Medical safety adverse event early warning method and computer equipment

Abstract

The invention provides a medical safety adverse event early warning method and computer equipment, and relates to the technical field of medical information, and the method comprises the steps: obtaining early warning rules of a plurality of preset medical safety adverse events under each clinical medical business system of a target medical institution; matching a plurality of clinical medical record files of each clinical medical service system in a preset historical time period by adopting the pre-warning rule of each preset medical safety adverse event to obtain a target clinical medical record file matched with the target pre-warning rule of the target medical safety adverse event; and according to the target early warning rule and the target clinical medical record file, generating an early warning message of the target medical safety adverse event. According to the method and the device, the early warning message of the medical adverse safety event is automatically generated, and the department inpatient area with missing report is effectively supervised, so that the medical quality is improved.

Description

Technical Field

[0001] The present application relates to the field of medical information technology, and in particular to a method for early warning of adverse medical safety events and a computer device. Background Art

[0002] With the development of medical technology and the increase in the amount of medical services, the types and number of adverse medical safety events are also increasing. These adverse events may involve adverse drug reactions, medical device failures, diagnostic errors and other aspects, and are highly prevalent and complex. Therefore, how to use advanced technology to improve the early warning ability of adverse medical safety events has become an urgent problem to be solved in the current medical field.

[0003] Currently, when medical staff discover possible adverse reactions or complications in patients during diagnosis and treatment, they need to conduct a preliminary assessment of the event and report it through the system or manually as required after the adverse medical safety event occurs.

[0004] However, the manual reporting process cannot be deeply linked with the clinical system, resulting in nurses taking a long time to fill out the report, forgetting or even concealing the report. It is impossible to effectively monitor the adverse events that have occurred, thus affecting the quality of medical care. Summary of the invention

[0005] The purpose of this application is to provide a medical safety adverse event warning method and computer equipment to address the deficiencies in the above-mentioned prior art, automatically generate warning messages for medical adverse safety events, effectively supervise departments and wards that have missed reports, and thus improve medical quality.

[0006] To achieve the above purpose, the technical solution adopted in the embodiment of the present application is as follows:

[0007] In a first aspect, an embodiment of the present application provides a method for early warning of adverse medical safety events, the method comprising:

[0008] Obtain early warning rules for multiple preset adverse medical safety events under each clinical medical business system of the target medical institution;

[0009] Using each preset warning rule for adverse medical safety events, multiple clinical medical record files of each clinical medical business system within a preset historical time period are matched to obtain a target clinical medical record file that matches the target warning rule for the target adverse medical safety event;

[0010] According to the target early warning rule and the target clinical medical record file, an early warning message of the target medical safety adverse event is generated.

[0011] Optionally, each preset warning rule for adverse medical safety events includes: warning execution time information, warning frequency information, rule description information, warning condition setting information corresponding to the rule description information, and data source configuration information; the data source configuration information includes: multiple preset data elements;

[0012] The method uses the pre-set warning rules for adverse medical safety events to match multiple clinical medical record files of each clinical medical service system within a pre-set historical time period to obtain a target clinical medical record file that matches the target warning rule for the target adverse medical safety event, including:

[0013] Using the warning execution time information and warning frequency information of each preset medical safety adverse event, the multiple clinical medical record files of each clinical medical business system within the preset historical time period are acquired;

[0014] The rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information are used to match the multiple clinical medical record files to obtain the target clinical medical record file, wherein the target clinical medical record file is a clinical medical record file that matches the rule description information of the target adverse medical safety event and the corresponding warning condition setting information;

[0015] Generating a warning message of the target adverse medical safety event according to the target warning rule and the target clinical medical record file includes:

[0016] According to the target data source configuration information in the target warning rule, the field values ​​of each preset data element in the target data source configuration information are extracted from the target clinical medical record file, and based on the extracted field values ​​of each preset data element, a warning message of the target medical safety adverse event is generated.

[0017] Optionally, the warning rule for each preset adverse medical safety event further includes: warning source information, and warning subject information, wherein the warning source information is used to indicate the target medical document category corresponding to each preset adverse medical safety event, and the warning subject information is used to indicate the warning object under the target medical document category;

[0018] Before matching the plurality of clinical medical record files by using the rule description information of each preset medical safety adverse event and the warning condition setting information corresponding to the rule description information to obtain the target clinical medical record file, the method further includes:

[0019] Using the warning source information of each preset adverse medical safety event, determine a plurality of to-be-monitored medical record files of the target medical record type from the plurality of clinical medical record files;

[0020] Determining target medical record information corresponding to the warning subject information in the plurality of medical record files to be monitored according to the warning subject information of each preset medical safety adverse event;

[0021] The method of using the rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information to match the multiple clinical medical record files to obtain the target clinical medical record file includes:

[0022] The rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information are used to match the target medical record information corresponding to the warning subject information in the multiple medical record files to be monitored to obtain the target clinical medical record file.

[0023] Optionally, the method further comprises:

[0024] According to the plurality of warning messages, a plurality of warning record information to be processed is generated and displayed on a first warning information page;

[0025] Among them, each piece of pending warning record information includes: the name information of the corresponding warning rule, the time when the warning record information was generated, the event type of the corresponding target medical safety adverse event, the warning data source information, and the warning patient information; the warning data source information is used to indicate the target medical record file.

[0026] Optionally, each of the preset warning rules for adverse medical safety events further includes: distribution configuration information, the distribution configuration information is used to indicate the user role to be processed;

[0027] The method further comprises:

[0028] According to the reporting processing instruction input through the first warning information page, executing the reporting processing operation on the first warning record information selected by the reporting processing instruction;

[0029] And / or, based on the distribution processing instructions input through the first warning information page and the distribution configuration information in the corresponding warning rule in the second warning record information selected by the distribution processing instructions, the distribution processing operation of the second warning record information is performed to distribute the second warning event information to the target medical user under the user role to be processed indicated by the distribution configuration information in the corresponding warning rule.

[0030] Optionally, the method further comprises:

[0031] Display multiple processed warning record information of the current medical user on the second warning information page;

[0032] According to the first viewing instruction input through the second warning information page, the second warning information page is jumped to the third warning information page, and the reported warning record information of the current medical user is displayed on the third warning information page;

[0033] According to the second viewing instruction input through the second warning information page, the operation log of the third warning record information corresponding to the second viewing instruction is displayed on the second warning information page, and the operation log records: the processing information of each processing stage of the third warning record information from generation to completion of processing.

[0034] Optionally, the method further comprises:

[0035] Displaying the pre-configured warning rules for the plurality of preset adverse medical safety events on the rule information page;

[0036] According to the rule modification instruction input through the rule information page, a rule setting page is triggered to be displayed, and the target warning rule targeted by the rule modification instruction is modified through the rule setting page.

[0037] Optionally, the method further comprises:

[0038] According to the first log query instruction input through the rule information page, the rule information page is jumped to the first rule log page to display the execution log of the first warning rule selected by the first log query instruction;

[0039] According to the second log query instruction input through the rule information page, the rule information page is jumped to a second rule log page to display the modification log of the first warning rule selected by the second log query instruction.

