CN111627536A - Adverse event management system and method for hospital - Google Patents
Adverse event management system and method for hospital Download PDFInfo
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- CN111627536A CN111627536A CN202010405063.0A CN202010405063A CN111627536A CN 111627536 A CN111627536 A CN 111627536A CN 202010405063 A CN202010405063 A CN 202010405063A CN 111627536 A CN111627536 A CN 111627536A
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- 238000000034 method Methods 0.000 title claims abstract description 21
- 230000002411 adverse Effects 0.000 claims abstract description 80
- 238000007726 management method Methods 0.000 claims description 130
- 238000012550 audit Methods 0.000 claims description 12
- 238000013523 data management Methods 0.000 claims description 9
- 238000012544 monitoring process Methods 0.000 claims description 8
- 230000004048 modification Effects 0.000 claims description 6
- 238000012986 modification Methods 0.000 claims description 6
- 238000012163 sequencing technique Methods 0.000 claims description 3
- 206010060933 Adverse event Diseases 0.000 description 79
- 230000000474 nursing effect Effects 0.000 description 4
- 230000009286 beneficial effect Effects 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000003745 diagnosis Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 230000032683 aging Effects 0.000 description 1
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/20—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
Abstract
The invention discloses an adverse event management system for a hospital, which is based on a management system method and comprises the steps of collecting adverse event information, inputting the adverse event information into an adverse event management system, and taking emergency measures for the adverse event information; the adverse events are transmitted to an event reporting management module, the adverse events are audited, the adverse events which are approved are analyzed through an event analysis management module, adverse event rectification and distribution are carried out according to the analysis results, the rectification process is monitored, and rectification results are obtained; and generating an adverse event statistical table through the report management module according to the adverse event information and the rectification result, and storing the adverse event statistical table through a report storage unit in the report management module. The invention can effectively manage and monitor the adverse events, realizes the traceability and closed-loop management of the adverse events, ensures the accuracy of the analysis of the adverse events and can effectively avoid the occurrence of the adverse events of the same kind.
Description
Technical Field
The invention belongs to the field of information management, and particularly relates to an adverse event management system and method for a hospital.
Background
Nursing adverse events refer to nursing-related injuries, and any event which may affect the diagnosis and treatment results of patients, increase the pain and burden of patients, and possibly cause nursing disputes or accidents in the diagnosis and treatment process. Nursing adverse events include preventable and unpredictable adverse events. Unforeseeable adverse events refer to unforeseeable damage caused by proper care actions; preventable adverse events refer to injuries in care that result from unsupervised errors or equipment failures. Adverse events are inevitable, and the length of the treatment aging and the quality of the treatment result of the adverse events determine the negative effects.
Disclosure of Invention
The adverse event management system and the adverse event management method for the hospital ensure the timeliness of the adverse event treatment, can treat the adverse event through historical data, and can effectively reduce the negative effects caused by the adverse event.
In order to achieve the purpose of the invention, the invention adopts the technical scheme that: an adverse event management system for a hospital comprises an event configuration management module, an event reporting management module, an event analysis management module, an event rectification management module, a patient data management module and a report management module;
the event configuration management module is used for configuring the information of the adverse events, transmitting the configured adverse events to the event reporting management module and providing data support for the report management module; the event reporting management module is used for checking and managing the reported adverse events and transmitting the checked adverse events to the event analysis management module; the event analysis management module is used for analyzing, analyzing and auditing adverse events, storing analysis results and providing the analysis results to the event rectification management module; the event rectification management module is used for rectifying adverse events, monitoring implementation progress and rectifying and evaluating according to analysis results and providing data support for the report management module; the patient data management module is used for recording personal information and medical data of the patient and providing data support for the event configuration management module; the report management module is used for carrying out report statistics on adverse events and providing data support for the event analysis management module.
Further, the event configuration management module comprises an event information configuration unit and an event content configuration unit;
the event information configuration unit is used for configuring the name, type, timeliness and event result of the newly added adverse event to generate a list; the event content configuration unit is used for editing the specific content of the adverse events in the list.
Furthermore, the event reporting management module comprises an event reporting unit and a reporting event management unit; the event reporting unit is used for auditing the adverse events, and the reported event management unit is used for canceling, modifying or deleting the adverse events.
Furthermore, the event rectification management module comprises a reporting event rectification unit and a rectification event supervision unit; the reported event rectification unit is used for assigning a rectification event and generating a state monitoring table of the rectification event; and the reported event supervision unit is used for modifying the state of the modification event and entering the progress.
Further, the report management module comprises a report reading and writing unit and a report storage unit, wherein the report reading and writing unit is used for writing and reading the report, and the report storage unit is used for storing the written report.
