Instrument management method, system, electronic device, and storage medium

Abstract

The application discloses an instrument management method and system, an electronic device and a storage medium, comprising: acquiring an instrument image; determining instrument basic information and instrument associated information according to the instrument image; determining cleaning, disinfecting and sterilizing treatment instructions according to the instrument basic information and a preset instrument reprocessing instruction library; and generating target business information according to the instrument basic information, the instrument associated information and the cleaning, disinfecting and sterilizing treatment instructions. Based on the instrument image, the related information of the instrument can be recognized, and the accuracy of instrument recognition can be effectively ensured. The instrument basic information is determined to facilitate the determination of the instrument status, and based on the instrument basic information and the instrument associated information, the instrument management efficiency can be improved. According to the instrument basic information, the instrument associated information and the cleaning, disinfecting and sterilizing treatment instructions, the target business information is generated, so that the instrument can be processed according to the target business information, and the reliability of instrument management can be effectively improved.

Description

Technical Field

[0001] This application relates to, but is not limited to, the field of medical device management technology, and in particular to a medical device management method, system, electronic device, and storage medium. Background Technology

[0002] Cleaning, disinfection, and sterilization of medical devices are key means of preventing and controlling hospital-acquired infections and ensuring medical quality. Medical devices are generally managed centrally, with the Central Sterile Supply Department (CSSD) responsible for the collection, cleaning, disinfection, sterilization, and supply of all reusable medical devices requiring disinfection or sterilization. With the continuous development of medical technology, the types of medical devices are increasing, their structures are becoming more complex, and their precision is increasing, leading to higher requirements for their management. In related technologies, it is often necessary to manually master the names of individual devices, the names of the entire set of devices, the current status of individual devices, the status of different devices within the entire set, the status of other basic packages within the same type of device set, and the ongoing modifications to the device set. This requires manual identification of device information and processing of the devices based on memory. However, the procedures for handling instruments are numerous, and the procedures for handling different instruments and instrument sets are different. Different instruments require different handling procedures. Using manual identification of instruments and accurate cleaning, disinfection, assembly and sterilization can easily lead to identification errors, resulting in incorrect instrument pack configuration, low reliability of instrument management, insufficient cleaning of instruments affecting sterilization effect, and use of incorrect disinfection and sterilization methods can damage instruments and lead to unqualified sterilization and incorrect instrument assembly, which can affect the operation. Summary of the Invention

[0003] This application provides a device management method, system, electronic device, and storage medium that can effectively improve the reliability of device management.

[0004] In a first aspect, embodiments of this application provide a medical device management method, including:

[0005] Acquire instrument images;

[0006] Determine the basic information and associated information of the device based on the device image;

[0007] The cleaning, disinfection, and sterilization instructions are determined based on the basic information of the instrument and the preset instrument reprocessing instruction library.

[0008] Target business information is generated based on the basic information of the device, the associated information of the device, and the cleaning, disinfection, and sterilization instructions.

[0009] The medical device management method according to the first aspect of this application has at least the following beneficial effects: It acquires medical device images to facilitate the determination of basic medical device information and related information. Identifying relevant medical device information based on medical device images effectively ensures the accuracy of medical device identification. Determining basic medical device information facilitates the identification of the device's name, the name of the entire set of medical devices, the current status of the device, and the current status of different devices within the entire set. Determining related information facilitates the identification of the current status of other basic packages of medical devices within the same type of medical device set, or the current status of similar medical devices. Based on basic medical device information and related information, it is beneficial to improve the efficiency of medical device management. Different medical devices and their conditions require different cleaning, disinfection, and sterilization procedures. Determining cleaning, disinfection, and sterilization procedures based on basic medical device information and a pre-set medical device reprocessing instruction library allows for the determination of the correct procedures for different medical devices and their conditions. Processing medical devices based on these procedures promotes the standardization and homogenization of medical device management. Target business information is generated based on the basic information of the device, the associated information of the device, and the cleaning, disinfection and sterilization instructions. This allows for the processing of the device according to the target business information, avoiding errors in device processing or incorrect configuration of the device package. Compared with related technologies where the device information is identified and processed manually based on memory, this method can effectively improve the reliability of device management.

[0010] According to some embodiments of the first aspect of this application, determining the basic information of the device and the device association information based on the device image includes:

[0011] The instrument image is identified to obtain basic information about the instrument.

[0012] The device association information is determined based on the device's basic information and the preset device classification information.

[0013] According to some embodiments of the first aspect of this application, the step of recognizing the device image to obtain basic device information includes:

[0014] The instrument image is preprocessed to obtain the target image;

[0015] Determine the device identifier based on the target image;

[0016] The initial image of the device is determined based on the device identifier and preset image information;

[0017] The device status information is determined by comparing the initial image of the device with the target image;

[0018] The device product information and device management information are determined based on the device identifier and the preset device information database;

[0019] The basic information of the device is obtained based on the device status information, the device product information, and the device management information.

[0020] According to some embodiments of the first aspect of this application, the step of generating target business information based on the basic device information, the device association information, and the cleaning, disinfection, and sterilization treatment instructions includes:

[0021] When the device status information indicates that the device is in the process of being processed in the sterilization supply center;

[0022] Obtain instrument processing flow information;

[0023] The target cleaning, disinfection and sterilization information is determined based on the instrument processing procedure information, the basic information of the instrument, and the cleaning, disinfection and sterilization treatment instructions.