[0040] Optionally, the method further comprises:

[0041] According to the information of each data element in the preset warning data element knowledge base, the warning rules for each preset medical safety adverse event are configured.

[0042] In a second aspect, another embodiment of the present application provides a medical safety adverse event warning device, the device comprising:

[0043] An acquisition module is used to obtain early warning rules for multiple preset adverse medical safety events under each clinical medical business system of the target medical institution;

[0044] A matching module, used to match multiple clinical medical record files of each clinical medical business system within a preset historical time period using each preset warning rule of medical safety adverse events, and obtain a target clinical medical record file that matches the target warning rule of the target medical safety adverse event;

[0045] A generation module is used to generate a warning message of the target adverse medical safety event according to the target warning rule and the target clinical medical record file.

[0046] In the third aspect, another embodiment of the present application provides a computer device, comprising: a processor and a memory, wherein the memory stores program instructions executable by the processor, and when the computer device is running, the processor communicates with the memory, and the processor executes the program instructions to perform the steps of any medical safety adverse event warning method described in the first aspect above.

[0047] In a fourth aspect, another embodiment of the present application provides a storage medium having a computer program stored thereon, and when the computer program is executed by a processor, the steps of the medical safety adverse event warning method as described in any one of the above-mentioned first aspects are executed.

[0048] The beneficial effects of this application are:

[0049] The present application provides a method for warning of adverse medical safety events and a computer device. First, a plurality of preset warning rules for adverse medical safety events under each clinical medical business system of a target medical institution are obtained, and the warning rules for each preset adverse medical safety event are used to match multiple clinical medical record files of each clinical medical business system within a preset historical time period, so as to obtain a target clinical medical record file that matches the target warning rule for the target adverse medical safety event, and generate a warning message for the target adverse medical safety event according to the target warning rule and the target clinical medical record file. The method for warning of adverse medical safety events in the present application matches multiple clinical medical record files of each clinical medical business system within a preset historical time period according to the warning rules for multiple preset adverse medical safety events under the clinical medical business system, without the need to manually match the warning rules for adverse medical safety events, thereby ensuring that the matching of the warning rules for adverse medical safety events is more accurate, and at the same time, multiple clinical medical record files of each clinical medical business system within a preset historical time period are matched, so that the matching range is more accurate, the amount of calculation in the matching process is reduced, and the matching speed is improved. According to the target warning rules and target clinical medical record files, warning messages of target adverse medical safety events are generated. The reasons for the warning can be explained through the warning messages, and the adverse safety warning events that have occurred can be effectively monitored. The underreporting of adverse medical safety events reported in the hospital can be counted, and the underreporting rate can be calculated according to the department or ward, so as to effectively supervise the departments and wards with underreporting, thereby improving the quality of medical care. BRIEF DESCRIPTION OF THE DRAWINGS

[0050] In order to more clearly illustrate the technical solutions of the embodiments of the present application, the drawings required for use in the embodiments will be briefly introduced below. It should be understood that the following drawings only show certain embodiments of the present application and therefore should not be regarded as limiting the scope. For ordinary technicians in this field, other related drawings can be obtained based on these drawings without paying creative work.

[0051] Figure 1 A flowchart of a method for early warning of adverse medical safety events provided in an embodiment of the present application;

[0052] Figure 2 A schematic diagram of a process for generating a warning message of a target medical safety adverse event provided in an embodiment of the present application;

[0053] Figure 3 A schematic diagram of a process for determining a target clinical medical record file in a method for early warning of adverse medical safety events provided in an embodiment of the present application;

[0054] Figure 4 A schematic diagram of a first warning information page provided in an embodiment of the present application;

[0055] Figure 5 A schematic diagram of a second first warning information page provided in an embodiment of the present application;

[0056] Figure 6 A schematic diagram of an operation flow for distributing configuration information in a method for early warning of adverse medical safety events provided in an embodiment of the present application;

[0057] Figure 7 A schematic diagram of a second warning information page provided in an embodiment of the present application;

[0058] Figure 8 A schematic diagram of an operation log of a third warning record information provided in an embodiment of the present application;

[0059] Fig. 9 A schematic diagram of the operation flow for a rule information page in a medical safety adverse event warning method provided in an embodiment of the present application;

[0060] Fig.10 A schematic diagram of a rule information page provided in an embodiment of the present application;

[0061] Fig.11 A schematic diagram of a rule setting page provided in an embodiment of the present application;

[0062] Fig.12 A schematic diagram of an execution log of a first warning rule provided in an embodiment of the present application;

[0063] Fig.13 A schematic diagram of a modification log of a first warning rule provided in an embodiment of the present application;

[0064] Fig.14 A schematic diagram of a warning data element knowledge base provided in an embodiment of the present application;

[0065] Fig.15 A schematic diagram of modifying a data element provided in an embodiment of the present application;

[0066] Fig.16 A schematic diagram of the structure of a medical safety adverse event warning device provided in an embodiment of the present application;

[0067] Fig.17 A schematic diagram of the structure of a computer device provided in an embodiment of the present application. DETAILED DESCRIPTION

[0068] To make the purpose, technical scheme and advantages of the embodiments of the present application clearer, the technical scheme in the embodiments of the present application will be clearly and completely described below in conjunction with the drawings in the embodiments of the present application. It should be understood that the drawings in the present application only serve the purpose of explanation and description and are not used to limit the scope of protection of the present application. In addition, it should be understood that the schematic drawings are not drawn in real proportion. The flowchart used in this application shows the operations implemented according to some embodiments of the present application. It should be understood that the operations of the flowchart can be implemented out of sequence, and the steps without logical context can be reversed in order or implemented simultaneously. In addition, those skilled in the art can add one or more other operations to the flowchart under the guidance of the content of the present application, or remove one or more operations from the flowchart.

[0069] In addition, the described embodiments are only a part of the embodiments of the present application, rather than all the embodiments. The components of the embodiments of the present application described and shown in the drawings here can be arranged and designed in various configurations. Therefore, the following detailed description of the embodiments of the present application provided in the drawings is not intended to limit the scope of the application claimed for protection, but merely represents the selected embodiments of the present application. Based on the embodiments of the present application, all other embodiments obtained by those skilled in the art without making creative work belong to the scope of protection of the present application.

[0070] It should be noted that the term "comprising" will be used in the embodiments of the present application to indicate the existence of the features declared thereafter, but does not exclude the addition of other features.

[0071] In order to clearly describe a medical safety adverse event warning method provided in an embodiment of the present application, the method for warning of medical safety adverse events provided in the present application is described below in combination with multiple figures. The medical safety adverse event warning method in the present application can be applied to any electronic device with processing functions, such as: personal computers, mobile terminals and other devices, and the present application embodiment does not limit this. Therefore, the medical safety adverse event warning method in the present application supports multi-channel push, and can remind the user roles to be processed in all directions, so that the user roles to be processed, especially the management personnel, are free from the limitations of venue and time, and can receive and process various non-warning messages anytime and anywhere. Figure 1 A flowchart of a method for early warning of adverse medical safety events provided in an embodiment of the present application is shown in FIG. Figure 1 As shown, the method includes:

[0072] Step 101: Acquire multiple preset warning rules for adverse medical safety events under each clinical medical business system of the target medical institution.

