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Pregnancy and Virologic Response to Antiretroviral Therapy in South Africa

BACKGROUND: Although women of reproductive age are the largest group of HIV-infected individuals in sub-Saharan Africa, little is known about the impact of pregnancy on response to highly active antiretroviral therapy (HAART) in that setting. We examined the effect of incident pregnancy after HAART...

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Autores principales: Westreich, Daniel, Cole, Stephen R., Nagar, Shashi, Maskew, Mhairi, van der Horst, Charles, Sanne, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149058/
https://www.ncbi.nlm.nih.gov/pubmed/21829650
http://dx.doi.org/10.1371/journal.pone.0022778
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author Westreich, Daniel
Cole, Stephen R.
Nagar, Shashi
Maskew, Mhairi
van der Horst, Charles
Sanne, Ian
author_facet Westreich, Daniel
Cole, Stephen R.
Nagar, Shashi
Maskew, Mhairi
van der Horst, Charles
Sanne, Ian
author_sort Westreich, Daniel
collection PubMed
description BACKGROUND: Although women of reproductive age are the largest group of HIV-infected individuals in sub-Saharan Africa, little is known about the impact of pregnancy on response to highly active antiretroviral therapy (HAART) in that setting. We examined the effect of incident pregnancy after HAART initiation on virologic response to HAART. METHODS AND FINDINGS: We evaluated a prospective clinical cohort of adult women who initiated HAART in Johannesburg, South Africa between 1 April 2004 and 30 September 2009, and followed up until an event, death, transfer, drop-out, or administrative end of follow-up on 31 March 2010. Women over age 45 and women who were pregnant at HAART initiation were excluded from the study; final sample size for analysis was 5,494 women. Main exposure was incident pregnancy, experienced by 541 women; main outcome was virologic failure, defined as a failure to suppress virus to ≤400 copies/ml by six months or virologic rebound >400 copies/ml thereafter. We calculated adjusted hazard ratios using marginal structural Cox proportional hazards models and weighted lifetable analysis to calculate adjusted five-year risk differences. The weighted hazard ratio for the effect of pregnancy on time to virologic failure was 1.34 (95% confidence limit [CL] 1.02, 1.78). Sensitivity analyses generally confirmed these main results. CONCLUSIONS: Incident pregnancy after HAART initiation was associated with modest increases in both relative and absolute risks of virologic failure, although uncontrolled confounding cannot be ruled out. Nonetheless, these results reinforce that family planning is an essential part of care for HIV-positive women in sub-Saharan Africa. More work is needed to confirm these findings and to explore specific etiologic pathways by which such effects may operate.
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spelling pubmed-31490582011-08-09 Pregnancy and Virologic Response to Antiretroviral Therapy in South Africa Westreich, Daniel Cole, Stephen R. Nagar, Shashi Maskew, Mhairi van der Horst, Charles Sanne, Ian PLoS One Research Article BACKGROUND: Although women of reproductive age are the largest group of HIV-infected individuals in sub-Saharan Africa, little is known about the impact of pregnancy on response to highly active antiretroviral therapy (HAART) in that setting. We examined the effect of incident pregnancy after HAART initiation on virologic response to HAART. METHODS AND FINDINGS: We evaluated a prospective clinical cohort of adult women who initiated HAART in Johannesburg, South Africa between 1 April 2004 and 30 September 2009, and followed up until an event, death, transfer, drop-out, or administrative end of follow-up on 31 March 2010. Women over age 45 and women who were pregnant at HAART initiation were excluded from the study; final sample size for analysis was 5,494 women. Main exposure was incident pregnancy, experienced by 541 women; main outcome was virologic failure, defined as a failure to suppress virus to ≤400 copies/ml by six months or virologic rebound >400 copies/ml thereafter. We calculated adjusted hazard ratios using marginal structural Cox proportional hazards models and weighted lifetable analysis to calculate adjusted five-year risk differences. The weighted hazard ratio for the effect of pregnancy on time to virologic failure was 1.34 (95% confidence limit [CL] 1.02, 1.78). Sensitivity analyses generally confirmed these main results. CONCLUSIONS: Incident pregnancy after HAART initiation was associated with modest increases in both relative and absolute risks of virologic failure, although uncontrolled confounding cannot be ruled out. Nonetheless, these results reinforce that family planning is an essential part of care for HIV-positive women in sub-Saharan Africa. More work is needed to confirm these findings and to explore specific etiologic pathways by which such effects may operate. Public Library of Science 2011-08-02 /pmc/articles/PMC3149058/ /pubmed/21829650 http://dx.doi.org/10.1371/journal.pone.0022778 Text en Westreich et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Westreich, Daniel
Cole, Stephen R.
Nagar, Shashi
Maskew, Mhairi
van der Horst, Charles
Sanne, Ian
Pregnancy and Virologic Response to Antiretroviral Therapy in South Africa
title Pregnancy and Virologic Response to Antiretroviral Therapy in South Africa
title_full Pregnancy and Virologic Response to Antiretroviral Therapy in South Africa
title_fullStr Pregnancy and Virologic Response to Antiretroviral Therapy in South Africa
title_full_unstemmed Pregnancy and Virologic Response to Antiretroviral Therapy in South Africa
title_short Pregnancy and Virologic Response to Antiretroviral Therapy in South Africa
title_sort pregnancy and virologic response to antiretroviral therapy in south africa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149058/
https://www.ncbi.nlm.nih.gov/pubmed/21829650
http://dx.doi.org/10.1371/journal.pone.0022778
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