WO2017061579A1

WO2017061579A1 - Screening assistance device, screening assistance method, and screening assistance system

Info

Publication number: WO2017061579A1
Application number: PCT/JP2016/079870
Authority: WO
Inventors: 学司後藤; 勇一郎高木
Original assignee: 株式会社湯山製作所
Priority date: 2015-10-08
Filing date: 2016-10-06
Publication date: 2017-04-13
Also published as: JP2022116317A; JP6809475B2; JPWO2017061579A1; JP7260040B2; JP2020189216A; JP7120278B2

Abstract

[Problem] To provide a screening assistance device and screening assistance method which are capable of assisting with screening work in which drugs are screened in a state wherein a plurality of first packaging materials in which a plurality of drugs is contained is collectively contained in a second packaging material. [Solution] Provided is a screening assistance device 100 in which, on the basis of both the number of drugs in a second packaging material which contains a plurality of first packaging materials that contains a plurality of drugs and the total weight of the second packaging material which contains the plurality of first packaging materials, if the difference between the weighed values of balance units 51-54 and the nearest approximate weights to the weighed values of the balance units 51-54, among integer multiple weights of the total weight of the second packaging material, falls within a preset allowable range, then a control unit 10 is capable of comparing prescription data with, as a balance result, the total number of drugs which the second packaging material contains, which is a quantity corresponding to the integer multiple.

Description

Inspection support device, inspection support method, inspection support system

The present invention relates to an inspection support apparatus and an inspection support method used for supporting the work of a pharmacist or the like that inspects a medicine dispensed based on prescription data.

In general, an inspection support apparatus is known that is used to support the work of a pharmacist or the like that inspects a medicine dispensed with a medicine based on prescription data. For example, a dispensing inspection system is known in which the suitability of dispensing contents is determined based on the total amount of medicines placed on a plurality of weighing units (see, for example, Patent Document 1).

JP 2013-42795 A

By the way, a plurality of first packaging materials such as PTP sheets or heat seals containing a plurality of medicines are collectively provided to a patient in a second packaging material such as an aluminum packaging material or a medicine box. Sometimes. In this case, in order to perform inspection work using the above-described dispensing inspection system, for example, after the first packaging material is taken out from the second packaging material and inspected, the first packaging material is again used as the second packaging material. The work of housing is required.

An object of the present invention is to provide an inspection support apparatus capable of supporting an inspection operation for inspecting a medicine in a state where a plurality of first packaging materials containing a plurality of medicines are accommodated in a second packaging material. The purpose is to provide inspection support methods.

The inspection support apparatus according to the present invention includes: a weighing unit; a selection processing unit that selects a drug to be weighed by the weighing unit; and a first packaging material that stores a plurality of the drugs selected by the selection processing unit. An acquisition processing unit that acquires the number of the medicines in the plurality of second packaging materials accommodated and the total weight of the second packaging material in which the plurality of first packaging materials are accommodated, and a weighing result by the weighing unit And a collation processing unit that collates the prescription data. And based on the number of the medicines acquired by the acquisition processing unit and the total weight of the second packaging material, the verification processing unit is based on the integral weight of the total weight of the second packaging material. When the difference between the approximate weight closest to the weighing value of the weighing unit and the weighing value of the weighing unit is within a preset allowable range, it is accommodated in the second packaging material in a number corresponding to the integral multiple. The total number of the medicines can be compared with the prescription data as a weighing result.

Further, the inspection support method according to the present invention is an inspection support method in an inspection support apparatus including a weighing unit, the selection step of selecting a drug to be weighed by the weighing unit, and the drug selected in the selection step The number of the medicines in the second packaging material in which a plurality of first packaging materials are accommodated and the total weight of the second packaging material in which the plurality of first packaging materials are accommodated are obtained. An acquisition step, and a collation step of collating the weighing result obtained by the weighing unit with the prescription data. And in the collation step, the weighing unit out of the weight of an integral multiple of the total weight of the second packaging material based on the number of the medicines acquired by the acquisition step and the total weight of the second packaging material When the difference between the approximate weight closest to the weighed value and the weighed value of the weighed portion is within a preset allowable range, the medicine contained in the second packaging material in a number corresponding to the integer multiple This is the inspection support method in which the total number is collated with the prescription data as a weighing result.

The inspection support system according to the present invention includes a plurality of the inspection support devices and an information processing device capable of communicating with each of the inspection support devices. And each said inspection support apparatus transmits the information of the weight of the said 1st packaging material or the said 2nd packaging material used by the collation by the said collation process part to the said information processing apparatus at a predetermined timing. Is provided. The information processing apparatus includes a weight setting processing unit that sets a reference value of the weight for each medicine based on the weight information acquired from each of the inspection support apparatuses. And each said inspection assistance apparatus can acquire the reference value of the said weight from the said information processing apparatus.

Further, the inspection support method according to the present invention is an inspection support method in an inspection support apparatus including a weighing unit, the selection step of selecting a drug to be weighed by the weighing unit, and the drug selected in the selection step The number of the medicines in the second packaging material in which a plurality of first packaging materials are accommodated and the total weight of the second packaging material in which the plurality of first packaging materials are accommodated are obtained. An obtaining step, and a collating step for collating the weighing result by the weighing unit and the prescription data, and in the collating step, the number of the medicines obtained by the obtaining step and the total weight of the second packaging material Based on the above, the difference between the approximate weight closest to the weighing value of the weighing part and the weighing value of the weighing part among the integral multiples of the total weight of the second packaging material is within a preset allowable range. Place The total number of the chemicals contained in the second packaging material number corresponding to the integer multiple is inspecting support method are matched to the prescription data resulting weighed.

Further, the inspection support apparatus according to the present invention includes a weighing unit, a matching processing unit that compares the amount of medicine calculated based on the weighing result by the weighing section and a target value of the medicine in the prescription data, and the matching A notification processing unit that notifies an error when the verification result by the processing unit is inconsistent. When the collation result by the collation processing unit satisfies a preset condition, the notification processing unit calculates the amount of the medicine calculated based on the weighing result by the weighing unit and the target value of the medicine in the prescription data. The error is not notified when the difference is within an error range set in advance for each medicine, and the error is notified when the error exceeds the error range.

According to the present invention, an inspection support apparatus capable of supporting an inspection operation for inspecting a medicine in a state where a plurality of first packaging materials containing a plurality of medicines are accommodated in the second packaging material, and Inspection support methods are provided.

FIG. 1 is a block diagram showing a configuration of an inspection support apparatus according to an embodiment of the present invention. FIG. 2 is a diagram showing the configuration of the inspection support apparatus according to the embodiment of the present invention. FIG. 3 is a diagram illustrating the configuration of the inspection support apparatus according to the embodiment of the present invention. FIG. 4 is a diagram showing the configuration of the inspection support apparatus according to the embodiment of the present invention. FIG. 5 is a diagram showing the configuration of the inspection support apparatus according to the embodiment of the present invention. FIG. 6 is a diagram showing the configuration of the inspection support apparatus according to the embodiment of the present invention. FIG. 7 is a flowchart showing an example of inspection support processing executed by the inspection support apparatus according to the embodiment of the present invention. FIG. 8 is a diagram illustrating an example of a display screen of the inspection support apparatus according to the embodiment of the present invention. FIG. 9 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 10 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 11 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 12 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 13 is a flowchart illustrating an example of the procedure of the weighing inspection process executed by the inspection support apparatus according to the embodiment of the present invention. FIG. 14 is a diagram illustrating an example of a master maintenance screen of the inspection support device according to the embodiment of the present invention. FIG. 15 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 16 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 17 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 18 is a diagram illustrating an example of a display screen of the inspection support apparatus according to the embodiment of the present invention. FIG. 19 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 20 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 21 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 22 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 23 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 24 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 25 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 26 is a diagram illustrating an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 27 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 28 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 29 is a flowchart illustrating an example of a procedure of master update processing executed by the inspection support device according to the embodiment of the present invention. FIG. 30 is a flowchart illustrating an example of a procedure of a prior inspection control process executed by the inspection support apparatus according to the embodiment of the present invention. FIG. 31 is a diagram illustrating an example of a printing result in the preliminary inspection control process executed by the inspection support apparatus according to the embodiment of the present invention. FIG. 32 is a flowchart illustrating an example of a procedure of a prior inspection application process executed by the inspection support apparatus according to the embodiment of the present invention. FIG. 33 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 34 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 35 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention.

Hereinafter, embodiments of the present invention will be described with reference to the accompanying drawings for understanding of the present invention. In addition, the following embodiment is an example which actualized this invention, Comprising: The thing of the character which limits the technical scope of this invention is not.

[Medical system 1]

As shown in FIG. 1, the medical system 1 includes an inspection support device 100, a dispensing support system 200, a reception system 300, and the like. The inspection support device 100, the dispensing support system 200, and the reception system 300 are communicably connected via a network N1 such as a LAN or the Internet. Note that a plurality of inspection support devices 100 can be connected to the medical system 1.

[Dispensing support system 200]

The dispensing support system 200 receives prescription data from a host system such as an electronic medical record system or a prescription order system. The prescription data includes, for example, basic information such as patient ID, patient name, gender, age, ward, doctor in charge, pharmacist in charge, and the type of medicine prescribed to the patient (drug name, medicine ID, YJ code, GS1 code, etc. ), Medication information such as dose, usage, start date of taking, duration of taking, and end date of taking. And the said dispensing assistance system 200 produces | generates the dispensing data used with dispensing apparatuses, such as a tablet packaging machine and a powder packaging machine, based on the said prescription data, and transmits to the said dispensing apparatus. The tablet packaging machine is capable of packaging one or more kinds of tablets into a wrapping paper at each time of taking, and the powder medicine dispensing machine separates one or more kinds of powder at each time of taking. It is possible to wrap it into wrapping paper. In addition, the tablet packaging machine or the powder packaging machine capable of packaging tablets and powders in the same wrapping paper is also known. Note that the wrapping paper is formed of a transparent or translucent material, and the medicine contained in the wrapping paper is visible from the outside. The tablet packaging machine or the powder packaging machine also includes a packaging printer that records a patient name, a medication time, a medicine name, and the like on the packaging paper.

Here, the dispensing support system 200 stores the prescription data in a sharable state in a preset storage device. Thereby, the inspection support device 100 can acquire the prescription data from the storage device of the dispensing support system 200. It is also conceivable that the prescription data is actively transmitted from the dispensing support system 200 to the inspection support device 100. The prescription data acquired from the dispensing support system 200 may be data in an original format edited by the dispensing support system, for example. The prescription data acquired by the inspection support device 100 is not limited to prescription data acquired from the higher-level system by the dispensing support system 200, and the dispensing generated by the dispensing support system 200 based on the prescription data. It may be data.

[Receive system 300]

The receipt system 300 receives medical data such as medical contents and prescription data from a host system such as an electronic medical record system or a prescription order system. The receipt system 300 is used to support a reception service such as calculation of medical expenses based on the medical data and issuance of a bill.

Here, the reception system 300 stores the prescription data in a sharable state in a preset storage device. Thereby, the inspection support device 100 can acquire the prescription data from the storage device of the reception system 300. In addition, the prescription data may be actively transmitted from the receipt system 300 to the inspection support device 100. The prescription data acquired from the reception system 300 is, for example, a text file format defined by NSIPS specifications.

[Inspection support device 100]

As shown in FIGS. 1 and 2, the inspection support device 100 includes a control unit 10, a display unit 20, an operation unit 30, a storage unit 40, a weighing device 50, an information reading unit 60, and a photographing unit 70. The inspection support device 100 is used to support the work of a medical worker such as a pharmacist who performs a final inspection of a medicine dispensed based on the prescription data in a medical institution such as a hospital, a health facility, or a pharmacy. . The weighing device 50, the information reading unit 60, and the photographing unit 70 are communicably connected to the control unit 10 in accordance with a communication standard such as USB, RS232C, or Bluetooth (registered trademark).

In the present embodiment, the inspection support device 100 includes a tablet terminal 80 including the control unit 10, the display unit 20, the operation unit 30, and the storage unit 40. Thereby, size reduction of the said inspection assistance apparatus 100 can be achieved. A configuration in which the inspection support device 100 includes the control unit 10, the display unit 20, the operation unit 30, and the storage unit 40 individually is also conceivable as another embodiment.

The inspection support device 100 is connected to a commercial AC power source by a power cord (not shown) and is operated by electric power supplied from the commercial AC power source. The tablet terminal 80 has a built-in secondary battery and is charged by the commercial AC power source. Therefore, even when the commercial AC power is cut off, the tablet terminal 80 can be operated for a certain period of time by the secondary battery, and for example, data backup at the time of a power failure is possible.

The control unit 10 includes a CPU, a ROM, a RAM, an EEPROM (registered trademark), and the like. The CPU is a processor that executes various arithmetic processes according to various control programs. The ROM is a non-volatile memory in which programs such as BIOS executed by the CPU are stored in advance. The RAM and the EEPROM are a volatile memory and a non-volatile memory used for development of various control programs and temporary storage of data by the CPU.

The display unit 20 and the operation unit 30 are user interfaces that are controlled by the control unit 10 to display information to the user and receive user operations. The display unit 20 includes a liquid crystal display or an organic EL display, and the operation unit 30 includes a touch panel disposed on the display unit 20. Specifically, in the inspection support apparatus 100, the control unit 10 displays various operation keys on the display unit 20, and detects the operation of the operation keys with the touch panel included in the operation unit 30. Accept the operation. The operation unit 30 may include a mouse or a keyboard. Furthermore, the operation unit 30 may include a voice operation input unit that receives input of various types of information by voice recognition.

Further, the inspection support apparatus 100 includes a cover member 90 that can be opened and closed with respect to the inspection support apparatus 100 as shown in FIGS. 2 and 3. Specifically, the cover member 90 can be opened and closed with respect to the inspection support device 100 by being rotatably supported by a rotation support portion 91 at one end of the weighing device 50. The tablet terminal 80 is disposed on the cover member 90. Thus, in the inspection support apparatus 100, the inspection support apparatus 100 is downsized by arranging the tablet terminal 80 on the cover member 90.

Here, the tablet terminal 80 is supported by the cover member 90 such that the display surface of the display unit 20 is exposed to the inner surface side of the cover member 90. In particular, the tablet terminal 80 is configured such that when the cover member 90 shown in FIG. 3 is closed, the display surface of the display unit 20 faces the weighing units 51 to 54 described later provided in the weighing device 50. It is supported by the cover member 90. Thus, as shown in FIG. 2, when the cover member 90 is opened, the display unit 20 and the operation unit 30 are in a state of facing the weighing units 51 to 54 of the weighing device 50. . Therefore, the user can perform the inspection work without moving the line of sight in a state where the display unit 20 and the operation unit 30 and the weighing units 51 to 54 of the weighing device 50 can be looked over at a time.

The storage unit 40 is a storage device such as a solid state drive or a flash memory in which various application programs executed by the control unit 10 and various data are stored. The storage unit 40 may be a hard disk drive externally connected to the control unit 10.

The storage unit 40 stores the prescription data acquired from the dispensing support system 200 or the reception system 300 by the control unit 10. For example, the control unit 10 refers to a shared folder in a storage device such as the dispensing support system 200 or the reception system 300 at a predetermined timing, and there is unacquired prescription data in the shared folder. Get the prescription data.

The storage unit 40 stores various databases such as a pharmaceutical master and a patient master. The medicine master and the patient master can be updated by interlocking with the dispensing support system 200 or the reception system 300. The medicine master includes medicine code, standard amount, host code, medicine name, medicine general name, JAN code, RSS code, YJ code (individual medicine code), GS1 code, medicine bottle code, dosage form code (powder, tablet) , Liquid medicine, topical medicine, etc.), form code, powerful medicine / managed medicine type (psychotropic drug, narcotic), management (vehicle height, safe, cold place, etc.), and unit (dispensing unit). In addition, the pharmaceutical master includes a weight per unit amount (single), a weight per PTP sheet, a weight with ears for one upper PTP tablet, a weight without ears for one upper PTP tablet, Information such as the number per PTP sheet and the file name of a medicine image (naked drug, packaged product) is also included. The PTP sheet is a packaging material in which a plurality of tablets or a plurality of capsules are individually accommodated. In this embodiment, a PTP sheet will be described as an example. For example, a heat seal in which a predetermined amount of tablets or powders are stored in advance is an example of a packaging material. Meanwhile, the patient master includes information such as the patient code, patient name, date of birth, and sex of each patient.

FIG. 14 is a diagram showing an example of a master maintenance screen D13 for referring to or editing the medicine master. The control unit 10 can display the master maintenance screen D13 on the display unit 20 according to a user operation. FIG. 14 shows a state where the drug master is displayed on the master maintenance screen D13. In addition, the control unit 10 can change the contents of the pharmaceutical master, the patient master, and the like according to a user operation. By the way, the control unit 10 is based on a user ID, a password, and the like input using the display unit 20 and the operation unit 30 when the inspection support apparatus 100 is turned on or returned from the power saving mode. The user of the inspection support apparatus 100 can be specified by executing user authentication. Further, in the inspection support apparatus 100, the control unit 10 can set a use authority for each user in advance according to a user operation or the like. For example, it is conceivable to set authority types such as “general”, “manager”, “maintenance manager”, “support”, “training”, and “technician” for each user. And it is possible that the said control part 10 changes the process which can be performed with the said inspection assistance apparatus 100 according to the said authority kind corresponding to the user specified as the said user. For example, master maintenance for editing the pharmaceutical product master, daily update operation, inspection history inquiry operation, etc. can be executed only by “General”, “Administrator”, or “Maintenance Manager” among the above authority types It is. Also, software setting, hardware setting, mother master periodic update, and the like can be executed only by “manager” or “maintenance manager” of the authority types. The mother master is a drug database provided by, for example, the manufacturer of the inspection support apparatus 100. It is also conceivable that only a part of each process can be executed depending on the authority type. For example, regarding the setting of the hardware, it is conceivable that the “manager” of the authority types is set to use only balance calibration. A configuration is also conceivable in which the control unit 10 can set a process that can be executed for each user, not for each authority type.

Further, the storage unit 40 stores an inspection support program executed by the control unit 10. The inspection support program is downloaded via the network N1, for example, or read from a recording medium by a disk drive and installed in the storage unit 40. And the said control part 10 performs various processes according to the said inspection assistance program, The weighing specific part 11, the unit weight acquisition part 12, the unit conversion process part 13, the collation process part 14, the visual inspection process part 15, It functions as an inspection completion notification unit 16, a display processing unit 17, and a photographing processing unit 18. Further, part or all of the control unit 10 may be an electronic circuit such as an ASIC. In addition, operation | movement of each process part which the said control part 10 has is demonstrated with a flowchart of a back | latter stage.

The weighing device 50 includes four weighing units 51 to 54 and is used for weighing the weight of the medicine. The results of weighing by the weighing units 51 to 54 are input to the control unit 10. Hereinafter, in the present embodiment, for convenience of explanation, the unspecified weighing units 51 to 54 may be referred to as “the weighing unit 5N”. In the present embodiment, the weighing device 50 will be described by taking as an example a configuration including four weighing units 51 to 54. However, the weighing device 50 may include at least two weighing units. That's fine.

As shown in FIGS. 2, 4, and 5, the weighing unit 5 N includes a weighing pan 55, a load cell 56, and a placement unit 57. 4 is a view showing a state in which the weighing pan 55 has been removed, and FIG. 5 is a view showing a state in which the weighing pan 55, the placing portion 57, and the upper surface 501 of the weighing apparatus 50 have been removed. .

The weighing pan 55 is used by being placed on the placement portion 57, and the weighing target chemical is placed on the weighing pan 55. In addition, as shown in FIG. 2, each of the weighing dishes 55 has a different radius of roundness between a corner portion 551 on one diagonal line and a corner portion 552 on the other diagonal line. Specifically, the pair of corner portions 551 have a smaller radius than the corner portions 552. For example, one corner portion 551 is gripped when the weighing pan 55 is lifted by a user, and the other corner portion 551 is held. 551 is inserted into the medicine bag when the medicine on the weighing pan 55 is stored in the medicine bag. The weighing pan 55 may have a configuration in which the corner portion 551 and the corner portion 552 are rounded with the same radius.

Further, an anti-slip member for increasing the frictional resistance between the bottom surface of the weighing pan 55 and the top surface of the mounting portion 57 on one or both of the bottom surface of the weighing pan 55 and the top surface of the mounting portion 57. Is considered to be provided. Thereby, in the said inspection assistance apparatus 100, the shaking of the said weighing pan 55 mounted in the said mounting part 57 is suppressed, and the weighing using the said weighing pan 55 can be performed stably. When the anti-slip member is provided on the weighing pan 55, the anti-slip member is provided on a part or all of the bottom surface of the weighing pan 55. Similarly, when the mounting member 57 is provided with the anti-slip member, the anti-slip member is provided on a part or all of the upper surface of the mounting unit 57. Furthermore, it is conceivable that the anti-slip member is an adhesive sheet. As a result, the weighing pan 55 and the placing portion 57 are temporarily fixed by the anti-slip member, and the shaking of the weighing pan 55 is further suppressed. For example, the weighing by the weighing portion 5N is not stable. Is avoided. The anti-slip member may be provided on a later-described platter 58.

The load cell 56 is a load converter that supports the placing portion 57 and measures the weight of the weighing object placed on the placing portion 57. In the inspection support apparatus 100, the weight of the medicine placed on the weighing dish 55 is weighed by the load cell 56 by placing the weighing dish 55 on the placement unit 57. As the load cell 56, for example, a load cell having a small rated capacity of 300 g or 500 g and high weighing accuracy is used. In addition, it is also possible as another embodiment that the weighing pan 55 and the placing portion 57 are integrally configured.

The placing portion 57 is supported by the load cell 56, and the weighing pan 55 is placed on the upper surface. In addition, a concave portion for stably placing the bottom surface of the weighing pan 55 is formed on the upper surface of the placing portion 57 described above. By the way, it is also conceivable that the load cell 56 and the mounting portion 57 are connected below the upper surface 501 of the weighing device 50, and a large-sized opening corresponding to the mounting portion 57 is formed in the upper surface 501. . However, in this case, a wide gap is generated between the upper surface 501 and the mounting portion 57, and there is a problem that dust or the like easily enters from the gap. On the other hand, in the weighing device 50, the load cell 56 and the mounting portion 57 are connected above the upper surface 501, and a small opening corresponding to the connection location is formed on the upper surface 501. . Thereby, in the weighing device 50, a structure in which dust or the like is difficult to enter from the opening of the upper surface 501 is realized.

