CN111755095A - Drug storage device management method and related device - Google Patents
Drug storage device management method and related device Download PDFInfo
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Abstract
The application discloses a medicine storage device management method and a related device, wherein the medicine storage device management method comprises the following steps: the medicine using device acquires the identification mark of the loaded medicine storage device; acquiring current accumulated use information of the medicine storage device and rated use information of the medicine storage device by using the identification mark; based on the cumulative usage information and the rated usage information, it is determined whether to stop using the medicine storage device. Above-mentioned scheme can improve the management effect and the efficiency of medicine storage device.
Description
Technical Field
The present application relates to the field of medical device technology, and in particular, to a method for managing a drug storage device and a related device.
Background
In the field of medical applications, to ensure sterile use, drug storage devices such as drug cassettes, infusion bags and the like often have strict usage regulations during use, e.g., the reuse of drug storage devices and the like is strictly prohibited. Therefore, it is necessary to perform supervision and management during the use of the medicine storage device, and manual management consumes a lot of human resources, and often cannot achieve seamless management in the whole process, thereby resulting in poor management effect and low efficiency of the medicine storage device. In view of the above, how to improve the management effect and efficiency of the drug storage device is a problem to be solved urgently.
Disclosure of Invention
The technical problem that the application mainly solves is to provide a medicine storage device management method and a related device, and the management effect and efficiency of the medicine storage device can be improved.
In order to solve the above technical problem, a first aspect of the present application provides a method for managing a drug storage device, including: the medicine using device acquires the identification mark of the loaded medicine storage device; acquiring current accumulated use information of the medicine storage device and rated use information of the medicine storage device by using the identification mark; based on the cumulative usage information and the rated usage information, it is determined whether to stop using the medicine storage device.
In order to solve the above technical problem, a second aspect of the present application provides a medication administering device, which includes a memory and a processor coupled to each other, wherein the memory stores program instructions for execution by the processor to implement the method for managing the medication administering device in the first aspect.
Above-mentioned scheme, the identification sign of medicine device through acquireing the storage medicine device that loads is used to the medicine device, acquire the current accumulative total service information of medicine device and the rated service information of medicine device storage, thereby based on accumulative total service information and rated service information, whether confirm to stop using the storage medicine device, the event can be in the use of medicine device, utilize the rated service information automatic supervision's of medicine device storage accumulative total service information, and can be favorable to forbidding storage medicine device reuse, thereby can need not artifical supervision and can realize the seamless supervision to storage medicine device, and then can improve the management effect and the efficiency of storage medicine device.
Drawings
In order to more clearly illustrate the technical solutions in the present application, the drawings required in the description of the embodiments will be briefly introduced below, and it is obvious that the drawings described below are only some embodiments of the present application, and it is obvious for those skilled in the art that other drawings can be obtained according to the drawings without inventive labor. Wherein:
FIG. 1 is a schematic flow chart illustrating an embodiment of a method for managing a medication storage device according to the present application;
FIG. 2 is a schematic flow chart illustrating another embodiment of a method for managing a medication storage device according to the present application;
FIG. 3 is a block diagram of an embodiment of a medication device according to the present application;
FIG. 4 is a block diagram of an embodiment of a computer-readable storage medium of the present application.
Detailed Description
The technical solutions in the embodiments of the present application are clearly and completely described below with reference to the drawings in the embodiments of the present application, and it is obvious that the described embodiments are only a part of the embodiments of the present application, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present application.
Referring to fig. 1, fig. 1 is a schematic flow chart illustrating an embodiment of a method for managing a medicine storage device according to the present application. Specifically, the method may include the steps of:
step S11: the medication device obtains an identification of the loaded medication storage device.
The medicine device and the medicine storage device can be set according to specific application scenes. For example, in a conventional infusion scenario, the medication device may also be an infusion pump, and the medication storage device may be a drug cassette, and in a specific implementation scenario, in an analgesic application scenario, the medication device may specifically be an analgesic pump, and the medication storage device may specifically be a drug cassette containing an anesthetic drug. In addition, the medicine taking device can also be a syringe pump, and the medicine storage device can also be a medicine box containing injection; the medication device may also be a nutrition pump, and the medicine storage device may also be a medicine box containing a nutrition liquid, which is not limited herein.
In an implementation scenario, an electronic tag may be disposed on the drug storage device, the electronic tag may be a Radio Frequency Identification (RFID), and the drug administration device may obtain the Identification identifier of the drug storage device by scanning the electronic tag. The identification mark of the medicine storage device is the unique identification mark of the medicine storage device, and the identification marks of the medicine storage devices of different types and different batches are different. In a specific implementation scenario, when the electronic tag is disposed on the drug storage device, the drug delivery device is correspondingly disposed with a card reader for reading the electronic tag to obtain the identification of the drug storage device. In another specific implementation scenario, in order to prevent the electronic tag from being damaged by external force, a protection component may be further disposed on the drug storage device, and the electronic tag is protected by the protection component, so that the probability of damage to the electronic tag is reduced.
In another implementation scenario, an identification code (e.g., a two-dimensional code, etc.) may be further set on the medicine storage device, and the medicine administration device may further obtain the identification identifier of the medicine storage device by scanning the identification code, which is not limited herein.
