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Early infant diagnosis of HIV infection using DNA-PCR at a referral center: an 8 years retrospective analysis

BACKGROUND: Over the last decade, Ethiopia adopted different strategies of prevention of mother to child transmission of HIV (PMTCT). Prior to implementation of Option A in 2011, there was no provision of prophylaxis for PMTCT. With ‘Option A’, PMTCT interventions relied on maternal CD4 count. In ea...

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Autores principales: Olana, Tolessa, Bacha, Tigist, Worku, Walelign, Tadesse, Birkneh Tilahun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016933/
https://www.ncbi.nlm.nih.gov/pubmed/27617023
http://dx.doi.org/10.1186/s12981-016-0112-0
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author Olana, Tolessa
Bacha, Tigist
Worku, Walelign
Tadesse, Birkneh Tilahun
author_facet Olana, Tolessa
Bacha, Tigist
Worku, Walelign
Tadesse, Birkneh Tilahun
author_sort Olana, Tolessa
collection PubMed
description BACKGROUND: Over the last decade, Ethiopia adopted different strategies of prevention of mother to child transmission of HIV (PMTCT). Prior to implementation of Option A in 2011, there was no provision of prophylaxis for PMTCT. With ‘Option A’, PMTCT interventions relied on maternal CD4 count. In early 2013, ‘‘Option B+’’ has been started; with this option, antiretroviral therapy is started and continued for life to any HIV positive pregnant mother irrespective of CD4 count with an enhanced treatment for the baby. Though there are a number of studies which evaluated the effectiveness of PMTCT interventions, the current study assessed the real-world effectiveness of PMTCT options in a setting where there is limitation of resources. OBJECTIVE: This study tried to address three questions: what proportion of babies tested by DNA-PCR are HIV infected in the first 2 months of life? How does the type of PMTCT intervention affect presence of HIV infection at this age? What are the factors affecting HIV transmission, after controlling for type of PMCT-HIV intervention? METHODS: We assessed records of 624 registered HIV exposed infants and 412 mothers who were delivered at Bishoftu Hospital from May 2006 to August 2014. Presence of HIV infection at 6–8 weeks of age was assessed from the records. Maternal and infant risk factors for infection at this age were analyzed. Data were collected using standard data abstraction format and were analyzed using SPSS version 20. RESULTS: Among all the infants who were delivered at the hospital during the study period, 624/936 (66.7 %) had undergone early infant diagnosis at 6–8 weeks. Twenty-seven (4.3 %) were positive for HIV DNA PCR at the age of 6–8 weeks. None of the infants who received ‘‘Option B+’’ had a positive HIV DNA PCR result. HIV infection rate was highest among those who took either no prophylaxis or single dose Nevirapine (11.5 and 11.1 % respectively). Those who took single dose Nevirapine and Zidovudine had HIV positivity rate of 3.9 %. Many of the covariates which were shown to be predictors on bivariate analysis were found not to be independent predictors on multivariate analysis. CONCLUSION: PMTCT ‘’Option B+’’ resulted in zero HIV infection rates among the included infants. There was a high loss to follow up rate at 6–8 weeks of age. The authors recommend that a better strategy of linkage to care and treatment should be devised for HIV exposed infants.
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spelling pubmed-50169332016-09-10 Early infant diagnosis of HIV infection using DNA-PCR at a referral center: an 8 years retrospective analysis Olana, Tolessa Bacha, Tigist Worku, Walelign Tadesse, Birkneh Tilahun AIDS Res Ther Research BACKGROUND: Over the last decade, Ethiopia adopted different strategies of prevention of mother to child transmission of HIV (PMTCT). Prior to implementation of Option A in 2011, there was no provision of prophylaxis for PMTCT. With ‘Option A’, PMTCT interventions relied on maternal CD4 count. In early 2013, ‘‘Option B+’’ has been started; with this option, antiretroviral therapy is started and continued for life to any HIV positive pregnant mother irrespective of CD4 count with an enhanced treatment for the baby. Though there are a number of studies which evaluated the effectiveness of PMTCT interventions, the current study assessed the real-world effectiveness of PMTCT options in a setting where there is limitation of resources. OBJECTIVE: This study tried to address three questions: what proportion of babies tested by DNA-PCR are HIV infected in the first 2 months of life? How does the type of PMTCT intervention affect presence of HIV infection at this age? What are the factors affecting HIV transmission, after controlling for type of PMCT-HIV intervention? METHODS: We assessed records of 624 registered HIV exposed infants and 412 mothers who were delivered at Bishoftu Hospital from May 2006 to August 2014. Presence of HIV infection at 6–8 weeks of age was assessed from the records. Maternal and infant risk factors for infection at this age were analyzed. Data were collected using standard data abstraction format and were analyzed using SPSS version 20. RESULTS: Among all the infants who were delivered at the hospital during the study period, 624/936 (66.7 %) had undergone early infant diagnosis at 6–8 weeks. Twenty-seven (4.3 %) were positive for HIV DNA PCR at the age of 6–8 weeks. None of the infants who received ‘‘Option B+’’ had a positive HIV DNA PCR result. HIV infection rate was highest among those who took either no prophylaxis or single dose Nevirapine (11.5 and 11.1 % respectively). Those who took single dose Nevirapine and Zidovudine had HIV positivity rate of 3.9 %. Many of the covariates which were shown to be predictors on bivariate analysis were found not to be independent predictors on multivariate analysis. CONCLUSION: PMTCT ‘’Option B+’’ resulted in zero HIV infection rates among the included infants. There was a high loss to follow up rate at 6–8 weeks of age. The authors recommend that a better strategy of linkage to care and treatment should be devised for HIV exposed infants. BioMed Central 2016-09-08 /pmc/articles/PMC5016933/ /pubmed/27617023 http://dx.doi.org/10.1186/s12981-016-0112-0 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Olana, Tolessa
Bacha, Tigist
Worku, Walelign
Tadesse, Birkneh Tilahun
Early infant diagnosis of HIV infection using DNA-PCR at a referral center: an 8 years retrospective analysis
title Early infant diagnosis of HIV infection using DNA-PCR at a referral center: an 8 years retrospective analysis
title_full Early infant diagnosis of HIV infection using DNA-PCR at a referral center: an 8 years retrospective analysis
title_fullStr Early infant diagnosis of HIV infection using DNA-PCR at a referral center: an 8 years retrospective analysis
title_full_unstemmed Early infant diagnosis of HIV infection using DNA-PCR at a referral center: an 8 years retrospective analysis
title_short Early infant diagnosis of HIV infection using DNA-PCR at a referral center: an 8 years retrospective analysis
title_sort early infant diagnosis of hiv infection using dna-pcr at a referral center: an 8 years retrospective analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016933/
https://www.ncbi.nlm.nih.gov/pubmed/27617023
http://dx.doi.org/10.1186/s12981-016-0112-0
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