The invention has the beneficial effects that: the system can effectively manage and correct the adverse events, improves the treatment efficiency of medical personnel on the adverse events, ensures the timeliness of the adverse event treatment, and reduces the repeated work of reporting the adverse events. By analyzing and monitoring the adverse events, the invention can know the adverse events of each department of the hospital in real time and provide visual data for reducing the occurrence of the adverse events.
An adverse event management method based on an adverse event management system, comprising the steps of:
s1, collecting adverse event information, inputting the adverse event information into an adverse event management system through an event configuration management module, and taking emergency measures for the adverse event;
s2, transmitting the adverse event to the event reporting management module, auditing the adverse event through the reporting management module, and judging whether the audit is passed, if yes, entering the step S3, otherwise, canceling the reported adverse event, and ending the management process;
s3, analyzing the adverse events which pass the audit by the event analysis management module to obtain an analysis result;
s4, according to the analysis result, the adverse event rectification management module is used for conducting adverse event rectification distribution, and the rectification process is monitored, and rectification results are obtained;
and S5, generating an adverse event statistical table through the report management module according to the adverse event information and the rectification result, and storing the adverse event statistical table through a report storage unit in the report management module.
Further, the adverse event information in step S1 includes personal information and medical data of the patient, and both the personal information and the medical data of the patient are acquired by the patient data management module.
Further, the specific steps of taking emergency measures for the adverse event in step S1 are as follows:
s1.1, collecting a plurality of adverse events as samples, classifying the adverse events, configuring emergency measures for each adverse event based on prior experience, and generating an emergency measure knowledge base;
and S1.2, acquiring corresponding classification through the adverse event information, and matching the classification with data in an emergency measure knowledge base to obtain emergency measures.
Further, the specific method for matching the classification information with the data in the emergency measure knowledge base in step S1.2 is as follows:
s1.21, randomly sequencing all classifications in an emergency measure knowledge base, and forming a character sequence by the randomly sequenced classification names;
s1.22, converting the character sequence into a character string to obtain a main string with the length of n, and converting a classification name corresponding to the adverse event information into the character string to obtain a mode string with the length of m;
s1.23, respectively obtaining the hash values of the main string and the pattern string through a hash algorithm, comparing the hash values of the pattern string and the main string one by using a traversal method, judging whether the hash value of the pattern string is the same as a certain hash value of the main string, if so, obtaining a classification corresponding to the certain hash value, and taking the classification as a matching result, otherwise, repeating the step S1.23.
Further, the step S3 is specifically: according to the adverse events which pass the audit, inquiring an adverse event statistical table in a report storage unit through an event analysis management module, searching the same events as the adverse events which pass the audit in the adverse event statistical table by adopting a traversal algorithm, and extracting the reasons, countermeasures and rectification processes of the same events;
the adverse event statistics table in step S5 includes an adverse event list, an adverse event department summary table, an adverse event occurrence rate summary table, an adverse event cause statistics table, and an adverse event modification statistics table, where the adverse event list includes the number, name, category, occurrence, and information of the reporter and the patient of the adverse event.
The invention has the beneficial effects that:
(1) the invention can effectively manage and monitor the adverse events, and realizes the traceability and closed-loop management of the adverse events.
(2) According to the invention, the adverse event statistical table is stored through the report storage unit in the report management module, and the adverse event statistical table is called during reason analysis, so that the accuracy of adverse event analysis is ensured, and the occurrence of similar adverse events can be effectively avoided.
Drawings
Fig. 1 is a block diagram of an adverse event management system for a hospital according to the present invention;
fig. 2 is a flowchart of an adverse event management method based on an adverse event management system according to the present invention.
Detailed Description
The following description of the embodiments of the present invention is provided to facilitate the understanding of the present invention by those skilled in the art, but it should be understood that the present invention is not limited to the scope of the embodiments, and it will be apparent to those skilled in the art that various changes may be made without departing from the spirit and scope of the invention as defined and defined in the appended claims, and all matters produced by the invention using the inventive concept are protected.
Embodiments of the present invention will be described in detail below with reference to the accompanying drawings.
As shown in fig. 1, an adverse event management system for a hospital is characterized by comprising an event configuration management module, an event reporting management module, an event analysis management module, an event rectification management module, a patient data management module and a report management module;
the event configuration management module is used for configuring the information of the adverse events, transmitting the configured adverse events to the event reporting management module and providing data support for the report management module; the event reporting management module is used for checking and managing the reported adverse events and transmitting the checked adverse events to the event analysis management module; the event analysis management module is used for analyzing, analyzing and auditing adverse events, storing analysis results and providing the analysis results to the event rectification management module; the event rectification management module is used for rectifying adverse events, monitoring implementation progress and rectifying and evaluating according to analysis results and providing data support for the report management module; the patient data management module is used for recording personal information and medical data of the patient and providing data support for the event configuration management module; the report management module is used for carrying out report statistics on adverse events and providing data support for the event analysis management module.