Step S12: and acquiring the current accumulated use information of the medicine storage device and the rated use information of the medicine storage device by using the identification mark.
In one implementation scenario, the cumulative usage information may include a cumulative usage duration, where the cumulative usage duration represents a sum of the time duration of usage of the medication reservoir since activation to the current history. Specifically, when the medicine storage device is loaded, the historical use duration corresponding to the identification mark can be obtained through inquiry, the historical use duration represents the sum of the use durations of the medicine storage device before the medicine storage device is loaded at the present time, the current use duration of the medicine storage device is counted, and the current use duration represents the use duration of the medicine storage device after the medicine storage device is loaded at the present time, so that the accumulated use duration is obtained by using the historical use duration and the current use duration, and specifically, the sum of the historical use duration and the current use duration can be used as the accumulated use duration. In the embodiment of the application, the time when the medicine storage device is loaded indicates the time when the medicine storage device is started to be used by the medicine taking device, the time when the medicine storage device is stopped or used is suspended indicates the end of the loading of the medicine taking device, and the time when the medicine storage device is restarted or used is resumed indicates the start of the loading of a new time.
In a specific implementation scenario, if the current time is the time when the medicine storage device starts to be loaded, the current usage time of the medicine storage device is 0. In thatIn another specific implementation scenario, if it is T (e.g., 0.5) hours after the medicine storage device is loaded this time, the current usage time of the medicine storage device is T. In a further specific implementation scenario, the drug storage device is activated and used M times, and the 1 st use time is t1The 2 nd use time is t2By analogy, the duration of the M-1 time use is tM-1The use time is Mth time, and the used time from the current loading of the medicine storage device to the current time is tMI.e. the current use duration is tMSo the accumulated usage time t of the medicine storage devicesumCan be expressed asIn another specific implementation scenario, the current usage duration of the drug storage device may be counted according to a preset frequency, for example, the preset frequency may be set to 15 seconds/time, 30 seconds/time, 1 minute/time, and the like, and may be specifically set according to an actual application situation, which is not limited herein.
In another implementation scenario, the cumulative usage information may further include a cumulative usage dose, wherein the cumulative usage dose represents a sum of the drug storage device's activation to a current past usage dose. Specifically, when the medicine storage device is loaded, the historical usage dose corresponding to the identification mark can be obtained through inquiry, the historical usage dose represents the rated sum of usage doses of the medicine storage device before the medicine storage device is loaded at this time, the current usage dose of the medicine storage device is counted, and the current usage dose represents the usage dose of the medicine storage device after the medicine storage device is loaded at this time, so that the accumulated usage dose is obtained by utilizing the historical usage dose and the current usage dose, and specifically, the sum of the historical usage dose and the current usage dose can be used as the accumulated usage dose. In the embodiment of the application, the time when the medicine storage device is loaded indicates the time when the medicine storage device is started to be used by the medicine taking device, the time when the medicine storage device is stopped or used is suspended indicates the end of the loading of the medicine taking device, and the time when the medicine storage device is restarted or used is resumed indicates the start of the loading of a new time.
In one specific implementation scenario, the drug storage device is started to fill if it is currently the current drug storage deviceAnd at the loading moment, the currently used dosage of the medicine storage device is 0. In another specific implementation scenario, if L (e.g., 10, etc.) milliliters of the drug reservoir has been currently used after the drug reservoir is loaded for the present time, then the currently used dose of the drug reservoir is L. In a further specific embodiment, the drug reservoir is activated M times, and the 1 st dose is l1The 2 nd dose is l2By analogy, the dosage of the M-1 time is lM-1And the used dosage from the current loading of the medicine storage device to the current time is lMI.e. the current dose is lMSo the cumulative dosage l of the medicine storage devicesumCan be expressed asIn a further specific implementation scenario, the current dosage of the drug storage device may be counted according to a preset frequency, for example, the preset frequency may be set to 15 seconds/time, 30 seconds/time, 1 minute/time, and the like, and may be specifically set according to an actual application, which is not limited herein.
In yet another implementation scenario, the cumulative usage information may include both a cumulative usage duration and a cumulative dosage. Specifically, reference may be made to the description in the foregoing implementation scenario, which is not repeated herein.
In one implementation scenario, the nominal usage information may include a nominal usage duration, wherein the nominal usage duration represents a total duration of time that the medication reservoir is enabled for use. For example, the rated usage time of the drug storage device is 2 hours, which means that the sum of the usage time of the drug storage device after activation cannot exceed 2 hours, and the rated usage time may also be set to other values according to practical application, for example, 3 hours, 4 hours, and the like, which is not limited herein.
In another implementation scenario, the nominal usage information may further include a nominal usage dose, wherein the nominal usage dose represents a total dose that can be used after the drug storage device is activated. For example, the rated usage dose of the drug storage device is 100 ml, which means that the sum of the usage doses after the drug storage device is activated cannot exceed 100 ml, and the rated usage dose may be set to other values according to practical application, for example, 200 ml, 250 ml, and the like, which is not limited herein.
In a further embodiment, the nominal usage information can comprise both the nominal duration of use and the nominal dosage. Specifically, reference may be made to the description in the foregoing implementation scenario, which is not repeated herein.
