Evaluation of Rapid Prenatal Human Immunodeficiency Virus Testing in Rural Cameroon

Author:

Granade Timothy C.123,Parekh Bharat S.123,Tih Pius M.123,Welty Thomas123,Welty Edith123,Bulterys Marc123,Ndikintum George123,Nkuoh Godlove123,Tancho Samuel123

Affiliation:

1. HIV Laboratory Branch, Division of HIV/AIDS Prevention, National Center for HIV, STD, and TB Prevention

2. Epidemiology Branch, Division of HIV/AIDS Prevention, National Center for HIV, STD and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA 30333

3. Cameroon Baptist Convention Health Board, P.O. Box 9, Nso, Northwest Province, Cameroon

Abstract

ABSTRACT Pregnant women ( n = 859) in rural Cameroonian prenatal clinics were screened by two rapid human immunodeficiency virus (HIV) antibody tests (rapid tests [RT]) (Determine and Hema-Strip) using either whole blood or plasma. One additional RT (Capillus, HIV-CHEK, or Sero-Card) was used to resolve discordant results. RT results were compared with HIV-1 enzyme immunoassay (EIA) and Western blot (WB) results of matched dried blood spots (DBS) to assess the accuracy of HIV RTs. DBS EIA/WB identified 83 HIV antibody-reactive, 763 HIV antibody-nonreactive, and 13 indeterminate specimens. RT results were evaluated in serial (two consecutive tests) or parallel (two simultaneous tests) testing algorithms. A serial algorithm using Determine and Hema-Strip yielded sensitivity and specificity results of 97.6% and 99.7%, respectively, whereas a parallel RT algorithm using Determine plus a second RT produced a sensitivity and specificity of 100% and 99.7%, respectively. HIV RTs provide excellent alternatives for identifying HIV infection, and their field performance could be monitored using DBS testing strategies.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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