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阿立哌唑治疗对扭转型室速高危患者的心脏安全性:一项采用荟萃分析方法的系统评价

The cardiac safety of aripiprazole treatment in patients at high risk for torsade: a systematic review with a meta-analytic approach.

作者信息

Polcwiartek Christoffer, Sneider Benjamin, Graff Claus, Taylor David, Meyer Jonathan, Kanters Jørgen K, Nielsen Jimmi

机构信息

Department of Psychiatry, Aalborg University Hospital, Aalborg, Denmark.

出版信息

Psychopharmacology (Berl). 2015 Sep;232(18):3297-308. doi: 10.1007/s00213-015-4024-9. Epub 2015 Aug 1.

Abstract

RATIONALE

Certain antipsychotics increase the risk of heart rate-corrected QT (QTc) prolongation and consequently Torsades de Pointes (TdP) and sudden cardiac death (SCD). Drug-induced Brugada syndrome (BrS) is also associated with SCD. Most SCDs occur in patients with additional cardiac risk factors.

OBJECTIVES

Aripiprazole's cardiac safety has not been assessed in patients at high risk for torsade, where QTc prolongation risk is highly increased.

METHODS

MEDLINE, Embase, and The Cochrane Library were searched for preclinical, clinical, and epidemiological studies. Eligible studies were reviewed and cardiac safety data were extracted. Continuous and dichotomous QTc data were used in the meta-analysis.

RESULTS

Preclinical studies suggested that aripiprazole has limited affinity for the delayed rectifier potassium current. TdP was reported in two case reports and SCD was reported in one case report and one case series. No clinical studies assessing aripiprazole's cardiac safety in patients at high risk for torsade were found. No thorough QT (TQT) study with aripiprazole was found. The meta-analysis revealed that the mean ΔQTc interval was decreased with aripiprazole and QTc prolongation risk was lower compared with placebo and active controls. Epidemiological studies linked aripiprazole to weak/moderate torsadogenicity. No studies were found associating aripiprazole with BrS suggesting low affinity for the fast sodium current.

CONCLUSIONS

Aripiprazole is a low-risk antipsychotic regarding cardiac safety in healthy patients. However, baseline and steady state electrocardiogram is recommended in patients at high risk for torsade due to marked QTc prolongation, absence of a TQT study, and lack of data in this group.

摘要

理论依据

某些抗精神病药物会增加心率校正QT(QTc)延长的风险,进而导致尖端扭转型室速(TdP)和心源性猝死(SCD)。药物性 Brugada 综合征(BrS)也与 SCD 相关。大多数 SCD 发生在有其他心脏危险因素的患者中。

目的

阿立哌唑在有高度增加的QTc延长风险的尖端扭转型室速高危患者中的心脏安全性尚未得到评估。

方法

检索了 MEDLINE、Embase 和 Cochrane 图书馆中的临床前、临床和流行病学研究。对符合条件的研究进行了综述,并提取了心脏安全性数据。在荟萃分析中使用了连续和二分法的QTc数据。

结果

临床前研究表明,阿立哌唑对延迟整流钾电流的亲和力有限。在两篇病例报告中报告了TdP,在一篇病例报告和一篇病例系列中报告了SCD。未发现评估阿立哌唑在尖端扭转型室速高危患者中的心脏安全性的临床研究。未发现有关阿立哌唑的全面QT(TQT)研究。荟萃分析显示,与安慰剂和活性对照相比,阿立哌唑使平均ΔQTc间期缩短,QTc延长风险更低。流行病学研究将阿立哌唑与弱/中度致尖端扭转型室速性联系起来。未发现将阿立哌唑与BrS相关联的研究,表明其对快速钠电流的亲和力较低。

结论

对于健康患者,阿立哌唑在心脏安全性方面是一种低风险的抗精神病药物。然而,由于明显的QTc延长、缺乏TQT研究以及该组缺乏数据,建议对尖端扭转型室速高危患者进行基线和稳态心电图检查。

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