In the weighing device 50, the results of weighing by the load cell 56 include the weights of the weighing pan 55 and the placing portion 57 described above. Therefore, the control unit 10 performs taring at the time of weighing using the load cell 56, and subtracts the tare weights of the weighing pan 55 and the placement unit 57 from the weighing result of the load cell 56 to determine the weighing. Obtained as a result of weighing the chemicals placed on the plate 55. The tare weight is initially set when the inspection support apparatus 100 is shipped, but the inspection support apparatus 100 can reset the tare weight at an arbitrary timing. As described above, when the anti-slip member is provided on one or both of the weighing pan 55 and the mounting portion 57, the weight of the anti-slip member is also included in the tare weight.

In addition, as shown in FIG. 6, in the weighing apparatus 50, the weighing of the medicine is performed using a large plate 58 (an example of an extended placement unit) that is larger than the weighing plate 55 instead of the plurality of the weighing plates 55. Is possible. The platter 58 can be placed across the plurality of weighing units 51 to 54. Specifically, a convex portion 581 is provided on the bottom surface of the platter 58 at a position corresponding to the placement portion 57 of the plurality of weighing portions 51 to 54. In the weighing device 50, after the weighing pan 55 is removed as shown in FIG. 4, the convex portions 581 of the platter 58 are arranged in front of the plurality of weighing portions 51 to 54 as shown in FIG. It is placed on each of the placement units 57. Thus, for example, when the rated capacity of the load cell 56 of the weighing units 51 to 54 is 500 g, the weighing device 50 can weigh up to a total of 2.0 kg by using the platter 58. Further, the platter 58 is not limited to the usage form in which the platters 58 are placed on the placing units 57 of the weighing units 51 to 54 in place of the plurality of weighing pans 55, and the plurality of weighing pans 55 are described above. It is also conceivable that the plurality of weighing pans 55 are placed on the placing portion 57 while being placed on the placing portion 57. Thereby, since the user does not need to attach and detach each weighing pan 55, the convenience is improved. The convex portion 581 of the platter 58, the mounting portion 57, and the weighing pan 55 are placed on the mounting portion 57 of the four weighing portions 51 to 54 or the weighing pan 55. It has a shape that is stable in the applied state.

Further, a cross portion 582 indicating the center position of the platter 58 is formed in the platter 58. Accordingly, the cross portion 582 serves as an index for setting the medicine in the center of the platter 58, and can prompt the user to set the medicine in the center of the platter 58. Further, when no medicine is placed in the center of the platter 58, the load acting on the weighing units 51 to 54 from the platter 58 is biased, and only the weighing value of any of the weighing units 51 to 54 is obtained. It is possible to exceed the rated capacity. For example, when the rated capacity of each of the weighing units 51 to 54 is 200 g, and when 500 g of medicine is placed on the platter 58, one or more weighing values of the weighing units 51 to 54 are used. May exceed the rated capacity of 200 g. For this reason, when the platter 58 is used, the control unit 10 determines that the difference between the weighing values of the weighing units 51 to 54 exceeds a predetermined range, that is, the load is applied evenly. If not, it is possible to display a caution message such as “Please bring it to the center”.

Further, the cross portion 582 serves as an index for setting the platter 58 at the center of the weighing units 51 to 54 so that a load is applied to the weighing units 51 to 54 evenly. It is also conceivable that it can be easily set at the center of the weighing parts 51 to 54. For example, it is conceivable that an index part for determining the center positions of the weighing parts 51 to 54 is formed on the upper surface 501, and in this case, referring to the cross part 582 and the index part. However, it becomes easier to set the platter 58 at the center of the weighing parts 51 to 54. In addition, a concave portion 583 is formed on the inner wall surface of the platter 58 to indicate a vertical center position and a horizontal center position of the platter 58 in plan view. Therefore, even if the cross portion 582 is hidden by the medicine in the platter 58, the center position of the platter 58 can be estimated with reference to the recess 583, and the user can measure the platter 58 in the weighing mode. It becomes easy to set in the center of the parts 51 to 54. Further, when the platter 58 is photographed by the photographing unit 70, the control unit 10 determines the center position of the platter 58 based on the position and shape of the cross portion 582 or the concave portion 583 included in the photographed image. Can be detected. For example, the control unit 10 may display a warning on the display unit 20 when the center position of the platter 58 is out of a predetermined range.

The information reading unit 60 can read identification information such as a one-dimensional code such as a barcode (JAN, GS1) or a two-dimensional code such as a QR code (registered trademark). It is a barcode reader that is input to the control unit 10.

Specifically, the information reading unit 60 is used when reading identification information (hereinafter referred to as “prescription identification information”) written on a medicine bag in order to identify prescription data. The prescription identification information is printed on the medicine bag by the dispensing support system 200. For example, in the prescription identification information, a prescription number for identifying the prescription data and prescription data (hereinafter referred to as Rp data) of the same usage unit to be stored in the same medicine bag included in the prescription data, and Rp number and the like are included. The prescription identification information may be other information such as order information as long as the prescription data and the Rp data can be identified.

The information reading unit 60 is also used to read identification information (hereinafter referred to as “medicine identification information”) written on a packaging material of medicine such as wrapping paper or PTP sheet in order to identify the medicine. It is done. The medicine identification information is, for example, a JAN code, RSS code, YJ code, or GS1 code.

And the said control part 10 can acquire the prescription data corresponding to the said prescription identification information from the said memory | storage part 40, when the said prescription identification information is read by the said information reading part 60 from the said medicine bag. . Moreover, the said control part 10 specifies the kind of chemical | medical agent corresponding to the said chemical | medical agent identification information based on the said pharmaceutical master, when the said chemical | drug | medicine identification information is read by the said information reading part 60 from the said packaging material. Is possible. Furthermore, the control unit 10 can select any one of the medicines registered in advance in the medicine master in accordance with a medicine selection operation in a prescription display area A15 (see FIG. 8) described later by the operator. It is. In addition, in the kind of chemical | medical agent, the same chemical | medical agent from which standard amount differs is also included as a different kind of chemical | medical agent. For example, “Memary Tablets 5 mg”, “Memary Tablets 10 mg”, and “Memary Tablets 20 mg” have the same drug name but different standard amounts and are therefore treated as different types of drugs.

As shown in FIG. 2, the photographing unit 70 includes a camera body 710 and a holding member 720 that holds the camera body 710. The camera body 710 is a digital camera used for taking a still image or a moving image of a subject. In the inspection support device 100, an image is taken by the photographing unit 70 in accordance with a control instruction from the control unit 10, and a photographed image is transmitted from the photographing unit 70 to the control unit 10. Note that it is also conceivable that moving image information of the shooting range captured by the shooting unit 70 is input to the control unit 10 and a still image is acquired from the moving image information by the control unit 10. In this case, the control unit 10 can determine the situation within the shooting range of the shooting unit 70 at any time based on the moving image information.

Here, it is conceivable that the photographing unit 70 is arranged at a position and orientation in which the weighing units 51 to 54 of the weighing device 50 and the display unit 20 can be photographed simultaneously. By the way, in the photographing unit 70, the camera body 710 is held by the holding member 720 by holding the connecting portion 711 provided in the camera body 710 by the holding member 720. At this time, the holding member 720 holds the camera body 710 in a state where the shooting range by the camera body 710 can be adjusted within a predetermined range (for example, about 1 mm). For example, the holding member 720 includes a swing mechanism that can swing a holding portion that holds the connecting portion 711 of the camera main body 710 within a range of a predetermined width. Thereby, in the inspection support device 100, it is possible to easily adjust the photographing range photographed by the photographing unit 70 by finely adjusting the direction of the camera main body 710 held by the holding member 720. It is. The photographing unit 70 only needs to be able to photograph at least the weighing units 51 to 54, and it is also conceivable as another embodiment that the display unit 20 is not included in the photographing range. Further, the photographing unit 70 may be fixed to the cover member 90.

As shown in FIG. 2, the photographing unit 70 is supported by the support arm 71 by fixing the holding member 720 to the support arm 71, and the support arm 71 supports the rotation support unit 72. Via the support arm 73, the support arm 73 is rotatably connected. Accordingly, the user can finely adjust the shooting range of the shooting unit 70 by rotating the support arm 71. On the other hand, the support arm 73 is fixed to the weighing device 50. In another embodiment, the support arm 73 is rotatably supported by the weighing device 50 and can be folded compactly by rotating the support arm 73 when the cover member 90 is closed. Conceivable.

[Inspection support processing]

Hereinafter, an example of the procedure of inspection support processing executed by the control unit 10 in accordance with the inspection support program in the inspection support apparatus 100 will be described with reference to the flowchart of FIG. Specifically, the inspection support process is started by the control unit 10 when the inspection support apparatus 100 is turned on or returned from the power saving mode. The inspection support process ends when the inspection support apparatus 100 is shut down or when there is no operation for a predetermined time or more and the mode is shifted to the power saving mode. When the inspection support device 100 is turned on or returned from the power saving mode, the control unit 10 performs user authentication by inputting a user ID and a password using the display unit 20 and the operation unit 30. Thus, the user of the inspection support apparatus 100 is specified.

<Step S11>

First, in step S11, the control unit 10 causes the display unit 20 to display a predetermined prescription inspection screen D10. FIG. 8 is a diagram showing an example of the prescription inspection screen D10. As shown in FIG. 8, the prescription inspection screen D10 includes an unprocessed information key K11, a wrapping paper selection key K12, a visual inspection key K13, a platter use key K14, a tare key K15, a menu key K16, and an inspection completion key. Operation keys such as K17, shooting key K18, and image display key K19 are displayed. The prescription inspection screen D10 displays weighing display areas A11 to A14 and a prescription display area A15. In the prescription inspection screen D10, the name of the user authenticated by the user authentication is also displayed as the authenticator. Further, the control unit 10 displays an authentication screen for performing the user authentication again when, for example, the vicinity of the user's name is operated, and the certifier is selected according to the subsequent input of the user ID and password. It is possible to switch.

The unprocessed information key K11 is an operation key for displaying a list of unprocessed prescription data for which inspection has not been completed on the prescription inspection screen D10. In response to the operation of the unprocessed information key K11, the control unit 10 displays an unprocessed display area A21 in which a list of unprocessed prescription data is displayed on the prescription inspection screen D10 as shown in FIG. In the unprocessed display area A21, information such as a prescription date, a patient name, the total number of Rp, and a voucher number is displayed as a list as information for identifying unprocessed prescription data.

In the unprocessed display area A21, a search operation area A22 and a detail display key K21 are displayed. The control unit 10 searches the prescription data according to the item selected in the search operation area A22 and the input characters input in the search operation area A22, and displays the search results. For example, FIG. 9 shows a display example when the item “date” is selected in the search operation area A22 and the character “20131130” is input. A list of prescription data whose date is November 30, 2013 is displayed as a search result. On the other hand, when the detail display key K21 is operated, the control unit 10 displays detailed information on the prescription data at the location where the detail display key K21 is displayed. The detailed information includes, for example, each content of Rp data of one or more same usage units included in the prescription data (medicine name, usage, daily dose, etc.). Each of the Rp data includes information on one or more types of prescription drugs that have the same usage and are contained in the same medicine bag.

Returning to FIG. 8, when the medicine identification information is read from the packaging paper by the information reading unit 60, the packaging paper selection key K 12 does not include preset specific information. And an operation key for designating the type of the wrapping paper used when weighing the wrapping paper. For example, there are 10 types of wrapping paper such as 60 mm, 70 mm, 76 mm, 80 mm, and 90 mm for each cellopoly and glassine. The control unit 10 displays a plurality of pre-registered wrapping papers as selection candidates according to the operation of the wrapping paper selection key K12, and presets corresponding to the wrapping paper selected from among them. The weight thus determined is set as the weight of the wrapping paper used in the weighing inspection process described later. The specific information is, for example, in a dispensing device such as a tablet packaging machine or a powder medicine packaging machine in which a packaging process using the packaging paper is performed, and the weight of the packaging paper is known, and the medicine identification information Is information for determining whether or not the weight of the wrapping paper is included in the weight per wrapping paper included in or the total weight of all the wrapping papers. For example, the specific information is information for specifying a manufacturer of the tablet packing machine or the powder packing machine.

The visual inspection key K13 is an operation key for executing a visual inspection process on the prescription data displayed in the prescription display area A15. When the visual inspection key K13 is operated in a state where one or more medicines included in the prescription data are selected, the control unit 10 is selected in the prescription display area A15 as shown in FIG. A visual inspection screen D 11 for performing visual inspection for each of the medicines being displayed is displayed on the display unit 20. As shown in FIG. 10, the visual inspection screen D11 displays a medicine information display area A31, a medicine image display area A32, a target value display area A33, and an inspection time input area A34 corresponding to each medicine. Yes.

Specifically, the control unit 10 reads the medicine name of the medicine to be visually inspected selected on the prescription display screen D10 from the prescription data or Rp data and displays it in the medicine information display area 31. Moreover, the said control part 10 reads the chemical | medical agent image of the said visual inspection object chemical | medical agent from the said pharmaceutical master, and displays it on the said chemical | medical agent image display area A32. Furthermore, the said control part 10 reads the target value of the said visual inspection object chemical | medical agent from prescription data or Rp data, and displays it. In addition, the said control part 10 matches the numerical value input into the said input area A34 at the time of inspection with the said chemical | medical agent for visual inspection, and memorize | stores it in the said memory | storage part 40 as inspection history. Here, the units such as “lock”, “g”, “pack”, “capsule” and the like displayed in the inspection input area A34 are units set in advance for each medicine in the pharmaceutical master. In addition, when all the said visual inspection object chemical | medical agents cannot be displayed on the said visual inspection screen D11, the said control part 10 is the said visual inspection object according to the left and right flick operation in the said visual inspection screen D11, or operation of an arrow key. Scroll the medicine display.

When the confirmation key K31 is operated on the visual inspection screen D11, the control unit 10 processes that the visual inspection of the visual inspection target medicine being displayed on the visual inspection screen D11 is completed, and It memorize | stores in the memory | storage part 40 as inspection history. Thus, in the visual inspection process, information such as the drug name, drug image, and target value of the drug to be visually inspected is displayed on the visual inspection screen D11. Therefore, the user refers to the visual inspection screen D11. Visual inspection of the visual inspection target chemical can be easily performed.

Returning to FIG. 8, the platter use key K 14 is an operation key for executing the weighing inspection process using the platter 58. In response to the operation of the platter use key K14, the control unit 10 displays one weighing display area A41 on the prescription inspection screen D10 instead of the weighing display areas A11 to A14 as shown in FIG. . Note that, for example, the control unit 10 may gray out or hide the weighing display areas A11 to A14. In the weighing display area A41, the total of all weighing values of the weighing units 51 to 54 is displayed as a weighing result. Further, in the weighing display area A41, a matching result between the weighing result when the platter 58 is used and the prescription data is displayed in the weighing inspection process described later. Accordingly, the inspection support apparatus 100 can execute the weighing inspection using the platter 58 even with a large amount of medicine that is difficult to weigh in each of the weighing dishes 55 or a medicine with a large size.

The tare key K15 is used for a taring process start operation for updating the set value of the tare weight of the tare weight corresponding to each of the weighing units 51 to 54 in the weighing device 50. For example, when using the platter 58, the user operates the tare key K15 after placing the platter 58 on the weighing units 51-54. Accordingly, the control unit 10 sets the current weighing value of each of the weighing units 51 to 54 as the tare weight of each of the weighing units 51 to 54. Therefore, the control unit 10 can weigh the chemical placed on the weighing pan 58 by subtracting the tare weight from the weighing value weighed by the weighing units 51 to 54. At this time, when the platter 58 is placed on each of the weighing dishes 55, the weight of the four weighing dishes 55 is included in the tare weight. Even when the platter 58 is changed to the weighing pan 55, the tare weight key K15 is operated to set the tare weight corresponding to the weighing pan 55.

The menu key K16 is an operation key for displaying a menu of various functions of the inspection support apparatus 100. The control unit 10 displays a menu screen for performing operations such as initial setting, master registration, environment setting, software version update, or history inquiry according to the operation of the menu key K16.

The inspection completion key K17 executes a visual inspection process or a weighing inspection process, which will be described later, for a drug whose inspection has not been completed among the Rp data currently displayed on the prescription inspection screen D10 in the inspection support apparatus 100. It is operated when the inspection is completed without any problem. In response to the operation of the inspection completion key K17, the control unit 10 completes the inspection of medicines that have not been inspected among the Rp data currently displayed on the prescription inspection screen D10, and records the history thereof as described above. After memorize | storing in the memory | storage part 40, the inspection of the said Rp data is complete | finished. As a result, even if unexamined medicine that can be judged visually appropriate by the pharmacist remains, the inspection service is completed by operating the inspection completion key K17 to complete the inspection of the displayed Rp data. It is possible to speed up the process. When the inspection is forcibly completed by operating the inspection completion key K17, the control unit 10 may display an inspection completion screen indicating that the inspection is completed on the display unit 20. Conceivable. In the inspection completion screen, a predetermined first color check mark is attached to the weighed and inspected medicine inspected in the later-described weighing inspection process in the Rp data, and the visual inspection performed in the later-described visual inspection process. The inspected medicine is given a predetermined second color check mark different from the first color. Moreover, about the uninspected medicine which is not inspected by the said weighing inspection process or the said visual inspection process among the said Rp data, in the aspect (for example, there is no check mark) which can be distinguished from the said weighing inspection medicine and the said visual inspection medicine. Is displayed. In the inspection completion screen, it is only necessary to distinguish the medicines weighed, the visual inspections, and the uninspected medicines on the inspection completion screen. For example, each background color may be different. .

The photographing key K18 is an operation key for recording a photographed image by the photographing unit 70. The control unit 10 causes the photographing unit 70 to take an image in response to an operation of the photographing key K18. Then, the control unit 10 records the captured image in the storage unit 40 as an inspection history in association with the prescription data to which the Rp data currently displayed on the prescription inspection screen D10 belongs. Thereby, the said control part 10 can display the said picked-up image memorize | stored in the said memory | storage part 40 for every said prescription data. In addition, it is also conceivable as another embodiment that the control unit 10 associates the captured image with each Rp data and stores it in the storage unit 40. Further, as another usage method, after the inspection of the medicine using the inspection support device 100 is completed, the prescription, the medicine bag, and the medicine corresponding to the prescription data that is the object of the inspection are obtained by the user. It is conceivable that the photographing key K18 is operated after being placed within the photographing range of the photographing unit 70 such as the upper surface 501 of 50. Accordingly, the prescription, the medicine bag, and the medicine are photographed by the photographing unit 70, and the photographed image is recorded in the storage unit 40 as an inspection history in association with the prescription data.

FIG. 12 is a diagram showing an example of an inspection history inquiry screen D12 for referring to the inspection history in the inspection support device 100. In the inspection history inquiry screen D12, an extraction condition display area A51 in which conditions for extracting the inspection history stored in the storage unit 40 can be input, a list display area A52 for displaying extraction results, and the list display A history content display area A53 is displayed in which the contents of the inspection history selected in the area A52 are displayed. Specifically, in the extraction condition display area A51, it is possible to input an inspection period (inspection date / time), a prescription date, a patient name, a medicine name, a pharmacist name, and whether or not yellow is determined. And the said control part 10 reads the inspection log | history corresponding to the conditions input in the said extraction condition display area A51 from the said memory | storage part 40, and displays it as a list on the said inspection log | history inquiry screen D12. In the history content display area A53, the target column displays target values (values of tablets, capsules, sheets, etc.) corresponding to the prescription data, and the inspection column is weighed by the inspection support apparatus 100. A converted value (value of tablets, capsules, sheets, etc.) obtained by converting the measured weight value of the medicine into the unit of medicine is displayed. However, the word “visually” is displayed in the inspection column of the medicines that have been inspected by the visual inspection process described below among the prescription medicines. In the inspection history inquiry screen D12, thumbnail images of images taken by the photographing unit 70 stored in the storage unit 40 as the inspection history of the prescription data selected in the list display area A52 are displayed on the prescription inspection screen D10. Similarly, it is displayed as the image display key K19. When the prescription, the medicine bag, and the medicine are photographed by the photographing unit 70, a thumbnail image of the photographed image is also displayed as the image display key K19. In response to the operation of the image display key K19, the control unit 10 enlarges and displays the photographed image corresponding to the image display key K19 on the inspection history inquiry screen D12.

Returning to FIG. 8, the image display key K19 is a thumbnail image of a photographed image by the photographing unit 70 stored in the storage unit 40 as an inspection history of the prescription data displayed in the prescription display area A15. . 8 and 12, “Image 1” to “Image 4” are displayed as the thumbnail image names under the image display key K19, but “Rp number” and “Continuous” are displayed as the thumbnail image names. It is also conceivable that “No.” is used. For example, when the Rp number is “01”, the name of the first image is “01-1”, and the name of the second image is “01-2”. Further, the control unit 10 enlarges and displays the thumbnail image corresponding to the image display key K19 in accordance with the operation of the image display key K19.

The weighing display areas A11 to A14 are display areas corresponding to the weighing parts 51 to 54, respectively, and the weighing results by the weighing parts 51 to 54 are displayed in the weighing display areas A11 to A14. Here, in the display unit 20, the weighing display areas A11 to A14 are displayed on the display unit 20 in the same arrangement as the weighing units 51 to 54. For example, the weighing display area A11 corresponding to the weighing section 51 is arranged at the upper left as in the weighing section 51, and the weighing display area A12 corresponding to the weighing section 52 is arranged at the upper right as in the weighing section 52. Has been. Thus, the control unit 10 causes the display unit 20 to display the weighing display areas A11 to A14 corresponding to the weighing units 51 to 54 in the same arrangement as the weighing units 51 to 54, respectively. Such display processing is executed by the display processing unit 17 of the control unit 10. Hereinafter, in the present embodiment, for the sake of convenience of explanation, the unspecified weighing display areas A11 to A14 may be referred to as “weighing display areas A1M”.

