The failure of routine rapid HIV testing: a case study of improving low sensitivity in the field

被引:41
|
作者
Wolpaw, Benjamin J. [1 ]
Mathews, Catherine [1 ,2 ]
Chopra, Mickey [3 ]
Hardie, Diana [4 ,5 ]
de Azevedo, Virginia [6 ]
Jennings, Karen [6 ]
Lurie, Mark N. [7 ]
机构
[1] S African MRC, Hlth Syst Res Unit, Cape Town, South Africa
[2] Univ Publ Hlth, Sch Publ Hlth & Family Med, Cape Town, South Africa
[3] Univ Western Cape, Sch Publ Hlth, ZA-7535 Bellville, South Africa
[4] Univ Cape Town, Natl Hlth Lab Serv, ZA-7925 Cape Town, South Africa
[5] Univ Cape Town, Div Virol, ZA-7925 Cape Town, South Africa
[6] City Cape Town, Cape Town City Hlth Dept, Cape Town, South Africa
[7] Brown Univ, Sch Med, Dept Community Hlth, Providence, RI 02912 USA
来源
关键词
Rapid Test; Local Healthcare Facility; Quality Improvement Measure; Routine Clinic Testing; Rapid Test Result;
D O I
10.1186/1472-6963-10-73
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: The rapid HIV antibody test is the diagnostic tool of choice in low and middle-income countries. Previous evidence suggests that rapid HIV diagnostic tests may underperform in the field, failing to detect a substantial number of infections. A research study inadvertently discovered that a clinic rapid HIV testing process was failing to detect cases of established (high antibody titer) infection, exhibiting an estimated 68.7% sensitivity (95% CI [41.3%-89.0%]) over the course of the first three weeks of observation. The setting is a public service clinic that provides STI diagnosis and treatment in an impoverished, peri-urban community outside of Cape Town, South Africa. Methods: The researchers and local health administrators collaborated to investigate the cause of the poor test performance and make necessary corrections. The clinic changed the brand of rapid test being used and later introduced quality improvement measures. Observations were made of the clinic staff as they administered rapid HIV tests to real patients. Estimated testing sensitivity was calculated as the number of rapid HIV test positive individuals detected by the clinic divided by this number plus the number of PCR positive, highly reactive 3(rd) generation ELISA patients identified among those who were rapid test negative at the clinic. Results: In the period of five months after the clinic made the switch of rapid HIV tests, estimated sensitivity improved to 93.5% (95% CI [86.5%-97.6%]), during which time observations of counselors administering tests at the clinic found poor adherence to the recommended testing protocol. Quality improvement measures were implemented and estimated sensitivity rose to 95.1% (95% CI [83.5%-99.4%]) during the final two months of full observation. Conclusions: Poor testing procedure in the field can lead to exceedingly low levels of rapid HIV test sensitivity, making it imperative that stringent quality control measures are implemented where they do not already exist. Certain brands of rapid-testing kits may perform better than others when faced with sub-optimal use.
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页数:4
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