JP2019063626A - Audit support system, audit support device, and audit support program - Google Patents

Abstract

To provide a compounding audit device capable of efficiently performing an audit on a plurality of types of prescription medicines included in prescription data.SOLUTION: An audit support device 100 comprises: a plurality of weighing units 51 to 54; an information reading unit for reading medicine identification information from a packaging material of a medicine; a weighing specification unit for specifying one or more of the weighing units 51 to 54 to be mapped with the medicine identification information read by the information reading unit; and a collation processing unit that every time medicine identification information is read by the information reading unit, starts processing of collating prescription data with weighing results of the one or more of the weighing units specified by the weighing specification unit as weighing units corresponding to the medicine identification information.SELECTED DRAWING: Figure 2

Description

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

  Generally, an inspection support device used to support the work of a pharmacist or the like who inspects a medicine into which a medicine has been dispensed based on prescription data is known. For example, there is known a dispensing inspection system in which the propriety of the contents of dispensing is determined based on the total amount of medicines placed in a plurality of weighing units (see, for example, Patent Document 1).

JP, 2013-42795, A

  However, the above-mentioned dispensing inspection system leaves no evidence of inspection.

  An object of the present invention is to provide an inspection support device and an inspection support method capable of leaving inspection evidence.

The inspection support device according to the present invention includes a weighing unit, a collation processing unit that collates the weighing result of the weighing unit with prescription data, a photographing unit capable of photographing the weighing unit, and recording a photographed image by the photographing unit And an imaging processing unit.
In the inspection support method according to the present invention, the verification step of collating the measurement result of the weighing unit with the prescription data, and when the weighing value by the weighing unit is determined, the collation by the collation processing unit is completed, or Recording a photographed image by a photographing unit capable of photographing the weighing unit when a predetermined photographing operation is performed.

Also, the inspection support device according to the present invention includes one or more of the plurality of weighing units, an information reading unit that reads drug identification information from a packaging material of a drug, and the drug identification information read by the information reading unit. One or more of the weighing units identified by the weighing identification unit as a weighing unit corresponding to the medicine identification information each time the medicine identification information is read by the weighing identification unit that specifies the weighing unit and the information reading unit And a verification processing unit that starts verification processing of the weighing result of the and the prescription data.
Further, an inspection support method according to the present invention is an inspection support method in an inspection support device including a plurality of weighing units and an information reading unit that reads drug identification information from a packaging material of a drug, and read by the information reading unit. The weighing specification step as a weighing unit corresponding to the medicine identification information, the weighing specifying step specifying the one or more weighing units to be associated with the medicine identification information, and each time the medicine identification information is read by the information reading unit And a verification processing step of starting verification processing of the weighing result of one or more of the weighing units specified in the above and prescription data.

  According to the present invention, the verification process is started every reading of the medicine identification information, and inspections of prescription medicines included in the prescription data can be performed continuously and in parallel. Therefore, for example, the inspection operation of each of the prescription drugs and the storage operation of each of the prescription drugs in the medicine bag can be performed efficiently and accurately.

  Specifically, the weighing specifying unit specifies one or more of the weighing units whose weighing value is increased from zero after the information reading unit reads the medicine identification information as a weighing unit to be associated with the medicine identification information. Is considered. In particular, one or more of the one or more of which the weighing value has increased from 0 before the weighing unit reads the medicine identification information by the information reading unit until the medicine reading information which is different by the information reading unit is read It is conceivable to specify the weighing unit as a weighing unit to be associated with the medicine identification information. Thus, by placing the medicine on an arbitrary weighing unit after reading the medicine identification information, it is possible to easily execute the verification process using one or more of the weighing units.

  Here, it is considered that the prescription data is prescription data (Rp data described later) of the same usage unit. Thus, inspection can be performed continuously and in parallel for each prescription data of the same usage unit contained in the same medicine bag, and erroneous insertion of the prescription medicine into the medicine bag can be suppressed.

  By the way, it is conceivable that the verification processing unit can acquire the prescription data to be inspected based on the prescription identification information described in the medicine bag read by the information reading unit. Further, it is conceivable that the verification processing unit can select the prescription data to be inspected from a plurality of the prescription data in accordance with a user operation.

  Further, the inspection support device causes the display unit to display a display unit and weighing display areas corresponding to the weighing units in the same arrangement as that of the weighing units, and the weighing result by the weighing unit and the collation processing unit It is possible to provide the display processing part which displays the collation result by B in the said measurement display area. Thus, the user can intuitively check the weighing result of each of the weighing units in the weighing display area.

  In addition, the inspection support device acquires a unit weight acquisition unit that acquires a weight per unit amount predetermined for each type of medicine, and the unit amount acquired by the unit weight acquisition unit as a result of weighing by the weighing unit. It is conceivable to provide a unit conversion processing unit that converts into a predetermined unit based on the weight of the hit. In this case, it is conceivable that the display processing unit causes the weighing display area to display the weighing result converted by the unit conversion processing unit. This allows the user to display the drug in a predetermined unit such as "tablet", "capsule" or "package" instead of "mg" indicating weight, for example. It is easy to grasp the propriety of the quantity.

  Furthermore, it is conceivable that the collation processing unit collates the measurement result converted by the unit conversion processing unit with the prescription data. Thereby, since the collation processing unit can use the weighing result converted by the unit conversion processing unit, for example, a unit of medicine indicated in the prescription data without using the weighing result. The processing is simplified as compared to the case of converting into a unit of weight and performing collation.

  The inspection support device may be provided with a cover member which is provided so as to be openable and closable with respect to the inspection support device and which supports the display unit. Thereby, since the display unit is integrated with the cover member, the inspection support device can be miniaturized.

  Further, the cover member is rotatably supported by the rotation support portion with respect to the inspection support device, and the display portion is in a posture in which the display surface faces the weighing portion when the cover member is closed. It is conceivable that the support member is supported by the cover member. Thereby, for example, the user can perform inspection work without moving the sight line in a state where the cover member can be opened and the weighing unit and the display unit can be overlooked at one time.

  By the way, it is conceivable that the inspection support device includes an extended placement unit that can be placed across a plurality of the weighing units. In this case, it is conceivable that the collation processing unit can collate the sum of the measurement results of the plurality of weighing units on which the extended mounting unit is placed and the prescription data. As a result, inspection work can be performed with the inspection support device by using the extended placement unit even for a large amount of medicine or a large size medicine.

  Further, the display processing unit displays an extended weighing display area corresponding to the extended placement unit in place of the plurality of weighing display areas, and displays the collation result of the collation processing unit in the expanded weighing display area. It is conceivable. As a result, compared to, for example, the case where the comparison result is displayed in a plurality of weighing table areas, the portion to be viewed by the user is limited to the expanded weighing display area, and the work efficiency of the user can be enhanced.

  Further, the inspection support device displays a medicine name, a medicine image, and a prescription amount corresponding to a visual inspection target medicine specified in advance among one or more kinds of medicines contained as prescription medicine in the prescription data. It is conceivable to provide a visual inspection processing unit that completes the inspection of the medicine targeted for visual inspection according to a predetermined confirmation operation. Thus, even when the prescription data includes a prescription medicine that is not appropriate to perform weighing inspection using the weighing unit, the inspection support device is used to check the prescription medicine included in the prescription data. It can be completed.

  Furthermore, the inspection support device notifies that the inspection of the prescription data is completed when the collation processing unit performs collation by the collation processing unit or inspection completion by the visual inspection processing unit for all the medicines included in the prescription data as the prescription medicine. It is possible to provide an inspection completion notification unit. Thereby, the user can clearly recognize that the inspection of the prescription drug included in the prescription data is finished.

  Further, it is conceivable that the inspection support device includes a photographing unit capable of photographing the weighing unit, and a photographing processing unit which records a photographed image by the photographing unit. More specifically, when the measured values by all the weighing units are determined, the photographing processing unit determines that all the medicines included in the prescription data have been checked by the matching processing unit, or is determined in advance. When a shooting operation is performed, it is conceivable to record a shot image by the shooting unit. Thereby, it is possible to record and record the state of the weighing unit in the inspection operation performed using the inspection support device. The imaging unit may be capable of imaging a range including the weighing display area. In particular, when the imaging processing unit determines that the measured values by all the weighing units have been determined, or when the collation processing unit completes the collation for all the medicines included in the prescription data, or the imaging operation determined in advance is In the case where it is performed, it is conceivable to cause the photographing unit to photograph the weighing unit after a predetermined standby time has elapsed after displaying the start of photographing on the display unit. This increases the possibility that shooting will be performed at the timing when the user withdraws a hand or the like out of the shooting range by the shooting unit, and useless shooting is suppressed.

  Further, a mark line formed continuously or intermittently outside the plurality of weighing parts is provided in the inspection support device, and the photographing processing part shields the mark line in the image taken by the photographing part. It is conceivable to record a photographed image by the photographing unit on condition that there is no shielding object. Thus, for example, the photographed image by the photographing unit is not recorded in a state where the user's hand or the like is in the photographing range of the photographing unit.

  In particular, the photographing processing unit records the photographed image by the photographing unit on the condition that a length or an area of a shield blocking the mark line in the photographed image by the photographing unit is less than a predetermined threshold. It is conceivable. Thereby, the recording of the photographed image is limited only when there is a shield having a certain area such as the user's hand, and the shield such as dust shields the mark line. The captured image can be recorded without any problem.

  Here, it is conceivable that a part or all of the mark line is formed in the weighing plate provided in the weighing unit or the extended placement unit placed over the plurality of weighing units. As a result, it is possible to record a photographed image in a state where the mark line of the weighing dish or the extended placement unit is not shielded.

  By the way, it is conceivable that the photographing unit is provided in a posture for photographing the weighing unit from an oblique direction, because the photographing unit interferes with inspection work if it is directly above the weighing unit, but in this case The image of the weighing unit is captured in a trapezoidal shape. Therefore, a plurality of correction index parts separated from each other are provided in the inspection support device, and the photographing processing part is based on the plurality of correction index parts present in the photographed image by the photographing part. It is conceivable to perform keystone correction of a captured image. As a result, the photographed image by the photographing unit is corrected, and it is possible to obtain a photographed image similar to the case where the weighing unit is photographed from directly above. Further, it is conceivable that the photographing unit can photograph all the weighing units at the same time.

  In the present invention, a plurality of weighing units, a second weighing specification unit for specifying drug identification information to be associated with each of the weighing units based on weighing results and prescription data by each of the weighing units, and a packaging material for medicine An information reading unit for reading medicine identification information, and inspection of the medicine identification information specified by the second weighing specification unit when the medicine identification information is read by the information reading unit after determination of the measurement result by the weighing unit And an inspection completion processing unit that completes the inspection support device.

  Further, the present invention is an inspection support method in an inspection support apparatus including a plurality of weighing units and an information reading unit for reading drug identification information from a packaging material of a drug, wherein weighing results by each of the weighing units and prescription data A second weighing specifying step of specifying drug identification information to be associated with each of the weighing units, and the second weighing specifying when the drug identification information is read by the information reading unit after determination of the weighing result by the weighing unit The method may be regarded as an inspection support method including an inspection completion step of completing the inspection of the medicine identification information specified in the step.

  Specifically, the system further comprises a unit weight obtaining unit for obtaining a weight per unit amount predetermined for each type of medicine, and the second weighing identifying unit determines the quantity of medicine contained in the prescription data as the unit weight It is considered to associate the weighing unit for which the weighing result is obtained that matches or most closely matches the weight of the medicine converted based on the unit weight of the medicine acquired by the acquiring unit and the medicine identification information of the medicine Be In the inspection support apparatus configured as described above, after the user first places the medicine on the weighing unit, the information reading unit reads the medicine identification information to check the medicine in the weighing inspection. It is possible to complete the

  Further, the system further includes a unit weight acquisition unit that acquires a weight per unit amount predetermined for each type of medicine, and the second weighing identification unit acquires the weighing value of the medicine by the unit weight acquisition unit. Associating the medicine identification information of the medicine with the weighing unit for which the weighing result is obtained that the quantity of the medicine converted based on the unit weight of the medicine matches or most closely matches the quantity of the medicine included in the prescription data It is also conceivable. Even in the inspection support device configured as described above, after the user first places the medicine on the weighing unit, and then causes the information reading unit to read the medicine identification information, the weighing inspection of the medicine is performed. It is possible to complete the

  According to the present invention, an inspection support device and an inspection support method capable of efficiently and accurately inspecting a plurality of types of prescription drugs contained in prescription data are provided.

FIG. 1 is a block diagram showing the configuration of an inspection support device according to an embodiment of the present invention. FIG. 2 is a view showing the configuration of the inspection support device according to the embodiment of the present invention. FIG. 3 is a diagram showing the configuration of the inspection support device according to the embodiment of the present invention. FIG. 4 is a view showing the configuration of the inspection support device according to the embodiment of the present invention. FIG. 5 is a view showing the configuration of the inspection support device according to the embodiment of the present invention. FIG. 6 is a view showing the configuration of the inspection support device according to the embodiment of the present invention. FIG. 7 is a flowchart showing an example of the inspection support process executed by the inspection support device according to the embodiment of the present invention. FIG. 8 is a view showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 9 is a view showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 10 is a view showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 11 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 12 is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 13 is a flowchart showing an example of the procedure of the weighing inspection process executed by the inspection support device according to the embodiment of the present invention. FIG. 14 is a view for explaining the keystone correction function of the inspection support device according to the embodiment of the present invention. FIG. 15 is a diagram for explaining the keystone correction function of the inspection support device according to the embodiment of the present invention. FIG. 16 is a diagram for explaining the keystone correction function of the inspection support device according to the embodiment of the present invention. FIG. 17 is a view for explaining a photographing control function of the inspection support device according to the embodiment of the present invention. FIG. 18 is a view for explaining a photographing control function of the inspection support device according to the embodiment of the present invention. FIG. 19 is a view showing the configuration of a check supporting device according to another embodiment of the present invention. FIG. 20 is a view showing the configuration of a check support device according to another embodiment of the present invention. FIG. 21 is a view showing the configuration of a checkup support apparatus according to another 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 view for explaining another example of the photographing control function of the inspection support device according to the embodiment of the present invention. FIG. 24 is a view for explaining another example of the photographing control function of the inspection support device according to the embodiment of the present invention. FIG. 25 is a view for explaining another example of the photographing control function of the inspection support device according to the embodiment of the present invention. FIG. 26 is a view for explaining another example of the weighing pan and the platter of the inspection support device according to the embodiment of the present invention. FIG. 27 is a view for explaining another example of the keystone correction function of the inspection support device according to the embodiment of the present invention. FIG. 28 is a view for explaining another example of the keystone correction function of the inspection support device according to the embodiment of the present invention. FIG. 29 is a block diagram showing the configuration of the inspection support device according to the embodiment of the present invention. FIG. 30A is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 30B is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 30C is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 30D is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 30E is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 31A is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 31A is a diagram showing an example of a display screen of the inspection support device according to the embodiment of the present invention. FIG. 32 is a view showing an example of a display screen of the inspection support device according to the embodiment of the present invention.

First Embodiment
Hereinafter, embodiments of the present invention will be described with reference to the accompanying drawings for understanding of the present invention. The following embodiments are merely specific examples of the present invention, and are not of the nature to limit the technical scope of the present invention.

[Medical system 1]
As shown in FIG. 1, the medical system 1 includes an inspection support device 100, a dispensing support system 200, a receipt system 300, and the like. The inspection support device 100, the dispensing support system 200, and the receipt system 300 are communicably connected via a network N1 such as a LAN or the Internet.

[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 ordering system. Then, the dispensing support system 200 generates dispensing data to be used by dispensing devices such as a tablet packaging machine and a powder dispensing packaging machine based on the prescription data, and transmits it to the dispensing device. The tablet dispensing machine can package one or more types of tablets into dispensing papers at each dosing stage, and the powder packager can dispense one or more types of powders at each dosing stage. It is possible to divide into packing paper. There is also known a tablet packaging machine or a powder packaging machine which can package tablets and powders into the same paper package. The packing paper is formed of a transparent or translucent material, and the medicine contained in the packing paper is visible from the outside. Further, the tablet dispensing machine or the powder dispensing machine also includes a dispensing printer or the like in which a patient name, a dosing timing, a drug name and the like are described on the packaging sheet.

  Here, the dispensing support system 200 stores the prescription data in a pre-setable storage device in a sharable manner. 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 apparatus 100. The prescription data acquired from the dispensing support system 200 may be, for example, data in an original format edited by the dispensing support system. The prescription data acquired by the inspection support device 100 is not limited to the prescription data acquired by the dispensing support system 200 from the upper system, and the dispensing generated by the dispensing support system 200 based on the prescription data It may be data.

[Reception system 300]
The medical treatment system 300 receives medical treatment data such as medical treatment contents and prescription data from a host system such as an electronic medical record system or a prescription ordering system. And, the receipt system 300 is used to support receipt operations such as calculation of medical expenses and issuance of a bill based on the medical care data.

  Here, the receipt system 300 stores the prescription data in a pre-setable storage device in a sharable manner. Thereby, the inspection support device 100 can acquire the prescription data from the storage device of the receipt system 300. It is also conceivable that the prescription data is actively transmitted from the receipt system 300 to the inspection support device 100. The prescription data acquired from the receipt system 300 is, for example, a text file format defined by the NSIPS specification.

[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, an imaging unit 70, and the like. The inspection support device 100 is used to support the work of a medical worker such as a pharmacist who carries out a final inspection of the medicine dispensed based on the prescription data in a medical institution such as a hospital, health care facility or pharmacy. . The weighing device 50, the information reading unit 60, and the photographing unit 70 are communicably connected to the control unit 10 according to 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. Thus, the inspection support device 100 can be miniaturized. A configuration in which the inspection support device 100 individually includes the control unit 10, the display unit 20, the operation unit 30, and the storage unit 40 is also conceivable as another embodiment.

  The inspection support device 100 is connected to a commercial AC power supply by a power cord (not shown), and is operated by the power supplied from the commercial AC power supply. In addition, the tablet terminal 80 incorporates a secondary battery, and is charged by the commercial AC power supply. Therefore, even when the commercial AC power is shut off, the tablet terminal 80 can be operated by the secondary battery for a certain period of time, for example, data backup at the time of a power failure can be performed.