In one implementation scenario, the medication device may be in communication connection with a server, and the server may store a correspondence between the identification mark of the medication device and the cumulative usage information and the rated usage information of the medication device, so that the cumulative usage information and the rated usage information of the medication device may be queried and obtained in the server. For example, the identification mark of the drug storage device a can be used for inquiring to obtain that the drug storage device a is an anesthetic drug box, the corresponding cumulative use duration is 30 minutes, the rated use duration is 1 hour, or the cumulative use dose is 50 milliliters, and the rated use dose is 100 milliliters, or the corresponding cumulative use duration is 30 minutes, the rated use duration is 1 hour, the cumulative use dose is 50 milliliters, and the rated use dose is 100 milliliters, and other scenes can be analogized, which is not illustrated one by one.
In another implementation scenario, the medication devices may further form a Mesh network in an ad hoc manner, for example, a SigMesh network is formed by using a SigMesh protocol, and SigMesh is a Bluetooth Mesh standard proposed by the Bluetooth technical association (Bluetooth SIG), so that the medication devices can broadcast the identification of the medication device loaded by the medication device through the SigMesh network, and broadcast at least one of the duration of each use and the dose of each use, so that each medication device in the SigMesh network can synchronize at least one of the duration of each use and the dose of each use of the medication device loaded by all the medication devices, and further obtain at least one of the historical duration of each use and the historical dose of the medication device through at least one of the duration of each use and the dose of each use of the medication device. For example, the SigMesh network includes the medication device 1, the medication device 2, and the medication device 3, the medication device 1 is loaded with the medicine storage device a, the medication device 2 is loaded with the medicine storage device B, and the medication device 3 is loaded with the medicine storage device C, so the medication device 1, the medication device 2, and the medication device 3 can broadcast the medicine storage device a, the medicine storage device B, the medicine storage device C for each use time and the dosage for each use in the network, respectively, so that the medication device 1 can store not only the accumulated use time and the accumulated use dosage of the medicine storage device a, but also the accumulated use time and the accumulated use dosage of the medicine storage device B and the medicine storage device C, and the medication device 2 and the medication device 3 can store the accumulated use time and the accumulated use dosage of the medicine storage device a, the accumulated use time and the accumulated use dosage of the medicine storage device B and the medicine storage device C in the.
In another implementation scenario, when the electronic tag is disposed on the drug storage device, the rated usage information of the drug storage device can be written into the electronic tag along with the identification mark, so that the drug administration device can obtain the identification mark and the rated usage information of the drug storage device by scanning the electronic tag.
Step S13: based on the cumulative usage information and the rated usage information, it is determined whether to stop using the medicine storage device.
In one implementation scenario, the accumulated usage information may include an accumulated usage duration, and the rated usage information may include a rated usage duration, so that it may be determined whether the accumulated usage duration is longer than the rated usage duration, and if the accumulated usage duration is longer than the rated usage duration, it may be determined to stop using the drug storage device. For example, the cumulative usage time of the drug storage device from activation to the present time is zero 1 minute for 5 hours, and the rated usage time of the drug storage device is 5 hours, it may be determined to stop using the drug storage device. In a specific implementation scenario, whether the accumulated usage duration is greater than the rated usage duration may be determined with a preset frequency, and the preset frequency may be set according to an actual application, for example, may be set to 10 seconds/time, 30 seconds/time, and the like, and is not limited herein. In another specific implementation scenario, after the accumulated usage duration is longer than the rated usage duration and the usage of the medicine storage device is determined to stop, a prompt message may be further output to prompt that the accumulated usage duration of the medicine storage device exceeds the rated usage duration. The prompting message may be in the form of voice, text, picture, etc., and is not limited herein. In addition, can also send prompt message to medical personnel in time change and store up medicine device. Therefore, when the medicine storage device is used at the beginning or in the using process of the medicine taking device, as long as the accumulated using time of the medicine storage device is longer than the rated using time, the medicine storage device is determined to be stopped, the medicine storage device can be forbidden from being reused, and the seamless management of the medicine storage device is realized.
In another implementation scenario, the accumulated usage information may further include an accumulated usage dose, and the rated usage information may include a rated usage dose, so that it may be determined whether the accumulated usage dose is greater than the rated usage dose, and if the accumulated usage dose is greater than the rated usage dose, it may be determined to stop using the drug storage device. For example, the cumulative dosage of the drug storage device from the activation to the current time is 100.1 ml, and the rated dosage of the drug storage device is 100 ml, it can be determined to stop using the drug storage device. In a specific implementation scenario, whether the accumulated usage amount is greater than the rated usage amount may be determined at a preset frequency, and the preset frequency may be set according to an actual application situation, for example, may be set to 10 seconds/time, 30 seconds/time, and the like, and is not limited herein. In another specific implementation scenario, when the accumulated usage dose is greater than the rated usage dose and it is determined to stop using the drug storage device, a prompt message may be output to prompt that the accumulated usage dose of the drug storage device exceeds the rated usage dose. The prompting message may be in the form of voice, text, picture, etc., and is not limited herein. In addition, can also send prompt message to medical personnel in time change and store up medicine device. Therefore, when the medicine storage device is used at the beginning or in the using process of the medicine taking device, the medicine storage device is determined to be stopped as long as the accumulated using dose of the medicine storage device is larger than the rated using dose, the recycling of the medicine storage device can be forbidden, and the seamless management of the medicine storage device is realized.