[0024] The target business information is determined based on the target cleaning, disinfection, and sterilization information and the instrument association information;

[0025] or,

[0026] When the device status information indicates that the device is in a state to be recycled, the target recycling information is determined based on the basic device information and the cleaning, disinfection and sterilization treatment instructions.

[0027] According to some embodiments of the first aspect of this application, the device status information includes damage information and quantity information, and the step of determining the target cleaning, disinfection, and sterilization information based on the device processing flow information, the basic device information, and the cleaning, disinfection, and sterilization treatment instructions includes:

[0028] Based on the damage information and the quantity information, determine the instrument update information;

[0029] Historical cleaning, disinfection, and sterilization information is determined based on the aforementioned medical device management information;

[0030] When the instrument processing information indicates that the instrument is in the first cleaning, disinfection and sterilization process, the first cleaning, disinfection and sterilization instructions are determined according to the first cleaning, disinfection and sterilization process and the cleaning, disinfection and sterilization instructions.

[0031] The target cleaning, disinfection and sterilization information is obtained based on the instrument update information, the historical cleaning, disinfection and sterilization information and the first cleaning, disinfection and sterilization instructions.

[0032] or,

[0033] When the instrument processing flow information indicates that the instrument is in the second cleaning, disinfection and sterilization process, the second cleaning, disinfection and sterilization instructions are determined according to the second cleaning, disinfection and sterilization process and the cleaning, disinfection and sterilization instructions.

[0034] The target cleaning, disinfection, and sterilization information is obtained based on the instrument update information, the historical cleaning, disinfection, and sterilization information, and the second cleaning, disinfection, and sterilization instructions.

[0035] According to some embodiments of the first aspect of this application, determining the target recovery information based on the basic device information includes:

[0036] The recycling guidelines are determined based on the aforementioned medical device product information;

[0037] The device management information is used to determine the recycling contact information;

[0038] The target recycling information is obtained based on the recycling specification information and the recycling contact information.

[0039] According to some embodiments of the first aspect of this application, after generating target business information based on the basic device information and the device association information, the method further includes:

[0040] When the business status corresponding to the target business information indicates that it has been completed, the preset medical device information database is updated according to the target business information;

[0041] When the business status corresponding to the target business information indicates that it is not completed, a reminder message is generated based on the target business information.

[0042] Secondly, embodiments of this application provide a medical device management system, the system comprising:

[0043] An image acquisition module, wherein the image acquisition module is used to acquire instrument images;

[0044] A device information determination module, which is used to determine basic device information and device association information based on the device image;

[0045] The cleaning, disinfection and sterilization instruction manual determination module is used to determine the cleaning, disinfection and sterilization instruction manual based on the basic information of the instrument and a preset instrument reprocessing instruction manual library.

[0046] The target business information generation module is used to generate target business information based on the basic instrument information, the instrument association information, and the cleaning, disinfection, and sterilization instructions.

[0047] Thirdly, embodiments of this application provide an electronic device, including: a memory, a processor, and a computer program stored in the memory and executable on the processor, wherein the processor executes the computer program to implement the device management method as described in the first aspect.

[0048] Fourthly, embodiments of this application provide a computer-readable storage medium storing computer-executable instructions for causing a computer to perform the medical device management method as described in the first aspect. Attached Figure Description

[0049] The accompanying drawings are provided to further understand the technical solutions of the present invention and constitute a part of the specification. They are used together with the embodiments of the present invention to explain the technical solutions of the present invention, and do not constitute a limitation on the technical solutions of the present invention.

[0050] Figure 1 This is an optional flowchart of the medical device management method provided in the embodiments of this application;

[0051] Figure 2 This is a flowchart of an optional step in the method for determining device association information provided in the embodiments of this application;

[0052] Figure 3 This is an optional flowchart of the method for determining basic device information provided in the embodiments of this application;

[0053] Figure 4 This is an optional flowchart of the method for generating target business information provided in the embodiments of this application;

[0054] Figure 5 This is an optional flowchart of the method for determining target cleaning, disinfection and sterilization information provided in the embodiments of this application;

[0055] Figure 6 This is a flowchart of an optional step in the method for determining target recovery information provided in the embodiments of this application;

[0056] Figure 7 This is another optional flowchart of the medical device management method provided in the embodiments of this application;

[0057] Figure 8 This is a schematic diagram of an optional module of the medical device management system provided in an embodiment of this application;

[0058] Figure 9 This is a schematic diagram of the hardware structure of the electronic device provided in the embodiments of this application. Detailed Implementation

[0059] To make the objectives, technical solutions, and advantages of this application clearer, the following detailed description is provided in conjunction with the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative and not intended to limit the scope of this application.

[0060] In the description of this application, "several" means one or more, "multiple" means two or more, "greater than", "less than", "exceeding" etc. are understood to exclude the number itself, and "above", "below", "within" etc. are understood to include the number itself.

[0061] It should be noted that although functional modules are divided in the device schematic diagram and a logical order is shown in the flowchart, in some cases, the steps shown or described may be performed in a different order than the module division in the device or the order in the flowchart. The terms "first," "second," etc., in the specification, claims, or the aforementioned drawings are used to distinguish similar objects and are not necessarily used to describe a specific order or sequence.

