Gerber A R, Valdiserri R O, Johnson C A, Schwartz R E, Hancock J S, Hearn T L
Division of Laboratory Systems, Centers for Disease Control, Atlanta, Ga 30333.
Arch Pathol Lab Med. 1991 Nov;115(11):1091-6.
In May 1988, the Centers for Disease Control's Model Performance Evaluation Program (Atlanta, Ga) surveyed 1092 laboratories that performed enzyme immunoassays and Western blot tests for human immunodeficiency virus type 1 antibody on mailed plasma samples of known human immunodeficiency virus type 1 antibody reactivity and that described their laboratory characteristics and testing practices. The study objective was to evaluate the quality of laboratory performance in testing for human immunodeficiency virus type 1 antibody. After identifying relevant variables in univariate analyses, multivariate analyses were performed using stepwise logistic models. Human immunodeficiency virus type 1 antibody test performance was independently associated with analytic variables such as commercial test kit used and with nonanalytic variables such as experience, training, and degree requirements of laboratory personnel. These results validate the importance of nonanalytic variables to the quality of outcomes in laboratory testing.
1988年5月,疾病控制中心的模型性能评估项目(佐治亚州亚特兰大)对1092家实验室进行了调查,这些实验室对邮寄的已知1型人类免疫缺陷病毒抗体反应性的血浆样本进行1型人类免疫缺陷病毒抗体的酶免疫测定和蛋白质印迹检测,并描述了它们的实验室特征和检测方法。研究目的是评估1型人类免疫缺陷病毒抗体检测中实验室检测性能的质量。在单变量分析中确定相关变量后,使用逐步逻辑模型进行多变量分析。1型人类免疫缺陷病毒抗体检测性能与诸如所使用的商业检测试剂盒等分析变量以及诸如实验室人员的经验、培训和学历要求等非分析变量独立相关。这些结果证实了非分析变量对实验室检测结果质量的重要性。