In yet another implementation scenario, the medication administering device may further obtain a rated lifespan of the medication storage device (i.e., a lifespan of the medication storage device), determine whether the current time exceeds the rated lifespan, and determine to stop using the medication storage device if the current time exceeds the rated lifespan. For example, if the rated life of the drug storage device is 12/31/2019 and the current time is 1/2010, it can be determined that the drug storage device is not used. In a specific implementation scenario, the medication device may obtain the rated service life of the medication storage device by scanning the electronic tag, querying the server, and the like, which refer to the relevant steps in the implementation scenario specifically, and are not described herein again. In another specific implementation scenario, when the current time exceeds the rated service life and the use of the medicine storage device is determined to be stopped, a prompt message can be output to prompt that the medicine storage device has passed the rated service life. The prompting message may be in the form of voice, text, picture, etc., and is not limited herein. In addition, can also send prompt message to medical personnel in time change and store up medicine device. Therefore, the medicine storage device is determined to be stopped when the medicine taking device starts to use the medicine storage device or when the medicine taking device is used and the current time exceeds the rated service life of the medicine storage device, the medicine storage device can be prohibited from being reused, and seamless management of the medicine storage device is achieved.
In another implementation scenario, the step of determining whether the accumulated usage time period is longer than the rated usage time period, whether the accumulated usage dose is longer than the rated usage dose, and whether the current time exceeds the rated usage time period may be performed simultaneously, and when at least one of the determination results is yes, the usage of the drug storage device is determined to be stopped. For example, when any one of the determination results is yes, the use of the medicine storage device is determined to be stopped, which may be specifically set according to the actual application, and is not limited herein.
In an implementation scenario, in order to remind that the accumulated use duration of the medicine storage device is close to the rated use duration, the medicine storage device can be replaced in time, whether the accumulated use duration is not greater than the rated use duration or not can be judged, and whether the duration difference between the rated use duration and the accumulated use duration is smaller than a preset duration or not can be judged, if yes, a prompt message can be output to prompt that the accumulated use duration of the medicine storage device is close to the rated use duration. Specifically, the preset time period may be set according to an actual application, for example, the preset time period may be set to 5 minutes, 10 minutes, and the like, and is not limited herein. The prompting message may be in the form of voice, text, picture, etc., and is not limited herein. In addition, can also send prompt message to medical personnel in time change and store up medicine device.
In another implementation scenario, in order to remind when the accumulated usage dose of the drug storage device is close to the rated usage dose, the drug storage device is convenient to replace in time, whether the accumulated usage dose is not greater than the rated usage dose or not can be judged, and whether the dose difference between the rated usage dose and the accumulated usage dose is smaller than a preset dose or not can be judged, if yes, a prompt message can be output to prompt that the accumulated usage dose of the drug storage device is close to the rated usage dose. Specifically, the preset dose may be set according to actual practice, for example, the preset dose may be set to 5 ml, 10 ml, etc., and is not limited herein. The prompting message may be in the form of voice, text, picture, etc., and is not limited herein. In addition, can also send prompt message to medical personnel in time change and store up medicine device.
Above-mentioned scheme, the identification sign of medicine device through acquireing the storage medicine device that loads is used to the medicine device, acquire the current accumulative total service information of medicine device and the rated service information of medicine device storage, thereby based on accumulative total service information and rated service information, whether confirm to stop using the storage medicine device, the event can be in the use of medicine device, utilize the rated service information automatic supervision's of medicine device storage accumulative total service information, and can be favorable to forbidding storage medicine device reuse, thereby can need not artifical supervision and can realize the seamless supervision to storage medicine device, and then can improve the management effect and the efficiency of storage medicine device.
Referring to fig. 2, fig. 2 is a schematic flow chart illustrating another embodiment of a method for managing a medicine storage device according to the present application. Specifically, the method may include the steps of:
step S21: and uploading the identification mark and the accumulated use information of the medicine storage device to a server.
The medication device may upload the identification and the cumulative usage information of the medication device to the server after each use of the medication device is completed. In one implementation scenario, the cumulative usage information may include at least one of a cumulative usage duration and a cumulative usage dosage, which is not limited herein. The obtaining method of the cumulative duration of use and the cumulative dosage of use may refer to the related steps in the foregoing embodiments, and will not be described herein again. Alternatively, the medication device may also upload the accumulated usage information and the identification thereof during the last use of the medication storage device to the server at a preset time interval, which is not limited herein. Specifically, the preset time period may be daily, weekly, etc., and is not limited herein.
Step S22: and receiving analysis result information obtained by analyzing the identification mark and the accumulated use information by the server.
In one implementation scenario, the accumulated usage information includes at least one of an accumulated usage amount and an accumulated usage duration, and the analysis result information includes an estimated stock quantity generated by using a shipment list stored by the server and the received accumulated usage information, where the shipment list may specifically include at least one of a total vector amount and a total usage duration of all the drug storage devices issued to the customer. Therefore, the stock quantity can be estimated according to the using quantity and the delivery quantity of the medicine storage device, and the customer service satisfaction can be favorably improved.