  The control unit 10 includes a CPU, a ROM, a RAM, an EEPROM, and the like. The CPU is a processor that executes various arithmetic processing in accordance with various control programs. The ROM is a non-volatile memory in which a program such as a BIOS executed by the CPU is stored in advance. The RAM and the EEPROM are a volatile memory and a non-volatile memory used for the expansion of various control programs by the CPU and the temporary storage of data.

  The display unit 20 and the operation unit 30 are user interfaces that display information for the user and receive user's operations under the control of the control unit 10. 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 device 100, the control unit 10 causes the display unit 20 to display various operation keys, and detects the operation of the operation keys by using the touch panel of the operation unit 30. Accept the operation. The operation unit 30 may include a mouse or a keyboard. Furthermore, the operation unit 30 may have a voice operation input unit that receives input of various information by voice recognition.

  Further, as shown in FIGS. 2 and 3, the inspection support device 100 includes a cover member 90 which can be opened and closed with respect to the inspection support device 100. Specifically, the cover member 90 is pivotably supported by the pivot support portion 91 at one end of the weighing device 50 so that the cover member 90 can be opened and closed with respect to the inspection support device 100. The tablet terminal 80 is disposed on the cover member 90. As described above, in the inspection support device 100, the tablet terminal 80 is disposed on the cover member 90, whereby the inspection support device 100 is miniaturized.

  Here, the tablet terminal 80 is supported by the cover member 90 in a posture in which the display surface of the display unit 20 is exposed to the inner surface side of the cover member 90. In particular, when the tablet terminal 80 closes the cover member 90 shown in FIG. 3, the display surface of the display unit 20 faces the below-described weighing units 51 to 54 provided on the weighing device 50. It is supported by a cover member 90. Thereby, as shown in FIG. 2, when the cover member 90 is opened, the display unit 20 and the operation unit 30 face the weighing units 51 to 54 of the weighing device 50. . Therefore, the user can perform inspection work without moving the line of sight in a state in which the display unit 20 and the operation unit 30 and the weighing units 51 to 54 of the weighing device 50 can be overlooked at one 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 or the like externally connected to the control unit 10.

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

  The storage unit 40 also stores various databases such as a medicine 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 receipt system 300 or the like. The drug master includes drug code, specification amount, host code, drug name, drug common name, JAN code, RSS code, YJ code (individual drug code), GS1 code, vial code, dosage form code (powder, tablet) , Liquid medicine, external medicine, etc., form code, kind of potent medicine / managed medicine (psychotropic drug, narcotic drug), management (car height, safe, cold place etc.), unit (dispensing unit), etc. is included. In addition, the drug master includes a weight per unit amount (single) (naked tablet), a weight per PTP sheet, a weight with one PTP upper ear, a weight without one ear with PTP upper tablet, It also includes information such as the number per PTP sheet and the file name of a drug image (naked medicine, package). The PTP sheet is a packaging material in which a plurality of tablets or a plurality of capsules are individually stored. In the present embodiment, a PTP sheet is described as an example, but for example, a heat seal in which a predetermined amount of tablets or powders are stored in advance is also an example of the packaging material. On the other hand, the patient master includes information such as patient code of each patient, patient name, date of birth, and gender. FIG. 22 is a view 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. 22 shows a state in which the medicine master is displayed on the master maintenance screen D13. The control unit 10 can also change the contents of the medicine master, the patient master, and the like according to the 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 device 100 is powered on or returned from the power saving mode. It is possible to identify the user of the inspection support device 100 by executing user authentication. Further, in the inspection support device 100, the control unit 10 can set the use authority for each user in advance according to the user operation or the like. For example, it is possible to set authority types such as “general”, “administrator”, “maintenance manager”, “support”, “training”, and “technician” for each user. Then, it is conceivable that the control unit 10 changes the process that can be executed by the inspection support device 100 according to the authority type corresponding to the user specified as the user. For example, the master maintenance for editing the pharmaceutical master, the daily update operation, the inspection operation of inspection history, etc. can be executed only by “general”, “manager” or “maintenance manager” among the authority types. It is. Furthermore, software settings, hardware settings, and mother master periodic updates can be executed only by the “administrator” or the “maintenance administrator” of the authority types. The mother master is, for example, a database of medicines provided by the manufacturer of the inspection support device 100 or the like. Further, it is also conceivable that only a part of each process can be executed according to the authority type. For example, with regard to the setting of the hardware, it is conceivable that “manager” of the authority types is set to be able to use only the balance calibration. Further, a configuration is also conceivable in which the control unit 10 can set a process that can be executed for each user instead of for each type of authority.

  Further, the storage unit 40 stores an inspection support program executed by the control unit 10. The inspection support program is downloaded, for example, via the network N1, or read from a recording medium by a disk drive and installed in the storage unit 40. Then, the control unit 10 executes various processes in accordance with the inspection support program, whereby the weighing specification unit 11, unit weight acquisition unit 12, unit conversion processing unit 13, verification processing unit 14, visual inspection processing unit 15, It functions as the inspection completion notification unit 16, the display processing unit 17, and the photographing processing unit 18. In addition, a part or all of the control unit 10 may be an electronic circuit such as an ASIC. The operation of each processing unit included in the control unit 10 will be described in conjunction with a flowchart in a later stage.

  The weighing device 50 includes four weighing units 51 to 54, and is used to weigh the weight of medicine. The weighing results by the weighing units 51 to 54 are input to the control unit 10. Hereinafter, in the present embodiment, for the sake of convenience of description, when the non-specific weighing units 51 to 54 are shown, the “weighing unit 5N” may be referred to. In the present embodiment, the weighing device 50 will be described as an example having a configuration including four weighing units 51 to 54. However, the weighing device 50 may include at least two or more weighing units. Just do it.

  As shown in FIG. 2, FIG. 4 and FIG. 5, the weighing unit 5 N includes a weighing dish 55, a load cell 56, and a placing unit 57. 4 is a view showing a state in which the weighing dish 55 is removed, and FIG. 5 is a view showing a state in which the weighing dish 55, the placing portion 57 described above, and the upper surface 501 of the weighing device 50 are removed. .

  The weighing dish 55 is placed on the placing section 57 and used, and the medicine to be weighed is placed on the weighing dish 55. As shown in FIG. 2, each of the weighing dishes 55 has a different radius of roundness between the corner 551 on one diagonal and the corner 552 on the other diagonal. Specifically, the pair of corner portions 551 has a smaller radius than the corner portion 552, for example, one of the corner portions 551 is gripped by the user when the weighing pan 55 is lifted, and the other corner portion 551 is inserted into the medicine bag when the medicine on the weighing dish 55 is contained in the medicine bag. The weighing pan 55 may have a configuration in which the corner 551 and the corner 552 have the same radius.

  Further, a non-slip member for increasing the frictional resistance between the bottom surface of the weighing dish 55 and the upper surface of the placing section 57 on one or both of the bottom surface of the weighing dish 55 and the top surface of the placing section 57. Is considered to be provided. Thereby, in the inspection support device 100, the shaking of the weighing pan 55 placed on the placing portion 57 can be suppressed, and the weighing using the weighing pan 55 can be stably performed. When the anti-slip member is provided on the weighing pan 55, the anti-slip member is provided on part or all of the bottom surface of the weighing pan 55. Similarly, when the mounting portion 57 is provided with the anti-slip member, the anti-slip member is provided on part or all of the upper surface of the mounting portion 57. Furthermore, it is considered that the non-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 section 5N is not stable Is avoided. The anti-slip member may be provided on a large plate 58 described later.

  The load cell 56 is a load converter which supports the placing portion 57 and measures the weight of the object to be weighed placed on the placing portion 57. In the inspection support device 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 placing portion 57. As the load cell 56, for example, a load cell having a small rated capacity of 300 g or 500 g and a high weighing accuracy is used. In addition, it can be considered 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 top surface. Further, on the upper surface of the placing portion 57, a concave portion for stably placing the bottom surface of the weighing pan 55 is formed. By the way, it is also conceivable that the load cell 56 and the placing portion 57 are connected below the upper surface 501 of the weighing device 50, and a large sized opening corresponding to the placing 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 placing portion 57, and there is a problem that dust and the like are easily introduced into the inside from the gap. On the other hand, in the weighing device 50, the load cell 56 and the placing portion 57 are connected above the upper surface 501, and the upper surface 501 is formed with a small opening corresponding to the connection point. . Thereby, in the weighing device 50, a structure in which dust and the like are less likely to enter from the opening of the upper surface 501 is realized.

  In the weighing device 50, the weighing result by the load cell 56 includes the weight of the weighing dish 55 and the placing portion 57. Therefore, the control unit 10 performs taring at the time of weighing using the load cell 56, and weighs a value obtained by subtracting the tare weight of the weighing tray 55, the placing portion 57, and the like from the weighing result of the load cell 56. Acquired as a result of weighing of the medicine placed on the plate 55. Although the tare weight is initially set at the time of shipment of the inspection support device 100, the inspection support device 100 can also reset the tare weight at an arbitrary timing. When the anti-slip member is provided on one or both of the weighing pan 55 and the placing portion 57 as described above, the weight of the anti-slip member is also included in the tare weight.

  Further, as shown in FIG. 6, in the weighing device 50, instead of the plurality of weighing dishes 55, weighing of the drug is performed using a large plate 58 (an example of the extended placement unit) larger than the weighing dishes 55. It is possible to do. The large plate 58 can be placed over the plurality of weighing units 51 to 54. Specifically, a convex portion 581 is provided on the bottom surface of the large plate 58 at a position corresponding to the placing portion 57 of the plurality of weighing portions 51 to 54. Then, in the weighing device 50, after the weighing pan 55 is removed as shown in FIG. 4, each of the convex portions 581 of the platter 58 is in front of the plurality of weighing portions 51 to 54 as shown in FIG. The information is placed on each of the placement units 57. Thereby, 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 2.0 kg in total by using the large plate 58. Further, the platter 58 is not limited to the usage form in which the plurality of weighing trays 55 is replaced with the plurality of weighing units 51 to 54 and the plurality of weighing trays 55 are described above. It is also conceivable to be placed over the plurality of weighing dishes 55 in the state of being placed on the placing portion 57. Thereby, the user does not have to attach and detach each of the weighing pans 55, which improves the convenience. The convex portion 581 of the platter 58 and the placing portion 57 and the weighing pan 55 are placed on the placing portion 57 of the four weighing portions 51 to 54 or the weighing pan 55. It has a shape that stabilizes in the closed state.

  Furthermore, in the large plate 58, a cross portion 582 indicating the center position of the large plate 58 is formed. As a result, 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. Furthermore, when no medicine is placed on the center of the large plate 58, the load acting on the weighing units 51 to 54 from the large plate 58 is biased, and only the weighing value of any of the weighing units 51 to 54 is It is conceivable to exceed the rated capacity. For example, when the rated capacity of each of the weighing units 51 to 54 is 200 g and 500 g of the medicine is placed on the large plate 58, any one or more of the weighing values of the weighing units 51 to 54 can be obtained. May exceed the rated capacity of 200 g. Therefore, when the control unit 10 uses the large plate 58, the load is equally applied when the difference in the weighing value by each of the weighing units 51 to 54 exceeds a predetermined range. If not, it is possible to display a warning message such as “Please center”.

  Further, the cross portion 582 serves as an index for setting the platter 58 at the center of the weighing portions 51 to 54 so that the load acts evenly on the weighing portions 51 to 54, and the user operates the platter 58 It is also considered that it becomes easy to set to the center of the said weighing parts 51-54. For example, it is also conceivable that an index portion for determining the center position of the weighing portions 51 to 54 is formed on the upper surface 501. In this case, reference is made to the cross portion 582 and the index portion. At the same time, it becomes easier to set the platter 58 at the center of the weighing parts 51-54. Further, on the inner wall surface of the large plate 58, a recessed portion 583 is formed which indicates the central position in the longitudinal direction and the central position in the lateral direction in a plan view of the large plate 58. Therefore, even when the cross portion 582 is hidden by the medicine in the large plate 58, the central position of the large plate 58 can be estimated with reference to the concave portion 583, and the user weighs the large plate 58. It becomes easy to set to the center of the parts 51-54. Furthermore, when the large plate 58 is photographed by the photographing unit 70, the control unit 10 determines the center position of the large plate 58 based on the position and shape of the cross portion 582 or the concave portion 583 included in the photographed image. It is possible to detect For example, it is conceivable that the control unit 10 displays a warning on the display unit 20 when the center position of the large plate 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 bar code (JAN, GS1) or a two-dimensional code such as a QR code (registered trademark). It is a barcode reader to be 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”) described in 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, and the prescription identification information includes a prescription number and an Rp number for identifying Rp data of the same usage unit to be accommodated in the same medicine bag. And so on. The prescription identification information may be other information such as order information as long as the information can identify the Rp data.

  In addition, the information reading unit 60 is also used to read identification information (hereinafter referred to as “drug identification information”) described in a medicine packaging material such as a packaging paper or a PTP sheet in order to identify the medicine. Be The medicine identification information is, for example, a JAN code, an RSS code, a YJ code, or a GS1 code.

  Then, when the prescription identification information is read from the medicine bag by the information reading unit 60, the control unit 10 can obtain prescription data corresponding to the prescription identification information from the storage unit 40. . In addition, when the medicine identification information is read from the packaging material by the information reading unit 60, the control unit 10 specifies the type of medicine corresponding to the medicine identification information based on the medicine master. It is possible. In addition, in the kind of medicine, the same medicine in which specification quantity differs is also contained as a medicine of a different kind. For example, "Memary tablet 5 mg", "Memary tablet 10 mg", and "Memary tablet 20 mg" are treated as different types of drugs because they have the same drug name but different specification amounts.

  The imaging unit 70 includes a camera body 710 and a holding member 720 for holding the camera body 710, as shown in FIG. The camera body 710 is a digital camera used to capture a still image or a moving image of a subject. In the inspection support device 100, the imaging unit 70 captures an image according to a control instruction from the control unit 10, and the captured image is transmitted from the imaging unit 70 to the control unit 10. It is also conceivable that moving image information of a shooting range captured by the shooting unit 70 is input to the control unit 10, and the control unit 10 acquires a still image from the moving image information. In this case, the control unit 10 can determine the situation within the imaging range of the imaging unit 70 as needed based on the moving image information.

  Here, it is conceivable that the photographing unit 70 is disposed at a position and an orientation at which the weighing units 51 to 54 of the weighing device 50 and the display unit 20 can be photographed at the same time. By the way, in the photographing unit 70, the connecting portion 711 provided on the camera main body 710 is held by the holding member 720, whereby the camera main body 710 is held by the holding member 720. At this time, the holding member 720 holds the camera body 710 in a state in which the photographing range of the camera body 710 can be adjusted within a predetermined predetermined range (for example, about 1 mm). For example, the holding member 720 has a swing mechanism capable of swinging the holding portion for holding the connecting portion 711 of the camera body 710 within a predetermined width range. As a result, in the inspection support device 100, by finely adjusting the direction of the camera main body 710 held by the holding member 720, it is possible to easily adjust the photographing range photographed by the photographing unit 70. It is. In addition, the imaging unit 70 may be capable of imaging at least the weighing units 51 to 54, and the display unit 20 may not be included in the imaging range as another embodiment. Furthermore, the imaging unit 70 may be fixed to the cover member 90.

  Note that, 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 is mounted on the rotation support unit 72. It is rotatably coupled to the support arm 73 via the support arm 73. Thereby, the user can also finely adjust the imaging range of the imaging unit 70 by rotating the support arm 71. On the other hand, the support arm 73 is fixed to the weighing device 50. In addition, as the other embodiment, the support arm 73 is rotatably supported by the weighing device 50, and when the cover member 90 is closed, the support arm 73 can be rotated to be compactly folded. Conceivable.

[Inspection support processing]
Hereinafter, an example of the procedure of the inspection support process executed by the control unit 10 according to the inspection support program in the inspection support device 100 will be described with reference to the flowchart of FIG. 7. Specifically, the inspection support process is started by the control unit 10 when the inspection support device 100 is powered on or returned from the power saving mode. In addition, the inspection support process ends when the inspection support device 100 is shut down, or when there is no operation for a predetermined time or more and the power saving mode is entered. 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. By doing this, the user of the inspection support device 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. Here, FIG. 8 is a view 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 paper package selection key K12, a visual inspection key K13, a platter use key K14, a tare weight withdrawal 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. Further, on the prescription inspection screen D10, weighing display areas A11 to A14 and a prescription display area A15 are displayed. The name of the user authenticated by the user authentication is also displayed as the certifier on the prescription inspection screen D10. The control unit 10 also displays an authentication screen for performing the user authentication again, for example, when the vicinity of the user's name is operated, and the certifier is displayed according to the subsequent input of the user ID, password, etc. It is possible to switch.

  The unprocessed information key K11 is an operation key for displaying a list of unprocessed prescription data whose 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 causes the prescription inspection screen D10 to display an unprocessed display area A21 in which a list of unprocessed prescription data is shown as shown in FIG. In the unprocessed display area A21, information such as a prescription date, a patient name, a total Rp number, and a voucher number is displayed in a list as information for identifying unprocessed prescription data.

  A search operation area A22 and a detail display key K21 are displayed in the unprocessed display area A21. The control unit 10 searches the prescription data according to the item selected in the search operation area A22 and the input character input in the search operation area A22, and displays the search result. 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, and the unprocessed display area A21 is a prescription. The list of prescription data on 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 causes the detail information to be displayed for the prescription data of the portion where the detail display key K21 is displayed. The detailed information includes, for example, contents (drug name, usage, daily dose, etc.) of prescription data (hereinafter referred to as “Rp data”) of one or more same usage units included in the prescription data. Each of the Rp data includes one or more types of prescription drugs which are contained in the same medicine bag and have the same usage.

  Referring back to FIG. 8, when the medicine identification information is read from the packing paper by the information reading unit 60, the packing paper selection key K12 does not include specific information set in advance in the medicine identification information. It is an operation key for designating the type of the packing paper to be used when weighing the packing paper. For example, there are ten types of the packaging paper, such as 60 mm, 70 mm, 76 mm, 80 mm, and 90 mm for each of the cellopoly and the glassine. The control unit 10 displays, in response to the operation of the packing paper selection key K12, a plurality of packing papers registered in advance as selection candidates, and sets in advance corresponding to the packing paper selected therefrom. The set weight is set as the weight of the packaging paper used in weighing inspection processing described later. The specific information is, for example, in a dispensing device such as a tablet packing machine or a powder medicine packing machine where the packing process using the packing paper is performed, the weight of the packing paper is known, and the medicine identification information It is information for determining whether or not the weight of the packing paper is included in the weight per packing paper of the packing paper included in or the total weight of all the packing papers. For example, the specific information is information for specifying the maker of the tablet dispensing machine or the powder dispensing machine.

