Bérard Anick, Iessa Noha, Chaabane Sonia, Muanda Flory T, Boukhris Takoua, Zhao Jin-Ping
Research Center, CHU Ste-Justine, Montreal, Quebec.
Faculty of Pharmacy, University of Montreal, Montreal, Quebec, Canada.
Br J Clin Pharmacol. 2016 Apr;81(4):589-604. doi: 10.1111/bcp.12849. Epub 2016 Jan 26.
The aim of this study was to perform an up-to-date meta-analysis on the risk of cardiac malformations associated with gestational exposure to paroxetine, taking into account indication, study design and reference category.
A systematic review of studies published between 1966 and November 2015 was conducted using embase and MEDLINE. Studies reporting major malformations with first trimester exposure to paroxetine were included. Potentially relevant articles were assessed and relevant data extracted to calculate risk estimates. Outcomes included any major malformations and major cardiac malformations. Pooled odds ratios and 95% confidence intervals were calculated using random-effects models.
Twenty-three studies were included. Compared with non-exposure to paroxetine, first trimester use of paroxetine was associated with an increased risk of any major congenital malformations combined (pooled OR 1.23, 95% CI 1.10, 1.38; n = 15 studies), major cardiac malformations (pooled OR 1.28, 95% CI 1.11, 1.47; n = 18 studies), specifically bulbus cordis anomalies and anomalies of cardiac septal closure (pooled OR 1.42, 95% CI 1.07, 1.89; n = 8 studies), atrial septal defects (pooled OR 2.38, 95% CI 1.14, 4.97; n = 4 studies) and right ventricular outflow track defect (pooled OR 2.29, 95% CI 1.06, 4.93; n = 4 studies). Although the estimates varied depending on the comparator group, study design and malformation detection period, a trend towards increased risk was observed.
Paroxetine use during the first trimester of pregnancy is associated with an increased risk of any major congenital malformations and cardiac malformations. The increase in risk is not dependent on the study method or population.
本研究旨在进行一项最新的荟萃分析,以探讨孕期暴露于帕罗西汀与心脏畸形风险之间的关系,并考虑适应症、研究设计和参照类别。
利用Embase和MEDLINE对1966年至2015年11月期间发表的研究进行系统综述。纳入报告孕早期暴露于帕罗西汀后出现重大畸形的研究。对潜在相关文章进行评估并提取相关数据以计算风险估计值。结局包括任何重大畸形和重大心脏畸形。采用随机效应模型计算合并比值比和95%置信区间。
共纳入23项研究。与未暴露于帕罗西汀相比,孕早期使用帕罗西汀与任何重大先天性畸形合并症(合并比值比1.23,95%置信区间1.10, 1.38;n = 15项研究)、重大心脏畸形(合并比值比1.28,95%置信区间1.11, 1.47;n = 18项研究)风险增加相关,具体为心球异常和心脏间隔闭合异常(合并比值比1.42,95%置信区间1.07, 1.89;n = 8项研究)、房间隔缺损(合并比值比2.38,95%置信区间1.14, 4.97;n = 4项研究)和右心室流出道缺损(合并比值比2.29,95%置信区间1.06, 4.93;n = 4项研究)。尽管估计值因比较组、研究设计和畸形检测期而异,但观察到风险增加的趋势。
孕期头三个月使用帕罗西汀与任何重大先天性畸形和心脏畸形风险增加相关。风险增加不依赖于研究方法或人群。