Reliability of HIV rapid diagnostic tests for self-testing compared with testing by health-care workers: a systematic review and meta-analysis

被引:150
作者
Figueroa, Carmen [1 ]
Johnson, Cheryl [1 ,3 ]
Ford, Nathan [1 ]
Sands, Anita [2 ]
Dalal, Shona [1 ]
Meurant, Robyn [2 ]
Prat, Irena [2 ]
Hatzold, Karin [4 ]
Urassa, Willy [2 ]
Baggaley, Rachel [1 ]
机构
[1] WHO, Dept HIV, CH-1201 Geneva, Switzerland
[2] WHO, Dept Essential Med & Hlth Prod, Geneva, Switzerland
[3] London Sch Hyg & Trop Med, Dept Clin Res, London, England
[4] PSI Zimbabwe, Harare, Zimbabwe
来源
LANCET HIV | 2018年 / 5卷 / 06期
基金
比尔及梅琳达.盖茨基金会;
关键词
EMERGENCY-DEPARTMENT; ACCEPTABILITY; ACCURACY; FEASIBILITY; POPULATIONS; PERFORM; KENYA;
D O I
10.1016/S2352-3018(18)30044-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background The ability of individuals to use HIV self-tests correctly is debated. To inform the 2016 WHO recommendation on HIV self-testing, we assessed the reliability and performance of HIV rapid diagnostic tests when used by self-testers. Methods In this systematic review and meta-analysis, we searched PubMed, PopLine, and Embase, conference abstracts, and additional grey literature between Jan 1, 1995, and April 30, 2016, for observational and experimental studies reporting on HIV self-testing performance. We excluded studies evaluating home specimen collection because patients did not interpret their own test results. We extracted data independently, using standardised extraction forms. Outcomes of interest were agreement between self-testers and health-care workers, sensitivity, and specificity. We calculated. to establish the level of agreement and pooled. estimates using a random-effects model, by approach (directly assisted or unassisted) and type of specimen (blood or oral fluid). We examined heterogeneity with the I (2) statistic. Findings 25 studies met inclusion criteria (22 to 5662 participants). Quality assessment with QUADAS-2 showed studies had low risk of bias and incomplete reporting in accordance with the STARD checklist. Raw proportion of agreement ranged from 85.4% to 100%, and reported. ranged from fair (kappa 0.277, p<0.001) to almost perfect (kappa 0.99, n=25). Pooled. suggested almost perfect agreement for both types of approaches (directly assisted 0.98, 95% CI 0.96-0.99 and unassisted 0.97, 0.96-0.98; I-2 = 34.5%, 0-97.8). Excluding two outliers, sensitivity and specificity was higher for blood-based rapid diagnostic tests (4/16) compared with oral fluid rapid diagnostic tests (13/16). The most common error that affected test performance was incorrect specimen collection (oral swab or finger prick). Study limitations included the use of different reference standards and no disaggregation of results by individuals taking antiretrovirals. Interpretation Self-testers can reliably and accurately do HIV rapid diagnostic tests, as compared with trained healthcare workers. Errors in performance might be reduced through the improvement of rapid diagnostic tests for self-testing, particularly to make sample collection easier and to simplify instructions for use.
引用
收藏
页码:E277 / E290
页数:14
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