Department of Obstetrics and Gynecology, Medical University of South Carolina, Charleston, SC; and.
Department of Medicine, Medical University of South Carolina, Charleston, SC.
J Acquir Immune Defic Syndr. 2022 Apr 1;89(4):448-453. doi: 10.1097/QAI.0000000000002882.
We sought to determine whether pregnant women with HIV prescribed integrase strand transfer inhibitor (INSTI) were more likely to have viral suppression at delivery and any increased risk of adverse infant outcomes.
This was a retrospective, statewide cohort study of women with HIV and their HIV-exposed infants who delivered in South Carolina from 2008 to 2019. Women's antenatal AVRs were classified as INSTI or non-INSTI. We compared the percentage of women with undetectable HIV RNA viral load (<40 copies/mL) at delivery between groups. We compared the percentage of HIV-exposed singleton infants who were born preterm delivery, low birth weight, and small for gestational age and had confirmed perinatal HIV infection. Categorical outcomes were compared using the χ2 test or Fischer exact test.
A total of 832 infants, including 11 sets of twins, were exposed to maternal HIV. Detailed antiretroviral regimens were available for analysis in a third of mother-infant pairs (n = 315). Half of the infants were exposed to INSTI (159) and half to non-INSTI antiretrovirals (156). Most women had an undetectable viral load at delivery (80% INSTI and 73% non-INSTI, P= 0.11). The percentage of singleton infants with adverse outcomes was similar between INSTI and non-INSTI groups: preterm delivery (21% and 16%, P = 0.3), low birth weight (19% and 21%, P = 0.7), small for gestational age (11% vs 9%, P = 0.5), and perinatal HIV infection (2.5% and 1.3%, P = 0.7).
We observed that viral suppression before delivery was similar between pregnant women prescribed INSTI and non-INSTI antiretroviral therapy. The percentage of infants with adverse outcomes was similar when exposed to INSTI and non-INSTI antiretroviral therapy.
本研究旨在确定接受整合酶抑制剂(INSTI)治疗的 HIV 感染孕妇在分娩时是否更有可能实现病毒抑制,以及是否会增加婴儿不良结局的风险。
这是一项回顾性的、全州性的队列研究,纳入了 2008 年至 2019 年在南卡罗来纳州分娩的 HIV 感染孕妇及其 HIV 暴露婴儿。将女性的产前 AVR 分为 INSTI 或非 INSTI。我们比较了两组孕妇在分娩时 HIV RNA 病毒载量(<40 拷贝/mL)不可检测的比例。我们比较了 HIV 暴露的单胎婴儿中早产儿、低出生体重儿、小于胎龄儿以及围产期 HIV 感染确诊婴儿的比例。使用 χ2 检验或 Fischer 精确检验比较分类结局。
共纳入 832 名婴儿(包括 11 对双胞胎),其中 11 对为双胎。159 名婴儿的母亲-婴儿对接受了详细的抗逆转录病毒治疗方案分析,占三分之一。一半的婴儿暴露于 INSTI(159 名),一半暴露于非 INSTI 抗逆转录病毒药物(156 名)。大多数女性在分娩时病毒载量不可检测(INSTI 组 80%,非 INSTI 组 73%,P=0.11)。INSTI 组和非 INSTI 组的不良结局婴儿比例相似:早产(21%和 16%,P=0.3)、低出生体重(19%和 21%,P=0.7)、小于胎龄儿(11%和 9%,P=0.5)和围产期 HIV 感染(2.5%和 1.3%,P=0.7)。
我们观察到,接受 INSTI 和非 INSTI 抗逆转录病毒治疗的孕妇在分娩前的病毒抑制率相似。当婴儿暴露于 INSTI 和非 INSTI 抗逆转录病毒药物时,其不良结局的比例相似。