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Antidepressants metoprolol and the risk of bradycardia

机译:抗抑郁药美托洛尔和心动过缓的风险

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摘要

Case reports and pharmacologic theory suggest that some antidepressants can interfere with the hepatic metabolism of metoprolol by cytochrome P450 2D6 (CYP2D6), potentially increasing the risk of bradycardia. The objective of this study was to characterize the clinical consequences of this potential drug interaction at the population level. We conducted a population-based, nested case–control study of Ontario residents 66 years of age or older receiving metoprolol. Cases hospitalized for bradycardia were compared with matched controls (4:1) to explore the odds ratio for initiation of antidepressants that inhibit CYP2D6 (fluoxetine and paroxetine) and those that do not inhibit CYP2D6 (fluvoxamine, citalopram, venlafaxine, and sertraline) 30 days before hospitalization. From April 1997 to March 2009, we identified 332,254 older patients continuously receiving metoprolol, of whom 8232 (2.5%) were treated in hospital for bradycardia. The adjusted odds ratio for exposure to fluoxetine or paroxetine compared with other antidepressants 30 days prior to hospitalization for bradycardia was 0.76 (95% confidence interval 0.42–1.37). Among older patients receiving metoprolol, the initiation of antidepressants that inhibit CYP2D6 was not associated with a significant increase in the risk of bradycardia compared with antidepressants that do not inhibit CYP2D6.
机译:病例报告和药理学理论表明,某些抗抑郁药可通过细胞色素P450 2D6(CYP2D6)干扰美托洛尔的肝代谢,从而可能增加心动过缓的风险。这项研究的目的是在人群水平上表征这种潜在药物相互作用的临床后果。我们对66岁或以上接受美托洛尔的安大略省居民进行了基于人群的嵌套病例对照研究。将住院的心动过缓患者与对照组(4:1)进行比较,以探讨抑制CYP2D6(氟西汀和帕罗西汀)和不抑制CYP2D6(氟伏沙明,西酞普兰,文拉法辛和舍曲林)的抗抑郁药启动的几率住院前。从1997年4月至2009年3月,我们确定了332254例持续接受美托洛尔的老年患者,其中8232例(占2.5%)在医院接受了心动过缓的治疗。心动过缓住院前30天与其他抗抑郁药相比,氟西汀或帕罗西汀暴露的校正后优势比为0.76(95%置信区间0.42-1.37)。在接受美托洛尔的老年患者中,与不抑制CYP2D6的抗抑郁药相比,抑制CYP2D6的抗抑郁药的启动与心动过缓风险的显着增加无关。

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