5490140B2 (ja) 2009-10-14 2010-10-06 薬液調製支援システムおよび薬液調製支援方法
US13/501,404 US20120199239A1 (en) 2009-10-14 2010-10-06 System for assisting medicinal liquid preparation and method for assisting medicinal liquid preparation

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2009236932 2009-10-14
JP2009-236932 2009-10-14

Publications (1)

Publication Number Publication Date
WO2011045906A1 true WO2011045906A1 (ja) 2011-04-21

Family

ID=43875962

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2010/005979 WO2011045906A1 (ja) 2009-10-14 2010-10-06 薬液調製支援システムおよび薬液調製支援方法

Country Status (5)

Country Link
US (1) US20120199239A1 (zh)
EP (1) EP2489343A1 (zh)
JP (1) JP5490140B2 (zh)
CN (1) CN102665643A (zh)
WO (1) WO2011045906A1 (zh)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103070772A (zh) * 2011-10-25 2013-05-01 深圳市卫邦科技有限公司 自动配药机器人及其控制系统
JP2014014428A (ja) * 2012-07-06 2014-01-30 Takazono Technology Inc 水剤供給装置
JP2016523143A (ja) * 2013-06-20 2016-08-08 エウレカＥｕｒｅｋａｍ 医薬調剤の安全な製作のための撮影方法および装置、関連する被写体位置決め台
CN103070772B (zh) * 2011-10-25 2016-12-14 深圳市卫邦科技有限公司 自动配药机器人及其控制系统
CN108553308A (zh) * 2017-12-31 2018-09-21 孔祥慧 一种神经内科用自动供药设备
JP2019033790A (ja) * 2017-08-10 2019-03-07 株式会社湯山製作所 混注制御装置、混注装置、混注制御プログラム
JP7094585B1 (ja) * 2021-03-30 2022-07-04 株式会社ソルブ 調剤支援プログラム

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9930297B2 (en) 2010-04-30 2018-03-27 Becton, Dickinson And Company System and method for acquiring images of medication preparations
JP2014018381A (ja) * 2012-07-17 2014-02-03 Toshiba Tec Corp 薬剤混合調製管理装置、薬剤混合調製管理システム及び制御プログラム
EP3453377A1 (en) * 2012-10-26 2019-03-13 Baxter Corporation Englewood Improved work station for medical dose preparation system
FR3001126B1 (fr) * 2013-01-24 2016-02-12 Jce Biotechnology Appareil a main d'aide au remplissage d'une poche ou similaire, telle qu'un infuseur
CN105277730B (zh) * 2015-10-27 2017-11-07 舟山医院 一种外周血特异性早期肺癌诊断辅助装置
EP4218709A1 (de) * 2016-03-15 2023-08-02 Fresenius Kabi Deutschland GmbH Verfahren zur herstellung einer medizinischen zubereitung
WO2017158009A1 (de) * 2016-03-15 2017-09-21 Fresenius Kabi Deutschland Gmbh Anlage zur herstellung einer medizinischen zubereitung
CN106901985A (zh) * 2017-02-09 2017-06-30 深圳市卫邦科技有限公司 药品配制控制方法及装置
CN107041843B (zh) * 2017-02-09 2021-03-26 深圳市卫邦科技有限公司 药品抽吸控制方法及装置
CN106924043A (zh) * 2017-02-09 2017-07-07 深圳市卫邦科技有限公司 药品定量抽吸控制方法及装置
US10751259B1 (en) * 2017-10-09 2020-08-25 Banpil Photonics, Inc. Smart bottle system and methods thereof
US10991264B2 (en) 2017-11-23 2021-04-27 Omnicell, Inc. Multi-camera imaging for IV compounding
US10596319B2 (en) 2017-11-23 2020-03-24 Aesynt Incorporated Compounding device system
US11335444B2 (en) 2017-11-30 2022-05-17 Omnicell, Inc. IV compounding systems and methods
US10664987B2 (en) 2018-02-02 2020-05-26 Aic Innovations Group, Inc. Apparatus and method for object recognition
CN115531661B (zh) * 2022-10-28 2023-07-18 巨翊医疗科技(苏州)有限公司 一种抗干扰静脉输液流速测量方法、装置及系统

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005279228A (ja) 2004-03-29 2005-10-13 Konishi Seisakusho:Kk 薬品監査装置
JP2006167145A (ja) * 2004-12-15 2006-06-29 Micro Denshi System:Kk 調剤事故防止システム
JP2006296912A (ja) * 2005-04-25 2006-11-02 Tosho Inc 処方薬調剤支援システム
JP2009504199A (ja) * 2005-05-16 2009-02-05 インテリジェント ホスピタル システムズ リミテッド 自動薬局混合システム（ａｐａｓ）

