Peddecord K M, Benenson A S, Hofherr L K, Garfein R S, Francis D P, Hewitt D J, Ferran K L, Schalla W O, Hearn T L
College of Health and Human Services, San Diego State University, CA 92182.
Clin Lab Sci. 1992 May-Jun;5(3):172-6.
Blind proficiency testing was used to examine nonanalytic performance indicators for human immunodeficiency virus type 1 (HIV-1) antibody testing. Physician offices, clinics, and hospitals located throughout Southern California submitted simulated patient specimens to laboratories as routine test requests. A total of 32 laboratories were involved during five blind proficiency testing surveys. Turnaround time for a reactive specimen ranged from three to 17 days. Laboratory charges for evaluating a reactive specimen varied depending on the volume of testing, prevalence of reactive specimens, and whether screening and confirmatory tests were billed separately or as a package price. Charges for an enzyme immunoassay screening test plus supplemental tests ranged from $11.75 to $114.50, with a median of $31.00 for 24 laboratories that participated in one of the five surveys. Evaluation of laboratory report content revealed that 37% of the 16 screening reports and 71% of the 14 supplemental reports contained information that was unrelated to the patient results. Evaluation of the testing system documents the need to monitor multiple outcomes of the total laboratory testing process, not just the analytic testing phase.
采用盲法能力验证来检测1型人类免疫缺陷病毒(HIV-1)抗体检测的非分析性能指标。南加州各地的医生办公室、诊所和医院将模拟患者标本作为常规检测请求提交给实验室。在五次盲法能力验证调查中,共有32家实验室参与。反应性标本的周转时间为3至17天。评估反应性标本的实验室收费因检测量、反应性标本的流行率以及筛查和确认试验是单独计费还是按套餐价格计费而异。酶免疫分析筛查试验加补充试验的收费从11.75美元到114.50美元不等,参与五项调查之一的24家实验室的中位数为31.00美元。对实验室报告内容的评估显示,16份筛查报告中有37%以及14份补充报告中有71%包含与患者结果无关的信息。对检测系统的评估表明,有必要监测整个实验室检测过程的多个结果,而不仅仅是分析检测阶段。