The impact of adjunctive aripiprazole on QT interval: A 12-week open label study in patients on olanzapine, clozapine or risperidone

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY Human Psychopharmacology: Clinical and Experimental Pub Date : 2023-02-22 DOI:10.1002/hup.2863
Thanita Pilunthanakul, Mable Quek Jing Ting, Jimmy Lee, Bhanu Gupta
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Abstract

Objective

To evaluate the effect of adjunct aripiprazole on QT of patients clinically stabilized on atypical antipsychotics.

Methods

The dataset was from an open-label 12-week prospective trial that evaluated adjunctive use of 5 mg/day of aripiprazole on metabolic profile in patients with schizophrenia, or schizoaffective disorder stabilized on olanzapine, clozapine, or risperidone. Bazett-corrected QT (QTc) was manually calculated from ECGs measured at baseline (before aripiprazole) and week 12, by two doctors blind to the diagnosis and atypical antipsychotic. The change in QTc (∆QTc: baseline QTc–week 12 QTc) and the number of participants in normal, borderline, prolonged, and pathological groups after 12 weeks were analyzed.

Results

Fifty-five participants, mean age of 39.3 (SD 8.2) years, were analyzed. The ∆QTc after 12 weeks was 5.9 ms (p = 0.143) for the whole sample; 16.4 ms (p = 0.762), 3.7 ms (p = 0.480) and 0.5 ms (p = 0.449), for the clozapine, risperidone and olanzapine group, respectively. There was no significant statistical difference comparing the change in QTc overall, and between atypical antipsychotic groups, when evaluating from baseline to endpoint. However, stratifying the sample based on sex-dependent QTc cut-offs showed a 45% decrease in abnormal QTc readings (p = 0.049) after aripiprazole initiation; 20 subjects had abnormal QTc at baseline, while only 11 subjects had abnormal QTc at 12 weeks. 25.5% of participants showed a reduction in at least one QTc severity group, while 65.5% had no change and 9.0% worsened in QTc group, after 12 weeks of adjunct aripiprazole.

Conclusion

Low-dose adjunctive aripiprazole did not prolong QTc in patients stabilized on either olanzapine, risperidone, or clozapine. More controlled studies evaluating the QTc effect of adjunctive aripiprazole should be done to confirm and support these findings.

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辅助阿立哌唑对QT间期的影响:奥氮平、氯氮平或利培酮患者的12周开放标签研究
目的评价阿立哌唑对非典型抗精神病药物临床稳定患者QT的影响。方法数据集来自一项为期12周的开放标签前瞻性试验,该试验评估了5 mg/天阿立哌唑对精神分裂症或稳定于奥氮平、氯氮平或利培酮的分裂情感障碍患者代谢谱的辅助使用。Bazett校正的QT(QTc)由两名对诊断和非典型抗精神病药物视而不见的医生根据基线(阿立哌唑之前)和第12周测量的心电图手动计算。分析QTc的变化(∆QTc:基线QTc–第12周QTc)以及12周后正常组、临界组、延长组和病理组的参与者人数。结果分析了55名参与者,平均年龄39.3岁(SD 8.2)。12周后,整个样本的∆QTc为5.9 ms(p=0.143);氯氮平组、利培酮组和奥氮平组分别为16.4ms(p=0.762)、3.7ms(p=0.480)和0.5ms(p=0.449)。当从基线到终点进行评估时,比较QTc的总体变化以及非典型抗精神病药物组之间的变化没有显著的统计学差异。然而,根据性别依赖性QTc截断值对样本进行分层显示,阿立哌唑引发后,异常QTc读数下降了45%(p=0.049);20名受试者在基线时QTc异常,而在12周时只有11名受试人QTc异常。25.5%的参与者在至少一个QTc严重程度组中表现出降低,而在服用阿立哌唑12周后,65.5%的参与者没有变化,9.0%的参与者QTc组病情恶化。结论小剂量阿立哌唑辅助治疗奥氮平、利培酮或氯氮平稳定期患者的QTc不延长。应该进行更多的对照研究来评估辅助阿立哌唑的QTc效应,以证实和支持这些发现。
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
34
审稿时长
6-12 weeks
期刊介绍: Human Psychopharmacology: Clinical and Experimental provides a forum for the evaluation of clinical and experimental research on both new and established psychotropic medicines. Experimental studies of other centrally active drugs, including herbal products, in clinical, social and psychological contexts, as well as clinical/scientific papers on drugs of abuse and drug dependency will also be considered. While the primary purpose of the Journal is to publish the results of clinical research, the results of animal studies relevant to human psychopharmacology are welcome. The following topics are of special interest to the editors and readers of the Journal: -All aspects of clinical psychopharmacology- Efficacy and safety studies of novel and standard psychotropic drugs- Studies of the adverse effects of psychotropic drugs- Effects of psychotropic drugs on normal physiological processes- Geriatric and paediatric psychopharmacology- Ethical and psychosocial aspects of drug use and misuse- Psychopharmacological aspects of sleep and chronobiology- Neuroimaging and psychoactive drugs- Phytopharmacology and psychoactive substances- Drug treatment of neurological disorders- Mechanisms of action of psychotropic drugs- Ethnopsychopharmacology- Pharmacogenetic aspects of mental illness and drug response- Psychometrics: psychopharmacological methods and experimental design
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