P16.31 Improving timely hiv results in key populations: rapid test antibody evaluation for hiv diagnosis in guatemala, 2012–2013. (13th September 2015)
- Record Type:
- Journal Article
- Title:
- P16.31 Improving timely hiv results in key populations: rapid test antibody evaluation for hiv diagnosis in guatemala, 2012–2013. (13th September 2015)
- Main Title:
- P16.31 Improving timely hiv results in key populations: rapid test antibody evaluation for hiv diagnosis in guatemala, 2012–2013
- Authors:
- Arana Flora, E
Castillo-Signor, L
Marchorro, P
Girón, V
Lopez, A
Escobar, C
Vargas, C
Mendizabal-Burastero, R
Morales-Miranda, S - Abstract:
- Abstract : Introduction: Guatemala has a concentrated HIV epidemic among key populations; in 2003, the first rapid test validation in Central America was performed. A national HIV testing algorithm with a rapid test and a second test using an enzyme immunoassay (EIA) was developed (average turnaround time of 2 weeks). Given the changes in the market since 2003, we present results of a second rapid test validation to update the Guatemalan algorithm. Methods: Validation was performed in 2012–2013, evaluating a total of 10 rapid tests in two phases: 1) with serum, HIV-negative samples were obtained from blood banks, and positive samples from HIV care units; 2) with whole blood, negative samples were obtained from antenatal care services and positive samples from HIV care units. We tested 452 serum samples [244 HIV+, 208 HIV-] and 432 whole blood samples (10 HIV positive, 422 HIV negative) using two EIA (Roche ELECSYS HIV Combi and Abbott AXSYM HIV Ag/Ab Combo). Discordant results were evaluated with HIV-1 Western Blot. For fourth generation rapid tests, only antibody was evaluated. Data was analysed using OpenEpi. Results: Six HIV rapid tests were included for both phases. All tests (except Double Check Gold) reported sensitivity higher than 99% and specificity higher than 95%. Determine HIV 1/2 and HIV Ag/Ab reported the highest results for sensitivity (100%). Hexagon HIV (100%) and Accu-Tell (99.5%) reported the highest results for specificity. All rapid tests that alsoAbstract : Introduction: Guatemala has a concentrated HIV epidemic among key populations; in 2003, the first rapid test validation in Central America was performed. A national HIV testing algorithm with a rapid test and a second test using an enzyme immunoassay (EIA) was developed (average turnaround time of 2 weeks). Given the changes in the market since 2003, we present results of a second rapid test validation to update the Guatemalan algorithm. Methods: Validation was performed in 2012–2013, evaluating a total of 10 rapid tests in two phases: 1) with serum, HIV-negative samples were obtained from blood banks, and positive samples from HIV care units; 2) with whole blood, negative samples were obtained from antenatal care services and positive samples from HIV care units. We tested 452 serum samples [244 HIV+, 208 HIV-] and 432 whole blood samples (10 HIV positive, 422 HIV negative) using two EIA (Roche ELECSYS HIV Combi and Abbott AXSYM HIV Ag/Ab Combo). Discordant results were evaluated with HIV-1 Western Blot. For fourth generation rapid tests, only antibody was evaluated. Data was analysed using OpenEpi. Results: Six HIV rapid tests were included for both phases. All tests (except Double Check Gold) reported sensitivity higher than 99% and specificity higher than 95%. Determine HIV 1/2 and HIV Ag/Ab reported the highest results for sensitivity (100%). Hexagon HIV (100%) and Accu-Tell (99.5%) reported the highest results for specificity. All rapid tests that also included HIV-2 detection, showed cross-reactivity, ranging from 37% of HIV cases for Anarapid HIV 1/2/O Tri-line to 15% for Rapid HIV 1/2/O Tri-Line. Conclusion: Our results show that Determine HIV½ and HIV Ag/Ab should be recommended as a screening test while Hexagon HIV and Accu-Tell should be recommended as second test. Rapid test validation provides valuable information for on-site confirmation of reactive results improving diagnosis turnaround time. Disclosure of interest statement: We declare that we have no conflicts of interest. … (more)
- Is Part Of:
- Sexually transmitted infections. Volume 91(2015)Supplement 2
- Journal:
- Sexually transmitted infections
- Issue:
- Volume 91(2015)Supplement 2
- Issue Display:
- Volume 91, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 91
- Issue:
- 2
- Issue Sort Value:
- 2015-0091-0002-0000
- Page Start:
- A222
- Page End:
- A223
- Publication Date:
- 2015-09-13
- Subjects:
- Sexually transmitted diseases -- Periodicals
HIV infections -- Periodicals
616.951005 - Journal URLs:
- http://sti.bmj.com/ ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/176/ ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/sextrans-2015-052270.578 ↗
- Languages:
- English
- ISSNs:
- 1368-4973
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18096.xml