The prescription display area A15 is a display area in which a list of medicine names and medicine images of prescription medicines included in Rp data to be displayed is displayed together with a patient name and a patient code. For a medicine whose medicine image is not registered in the medicine master, a character “no image” is displayed instead of the medicine image. In the prescription display area A15, prescription medicines included in the Rp data can be selected as inspection targets, and one or a plurality of selected prescription medicines are selected with a check mark. In addition, even when the drug identification information is read by the information reading unit 60, the prescription drug corresponding to the drug identification information is added with a check mark and selected as an inspection target. Of the prescription medicines displayed in the prescription display area A15, the medicines that have already been inspected by the visual inspection process described later are displayed in a color different from other medicines.

<Steps S12 to S13>

Next, in steps S12 to S13, the control unit 10 determines whether or not an operation for specifying prescription data to be inspected in the inspection support apparatus 100 has been executed. Specifically, in step S12, the control unit 10 determines whether or not the information reading unit 60 has read the prescription identification information described in the medicine bag. Moreover, in the said step S13, the said control part 10 judges whether operation which selects prescription data from an unprocessed list was performed. And the said control part 10 will transfer a process to step S14, if the said prescription data are specified (S12 or S13: Yes side).

<Step S14>

In step S14, the control unit 10 reads the prescription data specified in step S12 or step S13. Specifically, when the prescription identification information is read from the medicine bag in step S12, the control unit 10 reads the Rp data corresponding to the prescription identification information from the storage unit 40. That is, the control unit 10 can acquire the prescription data to be inspected based on the prescription identification information of the medicine bag read by the information reading unit 60. This processing is executed by the verification processing unit 14 of the control unit 10. In addition, the said control part 10 specifies the Rp data as inspection object, when Rp data is selected in the said detailed information displayed according to operation of the said detailed display key K21 of the said unprocessed display area A21. It is also possible.

When unprocessed prescription data is selected in step S13, the control unit 10 reads the selected prescription data from the storage unit 40. That is, the control unit 10 can select the prescription data to be inspected from a plurality of the prescription data in accordance with a user operation. This processing is executed by the verification processing unit 14 of the control unit 10.

FIG. 8 is a display example of the prescription inspection screen D10 when unprocessed prescription data is selected in step S13. When the prescription data is selected in step S13, the Rp data to be inspected is not specified even when the prescription data includes a plurality of Rp data. Therefore, as shown in FIG. 8, in the prescription display area A15, among the Rp data included in the prescription data, the designated RpNo. “1/3” is displayed.

For example, the designated RpNo. “1/3” indicates that the prescription data includes three Rp data, and the first Rp data is currently displayed. Then, the control unit 10 performs the designation RpNo. By the operation of “+” and “−” displayed in the prescription display area A15 or the direct input operation of the numerical value. And change the designated RpNo. Rp data corresponding to is displayed in the prescription display area A15. Further, the control unit 10 corresponds to the medicine identification information from the prescription data displayed in the prescription display area A15 when the medicine identification information is read from the medicine packaging material by the information reading unit 60. Rp data including the medicine to be searched is retrieved, and the Rp data is displayed in the prescription display area A15.

On the other hand, when the prescription identification information is read from the medicine bag in the step S12, the Rp data to be inspected can be specified by the prescription identification information. Therefore, when the prescription identification information is read from the medicine bag in step S12, Rp data corresponding to the prescription identification information is displayed on the prescription inspection screen D10, and the designated RpNo. The display of is omitted.

<Step S15>

Subsequently, in step S15, when the control unit 10 has a visual inspection setting medicine set in advance as a medicine to be inspected by visual inspection processing in the prescription data or the Rp data (S15: Yes side), The process proceeds to step S151, and a visual inspection process described later is executed. In this case, the said visual inspection setting chemical | medical agent is specified as a visual inspection object chemical | medical agent used as the object of visual inspection. The visual inspection setting medicine is, for example, a medicine in which a barcode is not attached to a medicine packaging material, or a medicine in which water and kneaded materials are mixed and dispensed. In addition, when the chemical | medical agent handled as the said visual inspection object chemical | medical agent does not exist in the said prescription data or the said Rp data (S15: No side), a process transfers to step S16. Further, the omission of step S15 can be considered as another embodiment.

<Step S16>

In step S16, when an operation for starting visual inspection is performed (S16: Yes side), the control unit 10 must move the process to step S151 and perform an operation for starting visual inspection. If it is (S16: No side), the process proceeds to step S17. Specifically, the control unit 10 starts the visual inspection when the visual inspection key K13 is operated in a state where one or more prescription medicines displayed on the prescription inspection screen D10 are selected. It is determined that an operation has been performed. In this case, one or a plurality of prescription medicines selected on the prescription inspection screen D10 are specified as visual inspection target medicines.

<Step S17>

In step S17, when the medicine identification information is read from the wrapping paper that is a medicine packaging material (S17: Yes side), the control unit 10 shifts the process to step S171 and performs a visual inspection process described later. Execute. For example, the medicine identification information corresponding to the medicine packaged by the packaging paper is recorded on the packaging paper by a code such as a QR code (registered trademark). Moreover, the said control part 10 makes a process transfer to step S18, when the said chemical | drug | medicine identification information is not read from the wrapping paper (S17: No side).

<Step S18>

In Step S18, when the medicine identification information is read from the PTP sheet which is a medicine packaging material (S18: Yes side), the control unit 10 sets the prescription medicine corresponding to the medicine identification information as a weighing inspection target medicine. The process is shifted to step S19, and a weighing inspection process described later is executed. Moreover, the said control part 10 returns a process to the said step S16, when the said chemical | drug | medicine identification information is not read from the PTP sheet (S18: No side). Even when the medicine identification information is read, the medicine corresponding to the medicine identification information is registered in advance as a medicine that does not undergo weighing inspection processing, or the medicine corresponding to the medicine identification information When the weight per unit amount is not stored in the pharmaceutical master, the control unit 10 may shift the process to step S151 as another embodiment.

In addition, even when the medicine identification information is not read (S18: No side), the control unit 10 selects only one medicine displayed on the prescription inspection screen D10 and is predetermined. When the weighing inspection processing start operation is performed, it is also possible to shift the processing to step S19 and execute the weighing inspection processing for the medicine. For example, the operation for starting the weighing inspection process is an operation of long-pressing the display area of the medicine or an operation of a weighing inspection key (not shown) displayed on the prescription inspection screen D10. On the other hand, if the weighing inspection process is not started, the process returns to step S16. The target drug for which the weighing inspection processing start operation is arbitrarily performed includes, for example, a drug in which the drug identification information is not attached to a packaging material, a drug in which a plurality of sheets are in one package, and a tablet component. This is medicine after packaging that is packaged by a packaging machine.

<Steps S151 and S171>

In step S151 or step S171, the control unit 10 executes a visual inspection process that supports a task for a user to visually confirm a medicine image for the visual inspection target medicine. Here, the visual inspection processing is executed by the visual inspection processing unit 15 of the control unit 10.

In the visual inspection process, the control unit 10 first displays the visual inspection screen D11 (see FIG. 10) on the display unit 20. The control unit 10 causes the visual inspection screen D11 to display one or a plurality of prescription drugs specified in the steps S15 to S17 as the visual inspection target chemicals. Specifically, when the medicine identification information of the wrapping paper is read in the step S17, the control unit 10 includes one or a plurality of pieces stored in the wrapping paper based on the medicine identification information. A medicine is specified as the medicine to be visually inspected. And the said control part 10 reads the chemical | medical agent name of the said chemical | medical agent for visual inspection, a chemical | medical agent image (bare tablet image), a target value, etc. from the said prescription data, the said Rp data, or the said pharmaceutical master, and the said visual inspection screen D11 is displayed. Thereafter, when the confirmation key K31 on the visual inspection screen D11 is operated, the control unit 10 processes that the visual inspection of the visual inspection target drug being displayed on the visual inspection screen D11 is completed, It memorize | stores in the memory | storage part 40 as inspection history. In addition, the control unit 10 may automatically delete the visual inspection screen D11 by determining that the visual inspection has ended when a predetermined time has elapsed after the display of the visual inspection screen D11. It is done. Furthermore, after the said control part 10 displays the said visual inspection screen D11, it is also considered that the enlarged screen of each said medicine image is automatically popped up in order, and it erase | eliminates after predetermined time.

By the way, when the control unit 10 reads the medicine identification information from the PTP sheet by the information reading unit 60 during the display of the visual inspection screen D11, among the medicines displayed on the visual inspection screen D11 Regarding the medicine corresponding to the medicine identification information, it may be possible to store in the storage unit 40 as an inspection history that the collation by the medicine identification information has been performed. Thereby, for example, when a medicine unpacked from a PTP sheet is packaged in the wrapping paper by a tablet wrapping machine or a powder wrapping machine, the GS1 code or the like is read from the PTP sheet after the wrapping. By reading by 60, the labor of visual inspection for at least some of the medicines packaged with the wrapping paper is reduced. For example, the result of the verification process of the medicine identification information in the visual inspection is reflected in the result of “bar code confirmation” in the history display area A53 in FIG.

When the medicine identification information on the wrapping paper is read in step S17, in the visual inspection process, the user performs inspection with reference to the medicine in the wrapping paper and the visual inspection screen D11. There is a need. On the other hand, for example, in the medicine identification information printed on the wrapping paper in a dispensing device such as the tablet wrapping machine or the powder wrapping machine, the medicine names and dosage forms of all the medicines contained in the wrapping paper It is conceivable that packaging information regarding contents such as dispensing amount (weight or quantity) and patient information is included. Therefore, when the medicine identification information of the wrapping paper is read in step S17, the control unit 10 collates the packaging information included in the medicine identification information with the prescription data, and the collation result If they match, it is conceivable that the inspection of each medicine contained in the wrapping paper is completed without executing the visual inspection process and the weighing inspection process. Thereby, the labor of the visual inspection about the chemical | medical agent packaged by the said wrapping paper with the said dispensing apparatus can be reduced.

<Step S172>

After execution of step S171, in step S172, the control unit 10 determines whether or not the weighing inspection setting is set to ON. If the weighing inspection setting is set to ON (S172: Yes) Side), the process proceeds to step S19. On the other hand, when the weighing inspection setting is set to OFF (S172: No side), the control unit 10 shifts the process to step S20. The weighing inspection setting is a setting relating to whether or not the weighing inspection processing using the weighing device 50 is executed together with the visual inspection processing when the medicine identification information is read from the wrapping paper in the step S17. The control unit 10 can arbitrarily change the contents of the weighing inspection setting according to a user operation at the time of setting the environment of the inspection support device 100. In addition, when the medicine identification information is read from the wrapping paper in the step S17, the control unit 10 may switch whether or not to execute the weighing inspection process according to a subsequent user operation. . Furthermore, it is considered that the weighing inspection setting is effective not only when the medicine identification information is read from the wrapping paper but also for a medicine that is predetermined as a medicine that can be weighed by the inspection support device 100. It is done.

<Step S19>

And in step S19, the said control part 10 performs the weighing | inspection inspection process including the collation process which collates the weighing result by the said weighing part 5N, and the said prescription data. This process is an example of a collation step, and is executed by the collation processing unit 14. Specifically, in step S19, the control unit 10 starts the new weighing inspection process corresponding to the medicine identification information, and then shifts the process to step S20. That is, the control unit 10 individually starts the weighing inspection process corresponding to the medicine identification information every time the medicine identification information is read in step S18. Therefore, when the medicine identification information is sequentially read from a plurality of PTP sheets, a plurality of the weighing inspection processes are started by the control unit 10, and the weighing inspection processes are executed in parallel. Become. Further, when the weighing inspection setting is ON, the weighing inspection processing is individually started each time the medicine identification information is read from the wrapping paper.

By the way, when the medicine identification information of the wrapping paper includes the weight of one wrap including the weight of the wrapping paper or the total weight of all the wrapping paper, In the weighing inspection process of step S19 executed when the medicine identification information is read, the weighing result by the weighing unit 5N is included in one package including the weight of the wrapping paper included in the medicine identification information. It is conceivable to check against the weight of the minute or the total weight of all the wrapping papers. The dispensing data or the packaging data at the time of dispensing executed based on the prescription data as described above is also an example of the prescription data. When the medicine identification information of the wrapping paper does not include the weight of one wrapping paper including the weight of the wrapping paper or the total weight of all the wrapping papers, the control unit 10 The number of wrapping paper selected after the operation of the wrapping paper selection key K12 or the initial setting of the wrapping paper type and the weight corresponding to the number of sachets to be weighed and the wrapping paper for inspection It is conceivable to execute the weighing inspection process by adding to the value. Further, when the medicine identification information of the wrapping paper does not include the weight of one wrap including the weight of the wrapping paper or the total weight of all the wrapping paper, the control unit 10 It is also conceivable to calculate the total weight based on the name of the medicine, YJ code, fraction, etc. packaged in the wrapping paper, and collate the value with the weighing result by the weighing unit 5N.

<Step S20>

Thereafter, in step S20, the control unit 10 determines whether or not the inspection has been completed for all of the prescription drugs included in the Rp data specified in step S12 or the prescription data specified in step S13. Determine whether. Specifically, the control unit 10 determines whether inspection by any of the visual inspection process and the weighing inspection process has been completed for all medicines included in the Rp data or the prescription data. Here, if the said control part 10 judges that the inspection was completed about all the said prescription medicines (S20: Yes side), it will transfer a process to step S21. Moreover, if the said control part 10 judges that the prescription medicine which inspection has not been completed remains (S20: No side), a process will be returned to said step S16.

<Step S21>

In step S21, the control unit 10 causes the display unit 20 to display an inspection completion notification indicating that the inspection of the Rp data or the prescription data has been completed, and returns the process to step S11. This processing is executed by the inspection completion notification unit 16 of the control unit 10. Thereby, the user can grasp | ascertain clearly that the inspection of the said Rp data or the said prescription data was completed by referring the display of the said display part 20. FIG. It is also conceivable that the inspection support device 100 is connected to a printer via the network N1. In this case, it is considered that the control unit 10 can print the inspection record of the Rp data or the prescription data for which the inspection is completed using the printer in the step S21. The inspection record includes, for example, patient information (patient name, patient ID, age, sex, etc.), usage, medicine, inspection result (weighing result, target value, verification result, etc.) and the like. Specifically, the control unit 10 automatically prints the inspection execution record in the step S21 or prints the inspection execution record in response to a user operation on the screen on which the inspection completion notification is displayed. It is possible. Note that the control unit 10 can also set in advance according to a user operation whether or not to automatically print the inspection execution record. Moreover, it is also conceivable that the control unit 10 can print a medicine bag based on the Rp data or the prescription data using the printer.

In addition, when the said prescription data is specified by the said step S13, the said control part 10 displays the inspection completion notice on the said display part 20 whenever inspection about Rp data contained in the said prescription data is completed. Is also possible. As a result, the inspection is performed in units of the Rp data, and it is possible to perform the inspection collectively for each prescription drug to be accommodated in the same medicine bag.

[Weighing inspection process]

Next, the weighing inspection process started in step S19 will be described with reference to FIG.

<Step S30>

First, in step S30, the control unit 10 determines that the medicine corresponding to the medicine identification information read from the PTP sheet or the wrapping paper is the prescription data to be inspected displayed in the prescription display area A15 or It is determined whether it is included in the Rp data. Here, if it is determined that the medicine corresponding to the medicine identification information is included in the prescription data or Rp data to be inspected (S30: Yes side), the process proceeds to step S31. On the other hand, when it is determined that the medicine corresponding to the medicine identification information is not included in the prescription data or Rp data to be inspected (S30: No side), the control unit 10 proceeds to step S301. In addition, even when the inspection target is prescription data, if the setting for executing the inspection for each Rp data has been performed in advance, the control unit 10 reads the step S30. It is conceivable to determine whether or not a medicine corresponding to medicine identification information is included in the Rp data currently displayed in the prescription display area A15.

<Step S301>

In step S301, the control unit 10 displays an error message on the display unit 20, and then ends the weighing inspection process. For example, the error message includes a warning that the medicine identification information read by the information reading unit 60 does not match the prescription data or the Rp data.

<Step S31>

In step S31, the control unit 10 stores the weight per unit amount of medicine corresponding to the medicine identification information read in step S17 or step S18 (hereinafter referred to as “unit weight”) in the storage unit 40. Obtain from the said pharmaceutical master. This process is executed by the unit weight acquisition unit 12 of the control unit 10. The control unit 10 may acquire a unit weight of the medicine from an external storage device. For example, when the medicine identification information is a tablet, the weight per unit amount of the tablet is read from the medicine master.

By the way, when the unit weight is less than 1.6 g, the influence of error becomes large. Therefore, when the unit weight acquired in step S31 is less than a predetermined value such as 1.6 g, the control unit 10 sets the background color of the weighing display areas A11 to A14 to a light yellow color determined in advance. It is possible to change. Thereby, the user can perform inspection work paying attention to the fact that the unit weight is small. Moreover, it is possible that the same chemical | medical agent from which dosage or usage differs is contained in the said prescription data or the said Rp data. In this case, for example, the control unit 10 first specifies the topmost medicine displayed in the prescription display area A15 among the same medicine corresponding to the medicine identification information as the medicine to be weighed and the subsequent inspections. Among the unfinished medicines, the top medicine displayed in the prescription display area A15 is specified as the medicine for weighing inspection. As another embodiment, the control unit 10 similarly sets the background color of the weighing display areas A11 to A14 when the unit weight acquired in the step S31 is equal to or larger than a preset allowable maximum value. It is conceivable to change the color to a predetermined light yellow color.

<Step S32>

Next, in step S32, the control unit 10 determines whether any of the weighing values of the weighing unit 5N has increased from zero. Here, when the control unit 10 determines that the weighing value of any of the weighing units 5N of the weighing units 51 to 54 has increased from 0 (S32: Yes side), the process proceeds to step S33. On the other hand, when the control unit 10 determines that the weighing values of the weighing units 51 to 54 have not changed from 0 (S32: No side), the process proceeds to step S35.

<Step S33>

In step S33, the control unit 10 specifies the weighing unit 5N whose weighing value has increased from 0 in step S32 as the weighing unit associated with the medicine identification information identified in step S17 or S18. That is, the control unit 10 specifies one or a plurality of the weighing units 5N whose weighing values have increased from 0 after the reading of the drug identification information by the information reading unit 60 as the weighing units associated with the drug identification information. The specifying process is an example of a weighing specifying step, and is executed by the weighing specifying unit 11 of the control unit 10. For example, when the weighing values of the plurality of weighing units 5N increase from 0 after the medicine identification information is read and before the next medicine identification information is read, the plurality of weighing units 5N Is associated with the medicine identification information that has been read first. Thereby, the user can divide a bundle of the same kind of medicines into a plurality of parts and place them on the weighing unit 5N.

In the inspection support apparatus 100 configured as described above, when the control unit 10 includes a weighing unit whose weighing value is increased from a value larger than 0 in the weighing unit 5N (S32: No side). The weighing unit is not specified as the weighing unit associated with the medicine identification information. Accordingly, the control unit 10 determines whether the weighing by the weighing unit 5N to be associated with the previously read medicine identification information and the weighing by the weighing unit 5N to be associated with the next medicine identification information read. Even when proceeding simultaneously, it is possible to distinguish these weighing parts 5N and associate them with the medicine identification information.

In addition, after the weighing unit 5N corresponding to the medicine identification information is specified in the step S33, the control unit 10 determines the weighing unit 5N corresponding to the medicine identification information in a later-described step S35 or S36. If the weighing value of the weighing unit 5N returns to 0 in the meantime, the association between the weighing unit 5N and the medicine identification information is canceled. In this case, the control unit 10 also resets the display in the weighing display area A1M corresponding to the weighing unit 5N.

<Step S34>

In step S34, the control unit 10 starts displaying the chemical amount according to the weighing value by the weighing unit 5N specified in step S33. Specifically, the control unit 10 converts the weighing result of the weighing unit 5N into a predetermined unit and displays it in the weighing display area A1M corresponding to the weighing unit 5N. Thereafter, the weighing result of the weighing unit 5N is continuously updated and displayed in the weighing display area A1M. The real-time update of the weighing result display is executed until the weighing result of the weighing unit 5N is stably determined. Here, the process of converting the weighing result by the weighing unit 5N into a predetermined unit based on the unit weight acquired in the step S31 is executed by the unit conversion processing unit 13 of the control unit 10. . Further, the display processing unit 17 of the control unit 10 executes a process of displaying the weighing result by the weighing unit 5N converted into a predetermined unit in the weighing display area A1M. The unit of the drug after conversion of the weighing result (tablet, capsule, package, sheet, g, etc.) is the same as the unit of drug (tablet, capsule, package, sheet, g, etc.) used in the prescription data, for example. It is.

By the way, in the said inspection assistance apparatus 100, it is possible that the precision (range) of the weighing by the said weighing part 5N can be switched. Specifically, it is conceivable that the weighing unit 5N includes a weighing control unit that inputs a weighing value to be weighed using the load cell 56 to the control unit 10. The weighing control unit is a control unit such as ASIC or MPU. The weighing control unit changes the number of digits of the decimal point of the weighing value input to the control unit 10 as the weighing result of the load cell 56 of the weighing unit 5N according to the control instruction from the control unit 10. Can be considered. For example, the weighing control unit is configured to input a weighing value to the control unit 10 with accuracy up to the first decimal point in accordance with a control instruction from the control unit 10, and to the second decimal point. It is conceivable that the second range mode in which the weighing value is input to the control unit 10 with high accuracy can be switched and executed.

In such a configuration, the control unit 10 can switch the operation mode of the weighing control unit to the first range mode or the second range mode depending on the situation. For example, the control unit 10 normally obtains a weighing value with accuracy from the weighing unit 5N to the second decimal place by operating the weighing control unit of the weighing unit 5N in the second range mode. . On the other hand, as the usage environment of the inspection support apparatus 100, for example, an environment in which the value of the second decimal place of the weighing value of the weighing unit 5N is difficult to be stabilized due to the influence of wind or vibration is assumed. Therefore, if the second decimal place value of the weighing value of the weighing unit 5N is not stable even after a preset predetermined time has elapsed, the control unit 10 turns the weighing control unit of the weighing unit 5N on. By operating in the first range mode, it is conceivable to obtain a weighing value with accuracy from the weighing unit 5N to the first decimal place. In this case, when the first decimal place of the weighing value of the weighing unit 5N is stabilized, the control unit 10 acquires the weighing value as a weighing result. In addition, when the situation where the value of the second decimal place of the weighing value of the weighing unit 5N is not stable after the lapse of the predetermined time has occurred repeatedly for a predetermined number of times during the predetermined period, the control unit 10 It is also conceivable to change the normal initial operation mode of the weighing control unit of the unit 5N from the second range mode to the first range mode.