[0073] Among them, the medical institution can be a hospital, health service center, health center or other health institution engaged in disease diagnosis and treatment activities, and the embodiments of the present application do not limit this. The clinical medical business system can be any business system related to the medical institution, such as a resident doctor station system, a nursing system, a medical management system, etc., and the embodiments of the present application do not limit this. The early warning rules for adverse medical safety events are used to warn of adverse medical safety events. Different clinical medical business systems correspond to different adverse medical safety events, and accordingly, different clinical medical business systems correspond to different early warning rules.

[0074] Optionally, the clinical medical business systems of the target medical institution are determined, and warning rules for multiple preset adverse medical safety events under different clinical business systems are determined according to different clinical business systems, thereby obtaining warning rules for multiple preset adverse medical safety events under the clinical medical business systems of the target medical institution.

[0075] Step 102: using the pre-set warning rules for adverse medical safety events, multiple clinical medical record files of each clinical medical business system within a pre-set historical time period are matched to obtain target clinical medical record files that match the target warning rules for the target adverse medical safety events.

[0076] Among them, the preset time period can be determined according to specific needs, for example, it can be one hour, one day, etc., and the embodiments of the present application do not limit this. The multiple clinical medical record files of each clinical medical business system within the preset historical time period are the multiple clinical medical record files newly added to each clinical medical business system within the preset historical time period. Clinical medical record files are formal documents that record the patient's health status, diagnosis, treatment and nursing process during the medical process. Clinical medical record files can be: nursing document record sheets, medical management medical records and other record files. The embodiments of the present application do not limit this. Clinical medical record files may include: patient basic information, patient current medical history, patient treatment plan, etc. The embodiments of the present application do not limit this, and it is determined according to actual usage.

[0077] Optionally, using each preset warning rule for adverse medical safety events, the record information in multiple clinical medical record files of each clinical medical business system within a preset historical time period is matched to determine whether the record information in multiple clinical medical record files conforms to each preset warning rule for adverse medical safety events. If the record information in multiple clinical medical record files conforms to each preset warning rule for adverse medical safety events, a target clinical medical record file matching the target warning rule for the target adverse medical safety event is obtained. If the record information in multiple clinical medical record files does not conform to each preset warning rule for adverse medical safety events, a target clinical medical record file matching the target warning rule for the target adverse medical safety event cannot be obtained.

[0078] Step 103: Generate a warning message of a target adverse medical safety event according to the target warning rule and the target clinical medical record file.

[0079] Among them, the warning message of the target adverse medical safety event is used to display the warning details after the warning is generated, and serves as the data basis for the reviewer to process.

[0080] Optionally, according to the target warning rule, information related to the target warning rule is determined from the target clinical medical record file, and a warning message of the target medical safety adverse event is generated based on the information related to the target warning rule determined in the target clinical medical record file.

[0081] The present application provides a method for early warning of adverse medical safety events. First, early warning rules for multiple preset adverse medical safety events under each clinical medical business system of a target medical institution are obtained, and the early warning rules for each preset adverse medical safety event are used to match multiple clinical medical record files of each clinical medical business system within a preset historical time period, so as to obtain a target clinical medical record file that matches the target early warning rule of the target adverse medical safety event, and generate an early warning message of the target adverse medical safety event according to the target early warning rule and the target clinical medical record file. The method for early warning of adverse medical safety events in the present application matches multiple clinical medical record files of each clinical medical business system within a preset historical time period according to the early warning rules for multiple preset adverse medical safety events under the clinical medical business system, without the need to manually match the early warning rules for adverse medical safety events, thereby ensuring that the early warning rules for adverse medical safety events are matched more accurately, and at the same time, multiple clinical medical record files of each clinical medical business system within a preset historical time period are matched, so that the matching range is more accurate, the amount of calculation in the matching process is reduced, and the matching speed is improved. According to the target warning rules and target clinical medical record files, warning messages of target adverse medical safety events are generated. The reasons for the warning can be explained through the warning messages, and the adverse safety warning events that have occurred can be effectively monitored. The underreporting of adverse medical safety events reported in the hospital can be counted, and the underreporting rate can be calculated according to the department or ward, so as to effectively supervise the departments and wards with underreporting, thereby improving the quality of medical care.

[0082] Based on the above embodiments, each preset warning rule for adverse medical safety events includes: warning execution time information, warning frequency information, rule description information, warning condition setting information corresponding to the rule description information, and data source configuration information. To this end, the present application provides a process for generating warning messages for target adverse medical safety events. Figure 2 A schematic diagram of a process for generating a warning message of a target medical safety adverse event provided in an embodiment of the present application, such as Figure 2 As shown, in the above step 102, each preset warning rule for adverse medical safety events is used to match multiple clinical medical record files of each clinical medical business system within a preset historical time period, and a target clinical medical record file matching the target warning rule for the target adverse medical safety event is obtained, including:

[0083] Step 201: using the warning execution time information and warning frequency information of each preset adverse medical safety event, a plurality of clinical medical record files of each clinical medical service system within a preset historical time period are obtained.

[0084] Among them, the warning execution time information is used to indicate the start time of the preset warning rule for medical safety adverse events, and the warning frequency information is used to indicate the frequency of the preset warning rule for medical safety adverse events. It can be flexibly set according to the importance level of the medical safety adverse event, either by day or by hour, and the embodiment of the present application does not limit this. For example, the warning execution time information is "2024-08-3000:00:00", and the warning frequency information is "one day". At this time, the preset historical time period is "2024-08-3000:00:00 to 2024-08-31 00:00:00".

[0085] Optionally, the warning execution time information and warning frequency information of each preset medical safety adverse event are used to determine the corresponding preset historical time period, so as to obtain multiple clinical medical record files from each clinical medical business system according to the preset historical time period.

[0086] Step 202: using the rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information, multiple clinical medical record files are matched to obtain a target clinical medical record file.

[0087] Among them, the target clinical medical record file is: a clinical medical record file that matches the rule description information of the target adverse medical safety event and the corresponding warning condition setting information. The rule description information is used to describe what kind of data or event combination will be considered by the system as a potential adverse medical safety event and requires an early warning. The early warning condition setting information is used to clarify which physiological parameters, laboratory test results, clinical symptoms, etc. will be monitored and used as the basis for triggering early warnings. For example, the early warning condition setting can set specific numerical thresholds for each early warning trigger indicator. Exceeding or falling below these thresholds will trigger an early warning, which can be determined based on the rule description information, and the embodiments of the present application are not limited to this.

[0088] Optionally, the rule description information of each preset adverse medical safety event is used to match multiple clinical medical record files, and the matching results are compared with the warning condition setting information corresponding to the rule description information. If the warning condition setting information corresponding to the rule description information is met, the target clinical medical record file is obtained; if the warning condition setting information corresponding to the rule description information is not met, no warning is issued.

[0089] As in the above step 103, according to the target warning rule and the target clinical medical record file, a warning message of the target medical safety adverse event is generated, including:

[0090] Step 203: According to the target data source configuration information in the target warning rule, the field values ​​of each preset data element in the target data source configuration information are extracted from the target clinical medical record file, and a warning message of the target medical safety adverse event is generated according to the extracted field values ​​of each preset data element.

