QT interval prolongation, torsades de pointes and psychotropic medication

T. Kyziridis
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Abstract

QT interval reflects the duration of action potential of myocardial cells. Its prolongation in electrocardiogram is related to risk of torsades de pointes (TdP), a form of polymorphous ventricular tachycardia, and sudden cardiac death, which is one of the main causes of early mortality in psychiatric patients. The fact that only a proportion of patients with drug-induced QT prolongation manifest TdP or die shows that QT prolongation alone is not the perfect biological predictive marker of arrhythmia manifestation. Yet, it continues to be useful but needs to be combined with other known risk factors. This paper is a narrative review based on search in reference books and in PubMed and ScienceDirect databases using the terms [Torsades de pointes OR QT prolongation] AND [Psychotropic drugs OR antipsychotics OR antidepressants]. Its aim is to present basic knowledge about the pathophysiology of TdP arrhythmia and QT prolongation and their relationship with psychotropic drugs. TdP is a relatively slow-rate tachycardia and, in some cases, may stop abruptly without manifestation of clinical symptoms. The diagnosis is based on electrocardiographic findings, the symptoms are similar to those of any tachyarrhythmia and they are related to heart rate and its effects on arterial pressure and cardiac work. QT interval prolongation and TdP result from structural and functional disorders of ion channels and related proteins which are implicated in the process of ventricular repolarization. Psychotropic drugs are commonly used not only in psychiatric patients but in many patients with somatic disease as well. They can affect transmission of electrical impulses from sinus node to ventricular myocardium in various ways and most of its classes prolong QT interval in therapeutic doses or in cases of intoxication. Thus, their careful administration and monitoring of patients, especially hospitalized ones, are of vital importance. More data is available concerning the effects of antipsychotic and antidepressant medication. Among the first group, first generation, classical antipsychotics, especially the lower potency drugs, are considered to carry greater risk. Caution should be exercised when administering thioridazine, haloperidol, pimozide, sertindole and ziprasidone. Among antidepressants, caution is warranted when administering tricyclic antidepressants, citalopram and escitalopram. Among the other psychotropics, much information is available about methadone.
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QT间期延长、点扭转和精神药物治疗
QT间期反映心肌细胞动作电位的持续时间。它在心电图上的延长与点扭转(TdP)(一种多形态室性心动过速)和心源性猝死的风险有关,这是精神病人早期死亡的主要原因之一。只有一部分药物性QT间期延长患者出现TdP或死亡,这表明单独QT间期延长并不是心律失常表现的完美生物学预测指标。然而,它仍然是有用的,但需要与其他已知的风险因素相结合。本文是基于参考书籍和PubMed和ScienceDirect数据库的检索,使用术语[QT间期延长或QT间期延长]和[精神药物或抗精神病药物或抗抑郁药物]进行的叙述性综述。其目的是介绍TdP心律失常和QT间期延长的病理生理基础知识及其与精神药物的关系。TdP是一种相对慢速的心动过速,在某些情况下,可突然停止而无临床症状表现。诊断是基于心电图的结果,症状与任何速性心律失常相似,它们与心率及其对动脉压和心脏工作的影响有关。QT间期延长和TdP是由参与心室复极过程的离子通道和相关蛋白的结构和功能紊乱引起的。精神药物不仅广泛应用于精神病患者,也广泛应用于躯体疾病患者。它们可以以各种方式影响窦房结到心室心肌的电脉冲传递,并且在治疗剂量或中毒情况下,大多数该类药物延长QT间期。因此,对病人,特别是住院病人的仔细管理和监测是至关重要的。关于抗精神病药物和抗抑郁药物的作用有更多的数据可用。在第一组中,第一代,经典抗精神病药物,特别是效力较低的药物,被认为具有更大的风险。在使用硫硝嗪、氟哌啶醇、吡莫齐、塞替多尔和齐拉西酮时应谨慎。在抗抑郁药中,使用三环抗抑郁药、西酞普兰和艾司西酞普兰时要谨慎。在其他精神药物中,有很多关于美沙酮的信息。
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