Hepatitis B virus surface antigen and anti-hepatitis C virus rapid tests underestimate hepatitis prevalence among HIV-infected patients

被引:13
作者
Honge, B. L. [1 ,2 ]
Jespersen, S. [1 ,2 ]
Medina, C. [3 ]
Te, D. S. [3 ]
da Silva, Z. J. [1 ,4 ]
Ostergaard, L. [2 ]
Laursen, A. L. [2 ]
Wejse, C. [1 ,2 ,5 ]
Krarup, H. [6 ]
Erikstrup, C. [7 ]
机构
[1] Bandim Hlth Project, Indepth Network, Bissau, Guinea Bissau
[2] Aarhus Univ Hosp, Dept Infect Dis, DK-8200 Aarhus, Denmark
[3] Minist Hlth, Natl HIV Programme, Bissau, Guinea Bissau
[4] Natl Publ Hlth Lab, Bissau, Guinea Bissau
[5] Aarhus Univ, Sch Publ Hlth, Ctr Global Hlth, GloHAU, Aarhus, Denmark
[6] Aalborg Univ Hosp, Dept Clin Biochem, Aalborg, Denmark
[7] Aarhus Univ Hosp, Dept Clin Immunol, DK-8000 Aarhus, Denmark
关键词
anti-hepatitis C virus; Guinea-Bissau; hepatitis B virus surface antigen; HIV; rapid tests; SEROPREVALENCE; COINFECTION; ANTIBODIES; ASSAYS;
D O I
10.1111/hiv.12158
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
ObjectivesIn the case of coinfection with HIV and hepatitis B virus (HBV) and/or hepatitis C virus (HCV), hepatic disease progression is often accelerated, with higher rates of liver cirrhosis and liver-related mortality. We aimed to evaluate the performance of the rapid tests used routinely to detect HBV surface antigen (HBsAg) and anti-HCV among HIV-infected patients in Guinea-Bissau. MethodsBlood samples from HIV-infected patients in Guinea-Bissau were stored after testing for HBsAg and anti-HCV with rapid tests. Samples were subsequently re-tested for HBsAg and anti-HCV in Denmark. ResultsTwo rapid tests were used in Guinea-Bissau: HBsAg Strip Ref 2034 (VEDA.LAB, Alencon, France; sensitivity 62.3%; specificity 99.2%) and HEPA-SCAN (Bhat Bio-Tech, Bangalore, India; sensitivity 57.1%; specificity 99.7%). In the two tests the ability to obtain the correct outcome depended on the antigen and antibody concentrations, respectively. Sex, age, CD4 cell count and antiretroviral therapy status did not differ between false negative and true positive samples in either of the tests. The study is limited by a low number of anti-HCV positive samples. ConclusionsNew diagnostic rapid tests should always be evaluated in the setting in which they will be used before implementation.
引用
收藏
页码:571 / 576
页数:6
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