Literature DB >> 15764963

Improved obstetric outcomes and few maternal toxicities are associated with antiretroviral therapy, including highly active antiretroviral therapy during pregnancy.

Ruth E Tuomala1, D Heather Watts, Daner Li, Mark Vajaranant, Jane Pitt, Hunter Hammill, Sheldon Landesman, Carmen Zorrilla, Bruce Thompson.   

Abstract

Data from 2543 HIV-infected women were analyzed to correlate antiretroviral therapy (ART) used during pregnancy with maternal and pregnancy outcomes. ART was analyzed according to class of agents used and according to monotherapy versus combination ART containing neither protease inhibitors (PIs) nor nonnucleoside reverse transcriptase inhibitors versus highly active ART. Timing of ART was classified according to early (recorded at or before 25-week gestation study visit) and late (recorded at 32-week gestation or delivery visit) use. Maternal outcomes assessed included hematologic, gastrointestinal, neurologic, renal, and dermatologic complications; gestational diabetes; lactic acidosis; and death. Adverse pregnancy outcomes assessed included hypertensive complications; pre-term labor or rupture of membranes; preterm delivery (PTD); low birth weight; and stillbirth. Logistic regression analyses controlling for multiple covariates revealed ART to be independently associated with few maternal complications: ART use was associated with anemia (odds ratio [OR] = 1.6, 95% confidence interval [CI]: 1.1-2.4), and late use of ART was associated with gestational diabetes (OR = 3.5, 95% CI: 1.2-10.1). Logistic regression analyses revealed an increase in PTD at <37 weeks for 10 women with late use of ART not containing zidovudine (ZDV; OR = 7.9, 95% CI: 1.4-44.6) and a decrease in adverse pregnancy outcomes as follows: late use of ART containing ZDV was associated with decreased risk for stillbirth and PTD at <37 weeks (OR = 0.06, 95% CI: 0.02-0.18; OR = 0.5, 95% CI: 0.3-0.8, respectively), and ART containing nucleoside reverse transcriptase inhibitors but not ZDV during early and late pregnancy was associated with decreased risk for PTD at <32 weeks (OR = 0.3, 95% CI: 0.2-0.7). Benefits of ART continue to outweigh observed risks.

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Year:  2005        PMID: 15764963     DOI: 10.1097/01.qai.0000139398.38236.4d

Source DB:  PubMed          Journal:  J Acquir Immune Defic Syndr        ISSN: 1525-4135            Impact factor:   3.731


  46 in total

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3.  Ten years of experience in the prevention of mother-to-child human immunodeficiency virus transmission in a university teaching hospital.

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4.  Highly active antiretroviral therapy and adverse birth outcomes among HIV-infected women in Botswana.

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5.  Pregnancy outcome in women infected with HIV-1 receiving combination antiretroviral therapy before versus after conception.

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Review 6.  Global report on preterm birth and stillbirth (3 of 7): evidence for effectiveness of interventions.

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Review 7.  Antiretroviral medications during pregnancy for therapy or prophylaxis.

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8.  Increased risk of hepatotoxicity in HIV-infected pregnant women receiving antiretroviral therapy independent of nevirapine exposure.

Authors:  David W Ouyang; David E Shapiro; Ming Lu; Susan B Brogly; Audrey L French; Robert M Leighty; Bruce Thompson; Ruth E Tuomala; Ronald C Hershow
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9.  Lack of increased hepatotoxicity in HIV-infected pregnant women receiving nevirapine compared with other antiretrovirals.

Authors:  David W Ouyang; Susan B Brogly; Ming Lu; David E Shapiro; Ronald C Hershow; Audrey L French; Robert M Leighty; Bruce Thompson; Ruth E Tuomala
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10.  Treatment interruption after pregnancy: effects on disease progression and laboratory findings.

Authors:  D H Watts; M Lu; B Thompson; R E Tuomala; W A Meyer; H Mendez; K Rich; C Hanson; P LaRussa; C Diaz; L M Mofenson
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