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Internal quality assurance in a clinical virology laboratory. I. Internal quality assessment.

机译:临床病毒学实验室的内部质量保证。一,内部质量评估。

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摘要

AIMS--In April 1991 an internal quality assessment scheme (IQAS) was introduced into the virology section of the Clinical Microbiology and Public Health Laboratory, Cambridge. The IQAS was established to identify recurring technical and procedural problems, to check the adequacy of current techniques, and to calculate the frequency of errors. METHODS--Between April 1991 and December 1993, 715 anonymous clinical serum samples were submitted to the laboratory to test 3245 individual procedures of diagnostic viral serology. RESULTS--A total of 485 (14.9%) procedural and 61 (1.9%) technical discrepancies were observed, the technical discrepancies mainly being recorded in complement fixation tests. Twenty two (0.7% of total procedures) of the technical discrepancies were diagnostically significant. CONCLUSIONS--Evaluation criteria developed with the introduction of IQAS to viral serology, and technical and procedural discrepancies are assessed. As yet, IQAS has not been introduced to other sections of the diagnostic virology laboratory (virus isolation, electron microscopy, immunofluorescence, and enzyme linked immunosorbent assays for viral and chlamydial antigens).
机译:目的-1991年4月,内部质量评估计划(IQAS)被引入剑桥大学临床微生物学和公共卫生实验室的病毒学部门。建立IQAS的目的是识别重复出现的技术和程序问题,检查当前技术的适当性并计算错误发生的频率。方法-在1991年4月至1993年12月之间,共向实验室提交了715份匿名临床血清样本,以测试3245条诊断性病毒血清学的个别程序。结果-总共观察到485(14.9%)的程序和61(1.9%)的技术差异,这些技术差异主要记录在补体固定测试中。 22项技术差异(占总程序的0.7%)具有诊断意义。结论-评估了将IQAS引入病毒血清学中制定的评估标准,以及技术和程序上的差异。迄今为止,IQAS尚未引入诊断病毒学实验室的其他部分(病毒和衣原体抗原的病毒分离,电子显微镜,免疫荧光和酶联免疫吸附测定)。

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