质量管理委员会明确要求：第一，各医技科室在确认检查结果出现“危急值”后

The Quality Management Committee clearly requires: <br><br>First, after confirming that the examination result has a "critical value", each medical technical department should immediately report the result to the clinical department where the patient is located. No concealment, omission or delay of the report shall be allowed, and relevant records shall be recorded Do it in detail. <br><br>Second, after the clinical department receives the "critical value" report, corresponding measures should be taken immediately to save the patient's life and ensure medical safety. <br><br>Third, communication should be carried out frequently between medical technical departments and clinicians, and clinicians' opinions on the quality management of "critical value" should be listened to in order to modify and formulate critical value report items and reporting thresholds that are more suitable for clinical use. <br><br>Members are sent to the department by the Quality Management Committee to conduct a quarterly inspection of critical value reports. The inspection content mainly involves whether the critical value registration records of the laboratory and clinical departments are complete, whether the critical value is under-reported, and the timely rate of critical value reports. <br><br>A meeting is held every six months by the Quality Management Committee, and a joint clinical laboratory joint meeting is composed of personnel from the Quality Control Department, Medical Department, Nursing Department, and Laboratory Department to provide feedback and discussion on the management of critical value reports in the Laboratory. <br><br>2) In the establishment of <br>the critical value quality management team of the clinical laboratory, the director of the laboratory serves as the team leader, and the deputy director serves as the deputy quality team leader to optimize the management of the critical value reporting system. The organization chart is shown in Figure 4. <br><br>Organization Chart of Critical Value Management Team of Laboratory

The Quality Management Committee specifically requires:<br><br>First, after confirming the "critical value" of the examination results, the medical and technical departments should immediately report the results to the clinical department where the patient is located, and shall not conceal, underreport or delay the report, and the relevant records should be done in detail.<br><br>Second, the clinical department received the "critical value" report, the corresponding measures should be taken immediately to save the lives of patients, to ensure medical safety.<br><br>Third, communication should often be conducted between the medical and technical department sandinum and clinician, clinicians on the "critical value" quality management should be listened to, in order to modify and develop more suitable clinical critical value report project and report boundary value.<br><br>Members are sent by the Quality Management Committee to the department on a quarterly basis to carry out a critical value report inspection, the contents of the inspection mainly related to the inspection department and clinical department critical value registration records are complete, whether the critical value is not reported, the critical value report timely rate.<br><br>A meeting by the Quality Management Committee every six months, by the quality control department, medical department, nursing department, inspection department of the relevant departments of the joint meeting of the clinical inspection of the inspection department critical value report management feedback and discussion.<br><br>2) The establishment of the critical value quality management team in the middle department of the inspection department.<br>The team is headed by the Director of the Inspection Section and the Deputy Director of Quality as the Deputy Head of the Critical Value Reporting System for the Optimization of management, as shown in Figure 4.<br><br>Organizational chart of the critical value management team of the Inspection Section.

The quality management committee clearly requires that:<br>First, each medical and technical department should report the results to the clinical department of the patient immediately after confirming the "critical value" of the examination results, and the relevant records should be made in detail.<br>Second, after the clinical departments receive the "critical value" report, the corresponding measures should be taken immediately to save the lives of patients and ensure medical safety.<br>Thirdly, communication should be carried out between medical technical departments and clinicians. Clinicians' opinions on the quality management of critical value should be listened to in order to modify and formulate more suitable critical value reporting items and reporting thresholds.<br>The members are sent by the quality management committee to the Department to inspect the critical value report once a quarter. The inspection contents mainly involve whether the emergency value registration records of the laboratory and clinical departments are complete, whether the critical value is not reported, and the timeliness rate of the critical value report.<br>A meeting is held by the quality management committee every half a year. It is composed of personnel from the quality control department, the medical department, the nursing department and the laboratory department. The clinical laboratory joint meeting provides feedback and Discussion on the management of critical value report in the laboratory.<br>2) Establishment of critical value quality management group in laboratory<br>The team leader is the director of the laboratory department, and the deputy director is the Deputy quality team leader to optimize the management of the critical value reporting system. The organization chart is shown in Figure 4.<br>Organization chart of critical value management group in laboratory<br>