Joseph K S, Sheehy Odile, Mehrabadi Azar, Urquia Marcelo L, Hutcheon Jennifer A, Kramer Michael, Bérard Anick
Department of Obstetrics and Gynaecology, School of Population and Public Health, Children's and Women's Hospital and Health Centre of British Columbia, University of British Columbia, Vancouver, British Columbia, Canada.
Paediatr Perinat Epidemiol. 2015 May;29(3):220-31. doi: 10.1111/ppe.12190. Epub 2015 Apr 5.
Rates of postpartum haemorrhage and atonic postpartum haemorrhage have increased in several high-income countries. We carried out a study to examine if drug use in pregnancy, or drug and other interactions, explained this increase in postpartum haemorrhage.
The linked administrative and hospital databases of the Québec Pregnancy Cohort were used to define a cohort of pregnant women in Québec, Canada, from 1998 to 2009 (n = 138,704). Case-control studies on any postpartum haemorrhage and atonic postpartum haemorrhage were carried out within this population, with up to five controls randomly selected for each case after matching on index date and hospital of delivery (incidence density sampling). Conditional logistic regression was used to estimate the effects of drug use on postpartum haemorrhage and atonic postpartum haemorrhage.
There was an unexpected non-linear, declining temporal pattern in postpartum haemorrhage and atonic postpartum haemorrhage between 1998 and 2009. Use of antidepressants (mainly selective serotonin reuptake inhibitors) was associated with higher rates of postpartum haemorrhage [adjusted rate ratio (aRR) 1.48, 95% confidence interval (CI) 1.23, 1.77] and atonic postpartum haemorrhage [aRR 1.40, 95% CI 1.13, 1.74]. Thrombocytopenia was also associated with higher rates of postpartum haemorrhage [aRR 1.52, 95% CI 1.16, 2.00]. There were no statistically significant drug interactions. Adjustment for maternal factors and drug use had little effect on temporal trends in postpartum haemorrhage and atonic postpartum haemorrhage.
Although antidepressant use and thrombocytopenia were associated with higher rates of atonic postpartum haemorrhage, antidepressant and other drug use did not explain temporal trends in postpartum haemorrhage.
在几个高收入国家,产后出血和宫缩乏力性产后出血的发生率有所上升。我们开展了一项研究,以检验孕期用药或药物及其他相互作用是否能解释产后出血的这种增加情况。
利用魁北克妊娠队列的关联行政和医院数据库,确定了1998年至2009年加拿大魁北克的一组孕妇(n = 138,704)。在该人群中开展了关于任何产后出血和宫缩乏力性产后出血的病例对照研究,在按索引日期和分娩医院匹配后,为每个病例随机选择多达5名对照(发病密度抽样)。采用条件逻辑回归来估计用药对产后出血和宫缩乏力性产后出血的影响。
1998年至2009年间,产后出血和宫缩乏力性产后出血出现了意外的非线性、下降的时间模式。使用抗抑郁药(主要是选择性5-羟色胺再摄取抑制剂)与较高的产后出血发生率相关[调整率比(aRR)1.48,95%置信区间(CI)1.23,1.77]以及宫缩乏力性产后出血发生率相关[aRR 1.40,95% CI 1.13,1.74]。血小板减少症也与较高的产后出血发生率相关[aRR 1.52,95% CI 1.16,2.00]。没有具有统计学意义的药物相互作用。对母亲因素和用药进行调整对产后出血和宫缩乏力性产后出血的时间趋势影响不大。
尽管使用抗抑郁药和血小板减少症与较高的宫缩乏力性产后出血发生率相关,但抗抑郁药和其他药物的使用并不能解释产后出血的时间趋势。