A field evaluation of a rapid dual immunoassay for human immunodeficiency virus and syphilis antibodies, Hanoi, Vietnam.
AIDS Serodiagnosis
/ methods
Adolescent
Adult
Antibodies, Bacterial
/ blood
Antibodies, Viral
/ blood
Female
HIV
/ immunology
HIV Infections
/ blood
Homosexuality, Male
Humans
Male
Mass Screening
/ methods
Middle Aged
Patient Acceptance of Health Care
Point-of-Care Systems
Point-of-Care Testing
Pregnancy
Pregnant Women
Prenatal Care
Sensitivity and Specificity
Syphilis
/ blood
Syphilis Serodiagnosis
/ methods
Treponema pallidum
/ immunology
Vietnam
None
HIV
Point of care
Vietnam
syphilis
Journal
International journal of STD & AIDS
ISSN: 1758-1052
Titre abrégé: Int J STD AIDS
Pays: England
ID NLM: 9007917
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
pubmed:
24
10
2018
medline:
3
9
2019
entrez:
24
10
2018
Statut:
ppublish
Résumé
The SD BIOLINE HIV/Syphilis Duo (SD BIOLINE DUO) rapid test is a dual rapid lateral flow immunoassay that detects antibodies to both human immunodeficiency virus (HIV) and Treponema pallidum (TP) 'syphilis' via fingerprick whole blood. We evaluated the field performance of the SD BIOLINE HIV/Syphilis Duo test among two populations in Hanoi, Vietnam - men who have sex with men (MSM) and pregnant women. We also surveyed factors that influence participants' willingness to test for HIV and syphilis. This test has the potential to increase HIV and syphilis screening in low-resource settings. Patients who received healthcare services at a sexual health clinic for MSM and a district antenatal care center in Hanoi, Vietnam were recruited for the study. Participants with HIV and syphilis were intentionally recruited for adequate test performance evaluation via convenience sampling. At each facility, venipuncture blood specimens were obtained for reference testing for HIV and TP using SD BIOLINE HIV 1/2 3.0 and TP particle agglutination, respectively. SD BIOLINE DUO was compared to the standard reference tests and sensitivity and specificity were calculated. We calculated 95% confidence interval (CI) using the exact binomial method. We used conjoint analysis to identify test attributes that are associated with participant likelihood to seek HIV and syphilis testing. Of 280 participants, 100 (35.7%) were MSM and 180 (64.3%) were pregnant women. Of MSM, 17 (17.0%) were HIV positive and 49 (49.0%) were TP seropositive. All women were negative for both HIV and syphilis antibodies. For HIV antibody testing, sensitivity and specificity were 100.0% (95% CI: 80.5-100.0%) and 100.0% (95% CI: 98.6-100.0%), respectively. For the syphilis antibody testing, sensitivity and specificity were 83.1% (95% CI: 71.0-91.6%) and 100.0% (95% CI: 98.3-100.0%), respectively. Potential for false positives, preference for one blood draw over two, and shorter wait time for testing results were the highest ranked attributes by participants according to their willingness to test. The SD BIOLINE HIV/Syphilis Duo rapid test demonstrated very good performance in this field setting and participants preferred attributes that aligned well with this test.
Identifiants
pubmed: 30348065
doi: 10.1177/0956462418802685
pmc: PMC7439759
mid: NIHMS1046991
doi:
Substances chimiques
Antibodies, Bacterial
0
Antibodies, Viral
0
Types de publication
Evaluation Study
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
173-180Subventions
Organisme : NIAID NIH HHS
ID : P30 AI028697
Pays : United States
Organisme : NIMH NIH HHS
ID : P30 MH058107
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI139265
Pays : United States
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