<Step S35>

In step S 35, the control unit 10 determines whether or not the drug identification information corresponding to another drug has been read by the information reading unit 60. Here, if the said control part 10 judges that the said chemical | medical agent identification information corresponding to another chemical | medical agent was read (S35: Yes side), it will transfer a process to step S351.

Moreover, if the said control part 10 judges that the said chemical | medical agent identification information corresponding to another chemical | medical agent is not read (S35: No side), a process will be transferred to step S36. Thereby, in the said weighing | inspection inspection process, the said control part 10 is after the said chemical | medical agent identification information is read by the said information reading part 60 after the said chemical | medical agent identification information is read by the said information reading part 60 (S35: Yes side), one or a plurality of the weighing parts 5N whose weighing values have increased from 0 are specified as weighing parts corresponding to the medicine identification information (S33). This processing is executed by the weighing specifying unit 11 of the control unit 10.

<Step S36>

In step S36, the control unit 10 determines whether or not a predetermined time has elapsed since the weighing unit 5N corresponding to the medicine identification information is specified in step S33. Here, if the said control part 10 judges that the said predetermined time passed (S36: Yes side), it will transfer a process to step S351, and until the said predetermined time passes (S36: No side), The process returns to step S32.

In the present embodiment, even when the predetermined time has elapsed, the process (S33) for assigning the weighing unit 5N to the weighing inspection target drug is not executed, and the weighing unit corresponding to the weighing inspection target drug Although the case where 5N is determined will be described, the present invention is not limited to this. For example, a configuration is also conceivable in which the control unit 10 can determine the weighing unit 5N corresponding to the weighing inspection target medicine in accordance with an operation of a predetermined confirmation key or the like. In addition, the control unit 10 executes a verification process described later in step S37 from time to time after step S33, and confirms that the weighing result of the weighing unit 5N corresponding to the drug for weighing inspection matches the prescription data. A configuration is also conceivable in which the weighing section 5N corresponding to the drug for weighing inspection can be determined under conditions.

<Step S351>

In step S351, the control unit 10 determines whether or not all the weighing values of one or a plurality of the weighing units 5N specified as the weighing unit corresponding to the medicine identification information in the step S33 have been determined. The weighing value of the weighing unit 5N is determined, for example, when the weighing value of the weighing unit 5N is stable without fluctuation for a predetermined time. Here, if the said control part 10 judges that the weighing value of all the said weighing parts was decided (S351: Yes side), it will transfer a process to step S37 and the weighing value of all the said weighing parts 5N will be decided. Until (S351: No side), the determination in step S351 is repeatedly executed.

<Step S37>

In step S37, the control unit 10 calculates the total of the weighing results by the one or more weighing units 5N specified as the weighing unit corresponding to the same medicine in step S33, and the total value and the prescription data And match. Specifically, the control unit 10 matches the prescription quantity, which is the target value indicated by the prescription data, in which the total weighing result of each of the weighing units 5N converted into the unit predetermined in step S34. Determine whether or not.

For example, when the target value of the weighing inspection target drug shown in the prescription data is 9 tablets and the unit weight of the weighing inspection target drug is 2.2 g, the weighing by the weighing unit 5N When the value is 19.8 g, the number of medicines placed on the weighing unit 5N is 9 tablets. On the other hand, the control unit 10 matches the collation result when the drug quantity calculated based on the weighing value by the weighing unit 5N and the unit weight is 8.5 to 9.4 tablets. If it is 8.4 tablets or less or 9.5 tablets or more, it may be determined that the verification results are inconsistent. That is, the control unit 10 may perform verification by rounding off the first decimal place of the chemical quantity. The error allowed by the control unit 10 in the verification process can be set in advance, and rounding off to the first decimal place is just one example. For example, it is conceivable that the control unit 10 determines that the collation results are the same when the weighing result is a target value ± 0.1 tablet or a target value ± 0.2 tablet.

In addition, when there are a plurality of weighing units 5N associated with the weighing inspection target drug, the control unit 10 includes the total number of tablets of the weighing inspection target drug in the prescription data or the Rp data, The total of the number of tablets into which the weighing value of the weighing unit 5N is converted is collated. As a result, even when a plurality of weighing units 5N are used for one drug to be weighed and inspected, the user can arbitrarily perform the same procedure as in the case of using one weighing unit 5N without requiring a special operation. It is possible to easily perform the weighing inspection by placing the weighing inspection target chemicals on the weighing portions 5N. As a verification method when there are a plurality of weighing units 5N associated with the weighing inspection target drug, the control unit 10 calculates the total number of tablets of the weighing inspection target drug in the prescription data or the Rp data. The total weight value obtained by multiplying the number of PTP sheets obtained by dividing by the number of PTP sheets corresponding to the drug to be weighed and inspected by the weight per PTP sheet, and the plurality of weighing units 5N It is also conceivable to determine whether or not the difference from the total weighing value is less than a predetermined tolerance.

By the way, when the medicine for weighing inspection is a tablet or a capsule, the control unit 10 stores the number per one PTP sheet stored in the medicine master corresponding to the medicine for weighing inspection and the prescription data. Alternatively, it is conceivable to calculate the number of PTP sheets of the drug to be weighed and the presence or absence of fractions less than one based on the Rp data. The control unit 10 may add a predetermined value set in advance as the weight of the ear of the PTP sheet to the target value in accordance with the number of PTP sheets and the presence or absence of fractions.

For example, when the fraction exists, the control unit 10 may determine that there is an ear and add the weight of the ear. Thereby, the target value approximates to a value considering the weight of the ear of the PTP sheet, and the matching is executed with high accuracy. In addition, when the fraction of a PTP sheet exists, the structure which can select beforehand whether it calculates with an ear | edge or without an ear | edge is also considered. In addition, the control unit 10 always changes the addition value to the target value with the ears with respect to the fraction of the PTP sheet. It is also conceivable to display a message suggesting the possibility that the collation result is inconsistent because the setting with the ear is set.

Further, in the inspection support apparatus 100, the control unit 10 displays “without ear” and “with ear” operation keys for inputting the presence / absence state of the ear in the fractional PTP sheet on the display unit 20. It can be considered. When an operation of the operation key “without ear” is detected by the operation unit 30, the control unit 10 assumes that there is no ear on the PTP sheet in which the fraction is generated, When operation of the operation key is detected by the operation unit 30, it is considered that the control unit 10 collates the measured value with the target value on the assumption that there is an ear in the PTP sheet having a fraction. It is done.

Further, it is conceivable that the control unit 10 adds a predetermined value set in advance as the weight of the rubber band to the target value according to the number of the PTP sheets. For example, when the number of PTP sheets is 0 or more and 2 or less, the weight of a predetermined small rubber band is set. When the number of PTP sheets is 3 or more and 5 or less, When the weight of the rubber band of the size and the number of PTP sheets are 6 or more and 10 or less, it is conceivable to add the weight of a predetermined large rubber band to the target value as the predetermined value. As a result, the target value approximates to a value that takes into account the weight of the rubber band that bundles the PTP sheets, and the verification is performed with high accuracy. For example, as an initial setting of the inspection support apparatus 100, the control unit 10 sets “weight of ear (0-99.99)”, “weight of rubber band (large) (0-99.99)”, “band rubber ( "Middle weight" (0-99.99) "," Rubber rubber (small) weight (0-99.99) "," Number of rubber band application sheets (small: 0.0-2.0, Medium: 3.0) -5.0, large: 6.0-10.0, etc.) "," single-pack weight inspection (performed, not performed, etc.) "," QR weight data (per day, per packet, etc.) "," “Inspection unit (RP unit, prescription unit, etc.)”, “Treatment of third decimal place when displaying g (rounding off, rounding off, etc.)”, “Rubber weight when reading packaged QR (adding, not adding, etc.)” Etc. can be set according to user operations. In addition, as an initial setting of the inspection support device 100, the control unit 10 sets the initial selection state of the rubber band at the time of weighing by each of the weighing unit 51 to the weighing unit 54, and “balance one wheel rubber selection default value”, “balance”. “2 wheel rubber selection default value”, “balance 3 wheel rubber selection default value”, “balance 4 wheel rubber selection default value”, “large dish rubber selection default value” indicating the initial selection state of rubber bands when weighing using the platter 58, “Weighing 1 fraction selection default value”, “Balance 2 fraction selection default value”, “Balance 3 fraction selection default value” indicating the initial selection state of the presence or absence of fractions when weighing by each of the weighing unit 51 to the weighing unit 54 ”,“ Balse 4 fraction selection default value ”, the number of drugs to be weighed when measuring the value per unit amount (single) of medicine“ Weighing when measuring per unit of medicine ” The number (0-999) "can be set and in response to a user operation.

Further, in the inspection support apparatus 100, the control unit 10 inputs “size of rubber”, “medium rubber”, “small rubber” for inputting the size or type of the rubber band for binding the PTP sheet to the display unit 20. An operation key such as “no rubber” may be displayed. In this case, the control unit 10 switches the size of the rubber band used for the PTP sheet in accordance with the operation of operation keys such as “large rubber”, “medium rubber”, “small rubber”, “no rubber”, and the like. It is possible. Thereby, the weighing value and the target value can be collated in consideration of the weight of the rubber band placed on the weighing unit 5N together with the PTP sheet. In particular, the size or type of the rubber band used for bundling the PTP sheets may differ depending on not only the number of PTP sheets but also the size of the PTP sheets. For this reason, the size or type of rubber band may not be uniquely determined only by the number of PTP sheets. On the other hand, as described above, in the configuration in which the size or type of the rubber band can be arbitrarily selected according to the operation of the operation keys such as “large rubber”, “medium rubber”, “small rubber”, “no rubber”, etc. The user can set the size or type of the rubber band by looking at the rubber band used in the actual PTP sheet. In addition, for example, when a plurality of PTP sheets are bundled with rubber bands, when the PTP sheet bundle is divided into a plurality of parts and placed on the plurality of weighing parts 5N, the rubber bands are provided only on one of the weighing parts 5N. It is possible to be placed. In particular, it is conceivable that the rubber band is placed on the weighing unit 5N where the number of PTP sheets not requiring the rubber band is placed. Further, even if the number of PTP sheets corresponds to “small rubber”, it is conceivable that the PTP sheet is placed on the weighing unit 5N together with the rubber rubber of “large rubber”. Even in this case, as described above, the size or type of the rubber band can be arbitrarily selected according to the operation of the operation keys such as “large rubber”, “medium rubber”, “small rubber”, “no rubber”, etc. Depending on whether or not the user puts the rubber band together with the actual PTP sheet, the presence / absence, size or type of the rubber band corresponding to each weighing unit 5N can be set.

In addition, since the reflection method (calculation method) with respect to the target value of the weight of the ear of the PTP sheet and the reflection method (calculation method) with respect to the target value of the weight of the rubber band are different for each pharmacy or medical institution, these It is conceivable that the reflection method can be set in advance. For example, as a method for reflecting the target value of the weight of the ear of the PTP sheet, a first arithmetic expression based on a first internal rule corresponding to the ear and a second arithmetic expression based on a second internal rule corresponding to the absence of the ear are set. And the control unit 10 corrects the target value or the weighing value based on the first arithmetic expression corresponding to the first internal rule when the PTP sheet is selected to have the ear, and the PTP sheet If no ear is selected, it is conceivable to correct the target value or the weighing value based on the second arithmetic expression corresponding to the second internal rule. In addition, as a method for dispensing the PTP sheet, for example, a method of leaving an ear may be defined such as “leave an ear in the case of one tablet”. Therefore, if the result of the comparison between the measured value and the target value is not appropriate according to the method of leaving the ears of the PTP sheet, the possibility that the method of leaving the ears is not appropriate is displayed on the display unit 20. It is conceivable to notify by For example, if there is a fraction of one tablet in the number of PTP sheets to be dispensed based on the prescription data, the ears should remain on the one tablet PTP sheet, so one tablet It is conceivable that the weighed value and the target value are collated on the assumption that there is an ear in the PTP sheet. Accordingly, it is possible to inform the user that there is a possibility that the method of leaving the ear of the PTP sheet is not observed, and an educational function can be realized.

<Step S38>

In step S38, if the collation result in step S37 is coincident (S38: Yes side), the control unit 10 moves the process to step S39, and if the collation result in step S37 is not coincident. (S38: No side), the process proceeds to step S381.

<Step S381>

In step S381, the control unit 10 displays an error message in the weighing display area A1M corresponding to each of the one or more weighing units 5N specified as the weighing unit corresponding to the same medicine in step S33. For example, the error message is “The measured value of the drug to be inspected exceeds (or is insufficient) the upper or lower limit value. Press the OK key to approve the inspection. Please press the cancel key ". The control unit 10 causes the display unit 20 to display an OK key and a cancel key together with the error message. Then, when the OK key is operated, the control unit 10 determines that the inspection of the weighing inspection target medicine is completed. On the other hand, when the cancel key is operated, the control unit 10 displays a message such as “Please take out the medicine to be inspected and weigh it again”, and the process proceeds to step S31.

<Step S39>

In step S39, the control unit 10 determines the weighing value in the weighing display area A1M corresponding to each of the weighing units 5N identified as the weighing unit corresponding to the same medicine in step S33. The quantity obtained by converting the weighing result corresponding to the weighing unit 5N into a predetermined unit is displayed, and the fact that the collation result is coincident is displayed. As described above, the display processing unit 17 of the control unit 10 executes the process of displaying the weighing result by the weighing unit 5N and the collation result by the step S38 in the weighing display area A1M. In addition, when the said platter 58 is used, the said control part 10 displays the said collation result on the said weighing display area A41 (refer FIG. 11). In step S39, the control unit 10 determines the weighing value as a weighing result of the weighing unit 5N, and a converted value obtained by converting the weighing value into a unit of medicine (value of units such as tablets, capsules, and sheets). Either or both of these are stored in the storage unit 40 together with the prescription data as an inspection history. Thereby, the said control part 10 can display the said measured value, the said conversion value, etc. with the content of the said prescription data, when displaying the said inspection history on the said inspection history inquiry screen D12.

Incidentally, it is conceivable that a printer is connected to the inspection support apparatus 100 in accordance with a communication standard such as USB, RS232C, or Bluetooth (registered trademark). In this case, it is conceivable that the control unit 10 causes the printer to print out the weighing result obtained in step S37 in step S39 or step S381. In addition, for example, inspection start date and time, prescription number, voucher number, patient ID, patient name, medical department, examiner, prescription data, and Rp data are printed in the journal output by the printout. In the journal, a JAN code may be printed as medicine identification information included in the prescription data or the Rp data. A configuration in which the control unit 10 can convert the GS1 code into a JAN code and print it out is also conceivable.

<Step S40>

Subsequently, in step S40, the control unit 10 waits for the recording timing of the captured image by the imaging unit 70 (S40: No side). Specifically, the control unit 10 performs the weighing inspection when all the weighing values of the four weighing units 51 to 54 are determined, or for all drugs included as prescription drugs in the prescription data or the Rp data. When the process is completed (when no other medicine remains in the prescription data or the Rp data as an inspection target), it is determined to record the captured image by the imaging unit 70 (S40: Yes side), and the process is performed. The process proceeds to S41. The case where the weighing inspection process is completed for all drugs included as prescription drugs in the prescription data or the Rp data is, for example, a case where six types of prescription drugs are included in the Rp data. This is a case where, after weighing the four types of prescription drugs using the weighing units 51 to 54, the remaining two types of prescription drugs are weighed using the two weighing units 5N. It is also conceivable that photographing by the photographing unit 70 is performed when the weighing values of all the weighing units 51 to 54 are stabilized instead of after the collation processing of all the weighing units 51 to 54 is completed.

<Step S41>

In step S41, the control unit 10 records a photographed image by the photographing unit 70, and associates the photographed image with the prescription data or the Rp data displayed on the prescription inspection screen D10 as the inspection history. The data is stored in the storage unit 40. Note that the photographing unit 70 photographs the weighing dishes 55 of all the weighing units 51 to 54 at the same time. When the platter 58 is placed on the weighing units 51 to 54, the platter 58 is photographed. This processing is executed by the photographing processing unit 18 of the control unit 10. Thereby, as described above, the photographed image can be confirmed when referring to the inspection history on the inspection history inquiry screen D12 or the like. By the way, when the control unit 10 determines that the recording timing has arrived in step S40, the control unit 10 displays on the display unit 20 a start of shooting such as “starts shooting” and then determines in advance. It is conceivable that the weighing unit 51 to 54 is photographed by the photographing unit 70 after a predetermined waiting time (for example, about 2 seconds) has elapsed. Thereby, it is expected that the user retreats the hand or the like out of the shooting range by the shooting unit 70, and useless shooting can be suppressed. The weighing inspection process is individually executed for each weighing unit 5N, but the photographing process in step S41 is executed as a common process. Since all the weighing units 51 to 54 are photographed at the same time after the weighing values of all the weighing units 51 to 54 are stabilized in this way, an effective photographed image is stored as evidence of inspection by the inspection support device 100. The That is, at the time when the recording timing comes, only one shooting is performed. In addition, it is also conceivable as another embodiment that photographing by the photographing unit 70 is performed at an individual timing for each weighing inspection process. In this case, the association between each of the weighing units 51 to 54 and the medicine identification information is individually released. For example, when the weighing value of the weighing unit 5N is decreased after the weighing value of the weighing unit 5N is confirmed and the collation process is completed, the association between the weighing unit 5N and the medicine identification information is released. It can be considered. Further, the photographing by the photographing unit 70 is performed at the timing when the photographing key K18 is operated after the weighing value of the weighing unit 5N is stabilized, and the association with the medicine identification information of the weighing unit 5N is released. It is also conceivable.

Further, the control unit 10 may record an image of a predetermined region corresponding to each of the weighing units 51 to 54 from the captured image after recording the image captured by the imaging unit 70. Considered as a form. In this case, the control unit 10 also extracts an image of each predetermined region corresponding to each of the weighing display regions A11 to A14. Then, the image corresponding to each of the weighing units 51 to 54 and the image corresponding to each of the weighing display areas A11 to A14 are stored in the storage unit 40 as individual image data. Note that the control unit 10 may store the moving image information received from the imaging unit 70 in the storage unit 40 in association with the prescription data as an inspection history.

In addition, after the collation process is completed, when it is determined in step S40 that the photographing key K18 displayed on the prescription inspection screen D10 has been operated, the control unit 10 performs photographing by the photographing unit 70. It is conceivable to record an image. In addition, it is also conceivable that a photographed image by the photographing unit 70 is recorded on the condition that collation with the prescription data of the weighing result of the weighing unit 5N corresponding to the medicine identification information is completed.

Further, a range in which a user using the inspection support apparatus 100 performs an operation for putting a medicine in a medicine bag is included in the imaging range of the imaging unit 70, and the predetermined time has elapsed after the occurrence of the event of the recording timing. It is also conceivable that a photographed image by the photographing unit 70 is recorded. Thereby, it is possible to image | photograph the operation | work which throws the chemical | medical agent inspected with the said inspection assistance apparatus 100 into a medicine bag with the said imaging | photography part 70. FIG.

<Step S42>

Thereafter, in step S42, the control unit 10 cancels the association between all the medicine identification information performed in step S33 and the weighing unit 5N. Thereby, the control unit 10 can execute the weighing inspection process for the next medicine by using the weighing unit 5N whose association with the medicine identification information is released. The control unit 10 resets (erases) the display of the weighing display area A1M corresponding to the weighing unit 5N that has been released from the association with the medicine identification information.

As described above, when the inspection support apparatus 100 is used, the weighing inspection process (S19) is started each time medicine identification information is read from a packaging material such as a medicine PTP sheet, and the prescription data or the Rp data is read. It is possible to carry out inspection of prescription medicines contained in a continuous and in parallel. Therefore, for example, it is possible to efficiently and accurately perform the inspection operation for each of the prescription drugs and the storage operation for each prescription drug in the medicine bag.

Further, in the weighing inspection process, the weighing unit in which the weighing value is increased from 0 after the medicine identification information is read from the medicine packaging material and before the medicine identification information is read from the different medicine packaging material. Is specified as a weighing unit corresponding to the drug for weighing inspection. Therefore, before the weighing value of the weighing unit 5N corresponding to the one medicine identification information is stabilized, the other reading information is read by the information reading unit 60 and the weighing by the other weighing unit 5N is started. It is possible to make it. Therefore, the user can efficiently and accurately perform inspection on a plurality of types of medicines included in the prescription data or the Rp data.

Specifically, the inspection support apparatus 100 includes four weighing units 51 to 54, and the weighing inspection process using the weighing units 51 to 54 is individually executed. For example, when four types of tablets are included as prescription drugs in the Rp data, the user reads the drug identification information of the PTP sheet of the first tablet with the information reading unit 60 and stores it in the weighing unit 5N. Place the PTP sheet. Thereafter, the user reads the drug identification information of the PTP sheet of the second tablet by the information reading unit 60 and places the PTP sheet on the weighing unit 5N. At this time, the medicine identification information on the PTP sheet of the second tablet may be read before the weighing value of the first weighing unit 5N is stabilized. In each of the weighing inspection processes started for each medicine identification information, the inspection result based on the weighing result by the weighing unit 5N is displayed in the weighing display area A1M. In addition, the user continues to read the medicine identification information of the PTP sheet of the third tablet by the information reading unit 60 and place the PTP sheet on the weighing unit 5N, and the PTP of the fourth tablet The medicine reading information of the sheet is read by the information reading unit 60, and the PTP sheet is placed on the weighing unit 5N. At this time, the comparison between the weighing result by each weighing unit 5N and the prescription data or the Rp data is started individually when the medicine identification information is read. Therefore, the collation process by each of the weighing units 5N is sequentially terminated. Accordingly, the last (fourth) PTP sheet is weighed as compared with the case where all the four types of PTP sheets are placed on the weighing unit 5N and the weighing results of all the weighing units 5N are compared. It is possible to shorten the time from the placement on the unit 5N to the end of the weighing inspection process by the inspection support device 100.