[0091] The data source configuration information includes: a plurality of preset data elements for generating warning messages, different warning rules corresponding to different data elements, which are specifically determined according to the warning rules, and the embodiments of the present application do not limit this. The field value of a data element refers to the actual data content of a specific field in a data element.

[0092] Optionally, based on the target data source configuration information in the target warning rule, the data element corresponding to the target warning rule is determined, so as to extract the field value of each preset data element in the target data source configuration information from the target clinical medical record file, and generate a warning message for the target medical safety adverse event based on the field value of the preset element.

[0093] In the embodiment of the present application, the early warning execution time information and early warning frequency information of each preset medical safety adverse event are used to obtain multiple clinical medical record files of each clinical medical business system within the preset historical time period, and the rule description information of each preset medical safety adverse event and the early warning condition setting information corresponding to the rule description information are used to match multiple clinical medical record files to obtain the target clinical medical record file, and according to the target data source configuration information in the target early warning rule, the field value of each preset data element in the target data source configuration information is extracted from the target clinical medical record file, and according to the field value of each preset data element extracted, the early warning message of the target medical safety adverse event is generated. Through the early warning rules of medical safety adverse events, the matching scope of each clinical medical business system can be narrowed, the amount of calculation can be reduced, and the matching speed can be improved. At the same time, the early warning rules of medical safety adverse events can generate early warning messages of target medical safety adverse events from the target clinical medical record files, which is helpful to prove responsibility and compliance when problems arise, thereby improving medical quality.

[0094] On the basis of the above embodiments, each preset warning rule for adverse medical safety events also includes: warning source information, and warning subject information. To this end, the present application provides a process for determining a target clinical medical record file in a method for warning adverse medical safety events. Figure 3 A schematic diagram of a process for determining a target clinical medical record file in a method for early warning of adverse medical safety events provided in an embodiment of the present application, such as Figure 3 As shown, as shown in the above step 202, the rule description information of each preset medical safety adverse event and the warning condition setting information corresponding to the rule description information are used to match multiple clinical medical record files, and before obtaining the target clinical medical record file, the method also includes:

[0095] Step 301: using the warning source information of each preset adverse medical safety event, a plurality of to-be-monitored medical record files of a target medical file type are determined from a plurality of clinical medical record files.

[0096] The warning source information is used to indicate the target medical file category corresponding to each preset medical safety adverse event. For example, the warning source information can be a drug prescription record, a postoperative care record, a blood transfusion record, etc., which is not limited in the present embodiment and is determined according to the warning rules.

[0097] Optionally, the warning source information of each preset adverse medical safety event is used to determine the target medical file category corresponding to each preset adverse medical safety event from multiple clinical medical record files, and the target medical file type corresponding to each preset adverse medical safety event is determined to determine multiple medical record files to be monitored of the target medical file type.

[0098] Step 302: According to the warning subject information of each preset medical safety adverse event, determine the target medical record information corresponding to the warning subject information in multiple medical record files to be monitored.

[0099] The warning subject information is used to indicate the warning object under the target medical file category. For example, the warning subject can be an operation record, a medical record, a medical code, etc., which is specifically determined according to the warning source information, and the present application embodiment does not limit this.

[0100] For example, when the warning source information is a nursing document record sheet and the warning subject information is a document code, the document codes in the plurality of nursing document records are determined as target medical record information according to the document codes.

[0101] As in the above step 202, the rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information are used to match multiple clinical medical record files to obtain the target clinical medical record file, including:

[0102] Step 303: using the rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information, match the target medical record information corresponding to the warning subject information in multiple medical record files to be monitored to obtain the target clinical medical record file.

[0103] Optionally, the rule description information of each preset medical safety adverse event is used to match the target medical record information corresponding to the warning subject information in multiple medical record files to be monitored. If the matching result satisfies the warning condition setting information corresponding to the rule description information, the target clinical medical record file is obtained. If the matching result does not satisfy the warning condition setting information corresponding to the rule description information, the target clinical medical record file cannot be obtained.

[0104] In an embodiment of the present application, the warning source information of each preset medical safety adverse event is used to determine multiple medical record files to be monitored of the target medical file type from multiple clinical medical record files, and the target medical record information corresponding to the warning subject information in the multiple medical record files to be monitored is determined according to the warning subject information of each preset medical safety adverse event, and the rule description information of each preset medical safety adverse event and the warning condition setting information corresponding to the rule description information are used to match the target medical record information corresponding to the warning subject information in the multiple medical record files to be monitored to obtain the target clinical medical record file. The present application can determine the target medical record information based on the warning source information and the warning subject information, and determine the target clinical medical record file using the rule description information of each preset medical safety adverse event and the warning condition setting information corresponding to the rule description information. It is ensured that the target medical record information is obtained more accurately, and the speed and accuracy of the matched target medical record information are improved.

[0105] On the basis of the above embodiment, the present application further provides a process for generating warning record information in a medical safety adverse event warning method. On the basis of the above steps 201 to 203, the method further includes: generating and displaying multiple pieces of pending warning record information on a first warning information page according to multiple warning messages;

[0106] Among them, each piece of pending warning record information includes: the name information of the corresponding warning rule, the time when the warning record information was generated, the event type of the corresponding target medical safety adverse event, the warning data source information, and the warning patient information.

[0107] Optionally, the first warning information page can be an unprocessed warning message page. The first warning information page is determined according to the user's client and can be a mobile phone page, which is not limited in this embodiment of the present application. The warning data source information is used to indicate the target medical record file. The warning record information generation time is the trigger time of the medical safety adverse event warning corresponding to the warning rule. The event type corresponding to the target medical safety adverse event is used to indicate the classification of various events that may cause patient harm during the medical process. For example, it can be drug care, etc., which is not limited in this embodiment of the present application. The warning patient information can be patient name, patient gender, patient age, patient hospital area, patient source, patient department, patient ward, bed number and other patient-related information, which is not limited in this embodiment of the present application.

[0108] For example, Figure 4 A schematic diagram of a first warning information page provided in an embodiment of the present application, such as Figure 4 As shown, the first warning information page includes: the name information of the corresponding warning rule, the time when the warning record information is generated, the event type of the corresponding target medical safety adverse event, the warning data source information, and the warning patient information. The first warning information page also includes a serial number for distinguishing different warning information.

[0109] In the embodiment of the present application, based on multiple warning messages, multiple warning record information to be processed is generated and displayed on the first warning information page, so that the warning message can be determined more intuitively and subsequent operations can be performed on the warning message. Medical safety adverse events can be warned in advance, so that measures can be taken to avoid accidents.

[0110] On the basis of the above embodiment, each preset warning rule for adverse medical safety events also includes: distribution configuration information, the present application also provides a process for processing in a method for warning adverse medical safety events, based on the above-mentioned generation and display of multiple pending warning record information on the first warning information page according to multiple warning messages, the method also includes: according to the reporting processing instruction input through the first warning information page, executing the reporting processing operation of the first warning record information selected by the reporting processing instruction. It is worth noting that the instructions in the present application can be manually selected or automatically triggered, and the embodiments of the present application are not limited to this.

