Risk of Cardiac Events Associated With Antidepressant Therapy in Patients With Long QT Syndrome

被引:7
作者
Wang, Meng [1 ,2 ]
Szepietowska, Barbara [1 ]
Polonsky, Bronislava [1 ]
McNitt, Scott [1 ]
Moss, Arthur J. [1 ]
Zareba, Wojciech [1 ]
Auerbach, David S. [3 ,4 ]
机构
[1] Univ Rochester, Med Ctr, Dept Med, Heart Res Followup Program, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Dept Publ Hlth Sci, Rochester, NY 14642 USA
[3] Univ Rochester, Med Ctr, Aab Cardiovasc Res Inst, Dept Med, Rochester, NY 14642 USA
[4] Univ Rochester, Med Ctr, Dept Pharmacol & Physiol, Rochester, NY 14642 USA
基金
美国国家卫生研究院;
关键词
TORSADE-DE-POINTES; INTERVAL PROLONGATION; CITALOPRAM; DEATH; ANTIPSYCHOTICS; ARRHYTHMIAS; NATIONWIDE; GENOTYPE; SAFETY; DRUGS;
D O I
10.1016/j.amjcard.2017.10.010
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Patients with long QT syndrome (LQTS) are at a high risk of cardiac events. Many patients with LQTS are treated with antidepressant drugs (ADs). We investigated the LQTS genotype-specific risk of recurrent cardiac arrhythmic events (CAEs) associated with AD therapy. The study included 59 LQT1 and 72 LQT2 patients from the Rochester-based I,QTS Registry with corrected QT (QT(c)) prolongation and a history,of AD therapy. Using multivariate Anderson-Gill models, we estimated the LQTS genotype-specific risk of recurrent CAEs (ventricular tachyarrhythmias, aborted cardiac arrest, or sudden cardiac death) associated with time-dependent ADs. Specifically, we examined the risk associated with all ADs, selective serotonin reuptake inhibitor (SSRI), and ADs classified on the CredibleMeds list (www.CredibleMeds.org) as "Conditional" or "Known risk of Torsades de pointes (TdP)" After adjusting for baseline QT, duration, sex, and time-dependent beta-blocker usage, there was an increased risk of recurrent CAEs associated with ADs in 1,QT1 patients (hazard ratio = 3.67, 95% confidence interval 1.98-6.82, p < 0.001) but not in LQT2 patients (hazard ratio = 0.89, 95% confidence interval 0.49-1.64, p = 0.716; LQTI vs LQT2 interaction, p < 0.001). Similarly, LQTI patients who were on SSRIs or ADs with "Known risk of TdP" had a higher risk of recurrent CAEs than those patients off all ADs, whereas there was no association in LQT2 patients. ADs with "Conditional risk of TdP" were not associated with the risk of recurrent CAEs in any of the groups. In conclusion, the risk of recurrent CAEs associated with time-dependent ADs is higher in LQT1 patients but not in LQT2 patients. Results suggest a LQTS genotype-specific effect of ADs on the risk of arrhythmic events. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:182 / 187
页数:6
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