Pregnancy, Pediatrics and HIV Infection:  Guidelines for Your Practice

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Short-Course Therapy

 

Short-course therapy may be provided to women in labor whose HIV status is unknown. Wade et al reported the highest transmission rate in women who did not use ZDV (26.6%).7   Short course AZT either intrapartum and in the neonate or only to the neonate was associated with decreased transmission when compared with no treatment at all, 10% and 9.3% respectively. The study concluded that short-course therapy markedly decreased perinatal HIV transmission, whether therapy was started intrapartum or within the first 48 hours.

Wade NA, Birkhead GS, Warren BL, et al. Abbreviated regimens of zidovudine prophylaxis and
perinatal transmission of the human immunodeficiency virus. N Engl J Med. 1998. 339:1409-1414.
Three international studies have shown the efficacy and safety of short course antiretroviral therapy as an alternative to the PACTG 076 regimen. A study conducted in Thailand in 1999 showed a 50% reduction in perinatal HIV transmission when 300 mg bid of ZDV was taken from 36 weeks gestation and every 3 hours during labor.8 Results of the PETRA trial revealed a 38% reduction in perinatal HIV transmission when antiretroviral therapy was provided from 36 weeks gestation.9 In Uganda, Guay et al found a 50% reduction in transmission when nevirapine was administered to women during labor and to infants 48 to 72 hours after birth.

Short-Course Regimens Reduce Perinatal HIV Transmission

Shaffer et al8: 50% reduction in transmission

  • ZDV 300 mg bid from 36 weeks gestation

  • 300 mg q3h during labor

PETRA Trial Study Team9: 38% reduction in transmission

  • Combivir (AZT & 3TC) 300 mg bid from 36 weeks gestation and during childbirth and 1 week postpartum

  • Combivir provided to the neonate for first week of life

Guay et al10: 50% reduction in transmission

  • 200mg oral neviripine to the woman during labor

  • 2mg/kg dose of oral neviripine to the neonate 48-72 hours after birth

 

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