In the post epidemic era of COVID-19 pneumonia, In the new era of information integration and intelligent development, How to innovate and develop quality control methods for clinical laboratories, To meet the requirements of national smart healthcare construction, New challenges in quality, safety, and cost control, Has become a focus of attention for quality researchers and practitioners both domestically and internationally.

With the rapid progress of clinical laboratory informationization and automation, Computer automated auditing is gradually receiving attention, The usage rate of automated laboratory audits in foreign countries is relatively high, But it has only been developed and used domestically in recent years, How to set standards, comprehensive, Comprehensive automatic review rules? What is the carrier setting? How to verify? How to manage? It has become a common problem that many laboratories planning to carry out automated audits are confused about and urgently need to grasp. This report mainly focuses on AUTO-10A Detailed interpretation and analysis of the guide, Elaborate and introduce the research progress of automatic review in different professional fields at home and abroad after the publication of the guidelines, Propose important insights, Provide reference and assistance for conducting automated audits in clinical laboratories.

With the rapid progress of clinical laboratory informationization and automation, Computer automated auditing is gradually receiving attention, The usage rate of automated laboratory audits in foreign countries is relatively high, But it has only been developed and used domestically in recent years, How to set standards, comprehensive, Comprehensive automatic review rules? What is the carrier setting? How to verify? How to manage? It has become a common problem that many laboratories planning to carry out automated audits are confused about and urgently need to grasp. This report mainly focuses on AUTO-10A Detailed interpretation and analysis of the guide, Elaborate and introduce the research progress of automatic review in different professional fields at home and abroad after the publication of the guidelines, Propose important insights, Provide reference and assistance for conducting automated audits in clinical laboratories.

With the rapid progress of clinical laboratory informationization and automation, Computer automated auditing is gradually receiving attention, The usage rate of automated laboratory audits in foreign countries is relatively high, But it has only been developed and used domestically in recent years, How to set standards, comprehensive, Comprehensive automatic review rules? What is the carrier setting? How to verify? How to manage? It has become a common problem that many laboratories planning to carry out automated audits are confused about and urgently need to grasp. This report mainly focuses on AUTO-10A Detailed interpretation and analysis of the guide, Elaborate and introduce the research progress of automatic review in different professional fields at home and abroad after the publication of the guidelines, Propose important insights, Provide reference and assistance for conducting automated audits in clinical laboratories.

In recent years, With the rapid development of laboratory medicine, Clinical testing plays an increasingly important role in clinical diagnosis and treatment work, Report review is a core link in the overall quality control of medical laboratories, Accuracy of audit results, Timeliness Direct Medical decisions that affect clinical practice, Safety and diagnostic effectiveness. At present, China's report review The conventional mode of nuclear testing is manual review, Manual review is based on the biological parameters of the inspection items Exam interval prompt, Clinical diagnosis, Historical results and professional theoretical knowledge of auditors Judging based on knowledge and work experience. The workload of manual review is high, Massive reports Not only is data time-consuming and laborious, Moreover, differences in personnel capabilities can result in delayed reporting time, Failure to timely detect and handle audit discrepancies such as anomalies or erroneous results.

In recent years, With the rapid development of laboratory medicine, Clinical testing plays an increasingly important role in clinical diagnosis and treatment work, Report review is a core link in the overall quality control of medical laboratories, Accuracy of audit results, Timeliness Direct Medical decisions that affect clinical practice, Safety and diagnostic effectiveness. At present, China's report review The conventional mode of nuclear testing is manual review, Manual review is based on the biological parameters of the inspection items Exam interval prompt, Clinical diagnosis, Historical results and professional theoretical knowledge of auditors Judging based on knowledge and work experience. The workload of manual review is high, Massive reports Not only is data time-consuming and laborious, Moreover, differences in personnel capabilities can result in delayed reporting time, Failure to timely detect and handle audit discrepancies such as anomalies or erroneous results.