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QT 延长、尖端扭转型室性心动过速与精神药物:5 年更新。

QT Prolongation, Torsades de Pointes, and Psychotropic Medications: A 5-Year Update.

机构信息

Harvard Medical School, Boston, MA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA.

Harvard Medical School, Boston, MA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA.

出版信息

Psychosomatics. 2018 Mar-Apr;59(2):105-122. doi: 10.1016/j.psym.2017.10.009. Epub 2017 Nov 3.

Abstract

BACKGROUND

Some psychotropic medications have been associated with prolongation of the QT interval and QT prolongation, especially in those with medical illness, and are linked to lethal ventricular arrhythmias, such as Torsades de Pointes (TdP). In 2013, we published a review of QT prolongation, TdP, and psychotropic medications.

OBJECTIVE

We provide an update over the past 5 years on the specific concerns most relevant to clinicians who see medically ill patients.

METHODS

In this nonsystematic review, we aimed to carefully and intensively identify new articles by utilizing a structured PubMed search from 2012-present.

RESULTS

QT prolongation remains an imperfect, though well-established marker of risk for TdP. Among antidepressant medications, citalopram does appear to prolong the QT interval more than other selective serotonin reuptake inhibitors, though the clinical significance of this prolongation remains unclear. Escitalopram appears to prolong the QT interval to a lesser extent. Haloperidol carries a risk for QT prolongation, but the assertion that intravenous haloperidol is inherently riskier may be confounded by its primary use in medically ill populations. Among atypical antipsychotic agents, ziprasidone-and possibly iloperidone-is associated with the greatest QT prolongation, whereas aripiprazole appears safest from this standpoint.

CONCLUSIONS

The evidence for clinically meaningful QT prolongation with most classes of psychiatric agents remains minimal. The most important risk-reducing intervention clinicians can make is undertaking a careful analysis of other QT risk factors when prescribing psychiatric medications.

摘要

背景

一些精神药物与 QT 间期延长和 QT 延长有关,特别是在患有医学疾病的患者中,并且与致命性室性心律失常如尖端扭转型室性心动过速(TdP)有关。2013 年,我们发表了一篇关于 QT 延长、TdP 和精神药物的综述。

目的

我们提供了过去 5 年来与治疗患有医学疾病的患者的临床医生最相关的具体问题的最新信息。

方法

在这项非系统性综述中,我们旨在通过使用 2012 年至今的结构化 PubMed 搜索,仔细和深入地识别新文章。

结果

QT 延长仍然是 TdP 风险的一个不完善但已确立的标志物。在抗抑郁药物中,西酞普兰似乎比其他选择性 5-羟色胺再摄取抑制剂更能延长 QT 间期,但这种延长的临床意义尚不清楚。艾司西酞普兰似乎延长 QT 间期的程度较小。氟哌啶醇存在 QT 延长的风险,但静脉用氟哌啶醇固有风险较高的说法可能因它主要用于患有医学疾病的人群而受到混淆。在非典型抗精神病药物中,齐拉西酮和(可能是依洛哌酮)与最大的 QT 延长有关,而阿立哌唑在这方面似乎是最安全的。

结论

大多数精神药物类别与临床有意义的 QT 延长相关的证据仍然很少。临床医生可以采取的最重要的降低风险干预措施是在开处方时仔细分析其他 QT 风险因素。

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