The source code of the hospital safety adverse event management system, and the adverse event is reported.As the conflict between doctors and patients becomes more and more prominent, and the attention to patient safety is getting higher and higher, the current level review requirements issued by the National Health Commission have raised patient safety to a new height. The hospital safety (adverse) event management system is to collect and deal with hospital safety related events that occur in the hospital for the purpose of improving the quality of hospital medical services, conduct statistical analysis, and continue to rectify and complete closed-loop managementIt provides information support for the improvement of the quality of hospital medical services.
The system includes medical safety adverse events, nursing safety adverse events, drug safety adverse events, blood transfusion adverse reaction events, hospital infection events, occupational exposure events, medical device adverse events, administrative safety adverse events, public facilities adverse events, fire and security adverse events, information security adverse events, etc.
Event Type:
Care-related events:(Fall incidents, bed fall incidents, pressure ulcer incidents, pipeline slippage events, drug delivery error events, burn and scald events, infusion reaction events, patient suicide events, patient lost incidents, disinfection ** events, and other events).
Medical-related events:(Surgical events, anesthesia events, diagnosis and treatment related events, medical ethics related to medical style, medical record management events, in-hospital unexpected cardiac arrest events, dosing errors, approximate dosing errors, doctor's orders or prescription errors).
Drug-related events:(drug storage-related, adverse drug reactions).
Device-related events:(Medical Device Report).
Hospital-related events:(Hospitalization gathering, occupational exposure, medical waste leakage incidents).
Blood transfusion-related events:(Blood safety, adverse reactions to blood transfusion).
Medical technology-related events:(medical technology related, examination events, pathological slice events).
Security Logistics Incidents:(public accidents, public security injuries, logistics-related incidents).
Information-related events:Information-related events:
Other Events:(Expense Events, Window Service Events).
The system has the following features:
1.Real-time escalation: Allow healthcare professionals to report adverse events anytime, anywhere, ensuring timely delivery of information.
2.Clear classification: For different types of medical adverse events, it provides clear event classification for easy retrieval and analysis.
3.Data analysis: Conduct data mining on reported adverse events to provide valuable information and recommendations for medical institutions.
4.Early warning function: Through intelligent analysis, early warning of possible adverse events can be carried out to prevent the occurrence of similar events.
5.Transparency and openness: Ensure that the reporting and handling results of adverse events are open and transparent, and enhance mutual trust between doctors and patients.
Value & Significance
The application of the medical adverse event reporting system is of great value and significance
1.Improve patient safety: Reduce medical risks and protect patients' lives and health by detecting and dealing with adverse events in a timely manner.
2.Improve the quality of medical care: Through the analysis of adverse events, find out the root cause of the problem, formulate targeted improvement measures, and improve the quality of medical care.
3.Enhance doctor-patient mutual trust: Transparent and open adverse event handling methods can help enhance doctor-patient mutual trust and build a harmonious doctor-patient relationship.
4.Promote the sustainable development of the medical industry: Promote the continuous progress of the entire industry and achieve the sustainable development of the medical industry by sharing experiences and lessons learned.
Conclusion
The medical adverse event reporting system is an important tool for medical institutions to improve management efficiency and ensure patient safety. Through real-time reporting, clear classification, data analysis and other functions, the system provides a comprehensive and effective management solution. At the same time, through the early warning function and the principle of transparency, the system helps to prevent the occurrence of similar adverse events, enhance the mutual trust between doctors and patients, and promote the sustainable development of the medical industry.