  The visual inspection key K13 is an operation key for executing visual inspection processing 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 D11 for performing visual inspection on each of the medicines being displayed is displayed on the display unit 20. As shown in FIG. 10, on the visual inspection screen D11, a medicine information display area A31, a medicine image display area A32, a target value display area A33, and an inspection input area A34 are displayed corresponding to each medicine. There is.

  Specifically, the control unit 10 reads out the medicine name or the like of the medicine for visual inspection to be selected on the prescription display screen D10 from the prescription data or Rp data, and displays the same on the medicine information display area 31. Further, the control unit 10 reads out the medicine image of the medicine to be visually inspected from the medicine master and displays it on the medicine image display area A32. Furthermore, the control unit 10 reads out and displays the target value of the medicine for visual inspection from prescription data or Rp data. The control unit 10 causes the storage unit 40 to store the numerical value input to the inspection input area A34 in association with the visual inspection target chemical as the inspection history. Here, units such as "lock", "g", "package", "capsule" and the like displayed in the inspection input area A34 are units set in advance for each medicine in the medicine master. In addition, when all the medicines for visual inspection can not be displayed on the visual inspection screen D11, the control unit 10 performs the visual inspection object according to the left and right flick operation on the visual inspection screen D11 or the operation of the arrow key. Scroll the drug display to make it appear.

  Then, when the confirmation key K31 is operated on the visual inspection screen D11, the control unit 10 processes as if visual inspection of the visual inspection target medicine displayed on the visual inspection screen D11 is completed, It stores in the storage unit 40 as an inspection history. As described above, in the visual inspection process, the information such as the medicine name, the medicine image, and the target value of the visual inspection target medicine is displayed on the visual inspection screen D11, so that the user refers to the visual inspection screen D11. The visual inspection of the medicine to be visually inspected can be easily performed.

  Referring back to FIG. 8, the platter use key K14 is an operation key for executing the weighing inspection process using the platter 58. The control unit 10 displays one weighing display area A41 on the prescription inspection screen D10 in place of the weighing display areas A11 to A14 as shown in FIG. 11 in response to the operation of the platter use key K14. . The control unit 10 may consider, for example, graying out or non-displaying the weighing display areas A11 to A14. In the weighing display area A41, the sum of all weighing values of the weighing units 51 to 54 is displayed as a weighing result. Further, in the weighing display area A41, in the weighing inspection process described later, the comparison result of the weighing result when the large plate 58 is used and the prescription data is displayed. As a result, in the inspection support device 100, it is possible to perform weighing inspection using the large plate 58 even for a large amount of medicine that is difficult to measure in each of the weighing trays 55 or a medicine having a large size.

  The tare weight pulling key K15 is used for the start operation of the tare weight pulling processing for updating the setting value of the tare weight of the tare weight pulling 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 pull key K15 after placing the platter 58 on the weighing units 51 to 54. Thereby, 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 measure the weight of the medicine placed on the weighing pan 58 by subtracting the tare weight from the weighing value measured by the weighing units 51 to 54. At this time, when the large dishes 58 are placed on each of the weighing dishes 55, the weight of the four weighing dishes 55 is also included in the tare weight. Even when the platter 58 is changed to the weighing tray 55, the tare weight pulling key K15 is operated to set the tare weight corresponding to the weighing tray 55.

  The menu key K16 is an operation key for displaying a menu of various functions of the inspection support device 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 in response to the operation of the menu key K16.

  The inspection completion key K17 executes, in the inspection support device 100, a visual inspection process or a weighing inspection process to be described later for the drug whose inspection is not completed among the Rp data currently displayed on the prescription inspection screen D10. It is operated when ending inspection without. According to the operation of the inspection completion key K17, the control unit 10 completes the inspection of the medicine for which the inspection has not been completed among the Rp data currently displayed on the prescription inspection screen D10, and the history is displayed as the history After storing in the storage unit 40, the inspection of the Rp data is ended. As a result, even if an unaudited drug which can be judged properly by the pharmacist by visual inspection remains, the inspection operation is performed by operating the inspection completion key K17 to complete inspection of the displayed Rp data. It is possible to speed up the When the inspection is compulsorily completed by operating the inspection completion key K17, the control unit 10 causes the display unit 20 to display an inspection completion screen indicating that the inspection is completed. Conceivable. On the inspection completion screen, a check mark of a first color determined in advance is attached to a weighed inspection inspected chemical inspected in a measurement inspection process described later among the Rp data, and a visual inspection inspected in a visual inspection process described later The checked medicine is marked with a check mark of a predetermined second color different from the first color. Moreover, about the unchecked medicine which is not checked by the said weighing inspection process or the said visual inspection process among the said Rp data, it is a mode (for example, without a check mark) distinguishable with the said weighing inspected medicine and the said visually inspected medicine. Is displayed. In the inspection completion screen, it is sufficient if the weighing inspection inspected drug, the visual inspection completed, and the unaudited medicine can be distinguished on the inspection completion screen, and, 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 imaging unit 70 to capture an image according to the operation of the imaging key K18. Then, the control unit 10 associates the photographed image with the prescription data to which the Rp data currently displayed on the prescription inspection screen D10 belongs, and records it in the storage unit 40 as an inspection history. Thereby, the control unit 10 can display the photographed image stored in the storage unit 40 for each of the prescription data. It is also conceivable as another embodiment that the control unit 10 associates the photographed image with each Rp data and stores the image in the storage unit 40. Further, as another method of use, the prescription, the medicine bag, and the medicine corresponding to the prescription data which is the subject of the inspection by the user after the inspection of the medicine using the inspection support device 100 is completed, the weighing device It is conceivable that the photographing key K 18 is operated after being placed within the photographing range of the photographing unit 70 such as the upper surface 501 of 50. Thereby, 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 view showing an example of the 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 an extraction result, and the list display A history content display area A53 in which the content of the inspection history selected in the area A52 is displayed is displayed. Specifically, in the extraction condition display area A51, it is possible to input an inspection period (inspection date and time), a prescription date, a patient name, a medicine name, a pharmacist name, and yellow determination presence or absence. Here, FIG. 32 is a view showing an example of an input screen of the inspection period. In the input screen shown in FIG. 32, the start date (year, month, day, hour, minute, second) of the inspection date and the end date (year, month, day, hour, minute, second) of the inspection date can be entered It is. Then, the control unit 10 reads out from the storage unit 40 the inspection history that matches the conditions input in the extraction condition display area A51, and displays a list on the inspection history inquiry screen D12. In the history content display area A53, the target column displays the target value (tablet, capsule, sheet, etc.) of the medicine corresponding to the prescription data, and the inspection column shows the weighing by the inspection support apparatus 100. The converted value (tablet, capsule, sheet, etc.) obtained by converting the weighed value of the medicine into the medicine unit is displayed. However, among the prescription medicines, the word “visual” is displayed in the inspection column of the medicine that has been inspected in the visual inspection process described later. Further, on the inspection history inquiry screen D12, a thumbnail image of the image taken by the imaging unit 70 stored in the storage unit 40 as the inspection history of the prescription data selected in the list display area A52 is 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. The control unit 10 enlarges and displays the photographed image corresponding to the image display key K19 on the inspection history inquiry screen D12 in response to the operation of the image display key K19.

  Referring back to FIG. 8, the image display key K 19 is a thumbnail image of a photographed image by the photographing unit 70 stored in the storage unit 40 as an inspection history of prescription data displayed in the prescription display area A 15. . In FIGS. 8 and 12, although "image 1" to "image 4" are displayed as the thumbnail image names under the image display key K19, "Rp No." and " It is also conceivable that a "number" 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, in response to the operation of the image display key K19, the control unit 10 enlarges and displays a thumbnail image corresponding to the image display key K19.

  The weighing display areas A11 to A14 are display areas respectively corresponding to the weighing parts 51 to 54, 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 unit 51 is disposed at the upper left similarly to the weighing unit 51, and the weighing display area A12 corresponding to the weighing unit 52 is disposed at the upper right as the weighing unit 52 It is done. As described above, 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. The display processing is performed by the display processing unit 17 of the control unit 10. Hereinafter, in the present embodiment, for the sake of convenience of description, when the weighing display areas A11 to A14 which are not specified are indicated, the “weighing display area A1M” may be referred to.

  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. In addition, about the medicine in which the medicine image is not registered into the said pharmaceutical master, it replaces with a medicine image and the character of "no image" is displayed. Further, in the prescription display area A15, the prescription medicine included in the Rp data can be selected, and the selected one or more prescription medicines are marked with a check mark to be in a selected state. Further, even when the drug identification information is read by the information reading unit 60, the prescribed drug corresponding to the drug identification information is marked with a check mark and is in a selected state. Note that among the prescription drugs displayed in the prescription display area A15, the medicine that has already been inspected in the visual inspection process described later is displayed in a color different from that of the other medicines in the background color.

<Steps S12 to S13>
Next, in steps S12 to S13, the control unit 10 determines whether an operation for specifying prescription data to be inspected in the inspection support device 100 has been performed. Specifically, in step S12, the control unit 10 determines whether the prescription identification information described in the medicine bag has been read by the information reading unit 60. In step S13, the control unit 10 determines whether an operation of selecting prescription data from the unprocessed list has been performed. Then, when the prescription data is specified (S12 or S13: Yes side), the control unit 10 shifts the process to step S14.

<Step S14>
In step S14, the control unit 10 reads out 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. Here, such processing is executed by the collation processing unit 14 of the control unit 10. When the Rp data is selected in the detailed information displayed according to the operation of the detail display key K21 of the unprocessed display area A21, the control unit 10 specifies the Rp data as an inspection target. It is also conceivable.

  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 the user operation. Here, such processing is executed by the collation 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. If the prescription data is selected in step S13, the Rp data to be inspected is not identified even if the prescription data includes a plurality of Rp data. Therefore, as shown in FIG. 8, in the prescription display area A15, a designation RpNo "1/3" for indicating the Rp data to be currently displayed among the Rp data included in the prescription data is displayed. There is.

  For example, the designation 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 changes 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 corresponds to the designation RpNo after the change. Rp data to be displayed is displayed on the prescription display area A15. Further, when the medicine identification information is read from the medicine packaging material by the information reading unit 60, the control unit 10 corresponds to the medicine identification information from the prescription data displayed in the prescription display area A15. The Rp data including the drug to be selected is searched, 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 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 the step S12, Rp data corresponding to the prescription identification information is displayed on the prescription inspection screen D10, and the indication of the designation RpNo in the prescription display area A15 is It is omitted.

<Step S15>
Subsequently, in step S15, when there is a visual inspection setting medicine set in advance as a medicine to be inspected in the visual inspection process in the prescription data or the Rp data (S15: Yes side), The process shifts to step S151 to execute visual inspection processing described later. In this case, the visual inspection set medicine is specified as the visual inspection target medicine targeted for visual inspection. The visual inspection setting medicine is, for example, a medicine having no bar code attached to a medicine packaging material, or a medicine prepared by mixing and dispensing water or a paste. In addition, when the chemical | medical agent handled as said chemical | medical agent for visual inspection does not exist in the said prescription data or said Rp data (S15: No side), a process transfers to step S16. In addition, omitting the step S15 is also considered as another embodiment.

<Step S16>
In step S16, when the operation for starting the visual inspection is performed (S16: Yes side), the control unit 10 shifts the process to step S151, and the operation for starting the visual inspection should not be performed. For example (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 the operation was performed. In this case, one or more 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 packaging paper which is a medicine packaging material (S17: Yes side), the control unit 10 shifts the process to step S171 and performs visual inspection processing described later. Run. For example, the medicine identification information corresponding to the medicine packaged in the packing paper is recorded in the packing paper by a code such as QR code (registered trademark). Further, when the medicine identification information is not read from the paper package (S17: No side), the control unit 10 shifts the process to step S18.

<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 medicine 10 sets the prescribed medicine corresponding to the medicine identification information as the weighing inspection medicine The process is specified, and the process proceeds to step S19 to execute the weighing inspection process described later. Further, when the medicine identification information is not read from the PTP sheet (S18: No side), the control unit 10 returns the process to the step S16. Even when the medicine identification information is read, if the medicine corresponding to the medicine identification information is registered in advance as a medicine for which the weighing inspection process is not performed, or if the medicine corresponding to the medicine identification information If 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.

  Further, 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 determined in advance. When the start operation of the weighing inspection process is performed, it is also possible to shift the process to step S19 and execute the weighing inspection process for the medicine. For example, the start operation of the weighing inspection process is a long press operation of the display area of the medicine, an operation of a weighing inspection key (not shown) displayed on the prescription inspection screen D10, or the like. On the other hand, when the start operation of the weighing inspection process is not performed, the process is returned to the step S16. The target medicines for which the start operation of the weighing inspection process is optionally performed are, for example, medicines in which the medicine identification information is not attached to the packaging material, medicines in which a plurality of sheets are in one package, and tablets. For example, medicine after packaging that is packaged in a packaging machine.

<Steps S151, S171>
In step S151 or step S171, the control unit 10 executes a visual inspection process for supporting a task for the 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 causes the display unit 20 to display the visual inspection screen D11 (see FIG. 10). The control unit 10 causes the visual inspection screen D11 to display the one or more prescription medicines specified in the steps S15 to S17 as the medicine for visual inspection. Specifically, when the medicine identification information of the packaging paper is read in the step S17, the control unit 10 selects one or more of the medicines stored in the packaging paper based on the medicine identification information. Identify the drug as the drug for visual inspection. Then, the control unit 10 reads out the medicine name, medicine image (naked tablet image), target value, etc. of the medicine for visual inspection, from the prescription data, the Rp data, or the medicine master, and the visual inspection screen Display on D11. Thereafter, when the confirmation key K31 of the visual inspection screen D11 is operated, the control unit 10 processes as if visual inspection of the visual inspection target medicine displayed on the visual inspection screen D11 is completed, It stores in the storage unit 40 as an inspection history. In addition, it is considered that the control unit 10 automatically dismisses the visual inspection screen D11 by judging that visual inspection has ended when a predetermined time set in advance has passed after the display of the visual inspection screen D11. Be Furthermore, after displaying the visual inspection screen D11, the control unit 10 may automatically cause the enlarged screens of the medicine images to pop-up in order and erase them after a predetermined time.

  By the way, when the medicine identification information is read from the PTP sheet by the information reading unit 60 while the control unit 10 is displaying the visual inspection screen D11, among the medicines displayed on the visual inspection screen D11 It is conceivable that, regarding the medicine corresponding to the medicine identification information, it is stored in the storage unit 40 as the inspection history that the verification based on the medicine identification information has been performed. Thereby, for example, when the medicine decapsulated from the PTP sheet is divided into the packing paper by the tablet packing machine or the powder packing machine, the GS1 code or the like from the PTP sheet after the packing is read from the information reading unit By reading at 60, the trouble of visual inspection of at least some of the medicines packaged in the packaging paper is reduced. For example, as described above, the result of the comparison process of the drug identification information in the visual inspection is reflected in the result of the "bar code confirmation" of the history display area A53 in FIG.

  When the medicine identification information on the packaging paper is read in the step S17, in the visual inspection process, the user performs inspection with reference to the medicine in the packaging paper and the visual inspection screen D11. There is a need. On the other hand, for the medicine identification information printed on the packing paper in a dispensing device such as the tablet packing machine or the powder packing machine, the drug names and dosage forms of all medicines contained in the packing paper It is conceivable that package information on contents such as dispensing amount (weight or quantity) and patient information is included. Therefore, when the medicine identification information of the packaging paper is read in the step S17, the control unit 10 collates the package information contained in the medicine identification information with the prescription data, and the collation result If they agree, it is conceivable to complete the inspection of each of the medicines contained in the paper without performing the visual inspection process and the weighing inspection process. As a result, it is possible to reduce the time and effort for visual inspection of the medicine that has been packaged in the packaging paper by the dispensing device.

<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, and if the weighing inspection setting is set to ON (S172: Yes Side) shifts the processing 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 related to whether or not the weighing inspection processing using the weighing device 50 is performed together with the visual inspection processing when the medicine identification information is read from the packing paper in the step S17. The control unit 10 can arbitrarily change the content of the weighing inspection setting according to a user operation at the time of setting the environment of the inspection support device 100 or the like. In addition, when the medicine identification information is read from the packing paper in the step S17, the control unit 10 may switch whether to execute the weighing inspection process according to the 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 packing paper but also for medicines predetermined as medicines that can be weighed by the inspection support device 100. Be

<Step S19>
Then, in step S19, the control unit 10 starts a weighing inspection process including a collation process of collating the measurement result by the weighing unit 5N with the prescription data. Here, the processing is an example of the collation processing step, and is executed by the collation processing unit 14. Specifically, in step S19, the control unit 10 shifts the process to step S20 after starting the new weighing inspection process corresponding to the medicine identification information. 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 the step S18. Therefore, when the medicine identification information is sequentially read from a plurality of PTP sheets, a plurality of weighing inspection processes are activated by the control unit 10, and the weighing inspection processes thereof are executed in parallel. Become. Also, when the weighing inspection setting is ON, the weighing inspection processing is individually started each time the medicine identification information is read from the packing sheet.

  By the way, when the medicine identification information of the packing paper includes the weight of one package including the weight of the packing paper or the total weight of all the packing paper, the packing paper from the packing paper In the weighing inspection process of step S19 executed when the drug identification information is read, the weighing result by the weighing unit 5N is included in one package including the weight of the packaging material included in the drug identification information. It is conceivable to check with the weight of the minutes or the total weight of all the paper sheets. Dispensing data or dispensing data at the time of dispensing performed based on the prescription data as described above is also an example of the prescription data. In addition, when the medicine identification information of the packaging paper does not include the weight of one package including the weight of the packaging paper or the total weight of all the packaging papers, the control unit 10 performs the distribution Set the number of packages for the weighing inspection object medicine and the weight corresponding to the package paper for the test according to the type of packing paper selected after the operation of the packing paper selection key K12 or the type of packing paper set in advance. It is conceivable to execute the weighing inspection process in addition to the value. Furthermore, when the medicine identification information of the packaging paper does not include the weight of one package including the weight of the packaging paper or the total weight of all the packaging papers, the control unit 10 performs the distribution It is also conceivable to calculate the total weight on the basis of the medicine name, YJ code, fraction and the like which are divided into the packaging paper, and to collate the value with the weighing result by the weighing unit 5N.