On the other hand, since the inspection support device 100 includes the four weighing units 51 to 54, when the five types of medicines are included in the Rp data as they are, the PTP sheet of the fifth medicine is the above-mentioned. Even if the medicine identification information is read by the information reading unit 60, the PTP sheet cannot be placed. Therefore, the control unit 10 may cancel the association between the weighing unit 5N and the medicine identification information every time the comparison between the weighing result by the weighing unit 5N and the prescription data or the Rp data is completed. It can be considered as an embodiment. As a result, even when five or more kinds of medicines more than the number of the weighing units 51 to 54 included in the inspection support device 100 are included in the Rp data, the weighing units 51 to 54 are repeatedly used. It is possible to sequentially carry out weighing inspections of five or more kinds of chemicals in parallel. That is, when the weighing inspection process corresponding to any one of the first to fourth medicines is completed, the user reads the medicine identification information of the fifth medicine by the information reading unit 60 and reads the weighing. The PTP sheet can be placed on the part 5N, and the medicine that has been inspected first can be stored in the medicine bag first. Therefore, the user can efficiently and accurately execute inspection of the types of the PTP sheets larger than the number of the weighing units 5N. However, in this case, it is not possible to perform photographing in steps S40 to S41. Therefore, this type of configuration is, for example, when the inspection support apparatus 100 does not have a recording function for recording a photographed image by the photographing unit 70, or when the recording function is set to be invalid, Is an operation of the photographing key K18, or when the recording timing of the photographed image is that the collation with the prescription data of the weighing result of the weighing unit 5N is completed.

[Other functions]

Hereinafter, other functions provided in the inspection support apparatus 100 will be described. In addition, the said inspection assistance apparatus 100 should just be provided with one or several functions among the following several functions.

[Packaging inspection function]

In the inspection support apparatus 100, the weighing inspection process can be executed in a state of being accommodated in a first packaging material such as a PTP (press through pack) sheet or a heat seal in which a plurality of medicines are accommodated. On the other hand, it is also conceivable that the object of the weighing inspection process is a medicine in which a plurality of the first packaging materials are accommodated in a second packaging material such as an aluminum packaging material or a medicine box. In this case, an operator such as a pharmacist takes out the first packaging material from the second packaging material in the inspection work using the inspection support device 100.

On the other hand, it is conceivable that the inspection support device 100 has a packaging inspection function capable of executing the weighing inspection process while a plurality of the first packaging materials are accommodated in the second packaging material. Specifically, the control unit 10 implements the package inspection function by executing various processes according to the inspection support program. Note that the word “first packaging material” used in the following description means a state in which a plurality of medicines are contained in the first packaging material as well as the first packaging material. The word “material” means not only the second packaging material but also a plurality of the first packaging materials contained in the second packaging material.

First, the medicine identification information such as the same GS1 code is given to the first packaging material and the second packaging material. Therefore, the control unit 10 weighs the prescription medicine corresponding to the medicine identification information when the medicine identification information is read from the first packaging material or the second packaging material in the inspection support processing step S18. It is possible to select it as a drug subject to inspection. In addition, the control unit 10 can select the drug for weighing inspection according to a user operation using the display unit 20 and the operation unit 30. Thus, the said control part 10 when performing the process for selecting the said measurement object chemical | medical agent which is the chemical | medical agent of the weighing object by the said weighing part 5N is an example of a selection process part.

Then, the control unit 10 sets the weighing units 51 to 54 in response to a user's operation input using the display unit 20 and the operation unit 30 at the time of initial setting in the inspection support device 100 or at the start of weighing inspection. It is possible to switch between valid and invalid of the package inspection function. Hereinafter, a state in which the packaging inspection function is valid is referred to as a packaging inspection mode, and a state in which the packaging inspection function is invalid is referred to as a normal mode.

For example, as shown in FIG. 15, an operation key K51 for switching between “with packaging” and “without packaging” is displayed in the weighing display areas A11 to A14 of the prescription inspection screen D10. Then, the control unit 10 switches between enabling and disabling the packaging inspection function for each of the weighing units 51 to 54 in accordance with the operation of the operation key K51 in each of the weighing display areas A11 to A14.

On the other hand, in the medicine master, as information corresponding to each medicine, the packaging weight indicating the unit weight (total weight) of the second packaging material and the number of medicines contained in the second packaging material The number is stored. FIG. 16 is a diagram showing an example of a registration screen D14 for registering barcode information in the pharmaceutical master. Specifically, the control unit 10 displays the registration screen D14 when an operation key for starting registration of barcode information is operated on the master maintenance screen D13 (see FIG. 14). In addition, in FIG. 16, the state in which three barcode information is registered about the medicine of the Magrax tablet 330 mg is shown. In the barcode information, information on each item of the type of barcode, the content of the barcode, the standard, the unit, the number in the PTP, the single weight, the number in the package, the package weight, the image, and the classification is the individual information of the medicine Included as

For example, in the first record of the registration screen D14 shown in FIG. 16, the number in the PTP indicating the number of medicines contained in one first packaging material is set to “10.00”. The single weight indicating the weight of one of the first packaging materials is set to “5.72 g”. Similarly, in the first record, the number in the packaging indicating the number of medicines contained in one second packaging material is set to “100”, indicating the weight of one second packaging material. The packaging weight is set to “62.20 g”.

The control unit 10 can set the number in the PTP, the single weight, the number in the packaging, the packaging weight, and the like according to a user operation on the registration screen D14. For example, the number in the PTP, the single weight, the number in the package, the package weight, etc. are set according to the numerical input operation by the user or updated based on the information of the mother master specified in advance. Also good.

In addition, it may replace with the number in the said package, and the number of the said 1st packaging materials accommodated in one said 2nd packaging material may be set. In this case, the control unit 10 is accommodated in one second packaging material based on the number of the first packaging materials accommodated in one second packaging material and the number in the PTP. It is possible to calculate the number of drugs.

Further, in the inspection support apparatus 100, it is possible to set the single weight of the first packaging material, the packaging weight of the second packaging material, and the like using the weighing unit 5N. Specifically, on the registration screen D14, an operation key K141 for starting the setting of the single weight of the first packaging material and an operation key for starting the setting of the packaging weight of the second packaging material. K142 is displayed corresponding to each record. In the example shown on the registration screen D14, the cells of the single weight and the package weight corresponding to each record function as the operation keys K141 and K142.

Then, when the operation key K141 is operated on the registration screen D14, the control unit 10 stores the first packaging material of the medicine in the record corresponding to the operation key K141 as shown in FIG. A notification screen D141 including a message that prompts the user to place only one on the weighing unit 5N is displayed. Accordingly, only two of the first packaging materials are placed on the weighing unit 5N by the operator. Thereafter, when the weighing result of the weighing unit 5N is determined, the control unit 10 calculates the weight per unit of the first packaging material by dividing the weighing result by two, and sets it as the single weight. . In addition, the said control part 10 can set arbitrarily the number of the said 1st packaging materials measured at the time of the setting of the said single weight beforehand according to user operation in the said registration screen D14. Further, the control unit 10 may have a learning function for updating the single weight based on the weighing results of the weighing units 51 to 54 by the daily inspection support apparatus 100. For example, the control unit 10 uses the bar code information as a single weight obtained by averaging a single weight calculated from a weighing result of each drug weighed using the weighing units 51 to 54 for each drug. Can be registered.

Similarly, when the operation key K142 is operated on the registration screen D14, the control unit 10 sets the second packaging material for the medicine in the record corresponding to the operation key K142 as shown in FIG. A notification screen D142 including a message prompting to put the weighing unit 5N on the weighing unit 5N is displayed. Accordingly, only one second packaging material is placed on the weighing unit 5N by the operator. Thereafter, when the weighing result of the weighing unit 5N is determined, the control unit 10 sets the weighing result as the packaging weight of the second packaging material. Further, the control unit 10 may have a learning function for updating the package weight based on the weighing results of the weighing units 51 to 54 by the daily inspection support apparatus 100. For example, the control unit 10 registers, in the barcode information, the value obtained by averaging the packaging weight calculated from the weighing result of each drug weighed using the weighing units 51 to 54 for each drug as the packaging weight. It is possible to do.

<Normal mode>

In the normal mode, in step S31 of the weighing inspection process (see FIG. 13), the control unit 10 determines the single weight and the number in the PTP of the medicine corresponding to the medicine identification information as the medicine master. Get from. In step S34, the control unit 10 starts displaying the chemical amount according to the weighing value, the single weight, and the number in the PTP by the weighing unit 5N specified in step S33. For example, as shown in the weighing display unit A14 in FIG. 15, the control unit 10 displays “35 tablets” as the weighing result of the weighing unit 54 set in the normal mode. And the said control part 10 collates the weighing result of the said weighing part 54, and the said Rp data in the said step S37.

<Packaging inspection mode>

On the other hand, in the packaging inspection mode, in the step S31 of the weighing inspection process (see FIG. 13), the control unit 10 determines the number of medicines in the packaging corresponding to the medicine identification information and the packaging weight. Get from. The said control part 10 when performing the acquisition process which concerns here is an example of an acquisition process part.

In step S34, the control unit 10 starts displaying the amount of medicine according to the weighing result by the weighing unit 5N specified in step S33, the previous number in the package, and the package weight. The display processing is executed by the display processing unit 17 of the control unit 10. Specifically, the control unit 10 includes the weighing unit 5N out of the weight of the weighing unit 5N and the weight of the packaging weight n times (n is an integer of 1 or more) that is the total weight of the second packaging material. It is determined whether or not the difference from the approximate weight closest to the weighed value is within a preset allowable range.

In addition, it is possible that the said tolerance | permissible_range is set by the ratio with respect to the weight of n times the total weight of a said 2nd packaging material. For example, it is conceivable that the allowable range is set as a range of ± 10% with respect to a weight n times the total weight of the second packaging material. That is, the lower limit allowable value of the allowable range is -10% of the approximate weight, and the upper limit allowable value is + 10% of the approximate weight. Here, the allowable range of ± 10% is a value set in advance in view of the fact that the weight error of one second packaging material generally guaranteed by a pharmaceutical manufacturer is ± 5%. Is a value obtained by adding ± 5% which is a value allowed as an error generated in the weighing result by the weighing unit 5N to ± 5% which is the weight error. Moreover, when the weight error of the said 2nd packaging material guaranteed for every pharmaceutical manufacturer or chemical | medical agent differs, the said tolerance | permissible_range may be set for every pharmaceutical manufacturer or chemical | medical agent. The control unit 10 can arbitrarily set the permissible range according to a user operation at the time of initial setting of the inspection support apparatus 100 or at the start of the inspection support process. The said control part 10 when performing the setting process which concerns here is an example of a setting process part.

As shown in the weighing display unit A13 in FIG. 15, the control unit 10 determines that the packaging inspection is performed when the difference between the weighing value by the weighing unit 53 and the approximate weight is within the allowable range. As the weighing result of the weighing unit 53 set in the mode, a chemical amount n times the number in the package is displayed. On the other hand, when the weighing value of the weighing unit 53 is smaller than the approximate weight and the difference between the measured value by the weighing unit 5N and the approximate weight is outside the allowable range, the number of n corresponding to n times that number. The total number of the medicines contained in the second packaging material, which is one less than the second packaging material, is displayed as the weighing result of the weighing unit 53. Further, when the weighing value of the weighing unit 53 is larger than the approximate weight and the difference between the approximate weight and the weighing value of the weighing unit 53 is out of the allowable range, the number of n corresponding to n times the number The total number of the medicines contained in the second packaging material is displayed as the weighing result.

For example, consider the display example of the weighing result when the number in the package is 100 tablets as described above (see FIG. 16). First, in the case where the approximate weight is one time the package weight, the weighing result of the weighing unit 53 is smaller than the approximate weight, and the difference between the weighing result of the weighing unit 53 and the approximate weight is When it exceeds 10% of the approximate weight, the weighing display unit A13 shows that the weighing result of the weighing unit 53 is 0 times the number in the package (a number smaller than 1 which is n) “0”. "Lock" is displayed. The approximate weight is twice the package weight, and the weighing result of the weighing unit 53 is smaller than the approximate weight, and the difference between the weighing result of the weighing unit 53 and the approximate weight is When it exceeds 10% of the approximate weight, the weighing display unit A13 has the weighing result of the weighing unit 53 as 1 times the number in the package (one less than 2 which is n) “100”. "Lock" is displayed.

Further, in the case where the approximate weight is one time the package weight, the weighing result of the weighing unit 53 is larger than the approximate weight, and the difference between the weighing result of the weighing unit 53 and the approximate weight is When it exceeds 10% of the approximate weight, “100 tablets” is displayed as the weighing result of the weighing unit 53 on the weighing display unit A13. The approximate weight is twice the package weight, and the weighing result of the weighing unit 53 is larger than the approximate weight, and the difference between the weighing result of the weighing unit 53 and the approximate weight is If it exceeds 10% of the approximate weight, “200 tablets” is displayed as the weighing result of the weighing unit 53 on the weighing display unit A13.

Thereafter, in the step S37, when the control unit 10 collates the weighing result by the weighing unit 5N with the prescription data, the total number of the medicines displayed as the weighing result in the step S34. And the prescription data. That is, when the difference between the approximate weight and the weighing value of the weighing unit 5N is within a preset allowable range based on the number in the package and the package weight, the control unit 10 The total number of the medicines contained in the second packaging material corresponding to an integer multiple is collated with the prescription data as a weighing result. On the other hand, when the difference between the approximate weight and the weighed value of the weighing unit is outside the allowable range, when the weighed value of the weighing unit 5N is smaller than the approximate weight, the number corresponding to the integral multiple is larger than The total number of the medicines contained in the second packaging material having a smaller number is collated with the prescription data as the weighing result, and when the weighing value of the weighing unit 5N is larger than the approximate weight, the integral multiple is used. The total number of the medicines contained in the corresponding number of the second packaging materials is collated with the prescription data as the weighing result.

And in the said step S37, the said control part 10 judges that a collation result is in agreement, when the total number of the said medicine and the target value (prescription amount) of the said medicine in Rp data of the said prescription data correspond. Further, when the total number of the medicines does not match the target value, it is determined that the matching results do not match. However, even if the control unit 10 determines in the step S37 that the collation result is the same, if the weight of the weighing result of the weighing unit 5N is outside the allowable range, The set warning message is displayed on the display unit 20 to notify the operator.

As shown in FIG. 15, when weighing is performed using a plurality of the weighing units 5N, the total number of chemicals corresponding to the weighing results by the plurality of weighing units 5N is the Rp data. The matching result is matched when it matches the target value of the medicine. For example, the target value of the drug in the Rp data is 135 tablets, the single weight of the drug is 5.72 g, the number in the PTP is 10 tablets, the package weight is 24.45 g, and the number in the package is 100 tablets. Consider a case where inspection work is performed using the two weighing units 53 and the weighing units 54. Further, it is assumed that the weighing unit 53 is set in the package inspection mode and the weighing unit 54 is set in the normal mode. In this case, when the weighing value by the weighing unit 53 is 23.98 g, the control unit 10 calculates 26.895, which is a weight of + 10% of 24.45 of the packaging weight, as an upper limit allowable value, The weight of 10% is calculated as 22.005 g as the lower limit allowable value. And since the 23.98 g which is the weighing value by the weighing unit 53 falls within the upper limit allowable value and the lower limit allowable value (22.005 <23.98 <26.895), the control unit 10 100 tablets, which are the number of medicines in the package, are specified as a result of weighing by the weighing unit 53. On the other hand, the control unit 10 calculates 20.02 g (weighing value) /5.72 g (single weight) × 10 (number in the PTP) when the weighing value by the weighing unit 54 is 20.02 g. The 35 tablets that are the results are specified as the results of weighing by the weighing unit 54. And the said control part 10 calculates 135 tablets which are the total of the weighing result of the said weighing part 53 and the said weighing part 54, and collation whether it corresponds with 135 which is the target value of the said medicine in the said Rp data Execute the process. That is, in the example described here, the matching result is determined to be coincident. On the other hand, if the weighing value by the weighing unit 53 does not fall between the upper limit allowable value and the lower limit allowable value, the weighing result by the weighing unit 53 becomes 0 tablets. The total weighing result of the unit 54 is 35 tablets, which does not coincide with 135 tablets, which is the target value of the medicine in the Rp data, and is determined to be inconsistent as the collation result. Of course, even if the weighing result by the weighing unit 54 is not 35 tablets, it does not coincide with 135 tablets which is the target value of the medicine in the Rp data.

As described above, in the inspection support apparatus 100, an inspection operation for inspecting a medicine in a state where a plurality of the first packaging materials containing a plurality of medicines are accommodated in the second packaging material is performed. It is possible to support. Therefore, the operator does not need to take out the first packaging material from the second packaging material, and the labor of inspection work is reduced.

[Prescription unit inspection function]

In the inspection support device 100, when the prescription data includes a plurality of Rp data, operation of the “+” and “−” operation keys displayed in the prescription display area A15, or direct numerical input operation The designated RpNo. Is changed, and the designated RpNo. Rp data corresponding to is displayed in the prescription display area A15. When the inspection of the selected Rp data is completed, the next Rp data is selected and the inspection is performed in the same manner. For example, when the Rp data of 10 is included in the prescription data, it is necessary to operate the “+” operation key every time the inspection of the Rp data is completed. Will be operated once.

On the other hand, it is considered that the inspection support device 100 has a prescription unit inspection function capable of performing inspection in units of the prescription data even when the prescription data includes a plurality of the Rp data. It is done. Specifically, the said prescription unit inspection function is embodied by the said control part 10 performing various processes according to the said inspection assistance program.

In addition, the said control part 10 is effective in the said prescription unit inspection function according to the user's operation input using the said display part 20 and the said operation part 30 at the time of the initialization in the said inspection assistance apparatus 100, or the time of the start of the weighing inspection. And invalid can be switched.

And when the said prescription unit inspection function is effective, the said control part 10 performs the following process in the said inspection assistance process (refer FIG. 7) and the said weighing inspection process (refer FIG. 13). Here, only differences from the inspection support process (see FIG. 7) and the weighing inspection process (see FIG. 13) will be described.

<Other examples of inspection support processing>

When the prescription data is specified in step S12 or step S13, the control unit 10 selects medicines in all the Rp data included in the prescription data as inspection targets in the step S14. Specifically, the control unit 10 displays a list of information on medicines in all the Rp data included in the prescription data in the prescription display area A15. That is, the medicines included in each of the Rp data are displayed as a list in the prescription data unit. Such processing is executed by the verification processing unit 14 of the control unit 10. If the information about each medicine cannot be displayed in the prescription display area A15 at one time, a scroll bar or the like is displayed in the prescription display area A15, and the information about each medicine is scrolled by operating the scroll bar or the like. Is displayed.

<Other examples of weighing inspection processing>

In step S40, the control unit 10 performs the weighing inspection process when all the weighing values of the four weighing units 51 to 54 are confirmed, or for all the drugs included in the prescription data as prescription drugs. Is completed, it is determined that it is the recording timing of the photographed image by the photographing unit 70, and the weighing units 51 to 54 are photographed by the photographing unit 70. That is, it is not determined that it is the recording timing of the photographed image just by completing the weighing inspection process for all the drugs included in the Rp data. Therefore, the photographed image photographed by the photographing unit 70 is not limited to a medicine image corresponding to one piece of Rp data, and may contain medicine images over a plurality of pieces of Rp data.

As explained above, according to the prescription unit inspection function, compared to the case where the weighing inspection process is executed in units of the Rp data, an operation for the operator to sequentially select the Rp data becomes unnecessary. The burden on the operator is reduced. Further, when all the weighing values of the four weighing units 51 to 54 are confirmed, or when the weighing inspection process is completed for all the drugs included in the prescription data as the prescription drug, The chemicals on the weighing units 51 to 54 are taken out together. Accordingly, the number of executions of the step of taking out the medicines on the weighing units 51 to 54 is reduced as compared with the case where the weighing inspection process is executed in Rp data units. Further, the control unit 10 determines when all the weighing values of the four weighing units 51 to 54 are confirmed, or when the weighing inspection process is completed for all drugs included in the prescription data as prescription drugs. The photographing by the photographing unit 70 is executed. Therefore, the time required for the inspection support process is shortened as compared with the case where photographing by the photographing unit 70 is executed in units of the Rp data.

For example, consider a case where three Rp data are included in the prescription data, and one drug is included in each Rp data. First, when the prescription unit inspection function is invalid and the weighing inspection process is executed in Rp data units, as shown in FIG. 19, the weighing inspection process is executed for each Rp data. Therefore, the medicine corresponding to each Rp data is sequentially displayed in the prescription display area A15 in the Rp data unit. In this case, the operation of taking out the medicine from the weighing units 51 to 54, the switching operation of the Rp data, and the imaging by the imaging unit 70 are performed twice.

On the other hand, when the prescription unit inspection function is effective and the weighing inspection process is executed in the prescription data unit, as shown in FIG. 20, the medicines corresponding to the three Rp data are Simultaneously displayed in the prescription display area A15 in units of prescription data. Therefore, the operation of taking out the medicine from the weighing units 51 to 54 and the imaging by the imaging unit 70 are executed only once, and the switching operation of the Rp data is unnecessary. In the case where three or more Rp data in the prescription data include four or more medicines in total, the medicines are taken out from the weighing units 51 to 54 at the end timing of the weighing inspection process for four medicines. The work, the switching operation of the Rp data, and the photographing by the photographing unit 70 are performed, but the number of times is smaller than that in the case where the weighing inspection process is performed in units of the Rp data.

[Inspection pending function]

The pharmacist starts the inspection work for the prescription data using the inspection support device 100, and if there is a missing item in the medicine included in the prescription data, the inspection support for the prescription data It is conceivable that the inspection support process is started again for the prescription data when the medicines corresponding to the prescription data are prepared after the process is stopped. However, in this case, since the inspection support process that was initially executed is stopped, even if the inspection support process for some medicines included in the prescription data has been completed, The inspection support process for prescription data needs to be executed.

On the other hand, it is conceivable that the inspection support device 100 has an inspection hold function capable of interrupting and holding the inspection support processing and resuming the inspection support processing from the middle. Specifically, the inspection suspension function is implemented by the control unit 10 executing various processes according to the inspection support program.

FIG. 21 is a diagram showing another example of the prescription inspection screen D10. As shown in FIG. 21, an inspection hold key K41 is displayed on the prescription inspection screen D10. And when the said control part 10 judges that the hold request | requirement was performed by operation of the said inspection hold key K41, as shown in FIG. 22, the prescription data which is the object of the said inspection support process currently being performed An operation screen D61 for confirming whether or not to put on-hold is displayed.