In a specific implementation scenario, the average usage duration of the medicine storage devices used by the customer on average each day may be obtained according to the accumulated usage duration and the date difference of delivery to the present, so that the estimated stock quantity may be generated using the average usage duration based on that the ratio of the remaining usage duration of all the medicine storage devices delivered to the customer to the average usage duration is less than a preset duration. For example, the cumulative usage time of all the medicine storage devices delivered to the customer from the shipment to the present is 500 hours, the date difference of the shipment to the present is 10 days, so the average usage time of the medicine storage devices used by the customer per day is 50 hours, and the total usage time of all the medicine storage devices delivered to the customer is 1000 hours (for example, the total usage time of 200 medicine storage devices rated for 5 hours is 1000 hours, or the total usage time of 500 medicine storage devices rated for 2 hours is 1000 hours), so the ratio of the remaining usage time of 500 hours (i.e., the total usage time minus the cumulative usage time already used) to the average usage time per day of 50 hours (i.e., 10 days) may be used as the estimated time for which the remaining medicine storage devices can be used, when the estimated time is less than the preset time (for example, 20 days), an estimated stock quantity may be generated for an average usage period of 50 hours, for example, the estimated stock quantity (i.e., 50 x 30/5-300) may be determined based on the average usage period per day (i.e., 50 hours), the number of days each stock can support usage (e.g., 30 days), and the rated usage period for each drug storage device (e.g., 5 hours).
In another specific implementation scenario, the average usage amount of the drug storage device used by the customer on average per day may be obtained according to the accumulated usage amount and the date difference of shipment up to now, so that the estimated stock quantity may be generated using the average usage amount based on the ratio between the remaining usage amount and the average usage amount of all the drug storage devices issued to the customer being less than a preset time period. For example, the total usage amount of all the medicine storage devices delivered to the customer from the self-delivery to the present is 5000 ml, the difference between the dates of delivery to the present is 10 days, so the average usage time period of the medicine storage devices used by the customer per day is 500 ml, and the total usage amount of all the medicine storage devices delivered to the customer is 10000 ml (for example, the total usage time period of 200 medicine storage devices rated for 50 ml is 10000 ml, or the total usage amount of 500 medicine storage devices rated for 20 ml is 10000 ml), so the ratio between the remaining usage amount of 5000 ml (namely, 10000 ml of the total usage amount minus 5000 ml of the used total usage amount) and the average usage amount of 500 ml per day (namely, 10 days) can be used as the estimated time period for which the remaining medicine storage devices can be used, when the estimated time period is less than the preset time period (for example, 20 days), an estimated stock quantity may be generated at an average use dose of 500 ml, which may be determined, for example, based on an average use dose per day (i.e., 500 ml), the number of days each stock can support use (e.g., 30 days), and a nominal use dose per drug storage device (e.g., 50 ml) (i.e., 500 × 30/50 — 300).
In another implementation scenario, the analysis result information may further include at least part of the identification identifiers obtained by removing the received identification identifiers from a delivery list stored in the server, where the delivery list includes identification identifiers of all the drug storage devices sent to the client, and a time difference between a rated lifespan corresponding to at least part of the identification identifiers and the current date is smaller than a preset time difference. Therefore, the reminding device can be beneficial to reminding the medicine storage device which is close to the rated service life in the residual medicine storage devices not used by the client. In one specific implementation scenario, the invoice contains the identifiers of all drug storage devices sent to the customer, e.g., a001, a002, a003, … …, a099, and the received identifiers may include: a001, a002, a003, … …, and a089, so the identifiers remaining after the received identifiers are rejected include: a090, a091, … … and a099, and may count a time difference between a rated service life corresponding to the identifiers and the current date, and filter out the identifiers having a time difference smaller than a preset time difference (e.g., 10 days), for example, the finally filtered identifiers include: a090, A091 and A092, the medicine storage devices corresponding to the identification marks can be reminded to be used as soon as possible.
In another implementation scenario, analysis may be performed according to the received cumulative usage information, the current production volume, and the inventory volume, so as to obtain analysis result information including production recommendations. For example, the accumulated usage dose of the customer may be counted, the average usage dose per day of the customer may be determined, and the performance of the stimulation plan, the reduction plan, or the maintenance plan may be determined using the average usage dose and the average single-day yield and inventory amount. For example, the average dosage is much larger than the sum of the average single-day yield and the inventory amount, and it may be determined to execute a yield increase plan, or the average dosage is much smaller than the sum of the average single-day yield and the inventory amount, and it may be determined to execute a yield decrease plan, or the average dosage is slightly smaller than the sum of the average single-day yield and the inventory amount, and it may be determined to execute a maintenance plan, and it may be specifically set as needed, and is not limited herein.
Step S23: and generating a corresponding prompt message based on the analysis result information.
In one implementation scenario, when the analysis result information includes an estimated stock quantity generated using the shipment list stored by the server and the received cumulative usage information, a prompt message including the estimated stock quantity may be generated to prompt confirmation of whether or not the stock device of the estimated stock quantity needs to be prepared. In one particular implementation scenario, after generating a prompt message containing the estimated quantity of stock, it may be forwarded to a healthcare facility manager (e.g., purchasing, logistics personnel) to remind the manager to confirm whether stock is needed.
