Departments of Psychiatry and Community Health Sciences, University of Calgary, Alberta, Canada.
Neuropsychiatr Dis Treat. 2010 Oct 29;6:711-7. doi: 10.2147/NDT.S13407.
There is a great need in the treatment of schizophrenia for a drug, or drug combinations, to improve clinical response with fewer serious side effects. The objective of this study was to explore the therapeutic effects and tolerability of the anticonvulsant gabapentin as an adjunctive in the treatment of patients with partially responsive schizophrenia.
Ten consenting patients with a confirmed Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision diagnosis of schizophrenia were identified. All patients failed at least one 12-week treatment trial with risperidone or olanzapine. Gabapentin was added to ongoing antipsychotic treatment with olanzapine or risperidone for eight weeks. The primary outcome measure was the Positive and Negative Syndrome Scale (PANSS). Other scales included the Calgary Depression Scale (CDSS) and the Abnormal Involuntary Movement Scale (AIMS). Repeated-measures multivariate analysis of variance was utilized to examine changes in outcome measures over time with adjunctive treatment with gabapentin.
There was a significant drop in the PANSS and CDSS scores at endpoint (week 8). There were no significant differences between the two treatment groups with regard to changes in all outcome measures or in AIMS score. The adjunctive treatments were well tolerated and side effects were transient.
Gabapentin could be used successfully as an adjunct to novel antipsychotics in partially responsive schizophrenia. However, large controlled studies are needed to examine the effectiveness of gabapentin in psychotic disorders.
在精神分裂症的治疗中,非常需要一种药物或药物组合,以在减少严重副作用的情况下改善临床反应。本研究的目的是探索抗惊厥药加巴喷丁作为辅助治疗部分反应性精神分裂症患者的治疗效果和耐受性。
确定了 10 名同意参加研究的、符合《精神障碍诊断与统计手册》第 4 版修订版(DSM-IV-TR)精神分裂症确诊的患者。所有患者均在使用利培酮或奥氮平治疗的至少 12 周治疗试验中失败。加巴喷丁被添加到正在进行的奥氮平或利培酮抗精神病治疗中,持续 8 周。主要结局指标是阳性和阴性症状量表(PANSS)。其他量表包括卡尔加里抑郁量表(CDSS)和异常不自主运动量表(AIMS)。采用重复测量多元方差分析来检验在加巴喷丁辅助治疗期间,结局测量值随时间的变化。
在终点(第 8 周)时,PANSS 和 CDSS 评分显著下降。在加巴喷丁治疗的所有结局指标或 AIMS 评分方面,两组之间没有显著差异。辅助治疗耐受性良好,副作用短暂。
加巴喷丁可成功用作部分反应性精神分裂症新型抗精神病药物的辅助药物。然而,需要进行大规模的对照研究来检验加巴喷丁在精神障碍中的有效性。