Zash Rebecca, Souda Sajini, Chen Jennifer Y, Binda Kelebogile, Dryden-Peterson Scott, Lockman Shahin, Mmalane Mompati, Makhema Joseph, Essex Max, Shapiro Roger
*Beth Israel Deaconess Medical Center, Boston, MA; †Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana; ‡Harvard School of Public Health, Boston, MA; §Faculty of Health Sciences, University of Botswana, Gaborone, Botswana; ‖Massachusetts General Hospital, Boston, MA; and ¶Brigham and Women's Hospital, Boston, MA.
J Acquir Immune Defic Syndr. 2016 Apr 1;71(4):428-36. doi: 10.1097/QAI.0000000000000847.
Before introduction of tenofovir/emtricitabine/efavirenz (TDF/FTC/EFV), 3-drug antiretroviral therapy (ART) was associated with increased adverse birth outcomes when used for prevention of mother-to-child HIV transmission (PMTCT) in Botswana.
We extracted obstetric records from all women at the 2 largest maternities in Botswana from 2009-2011 when Botswana National Guidelines recommended zidovudine (ZDV) from 28 weeks gestational age (GA) for CD4 ≥350 and ART for CD4 <350, and again in 2013-2014 after implementation of TDF/FTC/EFV for prevention of mother-to-child HIV transmission regardless of CD4 or GA. We compared the use of TDF/FTC/EFV in pregnancy with other 3-drug ART regimens, and with initiation of ZDV, among women with similar CD4 cell counts. Outcomes included small for gestational age (SGA), preterm delivery (PTD) (<37 weeks GA), and stillbirths (SB).
Among 9445 HIV-infected women delivering during the study period, 170 were on TDF/FTC/EFV at conception and 1468 initiated TDF/FTC/EFV during pregnancy. Adverse birth outcomes were high overall (3% SB, 21% PTD, and 18% SGA) and among women receiving TDF/FTC/EFV (3% SB, 22% PTD, and 12% SGA). There was no difference in PTD or SB among women initiating TDF/FTC/EFV compared with ZDV or other 3-drug ART, but initiating TDF/FTC/EFV was associated with fewer SGA infants than other 3-drug ART (adjusted odds ratio: 0.4, 95% confidence interval: 0.2 to 0.7).
Adverse birth outcomes remain high among HIV-infected women. TDF/FTC/EFV was at least as safe as other ART and associated with fewer SGA infants when initiated during pregnancy. Larger studies are needed to evaluate birth outcomes and congenital abnormalities among women on TDF/FTC/EFV at conception.
在替诺福韦/恩曲他滨/依非韦伦(TDF/FTC/EFV)引入之前,在博茨瓦纳用于预防母婴HIV传播(PMTCT)的三联抗逆转录病毒疗法(ART)与不良出生结局增加相关。
我们提取了博茨瓦纳2家最大妇产医院2009 - 2011年期间所有女性的产科记录,当时博茨瓦纳国家指南建议,对于CD4≥350的孕妇,从孕28周起使用齐多夫定(ZDV),对于CD4<350的孕妇使用ART;在2013 - 2014年,无论CD4或孕周如何,TDF/FTC/EFV用于预防母婴HIV传播后,再次提取产科记录。我们比较了孕期使用TDF/FTC/EFV与其他三联ART方案以及与开始使用ZDV的情况,这些孕妇的CD4细胞计数相似。结局包括小于胎龄儿(SGA)、早产(PTD,孕周<37周)和死产(SB)。
在研究期间分娩的9445名HIV感染女性中,170名在受孕时使用TDF/FTC/EFV,1468名在孕期开始使用TDF/FTC/EFV。总体不良出生结局较高(3%死产、21%早产和18%小于胎龄儿),在接受TDF/FTC/EFV的女性中也是如此(3%死产、22%早产和12%小于胎龄儿)。与开始使用ZDV或其他三联ART的女性相比,开始使用TDF/FTC/EFV的女性早产或死产情况没有差异,但与其他三联ART相比,开始使用TDF/FTC/EFV的女性小于胎龄儿较少(调整后的优势比:0.4,95%置信区间:0.2至0.7)。
HIV感染女性的不良出生结局仍然很高。TDF/FTC/EFV至少与其他ART一样安全,并且在孕期开始使用时与较少的小于胎龄儿相关。需要进行更大规模的研究来评估受孕时使用TDF/FTC/EFV的女性的出生结局和先天性异常情况。