[0062] Cleaning, disinfection, and sterilization of medical devices are key means of preventing and controlling hospital-acquired infections and ensuring medical quality. Medical devices are generally managed centrally, with the Central Sterile Supply Department (CSSD) responsible for the collection, cleaning, disinfection, sterilization, and supply of all reusable medical devices requiring disinfection or sterilization. With the continuous development of medical technology, the types of medical devices are increasing, their structures are becoming more complex, and their precision is increasing, leading to higher requirements for their management. Currently, it is often necessary to manually master the names of individual devices, the names of complete sets of devices, the current status of individual devices, the status of different devices within a complete set, and the status of other basic packages within similar sets. This manual identification and processing relies on memory. However, the device processing procedures are numerous, and different devices and sets require different procedures. Manual identification and accurate cleaning, disinfection, and sterilization are prone to errors, leading to incorrect device package configurations, low reliability of device management, insufficient cleaning affecting sterilization effectiveness, and the use of incorrect disinfection and sterilization methods, which can damage devices and result in sterilization failures.

[0063] To address the issue of low reliability in medical device management, this application provides a medical device management method, system, electronic device, and storage medium, including: acquiring medical device images; determining basic medical device information and associated medical device information based on the images; determining cleaning, disinfection, and sterilization instructions based on the basic medical device information and a pre-set medical device reprocessing instruction library; and generating target business information based on the basic medical device information, associated medical device information, and cleaning, disinfection, and sterilization instructions. Acquiring medical device images facilitates the determination of basic medical device information and associated medical device information. Identifying relevant medical device information based on medical device images effectively ensures the accuracy of medical device identification. Determining basic medical device information allows for the identification of the medical device name, the name of the entire medical device set, the current status of the medical device, and the current status of different medical devices within the entire medical device set. Determining associated medical device information allows for the identification of the current status of other basic packages of medical devices within the same type of medical device set or the current status of similar medical devices. Based on basic medical device information and associated medical device information, this improves the efficiency of medical device management. Different medical devices and their conditions require different cleaning, disinfection, and sterilization procedures. By determining the correct cleaning, disinfection, and sterilization instructions based on the device's basic information and a pre-defined medical device reprocessing instruction library, and processing the devices according to these instructions, the management of medical devices becomes more standardized and consistent. Target business information is generated based on the device's basic information, associated information, and the cleaning, disinfection, and sterilization instructions. This allows for the processing of medical devices according to the target business information, avoiding errors in device processing or incorrect device package configuration. Compared to related technologies where manual identification of device information and processing relies on memory, this approach significantly improves the reliability of medical device management.

[0064] The medical device management method, system, electronic device, and storage medium provided in this application are specifically described through the following embodiments. First, the medical device management method in this application is described. The medical device management method provided in this application relates to the field of medical device management technology. The medical device management method provided in this application can be applied to a terminal, a server, or software running on a terminal or server. In some embodiments, the terminal can be a smartphone, tablet computer, laptop computer, desktop computer, etc.; the server can be configured as an independent physical server, a server cluster or distributed system composed of multiple physical servers, or a cloud server providing basic cloud computing services such as cloud services, cloud databases, cloud computing, cloud functions, cloud storage, network services, cloud communication, middleware services, domain name services, security services, CDN, and big data and artificial intelligence platforms; the software can be an application that implements the medical device management method, but is not limited to the above forms.

[0065] This application can be used in a wide variety of general-purpose or special-purpose computer system environments or configurations. Examples include: personal computers, server computers, handheld or portable devices, tablet devices, multiprocessor systems, microprocessor-based systems, set-top boxes, programmable consumer electronics, network PCs, minicomputers, mainframe computers, and distributed computing environments including any of the above systems or devices. This application can be described in the general context of computer-executable instructions executed by a computer, such as program modules. Generally, program modules include routines, programs, objects, components, data structures, etc., that perform specific tasks or implement specific abstract data types. This application can also be practiced in distributed computing environments where tasks are performed by remote processing devices connected via a communication network. In distributed computing environments, program modules can reside in local and remote computer storage media, including storage devices.

[0066] It should be noted that in all specific embodiments of this application, when processing data related to user identity or characteristics, such as user information, user behavior data, user historical data, and user location information, user permission or consent is obtained first. Furthermore, the collection, use, and processing of this data comply with relevant laws, regulations, and standards. In addition, when embodiments of this application require access to sensitive personal information of users, separate permission or consent from the user is obtained through pop-ups or redirection to confirmation pages. Only after obtaining the user's separate permission or consent is the necessary user-related data required for the proper functioning of these embodiments acquired.

[0067] The embodiments of this application will be further described below with reference to the accompanying drawings.

[0068] Reference Figure 1 , Figure 1 This is an optional flowchart of the medical device management method provided in this application embodiment, which includes, but is not limited to, the following steps:

[0069] Step S110: Acquire instrument image;

[0070] Step S120: Determine the basic information and associated information of the device based on the device image;

[0071] Step S130: Determine the cleaning, disinfection and sterilization instructions based on the basic information of the instrument and the preset instrument reprocessing instruction library.

[0072] Step S140: Generate target business information based on basic device information, device association information, and cleaning, disinfection, and sterilization instructions.

[0073] It should be noted that the embodiments of this application do not limit the specific number of device images; they may include one device image or multiple device images. The embodiments of this application also do not limit the specific content of the device images; a device image may include one or more devices, or one or more device sets. It is understood that including a single device or a device set in a device image can effectively ensure the accuracy of image recognition.