<Step S20>
Thereafter, in step S20, the control unit 10 checks whether or not inspection of all of the Rp data specified in step S12 or all of the prescription medicines included in the prescription data specified in step S13 is completed. To judge. Specifically, the control unit 10 determines whether inspection by either the visual inspection process or the weighing inspection process has been completed for all the drugs included in the Rp data or the prescription data. Here, when the control unit 10 determines that the inspection has been completed for all the prescribed medicines (S20: Yes side), the control unit 10 shifts the process to step S21. In addition, when the control unit 10 determines that the prescription medicine whose inspection has not been completed remains (S20: No side), the process returns to the step S16.

<Step S21>
In step S21, the control unit 10 causes the display unit 20 to display an inspection completion notification indicating that inspection of the Rp data or the prescription data is completed, and returns the process to step S11. Here, the processing is executed by the inspection completion notification unit 16 of the control unit 10. Thereby, the user can clearly grasp that the inspection of the Rp data or the prescription data is completed by referring to the display of the display unit 20. It is also conceivable that the inspection support device 100 is connected to the printer via the network N1. In this case, it is conceivable that the control unit 10 can print the execution record of the inspection on the Rp data or the prescription data for which the inspection has been completed in the step S21 using the printer. The implementation record of the inspection includes, for example, patient information (patient name, patient ID, age, gender, etc.), usage, medicine, inspection result (weighing result, target value, collation result, etc.) and the like. Specifically, the control unit 10 automatically prints the inspection implementation record in the step S21, or prints the inspection implementation record according to the user operation on the screen on which the inspection completion notification is displayed. It is conceivable. The control unit 10 can also set in advance whether or not to automatically print the inspection execution record according to the user operation. Further, 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.

  Note that, when the prescription data is specified in step S13, the control unit 10 causes the display unit 20 to display an inspection completion notification each time inspection of the Rp data included in the prescription data is completed. Is also conceivable. As a result, inspection is performed in units of the Rp data, and inspection can be performed collectively for each prescription drug to be contained in the same medicine bag.

[Weighing check processing]
Subsequently, 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 packing sheet is the prescription data of the inspection target displayed in the prescription display area A15 or It is determined whether it is included in 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 shifts the process to step S301. In addition, even if the inspection target is prescription data, when the setting to execute the inspection for each Rp data is performed in advance, the control unit 10 reads the information read in step S30. It is conceivable to determine whether a drug corresponding to drug 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 causes the display unit 20 to display an error message, 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 in the storage unit 40 the weight per unit amount of medicine corresponding to the medicine identification information read in the step S17 or the step S18 (hereinafter referred to as "unit weight"). Acquired from the said pharmaceutical master. Here, the processing is performed by the unit weight acquisition unit 12 of the control unit 10. The control unit 10 may obtain the unit weight of the medicine from an external storage device. For example, when the drug identification information is a tablet, the weight per unit amount of the tablet is read from the pharmaceutical master.

  By the way, when the unit weight is less than 1.6 g, the influence of the error becomes large. Therefore, when the unit weight obtained in the step S31 is less than a predetermined value such as 1.6 g, the control unit 10 makes the background color of the weighing display area A11 to A14 a predetermined light yellow or the like. It is possible to change. Accordingly, the user can perform the inspection while paying attention to the small unit weight. In addition, it is conceivable that the prescription data or the Rp data may contain the same drug different in dose or usage. In this case, the control unit 10 specifies, for example, the topmost medicine displayed in the prescription display area A15 among the same medicine corresponding to the medicine identification information at the first time as the medicine for weighing inspection, and the inspection after the next time Among the uncompleted drugs, the topmost drug displayed in the prescription display area A15 is specified as the weighing inspection drug. Further, as another embodiment, the control unit 10 similarly sets the background color of the weighing display area A11 to A14 even when the unit weight acquired in the step S31 is equal to or larger than the preset allowable maximum value. It is conceivable to change to a predetermined light yellow or the like.

<Step S32>
Next, in step S32, the control unit 10 determines whether the weighing value of one of the weighing units 5N has increased from zero. Here, when the control unit 10 determines that the weighing value of the weighing unit 5N of any of the weighing units 51 to 54 has increased from 0 (S32: Yes side), the control unit 10 shifts the process 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 control unit 10 shifts the process 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 a weighing unit to be associated with the medicine identification information read in step S17 or S18. That is, the control unit 10 specifies one or more of the weighing units 5N whose weighing value is increased from 0 after the reading of the medicine identification information by the information reading unit 60 as a weighing unit to be associated with the medicine identification information. Here, the specifying process is an example of the 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 drug identification information is read and before the drug identification information is read next, the plurality of weighing units 5N are read. Is associated with the medicine identification information that has been read in advance. Thereby, the user can divide the bundle of the same kind of medicine into plural pieces and place the bundle on the weighing unit 5N.

  In the inspection support apparatus 100 configured as described above, when there is a weighing unit whose control value has increased from a value with a weighing value larger than 0 among the weighing units 5N (S32: No side) The weighing unit is not specified as a weighing unit to be associated with the drug identification information. Therefore, the control unit 10 measures the weighing by the weighing unit 5N to be associated with the medicine identification information read one before and the weighing by the weighing unit 5N to be associated with the medicine identification information read next. Even in the case of progressing at the same time, it is possible to distinguish the weighing units 5N and to associate them with the medicine identification information.

  Further, 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 steps S35 and S36 described later. 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 released. 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 the display of the amount of medicine according to the weighing value by the weighing unit 5N specified in the step S33. Specifically, the control unit 10 converts the measurement result of the weighing unit 5N into a predetermined unit, and displays the unit 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 updating of the display of the weighing result is executed until the weighing result of the weighing unit 5N is stably determined. Here, the unit conversion processing unit 13 of the control unit 10 executes a process of converting the measurement result by the weighing unit 5N into a unit determined in advance based on the unit weight acquired in the step S31. . Further, the processing of causing the weighing display area A1M to display the weighing result by the weighing unit 5N converted into a predetermined unit is executed by the display processing unit 17 of the control unit 10. The unit of medicine (tablet, capsule, package, sheet, g, etc.) after conversion of the weighing result is the same as the unit of drug (tablet, capsule, packet, sheet, g, etc.) used in the prescription data, for example. It is.

  By the way, in the inspection support device 100, it is conceivable that the accuracy (range) of weighing by the weighing unit 5N can be switched. Specifically, it is conceivable that the weighing unit 5N includes a weighing control unit that inputs a weighing value measured using the load cell 56 to the control unit 10. The weighing control unit is, for example, a control unit such as an ASIC or an MPU. Then, the weighing control unit changes the number of decimal places 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. Is considered. For example, according to a control instruction from the control unit 10, the weighing control unit may input a measurement value to the control unit 10 with accuracy up to the first decimal place, and a first range mode to the second decimal place. It is conceivable that switching can be performed by switching to the second range mode in which the measurement value is input to the control unit 10 with accuracy.

  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 according to the situation. For example, the control unit 10 normally obtains the measurement value from the measurement unit 5N to the second decimal place by operating the measurement control unit of the measurement unit 5N in the second range mode. . On the other hand, as a use environment of the inspection support device 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 stabilize due to the influence of wind or vibration is also assumed. Therefore, the control unit 10 controls the weighing control unit of the weighing unit 5N when the value of the second decimal place of the weighing value of the weighing unit 5N is not stable even after the preset predetermined time has elapsed. By operating in the first range mode, it is conceivable to acquire a weighing value with an accuracy to the first decimal place from the weighing unit 5N. 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 the weighing result. Further, the control unit 10 performs the weighing if the situation where the value of the second decimal place of the weighing value of the weighing unit 5N is not stable even after the predetermined time elapses repeatedly for a predetermined number of times during the predetermined period 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 S35, the control unit 10 determines whether the drug identification information corresponding to another drug has been read by the information reading unit 60 or not. Here, when the control unit 10 determines that the medicine identification information corresponding to another medicine is read (S35: Yes side), the control unit 10 shifts the process to step S351.

  When the control unit 10 determines that the medicine identification information corresponding to another medicine is not read (S35: No side), the control unit 10 shifts the process to step S36. Thereby, in the weighing inspection process, after the control unit 10 reads the medicine identification information by the information reading unit 60, the control reading unit 60 reads the different medicine identification information by the information reading unit 60 (S35: Yes), one or more of the weighing units 5N whose weighing value is increased from 0 is specified as a weighing unit corresponding to the medicine identification information (S33). Here, such processing is executed by the weighing specification unit 11 of the control unit 10.

<Step S36>
In step S36, the control unit 10 determines whether a predetermined time set in advance has passed since the weighing unit 5N corresponding to the medicine identification information is specified in step S33. Here, when the control unit 10 determines that the predetermined time has elapsed (S36: Yes side), the control unit 10 shifts the process to step S351, and until the predetermined time elapses (S36: No side), The process returns to step S32.

  In the present embodiment, the process (S33) for assigning the weighing unit 5N to the weighing inspection target drug is not performed even when the predetermined time has elapsed, and the weighing unit corresponding to the weighing inspection target drug is not executed. Although the case where 5N is determined will be described, it is not limited thereto. For example, a configuration is also conceivable in which the control unit 10 can determine the weighing unit 5N corresponding to the medicine for which the weighing inspection is to be performed in accordance with the operation of a predetermined confirmation key or the like. In addition, the control unit 10 executes the later-described checking process in the step S37 as needed from the step S33 onwards, and that the weighing result of the weighing unit 5N corresponding to the weighing inspection object medicine matches the prescription data. A configuration is also conceivable in which the weighing unit 5N corresponding to the weighing inspection target drug can be determined as the condition.

<Step S351>
In step S351, the control unit 10 determines whether or not all of the weighing values of one or more of the weighing units 5N specified as the weighing unit corresponding to the medicine identification information in 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, when the control unit 10 determines that the measurement values of all the measurement units have been determined (S 351: Yes side), the process proceeds to step S 37, and the measurement values of all the measurement units 5 N are determined. Until (S351: No side), the determination of the step S351 is repeatedly executed.

<Step S37>
In step S37, the control unit 10 calculates the sum of the weighing results by one or more of the weighing units 5N specified as the weighing unit corresponding to the same medicine in the step S33, and the total value and the prescription data Match against. Specifically, the control unit 10 is configured such that the total of the weighing results of each of the weighing units 5N converted into the unit determined in advance in the step S34 matches the prescription quantity that is the target value indicated by the prescription data. Determine if it is 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, when the medicine quantity calculated based on the weighing value by the weighing unit 5N and the unit weight is not less than 8.5 tablets and not more than 9.4 tablets, the control unit 10 matches the matching result. It can be considered that if it is not more than 8.4 tablets or not less than 9.5 tablets, it is judged that the collation results do not match. That is, it is conceivable that the control unit 10 performs verification by rounding off the first decimal place of the medicine quantity. In addition, it is possible to set beforehand the difference | error which the said control part 10 accept | permits in the said collation process, and the rounding off of the said 1st decimal place is only the example. For example, it can be considered that the control unit 10 determines that the comparison result is the same when the measurement result is the target value ± 0.1 tablet or the target value ± 0.2 tablet or the like.

  In addition, when there are a plurality of weighing units 5N associated with the weighing inspection target drug, the control unit 10 determines the total number of tablets of the weighing inspection target drug in the prescription data or the Rp data, The weighing value of the weighing unit 5N is collated with the total number of converted tablets. Thereby, even when the user uses a plurality of weighing units 5N for one weighing inspection target chemical, the user does not need any special operation, and does not have to follow the same procedure as the case where one weighing unit 5N is used. It is possible to easily carry out weighing inspection by placing the medicine for which the weighing inspection is to be performed on the number of weighing units 5N. In addition, as a collation method in the case where there are a plurality of weighing units 5N associated with the weighing inspection target drug, the control unit 10 determines 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 weight per PTP sheet by the number of PTP sheets obtained by dividing by the number per PTP sheet corresponding to the medicine for which the weighing inspection is performed, and a plurality of the weighing units 5N It is also conceivable to determine whether the difference with the sum of the weighing values is less than a predefined tolerance.

  By the way, when the medicine for which the weighing inspection is performed is a tablet or a capsule, the control unit 10 determines the number of pieces of the PTP sheet stored in the medicine master corresponding to the medicine for which the weighing inspection is performed and the prescription data. Alternatively, it is conceivable to calculate the number of PTP sheets of the medicine for which the weighing inspection is to be performed and the presence or absence of fractions smaller than one based on the Rp data. Then, it is conceivable that the control unit 10 adds a predetermined value preset as the weight of the ear of the PTP sheet to the target value in accordance with the number of sheets of the PTP sheet and the presence or absence of a fraction.

  For example, it is conceivable that the control unit 10 determines that there is an ear when the fraction is present, and adds the weight of the ear. Thereby, the target value approximates to a value in consideration of the weight of the ear of the PTP sheet, and the matching is performed with high accuracy. In addition, when the fraction of a PTP sheet exists, the structure which can be pre-selected whether it calculates with an ear or without an ear is also considered. In addition, the control unit 10 changes the added value to the target value with the ears always with respect to the fractions of the PTP sheet, and if there is no match as in the comparison result, "Does the ear exist in the fractions?" It is also conceivable to display a message suggesting that the matching result may not match because the setting with the ear is set.

  Further, in the inspection support device 100, the control unit 10 displays the “without ear” and “with ear” operation keys for inputting the presence / absence of the ear in the fractional PTP sheet on the display unit 20. It is conceivable that When the operation unit 30 detects the operation of the operation key “without ear”, it is assumed that the control unit 10 does not have an ear on the PTP sheet in which a fraction occurs, and “with the ear” When the operation of the operation key is detected by the operation unit 30, the control unit 10 considers that the measured value and the target value are compared on the assumption that the ear is present in the PTP sheet in which the fraction is generated. Be

  Furthermore, 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 in accordance with the number of PTP sheets. For example, when the number of PTP sheets is 0 or more and 2 or less, the weight of a predetermined small size rubber band, and when the number of PTP sheets is 3 or more and 5 or less, the predetermined weight It is conceivable to add the weight of the size rubber band and the weight of a predetermined large size rubber band as the predetermined value to the target value when the number of PTP sheets is 6 or more and 10 or less. Thereby, the target value approximates to a value in consideration of the weight of the rubber band that bundles the PTP sheet, and the matching is performed with high accuracy. For example, the control unit 10 sets “ear weight (0-99.99)”, “weight of rubber band (large) (0-99.99)”, “rubber band (0-99.99)” as initial setting of the inspection support device 100. Medium) weight (0-99.99), "weight of small rubber band (0-99.99)", "number of rubber rubber applied sheets (small: 0.0-2.0, middle: 3.0) -5.0, large: 6.0-10.0, etc.), "1 weight inspection (performed, not performed)", "QR weight data (per day, per package, etc.)", " Inspection unit (RP unit, prescription unit, etc.), "Treatment of the third decimal place when displaying g (rounding, rounding, etc.)", "Rubber rubber weight (added, not added, etc.) when reading packaged goods QR" Etc. can be set according to user operation. In addition, the control unit 10 sets the “weighbing rubber selection default value” indicating 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 as the initial setting of the inspection support device 100; 2 rubber band selection default value, 3 scale rubber selection default value, 4 scale rubber selection default value, the large pan rubber selection default value indicating the initial selection state of the rubber band at the time of weighing using the large plate 58, “Weigher 1 fraction presence / absence selection default value” indicating “weighing fraction presence / absence selection default value” indicating “weighing fraction presence / absence selection default value” indicating “weighing fraction presence / absence selection default value”, “weigher fraction presence / absence selection default value “Weigher 4 fractions presence / absence selection default value”, which indicates the number of medicines to be weighed when measuring the value per unit amount (single) of medicine “Weighing at the time of measurement per medicine single The number (0-999) "can be set and in response to a user operation.

  Further, in the inspection support device 100, "large rubber", "in rubber", and "small rubber" for inputting the size or type of the rubber band for bundling the PTP sheet to the display unit 20 by the control unit 10 , “No rubber”, etc. may be displayed. In this case, the control unit 10 switches the size of the rubber band used for the PTP sheet according to the operation of the operation keys such as "large rubber", "in rubber", "small rubber", "without rubber", etc. It is conceivable. Thereby, the weight value and the target value can be compared with each other in consideration of the weight of the rubber band placed on the weighing unit 5N together with the PTP sheet. In particular, it is conceivable that the size or type of the rubber band used when bundling the PTP sheets differs depending on not only the number of PTP sheets but also the size of the PTP sheets. Therefore, the size or type of the rubber band may not be uniquely determined only by the number of PTP sheets. On the other hand, as described above, according to the operation of the operation keys such as "large rubber", "in rubber", "small rubber", and "without rubber", the size or type of the rubber band can be arbitrarily selected. The user can set the size or type of the rubber band by looking at the rubber band used for the actual PTP sheet. Further, for example, in the case where a plurality of PTP sheets are bundled by a rubber band, when the bundle of PTP sheets is divided into a plurality and placed on a plurality of the weighing units 5N, the rubber band is only in one of the weighing units 5N. It is considered to be placed. In particular, it is conceivable that the rubber band is placed on the weighing unit 5N on which the number of PTP sheets not requiring the rubber band is placed. In addition, 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 "large rubber" rubber band. Even in this case, as described above, according to the operation of the operation keys such as "large rubber", "in rubber", "small rubber" and "without rubber", the size or type of rubber band can be arbitrarily selected. The user can set the presence, the size, the type, etc. of the rubber band corresponding to each of the weighing units 5N depending on whether the rubber band is placed together with the actual PTP sheet.