On the operation screen D61, operation keys K61 to K63 are displayed. The operation key K61 is operated when the inspection support process for the prescription data is interrupted after the photographing by the photographing unit 70. The operation key K62 is operated when the inspection support process for the prescription data is interrupted without performing the photographing by the photographing unit 70. The operation key K63 is operated when canceling the interruption of the prescription data inspection support process.

Then, when the operation key K61 is operated, the control unit 10 photographs the weighing units 51 to 54 by the photographing unit 70 and stores the photographed images in the storage unit 40 in association with the prescription data. To do. Here, the photographing process is executed by the photographing processing unit 18 of the control unit 10. Moreover, the said control part 10 memorize | stores the information under execution of the said inspection assistance process of the said prescription data as said hold information in the said memory | storage part 40, and sets the process state of the said prescription data to a hold state. The information during execution of the inspection support process includes the execution result of the weighing inspection process for some medicines executed up to the present time. Thereby, the control unit 10 can execute the inspection support process for the other prescription data. In addition, when the operation key K62 is operated, the control unit 10 stores information during execution of the inspection support process of the prescription data in the storage unit 40 without performing imaging by the imaging unit 70. And the processing state of the prescription data is set to the hold state.

When the unprocessed display area A21 is displayed, the control unit 10 converts the prescription data set in the hold state by the inspection hold function to other prescription data as shown in FIG. And a display mode (background color or character color) that can be identified. In the unprocessed display area A21, a hold selection key K42 for limiting prescription data to be displayed to the prescription data in the hold state is displayed. When the hold selection key K42 is operated, the control unit 10 displays the prescription data list in the hold state in the unprocessed display area A21. In the unprocessed display area A21, the pending Rp data is displayed in a display mode that can be distinguished from other Rp data.

Thereafter, when the prescription data in the pending state is selected in the unprocessed display area A21, the control unit 10 performs the inspection based on the processing state relating to the prescription data stored in the storage unit 40. Resume support processing. At this time, if there is a photographed image photographed when the prescription data is interrupted, the control unit 10 displays the image display key K19 corresponding to the photographed image as shown in FIG. . When the image display key K19 is operated, the control unit 10 enlarges and displays the captured image corresponding to the image display key K19 on the display unit 20. Thereby, the worker can easily grasp the suspension status of the inspection support processing for the prescription data.

As described above, in the inspection support apparatus 100, after the inspection support processing for one prescription data is interrupted by the inspection hold function and the inspection support processing for one or more other prescription data is executed. The inspection support process for the one prescription data can be resumed from the middle, and the efficiency of the inspection work can be improved.

[Standard selection function]

In the inspection support apparatus 100, the medicine to be inspected is selected by the information reading unit 60 reading the medicine identification information such as a barcode from the packaging material such as the PTP sheet. On the other hand, the medicine identification information may not be attached to a packaging material such as the PTP sheet. In this case, the operator performs an operation for selecting a medicine displayed in the prescription display area A15 when executing the inspection support process. On the other hand, in the medicine master, a plurality of medicine identification information are registered for one medicine, and any of the plurality of medicine identification information may be set as representative medicine identification information. And the said control part 10 selects the chemical | medical agent currently displayed on the said prescription display area | region A15 in the case of execution of the said inspection assistance process, and the said chemical | medical agent identification information corresponding to the selected chemical | medical agent is registered more than once in the said pharmaceutical master. If it is, the representative medicine identification information is selected and the inspection support process is executed.

However, in the configuration in which the representative medicine identification information is set in advance, even when there are a plurality of standards for the same medicine, for example, one preset representative medicine identification information is selected. . Therefore, when the inspection support apparatus 100 executes the inspection support process, a medicine displayed in the prescription display area A15 is selected, and a plurality of the medicine identification information is registered in the medicine master for the selected medicine. In the case where the information is used, it is conceivable to provide a standard selection function capable of arbitrarily selecting any one of the plurality of medicine identification information as information used in the collation process according to a user operation. Specifically, the standard selection function is implemented by the control unit 10 executing various processes according to the inspection support program.

For example, the control unit 10 can not set the representative medicine identification information even when a plurality of medicine identification information is registered as the medicine identification information of one medicine in the medicine master. And the said control part 10 selects the chemical | medical agent currently displayed on the said prescription display area | region A15 in the case of execution of the said inspection assistance process, and the said chemical | medical agent identification information corresponding to the selected chemical | medical agent is registered more than once in the said pharmaceutical master. If it is, an operation screen D62 for selecting any one of the plurality of medicine identification information is displayed on the display unit 20.

FIG. 25 shows an example of the operation screen D62. As shown in FIG. 25, the operation screen D62 displays a plurality of standards corresponding to a plurality of the medicine identification information. Then, the control unit 10 receives an operation for selecting any of the plurality of standards on the operation screen D62, and the medicine identification information corresponding to the selected standard is subjected to the inspection support process. It is selected as the medicine identification information of the medicine. Accordingly, in the weighing inspection process, in step S33, the control unit 10 specifies the weighing unit 5N whose weighing value has increased from 0 in step S32 as the weighing unit associated with the specified medicine identification information. To do.

As described above, in the inspection support device 100, when the standard selection function, for example, there are a plurality of standards for the same medicine, and a plurality of the medicine identification information is registered in the medicine master. It is possible to select an appropriate standard from the plurality of standards, and it is possible to appropriately execute the inspection support process.

[Exclusive control function]

Incidentally, as shown in FIG. 1, a plurality of the inspection support devices 100 may be connected to the medical system 1. In the medical system 1 configured as described above, the inspection support processing may be executed individually by each of the inspection support devices 100. In this case, the same inspection support device 100 is used. There is a possibility that the inspection support process for the prescription data may be executed and work efficiency may be reduced.

On the other hand, in each of the inspection support devices 100, it is possible to set whether the own device is a main device or a sub device. In any of the inspection support devices 100, it is possible to set whether each of the inspection support devices 100 is a main device or a sub device, and the setting contents may be transmitted to each of the inspection support devices 100. Good. Hereinafter, the inspection support device 100 set as the main device is referred to as a main inspection support device 100A, and the inspection support device 100 set as the sub device is referred to as a sub-inspection support device 100B.

For example, in each of the inspection support devices 100, the control unit 10 determines whether the main device is already registered in the medical system 1 when a registration operation as the main device is performed. It is conceivable to make an inquiry to each support device 100. And the said control part 10 permits setting an own machine as the said main apparatus, only when the said main apparatus is not registered. This prevents duplicate registration of the main device.

Then, the main inspection support device 100A acquires the prescription data from the dispensing support system 200 and the receipt system 300 and stores the prescription data in the storage unit 40. On the other hand, the control unit 10 of the sub-inspection support device 100B accesses the storage unit 40 of the main inspection support device 100A and performs the inspection support process for the prescription data stored in the storage unit 40 or The prescription data can be deleted. That is, it is conceivable that each of the sub-inspection support devices 100B does not acquire the prescription data from the dispensing support system 200 and the reception system 300.

However, even in this case, there is a possibility that inspection work for the same prescription data may be executed in parallel from a plurality of terminals such as the main inspection support device 100A and the sub inspection support device 100B. Therefore, it is conceivable that the medical system 1 includes an exclusive control function that exclusively controls access from the plurality of inspection support apparatuses 100 to the same prescription data. For example, the exclusive control function is implemented by the control unit 10 executing various processes according to the inspection support program.

Specifically, a processing folder and a processed folder may be provided in the storage unit 40 of the main inspection support apparatus 100A. And the said control part 10 of each said inspection assistance apparatus 100 is the said prescription identification which shows the selected said prescription data, when the said prescription data are selected as processing objects, such as the said inspection assistance process or the said deletion process Information is stored in the processing folder.

Accordingly, the control unit 10 of each of the inspection support devices 100 can determine that the prescription data is being processed based on the prescription identification information in the processing folder. Accordingly, in each of the inspection support devices 100, when the control unit 10 displays a list of unprocessed prescription data on the prescription inspection screen D10 (see FIG. 9), prescription data accessed from other terminals is displayed. It is possible not to display.

That is, when the prescription identification information indicating the prescription data to be processed is stored in the processing folder, the control unit 10 performs the inspection support process or the deletion process for the prescription data. Can not run. In addition, when the prescription identification information indicating the prescription data to be processed is not stored in the processing folder, the control unit 10 performs the inspection support process or the deletion process for the prescription data. Can be performed.

And each of the said control part 10 will move the said prescription identification information which shows the said prescription data to the said processed folder from the said folder during a process, when the said inspection support process or the said deletion process about the said prescription data is complete | finished. In addition, when the inspection support process or the deletion process for the prescription data is completed, the control unit 10 each sets the processing content and the processing result for the prescription data as the inspection history as the inspection history of the main inspection support apparatus 100A. The data is stored in the storage unit 40.

As described above, in the medical system 1, exclusive control is performed on the prescription data stored in the storage unit 40 of the main inspection support apparatus 100A by the exclusive control function, and thus a plurality of the inspections are performed. It is possible to prevent the processing for the same prescription data from being executed in parallel using the support device 100.

As another embodiment, the control unit 10 of the main inspection support apparatus 100A may manage the presence / absence of access to the prescription data by each of the inspection support apparatuses 100 connected to the medical system 1. It is done. In this case, when any one of the inspection support devices 100 accesses the prescription data, the control unit 10 of the main inspection support device 100A restricts access from the terminal to the prescription data. Thereby, in each said inspection assistance apparatus 100, when the said control part 10 displays the list of unprocessed prescription data on the said prescription inspection screen D10 (refer FIG. 9), the prescription data currently accessed from the other terminal Can not be displayed.

[Dish division function]

As described above, in the inspection support apparatus 100, by using the platter 58, it is possible to perform inspection work for drugs having a weight exceeding the rated capacity of the weighing unit 5N. However, even when the platter 58 is used, it is not possible to perform inspection work for drugs with an excess weight exceeding the total rated capacity of the four weighing units 5N. In particular, the maximum weight that can be used for the weighing inspection process using the platter 58 (hereinafter referred to as “maximum platter maximum weight”) is a predetermined value that is less than the total of the rated capacities of the four weighing units 5N. Is used. For example, when the rated capacity of the weighing unit 5N is 200 g, the total rated capacity of the four weighing dishes 5N is 800 g, whereas the maximum weight of the platter is set to about 600 g. .

On the other hand, it is conceivable that the inspection support apparatus 100 includes a platter dividing function that can execute the weighing inspection process for a medicine that exceeds the maximum weight of the platter using the platter 58. Specifically, the control unit 10 implements the platter dividing function by executing various processes according to the inspection support program. In addition, the control unit 10 can set validity and invalidity of the platter division weighing function according to a user operation in the initial setting of the inspection support apparatus 100 or the like. In addition, the control unit 10 may switch between enabling and disabling the platter divided weighing function according to a user operation during the execution of the weighing inspection process.

Specifically, when the platter divided weighing function is valid, the control unit 10 determines the medicine exceeding the platter maximum weight (hereinafter, “weight” based on the Rp data selected as an object of the weighing inspection process. It is determined whether or not “excess medicine” is included as a prescription medicine. And when the said overweight chemical | medical agent is contained as a prescription chemical | medical agent, the said control part 10 sets the execution mode of the said weighing | inspection inspection process about the said overweight chemical | medical agent to platter division | segmentation weighing mode.

In the platter divided weighing mode, the control unit 10 sets the drug corresponding to the weighing result every time the weighing drug is placed on the platter 58 and the weighing result by the weighing units 51 to 54 is determined. The amount is displayed in the weighing display area A41. In addition, the control unit 10 calculates and displays the remaining drug amount obtained by accumulating the drug amount corresponding to the weighing result by the weighing units 51 to 54 from the target value of the overweight drug in the Rp data. Let me.

FIG. 26 to FIG. 28 are diagrams showing display examples of the weighing display area A41 sequentially displayed on the prescription inspection screen D10 in the platter divided weighing mode.

As shown in FIG. 26, the control unit 10 calculates the amount of medicine obtained by converting the weight corresponding to the overweight medicine into the unit of the overweight medicine, and uses the amount of medicine as a weighing result to display the weight of the display unit 20. It is displayed in the weighing display area A41 of the prescription inspection screen D10. Further, as shown in FIGS. 27 and 28, the control unit 10 calculates the weighing result from the target value of the overweighted drug in the Rp data every time the weighing result by the weighing units 51 to 54 is determined. The remaining amount of medicine after accumulating the amount of medicine is displayed in the weighing display area A41 as a target quantity. As shown in FIGS. 26 to 28, the control unit 10 calculates the maximum number of medicines that can be weighed using the platter 58, and sets the number of medicines in the weighing display area A41 as the divided maximum number. It can also be displayed.

And the said control part 10 judges whether the weighing using the said platter 58 was repeatedly performed about the said overweight chemical | medical agent, and judged whether the said remaining chemical quantity reached | attained 0, and the weighing result by the said weighing part 5N and It is determined that the collation result with the prescription data matches. When the control unit 10 determines that the collation results are the same, the control unit 10 displays the fact on the display unit 20 and then ends the platter divided weighing mode, and determines that the collation results are inconsistent. While weighing, the weighing by the weighing unit 5N using the platter 58 is repeated. That is, the control unit 10 can collate the results of weighing a plurality of times by the plurality of weighing units 51 to 54 on which the platter 58 is placed with the prescription data.

As described above, in the inspection support apparatus 100, the weighing inspection process can be executed using the platter 58 for the overweight medicine exceeding the maximum weight of the platter by the platter dividing function. In addition, the control unit 10 displays the remaining amount of medicine with respect to the target value of the overweight medicine in the weighing display area A41 of the prescription inspection screen D10. Can be easily performed.

In the weighing inspection process, the control unit 10 may divide the data of the overweight medicine so that the weighing target value per time is not more than the maximum weight of the platter for the overweight medicine. It is done. For example, let us consider a case where the overweight medicine is a unit weight of 160 g (10 per bag), the amount to be dispensed is 60, and the maximum weight of the platter is 600 g. In this case, the weight corresponding to the excess drug is 960 g (160 g × 6 bags). In this case, it is conceivable that the control unit 10 sets the maximum weight of the platter 600 g and the remaining 360 g as two weighing target values. Further, the control unit 10 uses 480 g (3 bags) which is less than 600 g which is the maximum weight of the platter and is an integral multiple of the minimum payout unit, and the remaining 480 g (3 bags) as a target value for weighing twice. Dividing evenly is also conceivable.

Further, in the present embodiment, the case where the platter 58 placed over the plurality of weighing units 5N is used is described as an example. On the other hand, when the weighing pan 55 or the platter 58 is placed on one weighing unit 5N, the control unit 10 obtains a plurality of weighing results obtained by the one weighing unit 5N and the prescription data. It is also conceivable as another embodiment that collation is possible.

[Master update function]

In step S31 of the weighing inspection process, the unit weight of the medicine is acquired, but it is considered that the unit weight of the medicine is not registered in the medicine master. For example, unit weight information for a new drug may not be registered. On the other hand, it is conceivable that the inspection support device 100 has a master update function for updating the drug master. Specifically, the master update function is realized when the control unit 10 executes a master update process (see FIG. 29) described later in step S31. Here, the master update process will be described with reference to FIG. In addition, the said master update process is a process performed separately about each chemical | medical agent used as inspection object by the said weighing | inspection inspection process.

<Step S51>

In step S51, the control unit 10 determines whether or not information on a medicine to be inspected in the weighing inspection process is stored in the medicine master. In step S51, for the medicine, for example, information such as the unit weight of the medicine used in the weighing inspection process, the weight per PTP sheet, and the number per PTP sheet is stored in the medicine master. It is determined whether or not. Here, if it is determined that the drug information is stored in the drug master (S51: Yes), the process proceeds to step S55, and it is determined that the drug information is not stored in the drug master. If so (S51: No), the process proceeds to step S52.

<Step S52>

In step S 52, the control unit 10, with respect to the medicine to be inspected in the weighing inspection process, the mother master (second master) stored in the medicine master (an example of the first master) and a preset reference destination. It is determined whether or not there is a difference. The mother master includes the same type of information as the pharmaceutical master, and is downloaded in advance from a website, for example, or read from a recording medium such as a CD and stored in the storage unit 40. The mother master may be stored in the dispensing support system 200 or the reception system 300. The control unit 10 can set the reference destination of the mother master in advance according to a user operation at the initial setting of the inspection support apparatus 100 or at the start of the weighing inspection process. For example, the storage unit 40, the dispensing support system 200, the receipt system 300, or the like of the inspection support device 100 is set as the reference destination. Furthermore, the mother master sends the inspection support apparatus 100 to the inspection support apparatus 100 via the communication network N1 periodically or at an arbitrary timing from a server apparatus 400 (see FIG. 1) of the inspection support apparatus 100 or a drug manufacturer. It may be automatically distributed and stored in the storage unit 40.

For example, the control unit 10 extracts the number of barcode information associated with the medicine identification information such as the YJ code of the medicine to be inspected in the weighing inspection process as the individual information of the medicine for the medicine master. . Moreover, the said control part 10 extracts the number of the said barcode information matched with the identification information of the chemical | medical agent used as inspection object by the said weighing | inspection inspection process also about the said mother master. And the said control part 10 judges that the difference has arisen when the number of the said barcode information in each of the said pharmaceutical master and the said mother master does not correspond. For example, when there are three barcode information associated with the YJ code of a certain medicine in the medicine master and five in the mother master, the two barcode information that is the difference between them is the medicine master. Will be lacking. Further, the control unit 10 does not register the barcode information corresponding to the medicine identification information such as the YJ code of the medicine to be inspected in the weighing inspection process in the medicine master, and the mother master It is determined that there is a difference even if registered in. In addition, the control unit 10 is different even when there is a difference between the pharmaceutical master and the mother master in the content of the barcode information corresponding to the medicine (packaging weight or number in the packaging). Is determined to have occurred.

Here, if it is determined that there is a difference between the drug master and the mother master (S52: Yes), the process proceeds to step S53, and there is no difference between the drug master and the mother master. If it is determined (S52: No), the process proceeds to step S55. Note that, in step S52, instead of whether or not there is a difference between the pharmaceutical master and the mother master, whether or not information on the medicine to be inspected in the weighing inspection process is registered in the mother master. Simple processing for determining

<Step S53>

In step S53, the control unit 10 determines whether or not to update the medicine master based on the mother master. Specifically, the control unit 10 causes the display unit 20 to display an inquiry about whether or not the medicine master is updated, and determines whether or not the medicine master is updated according to a user operation for the inquiry. If it is determined that the pharmaceutical master is to be updated (S53: Yes), the process proceeds to step S54. If it is determined that the pharmaceutical master is not to be updated (S53: No), the process proceeds to step S55. To do.

<Step S54>

In step S54, the control unit 10 updates the medicine master based on the mother master. Specifically, the control unit 10 updates the information on the item that is different from the mother master to the information on the mother master by updating the information on the medicine master with the mother master. Synchronize. That is, the control unit 10 extracts a difference between the medicine master and the mother master. And when the number of the barcode information registered in association with the medicine is different between the medicine master and the mother master, the control unit 10 has the bar that the medicine master lacks. Code information is read from the mother master and registered in the pharmaceutical master. In addition, the control unit 10 does not register the barcode information corresponding to the medicine identification information such as the YJ code of the medicine to be inspected in the weighing inspection processing in the medicine master, and does not register it in the mother master. If registered, the barcode information is read from the mother master and registered in the pharmaceutical master. In addition, the control unit 10, when there is a difference between the drug master and the mother master, the content of the barcode information corresponding to the drug (packaging weight or number in the package), It is also possible to adopt the content of the barcode information in the mother master and update the content of the barcode information in the pharmaceutical master. The control unit 10 may be able to change the presence / absence of individual medicines in steps S53 to S54 according to a user operation for each medicine for which there is a difference between the mother master and the medicine master. . Further, the control unit 10 updates the information in the drug master to the information in the mother master only for the drug arbitrarily selected according to the user operation, or arbitrarily edits the information in the drug master. It may be possible.

In addition, when the said pharmaceutical master is updated based on the said mother master, the said control part 10 is matched with the said chemical | drug | medicine identification information in the said pharmaceutical master about the chemical | medical agent which becomes the inspection object by the said weighing | inspection inspection process. It is conceivable to perform a collation process to determine whether information such as a code or name matches information such as a YJ code or name of a medicine included in the prescription data. Thus, even if an error occurs in the correspondence between the medicine identification information and the medicine in the medicine master due to the update of the medicine master based on the mother master, the error can be found in the inspection support process. is there.

<Step S55>

Thereafter, in step S55, the control unit 10 acquires the unit weight of the medicine from the medicine master. In addition, when the unit weight of the medicine is not stored in either the medicine master or the mother master, a preset error message or the like is displayed. For example, if the barcode information is not registered in either the pharmaceutical master or the mother master for the medicine to be inspected in the weighing inspection process, the control unit 10 manually stores the barcode information. A warning prompting registration may be displayed on the display unit 20. In this case, the control unit 10 may start the registration process of the barcode information in response to a user operation of the operation unit 30 by subsequently displaying the registration screen D14.

As described above, in the master update process, when the information such as the unit weight of the medicine is not stored in the medicine master, the medicine master can be updated based on the mother master. Therefore, it is possible to update information such as the unit weight of the medicine without interrupting the weighing inspection process, and it is possible to continue the weighing inspection process.

It is also conceivable that the step S51 is omitted and whether or not there is a difference between the pharmaceutical master and the mother master each time the weighing inspection process is performed. Further, the step S53 may be omitted, and the medicine master may be automatically updated without a user operation during the weighing inspection process. Furthermore, the comparison between the drug master and the mother master and the update of the drug master based on the mother master may be automatically executed every preset period.

[Preliminary weighing inspection function]

In a medical facility such as a hospital or a pharmacy, the same medicine as that prescribed to the patient in the past may be prescribed to the patient (Do prescription). In such a case, an operator such as a pharmacist performs a medicine dispensing operation and an inspection operation based on a patient's visit schedule (reservation) or a visit frequency before the prescription data is input to the inspection support device 100. May be executed. However, if the prescription data is not input to the inspection support device 100, the inspection support device 100 cannot be used for the inspection work.