[0074] It is understandable that acquiring device images facilitates the determination of basic and related information about the devices. Identifying relevant device information based on images effectively ensures the accuracy of device identification. Determining basic device information allows for the identification of the device name, the overall name of the device set, the current status of the device, and the status of different devices within the set. Determining related information allows for the identification of the status of other basic sets of devices within the same device set, or the status of similar devices. This combination of basic and related information improves device management efficiency. Different devices and their conditions require different cleaning, disinfection, and sterilization procedures. Determining cleaning, disinfection, and sterilization instructions based on basic device information and a pre-set device reprocessing instruction library allows for the selection of the correct instructions for different devices and their conditions. Processing devices according to these instructions promotes standardization and homogenization of device management. Target business information is generated based on the basic information of the device, the associated information of the device, and the cleaning, disinfection and sterilization instructions. This allows for the processing of the device according to the target business information, avoiding errors in device processing or incorrect configuration of the device package. Compared with related technologies where manual identification of device information and cleaning, disinfection and sterilization are performed by memory, this method can effectively improve the reliability of device management.

[0075] Additionally, refer to Figure 2 In one embodiment, Figure 1 Step S120 in the illustrated embodiment also includes, but is not limited to, the following steps:

[0076] Step S210: Recognize the instrument image to obtain basic instrument information;

[0077] Step S220: Determine the device association information based on the basic device information and the preset device classification information.

[0078] It should be noted that the embodiments of this application do not limit the specific content of the preset device classification information. It can be device classification information set with reference to the medical device classification catalog, or it can be device classification information set according to actual individual needs. It is understood that device classification information may include the name, specification, classification of the device, and the names and specifications of other devices in the classification, etc.

[0079] It is understandable that recognizing medical device images to obtain basic information about the devices is necessary to determine the associated information of the devices based on the basic information and the preset device classification information. Based on the associated information, it is possible to determine the current status of other basic packages of devices within the same type of device set, as well as the current status of similar devices, which helps to improve the efficiency of device management.

[0080] Understandably, based on the associated information of medical devices, the quantity or combination of medical devices or sets of medical devices can be adjusted according to the current status of the devices or sets of medical devices to meet various medical device needs, which is conducive to improving the efficiency of medical device management.

[0081] Additionally, refer to Figure 3 In one embodiment, Figure 2 Step S210 in the illustrated embodiment also includes, but is not limited to, the following steps:

[0082] Step S310: Perform image preprocessing on the instrument image to obtain the target image;

[0083] Step S320: Determine the instrument identifier based on the target image;

[0084] Step S330: Determine the initial image of the device based on the device identifier and preset image information;

[0085] Step S340: Compare the initial image of the device with the target image to determine the device status information;

[0086] Step S350: Determine the device product information and device management information based on the device identification and the preset device information database;

[0087] Step S360: Obtain basic device information based on device status information, device product information, and device management information.

[0088] It should be noted that the embodiments of this application do not limit the specific method of image preprocessing, which may include image transformation, image enhancement and image feature extraction, etc., and can be adjusted according to actual needs.

[0089] It should be noted that the embodiments of this application do not limit the specific method of obtaining the preset image information. It can be an image taken when the device itself is in a fully functional and structurally complete state, or a reference standard image obtained from the network or image library based on the name of the device. The embodiments of this application also do not limit the specific content of the preset image information. It can be multi-angle images including various devices in a fully functional and structurally complete state, wherein the name of the device is stored corresponding to the multi-angle images.

[0090] It should be noted that the embodiments of this application do not limit the specific content of the preset medical device information database. It may include medical device product information and medical device management information, and may also include medical device information such as hospital information, department information, and current processing status information.

[0091] Understandably, image preprocessing of medical device images improves image recognizability, thereby ensuring the reliability of subsequent image recognition. The medical device identifier is determined based on the target image, facilitating the identification of device information, such as the device's name. An initial image of the device is then determined based on the identifier and pre-defined image information. This initial image is compared with the target image to identify the device's function, structure, and other status, obtaining its status information. Finally, the device product information and management information are determined based on the identifier and a pre-defined device information database, enabling the retrieval of basic device information from the status, product, and management data.

[0092] It should be noted that the device status information can also include information on whether the device is missing or damaged. That is, by comparing the initial image of the device with the target image, it can be determined whether the device is damaged or missing. In addition, when the device is damaged or missing, damage record information can be generated for medical staff to review.

[0093] Additionally, refer to Figure 4 In one embodiment, Figure 1 Step S130 in the illustrated embodiment also includes, but is not limited to, the following steps:

[0094] Step S410: When the device status information indicates that the device is in the sterilization supply center processing flow;

[0095] Step S420: Obtain instrument processing flow information;

[0096] Step S430: Determine the target cleaning, disinfection and sterilization information based on the instrument processing procedure information, basic instrument information and cleaning, disinfection and sterilization instructions;

[0097] Step S440: Determine the target business information based on the target cleaning, disinfection and sterilization information and the instrument association information;

[0098] Step S450: When the device status information indicates that the device is in a state to be recycled, determine the target recycling information based on the basic device information and the cleaning, disinfection and sterilization instructions.

[0099] Step S460: Determine the target business information based on the target recovery information and the device association information.

[0100] It should be noted that the embodiments of this application do not limit the specific content of the processing flow of the sterilization supply center. The processing flow of the sterilization supply center may include initial instrument washing, manual rinsing, automatic cleaning machine washing, chemical or thermal sterilization, drying cabinet drying, manual air gun drying, instrument assembly, instrument placement, placement of indicators in instrument packs, and placement of instruments in the sterilizer, etc., which can be adjusted according to actual needs. The embodiments of this application also do not limit the specific content of the cleaning, disinfection and sterilization processing instructions, which may include instructions related to the corresponding department for instrument processing, initial instrument washing, manual rinsing, automatic cleaning machine washing, chemical or thermal sterilization, drying cabinet drying, manual air gun drying, instrument assembly, instrument placement, placement of indicators in instrument packs, packaging materials for instrument packs, packaging effect of instrument packs, and the usual location of the sterilizer for placing instruments, etc., which can be adjusted according to actual needs.

