aDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of North Carolina School of Medicine, Chapel Hill, North Carolina bHarvard T.H. Chan School of Public Health, Center for Biostatistics in AIDS Research, Boston, Massachusetts, USA cCentre for AIDS Research in South Africa and Department of Obstetrics and Gynecology, School of Clinical Medicine, University of KwaZulu Natal, Durban, South Africa dByramiee Jeejeebhoy Government Medical College, Pune, India eMakerere University, Kampala, Uganda fWits Reproductive Health and HIV Institute, University of the Witwatersrand, Johannesburg, South Africa gDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland hDivision of Global Women's Health, Department of Obstetrics and Gynecology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
AIDS. 2019 Dec 1;33(15):2403-2413. doi: 10.1097/QAD.0000000000002367.
To evaluate the association between HIV antiretroviral therapy (ART) and preterm birth (PTB), when defined by gold standard antenatal ultrasound versus newborn exam.
A secondary analysis of the PROMISE 1077BF/1077FF randomized controlled trial, which compared antiretroviral strategies to reduce perinatal HIV transmission and improve maternal health. The trial used newborn exam (i.e. New Ballard Score, NBS) to assess gestational age. This analysis included liveborn singleton pregnancies with both newborn exam and ultrasound data. The primary exposure was the trial's antiretroviral strategies: zidovudine with intrapartum nevirapine ('ZDV alone'); zidovudine/lamivudine/lopinavir-ritonavir ('ZDV-based ART'); or tenofovir/emtricitabine/lopinavir-ritonavir ('TDF-based ART'). The primary outcome was PTB less than 37 and less than 34 weeks based on the gold standard of ultrasound dating. We evaluated the association between antiretroviral strategy and PTB. We fit multivariable logistic regression models, adjusting for maternal characteristics, obstetric history, and HIV disease severity.
Among 720 assessed pregnant women, PTB less than 37 weeks was 15.4% by NBS and 18.3% by ultrasound. The NBS was specific but not sensitive for PTB less than 37 weeks (92.0% and 48.5%). Women receiving ZDV-based and TDF-based ART had significantly higher odds of PTB less than 37 by ultrasound compared with ZDV alone (adjusted odds ratios: 1.68; 95% confidence interval 1.10-2.57, and 2.71; 95% confidence interval 1.39-5.29), as well as for PTB less than 34 weeks. These results held for ultrasounds performed less than 24 weeks, and were generally consistent with prior analyses from the PROMISE trial using the NBS.
Women starting HIV ART in pregnancy remained at higher risk of PTB when determined by ultrasound, consistent with prior data using newborn exam. However, newborn exam misclassified cases of PTB compared with gold standard ultrasound.
通过金标准产前超声与新生儿检查评估人类免疫缺陷病毒(HIV)抗逆转录病毒治疗(ART)与早产(PTB)之间的关系,当以此两种方法定义 PTB 时。
这是 PROMISE 1077BF/1077FF 随机对照试验的二次分析,该试验比较了抗逆转录病毒策略,以减少围产期 HIV 传播并改善产妇健康。该试验使用新生儿检查(即新生儿巴氏量表,NBS)来评估胎龄。本分析包括具有新生儿检查和超声数据的活产单胎妊娠。主要暴露因素是试验的抗逆转录病毒策略:齐多夫定联合分娩时奈韦拉平(“ZDV 单药”);齐多夫定/拉米夫定/洛匹那韦-利托那韦(“ZDV 为基础的 ART”);或替诺福韦/恩曲他滨/洛匹那韦-利托那韦(“TDF 为基础的 ART”)。主要结局是根据超声日期,PTB 小于 37 周和小于 34 周。我们评估了抗逆转录病毒策略与 PTB 之间的关系。我们拟合了多变量逻辑回归模型,调整了产妇特征、产科病史和 HIV 疾病严重程度。
在 720 名评估的孕妇中,NBS 测定的小于 37 周的 PTB 发生率为 15.4%,超声检查的发生率为 18.3%。NBS 测定 PTB 小于 37 周的特异性高,但敏感性低(92.0%和 48.5%)。与 ZDV 单药相比,接受 ZDV 为基础和 TDF 为基础的 ART 的女性发生超声检查小于 37 周的 PTB 的可能性明显更高(校正比值比:1.68;95%置信区间 1.10-2.57,和 2.71;95%置信区间 1.39-5.29),以及小于 34 周的 PTB。这些结果适用于在小于 24 周进行的超声检查,并且与使用新生儿检查的 PROMISE 试验的先前分析基本一致。
与使用新生儿检查相比,开始在妊娠期间接受 HIV ART 的女性的 PTB 风险仍较高,这与先前的数据一致。然而,与金标准超声相比,新生儿检查会错误分类 PTB 病例。