Kasper Siegfried, Lerman Mark N, McQuade Robert D, Saha Anutosh, Carson William H, Ali Mirza, Archibald Donald, Ingenito Gary, Marcus Ronald, Pigott Teresa
Department of General Psychiatry, University of Vienna, Vienna, Austria.
Int J Neuropsychopharmacol. 2003 Dec;6(4):325-37. doi: 10.1017/S1461145703003651.
Aripiprazole is a novel atypical antipsychotic for the treatment of schizophrenia. It is a D2 receptor partial agonist with partial agonist activity at 5-HT1A receptors and antagonist activity at 5-HT2A receptors. The long-term efficacy and safety of aripiprazole (30 mg/d) relative to haloperidol (10 mg/d) were investigated in two 52-wk, randomized, double-blind, multicentre studies (using similar protocols which were prospectively identified to be pooled for analysis) in 1294 patients in acute relapse with a diagnosis of chronic schizophrenia and who had previously responded to antipsychotic medications. Aripiprazole demonstrated long-term efficacy that was comparable or superior to haloperidol across all symptoms measures, including significantly greater improvements for PANSS negative subscale scores and MADRS total score (p<0.05). The time to discontinuation for any reason was significantly greater with aripiprazole than with haloperidol (p=0.0001). Time to discontinuation due to adverse events or lack of efficacy was significantly greater with aripiprazole than with haloperidol (p=0.0001). Aripiprazole was associated with significantly lower scores on all extrapyramidal symptoms assessments than haloperidol (p<0.001). In summary, aripiprazole demonstrated efficacy equivalent or superior to haloperidol with associated benefits for safety and tolerability. Aripiprazole represents a promising new option for the long-term treatment of schizophrenia.
阿立哌唑是一种用于治疗精神分裂症的新型非典型抗精神病药物。它是一种D2受体部分激动剂,对5-HT1A受体具有部分激动活性,对5-HT2A受体具有拮抗活性。在两项为期52周、随机、双盲、多中心研究(采用相似方案,经前瞻性确定可合并进行分析)中,对1294例诊断为慢性精神分裂症且既往对抗精神病药物有反应的急性复发患者,研究了阿立哌唑(30毫克/天)相对于氟哌啶醇(10毫克/天)的长期疗效和安全性。在所有症状测量指标上,阿立哌唑均显示出与氟哌啶醇相当或更优的长期疗效,包括阳性和阴性症状量表(PANSS)阴性分量表得分及蒙哥马利-阿斯伯格抑郁量表(MADRS)总分有显著更大改善(p<0.05)。阿立哌唑因任何原因停药的时间显著长于氟哌啶醇(p=0.0001)。因不良事件或缺乏疗效导致停药的时间,阿立哌唑也显著长于氟哌啶醇(p=0.