[0101] Understandably, when the device status information indicates that the device is in the sterilization supply center processing flow, the processing flow is complex, and different devices and their conditions require different procedures. Obtaining the device processing flow information helps determine the specific processing flow for each device. Based on the device processing flow information, basic device information, and cleaning, sterilization, and disinfection instructions, the target cleaning, sterilization, and disinfection information is determined. This allows for different cleaning, sterilization, and disinfection measures to be implemented according to different devices and their conditions, avoiding insufficient cleaning that affects sterilization effectiveness or improper cleaning, sterilization, and disinfection that leads to unqualified sterilization or even damage to the device. Based on the target cleaning, sterilization, and disinfection information and the device's associated information, the target business information is determined, enabling precise cleaning, sterilization, and disinfection of the device. When the device status information indicates that the device is in the awaiting recycling state, the target recycling information is determined based on the device's basic information and the cleaning, sterilization, and disinfection instructions. This allows for different recycling measures to be implemented for different devices. Based on the cleaning, sterilization, and disinfection instructions, damage to the device during recycling can be avoided. Based on the target recycling information and the device's associated information, the target business information is determined, effectively improving the recycling efficiency of the device. Based on different processing statuses of medical devices, corresponding target business information is generated, adapting to various usage scenarios and effectively improving the reliability and efficiency of medical device management. Standardized processing of medical devices based on cleaning, disinfection, and sterilization instructions avoids inconsistent processing quality, promoting standardized and homogenized medical device management and effectively improving its reliability.

[0102] Additionally, refer to Figure 5 In one embodiment, the device status information includes damage information and quantity information. Figure 4 Step S410 in the illustrated embodiment also includes, but is not limited to, the following steps:

[0103] Step S510: Determine the instrument update information based on the damage information and quantity information;

[0104] Step S520: Determine historical cleaning, disinfection, and sterilization information based on medical device management information;

[0105] Step S530: When the instrument processing flow information indicates that the instrument is in the first cleaning, disinfection and sterilization process, determine the first cleaning, disinfection and sterilization instructions according to the first cleaning, disinfection and sterilization process and the cleaning, disinfection and sterilization instructions.

[0106] Step S540: Obtain the target cleaning, disinfection and sterilization information based on the instrument update information, historical cleaning, disinfection and sterilization information and the first cleaning, disinfection and sterilization instructions.

[0107] Step S550: When the instrument processing flow information indicates that the instrument is in the second cleaning, disinfection and sterilization process, determine the second cleaning, disinfection and sterilization instructions according to the second cleaning, disinfection and sterilization process and the cleaning, disinfection and sterilization instructions.

[0108] Step S560: Obtain the target cleaning, disinfection and sterilization information based on the instrument update information, historical cleaning, disinfection and sterilization information, and the second cleaning, disinfection and sterilization instructions.

[0109] Understandably, determining instrument update information based on damage and quantity data allows for timely repair or replacement of instruments, preventing the reuse of damaged equipment and ensuring optimal performance. Furthermore, managing instruments based on quantity data avoids shortages and guarantees reliable management. Historical cleaning, disinfection, and sterilization information is also determined from the instrument management data. This information reveals best practices, errors, and the number of disinfection cycles, allowing for further optimization of cleaning, disinfection, and sterilization procedures, thus improving efficiency and reliability. When the instrument processing flow information indicates the instrument is in the first cleaning, disinfection, and sterilization process, the first cleaning, disinfection, and sterilization instruction manual is determined based on this process and the instruction manual. This specifies the corresponding cleaning, disinfection, and sterilization procedure for the instrument within the first process. Finally, by combining instrument update information, historical cleaning, disinfection, and sterilization information, and the first cleaning, disinfection, and sterilization instruction manual, the target cleaning, disinfection, and sterilization information is obtained, achieving precise cleaning, disinfection, and sterilization. When the device processing information indicates that the device is in the second cleaning, disinfection, and sterilization process, the second cleaning, disinfection, and sterilization instructions can be determined based on these instructions and the device's specific processing procedure within that process. By using updated device information, historical cleaning, disinfection, and sterilization data, and the second instructions, the target cleaning, disinfection, and sterilization information can be obtained, achieving precise cleaning, disinfection, and sterilization. By determining the specific processing procedure corresponding to each device in its different cleaning, disinfection, and sterilization stages, different personnel or different device processing systems can automatically, accurately, and systematically perform cleaning, disinfection, and sterilization based on the instructions. This promotes standardization and homogenization of device management, effectively improving its reliability.

[0110] Understandably, in one embodiment, when the device processing flow information indicates that the device is in the cleaning process of a fully automatic cleaning machine, the corresponding cleaning, disinfection, and sterilization instructions are determined based on the fully automatic cleaning machine's cleaning flow and cleaning, disinfection, and sterilization instructions. This allows the fully automatic cleaning machine to automatically and systematically clean the devices based on these instructions. When the device processing flow information indicates that the device is in the assembly process, the corresponding cleaning, disinfection, and sterilization instructions are determined based on the assembly flow and cleaning, disinfection, and sterilization instructions. This allows for assembly according to the instructions corresponding to the assembly process, avoiding problems such as incorrect device pack configuration, missing items, or excessive items being assembled.