  The method of reflecting the weight of the ear of the PTP sheet on the target value (calculation method) and the method of reflecting the weight of the rubber band on the target value (calculation method) differ depending on the pharmacy or medical institution. It is conceivable that the reflection method can be set in advance. For example, as a method of 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 earing and a second arithmetic expression based on a second internal rule corresponding to earless are set. If the earing of the PTP sheet is selected, the control unit 10 corrects the target value or the weighing value based on the first arithmetic expression corresponding to the first internal rule, and the PTP sheet is corrected. It is conceivable to correct the target value or the weighing value on the basis of the second arithmetic expression corresponding to the second internal rule when the no ear is selected. In addition, as a method of dispensing the PTP sheet, for example, the method of leaving the ear may be defined as “leave the ear in the case of one tablet”. Therefore, as a result of comparing the measurement value with the target value according to how the ear of the PTP sheet is left, if it is not appropriate, the possibility that the way of leaving the ear is not appropriate may be displayed on the display unit 20, etc. It is possible to notify by. For example, if the number of PTP sheets to be dispensed on the basis of prescription data is a fraction of one tablet, the PTP sheet of one tablet should have an ear, so one tablet It is conceivable that the weighing value and the target value are compared on the assumption that the ear is present in the PTP sheet. As a result, 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, when the collation result in step S37 is the same (S38: Yes side), the control unit 10 shifts the process to step S39, and when the collation result in the step S37 does not coincide. (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 the step S33. For example, the error message “The actual value of the inspection target chemical exceeds (or does not meet) the upper limit value or the lower limit value. Please press the OK key to approve the inspection. When re-weighing, Please press the cancel key. Further, 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 medicine for which the weighing inspection is to be completed 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 shifts the process to step S31.

<Step S39>
In step S39, the control unit 10 determines the weighing value determination in the weighing display area A1M corresponding to each of the one or more weighing units 5N identified as the weighing unit corresponding to the same medicine in the step S33. While displaying the quantity which converted the measurement result corresponding to the said measurement part 5N into the unit defined beforehand, it displays that the collation result is in agreement. As described above, the display processing unit 17 of the control unit 10 executes the process of displaying the measurement result by the measurement unit 5N and the comparison result at the step S38 in the measurement display area A1M. When the platter 58 is used, the control unit 10 displays the comparison result in the weighing display area A41 (see FIG. 11). Further, in the step S39, the control unit 10 determines the weighing value which is the weighing result of the weighing unit 5N, and the converted value obtained by converting the weighing value into a unit of medicine (table value of tablets, capsules, sheets, etc.) And either or both are stored in the storage unit 40 as inspection history together with the prescription data. Thus, when the inspection history is displayed on the inspection history inquiry screen D12, the control unit 10 can display the measurement value or the conversion value together with the content of the prescription data.

  Incidentally, it is also conceivable that a printer is connected to the inspection support device 100 according to 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 measurement result in step S37 in step S39 or step S381. In the journal output as the printout, for example, inspection start date, prescription number, voucher number, patient ID, patient ID, patient name, medical department, inspector, prescription data, and Rp data are printed. In the journal, it is conceivable that a JAN code is printed as medicine identification information included in the prescription data or the Rp data. A configuration is also conceivable in which the control unit 10 can convert the GS1 code into the JAN code and print out it.

<Step S40>
Subsequently, in step S40, the control unit 10 waits for the recording timing of the photographed image by the photographing unit 70 (S40: No side). Specifically, when all the weighing values of the four weighing units 51 to 54 are determined, the control unit 10 performs the weighing inspection process on all medicines included as prescription drugs in the prescription data or the Rp data. When it is determined that the image taken by the imaging unit 70 is to be recorded (S40: Yes side), the process is performed in step S41, if another medicine is not left as an inspection target in the prescription data or the Rp data. Migrate to The case where the weighing inspection process is completed for all the drugs contained as prescription drugs in the prescription data or the Rp data is, for example, the case where six types of prescription drugs are contained in the Rp data, and the four first In this case, after weighing on four types of prescription drugs is performed using the weighing units 51 to 54, weighing using the two weighing units 5N is performed on the remaining two prescription drugs. It is also conceivable that the photographing by the photographing unit 70 is performed when the weighing values of all of the weighing units 51 to 54 are stabilized instead of after the checking process of all the weighing units 51 to 54 is completed.

<Step S41>
In step S41, the control unit 10 records the 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 storage unit 40 stores the information. The photographing unit 70 photographs the weighing pans 55 of all the weighing units 51 to 54 at the same time. Further, when the large plate 58 is placed on the weighing units 51 to 54, the large plate 58 is photographed. Here, such processing is executed by the photographing processing unit 18 of the control unit 10. Thereby, as described above, when referring to the inspection history by the inspection history inquiry screen D12 or the like, it is possible to confirm the photographed image. By the way, when the control unit 10 determines that the recording timing has come in the step S40, the control unit 10 causes the display unit 20 to display an indication of the start of imaging such as "Start imaging", and then predetermine. It is conceivable to cause the photographing unit 70 to photograph the weighing units 51 to 54 after the waiting time (for example, about 2 seconds) has elapsed. As a result, it is expected that the user retracts a hand or the like out of the imaging range of the imaging unit 70, and unnecessary imaging can be suppressed. Although the weighing inspection process is performed individually for each of the weighing units 5N, the photographing process of step S41 is performed as a common process. Thus, 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, a photographed image effective as proof of inspection by the inspection support device 100 is stored. Ru. That is, only one shooting is performed when the recording timing arrives. In addition, it is also considered as another embodiment that the photographing by the photographing unit 70 is performed at an individual timing for each of the weighing inspection processing. In this case, the association between each of the weighing units 51 to 54 and the medicine identification information is released individually. For example, after the weighing value of the weighing unit 5N is determined and the checking process ends, when the weighing value of the weighing unit 5N decreases, the association between the weighing unit 5N and the medicine identification information is released. It is conceivable that Further, the photographing by the photographing unit 70 is performed at the timing when the photographing key K 18 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. Can also be considered.

In addition, the control unit 10 may extract an image of a predetermined region corresponding to each of the weighing units 51 to 54 from the photographed image after recording the photographed image by the photographing unit 70. It can be considered as a form. In this case, the control unit 10 also extracts an image of each of the predetermined areas corresponding to the respective weighing display areas 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. It is also conceivable that the control unit 10 stores 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.

  Further, after the end of the matching process, when it is determined in step S40 that the photographing key K 18 displayed on the prescription inspection screen D10 is operated, the control unit 10 causes the photographing unit 70 to perform photographing. It is conceivable to record an image. It is also conceivable that the photographed image by the photographing unit 70 is recorded on condition that the comparison with the prescription data of the weighing result of the weighing unit 5N corresponding to the medicine identification information is completed.

  Furthermore, the range in which the user using the inspection support apparatus 100 performs the operation for putting the medicine in the medicine bag is included in the imaging range of the imaging unit 70, and the predetermined time has elapsed since the occurrence of the recording timing event. It is also conceivable that a photographed image by the photographing unit 70 is recorded. As a result, it is possible to take an image of the operation of inserting the medicine after being inspected by the inspection support device 100 into the medicine bag by the imaging unit 70.

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

  As described above, when the inspection support device 100 is used, the weighing inspection process (S19) is started each time drug identification information is read from a packaging material such as a PTP sheet of the drug, and the prescription data or the Rp data It is possible to conduct inspections of prescribed medicines contained in a series and in parallel. Therefore, for example, the inspection operation of each of the prescription drugs and the storage operation of each of the prescription drugs in the medicine bag can be performed efficiently and accurately.

  Further, in the weighing inspection process, the weighing unit increases in weight value from 0 before the medicine identification information is read from the packaging materials of different medicines after the medicine identification information is read from the medicine packaging material. Is identified as the weighing unit corresponding to the medicine for which the weighing inspection is to be performed. Therefore, before the weighing value of the weighing unit 5N corresponding to one medicine identification information is stabilized, the information reading unit 60 reads the other medicine identification information and starts weighing by the other weighing unit 5N. It is possible to Therefore, the user can efficiently and accurately carry out inspections of multiple types of drugs included in the prescription data or the Rp data.

  Specifically, although the inspection support device 100 includes the four weighing units 51 to 54, the weighing inspection process using the weighing units 51 to 54 is individually performed. 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 by the information reading unit 60 and the weight unit 5N. Place the PTP sheet. Thereafter, the user reads the medicine 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 reading of the medicine identification information of the PTP sheet of the second tablet may be before the weighing value of the first weighing unit 5N is stabilized. Then, in each of the weighing inspection processes started for each of the 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 continuously reads the drug identification information of the PTP sheet of the third tablet by the information reading unit 60 and places the PTP sheet on the weighing unit 5N, and the PTP of the fourth tablet The medicine identification 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 of the weighing units 5N and the prescription data or the Rp data is individually started when the medicine identification information is read. Therefore, the collation processing by each of the weighing units 5N is sequentially ended. Therefore, the last (fourth) PTP sheet is weighed as compared to the case where the weighing results by all the weighing units 5N are checked after placing the PTP sheets of all four types of tablets in the weighing unit 5N. It is possible to shorten the time from the placement of the part 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, if five types of medicines are included in the Rp data as they are, the fifth PTP sheet of medicines is used. Even if the drug identification information is read by the information reading unit 60, the PTP sheet can not be placed. Therefore, the control unit 10 may release the association between the weighing unit 5N and the medicine identification information every time the comparison of the weighing result by the weighing unit 5N with the prescription data or the Rp data is completed. Can be considered as an embodiment of Thereby, 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, by repeatedly using the weighing units 51 to 54 It is possible to sequentially carry out weighing inspections of five or more kinds of drugs in parallel. That is, the user reads the medicine identification information of the fifth medicine by the information reading unit 60 when the weighing inspection process corresponding to any one of the first to fourth medicines is finished, and the weighing is performed. A PTP sheet can be placed on the section 5N, and medicines that have been inspected first can be stored in a medicine bag first. Therefore, the user can efficiently and accurately check the types of PTP sheets more than the number of weighing units 5N. However, in this case, the photographing at the steps S40 to S41 can not be performed. Therefore, this type of configuration is, for example, when the inspection support device 100 does not have the recording function of the photographed image by the photographing unit 70, the recording timing of the photographed image is set when the recording function is set to be invalid. Is the operation of the photographing key K18, or when the recording timing of the photographed image is the end of the comparison with the prescription data of the weighing result of the weighing unit 5N.

[Keystone correction function]
By the way, as shown in FIG. 2, the photographing unit 70 is provided to take an image in an oblique direction with respect to each of the weighing units 51 to 54. In this case, the image of each of the weighing units 51 to 54 photographed by the photographing unit 70 is deformed into a trapezoidal shape. Therefore, it is conceivable that the control unit 10 has a keystone correction function of executing keystone correction processing on the photographed image.

  For the keystone correction processing, a conventionally known technique may be used, but as shown in FIG. 14, for example, a plurality of mutually separated positions in the photographing range of the photographing unit 70 in the inspection support device 100. Correction index parts P1 to P4 are provided. Then, the control unit 10 executes a keystone correction process of the photographed image P0 by the photographing unit based on the plurality of correction index parts P1 to P4 present in the photographed image by the photographing unit 70. Here, such keystone correction processing is executed by the photographing processing unit 18 of the control unit 10. Specifically, the control unit 10 detects vertices P11 to P14 outside the correction index parts P1 to P4 by image matching or the like. Then, as shown in FIG. 15, the control unit 10 makes a trapezoidal shape by projective transformation of the photographed image P0 by the photographing unit 70 so that the positional relationship in which the vertices P11 to P14 become a predetermined rectangular vertex. Perform correction.

  It is also conceivable that the photographed image P0 of the entire photographing range of the photographing unit 70 includes an unnecessary area. Therefore, it is conceivable that the control unit 10 trims a predetermined range based on the positions of the vertices P11 to P14 after the execution of the keystone correction processing. Specifically, as shown in FIG. 15, the control unit 10 performs trimming of the captured image P0 by using the range of positions separated from the positions of the vertices P11 to P14 by distances L11 to L18 as effective images. Do. Thus, unnecessary portions are removed from the captured image P0 of the entire imaging range by the imaging unit 70, and it is possible to obtain a captured image P10 within a predetermined range as shown in FIG.

[Shooting control function]
Furthermore, in step S41, when a photographed object by the photographing unit 70 is recorded, if the shielding object such as the user's hand is present in the photographing range of the photographing unit 70, each of the weighing units 5N is photographed normally. I can not do it. Therefore, it is conceivable that the control unit 10 restricts the recording of the photographed image by the photographing unit 70 when the shield exists in the photographed image by the photographing unit 70.

  Specifically, as shown in FIG. 14, in the inspection support device 100, on the upper surface 501 of the weighing device 50, a mark line P5 continuously formed to surround the outside of the weighing portions 51 to 54 is provided. It is possible to be Then, the control unit 10 detects the mark line P5 from the photographed image by the photographing unit 70 in the step S41, and whether or not a shield for shielding the mark line P5 exists on the mark line P5. to decide. Here, when the shield does not exist, the control unit 10 stores the image captured by the imaging unit 70 in the storage unit 40 in association with the prescription data or the Rp data. On the other hand, when the shielding object is present, the control unit 10 causes the display unit 20 to display a shooting failure such as “shooting failure” and discards the shot image by the shooting unit 70, The imaging unit 70 causes the imaging unit 70 to image the weighing units 51 to 54 at predetermined intervals (for example, an interval of 2 seconds), and determines the presence or absence of a shield that shields the mark line P5 in the photographed image. Then, the photographing by the photographing unit 70 is repeatedly performed until a photographed image in which the shield does not exist is obtained. As a result, the photographed image unnecessary as evidence is deleted because the shield exists, and only the valid photographed image is recorded in the storage unit 40, so the amount of data stored in the storage unit 40 is reduced. . Note that the deletion timing of the captured image is, for example, when it is determined that the shield is present, or when a captured image without the shield is obtained. That is, the control unit 10 records a photographed image by the photographing unit 70 on the condition that there is no shield that shields the mark line P5. Here, the processing is executed by the photographing processing unit 18 of the control unit 10.

  Thus, the control unit 10 monitors the presence of the shield in the image captured by the imaging unit 70, and records the captured image by the imaging unit 70 at the timing when the shield does not exist. Thus, each of the weighing units 5N can be photographed normally by the photographing unit 70. Further, it is also conceivable that the control unit 10 displays a warning on the display unit 20 when a shield for shielding the mark line P5 is present on the mark line P5. Thus, the user can be urged to remove the shield from the imaging range, and the user can be prevented from taking out the medicine before the image taken by the imaging unit 70 is recorded. . In this case, the control unit 10 stops the photographing by the photographing unit 70 until the photographing key K18 is next operated by the user after the shield is detected, and the operation of the photographing key K18 is performed. According to the above, it is conceivable to cause the photographing unit 70 to photograph after a predetermined time (for example, 2 seconds) has elapsed. Thereby, unnecessary photographing by the photographing unit 70 is prevented. Further, the control unit 10 interrupts the photographing at predetermined time intervals when the photographed image without the shield can not be obtained even when the photographing by the photographing unit 70 is repeatedly performed a predetermined number of times. It is conceivable to resume shooting after the user operates the shooting key K18.

  However, when the recording of the photographed image is performed using the judgment index as to whether the mark line P5 is shielded, the photographed image by the photographing unit 70 even if the mark line P5 is slightly blocked by dust or the like. Records are limited. Therefore, the control unit 10 calculates the area of the shield present in the image captured by the imaging unit 70, and the image captured by the imaging unit 70 is calculated on the condition that the area is less than a predetermined threshold. It is conceivable to record.

  Specifically, the control unit 10 executes a binarization process based on a discriminant analysis method on the image captured by the imaging unit 70 and executes an image process for filling the area inside the mark line P5 with black. In addition, it is possible that the process which concerns is performed with respect to the said picked-up image P10 after being correct | amended by the said keystone correction process about the picked-up image of the said imaging | photography part 70. FIG. At this time, when the mark line P5 is not blocked, the entire mark line P5 in the photographed image P10 is painted out black.

  On the other hand, as shown in FIG. 17, when the mark line P5 is shielded by the shield H1 such as the user's hand in the photographed image P10, a part of the shield H1 is one of the mark lines P5. Will form a part. As a result, as shown in FIG. 18, in the photographed image P20 in which the inside of the mark line P5 is blacked out, the region H2 corresponding to the shield H1 becomes white. Then, the control unit 10 calculates the area of the region H2 corresponding to the shield H1. Here, when the area of the area H2 is less than a predetermined threshold, the control unit 10 records a photographed image by the photographing unit 70, and the area of the area H2 is equal to or more than the predetermined threshold. The control unit 10 stands by without recording a photographed image by the photographing unit 70.

  Thereafter, when the area of the region H2 is less than the threshold value, the control unit 10 records a photographed image by the photographing unit 70. As described above, the control unit 10 performs the photographing by the photographing unit 70 on the condition that the area of the area H1 corresponding to the shield H1 in the photographed image P20 by the photographing unit 70 is less than a predetermined threshold. Record the image. Here, the processing is executed by the photographing processing unit 18 of the control unit 10. Thereby, the recording of the photographed image by the photographing unit 70 is limited only when the shield H1 having a predetermined area is present, and the mark line P5 is shielded by a small dust Can record the photographed image by the photographing unit 70. Specifically, when there is a shield having a predetermined area on the mark line P5, the control unit 10 causes the display unit 20 to display an error message indicating that the shield exists. It is conceivable that after notification by the method described above, a predetermined time (for example, 2 seconds) elapses to acquire a photographed image by the photographing unit 70 and to judge again the presence or absence of the shield. . When the error repeatedly occurs a predetermined number of times, the control unit 10 displays, on the display unit 20, a message indicating that maintenance is necessary or that there is a risk of failure, instead of the error message. It is also conceivable to notify by means of a method such as Here, it is conceivable that the control unit 10 erases the photographed image photographed by the photographing unit 70 in the state in which the shield H1 exists, and stores only the photographed image in which the shield H1 does not exist. As a result, it is possible to reduce the storage capacity required for storing the photographed image.

  By the way, in the inspection support device 100, when dirt, a scratch, or the like occurs on a part of the mark line P5, the control unit 10 is always shielded by the shield H1 on the mark line P5 thereafter. It is possible to judge that Therefore, when the control unit 10 determines that the mark line P5 is shielded by the shield H1, it is considered that the position of the shield H1 is accumulated and stored as the history in the storage unit 40. Be Then, when the control unit 10 determines that the mark line P5 is shielded by the shielding object H1, the control unit 10 refers to the history stored in the storage unit 40, and sets a plurality of times in advance. When the shield H1 is detected in a certain range at the time of shooting by the shooting unit 70, it is conceivable to exclude the specific range from the detection targets of the shield H1. As a result, even when dirt, a scratch, or the like is generated on the mark line P5, it is possible to exclude the influence and perform inspection using the inspection support device 100.

