Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/68473
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dc.contributor.authorAhizechukwu C. Ekeen_US
dc.contributor.authorJiajia Wangen_US
dc.contributor.authorKhadija Aminen_US
dc.contributor.authorDavid E. Shapiroen_US
dc.contributor.authorAlice Steken_US
dc.contributor.authorElizabeth Smithen_US
dc.contributor.authorNahida Chakhtouraen_US
dc.contributor.authorMichael Basaren_US
dc.contributor.authorKathleen Georgeen_US
dc.contributor.authorKatherine M. Knappen_US
dc.contributor.authorEsaú C. Joãoen_US
dc.contributor.authorKittipong Rungruengthanakiten_US
dc.contributor.authorEdmund Capparellien_US
dc.contributor.authorSandra Burchetten_US
dc.contributor.authorMark Mirochnicken_US
dc.contributor.authorBrookie M. Besten_US
dc.date.accessioned2020-04-02T15:28:06Z-
dc.date.available2020-04-02T15:28:06Z-
dc.date.issued2020-03-24en_US
dc.identifier.issn10986596en_US
dc.identifier.other2-s2.0-85082393761en_US
dc.identifier.other10.1128/AAC.02260-19en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85082393761&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/68473-
dc.description.abstractCopyright © 2020 American Society for Microbiology. The purpose of this study was to evaluate the pharmacokinetics of ritonavir-boosted fosamprenavir during pregnancy and postpartum. Amprenavir (the active moiety of fosamprenavir) and ritonavir intensive pharmacokinetic evaluations were performed at steady state during the second and third trimesters of pregnancy and postpartum. Plasma concentrations of amprenavir and ritonavir were measured using high-performance liquid chromatography. The target amprenavir area under the concentration-versus-time curve (AUC) was higher than the 10th percentile (27.7 μg · h/ml) of the median area under the curve for ritonavir-boosted fosamprenavir in adults receiving twice-daily fosamprenavir-ritonavir at 700 mg/100 mg. Twenty-nine women were included in the analysis. The amprenavir AUC from time zero to 12 h (AUC0-12) was lower (geometric mean ratio [GMR], 0.60 [confidence interval {CI}, 0.49 to 0.72] [P < 0.001]) while its apparent oral clearance was higher (GMR, 1.68 [CI, 1.38 to 2.03] [P < 0.001]) in the third trimester than postpartum. Similarly, the ritonavir AUC0-12 was lower in the second (GMR, 0.51 [CI, 0.28 to 0.91] [P = 0.09]) and third (GMR, 0.72 [CI, 0.55 to 0.95] [P = 0.005]) trimesters than postpartum, while its apparent oral clearance was higher in the second (GMR, 1.98 [CI, 1.10 to 3.56] [P = 0.06]) and third (GMR, 1.38 [CI, 1.05 to 1.82] [P = 0.009]) trimesters than postpartum. The amprenavir area under the curve exceeded the target for 6/8 (75%) women in the 2nd trimester, 18/28 (64%) in the 3rd trimester, and 19/22 (86.4%) postpartum, and the trough concentrations (Cmin) of amprenavir were 4- to 16-fold above the mean amprenavir-protein-adjusted 50% inhibitory concentration (IC50) of 0.146 μg/ml. Although amprenavir plasma concentrations in women receiving ritonavir-boosted fosamprenavir were lower during pregnancy than postpartum, the reduced amprenavir concentrations were still above the exposures needed for viral suppression.en_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleFosamprenavir with Ritonavir Pharmacokinetics during Pregnancyen_US
dc.typeJournalen_US
article.title.sourcetitleAntimicrobial agents and chemotherapyen_US
article.volume64en_US
article.stream.affiliationsSkaggs School of Pharmacy &amp; Pharmaceutical Sciencesen_US
article.stream.affiliationsFHI 360en_US
article.stream.affiliationsFrontier Science &amp; Technology Research Foundation, Inc.en_US
article.stream.affiliationsUniversity of California, San Diegoen_US
article.stream.affiliationsChildren's Hospital Bostonen_US
article.stream.affiliationsHospital dos Servidores do Estadoen_US
article.stream.affiliationsSt. Jude Children's Research Hospitalen_US
article.stream.affiliationsNational Institute of Child Health and Human Developmenten_US
article.stream.affiliationsNational Institute of Allergy and Infectious Diseasesen_US
article.stream.affiliationsKeck School of Medicine of USCen_US
article.stream.affiliationsBoston University School of Medicineen_US
article.stream.affiliationsJohns Hopkins Bloomberg School of Public Healthen_US
article.stream.affiliationsCenter for Biostatistics in AIDS Researchen_US
article.stream.affiliationsJohns Hopkins School of Medicineen_US
article.stream.affiliationsChiang Mai Universityen_US
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