妊娠期选择性血清素再摄取抑制剂治疗和延迟新生儿适应:一项基于人群的队列研究

Marie-Coralie Cornet, Yvonne W Wu, Heather Forquer, Lyndsay A Avalos, Achyuth Sriram, Aaron W Scheffler, Thomas B Newman, Michael W Kuzniewicz
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摘要

目的:选择性血清素再摄取抑制剂(SSRI)在妊娠期的应用较为普遍。它与新生儿适应延迟有关。大多数先前的研究没有调整产妇精神健康障碍的严重程度,也没有检查SSRI类型和剂量的影响。我们研究了妊娠后期(20周后)使用SSRIs治疗是否与新生儿适应延迟相关,而不受母亲抑郁和焦虑的影响。设计、环境和患者2011-2019年在北加州15家Kaiser Permanente医院出生的28090名足月婴儿的回顾性人群出生队列。从电子病历中获取个人层面的药房、孕产妇、妊娠和新生儿数据。妊娠20周后配发母亲SSRI处方。新生儿延迟适应定义为5分钟Apgar评分≤5,出生时复苏或进入新生儿重症监护病房接受呼吸支持。次要结局包括主要结局的每个单独组成部分和更严重的新生儿结局(肺动脉高压、缺氧缺血性脑病和癫痫发作)。结果7573例(2.7%)婴儿在妊娠后期暴露于SSRIs。11.2%的暴露婴儿和4.4%的未暴露婴儿发生延迟新生儿适应(相对危险度2.52 (95% CI 2.36 - 2.70))。多变量校正后,SSRI暴露与新生儿延迟适应之间存在关联(校正OR为2.14 (95% CI 1.96 - 2.32))。这种关联是剂量依赖性的。艾司西酞普兰和氟西汀与延迟新生儿适应的最高风险相关。结论:暴露于SSRIs的婴儿延迟适应的风险增加呈类型和剂量依赖关系,表明存在因果关系。如有合理要求,可提供资料。本研究生成的数据集存储在KPNC研究部。在向通讯作者提出合理要求并获得KPNC机构审查委员会许可的情况下,可以提供已识别的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maternal treatment with selective serotonin reuptake inhibitors during pregnancy and delayed neonatal adaptation: a population-based cohort study
Objective Selective serotonin reuptake inhibitor (SSRI) use is common in pregnancy. It is associated with delayed neonatal adaptation. Most previous studies have not adjusted for the severity of maternal mental health disorders or examined the impact of SSRI type and dosage. We examined whether treatment with SSRIs in late pregnancy (after 20 weeks) is associated with delayed neonatal adaptation independent of maternal depression and anxiety. Design, setting and patients Retrospective population-based birth cohort of 280 090 term infants born at 15 Kaiser Permanente Northern California hospitals, 2011–2019. Individual-level pharmacy, maternal, pregnancy and neonatal data were obtained from electronic medical records. Exposure Dispensed maternal SSRI prescription after 20 weeks of pregnancy. Main outcome measures Delayed neonatal adaptation defined as a 5 min Apgar score ≤5, resuscitation at birth or admission to a neonatal intensive care unit for respiratory support. Secondary outcomes included each individual component of the primary outcome and more severe neonatal outcomes (pulmonary hypertension, hypoxic-ischaemic encephalopathy and seizures). Results 7573 (2.7%) infants were exposed to SSRIs in late pregnancy. Delayed neonatal adaptation occurred in 11.2% of exposed vs 4.4% of unexposed infants (relative risk 2.52 (95% CI 2.36 to 2.70)). After multivariable adjustment, there was an association between SSRI exposure and delayed neonatal adaptation (adjusted OR 2.14 (95% CI 1.96 to 2.32)). This association was dose dependent. Escitalopram and fluoxetine were associated with the highest risk of delayed neonatal adaptation. Conclusions Infants exposed to SSRIs have increased risks of delayed adaptation in a type and dose-dependent relationship, pointing toward a causal relationship. Data are available upon reasonable request. The datasets generated for this study are stored at the KPNC Division of Research. Deidentified data can be provided upon reasonable request to the corresponding author, and with permission from the KPNC Institutional Review Board.
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