The event configuration management module comprises an event information configuration unit and an event content configuration unit;
the event information configuration unit is used for configuring the name, type, timeliness and event result of the newly added adverse event to generate a list; the event content configuration unit is used for editing the specific content of the adverse events in the list.
The event reporting management module comprises an event reporting unit and a reporting event management unit; the event reporting unit is used for auditing the adverse events, and the reported event management unit is used for canceling, modifying or deleting the adverse events.
The event rectification management module comprises a reporting event rectification unit and a rectification event supervision unit; the reported event rectification unit is used for assigning a rectification event and generating a state monitoring table of the rectification event; and the reported event supervision unit is used for modifying the state of the modification event and entering the progress.
The report management module comprises a report reading and writing unit and a report storage unit, wherein the report reading and writing unit is used for writing and reading reports, and the report storage unit is used for storing the written reports.
The invention can effectively manage and correct the adverse events, improves the treatment efficiency of medical personnel on the adverse events, ensures the timeliness of the treatment of the adverse events and reduces the repeated work of reporting the adverse events. By analyzing and monitoring the adverse events, the invention can know the adverse events of each department of the hospital in real time and provide visual data for reducing the occurrence of the adverse events.
As shown in fig. 2, an adverse event management method based on an adverse event management system includes the following steps:
s1, collecting adverse event information, inputting the adverse event information into an adverse event management system through an event configuration management module, and taking emergency measures for the adverse event;
s2, transmitting the adverse event to the event reporting management module, auditing the adverse event through the reporting management module, and judging whether the audit is passed, if yes, entering the step S3, otherwise, canceling the reported adverse event, and ending the management process;
s3, analyzing the adverse events which pass the audit by the event analysis management module to obtain an analysis result;
s4, according to the analysis result, the adverse event rectification management module is used for conducting adverse event rectification distribution, and the rectification process is monitored, and rectification results are obtained;
and S5, generating an adverse event statistical table through the report management module according to the adverse event information and the rectification result, and storing the adverse event statistical table through a report storage unit in the report management module.
The adverse event information in step S1 includes personal information and medical data of the patient, and both the personal information and the medical data of the patient are acquired by the patient data management module.
The specific steps of taking emergency measures for the adverse event in step S1 are as follows:
s1.1, collecting a plurality of adverse events as samples, classifying the adverse events, configuring emergency measures for each adverse event based on prior experience, and generating an emergency measure knowledge base;
and S1.2, acquiring corresponding classification through the adverse event information, and matching the classification with data in an emergency measure knowledge base to obtain emergency measures.
The specific method for matching the classification information with the data in the emergency measure knowledge base in step S1.2 is as follows:
s1.21, randomly sequencing all classifications in an emergency measure knowledge base, and forming a character sequence by the randomly sequenced classification names;
s1.22, converting the character sequence into a character string to obtain a main string with the length of n, and converting a classification name corresponding to the adverse event information into the character string to obtain a mode string with the length of m;
s1.23, respectively obtaining the hash values of the main string and the pattern string through a hash algorithm, comparing the hash values of the pattern string and the main string one by using a traversal method, judging whether the hash value of the pattern string is the same as a certain hash value of the main string, if so, obtaining a classification corresponding to the certain hash value, and taking the classification as a matching result, otherwise, repeating the step S1.23.
The step S3 specifically includes: according to the adverse events which pass the audit, inquiring an adverse event statistical table in a report storage unit through an event analysis management module, searching the same events as the adverse events which pass the audit in the adverse event statistical table by adopting a traversal algorithm, and extracting the reasons, countermeasures and rectification processes of the same events;
the adverse event statistics table in step S5 includes an adverse event list, an adverse event department summary table, an adverse event occurrence rate summary table, an adverse event cause statistics table, and an adverse event modification statistics table, where the adverse event list includes the number, name, category, occurrence, and information of the reporter and the patient of the adverse event.
The invention has the beneficial effects that:
(1) the invention can effectively manage and monitor the adverse events, and realizes the traceability and closed-loop management of the adverse events.
(2) According to the invention, the adverse event statistical table is stored through the report storage unit in the report management module, and the adverse event statistical table is called during reason analysis, so that the accuracy of adverse event analysis is ensured, and the occurrence of similar adverse events can be effectively avoided.