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7783383B2 (en) * 2004-12-22 2010-08-24 Intelligent Hospital Systems Ltd. Automated pharmacy admixture system (APAS)
JP2006280916A (ja) * 2005-03-11 2006-10-19 Yuyama Manufacturing Co Ltd 薬品秤量装置
JP5044906B2 (ja) * 2005-08-25 2012-10-10 株式会社湯山製作所 薬剤払出装置
WO2009060872A1 (ja) * 2007-11-09 2009-05-14 Aloka Co., Ltd. 水薬調剤装置
US8225824B2 (en) * 2007-11-16 2012-07-24 Intelligent Hospital Systems, Ltd. Method and apparatus for automated fluid transfer operations
FR2932085B1 (fr) * 2008-06-06 2012-08-10 Pharmed Sam Station de travail automatisee pour la preparation securisee d'un produit final a usage medical ou pharmaceutique
US8400277B2 (en) * 2009-03-30 2013-03-19 Mckesson Automation Inc. Methods, apparatuses, and computer program products for monitoring a transfer of fluid between a syringe and a fluid reservoir
US8499919B2 (en) * 2010-08-30 2013-08-06 Health Robotics, S.r.l. Machine for the production of pharmaceutical products
US8539989B2 (en) * 2010-08-30 2013-09-24 Health Robotics, S.r.l. Method for the production of pharmaceutical products
US9033006B2 (en) * 2010-09-17 2015-05-19 Nicholas J. Perazzo Oral syringe packaging system for hospital pharmacies
US9563925B2 (en) * 2010-10-21 2017-02-07 Sami G. Y. Mikhaeil Method and apparatus for dispensing medicaments

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005279228A (ja) 2004-03-29 2005-10-13 Konishi Seisakusho:Kk 薬品監査装置
JP2006167145A (ja) * 2004-12-15 2006-06-29 Micro Denshi System:Kk 調剤事故防止システム
JP2006296912A (ja) * 2005-04-25 2006-11-02 Tosho Inc 処方薬調剤支援システム
JP2009504199A (ja) * 2005-05-16 2009-02-05 インテリジェント ホスピタル システムズ リミテッド 自動薬局混合システム（ａｐａｓ）

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103070772A (zh) * 2011-10-25 2013-05-01 深圳市卫邦科技有限公司 自动配药机器人及其控制系统
CN103070772B (zh) * 2011-10-25 2016-12-14 深圳市卫邦科技有限公司 自动配药机器人及其控制系统
JP2014014428A (ja) * 2012-07-06 2014-01-30 Takazono Technology Inc 水剤供給装置
JP2016523143A (ja) * 2013-06-20 2016-08-08 エウレカＥｕｒｅｋａｍ 医薬調剤の安全な製作のための撮影方法および装置、関連する被写体位置決め台
JP2019033790A (ja) * 2017-08-10 2019-03-07 株式会社湯山製作所 混注制御装置、混注装置、混注制御プログラム
CN108553308A (zh) * 2017-12-31 2018-09-21 孔祥慧 一种神经内科用自动供药设备
JP7094585B1 (ja) * 2021-03-30 2022-07-04 株式会社ソルブ 調剤支援プログラム

Also Published As

Publication number Publication date
CN102665643A (zh) 2012-09-12
JP5490140B2 (ja) 2014-05-14
US20120199239A1 (en) 2012-08-09
EP2489343A1 (en) 2012-08-22
JPWO2011045906A1 (ja) 2013-03-04

Similar Documents

Publication Publication Date Title
WO2011045906A1 (ja) 薬液調製支援システムおよび薬液調製支援方法
JP6586419B2 (ja) 薬剤を調合するロボットシステム
JP6965974B2 (ja) 混注装置、混注方法、混注制御プログラム
KR101382028B1 (ko) 혼합 주사 감사 시스템
KR102072025B1 (ko) 혼합 주사 장치
US8763651B2 (en) Dosage dispensing device
US8151835B2 (en) Automated drug delivery bag filling system
US20090154764A1 (en) Drug vial detection in an automated drug preparation system
EP2360609B1 (en) Digital assistant appliance for assisting an operator in the manual preparation of a liquid pharmaceutical composition
CN106102797B (zh) 注射针、注射器、混注装置、混注方法
WO2016088660A1 (ja) 混注装置
CN106901985A (zh) 药品配制控制方法及装置
EP2391543A1 (en) Dosage dispensing device

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 201080040908.5

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 10823174

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2011543932

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 13501404

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2010823174

Country of ref document: EP