Tuccori Marco, Testi Arianna, Antonioli Luca, Fornai Matteo, Montagnani Sabrina, Ghisu Narcisa, Colucci Rocchina, Corona Tiberio, Blandizzi Corrado, Del Tacca Mario
Division of Pharmacology and Chemotherapy, Department of Internal Medicine, University of Pisa, Pisa, Italy.
Clin Ther. 2009 Jun;31 Pt 1:1426-53. doi: 10.1016/j.clinthera.2009.07.009.
There is ongoing debate about the safety of selective serotonin reuptake inhibitors (SSRIs) and other serotonergic/noradrenergic antidepressants when used during pregnancy.
This article reviews the available literature on the main safety concerns associated with the use of SSRIs and other serotonergic/noradrenergic antidepressants (serotonin-norepinephrine reuptake inhibitors, norepinephrine reuptake inhibitors, noradrenergic and specific serotonergic antidepressants) during pregnancy.
English-language reports of analytical and descriptive studies, including case reports, case series, and meta-analyses, were identified through searches of MEDLINE, EMBASE, and PsycINFO (1966-April 2009). The search terms were fluoxetine, paroxetine, sertraline, Citalopram, escitalopram, fluvoxamine, venlafaxine, mirtazapine, reboxetine, duloxetine, SSRI, SNRI, NaSSA, and NRI in association with depression, pregnancy, prenatal exposure, miscarriage, spontaneous abortion, malformation, in utero exposure, and neonatal complications.
Paroxetine has been associated with significant risks of major malformation, particularly cardiac defects, when used during pregnancy. Significant associations between maternal exposure to SSRIs and both persistent pulmonary hypertension of the newborn and a self-limiting neonatal behavioral syndrome have been reported in a number of recent original studies and meta-analyses. Some studies have suggested a relationship between the use of SSRIs or other serotonergic/noradrenergic antidepressants and the occurrence of miscarriage, although these studies had methodologic limitations that affected the strength of the data. Evidence for a possible association between in utero exposure to SSRIs or other serotonergic/noradrenergic antidepressants and alterations in neurobehavioral development, bleeding, and QTc-interval prolongation is currently weak.
The available evidence suggests that SSRIs and other serotonergic/noradrenergic antidepressants should be used with caution during pregnancy, with careful follow-up of infants exposed to these agents in utero.
关于孕期使用选择性5-羟色胺再摄取抑制剂(SSRI)及其他5-羟色胺能/去甲肾上腺素能抗抑郁药的安全性,一直存在争议。
本文回顾了有关孕期使用SSRI及其他5-羟色胺能/去甲肾上腺素能抗抑郁药(5-羟色胺-去甲肾上腺素再摄取抑制剂、去甲肾上腺素再摄取抑制剂、去甲肾上腺素能及特异性5-羟色胺能抗抑郁药)的主要安全性问题的现有文献。
通过检索MEDLINE、EMBASE和PsycINFO(1966年至2009年4月),找出分析性和描述性研究的英文报告,包括病例报告、病例系列和荟萃分析。检索词为氟西汀、帕罗西汀、舍曲林、西酞普兰、艾司西酞普兰、氟伏沙明、文拉法辛、米氮平、瑞波西汀、度洛西汀、SSRI、SNRI、NaSSA和NRI,以及抑郁症、妊娠、产前暴露、流产、自然流产、畸形、子宫内暴露和新生儿并发症。
孕期使用帕罗西汀与重大畸形尤其是心脏缺陷的显著风险相关。近期一些原创研究和荟萃分析报告了母亲暴露于SSRI与新生儿持续性肺动脉高压及一种自限性新生儿行为综合征之间的显著关联。一些研究提示使用SSRI或其他5-羟色胺能/去甲肾上腺素能抗抑郁药与流产的发生之间存在关联,尽管这些研究存在方法学局限性,影响了数据的说服力。目前,子宫内暴露于SSRI或其他5-羟色胺能/去甲肾上腺素能抗抑郁药与神经行为发育改变、出血及QTc间期延长之间可能存在关联的证据尚不充分。
现有证据表明,孕期应谨慎使用SSRI及其他5-羟色胺能/去甲肾上腺素能抗抑郁药,应对子宫内暴露于这些药物的婴儿进行密切随访。