Department of Veterans Affairs, National Serious Mental Illness Treatment Resource and Evaluation Center, Ann Arbor, Michigan, USA.
Am J Psychiatry. 2013 Jun;170(6):642-50. doi: 10.1176/appi.ajp.2013.12030408.
A recent Food and Drug Administration (FDA) warning cautioned that citalopram dosages exceeding 40 mg/day may cause abnormal heart rhythms, including torsade de pointes. The authors assessed relationships between citalopram use and ventricular arrhythmias and mortality.
A cohort study was conducted using Veterans Health Administration data between 2004 and 2009 from depressed patients who received a prescription for citalopram (N=618,450) or for sertraline (N=365,898), a comparison medication with no FDA warning. Cox regression models, adjusted for demographic and clinical characteristics, were used to examine associations of antidepressant dosing with ventricular arrhythmia and cardiac, noncardiac, and all-cause mortality.
Citalopram daily doses >40 mg were associated with lower risks of ventricular arrhythmia (adjusted hazard ratio=0.68, 95% CI=0.61-0.76), all-cause mortality (adjusted hazard ratio=0.94, 95% CI=0.90-0.99), and noncardiac mortality (adjusted hazard ratio=0.90, 95% CI=0.86-0.96) compared with daily doses of 1-20 mg. No increased risks of cardiac mortality were found. Citalopram daily doses of 21-40 mg were associated with lower risks of ventricular arrhythmia (adjusted hazard ratio=0.80, 95% CI=0.74-0.86) compared with dosages of 1-20 mg/day but did not have significantly different risks of any cause of mortality. The sertraline cohort revealed similar findings, except there were no significant associations between daily dose and either all-cause or noncardiac mortality.
This large study found no elevated risks of ventricular arrhythmia or all-cause, cardiac, or noncardiac mortality associated with citalopram dosages >40 mg/day. Higher dosages were associated with fewer adverse outcomes, and similar findings were observed for a comparison medication, sertraline, not subject to the FDA warning. These results raise questions regarding the continued merit of the FDA warning.
美国食品和药物管理局(FDA)最近发布的一则警告提醒称,西酞普兰的日剂量超过 40 毫克可能会导致异常心律,包括尖端扭转型室性心动过速。作者评估了西酞普兰的使用与室性心律失常和死亡率之间的关系。
这是一项使用退伍军人健康管理局(VA)数据进行的队列研究,时间范围为 2004 年至 2009 年,参与者为接受西酞普兰(N=618450)或对照药物舍曲林(N=365898)处方的抑郁患者。该对照药物没有 FDA 警告。采用 Cox 回归模型,调整人口统计学和临床特征,以检查抗抑郁药剂量与室性心律失常以及心脏、非心脏和全因死亡率之间的关联。
与每日剂量为 1-20 毫克相比,西酞普兰日剂量>40 毫克与较低的室性心律失常(调整后的危险比=0.68,95%CI=0.61-0.76)、全因死亡率(调整后的危险比=0.94,95%CI=0.90-0.99)和非心脏死亡率(调整后的危险比=0.90,95%CI=0.86-0.96)相关。未发现心脏死亡率增加的风险。与每日剂量为 1-20 毫克相比,西酞普兰每日剂量为 21-40 毫克与较低的室性心律失常风险相关(调整后的危险比=0.80,95%CI=0.74-0.86),但与任何原因的死亡率无显著差异。舍曲林队列也得出了类似的结果,只是每日剂量与全因或非心脏死亡率之间没有显著关联。
这项大型研究发现,西酞普兰日剂量超过 40 毫克与室性心律失常或全因、心脏或非心脏死亡率升高无关。较高的剂量与较少的不良结局相关,对于不受 FDA 警告限制的对照药物舍曲林,也观察到了类似的结果。这些结果引发了对 FDA 警告是否继续合理的质疑。