Publication:
A trial of shortened zidovudine regimens to prevent mother-to-child transmission of human immunodeficiency virus type 1

dc.contributor.authorMarc Lallemanten_US
dc.contributor.authorGonzague Jourdainen_US
dc.contributor.authorSophie Le Coeuren_US
dc.contributor.authorKim Soyeonen_US
dc.contributor.authorSporn Koetsawangen_US
dc.contributor.authorAnne Marie Comeauen_US
dc.contributor.authorWiput Phoolcharoenen_US
dc.contributor.authorMax Essexen_US
dc.contributor.authorKenneth McIntoshen_US
dc.contributor.authorVicharn Vithayasaien_US
dc.contributor.otherIRD Institut de Recherche pour le Developpementen_US
dc.contributor.otherHarvard School of Public Healthen_US
dc.contributor.otherINED Institut National d' Etudes Demographiquesen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of Massachusetts Medical Schoolen_US
dc.contributor.otherThailand Ministry of Public Healthen_US
dc.contributor.otherChildren's Hospital Bostonen_US
dc.contributor.otherChiang Mai Universityen_US
dc.contributor.otherPHPTen_US
dc.date.accessioned2018-09-07T09:17:44Z
dc.date.available2018-09-07T09:17:44Z
dc.date.issued2000-10-05en_US
dc.description.abstractBackground: The optimal duration of zidovudine administration to prevent perinatal transmission of human immunodeficiency virus type 1 (HIV-1) should be determined to facilitate its use in areas where resources are limited. Methods: We conducted a randomized, double-blind equivalence trial of four regimens of zidovudine starting in the mother at 28 weeks' gestation, with 6 weeks of treatment in the infant (the long-long regimen), which is similar to protocol 076; zidovudine starting at 35 weeks' gestation, with 3 days of treatment in the infant (the short-short regimen); a long-short regimen; and a short-long regimen. The mothers received zidovudine orally during labor. The infants were fed formula and were tested for HIV DNA at 1, 45, 120, and 180 days. After the first interim analysis, the short-short regimen was stopped. Results: A total of 1437 women were enrolled. At the first interim analysis, the rates of HIV transmission were 4.1 percent for the long-long regimen and 10.5 percent for the short-short regimen (P=0.004); at this point the short-short regimen was stopped. For the entire study period, the transmission rates were 6.5 percent (95 percent confidence interval, 4.1 to 8.9 percent) for the long-long regimen, 4.7 percent (95 percent confidence interval, 2.4 to 7.0 percent) for the long-short regimen, and 8.6 percent (95 percent confidence interval, 5.6 to 11.6 percent) for the short-long regimen. The rate of in utero transmission was significantly higher with the two regimens with shorter maternal treatment (5.1 percent) than with the two with longer maternal treatment (1.6 percent). Conclusions: The short-short zidovudine regimen is inferior to the long-long regimen and leads to a higher rate of perinatal HIV transmission. The long-short, short-long, and long-long regimens had equivalent efficacy. However, the higher rate of in utero transmission with the short-long regimen suggests that longer treatment of the infant cannot substitute for longer treatment of the mother. (C) 2000, Massachusetts Medical Society.en_US
dc.identifier.citationNew England Journal of Medicine. Vol.343, No.14 (2000), 982-991en_US
dc.identifier.doi10.1056/NEJM200010053431401en_US
dc.identifier.issn00284793en_US
dc.identifier.other2-s2.0-0034610026en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/26157
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0034610026&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleA trial of shortened zidovudine regimens to prevent mother-to-child transmission of human immunodeficiency virus type 1en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0034610026&origin=inwarden_US

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