Your browser doesn't support javascript.
loading
Is intrapartum intravenous zidovudine for prevention of mother-to-child HIV-1 transmission still useful in the combination antiretroviral therapy era?
Briand, Nelly; Warszawski, Josiane; Mandelbrot, Laurent; Dollfus, Catherine; Pannier, Emmanuelle; Cravello, Ludovic; Nguyen, Rose; Matheron, Isabelle; Winer, Norbert; Tubiana, Roland; Rouzioux, Christine; Faye, Albert; Blanche, Stéphane.
Afiliação
  • Briand N; INSERM U1018, Centre for Research in Epidemiology and Population Health, Université Paris-Sud, Paris, France. nelly.briand@inserm.fr
Clin Infect Dis ; 57(6): 903-14, 2013 Sep.
Article em En | MEDLINE | ID: mdl-23728147
ABSTRACT

BACKGROUND:

Intrapartum intravenous zidovudine (ZDV) prophylaxis is a long-standing component of prevention of mother-to-child transmission (MTCT) of human immunodeficiency virus (HIV) in high-resource countries. In some recent guidelines, intravenous ZDV is no longer systematically recommended for mothers receiving combination antiretroviral therapy (cART) with low viral load. We evaluated the impact of intravenous ZDV according to viral load and obstetrical conditions.

METHODS:

All HIV-1-infected women delivering between 1 January 1997 and 31 December 2010 in the French Perinatal Cohort (ANRS-EPF) were analyzed if they received ART during pregnancy and did not breastfeed. We identified maternal and obstetrical characteristics related to lack of intravenous ZDV and compared its association with MTCT rate and other infant parameters, according to various risk factors.

RESULTS:

Intravenous ZDV was used in 95.2% of the 11 538 deliveries. Older age, multiparity, and preterm and vaginal delivery were associated with lack of intravenous ZDV (n = 554). In women who delivered with viral load ≥1000 copies/mL, the overall MTCT rate was higher without than with intravenous ZDV (7.5% vs 2.9%; P = .01); however, there was no such difference when the neonate received postnatal intensification therapy. Among them, 77% of women who had viral load <400 copies/mL, there was no difference in MTCT rate (0% without intravenous ZDV vs 0.6% with intravenous ZDV; P = .17). Intravenous ZDV was not associated with increased short-term hematological toxicity or lactate level.

CONCLUSIONS:

Intravenous ZDV remains an effective tool to reduce transmission in cases of virological failure, even in cART-treated women. However, for the vast majority of women with low viral loads at delivery, in the absence of obstetrical risk factors, systematic intravenous ZDV appears to be unnecessary.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Complicações Infecciosas na Gravidez / Zidovudina / Infecções por HIV / Transmissão Vertical de Doenças Infecciosas / Fármacos Anti-HIV Tipo de estudo: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Newborn / Pregnancy Idioma: En Revista: Clin Infect Dis Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Complicações Infecciosas na Gravidez / Zidovudina / Infecções por HIV / Transmissão Vertical de Doenças Infecciosas / Fármacos Anti-HIV Tipo de estudo: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Newborn / Pregnancy Idioma: En Revista: Clin Infect Dis Ano de publicação: 2013 Tipo de documento: Article