[0111] It is understood that, in one embodiment, high-quality and erroneous cleaning, disinfection, and sterilization procedures can be selected based on historical cleaning, disinfection, and sterilization information. These procedures can then be stored in a pre-defined instrument reprocessing instruction library to facilitate further optimization of the corresponding cleaning, disinfection, and sterilization instructions. Alternatively, new cleaning, disinfection, and sterilization instructions can be automatically generated based on high-quality procedures and existing instructions. Furthermore, instructions for the complete cleaning, disinfection, and sterilization process of the instrument can be automatically generated based on at least one piece of historical cleaning, disinfection, and sterilization information. The specific implementation can be adjusted according to actual needs.

[0112] By obtaining target cleaning, disinfection, and sterilization information based on instrument update information, cleaning, disinfection, and sterilization reference information, and historical cleaning, disinfection, and sterilization information, and then processing the instruments based on the target cleaning, disinfection, and sterilization information, the reliability of the processed instruments can be effectively guaranteed.

[0113] Additionally, refer to Figure 6 In one embodiment, Figure 4 Step S430 in the illustrated embodiment also includes, but is not limited to, the following steps:

[0114] Step S610: Determine the recycling specifications based on the medical device product information;

[0115] Step S620: Determine the recycling contact information based on the medical device management information;

[0116] Step S630: Obtain target recycling information based on recycling specification information and recycling contact information.

[0117] Understandably, determining recycling standards based on medical device product information allows for tailored recycling measures for different devices, preventing damage during the recycling process. Determining contact information based on medical device management information enables timely notification of recycling personnel for prompt device collection. Target recycling information, derived from both recycling standards and contact information, allows for effective recycling of devices, significantly improving recycling efficiency.

[0118] Additionally, refer to Figure 7 In one embodiment, in Figure 1 Following step S130 in the illustrated embodiment, the device management method further includes, but is not limited to, the following steps:

[0119] Step S710: When the business status corresponding to the target business information indicates that it has been completed, update the preset medical device information database according to the target business information.

[0120] Step S720: When the business status corresponding to the target business information indicates that it is not completed, a reminder message is generated based on the target business information.

[0121] Understandably, when the business status corresponding to the target business information indicates completion, the preset medical device information database is updated based on the target business information to facilitate subsequent information retrieval and management of medical devices, effectively ensuring the reliability of medical device management. When the business status corresponding to the target business information indicates incompleteness, a reminder message is generated based on the target business information, so that staff can promptly process the medical devices according to the target business information, effectively improving the efficiency of medical device management.

[0122] It is understood that, in one embodiment, after updating the preset medical device information database according to the target business information, the method further includes: generating a new medical device identifier according to the target business information, for example, after the medical devices are cleaned, disinfected and sterilized, they are reassembled into a new medical device set, and a new medical device identifier is generated to correspond to the new medical device set, so as to facilitate subsequent querying of the status of the medical device according to the new medical device identifier.

[0123] It is understood that, in one embodiment, after updating the preset medical device information database according to the target business information, the method further includes: obtaining search keywords and / or search time intervals, determining target information based on the medical device information database and / or search time intervals, and displaying the target information so that staff can access the basic information and management information of the medical devices.

[0124] It is understood that, in one embodiment, administrators can perform management operations such as information retrieval, modification, and addition in the medical device information database to facilitate timely correction and updates of medical device information.

[0125] Understandably, in one embodiment, the medical device information database also stores management traces such as information retrieval, information modification, and information addition, so as to facilitate full monitoring of the medical device management process and effectively ensure the reliability of medical device management.

[0126] It is understood that, in one embodiment, based on the medical device information database, information sharing can be achieved among multiple hospitals and medical device processing institutions, and each hospital or medical device processing institution can track and understand the status information of the medical devices.

[0127] It is understood that, in one embodiment, after generating target business information based on basic device information and device association information, the display module can be used to display the basic device information, device association information, and target business information so that staff can intuitively understand the relevant information of the device.

[0128] Additionally, refer to Figure 8 , Figure 8This is a schematic diagram of a device management system provided in one embodiment of this application. The device management system includes:

[0129] Image acquisition module 810, used to acquire instrument images;

[0130] The instrument information determination module 820 is used to determine the basic information and associated information of the instrument based on the instrument image.

[0131] Cleaning, disinfection and sterilization instruction manual determination module 830 is used to determine the cleaning, disinfection and sterilization instruction manual based on the basic information of the device and a preset device reprocessing instruction manual library.

[0132] The target business information generation module 840 is used to generate target business information based on the basic information of the device, the associated information of the device, and the cleaning, disinfection and sterilization instructions.

[0133] The specific implementation of the medical device management system in this application is basically the same as the specific implementation of the medical device management method described above, and will not be repeated here.

[0134] Additionally, refer to Figure 9 , Figure 9 The hardware structure of an electronic device according to another embodiment is illustrated. The electronic device includes:

[0135] The processor 901 can be implemented using a general-purpose CPU (Central Processing Unit), microprocessor, application-specific integrated circuit (ASIC), or one or more integrated circuits, and is used to execute relevant programs to implement the technical solutions provided in the embodiments of this application.

