Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Center for Biostatistics in AIDS Research, Harvard TH Chan School of Public Health, Boston, Massachusetts, USA.
Clin Infect Dis. 2024 Mar 20;78(3):667-673. doi: 10.1093/cid/ciad583.
Isoniazid preventive therapy (IPT) is recommended for tuberculosis prevention yet data on the safety of first-trimester pregnancy exposure are limited.
Planned secondary analysis in a TB prevention trial of adverse pregnancy outcomes among participants assigned to 9-month IPT who became pregnant during (IPT-exposed) or after (unexposed) IPT. Regression models compared binary outcomes of a composite adverse outcome (any non-live birth, excluding induced abortion); preterm delivery <37 weeks; and low birth weight <2500 g) among exposure groups. Models were adjusted for latent TB infection, maternal age, CD4 count, and antiretroviral therapy (ART).
In total, 128 participants had a known pregnancy outcome; 39 IPT-exposed and 89 unexposed. At pregnancy outcome, ART use was lower in IPT-exposed (79%) than unexposed women (98%). Overall, 29 pregnancies ended in a composite adverse outcome (25 spontaneous abortions, 2 stillbirths and 2 ectopic pregnancies), 15 preterm deliveries, and 10 infants with low birth weight. IPT was associated with the composite adverse outcome adjusting for covariates at enrollment (adjusted relative risk [aRR] 1.98; 95% confidence interval [CI] 1.15, 3.41), but the effect was attenuated when adjusted for covariates at pregnancy outcome (aRR 1.47; 95% CI .84, 2.55); IPT was not associated with preterm delivery (relative risk [RR] 0.87; 95% CI .32-2.42) or low birth weight (RR 1.01; 95% CI .29, 3.56).
First-trimester IPT exposure was associated with nearly two-fold increased risk of fetal demise, mostly spontaneous abortion, though the association was attenuated when adjusted for covariates proximal to pregnancy outcome including ART use. Further study is needed to inform TB prevention guidelines.
异烟肼预防治疗(IPT)被推荐用于结核病预防,但关于其在妊娠早期暴露的安全性的数据有限。
在一项结核病预防试验中,对接受 9 个月 IPT 并在 IPT 期间(IPT 暴露组)或之后(未暴露组)怀孕的参与者的不良妊娠结局进行了计划的二次分析。回归模型比较了复合不良结局(任何非活产,不包括人工流产)、早产 <37 周和低出生体重 <2500g)在暴露组之间的发生率。模型调整了潜伏性结核感染、产妇年龄、CD4 计数和抗逆转录病毒治疗(ART)。
共有 128 名参与者有明确的妊娠结局;39 名 IPT 暴露和 89 名未暴露。在妊娠结局时,IPT 暴露组(79%)使用 ART 的比例低于未暴露组(98%)。总体而言,29 例妊娠结局为复合不良结局(25 例自然流产、2 例死胎和 2 例异位妊娠)、15 例早产和 10 例低出生体重儿。在调整了入组时的协变量后,IPT 与复合不良结局相关(调整后的相对风险 [aRR] 1.98;95%置信区间 [CI] 1.15,3.41),但在调整了妊娠结局时的协变量后,这种相关性减弱(aRR 1.47;95% CI.84,2.55);IPT 与早产(RR 0.87;95% CI.32,2.42)或低出生体重(RR 1.01;95% CI.29,3.56)无关。
妊娠早期 IPT 暴露与胎儿死亡风险增加近两倍相关,主要是自然流产,但当调整与妊娠结局接近的协变量时,包括 ART 使用,这种相关性减弱。需要进一步研究为结核病预防指南提供信息。