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dc.contributor.authorTim R. Cresseyen_US
dc.contributor.authorAlice Steken_US
dc.contributor.authorEdmund Capparellien_US
dc.contributor.authorChureeratana Bowonwatanuwongen_US
dc.contributor.authorSinart Prommasen_US
dc.contributor.authorPannee Sirivatanapaen_US
dc.contributor.authorPrapap Yuthavisuthien_US
dc.contributor.authorChanon Neungtonen_US
dc.contributor.authorYanling Huoen_US
dc.contributor.authorElizabeth Smithen_US
dc.contributor.authorBrookie M. Besten_US
dc.contributor.authorMark Mirochnicken_US
dc.date.accessioned2018-09-04T06:11:58Z-
dc.date.available2018-09-04T06:11:58Z-
dc.date.issued2012-03-01en_US
dc.identifier.issn10779450en_US
dc.identifier.issn15254135en_US
dc.identifier.other2-s2.0-84859758788en_US
dc.identifier.other10.1097/QAI.0b013e31823ff052en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84859758788&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/51935-
dc.description.abstractBackground: The impact of pregnancy on efavirenz (EFV) pharmacokinetics is unknown. Methods: International Maternal Pediatric Adolescent AIDS Clinical Trials P1026s is an on-going, prospective, nonblinded study of antiretroviral pharmacokinetics in HIV-infected pregnant women that included a cohort receiving 600 mg EFV once daily as part of combination antiretroviral therapy. Intensive steady-state 24-hour blood sampling was performed during the third trimester and at 6-12 weeks postpartum. Maternal and umbilical cord blood samples were drawn at delivery. Pharmacokinetics targets were the estimated 10th percentile EFV area under the curve (AUC) in nonpregnant historical controls (40.0 mcghr?1mL?1) and a trough concentration of 1 mcg/mL. Results: Twenty-five women were enrolled during the third trimester: median (range) age was 29.3 (18.9-42.9) years, weight 69.0 (40-130) kg, and gestational age 32.9 (30.1-38.7) weeks. Median (range) EFV AUC0-24, Cmax, and C24 hourswere 55.4 mcghr?1mL?1(13.5-220.3), 5.4 mcg/mL (1.9-12.2), and 1.6 mcg/mL (0.23-8.13), respectively. EFV AUC and Cmax did not differ during pregnancy and postpartum but C24 hourswas lower during the third trimester (1.6 vs. 2.1 mcg/mL, P = 0.01). During the third trimester, 5 of 25 (20%) women had an EFV AUC below the target and 3 of 25 (12%) had a trough concentration below 1 mcg/mL. EFV cord blood/maternal concentration ratio was 0.49 (0.37-0.74). All women had a HIV-1 RNA viral load less than 400 copies per milliliter at delivery and 19 (76%) had a viral load below 50 copies per milliliter. One child was perinatally HIV infected. Three women were exposed to EFV throughout the first 6 weeks of pregnancy. EFV was well tolerated, and among the 25 infants, no congenital anomalies or newborn complications were reported. Conclusions: Changes in EFV pharmacokinetics during pregnancy compared with postpartum are not sufficiently large enough to warrant a dose adjustment during pregnancy. Copyright © 2012 by Lippincott Williams & Wilkins.en_US
dc.subjectMedicineen_US
dc.titleEfavirenz pharmacokinetics during the third trimester of pregnancy and postpartumen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Acquired Immune Deficiency Syndromesen_US
article.volume59en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsHarvard School of Public Healthen_US
article.stream.affiliationsIRD Institut de Recherche pour le Developpementen_US
article.stream.affiliationsKeck School of Medicine of USCen_US
article.stream.affiliationsUniversity of California, San Diegoen_US
article.stream.affiliationsChonburi Regional Hospitalen_US
article.stream.affiliationsBhumibol Adulyadej Hospitalen_US
article.stream.affiliationsPrapokklao Hospitalen_US
article.stream.affiliationsFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
article.stream.affiliationsNational Institute of Allergy and Infectious Diseasesen_US
article.stream.affiliationsBoston University School of Medicineen_US
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