[0136] The memory 902 can be implemented as a read-only memory (ROM), static storage device, dynamic storage device, or random access memory (RAM). The memory 902 can store the operating system and other application programs. When the technical solutions provided in the embodiments of this specification are implemented through software or firmware, the relevant program code is stored in the memory 902 and is called and executed by the processor 901 to execute the device management method of the embodiments of this application, for example, executing the above-described... Figure 1 Method steps S110 to S130 in the middle Figure 2 Method steps S210 to S220 in the middle Figure 3 Method steps S310 to S360 in the middle Figure 4 Method steps S410 to S440 in the middle Figure 5 Method steps S510 to S540 in the middle Figure 6 Method steps S610 to S630 and Figure 7 Method steps S710 to S720.

[0137] The input / output interface 903 is used to implement information input and output;

[0138] The communication interface 904 is used to enable communication and interaction between this device and other devices. Communication can be achieved through wired means (such as USB, Ethernet cable, etc.) or wireless means (such as mobile network, WIFI, Bluetooth, etc.).

[0139] The bus transmits information between various components of the device (e.g., processor 901, memory 902, input / output interface 903, and communication interface 904);

[0140] The processor 901, memory 902, input / output interface 903, and communication interface 904 communicate with each other within the device via a bus.

[0141] This application embodiment also provides a storage medium, which is a computer-readable storage medium for computer-readable storage. The storage medium stores one or more programs, which can be executed by one or more processors to implement the above-described device management method, for example, executing the above-described... Figure 1 Method steps S110 to S130 in the middle Figure 2 Method steps S210 to S220 in the middle Figure 3 Method steps S310 to S360 in the middle Figure 4 Method steps S410 to S440 in the middle Figure 5 Method steps S510 to S540 in the middle Figure 6 Method steps S610 to S630 and Figure 7 Method steps S710 to S720.

[0142] Memory, as a non-transitory computer-readable storage medium, can be used to store non-transitory software programs and non-transitory computer-executable programs. Furthermore, memory may include high-speed random access memory, and may also include non-transitory memory, such as at least one disk storage device, flash memory device, or other non-transitory solid-state storage device. In some embodiments, memory may optionally include memory remotely located relative to the processor, and these remote memories can be connected to the processor via a network. Examples of such networks include, but are not limited to, the Internet, intranets, local area networks, mobile communication networks, and combinations thereof.

[0143] The embodiments described in this application are for the purpose of more clearly illustrating the technical solutions of the embodiments of this application, and do not constitute a limitation on the technical solutions provided by the embodiments of this application. As those skilled in the art will know, with the evolution of technology and the emergence of new application scenarios, the technical solutions provided by the embodiments of this application are also applicable to similar technical problems.

[0144] It will be understood by those skilled in the art that Figures 1 to 7 The technical solutions shown do not constitute a limitation on the embodiments of this application, and may include more or fewer steps than shown, or combine certain steps, or different steps.

[0145] The device embodiments described above are merely illustrative. The units described as separate components may or may not be physically separate; that is, they may be located in one place or distributed across multiple network units. Some or all of the modules can be selected to achieve the purpose of this embodiment according to actual needs.

[0146] Those skilled in the art will understand that all or some of the steps in the methods disclosed above, as well as the functional modules / units in the systems and devices, can be implemented as software, firmware, hardware, or suitable combinations thereof.

[0147] The terms “first,” “second,” “third,” “fourth,” etc. (if present) in the specification and accompanying drawings of this application are used to distinguish similar objects and are not necessarily used to describe a specific order or sequence. It should be understood that such data can be interchanged where appropriate so that the embodiments of this application described herein can be implemented in orders other than those illustrated or described herein. Furthermore, the terms “comprising” and “having,” and any variations thereof, are intended to cover non-exclusive inclusion; for example, a process, method, system, product, or apparatus that comprises a series of steps or units is not necessarily limited to those steps or units explicitly listed, but may include other steps or units not explicitly listed or inherent to such processes, methods, products, or apparatus.

[0148] It should be understood that in this application, "at least one (item)" means one or more, and "more than" means two or more. "And / or" is used to describe the relationship between related objects, indicating that three relationships can exist. For example, "A and / or B" can represent three cases: only A exists, only B exists, and both A and B exist simultaneously, where A and B can be singular or plural. The character " / " generally indicates that the preceding and following related objects are in an "or" relationship. "At least one (item) of the following" or similar expressions refer to any combination of these items, including any combination of single or plural items. For example, at least one (item) of a, b, or c can represent: a, b, c, "a and b", "a and c", "b and c", or "a and b and c", where a, b, and c can be single or multiple.

[0149] In the several embodiments provided in this application, it should be understood that the disclosed apparatus and methods can be implemented in other ways. For example, the apparatus embodiments described above are merely illustrative; for instance, the division of the units described above is only a logical functional division, and in actual implementation, there may be other division methods. For example, multiple units or components may be combined or integrated into another system, or some features may be ignored or not executed. Furthermore, the coupling or direct coupling or communication connection shown or discussed may be through some interfaces; the indirect coupling or communication connection between apparatuses or units may be electrical, mechanical, or other forms.

[0150] The units described above as separate components may or may not be physically separate. The components shown as units may or may not be physical units; that is, they may be located in one place or distributed across multiple network units. Some or all of the units can be selected to achieve the purpose of this embodiment according to actual needs.

[0151] Furthermore, the functional units in the various embodiments of this application can be integrated into one processing unit, or each unit can exist physically separately, or two or more units can be integrated into one unit. The integrated unit can be implemented in hardware or as a software functional unit.