[0111] For example, Figure 5 This is a schematic diagram of a second first warning information page provided in an embodiment of the present application. The first warning information page also includes operation options, and the operation options include reporting, distribution, and exclusion.

[0112] Optionally, combined Figure 5It can be seen that when the operation selection is reporting, by selecting the reporting processing instruction input, the reporting processing operation of the first warning record information selected by the reporting processing instruction can be executed.

[0113] On the basis of the above embodiment, each preset warning rule for adverse medical safety events also includes: distribution configuration information. The present application also provides another processing flow in the method for warning adverse medical safety events. Based on the above-mentioned generation and display of multiple pending warning record information on the first warning information page according to multiple warning messages, the method also includes: according to the distribution processing instructions input through the first warning information page, and the distribution configuration information in the corresponding warning rule in the second warning record information selected by the distribution processing instructions, the distribution processing operation of the second warning record information is executed to distribute the second warning event information to the target medical user under the pending user role indicated by the distribution configuration information in the corresponding warning rule.

[0114] The target medical user may be a doctor, nurse, etc., which is not limited in the present embodiment and is specifically determined according to the early warning rules of medical safety adverse events.

[0115] Optionally, continue combining Figure 5 When the operation is selected as distribution, the distribution processing instruction is input. The distribution processing instruction is input through the first warning information page, and the distribution configuration information in the corresponding warning rule in the second warning record information selected by the distribution processing instruction is used to execute the distribution processing operation of the second warning record information to distribute the second warning event information to the target medical user under the user role to be processed indicated by the distribution configuration information in the corresponding warning rule.

[0116] Optionally, continue combining Figure 5 When the operation is selected as exclusion, it is determined whether the corresponding warning message can be excluded according to whether the target patient currently has an adverse medical safety event. If the target patient currently has no adverse medical safety event, the corresponding warning record information can be excluded.

[0117] In an embodiment of the present application, corresponding operations are performed according to different processing instructions input on the first warning information page to ensure the accuracy of the processing of the warning record information, and when distributing the warning record information, it is allocated according to the corresponding distribution configuration information to ensure that the allocated personnel are accurate, thereby improving the efficiency of the processing of the warning record information.

[0118] Based on the above embodiments, the present application also provides an operation flow for distributing configuration information in a medical safety adverse event warning method. Figure 6A schematic diagram of the operation flow for distributing configuration information in a method for early warning of adverse medical safety events provided in an embodiment of the present application is shown in FIG. Figure 6 As shown, based on the above steps 101 to 103, the method further includes:

[0119] Step 601: Display multiple processed warning record information of the current medical user on the second warning information page.

[0120] Among them, the second warning information page is a processed warning message page, which is used to display multiple processed warning record information of the current medical user. The processed warning record information includes: serial number, name information of the corresponding warning rule, warning processing status, warning event progress, warning data source information, event type of the corresponding target medical safety adverse event, warning record information generation time, and warning record information reporting time. The name information of the corresponding warning rule is a description of the logical rule for monitoring and warning specific medical safety risks. The warning processing status is used to indicate that the current warning record information is being processed or excluded. The warning event progress is used to indicate the specific progress of the current warning record information reporting. The warning data source information is used to indicate the target medical record file. The event type corresponding to the target medical safety adverse event is used to indicate the classification of various events that may cause patient harm during the medical process. The warning record information generation time is the trigger time of the medical safety adverse event warning corresponding to the warning rule. The warning record information reporting time is the time when the processing of the medical safety adverse event warning corresponding to the warning rule is completed.

[0121] For example, Figure 7 A schematic diagram of a second warning information page provided in an embodiment of the present application, such as Figure 7 As shown, the second warning information page includes: serial number, name information of the corresponding warning rule, warning processing status, warning event progress, warning data source information, event type corresponding to the target medical safety adverse event, warning record information generation time, and warning record information reporting time.

[0122] Step 602: according to the first viewing instruction input through the second warning information page, the second warning information page is jumped to the third warning information page, and the reported warning record information of the current medical user is displayed on the third warning information page.

[0123] The first viewing instruction is used to view the reported warning record information of the current medical user. The third warning information page is the reported warning record information of the current medical user.

[0124] For example, Figure 7 A schematic diagram of a second warning information page provided in an embodiment of the present application, such as Figure 7As shown, the second warning information page also includes: operation selection, the operation selection includes viewing, excluding and viewing logs, the first viewing instruction is the viewing operation, when the viewing operation is selected, the second warning information page can be jumped to the third warning information page through the first viewing instruction entered on the second warning information page, and the reported warning record information of the current medical user is displayed on the third warning information page.

[0125] Step 603: According to the second viewing instruction input through the second warning information page, the operation log of the third warning record information corresponding to the second viewing instruction is displayed on the second warning information page.

[0126] The operation log records include: processing information of each processing stage from the generation to the completion of the third warning record information. The operation log includes: distribution time, distribution operator, distribution operator department name, reporting reason, reporting time, reporting operator, reporting operator department name, reporting reason. The operation log may also include: exclusion time, exclusion operator, exclusion operator department name, and exclusion reason.

[0127] Optionally, the second viewing instruction is a log viewing operation. When the log viewing operation is selected, the second viewing instruction can be entered on the second warning information page to jump the second warning information page to the third warning information page, and the operation log of the third warning record information corresponding to the second viewing instruction is displayed on the second warning information page.

[0128] For example, Figure 8 A schematic diagram of an operation log of a third warning record information provided in an embodiment of the present application, such as Figure 8 As shown, the operation log includes: distribution time: 2024-05-11 10:18, distribution operator: Wang Wu, distribution operator department name: prescription 0320, reporting reason: none, reporting time: 2024-05-11 10:24, reporting operator: Wang Wu, reporting operator department name: prescription 0320, reporting reason: none.

[0129] In an embodiment of the present application, multiple processed warning record information of the current medical user is displayed on the second warning information page, and according to the first viewing instruction input through the second warning information page, the second warning information page is jumped to the third warning information page, and the reported warning record information of the current medical user is displayed on the third warning information page, and according to the second viewing instruction input through the second warning information page, the operation log of the third warning record information corresponding to the second viewing instruction is displayed on the second warning information page. By viewing different contents through different instructions, the processed warning messages can be traced, and the performance and responsibility of the warning issuing agency and relevant personnel in the incident can be evaluated, thereby improving the quality of medical care, effectively controlling the development trend of medical safety adverse events that have occurred, timely eliminating safety hazards, and reducing the negative impact of adverse events.

[0130] Based on the above embodiments, the present application also provides an operation flow for a rule information page in a medical safety adverse event warning method. Fig. 9 A schematic diagram of the operation flow for the rule information page in a medical safety adverse event warning method provided in an embodiment of the present application, such as Fig. 9 As shown, based on the above steps 201 to 203, the method further includes:

[0131] Step 901: Display multiple pre-configured warning rules for preset adverse medical safety events on the rule information page.