In another implementation scenario, when the analysis result information includes at least part of the identification marks after the received identification marks are removed from the shipment list stored in the server, a prompt message containing at least part of the identification marks may be generated to prompt that the medicine storage devices corresponding to at least part of the identification marks are used as soon as possible. In a specific implementation scenario, after the prompt message including at least part of the identification mark is generated, the prompt message may be forwarded to the medical care personnel to remind the medical care personnel to use the drug storage device corresponding to at least part of the identification mark as soon as possible.
Different from the embodiment, the identification mark and the accumulated use information of the medicine storage device are uploaded to the server, and the analysis result information obtained by analyzing the identification mark and the accumulated use information by the server is received, so that the corresponding prompt message is generated based on the analysis result information, the closed-loop management of the medicine storage device from production to use can be favorably realized, and the management effect of the medicine storage device is improved.
Referring to fig. 3, fig. 3 is a schematic diagram of a medication administering device 30 according to an embodiment of the present application. The medication administering device 30 comprises a memory 31 and a processor 32 coupled to each other, the memory 31 storing program instructions for execution by the processor 32 to perform the steps of any of the above-described embodiments of the medication administering method. Specifically, the medication administering device 30 may be an analgesia pump, an infusion pump, a nutrition pump, a syringe pump, etc., and is not limited thereto.
Specifically, the processor 32 is configured to control itself and the memory 31 to implement the steps in any of the above embodiments of the drug storage device management method. The processor 32 may also be referred to as a CPU (Central Processing Unit). The processor 32 may be an integrated circuit chip having signal processing capabilities. The Processor 32 may also be a general purpose Processor, a Digital Signal Processor (DSP), an Application Specific Integrated Circuit (ASIC), a Field Programmable Gate Array (FPGA) or other Programmable logic device, discrete gate or transistor logic, discrete hardware components. A general purpose processor may be a microprocessor or the processor may be any conventional processor or the like. In addition, processor 32 may be commonly implemented by a plurality of integrated circuit chips.
In this embodiment, the processor 32 is configured to obtain an identification of the loaded drug storage device; the processor 32 is used for acquiring the current accumulated use information of the medicine storage device and the rated use information of the medicine storage device by using the identification mark; the processor 32 is configured to determine whether to discontinue use of the medication storage device based on the cumulative usage information and the nominal usage information.
According to the scheme, the medicine storage device 30 acquires the current accumulated use information of the medicine storage device and the rated use information of the medicine storage device by acquiring the identification mark of the loaded medicine storage device, so that whether the medicine storage device is stopped to be used or not is determined based on the accumulated use information and the rated use information, the accumulated use information can be automatically supervised by utilizing the rated use information of the medicine storage device in the use process of the medicine storage device, the reuse of the medicine storage device can be favorably forbidden, the seamless supervision of the medicine storage device can be realized without manual supervision, and the management effect and the efficiency of the medicine storage device can be improved.
In some embodiments, the cumulative usage information includes at least one of a cumulative usage period and a cumulative usage dose, the nominal usage information includes at least one of a nominal usage period and a nominal usage dose, the processor 32 is configured to determine to discontinue use of the drug reservoir when the cumulative usage period is greater than the nominal usage period, and/or the processor 32 is configured to determine to discontinue use of the drug reservoir when the cumulative usage dose is greater than the nominal usage dose.
In contrast to the foregoing embodiment, the accumulated usage information is set to include at least one of the accumulated usage duration and the accumulated usage dose, the rated usage information is set to include at least one of the rated usage duration and the rated usage dose, and when the accumulated usage duration is longer than the rated usage duration, the drug storage device is determined to be stopped, and when the accumulated usage dose is longer than the rated usage dose, the drug storage device is determined to be stopped, which can be advantageous to inhibit the drug storage device from being reused, and thus can be advantageous to improve the management effect of the drug storage device.
In some embodiments, the processor 32 is configured to query, when the medicine storage device is loaded, a historical usage duration corresponding to the identification mark, count a current usage duration of the medicine storage device, and obtain a cumulative usage duration by using the historical usage duration and the current usage duration.
Different from the embodiment, when the medicine storage device is loaded, the historical use duration corresponding to the identification mark is obtained through inquiry, the current use duration of the medicine storage device is counted, the historical use duration and the current use duration are utilized, the accumulated use duration is obtained, the accumulated use duration can be favorably and accurately determined in the use process of the medicine storage device, the medicine storage device can be favorably prevented from being reused, and the management effect of the medicine storage device can be favorably improved.
In some embodiments, the processor 32 is configured to query for a historical usage dose corresponding to the identification mark when the drug storage device is loaded, count a current usage dose of the drug storage device, and obtain a cumulative usage dose using the historical usage dose and the current usage dose.
Different from the embodiment, when the medicine storage device is loaded, the historical use dosage corresponding to the identification mark is obtained through inquiry, the current use dosage of the medicine storage device is counted, the historical use dosage and the current use dosage are utilized, the accumulated use dosage is obtained, the accumulated use dosage can be favorably determined in the use process of the medicine storage device, the medicine storage device can be favorably prevented from being reused, and the management effect of the medicine storage device can be favorably improved.
In some embodiments, the processor 32 is configured to output a first prompt message to prompt that the accumulated usage time of the drug storage device is close to the rated usage time when the accumulated usage time is not greater than the rated usage time and a time difference between the rated usage time and the accumulated usage time is less than a preset time.
