Takeuchi Hiroyoshi, Suzuki Takefumi, Remington Gary, Uchida Hiroyuki
Post-doctoral Fellow, Schizophrenia Division, Complex Mental Illness Program, Centre for Addiction and Mental Health, Toronto, Ontario; Clinical Fellow, Department of Psychiatry, University of Toronto, Toronto, Ontario; Collaborative Researcher, Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Senior Lecturer, Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Can J Psychiatry. 2015 May;60(5):215-22. doi: 10.1177/070674371506000503.
It remains unclear whether antipsychotic polypharmacy, a common clinical practice, is related to an increased risk of corrected time between start of Q wave and end of T wave (QTc) interval prolongation. We conducted a systematic review of the literature to address this important issue.
A systematic literature search was conducted in October 2014, using MEDLINE, Embase, and PsycINFO. Studies and case reports were included if they reported QTc intervals or QTc interval changes before and after antipsychotic polypharmacy or QTc intervals in both antipsychotic polypharmacy and monotherapy groups.
A total of 21 articles (10 clinical trials, 4 observational studies, and 7 case reports) met inclusion criteria. The clinical trials have shown that a combination treatment with risperidone or pimozide is not obviously related to an increase in QTc interval, whereas ziprasidone or sertindole combined with clozapine may prolong QTc interval. Among the 4 observational studies, antipsychotic polypharmacy was not clearly associated with QTc prolongation in 3 studies, each cross-sectional. In contrast, one prospective study showed a significant increase in QTc interval following antipsychotic coadministration. The case reports indicated an increased risk of QTc prolongation in at least some patients receiving antipsychotic polypharmacy.
Currently available evidence fails to confirm that antipsychotic polypharmacy worsens QTc prolongation in general, although the evidence is scarce and inconsistent. Clinicians are advised to remain conservative in resorting to antipsychotic polypharmacy, as a combination of some QTc-prolongation liable antipsychotics may further prolong QTc interval, and efficacy supporting the clinical benefits of antipsychotic polypharmacy is equivocal, at best.
抗精神病药物联合使用是一种常见的临床做法,但其是否与校正Q波起始至T波结束时间(QTc)间期延长风险增加相关尚不清楚。我们对文献进行了系统综述以解决这一重要问题。
2014年10月使用MEDLINE、Embase和PsycINFO进行了系统的文献检索。纳入报告了抗精神病药物联合使用前后QTc间期或QTc间期变化的研究及病例报告,或抗精神病药物联合治疗组与单药治疗组的QTc间期。
共有21篇文章(10项临床试验、4项观察性研究和7篇病例报告)符合纳入标准。临床试验表明,利培酮或匹莫齐特联合治疗与QTc间期增加无明显关联,而齐拉西酮或舍吲哚联合氯氮平可能会延长QTc间期。在4项观察性研究中,3项横断面研究显示抗精神病药物联合使用与QTc延长无明显关联。相比之下,1项前瞻性研究显示抗精神病药物联合使用后QTc间期显著增加。病例报告表明,至少部分接受抗精神病药物联合治疗的患者QTc延长风险增加。
目前可得的证据未能证实抗精神病药物联合使用总体上会加重QTc延长,尽管证据稀少且不一致。建议临床医生在采用抗精神病药物联合使用时保持谨慎,因为一些易导致QTc延长的抗精神病药物联合使用可能会进一步延长QTc间期,而且支持抗精神病药物联合使用临床益处的疗效充其量也不明确。