[0132] Among them, the rule information page includes multiple preset warning rules for adverse medical safety events, and the preset warning rules for adverse medical safety events include: operation selection, status information, rule code, rule name, rule description, event type, event name, warning data source information, and warning record information effective time. The operation selection is used to determine the input instructions of the rule information page, the status information is used to determine whether the warning rules for adverse medical safety events are running, the rule code is used to distinguish different preset warning rules for adverse medical safety events, the rule description is used to specify the triggering conditions of the warning rules for adverse medical safety events, the event type is used to indicate the classification of various events that may cause patient harm during the medical process, the event name corresponds to the warning rule for adverse medical safety events, the warning data source information is used to indicate the target medical record file, and the warning record information effective time is the effective time of the medical safety adverse event warning corresponding to this warning rule.

[0133] For example, Fig.10 A schematic diagram of a rule information page provided in an embodiment of the present application, such as Fig.10As shown, the rule information page includes multiple warning rules for adverse medical safety events, as well as the operation selection, status information, rule code, rule name, rule description, event type, event name, warning data source information and warning record information effective time corresponding to the warning rules for adverse medical safety events.

[0134] When the warning rule for adverse medical safety events is unplanned extubation event warning, at this time, the status of the unplanned extubation event is open, the rule code is 1, the rule name is unplanned extubation event warning, and the rule description is the monitoring data source. When the patient's nursing document record contains keywords such as "tube detachment; catheter detachment", the event type is nursing, the event name is unplanned extubation event warning, the data source information is nursing document-record sheet, and the effective time is 2024-05-10 00:00.

[0135] Step 902: trigger the display of the rule setting page according to the rule modification instruction input through the rule information page, and modify the target warning rule targeted by the rule modification instruction through the rule setting page.

[0136] The rule modification instruction may be manually input, selected, or automatically triggered, which is not limited in the present embodiment and is determined according to the actual situation. The rule setting page is used to modify the warning rules.

[0137] For example, combined with Fig.10 It can be seen that when the rule modification instruction is selected, the input rule modification instruction can be received according to selecting modification through the rule information page, thereby triggering the display of the rule setting page.

[0138] For example, Fig.11 A schematic diagram of a rule setting page provided in an embodiment of the present application, such as Fig.11 As shown, the rule setting page includes: rule code, rule name, rule version, warning execution time information, that is, effective time, hospital district, hospitalization form, event type, event name, warning source information, warning subject information, warning frequency information, distribution configuration information, rule description information, warning condition setting information corresponding to the rule description information, and data source configuration information.

[0139] In an embodiment of the present application, a plurality of pre-configured warning rules for preset adverse medical safety events are displayed on the rule information page, and according to the rule modification instruction input through the rule information page, the rule setting page is triggered to display, and the target warning rule targeted by the rule modification instruction is modified through the rule setting page. Through the rule information page, the current plurality of preset warning rules for adverse medical safety events can be determined, and the corresponding warning rules can be modified according to the input rule modification instruction to ensure that the warning rules match the target medical institution, thereby improving the quality of medical treatment.

[0140] Based on the above embodiment, the present application also provides an operation flow for the rule information page in a second method for early warning of adverse medical safety events. Based on the above steps 901 and 902, the method further includes:

[0141] According to the first log query instruction input through the rule information page, the rule information page is jumped to the first rule log page to display the execution log of the first warning rule selected by the first log query instruction.

[0142] The first log query instruction is used to query the execution log of the first warning rule.

[0143] For example, combined with Fig.10 It can be seen that the first log query instruction is the execution log. By selecting the execution log through the rule information page, the input first log query instruction can be received, so that the rule information page jumps to the first rule log page to display the execution log of the first warning rule selected by the first log query instruction.

[0144] For example, Fig.12 A schematic diagram of an execution log of a first warning rule provided in an embodiment of the present application is shown as follows: Fig.12 As shown, the execution log of the first warning rule includes: rule code, rule name, warning execution time information, that is, effective time, data start position, data end position, whether to warn, and log information. Fig.12 It can be seen that when there is no warning, there is no corresponding data at the data start position, data end position, and corresponding log information.

[0145] Based on the above embodiment, the present application also provides an operation flow for the rule information page in a third method for early warning of adverse medical safety events. Based on the above steps 901 and 902, the method further includes:

[0146] According to the second log query instruction input through the rule information page, the rule information page is jumped to the second rule log page to display the modification log of the first warning rule selected by the second log query instruction.

[0147] The second log query instruction is used to query the modification log of the first warning rule.

[0148] For example, combined with Fig.10 It can be seen that the first log query instruction is to modify the log. By selecting to modify the log through the rule information page, the input second log query instruction can be received, so that the rule information page jumps to the second rule log page to display the modification log of the first warning rule selected by the second log query instruction.

[0149] For example, Fig.13 A schematic diagram of a modification log of a first warning rule provided in an embodiment of the present application is shown as follows: Fig.13 As shown, the modification log of the first warning rule includes: rule code, rule name, version number, operator, save time, effective time, total number of warnings, number of successful warnings, success rate, and operation selection. Fig.13 When the operation is selected as modification record, the modification record information is displayed, and the modification record includes all the information in the rule setting page. The specific modification content of the warning rule modification can be viewed in the operation column, and the content comparison before and after the version will be displayed in a table.

[0150] In an embodiment of the present application, according to the first log query instruction input through the rule information page, the rule information page is jumped to the first rule log page to display the execution log of the first warning rule selected by the first log query instruction, and according to the second log query instruction input through the rule information page, the rule information page is jumped to the second rule log page to display the modification log of the first warning rule selected by the second log query instruction. The present application can jump to different pages according to different input instructions on the rule information page, ensuring the traceability of each warning record and the precise source of responsibility, thereby improving the quality of medical care.

[0151] Based on the above embodiment, the present application also provides a process for configuring warning rules in a medical safety adverse event warning method. Based on the above steps 101 to 103, the method further includes:

[0152] According to the information of each data element in the preset warning data element knowledge base, the warning rules for each preset medical safety adverse event are configured.

[0153] Among them, the preset warning data element knowledge base can be a knowledge base configured in advance, and the knowledge base can be modified during the specific use process, which is not limited by the embodiment of the present application. The knowledge bases corresponding to different medical institutions are different, and the contents in the corresponding knowledge bases are also different. The warning data element knowledge base includes: element code, system name, module name, table name, field name, data element, and whether it is used as a warning subject. The system name is the system name corresponding to the element, the module name is the module name corresponding to the element, the table name is the table name corresponding to the element, the field name is the field name corresponding to the element, and the data element is a plurality of elements in the warning data element knowledge base. The data source configuration information in the warning rule can be modified by the system name, module name, table name, and field name, and the warning subject information in the warning rule can be modified by the information of whether it is used as the warning subject. When a data element is configured as unable to be used as a warning subject in the warning data element knowledge base, then the element cannot be used as a warning subject in the warning rule.

[0154] For example, Fig.14 A schematic diagram of a warning data element knowledge base provided in an embodiment of the present application is shown in FIG. Fig.14 As shown, the early warning data element knowledge base includes: element code, system name, module name, table name, field name, data element, and whether it is used as an early warning subject. When the data element is a medical record, the value of the field "BCJL" in the table name "ALARM_BIZ_EMR_BCJL" in the medical record module in the medical management system is the content corresponding to the medical record element. When the data element is an input report, the value of the field "DRBG" in the table name "ALARM_BIZ_NIS_HLWS" in the medical record module in the medical management system is the content corresponding to the input report element.