Claims (10)
1. An adverse event management system for a hospital is characterized by comprising an event configuration management module, an event reporting management module, an event analysis management module, an event rectification management module, a patient data management module and a report management module;
the event configuration management module is used for configuring the information of the adverse events, transmitting the configured adverse events to the event reporting management module and providing data support for the report management module; the event reporting management module is used for checking and managing the reported adverse events and transmitting the checked adverse events to the event analysis management module; the event analysis management module is used for analyzing, analyzing and auditing adverse events, storing analysis results and providing the analysis results to the event rectification management module; the event rectification management module is used for rectifying adverse events, monitoring implementation progress and rectifying and evaluating according to analysis results and providing data support for the report management module; the patient data management module is used for recording personal information and medical data of the patient and providing data support for the event configuration management module; the report management module is used for carrying out report statistics on adverse events and providing data support for the event analysis management module.
2. The adverse event management system for hospitals according to claim 1, characterized in that said event configuration management module comprises an event information configuration unit and an event content configuration unit;
the event information configuration unit is used for configuring the name, type, timeliness and event result of the newly added adverse event to generate a list; the event content configuration unit is used for editing the specific content of the adverse events in the list.
3. The system for managing adverse events for hospitals according to claim 1, wherein said event reporting management module comprises an event reporting unit and a reported event management unit; the event reporting unit is used for auditing the adverse events, and the reported event management unit is used for canceling, modifying or deleting the adverse events.
4. The adverse event management system for hospitals according to claim 1, wherein said event rectification management module comprises a reporting event rectification unit and a rectification event supervision unit; the reported event rectification unit is used for assigning a rectification event and generating a state monitoring table of the rectification event; and the reported event supervision unit is used for modifying the state of the modification event and entering the progress.
5. The system for managing the adverse events for hospitals according to claim 1, wherein the report management module comprises a report reading and writing unit and a report storage unit, the report reading and writing unit is used for writing and reading reports, and the report storage unit is used for storing written reports.
6. An adverse event management method based on the adverse event management system according to claim 1, comprising the steps of:
s1, collecting adverse event information, inputting the adverse event information into an adverse event management system through an event configuration management module, and taking emergency measures for the adverse event;
s2, transmitting the adverse event to the event reporting management module, auditing the adverse event through the reporting management module, and judging whether the audit is passed, if yes, entering the step S3, otherwise, canceling the reported adverse event, and ending the management process;
s3, analyzing the adverse events which pass the audit by the event analysis management module to obtain an analysis result;
s4, according to the analysis result, the adverse event rectification management module is used for conducting adverse event rectification distribution, and the rectification process is monitored, and rectification results are obtained;
and S5, generating an adverse event statistical table through the report management module according to the adverse event information and the rectification result, and storing the adverse event statistical table through a report storage unit in the report management module.
7. An adverse event management method based on the adverse event management system of claim 6, wherein the adverse event information in step S1 includes personal information and medical data of a patient, and the personal information and medical data of the patient are acquired by the patient data management module.
8. An adverse event management method based on the adverse event management system of claim 6, wherein the specific steps of taking emergency measures for the adverse event in step S1 are as follows:
s1.1, collecting a plurality of adverse events as samples, classifying the adverse events, configuring emergency measures for each adverse event based on prior experience, and generating an emergency measure knowledge base;
and S1.2, acquiring corresponding classification through the adverse event information, and matching the classification with data in an emergency measure knowledge base to obtain emergency measures.
9. An adverse event management method based on the adverse event management system of claim 8, wherein the specific method of matching the classification information with the data in the emergency measure knowledge base in step S1.2 is as follows:
s1.21, randomly sequencing all classifications in an emergency measure knowledge base, and forming a character sequence by the randomly sequenced classification names;
s1.22, converting the character sequence into a character string to obtain a main string with the length of n, and converting a classification name corresponding to the adverse event information into the character string to obtain a mode string with the length of m;
s1.23, respectively obtaining the hash values of the main string and the pattern string through a hash algorithm, comparing the hash values of the pattern string and the main string one by using a traversal method, judging whether the hash value of the pattern string is the same as a certain hash value of the main string, if so, obtaining a classification corresponding to the certain hash value, and taking the classification as a matching result, otherwise, repeating the step S1.23.
10. An adverse event management method based on the adverse event management system according to claim 6, wherein the step S3 specifically comprises: according to the adverse events which pass the audit, inquiring an adverse event statistical table in a report storage unit through an event analysis management module, searching the same events as the adverse events which pass the audit in the adverse event statistical table by adopting a traversal algorithm, and extracting the reasons, countermeasures and rectification processes of the same events;
the adverse event statistics table in step S5 includes an adverse event list, an adverse event department summary table, an adverse event occurrence rate summary table, an adverse event cause statistics table, and an adverse event modification statistics table, where the adverse event list includes the number, name, category, occurrence, and information of the reporter and the patient of the adverse event.
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Application publication date: 20200904 |