Different from the embodiment, when the accumulated use time is not longer than the rated use time and the time difference between the rated use time and the accumulated use time is less than the preset time, the first prompt message is output, so that the accumulated use time of the medicine storage device can be prompted to be close to the rated use time, and the medicine storage device can be replaced in time.
In some embodiments, the processor 32 is configured to output a second prompt message to prompt that the accumulated used dose of the drug storage device is close to the rated used dose when the accumulated used dose is not greater than the rated used dose and a dose difference between the rated used dose and the accumulated used dose is less than a preset dose.
Different from the previous embodiment, when the accumulated used dose is not larger than the rated used dose and the dose difference between the rated used dose and the accumulated used dose is smaller than the preset dose, the second prompt message is output, the accumulated used dose of the medicine storage device can be prompted to be close to the rated used dose, and therefore the medicine storage device can be replaced in time.
In some embodiments, the processor 32 is configured to output a third prompting message to prompt that the cumulative usage period of time of the medication storage device has exceeded the rated usage period of time after the cumulative usage period of time is greater than the rated usage period of time and it is determined that the medication storage device is to be taken out of use.
Different from the embodiment, the accumulated use time of the medicine storage device can be prompted to exceed the rated use time by outputting the third prompt message, so that early warning can be timely performed.
In some embodiments, the processor 32 is configured to output a fourth prompt message to prompt that the cumulative dose of medication for the medication reservoir has exceeded the nominal dose of medication after the cumulative dose of medication is greater than the nominal dose of medication and the reservoir is determined to be removed from use.
Different from the embodiment, the accumulated use dosage of the medicine storage device can be prompted to exceed the rated use dosage by outputting the fourth prompt message, so that early warning can be timely performed.
In some embodiments, the medication administration device 30 further comprises a communication circuit, and the processor 32 is configured to control the communication circuit to upload the identification and cumulative usage information of the medication storage device to the server; the processor 32 is used for controlling the communication circuit to receive the analysis result information obtained by the server through the identification mark and the accumulated use information; the processor 32 is configured to generate a corresponding prompt message based on the analysis result information.
Different from the embodiment, the identification mark and the accumulated use information of the medicine storage device are uploaded to the server, and the analysis result information obtained by analyzing the identification mark and the accumulated use information by the server is received, so that the corresponding prompt message is generated based on the analysis result information, the closed-loop management of the medicine storage device from production to use can be favorably realized, and the management effect of the medicine storage device is improved.
In some embodiments, the accumulated usage information includes an accumulated usage amount and/or an accumulated usage duration, the analysis result information includes an estimated stock quantity generated using a shipment list stored by the server and the received accumulated usage information, wherein the shipment list includes a total usage amount and/or a total usage duration of all the drug storage devices delivered to the customer, and the processor 32 is configured to generate a fifth prompt message including the estimated stock quantity to prompt confirmation of whether the drug storage devices of the estimated stock quantity need to be prepared.
In contrast to the foregoing embodiment, the stock provision indication can be implemented by setting the accumulated usage information to include the accumulated usage amount and/or the accumulated usage period, setting the analysis result information to include the estimated stock quantity generated using the shipment list stored by the server and the received accumulated usage information, and generating a fifth prompt message including the estimated stock quantity by prompting to confirm whether the stock device of the estimated stock quantity needs to be prepared by the shipment list including the total usage amount and/or the total usage period of all the stock devices issued to the customer.
In some embodiments, the analysis result information is set to include at least part of the identification marks after the received identification marks are removed from the shipment list stored in the server, the shipment list is set to include the identification marks of all the medicine storage devices sent to the client, and the time difference between the rated service life corresponding to at least part of the identification marks and the current date is smaller than the preset time difference, so that a sixth prompt message including at least part of the identification marks is generated to prompt that the medicine storage devices corresponding to at least part of the identification marks are used as soon as possible, and further prompt can be performed when the unused medicine storage devices are close to the validity period.
In some embodiments, the drug storage device is provided with an electronic tag, the medication administering device 30 further comprises a scanning circuit, and the processor 32 is configured to control the scanning circuit to scan the electronic tag to obtain the identification of the drug storage device.
Be different from aforementioned embodiment, through set up electronic tags on storing up the medicine device to scanning electronic tags acquires the identification of storing up the medicine device, can acquire the identification of storing up the medicine device fast, and then can be favorable to improving the managerial efficiency of storing up the medicine device.
In some embodiments, the administration device is an analgesic pump and the drug storage device is a drug cassette.
Referring to fig. 4, fig. 4 is a block diagram of an embodiment of a computer-readable storage medium 40 according to the present application. The computer readable storage medium 40 stores program instructions 401, and when the program instructions 401 are executed by the processor, the steps of any of the above-mentioned drug storage device management method embodiments may be implemented.
Above-mentioned scheme can improve the management effect and the efficiency of medicine storage device.
In the several embodiments provided in the present application, it should be understood that the disclosed method and apparatus may be implemented in other ways. For example, the above-described apparatus embodiments are merely illustrative, and for example, a division of a module or a unit is merely a logical division, and an actual implementation may have another division, for example, a plurality of units or components may be combined or integrated into another system, or some features may be omitted, or not executed. In addition, the shown or discussed mutual coupling or direct coupling or communication connection may be an indirect coupling or communication connection of devices or units through some interfaces, and may be in an electrical, mechanical or other form.