Therefore, it is conceivable that the inspection support apparatus 100 has a pre-weighing inspection function capable of executing the inspection support processing based on the past prescription data before the prescription data is newly issued. Specifically, the control unit 10 implements the pre-weighing inspection function by executing various processes in accordance with the inspection support program. Hereinafter, an example of the procedure of the pre-inspection control process and the pre-verification application process executed by the control unit 10 to implement the pre-weighing inspection function will be described with reference to FIG. The pre-inspection control process is a process that is executed before new prescription data is registered, for example, before a patient visit, and the pre-dispensed result is inspected based on past prescription data. It is a process to do. In addition, the pre-verification conforming process is a result of collating past prescription data and new prescription data without requiring weighing using the weighing unit 5N, and having been inspected in advance by the pre-inspection control process. Is a process for adopting as an inspection result of new prescription data.

<Step S61>

First, in step S61, the control unit 10 determines whether inspection has been completed for the prescription data that has been subject to inspection in the inspection support process, and when the inspection is completed (S61: Yes), The process proceeds to step S62. That is, the process of step S62 is performed every time the inspection support process for the prescription data is completed. If the inspection is not completed (S61: No), the process proceeds to step S63.

<Step S62>

In step S62, the control unit 10 stores a part or all of the information in the prescription data in the storage unit 40 as data for executing the weighing support process (hereinafter referred to as “pre-matching data”). To do. That is, the pre-collation data is a part of the prescription data generated based on the prescription data, or the prescription data itself. For example, the pre-collation data includes information such as a prescription ID, a patient ID (patient name), a medicine type, a usage, and a dose (total amount) corresponding to the prescription data.

The control unit 10 may determine whether or not the pre-verification data is stored for only prescription data satisfying a preset condition among the prescription data to be inspected in the inspection support process. It is done. For example, the condition is that the patient is preset, the preset medicine is not included, the type of the prescription data is a preset type (regular or temporary), and the like. Conceivable. Note that the control unit 10 may automatically delete the pre-collation data after a predetermined period of time has elapsed from the storage date and time of the pre-collation data. This makes it possible to effectively use the data capacity of the storage unit 40 and prohibit the use of the old pre-verification data.

<Step S63>

In step S63, the control unit 10 determines whether a user operation for using the pre-weighing inspection function has been performed. For example, when a predetermined pre-weighing inspection key is displayed on the prescription inspection screen D10 and the control unit 10 is operated, the pre-weighing inspection key is used. It is determined that a user operation has been performed. If it is determined that the user operation has been performed (S63: Yes), the process proceeds to step S64. If it is determined that the user operation has not been performed (S63: No), the process is performed as described above. The process returns to step S61.

<Step S64>

In step S 64, the control unit 10 displays a list of the pre-verification data stored in the storage unit 40 on the prescription inspection screen D 10 of the display unit 20. In the list of pre-collation data, a patient ID corresponding to each of the pre-collation data, a prescription ID of the prescription data that is the original of the pre-collation data, and the like are displayed. In step S64, the control unit 10 accepts an operation for selecting any of the pre-collation data from the pre-collation data list.

<Step S65>

In step S65, the control unit 10 determines whether or not the pre-collation data has been selected. If it is determined that the pre-collation data has been selected (S65: Yes), the process proceeds to step S66 until the pre-collation data is selected (S65: No). Waits in step S65.

<Step S66>

In step S66, the control unit 10 starts the inspection support process based on the preliminary collation data determined to be selected in step S65. Specifically, the control unit 10 determines that the preliminary verification data has been selected as an inspection target, and starts the process from step S15 in the inspection support process (see FIG. 7).

<Step S67>

In step S67, the control unit 10 determines whether or not the inspection support process for the pre-verification data has been completed, and determines that the inspection support process has ended (S67: Yes), the process is performed. The process proceeds to step S68 and waits for the process in step S67 until the inspection support process ends (S67: No).

<Step S68>

In step S68, the control unit 10 causes the storage unit 40 to store the result of the inspection support process for the preliminary verification data as the preliminary inspection result. Thereby, the said control part 10 can refer the said preliminary inspection result later. For example, the pre-examination result includes the prescription ID, patient ID (patient name), medicine type, usage, dose (total amount), weighing value, weighing result (quantity), matching result ( Information such as match, mismatch).

<Step S69>

In step S69, the control unit 10 prints information that can identify the preliminary inspection result by the printer. FIG. 31 is a diagram showing an example of the printing result in step S69. For example, as shown in FIG. 31, the control unit 10 prints, as the barcode B1, a pre-inspection record number assigned to the pre-inspection result by a serial number as identification information of the pre-inspection result. As shown in FIG. 31, information such as patient ID (patient name), usage, number of days, and total amount of each medicine is also printed in the print result in step S69.

And the said control part 10 performs the said prior collation application process in the back | latter stage of the said step S14 in the said inspection assistance process. Hereinafter, an example of the procedure of the pre-collation application process will be described with reference to FIG.

<Step S71>

In step S71, the control unit 10 determines whether or not the preliminary inspection record number has been read. Specifically, the control unit 10 determines that the preliminary inspection record number has been read when the barcode B1 is read by the information reading unit 60. If the pre-inspection record number has been read (S71: Yes), the process proceeds to step S72. If the pre-inspection record number has not been read (S71: No), the pre-inspection process ends. To do.

<Step S72>

In step S 72, the control unit 10 reads out the preliminary inspection result corresponding to the preliminary inspection record number from the storage unit 40. The control unit 10 may display a list of the preliminary inspection results, accept an arbitrary selection operation of the preliminary inspection results, and read the preliminary inspection results instead of the steps S71 to S72. Other embodiments are possible.

<Step S73>

In step S73, the control unit 10 determines whether or not the contents of the prescription data that are the targets of the inspection support process and the contents of the preliminary verification data included in the preliminary inspection results all match. Is matched. Specifically, the control unit 10 includes patient information such as patient ID (patient name) in the prescription data and the pre-verification data, drug information (YJ code, etc.), usage, dose (total amount), etc. It is determined whether or not all the drug information matches. In addition, the collation item in the said collation process should just be one or several preset items. In addition, for example, the control unit 10 determines whether or not the patient corresponding to the pre-verification data matches the patient corresponding to the prescription data, and then only when the patient matches If the patients do not match, it may be determined that the collation results do not match without determining whether the drug information matches.

<Step S74>

In step S74, when the control unit 10 determines that the collation result of the prescription data and the pre-collation data in step S73 is the same (S74: Yes), the process proceeds to step S75, and the collation is performed. If it is determined that the results do not match (S74: No), the process proceeds to step S76.

<Step S75>

In step S75, the control unit 10 uses the pre-inspection result executed in the pre-inspection control process as a target (verification target) of the inspection support process after the execution of the pre-inspection control process. Is stored in the storage unit 40, and the process proceeds to step S21. That is, the weighing inspection process for the prescription data is omitted, and the preliminary inspection result in the preliminary inspection control process performed based on the preliminary verification data is adopted as the inspection result of the prescription data. Will be.

<Step S76>

In step S76, the control unit 10 causes the display unit 20 to display a warning that the collation result between the preliminary inspection result and the prescription data is inconsistent. For example, messages such as “patient difference”, “drug difference”, “use difference”, and “dose difference” are displayed. In this case, the pre-collation process ends, and the process proceeds to step S15. That is, in this case, the preliminary inspection result is not adopted, the inspection support process for the prescription data is performed as usual, and the weighing unit 5N is compared with the prescription data in the weighing inspection process. Will be.

As described above, according to the pre-weighing inspection function, the inspection support process can be executed in advance for the pre-check data, and the dispensing operation and the inspection operation for the prescription data are performed in advance. Therefore, an operator such as a pharmacist can use time effectively. In addition, although it is conceivable that the pre-collation result is adopted only for the portion where the drug information in the prescription data and the pre-collation data matches, as described above, in the inspection support device 100, Since the pre-collation result is adopted only when all the drug information in the prescription data and the pre-collation data match, a highly safe inspection is realized.

In particular, for example, after collating only the total weight of a plurality of types of medicines in the pre-collation data and the weighing result by the weighing unit 5N, A method in which the inspection result by the pre-weighing inspection function is adopted as the inspection result for the prescription data when the total weights match is also considered as a comparative example. However, even if the total weight of the medicines is the same, the kind or number of medicines may be different, so that such a method is less reliable. On the other hand, in the inspection support apparatus 100, the weighing inspection process for a plurality of types of medicines in the preliminary collation data is individually executed for each medicine using the plurality of weighing units 5N. And only when the information of all the medicines in the data for pre-collation and the prescription data are in agreement, the pre-collation result is adopted. Therefore, in the inspection support apparatus 100, highly reliable inspection is realized.

In addition, it is possible that the said control part 10 restrict | limits utilization of the said inspection pending | holding function, when the said inspection assistance process is performed by the said prior weighing inspection function. For example, the control unit 10 may display the inspection hold key K41 on the prescription inspection screen D10 in gray out.

[Mother master update function]

As described above, the mother master is used for updating the drug master and the barcode information in the master update function. Here, when the mother master is distributed from the server device 400 to each of the inspection support devices 100, the mother master set in the server device 400 needs to have high reliability. On the other hand, the medical system 1 includes the server device 400 and a plurality of the inspection support devices 100 connected to the server device 400 via the communication network N1, and the inspection support device It is conceivable to have a mother master update function for updating the mother master based on information collected from each of 100. The medical system 1 is an example of an inspection support system according to the present invention. Further, the server device 400 may be the dispensing support system 200 or the reception system 300.

As described above, in the inspection support apparatus 100, the control unit 10 performs actual measurement using the weighing units 51 to 54 such as the single weight and the package weight in the barcode information. A value that can be calculated based on the value can be set based on the actual measurement value. And the said control part 10 outputs the said barcode information of each chemical | medical agent as data of predetermined formats, such as a CSV format, at the predetermined timings, such as at the time of starting of the said inspection assistance apparatus 100 or a shutdown. The identification information such as a MAC address that can identify the inspection support device 100 is transmitted to the server device 400 via the communication network N1. In addition, the said control part 10 when performing the transmission process which concerns is an example of a transmission process part. Accordingly, the server device 400 automatically collects a plurality of pieces of bar code information corresponding to each medicine from the plurality of inspection support devices 100. In addition, the said pharmaceutical master containing the said barcode information is transmitted to the said server apparatus 400 from each said inspection support apparatus 100, or only the information of the said single weight or the said packaging weight is the said each from the said inspection support apparatus 100. Transmission to the server apparatus 400 is also conceivable as another embodiment.

On the other hand, the server device 400 includes a control unit 401 including a CPU, a RAM, a ROM, and the like, and a non-volatile storage unit 402 such as a hard disk or an SSD. The storage unit 402 stores the barcode information acquired from the mother master and the inspection support device 100, respectively. And the said control part 401 calculates the said single weight and the said package weight of each chemical | medical agent based on the several said barcode information acquired from the said some inspection assistance apparatus 100, Each chemical | medical agent in the said mother master is calculated. Set as the single weight and the packaging weight. The said control part 401 when performing the setting process which concerns here is an example of a weight setting process part.

Accordingly, each of the inspection support devices 100 acquires the updated master master from the server device 400, and thereby sets the single weight set based on the information acquired from each of the inspection support devices 100 and the Package weight information can be acquired. Specifically, the server device 400 automatically distributes the mother master to each inspection support device 100 at a preset timing, or each of the inspection support devices 100 sets the server at a preset timing. It is conceivable to automatically obtain the mother master from the device 400. That is, in the medical system 1, the bar code information and the mother master are automatically transmitted and received between each of the inspection support devices 100 and the server device 400 without any user operation, so-called M2M. (Machine to Machine) is realized. The information acquired by each of the inspection support devices 100 may be only information corresponding to the barcode information in the mother master, or only information on the single weight or the packaging weight in the mother master. Good.

Here, an example of a method for calculating the single weight by the control unit 401 will be described. Note that the packaging weight may be calculated in the same manner as the single weight, and thus the description thereof is omitted here.

First, the control unit 401, for each medicine, has a center in a plurality of single weights, which is a combination of a plurality of single weights acquired from each of the inspection support devices 100 and a single weight currently registered in the mother master. The value is extracted as a reference single weight. As another embodiment, a single weight currently registered in the mother master may not be extracted.

Here, when the parameter of the single weight is an odd number, the median value is a value located in the center when the single weights are arranged in ascending order, and the number of the single weights is an even number. In this case, the median is the smaller of the two values located in the center when the single weights are arranged in ascending order. The median value when the number of single weights is an even number may be an average value of two values located at the center when the single weights are arranged in ascending order.

Next, the control unit 401 calculates a predetermined allowable range for the reference single weight for each medicine. The allowable range is a value for limiting the single weight so as not to fluctuate greatly in the mother master. For example, the allowable range is within ± 10% of the median.

And the said control part 401 extracts the single weight which belongs to the said tolerance | permissible_range among the said single weight acquired from the said some inspection assistance apparatus 100 for every chemical | medical agent. Thereafter, the control unit 401 calculates an average single weight obtained by dividing the total of the single weights within the allowable range by the number of data, and sets the average single weight as the single weight in the mother master.

Thus, according to the mother master update function, it is possible to update the single weight of each medicine in the mother master according to information collected from a plurality of the inspection support devices 100, It is possible to increase the accuracy of a single weight.

For example, three values of 2.43 g, 2.40 g, and 2.80 g are acquired as a single weight of a specific medicine from the three inspection support devices 100, and the unit currently registered in the mother master is acquired. When one weight is 2.42 g, 2.42 g which is the median value among the four values is extracted as the reference single weight. In this case, the allowable range is not less than 2.18 g of 2.42 g which is the reference single weight and 2.66 g or more and 2.66 g or less. Then, out of 2.43 g, 2.40 g, 2.42 g, and 2.80 g, 2.80 g outside the allowable range is excluded, and 2.43 g, 2.40 g, and 2.42 g within the allowable range are extracted. Then, 2.42 g which is a value obtained by dividing the sum of the three values by 3 of the number of data ((2.43 + 2.40 + 2.42) /3≈2.42) is calculated, and the mother master Is set as a single weight (reference value of the weight) of the specific medicine.

In the medical system 1, when the parameter of the single weight of the medicine collected in the server device 400 is small, the setting accuracy of the single weight in the mother master may be lowered. Therefore, when the parameter of the single weight acquired from each of the inspection support devices 100 is less than a preset threshold, the control unit 401 updates the mother master based on the single weight. It is possible not to execute.

Specifically, the control unit 401 stores the single weight of the medicine acquired from each of the inspection support devices 100 together with the identification information and the acquisition date and time of the inspection support device 100 in the storage unit 402. The single weight of the same medicine acquired from the same inspection support device 100 is overwritten and stored. Thereafter, when the control unit 401 acquires the single weight from the inspection support device 100, the single unit acquired for the same kind of medicine in a specific period set in advance such as the past seven days from the present, for example. It is determined whether the weight parameter is equal to or greater than the threshold value. And when the number of the said single weight is more than the said threshold value, the said single weight in the said mother master is updated based on those single weights as mentioned above. On the other hand, if the number of the single weights is less than the threshold value, the updating of the mother master based on the single weights is not performed. This prevents the single weight from being updated in a state where the parameter is small and the reliability is low.

By the way, when the control unit 401 updates the single weight and the packaging weight of the medicine collected in the server device 400, the barcode having the same medicine identification information such as the YJ code and the GS1 code. It is possible to average for each information. However, for the medicines sold by the manufacturer, the specifications of the packaging such as the PTP sheet, heat seal, or medicine box in which the medicine is accommodated are changed without changing the medicine identification information, and the unit weight of the medicine. Or individual information such as packaging weight may change. When the individual information changes in this way, the inspection result of the medicine before the change of the packaging specification in the inspection support device 100 in the barcode information collected from the inspection support device 100 to the server device 400. The barcode information updated based on the information and the barcode information updated based on the inspection result of the medicine after the change of the packaging specification by the inspection support device 100 are included. Therefore, the reliability of the single weight and the package weight for each barcode information set in the mother master may be lowered. Therefore, in the medical system 1, it is desirable to increase the reliability of the single weight and the package weight for each barcode information set in the mother master. Hereinafter, the single weight and the package weight will be described as an example of the individual information.

First, in the medicine master, for each of the barcode information, an external appearance photographed image in which a state corresponding to the barcode information is packaged with a plurality of types of packaging materials or an illustration depicting the state is drawn. A packaging state image such as an image can be registered together with packaging identification information such as a file name for identifying the packaging state image. The packaging state image and the packaging identification information are registered in advance in the mother master, for example, and are taken into the pharmaceutical master from the mother master. Specifically, the control unit 10 of the inspection support device 100 automatically registers the packaging state image and the packaging identification information registered in the mother master in the medicine master at a preset timing. It is possible. That is, when the packaging specification of the medicine is changed and the packaging state image and the packaging identification information of the medicine are newly registered in the mother master, the mother used in the inspection support apparatus 100 thereafter The master and the pharmaceutical product master are also updated to the latest state.

And in the said inspection assistance apparatus 100, the said control part 10 is the said packaging state image corresponding to each said barcode information in the said prescription inspection screen D10 displayed on the said inspection assistance apparatus 100, the said master maintenance screen D13, etc. A user operation for arbitrarily selecting the packaging identification information can be accepted. Specifically, when the operation key corresponding to the “bar code” on the master maintenance screen D13 (see FIG. 14) is operated, the control unit 10 displays the registration screen D14. Subsequently, the control unit 10 corresponds to the barcode information when the information reading unit 60 reads the barcode information of the medicine whose packaging specifications are new in a state where the registration screen D14 is displayed. The registration process is started with the drug information to be operated as the operation target. Specifically, the control unit 10 displays a display field corresponding to the read barcode information on the registration screen D14 so as to be identifiable in a display mode such as a preset color scheme.

Thereafter, when the “image” field is operated in the display field corresponding to the read barcode information, the control unit 10 displays the packaging state image registered in association with the barcode information. An image list screen D143 showing a list is displayed on the display unit 20. FIG. 33 shows an example of the image list screen D143. The selection of the barcode information to be operated may be performed according to a user operation on the operation unit 30. Next, when an arbitrary image is selected from the list of images displayed on the display unit 20 and a confirming operation is performed, the control unit 10 temporarily stores the selection state of the image and stores the image. The list screen D143 is closed and the registration screen D14 is displayed on the display unit 20. Thereafter, when a confirmation operation is performed on the registration screen D14, the control unit 10 displays the packaging identification information corresponding to the packaging state image selected on the image list screen D143 for the barcode information. Store in information.

Thereby, in the medical system 1, the packaging identification information stored in association with the barcode information is included in the barcode information collected by the server device 400 from the inspection support device 100. Therefore, in the server device 400, the control unit 401 determines that each of the single weight and the packaging weight for each barcode information in which the medicine identification information such as the YJ code and the GS1 code and the packaging identification information are the same. It is possible to calculate the average value of. And the said control part 401 sets the average value of the said single weight and the said package weight as the said single weight and the said package weight for every said package identification information corresponding to the said barcode information of the said mother master. That is, the control unit 401 identifies the packaging based on the single weight and the packaging weight that are the same in the packaging identification information among the single weight and the packaging weight acquired from each of the inspection support devices 100. A reference value of the single weight and the package weight corresponding to the information is set. The control unit 401 sets the latest package identification information among the package identification information associated with the barcode information in the mother master as the single weight and the package weight corresponding to the barcode information. It is also possible to do.

In the medical system 1 configured as described above, individual information such as the single weight and the packaging weight corresponding to the barcode information in the mother master is included in each medicine packaging specification corresponding to the barcode information. Updated to Thereby, the reliability of the single weight and the packaging weight for each barcode information set in the mother master is increased, and as a result, the inspection accuracy in the inspection support device 100 in which the barcode information is used. It is possible to increase. In the mother master, when a plurality of pieces of individual information corresponding to a plurality of pieces of packaging identification information are stored for each piece of barcode information, the control unit 10 of the inspection support device 100 performs the barcode information. It is conceivable to switch the individual information corresponding to the barcode information in accordance with a user operation for selecting the packaging identification information corresponding to the barcode information.

[History protection function]

Incidentally, in the inspection support apparatus 100, the control unit 10 stores the inspection history based on the weighing results of the weighing units 51 to 54 in the storage unit 40. Here, it is conceivable that the control unit 10 automatically deletes the inspection history stored in the storage unit 40 in order from the oldest in accordance with preset deletion conditions. The said control part 10 when performing the process which concerns here is an example of a memory | storage process part.

Specifically, the deletion condition is that the timing when a preset date / time has elapsed from the storage date / time of the inspection history has arrived, or that the storage capacity of the storage unit 40 has reached a lower limit value or less. is there. However, in this case, even if there is an inspection history that the user thinks important, the oldest one is deleted in order.

Therefore, in the inspection support apparatus 100, the control unit 10 may have a history protection function capable of protecting the inspection history. Here, the control unit 10 when executing the process for realizing the history protection function is an example of the protection processing unit. Specifically, the control unit 10 displays a list of the inspection history, and accepts a selection operation by an arbitrary user in a state where the list is displayed. For example, the control unit 10 can select the inspection history for each prescription according to a user operation, but the inspection history can be selected for each patient, for each date, for each drug, and for each pharmacist in charge. It is also possible to select. The inspection history includes a protection flag as protection information indicating the presence or absence of protection, and the protection flag is set to ON in the inspection history selected in accordance with a user operation. In addition, when conditions such as patient, date, medicine, and responsible pharmacist are selected in advance by the user, even if the inspection history corresponding to the conditions is subsequently generated, the protection flag in the inspection history is set. Set to ON.

And when the said inspection part deletes the said inspection log | history according to the said deletion conditions, the said inspection log | history selected beforehand according to a user operation and the said protection flag is set to ON is excluded from deletion object. Thereby, the user can refer to the inspection history in which the protection flag is set to ON at any time by performing the history inquiry operation with the inspection support device 100. The control unit 10 sets the protection flag to OFF in the same process as the inspection history protection setting, and thereafter, the inspection history is sequentially deleted at the deletion timing.

If the protection flag is set to ON for a large number of inspection histories, the storage capacity of the storage unit 40 may be saturated. Therefore, it is conceivable that the control unit 10 does not set the protection flag to ON when the number of inspection histories that can set the protection flag to ON exceeds a preset upper limit number. Therefore, when setting the protection of the inspection history, the user selects a target for setting the protection flag to ON while being aware of the upper limit number. The control unit 10 can also erase the inspection history in which the protection flag is set to ON after a longer period than usual. For example, when the inspection history with the protection flag OFF is deleted after 90 days, the inspection history with the protection flag ON is automatically deleted after one year has passed, or the user is notified after one year has passed. It is possible to delete the data after accepting the confirmation operation.

