School of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Graduate Institute of Clinical Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan; School of Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan; Department of Pharmacy, National Taiwan University Hospital, Taipei, Taiwan.
Am J Obstet Gynecol. 2021 Dec;225(6):672.e1-672.e11. doi: 10.1016/j.ajog.2021.06.003. Epub 2021 Jun 8.
Evidence for the association between prenatal antidepressant use and the development of hypertensive disorders of pregnancy is inconsistent. Previous studies have reported that antidepressant use during pregnancy increases the risk for gestational hypertension and preeclampsia, but the results of these studies are potentially confounded by important methodologic limitations. Furthermore, it remains unknown whether a higher cumulative dose of antidepressant increases the risk for hypertensive disorders of pregnancy.
This study aimed to investigate the association between prenatal antidepressant use and the risk for hypertensive disorders of pregnancy and the potential effect of a higher cumulative antidepressant dose.
This retrospective cohort study used data from the Health and Welfare Database in Taiwan. Pregnant women with depression aged 18 to 49 years were enrolled as part of the study population. Prenatal antidepressant use was defined as at least 1 dispensing record of an antidepressant between the conception date and 20 weeks of gestation. Antidepressant users were further divided into groups according to the cumulative defined daily dose based on whether they took the defined daily dose for ≤10 weeks (low cumulative dose group ≤70 cumulative defined daily dose) or for >10 weeks (high cumulative dose group >70 cumulative defined daily dose). The primary outcome was hypertensive disorders of pregnancy defined as the diagnosis of either gestational hypertension or preeclampsia during the period from 20 weeks of gestation to delivery. Propensity score matching and stabilized inverse probability of treatment weighting were used to balance the confounders between the comparison groups. A robust Cox regression model was used to evaluate the association between exposure and outcome.
A total of 5664 pregnant women with depression were included in the study (2832 antidepressant users matched to 2832 antidepressant nonusers). Prenatal antidepressant use was not associated with an increased risk for hypertensive disorders of pregnancy (adjusted hazard ratio, 0.89; 95% confidence interval, 0.67-1.18). However, among antidepressant users, the risk for hypertensive disorders of pregnancy was higher among women with a higher cumulative defined daily dose than among women with a lower cumulative defined daily dose (adjusted hazard ratio, 2.46; 95% confidence interval, 1.05-5.74).
No association was found between antidepressant use and the development of hypertensive disorders of pregnancy. However, women taking higher cumulative doses of antidepressants were at greater risk. More frequent or regular monitoring of blood pressure may be warranted in women on high cumulative doses of antidepressants.
产前使用抗抑郁药与妊娠高血压疾病发展之间的关联证据不一致。先前的研究报告称,怀孕期间使用抗抑郁药会增加妊娠高血压和子痫前期的风险,但这些研究的结果可能受到重要方法学局限性的影响。此外,目前尚不清楚抗抑郁药的累积剂量是否更高会增加妊娠高血压疾病的风险。
本研究旨在调查产前使用抗抑郁药与妊娠高血压疾病风险之间的关联,以及更高累积抗抑郁药剂量的潜在影响。
本回顾性队列研究使用了来自台湾健康与福利数据库的数据。将年龄在 18 至 49 岁之间患有抑郁症的孕妇纳入研究人群。产前使用抗抑郁药的定义为至少有 1 次抗抑郁药处方记录,时间在受孕日期至妊娠 20 周之间。根据是否使用规定的日剂量≥10 周(低累积剂量组≤70 个累积规定日剂量)或>10 周(高累积剂量组>70 个累积规定日剂量),将抗抑郁药使用者进一步分为两组。主要结局是妊娠 20 周后至分娩期间诊断为妊娠高血压或子痫前期的高血压疾病。使用倾向评分匹配和稳定逆概率处理权重来平衡对照组之间的混杂因素。使用稳健 Cox 回归模型评估暴露与结局之间的关联。
共有 5664 名患有抑郁症的孕妇纳入研究(2832 名抗抑郁药使用者与 2832 名抗抑郁药未使用者相匹配)。产前使用抗抑郁药与妊娠高血压疾病的风险增加无关(调整后的危险比,0.89;95%置信区间,0.67-1.18)。然而,在抗抑郁药使用者中,与低累积规定日剂量相比,高累积规定日剂量的女性发生妊娠高血压疾病的风险更高(调整后的危险比,2.46;95%置信区间,1.05-5.74)。
未发现抗抑郁药使用与妊娠高血压疾病的发展之间存在关联。然而,服用更高累积剂量抗抑郁药的女性风险更高。对于服用高累积剂量抗抑郁药的女性,可能需要更频繁或更定期监测血压。