  At this time, when the shield H1 is detected in the specific range, the control unit 10 displays a message screen or the like prompting removal or repair of dirt or a scratch or the like generated on the mark line P5. It is conceivable to display on 20. Thereby, it is expected that the user performs removal or repair of dirt, scratches, etc. occurring on the mark line P5. In addition, the control unit 10 causes the message screen to display an operation key for inputting whether or not dirt or a scratch or the like generated on the mark line P5 can not be removed or repaired. Is considered. Then, when the user operates the operation key corresponding to the case where the user can not remove or repair dirt, scratches, etc., the control unit 10 then detects the target object for detection of the shield H1. It is possible to exclude from. This makes it possible to interpose the selection of the user in the selection as to whether or not to exclude the specific range from the detection targets, and operation suitable for each user is possible. In addition, after the control unit 10 excludes the specific range from the detection target, the specific range is not detected when the shield H1 is not detected in the specific range in the image captured by the imaging unit 70. It is also conceivable to cancel the exclusion from the detection targets of

Second Embodiment
By the way, in the inspection support device 100, in order to measure the medicine with high accuracy by the weighing device 50, the rated capacity of the load cell 56 becomes small, and even when the large plate 58 is used, the large capacity is weighed. I can not do it. For example, when the rated capacity of the load cell 56 is 500 g, the weighing device 50 can weigh up to 2.0 kg in total, but the minimum accuracy is 0.1 g. On the other hand, when the rated capacity of the load cell 56 is 300 g, the minimum accuracy can be increased to 0.05 g, but the total weight of the weighing device 50 is up to 1.2 kg.

  Therefore, it is conceivable that the inspection support device 100 is provided with a plurality of sets of weighing scales having different rated capacities, and the combination of weighing scales used is variable according to the size of the weighing pan used. As a result, it is possible to selectively use weighing with high accuracy and weighing with large volume as needed.

  Specifically, in addition to the load cells 56 corresponding to the weighing units 51 to 54, the weighing device 50 has large-capacity load cells larger than the rated capacity of the load cells 56 on the left and right sides of the four load cells 56. It is conceivable to be provided. When the load cell 56 is used, the weighing pan 55 is used, and when the large capacity load cell is used, a large pan supported by the two large capacity load cells is used.

  For example, it is conceivable that the rated capacity of the load cell 56 is 300 g and the rated capacity of the large capacity load cell is 3 kg. As a result, in the case of performing weighing using the load cell 56, it is possible to carry out high-accuracy weighing with a small volume but a minimum accuracy of 0.05 g. On the other hand, when weighing using the large capacity load cell, although the minimum accuracy is 0.5 g, it is possible to carry out large capacity weighing.

Third Embodiment
By the way, in the inspection support device 100, the influence of wind from the surroundings may cause the weighing in the weighing device 50. Therefore, in the inspection support device 100, as shown in FIG. 19 and FIG. 20, it is considered that the windshield 92 and the windshield 93 can cover the periphery of the weighing units 51 to 54 of the weighing device 50. Be For example, the windshield 92 and the windshield 93 are a transparent resin such as an acrylic plate.

  Each of the windshields 92 can be accommodated inside the weighing device 50 through an elongated opening 502 formed on the upper surface 501 of the weighing device 50. In addition, the windshield 93 is rotatably supported by the cover member 90 via a pivot support portion 94. In the inspection support apparatus 100 according to the present embodiment, a photographing unit 74 mounted on the cover member 90 is provided in place of the photographing unit 70, and the windshield 93 is provided with the photographing unit 74. An opening 931 is formed at a position corresponding to the imaging range. Thus, even when the windshield 93 is used, photographing of the weighing units 51 to 54 by the photographing unit 74 is possible.

  The wind shield plate 93 can be turned to the inner surface side of the cover member 90 as needed by the user and disposed above the weighing parts 51 to 54 to prevent wind from above. It is. When the windshield 93 is unnecessary, as shown in FIG. 20, the windshield 93 can be folded by being pivoted to the outer surface side of the cover member 90.

  Although it is conceivable that the windshield 92 can be moved up and down with respect to the opening portion 502 of the weighing device 50 manually by the user, the windshield 92 is interlocked with the opening / closing operation of the cover member 90. It is also conceivable to go up and down. FIG. 21 is a schematic cross-sectional view for explaining an example of the lifting and lowering mechanism 503 for supporting the windshield 92 so as to be capable of lifting and lowering in the weighing device 50. As shown in FIG.

  As shown in FIG. 21, the lifting mechanism 503 has a wire 504, a pulley 505, and a weight 506. The weight 506 is suspended by the wire 504 via the pulley 505, and the end of the wire 504 opposite to the weight 506 is fixed to the lower end of the windshield 92. The weight of the weight 506 is larger than that of the windshield 92.

  In the elevating mechanism 503 configured as above, the cover member 90 is closed and the windshield 92 is pushed downward by the cover member 90, whereby the windshield 92 is inserted through the opening 502. It is housed in the weighing device 50. On the other hand, when the cover member 90 is opened, the weight 506 moves downward and the windshield 92 rises, and the windshield 92 protrudes upward from the weighing device 50 through the opening 502. It will be. Therefore, the user can raise and lower the windshield 92 simply by opening and closing the cover member 90. Further, in a case where the windshield plate 92 is not required to be used, a lock mechanism for locking the windshield plate 92 so as not to ascend when the cover member 90 is opened is provided in the elevating mechanism 503. Is also conceivable. In addition, the outer peripheral surface of the said weighing device 50 is a metal, and the structure which can attach or detach the windshield which has a magnet in the said outer peripheral surface is also considered as another embodiment.

Fourth Embodiment
Here, another example related to the photographing control function will be described with reference to FIGS.

  As shown in FIG. 23, on the upper surface 501 of the weighing device 50 of the inspection support device, the weighing plate placed on the placing portion 57 of the weighing portions 51 to 54 instead of the mark line P5. A plurality of mark lines P <b> 21 to P <b> 24 formed intermittently on the outer periphery of 55 are formed. In the upper surface 501, correction index parts P15 to P18 are formed instead of the correction index parts P1 to P4.

  Then, the control unit 10 determines whether any one of the mark lines P21 to P24 is shielded by a shield. Specifically, as shown in FIG. 25, the control unit 10 extracts the mark lines P21 to P24 from the photographed image by the photographing unit 70, and converts the area other than the mark lines P21 to P24 into white. Execute the digitization process. Here, FIG. 24 shows a state in which the mark line P23 is shielded by the shield H1 which is a user's finger. The extraction of the mark lines P21 to P24 can be realized, for example, by searching a line segment of a predetermined width or a line segment of a predetermined color by image processing.

  Thereafter, the control unit 10 determines whether the mark lines P21 to P24 in the photographed image after the binarization process are shielded by a shield. Specifically, the control unit 10 measures the length or area of the white region in the mark lines P21 to P24, and the mark line P21 to P24 when the length or area is equal to or greater than a predetermined threshold value. It is determined that any of P24 is shielded by the shield. Here, FIG. 25 is a view showing an example of the photographed image after the binarization processing, and in the example shown in FIG. 25, the control unit 10 detects a white region H3 on the mark line P23, It is determined that the mark line P23 is shielded. Then, as described above, when a photographed image in which any of the mark lines P21 to P24 is not blocked is obtained, the control unit 10 associates the photographed image with the prescription data or the Rp data. Is stored in the storage unit 40.

  By the way, even when the mark lines P21 to P24 are formed on the upper surface 501 of the weighing device 50, depending on the size of the weighing plate 55 or the large plate 58, the weighing plate 55 or the large plate 58 may be When placed on the weighing units 51 to 54, the mark lines P21 to P24 may be blocked by the weighing plate 55 or the large plate 58. Therefore, as shown in FIG. 26A, it is conceivable that a black mark line P19 is formed at the edge portion 553 of the weighing pan 55, similarly to the mark lines P21 to P24. Thereby, even when the mark lines P21 to P24 are interrupted by the weighing dish 55, the mark control lines can be effectively executed because the mark lines P21 to P24 are interpolated by the mark line P19. The control unit 10 determines whether the mark line P19 formed on each of the weighing dishes 55 is shielded, and the photographing is performed when the mark line P19 of the weighing dish 55 is not blocked. Allowing the unit 70 to execute photographing is also considered as another embodiment.

  Further, as shown in FIG. 26B, it is conceivable that black mark lines P21 to P24 are formed at the edge portion 581 of the large plate 58 similarly to the mark lines P21 to P24. Thereby, even when the mark lines P21 to P24 are interrupted by the large plate 58, the photographing control function can be effectively executed. Furthermore, when the large plate 58 is placed on the weighing units 51 to 54, when the correction indicator P15 to P18 is covered with the large plate 58, the trapezoid using the correction indicator P15 to P18 Correction processing can not be performed. Therefore, it is conceivable that correction index portions P25 to P28 similar to the correction index portions P15 to P18 are formed at the edge 581 of the large plate 58. Thereby, even when the correction indicator portions P15 to P18 are covered with the large plate 58, the keystone correction process can be effectively performed.

  Here, another example of the keystone correction process will be described with reference to FIGS. 27 and 28. FIG.

  In the keystone correction processing, the correction index parts P15 to P18 are extracted. At this time, when processing such as image matching is performed on the entire photographing range by the photographing part 70, the processing load Processing time will be longer. Therefore, in the keystone correction process, it is conceivable that the control unit 10 extracts only a specific search range determined in advance as a detection target.

  For example, as shown in FIG. 27, the control unit 10 detects a part of the detection range P31 to P34 defined by position coordinates predetermined in the photographed image P30 photographed by the photographing unit 70 as the detection target. The correction index parts P15 to P18 are extracted. For example, in FIG. 27, the detection range P31 to P34 is a specific rectangular range located inside by a predetermined distance determined in advance from the upper end, the lower end, the left end, the right end and the like of the captured image P30. It is. As a result, the control unit 10 may detect the correction index parts P15 to P18 with only the detection range P31 to P34 as a detection target, so processing compared to the case where the entire photographed image P30 is to be detected The load is reduced and the processing time is reduced.

  At this time, the control unit 10 executes binarization processing on each of the detection ranges P31 to P34 of the photographed image P30 photographed by the photographing unit 70, and from the image after the binarization processing. The correction indicator parts P15 to P18 are detected. Below, a binarization process is performed with respect to the said detection area P34 among the said detection area P31-P34 shown by FIG. 27, and the said correction index part P18 is detected from the image after the binarization process. Although the case will be described as an example, the same applies to the detection regions P31 to P33.

  In the inspection support device 100, as shown in FIG. 28A, the brightness of the background area or the like included in the detection range P34 of the captured image P30 changes according to the illuminance environment in which the inspection support device 100 is placed. Do. Therefore, when the binarization processing is performed using a predetermined fixed threshold, it is considered that the background region etc. becomes a black image when the brightness of the background region etc. is darker than the threshold. Be Therefore, it is preferable that the control unit 10 execute a binarization process based on a discriminant analysis method as the binarization process. The discriminant analysis method is a method of automatically determining the threshold so that the separation between the two classes in the histogram of the image is the best. Thus, for example, as shown in FIG. 28A, the control unit 10 has a different illuminance environment in which the inspection support device 100 is used, and the brightness of the background area or the like is different. As a similar result, as shown in FIG. 28B, it is possible to obtain a detection image P 341 after binarization in which the background area etc. is a white image.

  Further, in order to allow some positional fluctuation of the correction index part P18 in the detection image P341, the detection range P34 is set to be a range larger than the correction index part P18 to some extent. Therefore, as shown in FIG. 28B, in the detected image P341, a part such as the weighing dish 55, the mark line P23, the mark line P24, and the like as an unnecessary image which is not the correction index part P18. Will be included. Therefore, when the correction indicator portion P18 is detected from the detection range P34 by the control unit 10, there is a possibility that a portion of the unnecessary image is erroneously detected as the correction indicator portion P18. Therefore, it is conceivable that the control unit 10 detects the correction index unit P18 with only an element image of a specific range in which the area is predetermined among the element images included in the detected image P341 as a detection target. For example, when the area of the correction index portion P18 is α, the specific range is set as a range (α-β or more and α + β or less) equal to or smaller than a predetermined allowable value β.

  Thereby, an image whose area is smaller than the correction index part P18 by the allowance value β or more and an image larger than the correction index part P18 by the allowance value β or more are excluded from detection targets. Therefore, even if the detected image P341 includes an image other than the correction index part P18 as shown in FIG. 28B, only the correction index part P18 as shown in FIG. 28C. It is possible to extract

  Furthermore, as described above, the control unit 10 detects a vertex P181 of the correction indicator P18 in the keystone correction process. Here, as also shown in FIG. 23, the correction index part P18 is a right triangle including the vertex part P181 at one of the vertices. On the other hand, as shown in FIG. 28C, the control unit 10 generates a template image P343 including a rectangular portion including the apex portion P181 of the correction index portion P18 and a blank area outside the rectangular portion. It is conceivable to detect the vertex P181 by image matching using.

  Specifically, in the example shown in FIG. 28C, the template image P343 is a rectangular image in which the first quadrant is a black image and the second to fourth quadrants are white images. Thereby, it is possible to specify the center position of the template image P343 when the template image P343 and the correction index part P18 coincide with each other as the position coordinates of the vertex P181 in the correction index part P18. As described above, since the inspection support device 100 can extract each of the correction index parts P15 to P18 from the photographed image P30 and can specify the position coordinates of their vertexes with high accuracy, the photographed image P30 can be obtained. Can perform highly accurate keystone correction processing.

Fifth Embodiment
By the way, in each of the embodiments, in the inspection support device 100, the user first causes the information reading unit 60 to read the medicine identification information, and then the medicine is measured by the weighing unit 5N. The case where the weighing inspection of the medicine was performed was described. On the other hand, it is also conceivable that the user causes the information reading unit 60 to read the medicine identification information after placing the medicine on the weighing unit 5N first. That is, a configuration in which the order of the reading of the drug identification information and the placement of the drug can be reversed from that of each of the above embodiments is also conceivable.

  Specifically, in the inspection support device 100, the control unit 10 associates each of the weighing units 51 to 54 with each other based on the weighing result and the prescription data (or Rp data) by each of the plurality of weighing units 51 to 54. It is conceivable to identify drug identification information. Here, the process is an example of the second weighing specification unit, and the control unit 10 when the process is performed is an example of the second weighing specification unit. Then, when the medicine identification information is read by the information reading unit 60 after the measurement result by the weighing unit 5N is determined, the control unit 10 completes the inspection of the specified medicine identification information. Here, the process is an example of the inspection completion step, and the control unit 10 when the process is performed is an example of the inspection completion processing unit. That is, after the medicine is placed on the weighing unit 5N and the medicine identification information of the drug placed on the weighing unit 5N is tentatively specified among the drug identification information included in the prescription data, the information reading is performed. It is conceivable that the identification is confirmed by reading the medicine identification information by the part 60, and the weighing inspection of the medicine is completed. In this case, when the medicine is placed on the weighing unit 5N and the weighing value is determined, comparison between the weighing result of the medicine and the prescription data is performed.

  In particular, it is conceivable that the control unit 10 associates the weighing unit 5N and the medicine identification information of the medicine for which the weighing result is obtained that matches or most closely matches the number of medicines included in the prescription data. Specifically, the unit weight acquisition unit 12 reads out the weight per unit amount (unit weight) predetermined corresponding to the medicine identification information of each medicine included in the prescription data from the medicine master. Subsequently, the control unit 10 converts the quantity of medicine included in the prescription data into the weight of the medicine based on the unit weight. Then, the control unit 10 corresponds to the medicine identification information the weighing unit 5N, of the weighing units 51 to 54, a weighing value that is the same as or closest to the weight of the medicine after conversion is obtained as a weighing result. Identified as a weighing unit. That is, the control unit 10 associates the drug identification information included in the prescription data with the weighing unit 5N based on the prescription data, the medicine master, and the weighing result of the weighing unit 5N. Thereafter, after the control unit 10 causes the display unit 20 to display the correspondence between the medicine identification information and the weighing unit 5N, the medicine at the timing when the medicine identification information is read by the information reading unit 60. Complete inspection of identification information. At this time, the control unit 10 stores the correspondence between the drug identification information and the weighing result of the weighing unit 5N in the storage unit 40 as the inspection history of the prescription data.

  Thereby, for example, when only one type of medicine is included in the prescription data, or when the prescription data includes multiple kinds of medicines with extremely different weights, the medicine is first added to the weighing unit 5N. After setting, it is possible to perform operation such as reading the drug identification information of the drug by the information reading unit 60.

  In the inspection support device 100, the control unit 10 causes the display unit 20 to display the switching operation key, and the reading of the medicine identification information and the placement of the medicine are performed according to the operation of the switching operation key. It is conceivable that the order can be switched. That is, it is possible to switch and use both the first operation mode in which the drug identification information is read first and the second operation mode in which the drug is placed on the weighing unit 5N first. Is considered. Furthermore, the control unit 10 automatically switches the first operation mode and the second operation mode according to the relationship between the reading by the information reading unit 60 and the change in the weighing value of the weighing unit 5N. Is considered. Specifically, the control unit 10 executes the first operation mode when the medicine identification information is read by the information reading unit 60 before the measurement value of the measurement unit 5N changes, and the information It is conceivable to execute the second operation mode when the weighing value of the weighing unit 5N is changed before the medicine identification information is read by the reading unit 60. By this, it is possible to flexibly cope with different operations for each user, and work efficiency is improved.

  When the weighing result of the medicine set in the weighing unit 5N matches or approximates the weight of the plurality of medicines included in the prescription data, the control unit 10 indicates that and any medicine It is conceivable to display an operation key or the like for making the selection on the display unit 20, and to select medicine identification information to be associated with the weighing unit 5N according to the operation of the operation key. In this case, the control unit 10 completes the inspection of the medicine identification information at the timing when the medicine identification information is read by the information reading unit 60. Thus, inspection can be performed even when a plurality of medicines having similar total weights are included in the prescription data. On the other hand, the control unit 10 displays an error on the display unit 20 when the weighing result of the drug set in the weighing unit 5N does not match or approximate the weight of any drug contained in the prescription data. It is possible to do it.