[0155] Optionally, continue combining Fig.14 It can be seen that the element information in the warning data element knowledge base can be modified through operation instructions. Fig.15 A schematic diagram of modifying a data element provided in an embodiment of the present application, such as Fig.15 As shown, by selecting the warning source, you can generate the corresponding module name, fill in the table name and field name of the element, select the data type of the field, and select whether the data element is used as the warning subject, thereby determining whether the element can be used as the warning subject in the warning rule.

[0156] In the embodiment of the present application, the warning rules for each preset medical safety adverse event are configured according to the information of each data element in the preset warning data element knowledge base. The accuracy of the generated warning message can be guaranteed, while the matching degree with the target medical institution is improved, and the warning message can be viewed more intuitively.

[0157] Based on the same inventive concept, a medical safety adverse event warning device corresponding to the medical safety adverse event warning method is also provided in the embodiment of the present application. Since the principle of solving the problem by the device in the embodiment of the present application is similar to the above-mentioned medical safety adverse event warning method in the embodiment of the present application, the implementation of the device can refer to the implementation of the method, and the repeated parts will not be repeated.

[0158] Fig.16 A schematic diagram of the structure of a medical safety adverse event warning device provided in an embodiment of the present application, the device includes: an acquisition module 1601, which is used to obtain a plurality of preset medical safety adverse event warning rules under each clinical medical business system of a target medical institution;

[0159] A matching module 1602 is used to match multiple clinical medical record files of various clinical medical service systems within a preset historical time period using each preset warning rule of medical safety adverse events to obtain a target clinical medical record file that matches the target warning rule of the target medical safety adverse event;

[0160] The generation module 1603 is used to generate a warning message of a target adverse medical safety event according to a target warning rule and a target clinical medical record file.

[0161] In a possible implementation, each preset warning rule for adverse medical safety events includes: warning execution time information, warning frequency information, rule description information, warning condition setting information corresponding to the rule description information, and data source configuration information; the data source configuration information includes: multiple preset data elements; matching module 1602 is specifically used to: use each preset warning rule for adverse medical safety events to match multiple clinical medical record files of each clinical medical business system within a preset historical time period, and obtain a target clinical medical record file that matches the target warning rule for the target adverse medical safety event, including:

[0162] Using the early warning execution time information and early warning frequency information of each preset medical safety adverse event, multiple clinical medical record files of each clinical medical business system within a preset historical time period are obtained;

[0163] The rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information are used to match multiple clinical medical record files to obtain a target clinical medical record file. The target clinical medical record file is a clinical medical record file that matches the rule description information of the target adverse medical safety event and the corresponding warning condition setting information.

[0164] In one possible implementation, generation module 1603 is specifically used to: extract the field values ​​of each preset data element in the target data source configuration information from the target clinical medical record file according to the target data source configuration information in the target warning rule, and generate a warning message for the target medical safety adverse event based on the extracted field values ​​of each preset data element.

[0165] In a possible implementation, each pre-set medical safety adverse event warning rule further includes: warning source information, and warning subject information, wherein the warning source information is used to indicate the target medical file category corresponding to each pre-set medical safety adverse event, and the warning subject information is used to indicate the warning object under the target medical file category; the matching module 1602 is further used to: use the warning source information of each pre-set medical safety adverse event to determine multiple medical record files to be monitored of the target medical file type from multiple clinical medical record files;

[0166] According to the early warning subject information of each preset medical safety adverse event, the target medical record information corresponding to the early warning subject information in multiple medical record files to be monitored is determined.

[0167] In one possible implementation, the matching module 1602 is specifically used to: use the rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information to match the target medical record information corresponding to the warning subject information in multiple medical record files to be monitored, and obtain the target clinical medical record file.

[0168] In a possible implementation manner, the medical safety adverse warning device further includes: a display module, the display module being specifically used to: generate and display a plurality of to-be-processed warning record information on a first warning information page according to a plurality of warning messages;

[0169] Among them, each piece of pending warning record information includes: the name information of the corresponding warning rule, the time when the warning record information was generated, the event type of the corresponding target medical safety adverse event, the warning data source information, and the warning patient information; the warning data source information is used to indicate the target medical record file.

[0170] In a possible implementation, each preset warning rule for adverse medical safety events further includes: distribution configuration information, the distribution configuration information is used to indicate the user role to be processed; the display module is further used to: according to the reporting processing instruction input through the first warning information page, perform a reporting processing operation on the first warning record information selected by the reporting processing instruction;

[0171] And / or, based on the distribution processing instructions input through the first warning information page and the distribution configuration information in the corresponding warning rule in the second warning record information selected by the distribution processing instructions, the distribution processing operation of the second warning record information is performed to distribute the second warning event information to the target medical user under the user role to be processed indicated by the distribution configuration information in the corresponding warning rule.

[0172] In a possible implementation manner, the display module is further used to: display multiple processed warning record information of the current medical user on the second warning information page;

[0173] According to the first viewing instruction input through the second warning information page, the second warning information page is jumped to the third warning information page, and the reported warning record information of the current medical user is displayed on the third warning information page;

[0174] According to the second viewing instruction input through the second warning information page, the operation log of the third warning record information corresponding to the second viewing instruction is displayed on the second warning information page, and the operation log records: the processing information of each processing stage of the third warning record information from generation to completion of processing.

[0175] In a possible implementation manner, the display module is further used to: display a plurality of pre-configured warning rules for preset adverse medical safety events on the rule information page;

[0176] According to the rule modification instruction input through the rule information page, the rule setting page is triggered to display, and the target warning rule targeted by the rule modification instruction is modified through the rule setting page.

[0177] In a possible implementation, the display module is further used to: according to the first log query instruction input through the rule information page, jump the rule information page to the first rule log page to display the execution log of the first warning rule selected by the first log query instruction;

[0178] According to the second log query instruction input through the rule information page, the rule information page is jumped to the second rule log page to display the modification log of the first warning rule selected by the second log query instruction.

[0179] In a possible implementation manner, the display module is further used to configure the warning rules for each preset adverse medical safety event according to the information of each data element in the preset warning data element knowledge base.

[0180] For descriptions of the processing flow of each module in the device and the interaction flow between each module, reference may be made to the relevant descriptions in the above method embodiment, which will not be described in detail here.

[0181] The present application also provides a computer device, Fig.17 A schematic diagram of the structure of a computer device provided in an embodiment of the present application includes: a processor 1701 and a memory 1702. The memory 1702 stores machine-readable instructions executable by the processor 1701. When the computer device is running, the processor 1701 communicates with the memory 1702, and when the machine-readable instructions are executed by the processor 1701, the steps of the above-mentioned medical safety adverse event warning method are executed.

[0182] An embodiment of the present application also provides a computer-readable storage medium, on which a computer program is stored. When the computer program is executed by a processor, the steps of the above-mentioned medical safety adverse event warning method are executed.

