Aronow Wilbert S, Shamliyan Tatyana A
Department of Cardiology, Westchester Medical Center, New York Medical College, Valhalla, NY, USA.
Quality Assurance, Evidence-Based Medicine Center, Elsevier, Philadelphia, PA, USA.
Ann Transl Med. 2018 Apr;6(8):147. doi: 10.21037/atm.2018.03.17.
Drug-induced QT prolongation is associated with higher risk of cardiac arrhythmias and cardiovascular mortality. We investigated the effects of atypical antipsychotic drugs on QT interval in children and adults with mental disorders.
We conducted random-effects direct frequentist meta-analyses of aggregate data from randomized controlled trials (RCT) and appraised the quality of evidence using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) methodology. Our search in PubMed, EMBASE, the Cochrane Library, clinicaltrials.gov, and PharmaPendium up to October 2017 identified studies that examined aripiprazole, quetiapine, risperidone, olanzapine, ziprasidone and brexpiprazole.
Low quality evidence suggests that aripiprazole (four meta-analyses and twelve RCTs), brexpiprazole (one systematic review and four RCTs) or olanzapine (five meta-analyses and twenty RCTs) do not increase QT interval. Low quality evidence suggests that ziprasidone (five meta-analyses and 11 RCTs) increases QT interval and the rates of QT prolongation while risperidone (four meta-analyses, 70 RCTs) and quetiapine (two meta-analyses and seven RCTs) are associated with QT prolongation and greater odds of torsades de pointes ventricular tachycardia especially in cases of drug overdose.
The main conclusion of our study is that in people with mental disorders and under treatment with atypical antipsychotic drugs, in order to avoid QT prolongation and reduce the risk of ventricular tachycardia clinicians may recommend aripiprazole, brexpiprazole or olanzapine in licensed doses. Long-term comparative safety needs to be established.
药物性QT间期延长与心律失常及心血管疾病死亡率升高相关。我们研究了非典型抗精神病药物对患有精神障碍的儿童和成人QT间期的影响。
我们对随机对照试验(RCT)的汇总数据进行随机效应直接频率元分析,并使用推荐分级评估、制定和评价(GRADE)方法评估证据质量。我们检索了截至2017年10月的PubMed、EMBASE、Cochrane图书馆、clinicaltrials.gov和PharmaPendium,以确定研究阿立哌唑、喹硫平、利培酮、奥氮平、齐拉西酮和布雷斯哌唑的研究。
低质量证据表明,阿立哌唑(四项元分析和十二项RCT)、布雷斯哌唑(一项系统评价和四项RCT)或奥氮平(五项元分析和二十项RCT)不会增加QT间期。低质量证据表明,齐拉西酮(五项元分析和11项RCT)会增加QT间期和QT延长率,而利培酮(四项元分析,70项RCT)和喹硫平(两项元分析和七项RCT)与QT延长以及尖端扭转型室性心动过速的更高几率相关,尤其是在药物过量的情况下。
我们研究的主要结论是,对于患有精神障碍且正在接受非典型抗精神病药物治疗的患者,为避免QT延长并降低室性心动过速风险,临床医生可按许可剂量推荐使用阿立哌唑、布雷斯哌唑或奥氮平。需要确定长期的比较安全性。