Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Mar 21;11(3):e0150565.
doi: 10.1371/journal.pone.0150565. eCollection 2016.

Preterm Birth and Low Birth Weight after In Utero Exposure to Antiretrovirals Initiated during Pregnancy in Yaoundé, Cameroon

Affiliations

Preterm Birth and Low Birth Weight after In Utero Exposure to Antiretrovirals Initiated during Pregnancy in Yaoundé, Cameroon

Anne Esther Njom Nlend et al. PLoS One. .

Abstract

Background: Effects of antiretroviral therapy (ART) on birth outcomes remain controversial.

Objective: To assess the impact of antenatal exposure to ART on the occurrence of preterm birth (PTB) and low birth weight (LBW).

Methods: A cross-sectional study conducted at the Essos Hospital Center in Yaounde from 2008 to 2011 among HIV vertically exposed infants with two distinct maternal antiretroviral experiences: monotherapy group (Zidovudine, ZDV) and the combination ART group (cART). Mothers already receiving cART before pregnancy were ineligible. In both groups, events of PTB (<37 weeks) and LBW (<2,500g) were analyzed using univariate and multivariate logistic regression; with p<0.05 considered statistically significant.

Results: Of the 760 infants, 481 were born from cART-exposed mothers against 279 from maternal-ZDV. Median maternal CD4 count was 378 [interquartile range (IQR): 253-535] cells/mm3. Median duration of ART at onset of delivery was 13 [IQR: 10-17] weeks. In the cART-group, 64.9% (312/481) of mothers were exposed to Zidovudine/Lamuvidine/Nevirapine and only 2% (9/481) were on protease inhibitor-based regimens. Events of PTB were not significantly higher in the cART-group compared to the ZDV-group (10.2% vs. 6.4% respectively, p = 0.08), while onsets of LBW were significantly found in the cART-group compared to ZDV-group (11.6% vs. 7.2% respectively, p = 0.05). Other factors (parity, maternal age at delivery or CD4 cell count) were not associated with PTB.

Conclusion: cART, initiated during pregnancy, would be an independent factor of LBW. In the era of option B+ (lifelong ART to all HIV-pregnant women), further studies would guide towards measures limiting onsets of LBW.

PubMed Disclaimer

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Algorithm for ARV eligibility and type of PMTCT regimens at Essos Hospital Centre from 2008 to 2011, Cameroon.
Fig 2
Fig 2. Flowchart of the HIV-positive mothers enrolled in the study, 2008 to 2011, Cameroon.

References

    1. de Vincenzi I (2011) Triple antiretroviral compared with zidovudine and single-dose nevirapine prophylaxis during pregnancy and breastfeeding for prevention of mother-to-child transmission of HIV-1 (Kesho Bora study): a randomised controlled trial. Lancet Infect Dis 3: 171–80 - PubMed
    1. UNAIDS (2011) Global plan towards the elimination of new HIVinfections among children by 2015 and keeping their mothers alive Geneva: UNAIDS. - PubMed
    1. World Health Organization (2010) Antiretroviral drugs for treating pregnant women and preventing HIV infection in infants. Recommandations for a public health approach. Geneva. - PubMed
    1. Ministry of Public Health (2009) Recommandations for use of antiretroviral drugs during pregnancy Ministry of Public Health, Yaounde.
    1. Njom Nlend A E, Ekobo C Same, Bitoungui M J, Ekani B Bagfegue, Tchokoteu P, Lyeb S, et al. (2012) Early outcomes of HIV exposed children in the first district-wide programme using extended regimens for the prevention of mother-to-child transmission of HIV, in Yaounde, Cameroon. J Trop Pediatr 4: 297–302 - PubMed

Publication types

Substances