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母亲接受短程治疗后,HIV-1 感染的早产儿中拉替拉韦经胎盘转运的一个月药代动力学。

One-month transplacental pharmacokinetics of raltegravir in a premature newborn after short-course treatment of the HIV-1-infected mother.

机构信息

Infectious Diseases Unit, L.C. Fleming Hospital, Saint Martin, French West Indies.

出版信息

Antimicrob Agents Chemother. 2013 Dec;57(12):6393-4. doi: 10.1128/AAC.01349-13. Epub 2013 Sep 30.

DOI:10.1128/AAC.01349-13
PMID:24080650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3837897/
Abstract

We describe the pharmacokinetics of raltegravir of a preterm newborn after short-course treatment of the mother tested HIV + the day of delivery. At age 1 month, the circulating concentration of raltegravir in the newborn was 29 ng/ml (the IC95 of RAL against HIV-1 is 15 ng/ml). Raltegravir should therefore be considered a potential transplacental postexposure prophylaxis for HIV-1 and an alternative to the use of boosted lopinavir in this context.

摘要

我们描述了一例 HIV 阳性母亲于分娩当天接受短程治疗后,其早产儿的拉替拉韦药代动力学。1 月龄时,新生儿循环中的拉替拉韦浓度为 29ng/ml(拉替拉韦抗 HIV-1 的 IC95 为 15ng/ml)。因此,拉替拉韦应被视为 HIV-1 潜在的胎盘暴露后预防药物,可替代该背景下使用洛匹那韦利托那韦。

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Association of prenatal and postnatal exposure to lopinavir-ritonavir and adrenal dysfunction among uninfected infants of HIV-infected mothers.母亲感染 HIV 的未感染婴儿中,产前和产后暴露于洛匹那韦利托那韦与肾上腺功能障碍的相关性。
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