[0183] Those skilled in the art can clearly understand that, for the convenience and simplicity of description, the specific working process of the system and device described above can refer to the corresponding process in the method embodiment, and will not be repeated in this application. In the several embodiments provided in this application, it should be understood that the disclosed system, device and method can be implemented in other ways. The device embodiments described above are merely schematic. For example, the division of the modules is only a logical function division. There may be other division methods in actual implementation. For example, multiple modules or components can be combined or integrated into another system, or some features can be ignored or not executed. Another point is that the mutual coupling or direct coupling or communication connection shown or discussed can be through some communication interfaces, indirect coupling or communication connection of devices or modules, which can be electrical, mechanical or other forms.

[0184] In addition, each functional unit in each embodiment of the present application can be integrated into a processing unit, or each unit can exist physically separately, or two or more units can be integrated into one unit. If the function is implemented in the form of 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 the present invention is essentially or part of the technical solution that contributes to the prior art or part of the technical solution can be embodied in the form of a software product, and the computer software product is stored in a storage medium, including several instructions for a computer device (which can be a personal computer, a server, or a network device, etc.) to perform all or part of the steps of the method described in each embodiment of the present invention. The aforementioned storage medium includes: U disk, mobile hard disk, read-only memory (ROM, Read-Only Memory), random access memory (RAM, RandomAccess Memory), disk or optical disk and other media that can store program code.

[0185] The above are only specific implementation methods of the present application, but the protection scope of the present application is not limited thereto. Any technician familiar with the technical field can easily think of changes or substitutions within the technical scope disclosed in the present application, which should be covered by the protection scope of the present application.

Claims

1. A method for early warning of adverse medical safety events, characterized in that: The method comprises: Obtain early warning rules for multiple preset adverse medical safety events under each clinical medical business system of the target medical institution; Using each preset warning rule for adverse medical safety events, multiple clinical medical record files of each clinical medical business system within a preset historical time period are matched to obtain a target clinical medical record file that matches the target warning rule for the target adverse medical safety event; According to the target early warning rule and the target clinical medical record file, an early warning message of the target medical safety adverse event is generated.

2. The method for early warning of adverse medical safety events according to claim 1, characterized in that: Each pre-set warning rule for adverse medical safety events includes: warning execution time information, warning frequency information, rule description information, warning condition setting information corresponding to the rule description information, and data source configuration information; the data source configuration information includes: multiple pre-set data elements; The method uses the pre-set warning rules for adverse medical safety events to match multiple clinical medical record files of each clinical medical service system within a pre-set historical time period to obtain a target clinical medical record file that matches the target warning rule for the target adverse medical safety event, including: Using the warning execution time information and warning frequency information of each preset medical safety adverse event, the multiple clinical medical record files of each clinical medical business system within the preset historical time period are acquired; The rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information are used to match the multiple clinical medical record files to obtain the target clinical medical record file, wherein the target clinical medical record file is a clinical medical record file that matches the rule description information of the target adverse medical safety event and the corresponding warning condition setting information; Generating a warning message of the target adverse medical safety event according to the target warning rule and the target clinical medical record file includes: According to the target data source configuration information in the target warning rule, the field values ​​of each preset data element in the target data source configuration information are extracted from the target clinical medical record file, and based on the extracted field values ​​of each preset data element, a warning message of the target medical safety adverse event is generated.

3. The method for early warning of adverse medical safety events according to claim 2, characterized in that: The warning rule for each preset adverse medical safety event further includes: warning source information and warning subject information, wherein the warning source information is used to indicate the target medical document category corresponding to each preset adverse medical safety event, and the warning subject information is used to indicate the warning object under the target medical document category; Before matching the plurality of clinical medical record files by using the rule description information of each preset medical safety adverse event and the warning condition setting information corresponding to the rule description information to obtain the target clinical medical record file, the method further includes: Using the warning source information of each preset adverse medical safety event, determine a plurality of to-be-monitored medical record files of the target medical record type from the plurality of clinical medical record files; Determining target medical record information corresponding to the warning subject information in the plurality of medical record files to be monitored according to the warning subject information of each preset medical safety adverse event; The method of using the rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information to match the multiple clinical medical record files to obtain the target clinical medical record file includes: The rule description information of each preset adverse medical safety event and the warning condition setting information corresponding to the rule description information are used to match the target medical record information corresponding to the warning subject information in the multiple medical record files to be monitored to obtain the target clinical medical record file.

4. The method for early warning of adverse medical safety events according to claim 2, characterized in that: The method further comprises: According to the plurality of warning messages, a plurality of warning record information to be processed is generated and displayed on a first warning information page; Among them, each piece of pending warning record information includes: the name information of the corresponding warning rule, the time when the warning record information was generated, the event type of the corresponding target medical safety adverse event, the warning data source information, and the warning patient information; the warning data source information is used to indicate the target medical record file.

5. The method for early warning of adverse medical safety events according to claim 4, characterized in that: Each of the preset warning rules for adverse medical safety events also includes: distribution configuration information, the distribution configuration information is used to indicate the user role to be processed; The method further comprises: According to the reporting processing instruction input through the first warning information page, executing the reporting processing operation on the first warning record information selected by the reporting processing instruction; And / or, based on the distribution processing instructions input through the first warning information page and the distribution configuration information in the corresponding warning rule in the second warning record information selected by the distribution processing instructions, the distribution processing operation of the second warning record information is performed to distribute the second warning event information to the target medical user under the user role to be processed indicated by the distribution configuration information in the corresponding warning rule.

6. The method for early warning of adverse medical safety events according to claim 1, characterized in that: The method further comprises: Display multiple processed warning record information of the current medical user on the second warning information page; According to the first viewing instruction input through the second warning information page, the second warning information page is jumped to the third warning information page, and the reported warning record information of the current medical user is displayed on the third warning information page; According to the second viewing instruction input through the second warning information page, the operation log of the third warning record information corresponding to the second viewing instruction is displayed on the second warning information page, and the operation log records: the processing information of each processing stage of the third warning record information from generation to completion of processing.

7. The method for early warning of adverse medical safety events according to claim 2, characterized in that: The method further comprises: Displaying the pre-configured warning rules for the plurality of preset adverse medical safety events on the rule information page; According to the rule modification instruction input through the rule information page, a rule setting page is triggered to be displayed, and the target warning rule targeted by the rule modification instruction is modified through the rule setting page.

8. The method for early warning of adverse medical safety events according to claim 7, characterized in that: The method further comprises: According to the first log query instruction input through the rule information page, the rule information page is jumped to the first rule log page to display the execution log of the first warning rule selected by the first log query instruction; According to the second log query instruction input through the rule information page, the rule information page is jumped to a second rule log page to display the modification log of the first warning rule selected by the second log query instruction.

9. The method for early warning of adverse medical safety events according to claim 1, characterized in that: The method further comprises: According to the information of each data element in the preset warning data element knowledge base, the warning rules for each preset medical safety adverse event are configured.

10. A computer device, characterized in that: include: A processor and a memory, wherein the memory stores program instructions executable by the processor, and when the computer device is running, the processor communicates with the memory, and the processor executes the program instructions to perform the steps of the medical safety adverse event warning method as described in any one of claims 1 to 9.

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