Abstract

Clinical laboratory test-data report is not only an important basis for clinical diagnosis and treatment, but also an important medical evidence. However, at present, in clinical practice, there is a general situation that the medical test-data report have no pay necessary attention in medicine evidence. As a result, in cases of medical malpractise disputes, the medical test-data report often becomes the evidence of litigation against the hospital. This study aims to analyze the healthcare risks in clinical medical laboratory testing and propose effective risk management strategies. The article first identifies key risk points in clinical medical laboratory testing, including risks before, during, and after testing, as well as other related risks. It then discusses existing issues in healthcare risk management, such as non-standardized testing processes, inadequate risk warning mechanisms, and insufficient credibility of test results. Based on these analyses, the article puts forward targeted management strategies, including standardizing testing processes, improving warning mechanisms, and enhancing the credibility of test results. The purpose of this study is to enhance the safety and accuracy of clinical medical laboratory testing, reduce healthcare risks, and ensure patient safety.

Full Text
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