  Moreover, the following method is considered as another example of the method of matching the said measurement part 5N and the said chemical | medical agent identification information of the said chemical | medical agent. That is, the unit weight acquisition unit 12 reads out the weight (unit weight) per unit amount predetermined corresponding to the medicine identification information of each medicine included in the prescription data from the medicine master. Subsequently, the control unit 10 converts the weighing value of the weighing unit 5N of the weighing units 51 to 54 in which the weighing value is changed into the quantity of the medicine based on the unit weight. Then, the control unit 10 uses, as the medicine identification information, the weighing unit 5N in which, among the weighing units 51 to 54, the quantity of the medicine that matches or most closely matches the quantity of the drug after conversion is obtained as the weighing result. Identify as the corresponding weighing unit. At this time, when the medicine is placed on the weighing unit 5N and the weighing value is determined, comparison between the weighing result of the medicine and the prescription data is performed. Thereafter, after the control unit 10 causes the display unit 20 to display the correspondence between the medicine identification information and the weighing unit 5N, the medicine at the timing when the medicine identification information is read by the information reading unit 60. Complete inspection of identification information. At this time, the control unit 10 stores the correspondence between the drug identification information and the weighing result of the weighing unit 5N in the storage unit 40 as the inspection history of the prescription data. Even in this case, for example, when only one type of drug is included in the prescription data, or when the prescription data includes multiple types of drugs having extremely different weights, the medicine is first added to the weighing unit 5N. After setting, it is possible to perform operation such as reading the drug identification information of the drug by the information reading unit 60.

  Even when the weighing result of the medicine set in the weighing unit 5N matches or approximates the quantity of the plurality of medicines included in the prescription data, the control unit 10 indicates that and any medicine. It is conceivable to display an operation key or the like for making the selection on the display unit 20, and to select medicine identification information to be associated with the weighing unit 5N according to the operation of the operation key. In this case, the control unit 10 completes the inspection of the medicine identification information at the timing when the medicine identification information is read by the information reading unit 60. In this way, inspection can be performed even when a plurality of medicines close in total amount are included in the prescription data. On the other hand, the control unit 10 displays an error on the display unit 20 when the weighing result of the medicine set in the weighing unit 5N does not match or approximate the quantity of any medicine contained in the prescription data. It is possible to do it.

Sixth Embodiment
Further, as shown in FIG. 29, the inspection support device 100 automatically updates the weight per unit amount in the medicine master or the weight per PTP sheet according to the weighing value at the time of actual inspection. It is conceivable to include an automatic update processing unit 191 that executes update processing. Specifically, the control unit 10 functions as the automatic update processing unit 191 by executing various processes in accordance with the inspection support program.

  First, the control unit 10 executes the automatic update processing, for example, 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 enabling and disabling the automatic update function. For example, the control unit 10 sets an automatic update flag provided in the EEPROM in the control unit 10 to “1” when the automatic update function is enabled, and the automatic update function is disabled. Set to "0". Thereby, after that, the control unit 10 can determine whether the automatic update function is valid or invalid based on the value of the automatic update flag.

  Then, when the automatic update function is effective, the control unit 10 is included in the prescription data when it is determined in step S38 in the weighing inspection process (see FIG. 13) that the comparison result is the same. The storage unit 40 stores, for each medicine, the prescribed quantity (the number of tablets, etc.) which is the target value shown in the prescription data and the sum (weight) of the weighing results by one or more of the weighing units 5N. Remember. Thereby, the history of the prescribed quantity and the weighing result corresponding to each medicine is accumulated and stored in the storage unit 40. The control unit 10 accumulates and stores in the storage unit 40 the prescription quantity and the weighing result for a predetermined number of times (for example, about 50 to 100 times) set in advance, and data exceeding the predetermined number of times is Erase or overwrite old data sequentially. As another embodiment, it is also conceivable that the control unit 10 stores the total of the prescription quantity and the weighing result in the storage unit 40 in the step S37 or the like preceding to the step S38. In this case, for example, when it is determined in step S38 that the comparison result matches, the control unit 10 stores the total of the prescription quantity and the weighing result as it is, and the comparison result does not match in step S38. It is also conceivable to eliminate the sum of the prescribed quantity and the weighing result when it is determined that

  Thereafter, in step S21 in the inspection support process, the control unit 10 stores the prescribed quantity stored in the storage unit 40 and the weighing result for each medicine included in the prescription data. Based on the weight per unit amount stored in the medicine master or the weight per PTP sheet is updated. For example, the control unit 10 may calculate the integrated value D1 of the prescription quantity stored and stored in the storage unit 40 and the integrated value D2 of the sum of the weighing results stored and stored in the storage unit 40. And are calculated respectively. When the medicine is a medicine packaged in a PTP sheet, a value obtained by dividing the integrated value D2 by the integrated value D1 and indicating the weight per unit amount is multiplied by the number of pieces per PTP sheet. Update the contents of the medicine master as the weight per PTP sheet. If the medicine is not packaged in the PTP sheet, the contents of the medicine master are updated with the value obtained by dividing the integrated value D2 by the integrated value D1 as the weight per unit. Thereby, it is possible to suppress the influence of, for example, the error of the weighing value due to the aged deterioration of the weighing unit 5N or the error of the weighing result of the weighing unit 5N due to the use environment of the inspection support device 100.

Seventh Embodiment
Further, as shown in FIG. 29, when the medicine to be weighed is the medicine contained in the PTP sheet, the inspection support apparatus 100 compares the weighing result and the target value in units of the number of PTP sheets. It is conceivable to include a weighing reduction processing unit 192 that executes the weighing inspection process in the weighing reduction mode. Specifically, the control unit 10 functions as the weighing reduction processing unit 192 by executing various processes in accordance with the inspection support program.

  First, at the time of initial setting in the inspection support device 100 or at the start of weighing inspection, the control unit 10 responds to the user's operation input using the display unit 20 and the operation unit 30, for example. It is possible to switch to the normal mode in which the weighing reduction process is not performed. For example, the control unit 10 sets a mode flag provided in the EEPROM in the control unit 10 to "1" in the weighing reduction mode, and sets it to "0" in the normal mode. . Thereby, the control unit 10 can then determine the current operation mode based on the value of the mode flag. However, when the control unit 10 executes the weighing inspection process, even if the weighing reduction function is set to be effective, if the weighing target in the inspection support device 100 is not a PTP sheet, The weighing mode is not performed, and the weighing mode is performed only when the object to be weighed is a PTP sheet.

  By the way, in the weighing mode, it is not necessary to perform weighing by the weighing unit 5N with high accuracy. On the other hand, as described above, the control unit 10 transmits a control instruction to the weighing control unit of the weighing unit 5N to operate the weighing control unit in the first range mode and the second range mode. A configuration that can be switched to any of the above can be considered. Therefore, the control unit 10 sets the operation mode of the weighing control unit to the first range mode when the weighing reduction mode is set, and the operating mode of the weighing control unit when the normal mode is set. It is conceivable to set the second range mode. As a result, for example, the time until the weighing value of the weighing unit 5N in the weighing relaxation mode is stabilized can be shortened, and in the normal mode, a weighing value with high accuracy can be obtained as the weighing result of the weighing unit 5N.

<Normal mode>
First, an example of a specific processing flow when the weighing inspection process (see FIG. 13) is performed in the normal mode will be briefly described. Here, the case where the weighing reduction function is set to be invalid and the medicine identification information is read from the PTP sheet in step S18 will be described as an example.

  In the normal mode, in step S31, the control unit 10 determines the weight per PTP and the number per PTP of the medicine corresponding to the medicine identification information read in the step S17 or the step S18. Obtain from the master.

  Then, in step S37, the control unit 10 collates the total of the weighing results by the one or more weighing units 5N with the prescription data. First, the control unit 10 divides a value obtained by subtracting the weight of the rubber band according to the number of sheets of the PTP sheet from the sum of the weighing results by the one or more weighing units 5N by the weight per one PTP ( (Total of weighing results-Weight of rubber band) / Weight per PTP sheet) The number of sheets C1 actually measured is calculated. The weight of the rubber band is a predetermined value preset as, for example, the weight of the rubber rubber corresponding to the number of PTP sheets, and the number of PTP sheets is a target value indicated in the prescription data. And it is calculated based on the number of pieces per PTP sheet. In addition, the weight of the rubber band may be a constant value regardless of the number of PTP sheets. Then, the control unit 10 calculates a value obtained by multiplying the number of sheets C1 by the number of sheets per PTP sheet as the actually measured number of tablets C2, and rounds off the first decimal place of the number of tablets C2. The number of tablets C3 is calculated. Thereafter, the control unit 10 determines whether or not the tablet number C3 indicating the number of tablets actually weighed and the prescription quantity which is the target value indicated in the prescription data match. Perform matching of the results with the prescription data.

<Weighing relaxation mode>
Next, an example of a specific processing flow when the weighing inspection process (see FIG. 13) is performed in the weighing reduction mode will be described. Here, the case where the weighing reduction function is effectively set and the medicine identification information is read from the PTP sheet in step S18 will be described as an example.

  In the weighing reduction mode, in step S31, the control unit 10 determines the weight per PTP sheet and the number per PTP sheet of the medicine corresponding to the medicine identification information read in the step S18. Acquired from the pharmaceutical master stored in the storage unit 40. Further, in step S31, the control unit 10 divides the number of tablets (prescription quantity), which is the target value indicated in the prescription data, by the number of sheets per one PTP sheet, and the target number of sheets C11 is The sheet number C12 is calculated by rounding off the first decimal place of the sheet number C11. For example, when the number of tablets (prescribed number), which is the target value indicated in the prescription data, is 28 tablets and the number of tablets per PTP sheet is 10 tablets, the number of sheets C11 is 28/10 = The number of sheets C12 is 2.8, and the number of sheets C12 with the first decimal place rounded off is two.

  Then, in step S37, the control unit 10 collates the total of the weighing results by the one or more weighing units 5N with the prescription data. First, in the same manner as in the normal mode, the control unit 10 has a value obtained by subtracting the weight of the rubber band according to the number of PTP sheets from the total of the weighing results by one or more of the weighing units 5N The number of sheets C1 is calculated by dividing by the weight of ((total of weighing results-weight of rubber band) / weight per PTP). Then, the control unit 10 calculates the number C13 of sheets obtained by rounding off the first decimal place of the number C1 of sheets. Thereafter, the control unit 10 determines that the number C13 of sheets indicating the number of PTP sheets actually weighed and the number C12 of sheets indicating the number of PTP sheets corresponding to the target value indicated in the prescription data coincide with each other. By determining whether or not it is determined, comparison between the weighing result and the prescription data is performed. In the weighing reduction mode, in the weighing display areas A11 to A14, the unit displayed as the target value and the conversion value is changed to “sheet”.

<2nd weighing relaxation mode>
Here, a second weighing mode, which is another example of the weighing mode, will be described. Specifically, in the weighing reduction mode, it is conceivable that an operation button for designating whether or not the fraction of the PTP sheet is to be displayed is displayed in the weighing display area A11 to A14. Then, the control unit 10 executes the weighing reduction mode when designation of not removing the fraction is performed by the operation button, and designation of removing the fraction is performed by the operation button. The second weighing mode described below is executed.

  By the way, the EEPROM of the control unit 10 stores a threshold C31 used when calculating the number of sheets. The threshold C31 is a value less than 1 set in advance, and is set to, for example, 0.2 or 0.5. The control unit 10 can arbitrarily set the threshold value C31 according to, for example, a user's operation input using the display unit 20 and the operation unit 30 at the time of initial setting or start of weighing inspection in the inspection support device 100. It is.

  In the second weighing mode, the control unit 10 divides the number of tablets (prescription number), which is the target value indicated in the prescription data, by the number per one PTP sheet in the step S31. The number of sheets C11 is calculated, and the number of sheets C12 is calculated by rounding off the first decimal place of the number of sheets C11. At this time, the control unit 10 temporarily stores the fraction C111, which is the value of the first decimal place of the number of sheets C11, in the RAM or the EEPROM. The value of the number C11 of sheets may be stored as the fraction C111, as well as the value of the first decimal place and the value of the second decimal place, or the entire decimal part.

  Thereafter, in step S37, the control unit 10 collates the total of the weighing results by the one or more weighing units 5N with the prescription data. First, as described above, the control unit 10 divides the weight of the rubber band according to the number of PTP sheets from the measurement result of the weighing unit 5N by dividing it by the weight per PTP (( The total of the weighing results-the weight of the rubber band) / the weight per PTP) and the number of sheets C1 are calculated. Next, the control unit 10 calculates the number of sheets C4 which is a value obtained by removing the fraction C111 from the number of sheets C1. At this time, when a plurality of weighing units 5N are associated with the same medicine, the control unit 10 updates the fraction C111 in advance to a value obtained by dividing the number by the number of the weighing units 5N. When the number of sheets C1 is larger than “−0.5” and the number of sheets C4 is smaller than “0”, the control unit 10 sets the number of sheets C4 to “0”.

  Then, when the fractional part of the number of sheets C4 is smaller than the threshold C31, the control unit 10 calculates a value obtained by rounding off the first decimal place of the number of sheets C4 as the number of sheets C5. On the other hand, when the fractional part of the number of sheets C4 is the threshold C31 or more, the control unit 10 calculates a value obtained by rounding up the first decimal place of the number of sheets C4 as the number of sheets C5. Thereafter, the control unit 10 calculates the number of sheets C14 which is the total of the number of sheets C5 calculated based on the measurement result by the one or more weighing units 5N, and the number of sheets C14 becomes the number of sheets C12. On the other hand, if it is within a predetermined tolerance, it is determined that the matching result is a match. That is, if "the number of sheets C12-the previously set lower limit allowable value" 前 記 "the number of sheets C5" 前 記 "the number of sheets C12 + the previously set upper limit allowable value" Ru.

  Specifically, the target number of tablets is "21", the number per PTP sheet is "10", the weight per PTP sheet is "2 g", the threshold C31 is "0.2", the weighing section Consider the case where the measured value of 5N is “4.4 g”, the upper limit allowable value is “1”, and the lower limit allowable value is “1”. Here, it is assumed that one weighing unit 5N is associated with one medicine.

  In this case, first, the control unit 10 calculates “2.1” as the number of sheets C11 by dividing “21” which is the target value by “10” which is the number per PTP sheet, By rounding off the first decimal place of the number of sheets C11, "2" is calculated as the number of sheets C12. Further, the control unit 10 stores “0.1” which is a value of the first decimal place of the number of sheets C11 as the fraction C111.

  Next, the control unit 10 divides “4.4 g”, which is the weighing value of the weighing unit 5N, by “2 g,” which is the weight per PTP sheet, and thereby “2.2” as the number of sheets C1. Calculate Further, the control unit 10 calculates "2.1" as the number of sheets C4 by subtracting "0.1" which is the fraction C111 from the number of sheets C1.

  Thereafter, the control unit 10 truncates the first decimal place of the number C4 of sheets since the decimal part "0.1" of the number C4 of sheets is smaller than "0.2" which is the threshold C31. “2” is calculated as the number of sheets C5. If the fractional part of the number C4 of sheets is equal to or more than "0.2" which is the threshold C31, "3" obtained by rounding up the first decimal place of the number C4 of sheets is calculated as the number C5 of sheets Ru.

  Then, the control unit 10 sets a value “1” obtained by subtracting “1” which is the lower limit allowable value from “2” which is the number C12 of sheets to “2” or less which is the number C5 of sheets. Since the value “3” obtained by adding “1” which is the upper limit allowable value to “2” which is the number C12 is “2” or more which is the number C5 of sheets, it is determined that the collation result is identical. When the control unit 10 does not satisfy the condition of “the number of sheets C12−predetermined lower limit allowable value” ≦ “the number of sheets C5” ≦ “the number of sheets C12 + predetermined upper limit allowable value” , It is determined that the matching result is not consistent.

  By the way, when the number (for example, 3 tablets) smaller than the number (for example, 10 tablets) per PTP sheet is the target value in the weighing reduction mode or the second weighing reduction mode, a target sheet to be compared The number may be "0". On the other hand, after the medicine to be weighed is selected, before the medicine is placed on the weighing unit 5N, for example, when the user touches the weighing unit 5N or when it is affected by wind. The value of the weighing unit 5N may instantaneously increase and return to “0”. In this case, since the measurement result of the weighing unit 5N is “0 g” and the number of sheets is “0”, it is conceivable that the comparison result is judged to be identical. Therefore, when the control unit 10 returns to “0” within a predetermined time set in advance after the measurement value of the measurement unit 5N increases from “0”, the control unit 10 uses the measurement unit 5N. It is conceivable not to carry out verification based on the weighing results. As a result, for example, when the user touches the weighing unit 5N or when it is affected by the wind, it is possible to prevent the matching result from being judged to be a match. Further, after the weighing value of the weighing unit 5N increases from "0", the control unit 10 causes the weighing unit 5N to return to "0" without the weighing value of the weighing unit 5N becoming stable. It is also conceivable not to carry out a verification based on the weighing results.

  Further, after the weighing value of the weighing unit 5N increases from "0", the medicine is placed on the weighing unit 5N when the weighing value decreases and becomes stable at a predetermined value or more set in advance. Since there is a possibility, in such a case, the control unit 10 is considered to execute matching based on the stable weighing result. On the other hand, when the weighing value of the weighing unit 5N increases from “0” and then decreases to “0” after passing through the specific value, the control unit 10 checks the comparison based on the weighing result by the weighing unit 5N. Do not run The specific value may be, for example, a preset constant value. Further, the control unit 10 may use a value of a predetermined ratio of a target weight corresponding to a target value (such as the number of tablets) of the medicine associated with the weighing unit 5N, or a value obtained by subtracting a predetermined value from the target weight. It is also conceivable to calculate as the specific value each time. Also in this case, for example, when the hand of the user touches the weighing unit 5N or when it is affected by the wind, it is prevented that the comparison result is determined to be the same. Furthermore, it is also conceivable that the control unit 10 determines the presence or absence of the execution of the matching based on both the specific time and the specific value.

