Garcia Albert, Subbarao Shambavi, Zhang Guoqing, Parsons Linda, Nkengasong John, Ou Chin-Yih, Ellenberger Dennis
International Laboratory Branch, Division of Global HIV/AIDS, Center for Global Health, Centers for Disease Control and Prevention, U.S. Department of Health and Human Services, Atlanta, Georgia, USA.
J Clin Microbiol. 2014 Mar;52(3):773-80. doi: 10.1128/JCM.03097-13. Epub 2013 Dec 18.
A voluntary, cost-free external quality assessment (EQA) program established by the U.S. Centers for Disease Control and Prevention (CDC) was implemented to primarily monitor the performance of laboratories conducting HIV Early Infant Diagnosis (EID) from dried blood spots (DBS) in low- to middle-income countries since 2006. Ten blind DBS proficiency test (PT) specimens and 100 known HIV-positive and -negative DBS specimens (to be used as internal controls) were shipped triannually to participating laboratories with reports for the PT specimens due within 30 days. The participant's results and a summary of the performance of all participating laboratories and each diagnostic method were provided after each test cycle. Enrollment in the CDC PT program expanded progressively from 17 laboratories from 11 countries in 2006 to include 136 laboratories from 41 countries at the end of 2012. Despite external pressures to test and treat more children while expanding EID programs, mean PT test scores significantly improved over time as demonstrated by the upward trend from mid-2006 to the end of 2012 (P=0.001) and the increase in the percentage of laboratories scoring 100% (P=0.003). The mean test scores plateaued over the past 10 testing cycles, ranging between 98.2% and 99.7%, and discordant test results still occur but at a rate of no higher than 2.6%. Analysis of these test results suggests a positive impact of proficiency testing on the testing performance of the participating laboratories, and a continuous training program and proficiency testing participation may translate into laboratories improving their testing accuracy.
美国疾病控制与预防中心(CDC)设立了一项自愿、免费的外部质量评估(EQA)计划,自2006年起主要用于监测中低收入国家从干血斑(DBS)进行HIV早期婴儿诊断(EID)的实验室的表现。每三年向参与实验室运送10份盲法DBS能力验证(PT)标本和100份已知HIV阳性和阴性的DBS标本(用作内部对照),PT标本的报告应在30天内提交。每个测试周期后会提供参与者的结果以及所有参与实验室和每种诊断方法的表现总结。CDC PT计划的参与实验室从2006年来自11个国家的17个实验室逐步扩大,到2012年底包括来自41个国家的136个实验室。尽管在扩大EID计划的同时面临着对更多儿童进行检测和治疗的外部压力,但PT测试的平均分数随着时间的推移显著提高,如2006年年中至2012年底的上升趋势所示(P = 0.001),以及得分100%的实验室百分比增加(P = 0.003)。在过去10个测试周期中,平均测试分数趋于平稳,在98.2%至99.7%之间,不一致的测试结果仍然存在,但发生率不高于2.6%。对这些测试结果的分析表明,能力验证对参与实验室的测试表现有积极影响,持续培训计划和参与能力验证可能会使实验室提高其测试准确性。