[0152] If the integrated unit is implemented as a software functional unit and sold or used as an independent product, it can be stored in a computer-readable storage medium. Based on this understanding, the technical solution of this application, in essence, or the part that contributes to the prior art, or all or part of the technical solution, can be embodied in the form of a software product. This computer software product is stored in a storage medium and includes multiple instructions to cause a computer device (which may be a personal computer, server, or network device, etc.) to execute all or part of the steps of the methods of the various embodiments of this application. The aforementioned storage medium includes various media capable of storing programs, such as USB flash drives, portable hard drives, read-only memory (ROM), random access memory (RAM), magnetic disks, or optical disks.

[0153] The preferred embodiments of the present application have been described above with reference to the accompanying drawings, but this does not limit the scope of the claims of the present application. Any modifications, equivalent substitutions, and improvements made by those skilled in the art without departing from the scope and substance of the embodiments of the present application shall be within the scope of the claims of the present application.

Claims

1. A method for managing medical devices, characterized in that, include: Acquire instrument images; Determine the basic information and associated information of the device based on the device image; The cleaning, disinfection, and sterilization instructions are determined based on the basic information of the instrument and the preset instrument reprocessing instruction library. Target business information is generated based on the basic information of the device, the associated information of the device, and the cleaning, disinfection, and sterilization instructions.

2. The medical device management method according to claim 1, characterized in that, The step of determining the basic information and associated information of the device based on the device image includes: The instrument image is identified to obtain basic information about the instrument. The device association information is determined based on the device's basic information and the preset device classification information.

3. The medical device management method according to claim 2, characterized in that, The process of recognizing the device image to obtain basic device information includes: The instrument image is preprocessed to obtain the target image; Determine the device identifier based on the target image; The initial image of the device is determined based on the device identifier and preset image information; The device status information is determined by comparing the initial image of the device with the target image; The device product information and device management information are determined based on the device identifier and the preset device information database; The basic information of the device is obtained based on the device status information, the device product information, and the device management information.

4. The medical device management method according to claim 3, characterized in that, The generation of target business information based on the basic instrument information, the instrument association information, and the cleaning, disinfection, and sterilization instructions includes: When the device status information indicates that the device is in the process of being processed in the sterilization supply center; Obtain instrument processing flow information; The target cleaning, disinfection and sterilization information is determined based on the instrument processing procedure information, the basic information of the instrument, and the cleaning, disinfection and sterilization treatment instructions. The target business information is determined based on the target cleaning, disinfection, and sterilization information and the instrument association information; or, When the device status information indicates that the device is in a state to be recycled, the target recycling information is determined based on the basic device information and the cleaning, disinfection and sterilization treatment instructions. The target business information is determined based on the target recovery information and the device association information.

5. The medical device management method according to claim 4, characterized in that, The device status information includes damage information and quantity information. Determining the target cleaning, disinfection, and sterilization information based on the device processing procedure information, the device basic information, and the cleaning, disinfection, and sterilization instructions includes: Based on the damage information and the quantity information, determine the instrument update information; Historical cleaning, disinfection, and sterilization information is determined based on the aforementioned medical device management information; When the instrument processing information indicates that the instrument is in the first cleaning, disinfection and sterilization process, the first cleaning, disinfection and sterilization instructions are determined according to the first cleaning, disinfection and sterilization process and the cleaning, disinfection and sterilization instructions. The target cleaning, disinfection and sterilization information is obtained based on the instrument update information, the historical cleaning, disinfection and sterilization information and the first cleaning, disinfection and sterilization instructions. or, When the instrument processing flow information indicates that the instrument is in the second cleaning, disinfection and sterilization process, the second cleaning, disinfection and sterilization instructions are determined according to the second cleaning, disinfection and sterilization process and the cleaning, disinfection and sterilization instructions. The target cleaning, disinfection, and sterilization information is obtained based on the instrument update information, the historical cleaning, disinfection, and sterilization information, and the second cleaning, disinfection, and sterilization instructions.

6. The medical device management method according to claim 4, characterized in that, The step of determining the target recovery information based on the basic information of the device includes: The recycling guidelines are determined based on the aforementioned medical device product information; The recycling contact information is determined based on the aforementioned medical device management information; The target recycling information is obtained based on the recycling specification information and the recycling contact information.

7. The medical device management method according to claim 1, characterized in that, After generating target business information based on the device basic information and the device association information, the method further includes: When the business status corresponding to the target business information indicates that it has been completed, the preset medical device information database is updated according to the target business information; When the business status corresponding to the target business information indicates that it is not completed, a reminder message is generated based on the target business information.

8. A medical device management system, characterized in that, The system includes: Image acquisition module, the image acquisition module being used to acquire instrument images; A device information determination module, which is used to determine basic device information and device association information based on the device image; The cleaning, disinfection and sterilization instruction manual determination module is used to determine the cleaning, disinfection and sterilization instruction manual based on the basic information of the instrument and a preset instrument reprocessing instruction manual library. The target business information generation module is used to generate target business information based on the basic instrument information, the instrument association information, and the cleaning, disinfection, and sterilization instructions.

9. An electronic device, comprising: A memory, a processor, and a computer program stored in the memory and executable on the processor, characterized in that the processor, when executing the computer program, implements the device management method as described in any one of claims 1 to 7.

10. A computer-readable storage medium, characterized in that: The computer-readable storage medium stores computer-executable instructions for causing a computer to perform the device management method as described in any one of claims 1 to 7.

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