Eighth Embodiment
By the way, when checking the measurement results such as the number of tablets or the number of sheets measured by each of the weighing units 5N in step S37, the control unit 10 checks in advance the degree of the error included in the measurement results. It is conceivable to classify into a plurality of defined stages and execute processing according to the classification. Specifically, even if the weighing result matches the target value, the number of medicines or the number of sheets of the medicine calculated as the weighing result may be rounded off, rounded up, or cut off with respect to the actual value. It has been corrected. Therefore, even if the comparison result matches, depending on the contents of the correction, the number of medicines may not actually match the target value. Therefore, it is conceivable that the control unit 10 changes the display mode such as the background color of the weighing display area A1M according to the degree of the error included in the weighing result.

  For example, when the control unit 10 rounds off the medicine quantity obtained as the weighing result by the weighing unit 5N, a difference between the medicine quantity and the medicine quantity after the rounding (hereinafter referred to as "corrected medicine quantity") In the case where there is a high possibility that the post-correction medicine quantity is not appropriate, as in the case where the difference value C6 that is ± 0.5 or more (+0.5 or more or −0.5 or less), the weighing result is The background of the obtained weighing display area A1M is displayed in a first predetermined specific color such as transparent or red. Further, when the difference value C6 is ± 0.25 or more and less than ± 0.5 (+0.25 or more and less than +0.5, or −0.25 or less and −0.5). As in the case of large), when it is considered that the post-correction medicine quantity is likely to be appropriate but there is doubt about the judgment, the background of the weighing display area A1M from which the weighing result is obtained is grayed, etc. Is displayed in a second predetermined specific color. Then, as in the case where the difference value C6 is less than ± 0.25 (less than +0.25 and greater than −0.25), the control unit 10 may have the possibility that the corrected medicine quantity is appropriate. If it is high, the background of the weighing display area A1M for which the weighing result is obtained is displayed in a predetermined third specific color such as light green.

  Thereby, the user can determine whether the corrected medicine quantity is appropriate or not with reference to the color arrangement of the weighing display area A1M. For example, when the background color of the weighing display area A1M is the first specific color, the user determines that the post-correction medicine quantity is not appropriate, and when the background color is the second specific color, the correction It is possible to judge that it is necessary to carry out a visual check because there is a possibility that the post medicine quantity is not appropriate, and in the case of the third specific color, it is possible to judge that the medicine quantity after correction is appropriate. . The change of the display mode of the weighing display area A1M is not limited to the background color. For example, the color arrangement of the edge of the weighing display area A1M may be changed. Furthermore, the control unit 10 sets the color arrangement (character color or background color) of the area in the medicine display area A15 where the medicine associated with the weighing unit 5N for which the weighing result is obtained is displayed. It is also conceivable to change to a specific color, the second specific color, or the third specific color.

  Further, the control unit 10 may display on the display unit 20 a message set in advance according to the degree of the error included in the measurement result. For example, when the difference value C6 is ± 0.5 or more, the control unit 10 indicates that the possibility that the post-correction medicine quantity is not appropriate is high, or that the possibility of including an error factor is high. And the like can be displayed on the display unit 20. Further, when the difference value C6 is ± 0.25 or more and less than ± 0.5, the control unit 10 has a high possibility that the post-correction medicine quantity is appropriate, but the visual confirmation by the user is It is conceivable to display a prompt message or the like on the display unit 20. Furthermore, when the difference value C6 is less than ± 0.25, the control unit 10 may cause the display unit 20 to display that the possibility that the post-correction medicine quantity is appropriate is high. .

  Furthermore, the determination processing in the case where the control unit 10 is considered to have doubts about the suitability of the post-correction medicine quantity as in the case where the difference value C6 is ± 0.25 or more and less than ± 0.5 A configuration can be considered that can be set in advance according to the user operation in initial setting and the like. For example, as one example of the determination process, it may be considered that the amount of medicine after correction is determined to be appropriate, and the color arrangement of the weighing display area A1M is set as the second specific color.

  In addition, as another example of the determination process, an operation button for selecting whether or not the post-correction medicine quantity is appropriate is displayed together with a message indicating that the propriety of the post-correction medicine quantity is doubtful. It is conceivable. In this case, when an operation to the effect that the post-correction medicine quantity is appropriate is performed on the operation button, the control unit 10 determines that the post-correction medicine quantity is appropriate, and the weighing display area It is conceivable to set the color arrangement of A1M as the second specific color. On the other hand, when an operation to the effect that the post-correction medicine quantity is not appropriate is performed on the operation button, the control unit 10 determines that the post-correction medicine quantity is not appropriate, and the control by the weighing part 5N It is conceivable to start weighing and checking.

  Specifically, when the weight per PTP is "10 g", the number per PTP is "10 tablets", and the target value is "35 tablets", the following first condition is satisfied in the weighing units 51 to 53: A case where three types of weighing values of the third to third conditions are obtained will be considered. The said 1st conditions are weighing part 51: 10.1g, weighing part 52: 13g, and weighing part 53: 12.2g. The said 2nd conditions are weighing part 51: 10.1g, weighing part 52: 13.4g, and weighing part 53: 12.2g. The third condition is that the weight part 51: 10.1 g, the weight part 52: 13.4 g, and the weight part 53: 12.8 g. The control unit 10 calculates “1 g”, which is a value obtained by dividing the weight per PTP sheet by the number per one PTP sheet, as the weight per tablet, and executes the following processing.

<In the case of the first condition>
First, in the case of the first condition, the control unit 10 calculates the “10.1 tablets” as the medicine quantity because the weighing value of the weighing unit 51 is “10.1 g”, Calculate “10 tablets” as the post-correction medicine quantity. Similarly, the control unit 10 calculates “13.0 tablets” as the medicine quantity and then calculates “13 tablets” as the medicine quantity after correction since the measurement unit 52 is “13 g”. . In addition, since the control unit 10 is “12.2 g” for the weighing unit 53, after calculating “12.2 tablets” as the medicine quantity, “12 tablets” as the medicine quantity after correction calculate. In these cases, since the difference value C6 is “0.1 tablet”, “0.0 tablet”, and “0.2 tablet”, the weighing display area A11 to the weighing unit 51 correspond to the weighing units 51 to 53, respectively. The background of A13 is the third specific color. In the case of the first condition, since the total of the post-correction medicine quantity which is the weighing result is 35 tablets, the control unit 10 determines that the comparison result of the weighing result and the target value is identical. Do.

<In the case of the second condition>
On the other hand, in the case of the second condition, the control unit 10 calculates “13.4 tablets” as the medicine quantity since the weighing value of the weighing unit 52 is “13.4 g”, Calculate “13 tablets” as the post-correction medicine quantity. In this case, since the difference value C6 is "0.4 tablets", the background of the weighing display area A12 corresponding to the weighing unit 52 is the second specific color. In the case of the second condition, the weighing units 51 and 53 are the same as the first condition. In the case of the second condition, since the total of the post-correction medicine quantity which is the weighing result is 35 tablets, the control unit 10 determines that the comparison result of the weighing result and the target value is identical. However, the background color of the weighing display area A12 corresponding to the weighing unit 52 is displayed in the second specific color such as gray.

<In the case of the third condition>
Further, in the case of the third condition, the control unit 10 calculates “12.8 tablets” as the medicine quantity since the weighing value is “12.8 g” for the weighing unit 53, Calculate “13 tablets” as the post-correction medicine quantity. In this case, since the difference value C6 is "0.2 tablets", the background of the weighing display area A13 corresponding to the weighing unit 52 is the third specific color. In the case of the third condition, in the case of the third condition which is the same as the second condition for the weighing units 51, 52, the total of the post-correction medicine quantity which is the weighing result is 36 tablets, It differs from the target value. Therefore, the control unit 10 determines that the comparison result between the measurement result and the target value is not identical, and the background color of the measurement display area A12 corresponding to the measurement unit 52 is the second color such as gray. Display in a specific color.

  By the way, even if the control unit 10 does not match the matching result in the step S37, the user does not match the matching result due to the influence of the wind or the attachment of the medicine, and the like. When it is determined that it is clear that there is no problem even if the matching result is processed as a match and a predetermined user operation is performed, it is conceivable to process the matching result as a match. In this case, the control unit 10 changes the color arrangement (background color or border color) of the weighing display area A1M corresponding to the weighing unit 5N and the color arrangement (text color or color) of the area corresponding to the medicine in the prescription display area A15. It is conceivable to display the background color or the like in the first specific color or a predetermined fourth specific color. Furthermore, when the predetermined user operation is performed, the control unit 10 displays a comment field for inputting a reason for processing as matching with the matching result, and the comment input by the user in the comment field is displayed. It records in association with the prescription data. As described above, it is also conceivable that the background color of the visually inspected medicine in the prescription display area A15 is different from that of the other medicines in the visually inspected medicine. Furthermore, when the medicine after the visual inspection has been placed on the weighing unit 5N, the control unit 10 arranges the color arrangement (the background color or the border color) of the weighing display area A1M corresponding to the weighing unit 5B. May be displayed in a fifth specific color such as light blue.

[Ninth embodiment]
Further, as shown in FIG. 29, the inspection support device 100 is considered to include a calibration processing unit 193 capable of executing a calibration process for calibrating the weighing units 51 to 54. Specifically, the control unit 10 functions as the calibration processing unit 193 by executing various processes in accordance with the inspection support program. 30A to 30E are diagrams showing transition examples of the display screen when the calibration processing is performed by the calibration processing unit 193.

  Specifically, the calibration processing unit 193 performs operations for executing the initial setting of the inspection support device 100 and then performs a start operation of “balance calibration”, as shown in FIGS. 30A to 30E. Thus, the display unit 20 displays a navigation screen for performing calibration of any of the weighing units 51 to 54. In FIG. 30A to FIG. 30E, the contents of the calibration process are “1. designation of balance”, “2. preparation”, “3. put a weight on”, “4. remove weight”, and “5. completed” It is indicated that the procedure is included. Moreover, in FIG. 30A-FIG. 30E, the procedure currently performed in the calibration process is displayed by coloring of the location corresponding to the procedure. For example, in FIG. 30A, only portions corresponding to “1. designation of balance” are colored, and in FIG. 30B, portions corresponding to “1. designation of balance” and “2. preparation” are colored. . Hereinafter, display and processing of each procedure will be described.

  First, FIG. 30A is a first display screen corresponding to “1. designation of balance”. In the above first display screen, "calibrate A / D 100g correction weight width of balance. Select a balance to be calibrated, and click" Next "button. In addition to the message “,” “balance 1”, “balance 2”, “balance 3”, and “balance 4” corresponding to the weighing units 51 to 54 as options are displayed. Here, when one of “balance 1”, “balance 2”, “balance 3”, and “balance 4” is selected and the “next” operation key is operated, the calibration processing unit 193 The weighing unit (hereinafter, referred to as calibration target weighing unit) of the weighing units 51 to 54 corresponding to the selected balance is selected as a calibration target in the calibration process.

  Next, FIG. 30B is a second display screen corresponding to “2. Preparation”. On the second display screen, confirm that nothing is on the balance 1 and press the "Next" button. "" Message is displayed. Here, when the “next” operation key is operated, the calibration processing unit 193 determines that nothing is on the calibration target weighing unit (the weighing value is 0).

  Next, FIG. 30C is a third display screen corresponding to “3. Put a weight on”. In the 3rd display screen, put “weight (200 g) on balance 1 and press“ Next ”button. "" Message is displayed. Here, when the "next" operation key is operated, the calibration processing unit 193 determines that the weight (200 g) is placed on the calibration target weighing unit, and executes the weighing by the calibration target weighing unit. Do.

  After that, FIG. 30D is a fourth display screen corresponding to “4. Remove weight”. On the fourth display screen, remove the weight (200 g) from the balance 1 and press the "Next" button. "" Message is displayed. Here, when the “next” operation key is operated, the calibration processing unit 193 determines that nothing is on the calibration target weighing unit (the weighing value is 0). At this time, the calibration processing unit 193 weighs the calibration target based on the weighing result when the weight is placed on the calibration target weighing unit and the weighing result when the weight is not placed on the calibration target weighing unit. Calibrate the department. Specifically, the calibration processing unit 193 is configured to adjust the “A / D 100 g correction weight width (balance 1)”, “A / D 100 g correction weight width (balance 2)”, “A / D 100 g” corresponding to the weighing units 51 to 54. The set value corresponding to the calibration target weighing unit is updated among the corrected weight width (balance 3) and the A / D 100 g corrected weight width (balance 4). For example, when the weight is not loaded, the calibration processing unit 193 outputs the analog signal output from the load cell 56 of the calibration target weighing unit and the load cell of the calibration target weighing unit when the weight is loaded. The analog value per 1 g calculated by dividing the difference from the analog signal output from 56 by the weight (200 g) of the weight is recorded as the A / D 100 g correction weight width. Thereby, thereafter, in the inspection support device 100, the value of the analog signal output from the load cell 56 of the calibration target weighing unit using the value of the A / D 100g correction weight width calibrated by the calibration processing unit 193 Is converted to the weighing result of the digital signal.

  And FIG. 30E is a 5th display screen corresponding to "5. completion." On the fifth display screen, when the calibration by the calibration process is normally performed, a message of “calibration of balance 1 has been completed.” Is displayed. If an error occurs during calibration by the calibration process, a message of “Failure to calibrate the balance 1 has failed.” Is displayed on the fifth display screen. For example, when the calibration processing unit 193 obtains a weighing result equal to or more than a preset value in a state in which no weight is placed on the calibration target weighing unit, or the weight on the calibration target weighing unit (200 g It is judged as an error when weighing results outside the preset range are obtained in a state where the vehicle should be riding).

Tenth Embodiment
Further, the inspection support device 100 has a reception result inquiry function of inquiring the reception result of the prescription data received by the inspection support device 100. Specifically, the display processing unit 17 of the control unit 10 executes a reception result inquiry process for realizing the reception result inquiry function. In the inspection support device 100, the control unit 10 determines whether or not the prescription data received by the inspection support device 100 is normal, associates the determination result with the prescription data, and stores the storage unit. Remember to 40. For example, the control unit 10 lacks information necessary as the prescription data, such as when the prescription data does not include a drug name, or when the prescription data does not include a usage dose (fraction). If so, it is determined that the prescription data was not successfully received.

  Then, when the user operation for displaying the list of prescription data received by the inspection support device 100 is performed, the display processing unit 17 displays the unprocessed list screen illustrated in FIG. 31A and the unprocessed list screen illustrated in FIG. 31B. Among the list screens, a screen set in advance as an initial screen is displayed. In addition, the display processing unit 17 prescribes the display contents of the unprocessed list screen as a normal prescription in accordance with the operation of the operation key corresponding to “normal” in the unprocessed list screen and the operation key corresponding to “abnormal”. It switches to a list of data (FIG. 31A) and a list of prescription data with abnormality (FIG. 31B). In the unprocessed list screen shown in FIG. 31A, a prescription date, a patient name, a total Rp number, a voucher number, etc. are displayed for the prescription data normally received by the inspection support device 100. On the other hand, on the unprocessed list screen shown in FIG. 31B, the date and time of occurrence, the patient name, the reason for abnormality, and the like are displayed for prescription data having an abnormality that the inspection support device 100 could not receive normally. Further, the display processing unit 17 can search and display prescription data for items such as “date”, “ID”, “name”, or “refund ticket” on the unprocessed list screen. It is. For example, in FIG. 31A, search results of prescription data corresponding to the date of November 30, 2013 are displayed, and in FIG. 31B, search results of prescription data corresponding to the date of June 16, 2014 are displayed. It is done.

10: Control unit 20: Display unit 30: Operation unit 40: Storage unit 50: Weighing devices 51-54: Weighing unit 55: Weighing tray 56: Load cell 60: Information reading unit 70: Photographing unit 80: Tablet terminal 90: Cover member 100: Inspection support device

Claims (9)

A storage unit for storing one or more Rp data indicating prescription drugs contained in the same medicine bag;
An information reading unit capable of reading drug identification information for identifying the drug from the packaging material of the drug, and reading prescription identification information for identifying the Rp data corresponding to the drug bag from the drug bag;
Corresponds to the medicine identification information read by the information reading unit based on the medicine identification information read by the information reading unit, the prescription identification information read by the information reading unit, and the Rp data Control unit that determines whether the medicine to be used is a prescribed medicine stored in a medicine bag corresponding to the Rp data identified by the prescription identification information read by the information reading unit, and displays the determination result on the display unit When,
Inspection support system equipped with The prescription identification information includes a prescription number for identifying prescription data including the Rp data, and an Rp number for identifying the Rp data in the prescription data.
An inspection support system according to claim 1. Means for printing the prescription identification information on the medicine bag,
An inspection support system according to claim 1 or 2. A processor mounted on an inspection support device including a storage unit storing one or more Rp data indicating prescription drugs contained in the same medicine bag;
A first step of reading drug identification information for identifying the drug from a packaging material of the drug;
A second step of reading prescription identification information for identifying the Rp data corresponding to the medicine bag from the medicine bag;
Corresponds to the medicine identification information read in the first step based on the medicine identification information read in the first step, the prescription identification information read in the second step, and the Rp data A third step of determining whether the drug to be administered is a prescription drug contained in a medicine bag corresponding to the Rp data identified by the prescription identification information read in the second step;
A fourth step of displaying the determination result in the third step on a display unit;
Inspection support program to execute the program. A weighing specification unit for specifying the weighing unit to be associated with the medicine identification information among a plurality of weighing units after the drug identification information is read from the medicine or the packaging material for the drug;
When one or a plurality of weighing units to be associated with the medicine identification information is specified by the weighing specification unit, collation processing is started to collate the measurement result of the specified one or more weighing units with prescription data. A processing unit,
Inspection support device equipped with The weighing specification unit identifies the weighing unit whose weighing value has increased after the medicine identification information is read as the weighing unit to be associated with the medicine identification information.
An inspection support device according to claim 5. In the matching process, when the weighing result of one or more of the weighing units specified by the weighing specifying unit is determined, the weighing result is compared with the prescription data.
The inspection support device according to claim 5 or 6. The plurality of weighing units,
An information reading unit which reads the medicine identification information from a medicine or medicine packaging material;
Equipped with
The inspection support device according to any one of claims 5 to 7. A weighing specification step of specifying the weighing unit to be associated with the medicine identification information among a plurality of weighing units after the drug identification information is read from the medicine or the packaging material for the drug;
When one or a plurality of weighing units to be associated with the medicine identification information is specified in the weighing specifying step, collation processing is started to collate the weighing result of the specified one or more weighing units with prescription data. Step and
Inspection support program for making a computer execute.