Units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units, may be located in one place, or may be distributed on a plurality of network units. Some or all of the units can be selected according to actual needs to achieve the purpose of the embodiment.
In addition, functional units in the embodiments of the present application may be integrated into one processing unit, or each unit may exist alone physically, or two or more units are integrated into one unit. The integrated unit can be realized in a form of hardware, and can also be realized in a form of a software functional unit.
The integrated unit, if implemented in the form of a software functional unit and sold or used as a stand-alone product, may be stored in a computer readable storage medium. Based on such understanding, the technical solution of the present application may be substantially implemented or contributed to by the prior art, or all or part of the technical solution may be embodied in a software product, which is stored in a storage medium and includes instructions for causing a computer device (which may be a personal computer, a server, a network device, or the like) or a processor (processor) to execute all or part of the steps of the method according to the embodiments of the present application. And the aforementioned storage medium includes: a U-disk, a removable hard disk, a Read-Only Memory (ROM), a Random Access Memory (RAM), a magnetic disk or an optical disk, and other various media capable of storing program codes.
Claims (10)
1. A method of managing a medication storage device, comprising:
the medicine using device acquires the identification mark of the loaded medicine storage device;
acquiring current accumulated use information of the medicine storage device and rated use information of the medicine storage device by using the identification mark;
determining whether to stop using the medicine storage device based on the accumulated usage information and the rated usage information.
2. The method of claim 1, wherein the cumulative usage information comprises at least one of a cumulative usage duration and a cumulative usage dose, and the nominal usage information comprises at least one of a nominal usage duration and a nominal usage dose;
the determining whether to stop using the medicine storage device based on the accumulated usage information and the rated usage information includes:
if the accumulated use time is longer than the rated use time, determining to stop using the medicine storage device;
and/or determining to stop using the medicine storage device if the accumulated use dose is larger than the rated use dose.
3. The method of claim 2, wherein obtaining current cumulative usage information for the medication storage device using the identification tag comprises:
when the medicine storage device is loaded, inquiring to obtain the historical use time corresponding to the identification mark, counting the current use time of the medicine storage device, and obtaining the accumulated use time by using the historical use time and the current use time; and/or the presence of a gas in the gas,
when the medicine storage device is loaded, the historical usage dosage corresponding to the identification mark is obtained through inquiry, the current usage dosage of the medicine storage device is counted, and the accumulated usage dosage is obtained through the historical usage dosage and the current usage dosage.
4. The method of claim 2, further comprising:
if the accumulated use time is not longer than the rated use time and the time difference between the rated use time and the accumulated use time is less than the preset time, outputting a first prompt message to prompt that the accumulated use time of the medicine storage device is close to the rated use time;
and/or outputting a second prompt message to prompt that the accumulated used dose of the medicine storage device approaches the rated used dose if the accumulated used dose is not larger than the rated used dose and the dose difference between the rated used dose and the accumulated used dose is smaller than a preset dose.
5. The method of claim 2, wherein after determining to discontinue use of the medication storage device if the cumulative length of use is greater than the nominal length of use, the method further comprises:
outputting a third prompt message to prompt that the accumulated use time of the medicine storage device exceeds the rated use time;
and/or, after determining to stop using the medicine storage device if the accumulated usage dose is larger than the rated usage dose, the method further comprises:
outputting a fourth prompt message to prompt that the accumulated usage dose of the medicine storage device exceeds the rated usage dose.
6. The method of claim 1, further comprising:
uploading the identification mark and the accumulated use information of the medicine storage device to a server;
receiving analysis result information obtained by analyzing the server by using the identification mark and the accumulated use information;
and generating a corresponding prompt message based on the analysis result information.
7. The method according to claim 6, wherein the accumulated usage information includes accumulated usage amount and/or accumulated usage period, and the analysis result information includes estimated stock quantity generated by using a shipment list stored by the server and the received accumulated usage information, wherein the shipment list includes total usage amount and/or total usage period of all drug storage devices issued to the customer;
generating a corresponding prompt message based on the analysis result information, including:
and generating a fifth prompt message containing the estimated stock quantity to prompt the medicine storage device for confirming whether the estimated stock quantity needs to be prepared or not.
8. The method according to claim 6, wherein the analysis result information comprises at least part of identification marks after the received identification marks are removed from a delivery list stored by the server, wherein the delivery list comprises identification marks of all medicine storage devices sent to the client, and the time difference between the rated service life and the current date corresponding to the at least part of identification marks is smaller than a preset time difference;
generating a corresponding prompt message based on the analysis result information, including:
and generating a sixth prompt message containing the at least part of identification mark to prompt that the medicine storage device corresponding to the at least part of identification mark is used as soon as possible.
9. The method of claim 1, wherein the drug storage device is provided with an electronic tag; the medicine device obtains the identification mark of the loaded medicine storage device, and the method comprises the following steps:
and scanning the electronic tag to acquire the identification mark of the medicine storage device.
10. A medication device comprising a memory and a processor coupled to each other, the memory storing program instructions for execution by the processor to perform the medication device management method of any of claims 1 to 9.
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