[Continuous weighing function]

By the way, in the inspection support apparatus 100, when inspection is performed on five or more kinds of medicines using the four weighing units 51 to 54, any one or a plurality of the weighing units 51 to 54 are previously provided. It is necessary to take out the placed medicine and place a new medicine. In contrast, in the inspection support apparatus 100, when the control unit 10 performs inspection on five or more kinds of medicines using the four weighing units 51 to 54, the weighing units 51 to 54 are first performed. It is conceivable to have a continuous weighing function capable of carrying out inspection even if the next medicine to be inspected is placed on the weighing units 51 to 54 without taking out the medicine placed on the weighing machine.

Specifically, the control unit 10 has a continuous mode in which the continuous weighing function is enabled, and switches between a normal mode in which the continuous weighing function is disabled and the continuous mode in accordance with a user operation. Then, when the control unit 10 is in the continuous mode, the control unit 10 performs the current measurement by each of the weighing units 51 to 54 at a predetermined timing such as the timing at which the photographed image is recorded in the step S42 of the weighing inspection process. A taring setting process for performing so-called taring to adjust the weighing value to 0 is executed. The said control part 10 when performing the said tare pulling setting process is an example of a tare pulling setting process part here.

For example, in the tare setting process, the control unit 10 sets the current actual weighing value as the exceptional taring value. And the said control part 10 outputs the value which pulled the said exceptional tare subtraction value from the actual weighing result as a weighing result at the time of subsequent weighing. Thereby, in the weighing inspection process, even when the medicine is placed on the weighing units 51 to 54, the weighing value is adjusted to 0 when the photographed image is recorded. It is possible to continue the inspection based on the weight of the medicine newly placed on the parts 51 to 54. In addition, the said control part 10 complete | finishes the inspection about the chemical | medical agent contained in the said Rp data or the said prescription data, and performs the said tare subtraction setting process at the timing when the inspection about the said next Rp data or the said prescription data is started. Try again.

Therefore, according to the continuous weighing function, even when five or more kinds of medicines are to be inspected, the next medicine is removed without removing the four kinds of medicines placed on the weighing parts 51 to 54. It can be placed, and the efficiency of user work is realized.

The tare setting setting process is not limited to step S42, but for example, timing when the weighing values of the weighing units 51 to 54 are determined (step S351), timing when the weighing values of the weighing units 51 to 54 are verified (step S351). Step S37) may be executed at a predetermined timing such as a timing at which the comparison of the weighing values of the weighing units 51 to 54 is determined to be normal (Step S38: Yes). In the continuous mode, after the execution of step S42, the control unit 10 performs the tare subtraction setting process when the current weighing value of the weighing units 51 to 54 is equal to or greater than a preset upper limit value. It is also conceivable to display a preset message such as “Please take out the medicine” without executing it.

[Relaxation inspection function]

By the way, it is conceivable that the medicine weighed by the inspection support device 100 includes a medicine that is likely to cause an error in the weight per unit quantity such as one tablet or 0.1 sheet. In this case, in the configuration in which an error is notified each time when the amount of medicine calculated based on the weighing results by the weighing units 51 to 54 and the target value of the medicine in the prescription data do not match, Errors may occur frequently and the efficiency of inspection work may be reduced. On the other hand, it is considered that the inspection support device 100 has a relaxed inspection function that can improve the efficiency of inspection work by relaxing the inspection accuracy of drugs that are likely to cause an error in weight per unit amount. It is done. Hereinafter, the relaxation inspection function will be described.

First, in the inspection support apparatus 100, in the medicine master, a caution flag (ON: valid, OFF: invalid) indicating validity and invalidity of the relaxation examination function can be stored in association with each medicine. In addition, the control unit 10 may automatically set the caution flag for each medicine based on the inspection history of each medicine in the inspection support apparatus 100. For example, the control unit 10 displays an error message indicating that the verification results do not match in step S381 of the weighing inspection process (see FIG. 13) in the inspection support process executed in the inspection support apparatus 100. When the inspection approval operation (OK key operation) for the user to approve the inspection is performed, the fact that the conditional approval has been performed for the medicine and the error at that time are stored as the inspection history. Then, the control unit 10 automatically sets the caution flag to ON when the conditional approval is performed more than a predetermined number of times set in a predetermined specific period (for example, three months). It is possible. The control unit 10 displays an operation screen for allowing the user to select whether or not to set the attention flag to ON when the conditional approval is performed more than the specific number of times within the specific period. The caution flag may be set to ON according to a user operation. Further, the control unit 10 may arbitrarily set the caution flag according to a user operation.

Further, the pharmaceutical master can store target value lower limit number conversion, target value upper limit number conversion, target value lower limit sheet conversion, and target value upper limit sheet conversion in association with each drug. The target value lower limit number conversion and the target value upper limit number conversion are values that define a range that is allowed as an error when the amount of medicine is collated in units of number. The target value lower limit sheet conversion and the target value upper limit sheet conversion are values that define a range that is allowed as an error when the amount of medicine is collated in sheet units. The initial value of the target value lower limit number conversion, the target value upper limit number conversion, the target value lower limit sheet conversion, and the target value upper limit sheet conversion may be 0, for example.

In the inspection support apparatus 100, the control unit 10 performs the target value lower limit number conversion, the target value upper limit number conversion, the target value lower limit sheet conversion, and the target value upper limit sheet conversion in the pharmaceutical master according to a user operation. It can be set arbitrarily. However, in the inspection support device 100, it is possible to set the settable maximum number of the target value lower limit number conversion and the target value upper limit number conversion in common for all medicines, and the control unit 10 It is conceivable to limit the setting of the target value lower limit number conversion and the target value upper limit number conversion to the settable maximum number or less. Similarly, in the inspection support device 100, common to all medicines, the settable maximum number of sheets for the target value lower limit sheet conversion and the target value upper limit sheet conversion is set, and the control unit 10 It is conceivable to limit the setting of the target value lower limit sheet conversion and the target value upper limit sheet conversion of the medicine to the settable maximum number of sheets or less.

FIG. 34 is a diagram showing a display example of the master maintenance screen D13. As shown in FIG. 34, in the master maintenance screen D13, the target value lower limit number conversion, the target value upper limit number conversion, the target value lower limit sheet conversion, and the target value upper limit sheet conversion can be input. . The master maintenance screen D13 displays operation keys K33 to K36 for displaying an inspection history for the medicine selected on the master maintenance screen D13. Specifically, when the operation keys K33 and K34 are operated, the control unit 10 determines the number of errors that occurred when the inspection unit is the number and the conditional approval is performed, and the occurrence of the errors. Display percentages. In addition, when the operation keys K35 and K36 are operated, the control unit 10 generates an error in the number of sheets and the occurrence of the error when the inspection unit is the number of sheets and the conditional approval is performed. Display percentages.

For example, with regard to “A medicine”, the number of times that the conditional approval was made within the specific period is 15 cases, and the number of errors at that time is −1 tablet, 80%, −2 tablets In the case where there is 20%, such information is displayed on a pop-up screen D33 as shown in FIG. 34 in response to the operation of the operation key K33. In the case of “A medicine”, the number of times that the conditional approval is made within the specific period is 15 cases, and the number of errors at that time is +1 tablet, 80%, and +2 tablets Is 20%, these pieces of information are displayed according to the operation of the operation key K34. Similarly, for “B medicine”, the number of times that the conditional approval was made within the specific period was 15 cases, and the number of sheets with an error at that time was −0.1 sheets was 100%. In some cases, these pieces of information are displayed in response to the operation of the operation key K35.

In the case of “B medicine”, the number of times that the conditional approval is made within the specific period is 15 cases, and the number of error sheets at that time is +0.1 sheets is 100% The information is displayed according to the operation of the operation key K36. Note that the control unit 10 may calculate and display the error number and the ratio of the error sheet number as absolute values including shortage and excess. For example, in the case of the above-described example, when the operation key K33 or K34 is operated, 30 cases are displayed as the number of times that the conditional approval is performed, and the number of errors is 1 tablet 80% If there are 2 tablets, 20% is displayed. Similarly, when the operation key K35 or K36 is operated, 30 cases are displayed as the number of times that the conditional approval has been performed, and the number of error sheets is 0.1%. Is displayed.

In addition, the control unit 10 is based on the inspection history, the number of medicines or the number of sheets with the highest rate of conditional approval, the target value lower limit number conversion, the target value upper limit number conversion, It is also conceivable to automatically set each value for target value lower limit sheet conversion and target value upper limit sheet conversion.

Then, in step S37 of the weighing inspection process (see FIG. 13) in the inspection support process, the control unit 10 determines the weighing result when the caution flag is ON in the medicine master for the medicine to be inspected. When the error is within a preset error range, it is determined that the matching result is coincident. Specifically, when the inspection unit of the medicine to be inspected is the number, the control unit 10 calculates the number of medicines calculated based on the weighing result by the weighing part 5N and the target value in the prescription data. When the difference is equal to or greater than the target value lower limit number conversion set by the pharmaceutical master and equal to or less than the target value upper limit number conversion, it is determined that the matching results are the same. In addition, when the inspection unit of the medicine to be inspected is the number of sheets, the control unit 10 calculates the number of medicine sheets calculated based on the weighing result by the weighing unit 5N and the target value in the prescription data. When the difference is equal to or greater than the target value lower limit sheet conversion set by the pharmaceutical master and equal to or less than the target value upper limit sheet conversion, it is determined that the matching results are the same. That is, the controller 10 determines that the difference between the amount of the medicine calculated based on the weighing result by the weighing section 5N and the target value of the medicine in the prescription data is within an error range set in advance for each medicine. In some cases (S38: Yes), the error is not notified, and when the error range is exceeded (S38: No), the error is notified (S381).

As a result, the inspection support apparatus 100 allows inspection errors for medicines that are likely to have an error in weight per unit amount, and reduces the frequency of notification of errors, so that the efficiency of inspection work can be improved. . Here, a case has been described by way of example in which it is determined that the matching result is the same when the error between the weighing result and the target value is within the error range. On the other hand, if the error between the weighing result and the target value is within the error range, the collation result is determined to be inconsistent, but only the error notification in step S371 is not executed, and the process is performed in step S40. It is also conceivable as another embodiment to shift to.

In addition, the control unit 10 may display a precaution check mode that is set in advance in order to recognize that the medicine with the caution flag turned on is an easy-to-error medicine on the prescription inspection screen D10. Conceivable. For example, the caution display mode may be displayed in a preset character color, displayed in a preset background color, or a symbol or character such as a preset “!”, “*”, Or “caution” It may be possible to display the name with a chemical name. Thereby, the user can perform inspection while paying attention to the medicine displayed in the caution display mode.

[Other display examples of captured images]

By the way, in the inspection history inquiry screen D12 or the like, when a photographed image taken simultaneously with the weighing units 51 to 54 is displayed as an inspection history, it is possible to grasp the type of each medicine contained in the photographed image. Have difficulty. For example, the user needs to determine the type of medicine from the packaging material of each medicine contained in the photographed image. On the other hand, the display example of the said picked-up image which can identify each chemical | medical agent contained in the said picked-up image easily is demonstrated.

First, in the inspection support process, the control unit 10 includes, for each medicine to be inspected, image identification information such as a file name for identifying a photographed image by the photographing unit 70, and the medicine on which the medicine is placed. Weighing unit identification information such as a weighing unit number for identifying the weighing unit 5N is associated with and stored in the storage unit 40 as an inspection history. Thereafter, when the control unit 10 displays the inspection history on the inspection history inquiry screen D12 or the like (see FIG. 12), at least according to the selection operation of the display column of any medicine in the history content display area A53. An image display screen D121 on which a captured image of the image identification information corresponding to the medicine is displayed is displayed on the display unit 20. FIG. 35 shows an example of the image display screen D121. As shown in FIG. 35, on the image display screen D121, the photographed image of the selected medicine is displayed in an enlarged manner than the thumbnail image of the operation key K19. Note that the operation key K19 is not displayed on the inspection history inquiry screen D12, and the control unit 10 performs the image display screen D121 in response to a selection operation of an arbitrary medicine display field in the history content display area A53. It is also possible to display. Further, when the operation key K19 is operated, the captured image may be enlarged and displayed on the image display screen D121.

As described above, the history content display area A53 displayed in FIG. 12 is extracted on the basis of information such as the medicine name input in the extraction condition display area A51 and displayed in the list display area A52. The contents of the inspection history of a patient arbitrarily selected from the selected patient list are displayed. That is, the control unit 10 can search for a photographed image in which the medicine is photographed using an arbitrarily input medicine name as a keyword.

In addition, the control unit 10 can accept operations on the operation areas A121 to A124, which are separated by a dashed line shown in FIG. 35, on the image display screen D121. Each of the operation areas A121 to A124 is an area corresponding to each position of the weighing units 51 to 54. Then, the control unit 10 performs weighing with a weighing unit corresponding to one of the operation regions A121 to A124 operated among the weighing units 51 to 54 in response to any operation of the operation regions A121 to A124. Individual information on medicines including information such as medicine names that can identify the medicines that have been identified, and information indicating the amount of medicines (number of tablets, number of sheets, etc.) calculated based on the weighing results, is stored in the inspection history. Display based on. Such display processing is executed by the display processing unit 17 of the control unit 10. In addition, when the operation areas A121 to A124 are operated again, the control unit 10 ends the display of the individual drug information. In FIG. 35, the operation area A121 is operated, and the name and the number of tablets (number of sheets) weighed by the weighing unit 51 are displayed on the pop-up screen D122. Further, when the operation area A121 is operated, an enlarged image of the photographed image of the weighing unit 51 and the individual information on the medicine may be displayed on the pop-up screen D123. Note that the name of the medicine and the number of tablets (number of sheets) weighed by the weighing unit 51 may be transferred from the image display screen D121 to another screen and displayed.

10 Control unit

20 Display section

30 Operation unit

40 storage unit

50 Weighing device

51-54 Weighing section

55 Weighing pan

56 load cell

60 Information reader

70 Shooting Department

80 tablet devices

90 Cover member

100 Inspection support device

Claims

A weighing unit;

A selection processing unit for selecting medicines to be weighed by the weighing unit;

The number of the medicines in the second packaging material containing a plurality of first packaging materials containing a plurality of the medicines selected by the selection processing unit and the first packaging materials contained in the second packaging materials. 2 acquisition processing unit for acquiring the total weight of the packaging material;

A collation processing unit that collates the weighing result with the prescription data by the weighing unit;

With

Based on the number of the medicines acquired by the acquisition processing unit and the total weight of the second packaging material, the weighing processing unit is a weighing unit out of a weight that is an integral multiple of the total weight of the second packaging material. When the difference between the approximate weight closest to the weighed value and the weighed value of the weighed portion is within a preset allowable range, the medicine contained in the second packaging material in a number corresponding to the integer multiple An inspection support apparatus capable of collating the total number of the above data with the prescription data as a weighing result.
When the weighing value of the weighing unit is smaller than the approximate weight and the difference between the approximate weight and the measured value of the weighing unit is out of the allowable range, the collation processing unit has a number corresponding to the integer multiple. The inspection support device according to claim 1, wherein the total number of the medicines contained in the second packaging material that is smaller by one is collated with the prescription data as the weighing result.
When the weighing value of the weighing unit is larger than the approximate weight and the difference between the approximate weight and the weighing value of the weighing unit is out of the allowable range, the verification processing unit has a number corresponding to the integer multiple. The inspection support device according to claim 1 or 2, wherein the total number of the medicines contained in the second packaging material is collated with the prescription data as the weighing result.
The said collation process part alert | reports the warning set beforehand, when the difference of the said approximate weight and the weighing value of the said weighing part is outside the said tolerance | permissible_value, and the said collation result is in agreement. Inspection support device described in 1.
5. The inspection support device according to claim 1, further comprising a display processing unit capable of displaying the weighing result.
6. The inspection support apparatus according to claim 1, further comprising a setting processing unit capable of setting the allowable range in accordance with a user operation.
A plurality of the weighing units;

The inspection support device according to any one of claims 1 to 6, wherein the collation processing unit collates a weighing result obtained by one or a plurality of the weighing units and the prescription data.
The collation processing unit can select any one of the plurality of medicine identification information according to a user operation when a plurality of medicine identification information corresponding to a medicine selected by a user operation is registered. The inspection support device according to any one of 1 to 7.
A unit weight acquisition unit for acquiring a weight per unit amount predetermined for each type of medicine;

A unit conversion processing unit that converts a weighing result by the weighing unit into a predetermined unit based on the weight per unit amount obtained by the unit weight obtaining unit;

An update processing unit capable of updating the first master information in which the correspondence relationship between the type of the medicine and the weight per unit amount is preset based on the second master information set in advance;

A display processing unit for displaying the weighing result converted by the unit conversion processing unit in the weighing display area;

The inspection support device according to any one of claims 1 to 8, further comprising:
The update processing unit compares the first master with the second master to extract a difference, and registers the individual information registered in association with the medicine between the first master and the second master. If the numbers are different, the individual information that is lacking in the first master is read from the second master and registered in the information of the first master, and the individual information is not registered in the first master and the first master 10. The inspection support device according to claim 9, wherein the medicine registered in the second master is read out from the second master and registered in the first master.
The collation processing unit can display a list of medicines included in each Rp data in the prescription data unit when the prescription data includes a plurality of Rp data that are prescription data in the same usage unit. The inspection support device according to any one of 10.
A plurality of the weighing units, and a photographing unit capable of simultaneously photographing all the weighing units,

The collation processing unit photographs the weighing unit with the photographing unit when the weighing values by all the weighing units are confirmed and when collation by the collation processing unit is completed for all medicines included in the prescription data. The inspection support device according to claim 11.
The photographed image photographed by the photographing unit is displayed, and when an operation region corresponding to any one of the weighing units is operated in the photographed image, the weighing unit corresponding to the photographing region is weighed. The inspection support device according to claim 12, further comprising a display processing unit capable of displaying individual information including at least information capable of identifying the performed medicine on the display unit together with the captured image.
The inspection support device according to any one of claims 1 to 13, wherein the collation processing unit is capable of collating a plurality of weighing results obtained by the weighing unit with the prescription data.
A plurality of the weighing units, and an extended placement unit that can be placed across the plurality of weighing units,

The inspection support device according to claim 14, wherein the verification processing unit is capable of verifying a plurality of weighing results obtained by a plurality of the weighing units on which the respective survey parts are placed and the prescription data.
Whenever the weighing value of the weighing unit is determined, the verification processing unit can display the remaining drug amount obtained by accumulating the drug amount corresponding to the weighing value from the target value of the drug in the prescription data. The inspection support device according to claim 14 or 15.
The collation processing unit can execute a pre-inspection control process for collating pre-collation data including a part of the past prescription data or the past prescription data itself and a weighing result by the weighing unit, The collation result in the pre-inspection control process can be adopted as a collation result of prescription data corresponding to the same patient as the pre-collation data as a collation target by the collation processing unit after execution of the preliminary inspection control process. Item 17. The inspection support device according to any one of Items 1 to 16.
The collation processing unit is subject to collation by the collation processing unit after execution of the pre-inspection control process, and information on all medicines included in prescription data corresponding to the same patient as the pre-collation data is stored in advance. The matching result in the pre-inspection control process based on the pre-matching data is adopted as the matching result of the prescription data only when matching with the matching data. The inspection support apparatus according to claim 17, wherein a verification process for verifying a weighing result obtained by the weighing unit and the prescription data is performed without employing a matching result in the pre-article inspection control process.
A storage processing unit that stores an inspection history including a weighing result by the weighing unit in a storage unit, and sequentially deletes the inspection history stored in the storage unit according to a predetermined condition;

A protection processing unit that excludes the inspection history selected in response to a user operation from being erased by the storage processing unit;

The inspection support device according to any one of claims 1 to 18, further comprising:
One or more weighing units;

A tare setting setting processing unit capable of executing a tare setting setting process for adjusting the weighing value by the weighing unit to 0 at a predetermined timing after the collation start by the collation processing unit;

The inspection support device according to any one of claims 1 to 19, further comprising:
An inspection support system comprising a plurality of inspection support devices according to any one of claims 1 to 20 and an information processing device capable of communicating with each of the inspection support devices,

Each of the inspection support devices includes a transmission processing unit that transmits information on the weight of the first packaging material or the second packaging material used for collation by the collation processing unit to the information processing apparatus at a predetermined timing. ,

The information processing device includes a weight setting processing unit that sets a reference value of the weight for each medicine based on the weight information acquired from each of the inspection support devices,

An inspection support system in which each of the inspection support devices can acquire the reference value of the weight from the information processing device.
The transmission processing unit transmits information on the weight of the first packaging material or the second packaging material to the information processing apparatus together with packaging identification information capable of identifying the specification of the packaging of the first packaging material or the second packaging material. Send

The weight setting processing unit sets the reference value of the weight corresponding to the packaging identification information based on the weight information of which the packaging identification information is the same among the weight information acquired from each of the inspection support devices. To

The inspection support system according to claim 21.
An inspection support method in an inspection support apparatus including a weighing unit,

A selection step of selecting a drug to be weighed by the weighing unit;

The number of the medicines in the second packaging material in which a plurality of first packaging materials containing a plurality of the medicines selected in the selection step are accommodated and the second in which the plurality of first packaging materials are accommodated. An obtaining step for obtaining the total weight of the packaging material;

A collation step of collating the weighing result by the weighing unit with the prescription data;

Including

In the collating step, the weighing unit measures the weight out of an integer multiple of the total weight of the second packaging material based on the number of the medicines obtained in the obtaining step and the total weight of the second packaging material. When the difference between the approximate weight closest to the value and the weighing value of the weighing unit is within a preset allowable range, the total number of the medicines contained in the second packaging material corresponding to the integer multiple Is an inspection support method in which the weighing result is compared with the prescription data.
A weighing unit;

A collation processing unit for collating the amount of the medicine calculated based on the weighing result by the weighing section and the target value of the medicine in the prescription data;

A notification processing unit for reporting an error when the verification result by the verification processing unit is inconsistent;

With

When the collation result by the collation processing unit satisfies a preset condition, the notification processing unit calculates the amount of the medicine calculated based on the weighing result by the weighing unit and the target value of the medicine in the prescription data. An inspection support apparatus that does not notify the error when the difference is within an error range set in advance for each medicine but notifies the error when the difference exceeds the error range.