Khan Khalid, Zamora Javier, Lamont Ronald F, Van Geijn Hp Herman, Svare Jens, Santos-Jorge Carlos, Jacquemyn Yves, Husslein Peter, Helmer H Hanns, Dudenhausen Joachim, Di Renzo Gian Carlo, Roura Luis Cabero, Beattie Bryan
University of Birmingham Women's Hospital, Birmingham UK.
J Matern Fetal Neonatal Med. 2010 Sep;23(9):1030-8. doi: 10.3109/14767050903572182.
Calcium channel blockers (CCBs) are not licensed for use in pregnancy but are used without robust surveillance to treat hypertension in pregnancy and preterm labour. The objective of this study was to evaluate the fetomaternal safety of CCB in pregnancy by a quantitative systematic review.
Medline (1996-2005), EMBASE (1996-2003), BIOSIS (1993-2003), Current contents (1995-2003), DERWENT DRUGFILE (1983-2003) and Cochrane Library (2005: issue 3). The number of women reporting an adverse event was used to compute a percentage of the total number of women in whom the occurrence of that event or confirmation of its absence was reported. Meta-regression with generalised estimation equations modelling explored reasons for heterogeneity, seeking factors that increased the rates of the most commonly reported adverse events.
Of 269 relevant reports, including 5607 women, adverse fetomaternal events varied according to the total dose of nifedipine and study design. Adverse events were highest amongst women given more than 60 mg total dose of nifedipine [odds ratio (OR) 3.78, 95% confidence interval (CI) 1.27-11.2, p = 0.017] and in reports from case series compared to controlled studies (OR 2.45, 95% CI 1.17-5.15, p = 0.018).
Adverse event rates generated from this study provide an evidence base for clinical guidelines and informed patient consent for CCB use in pregnancy.
钙通道阻滞剂(CCB)未获许可用于孕期,但在缺乏有力监测的情况下被用于治疗孕期高血压和早产。本研究的目的是通过定量系统评价评估CCB在孕期的母婴安全性。
检索了Medline(1996 - 2005年)、EMBASE(1996 - 2003年)、BIOSIS(1993 - 2003年)、《现刊目次》(1995 - 2003年)、德温特药物档案(1983 - 2003年)以及Cochrane图书馆(2005年第3期)。报告不良事件的女性数量用于计算报告该事件发生或确认其未发生的女性总数的百分比。采用广义估计方程建模的Meta回归探讨异质性原因,寻找增加最常报告不良事件发生率的因素。
在269篇相关报告中,包括5607名女性,母婴不良事件因硝苯地平总剂量和研究设计而异。硝苯地平总剂量超过60mg的女性中不良事件发生率最高[比值比(OR)3.78,95%置信区间(CI)1.27 - 11.2,p = 0.017],与对照研究相比,病例系列报告中的不良事件发生率也较高(OR 2.45,95%CI 1.17 - 5.15,p = 0.018)。
本研究得出的不良事件发生率为临床指南以及患者在孕期使用CCB时的知情同意提供了证据基础。