Kane John M, Crandall David T, Marcus Ronald N, Eudicone James, Pikalov Andrei, Carson William H, Swyzen Wim
The Zucker Hillside Hospital, 75-59 263 St., Glen Oaks, NY 11004, USA.
Schizophr Res. 2007 Sep;95(1-3):143-50. doi: 10.1016/j.schres.2007.05.009. Epub 2007 Jul 17.
The Remission in Schizophrenia Working Group (RSWG) has defined criteria for symptomatic remission based on achieving and maintaining a consistently low symptom threshold for at least six consecutive months. This analysis examined symptomatic remission in acutely ill patients with schizophrenia receiving either aripiprazole or haloperidol for one year.
Pooled data from two 52-week, randomized, double-blind, multicenter, comparative trials of aripiprazole and haloperidol in acutely ill patients with schizophrenia were analyzed. Measures of symptomatic remission were calculated according to RSWG criteria.
Remission rates were significantly higher for patients treated with aripiprazole compared with haloperidol (32% vs 22%, respectively; p<0.001, LOCF). Among remitters, aripiprazole-treated patients achieved symptom criteria in a significantly shorter time than haloperidol-treated patients (log rank p=0.0024). For trial completers, remission rates were similarly high in both groups (aripiprazole, 77%; haloperidol, 74%). Regardless of treatment type, remitters received significantly higher global clinical ratings than nonremitters (p<0.0001). Aripiprazole was associated with a significantly lower rate of discontinuations due to adverse events (AEs) than haloperidol (8.0% vs 18.4%, respectively; p<0.001) as well as lower concomitant medication use for extrapyramidal symptoms (EPS) (23% vs 57%, respectively; p<0.001).
Acutely ill schizophrenia patients treated with aripiprazole demonstrated a significantly higher rate of symptomatic remission across 52 weeks compared with haloperidol-treated patients. The similar remission rates among trial completers in both treatment groups, combined with fewer AE-related discontinuations and lower EPS medication use in the aripiprazole group, suggest that better tolerability with aripiprazole may have contributed to superior overall remission rates.
精神分裂症缓解工作组(RSWG)已根据连续至少六个月达到并维持始终较低的症状阈值来定义症状缓解标准。本分析研究了接受阿立哌唑或氟哌啶醇治疗一年的急性精神分裂症患者的症状缓解情况。
对两项为期52周、随机、双盲、多中心、比较阿立哌唑和氟哌啶醇治疗急性精神分裂症患者的试验汇总数据进行分析。根据RSWG标准计算症状缓解指标。
与氟哌啶醇治疗的患者相比,阿立哌唑治疗的患者缓解率显著更高(分别为32%和22%;p<0.001,末次观测结转)。在缓解者中,阿立哌唑治疗的患者达到症状标准的时间明显短于氟哌啶醇治疗的患者(对数秩检验p=0.0024)。对于试验完成者,两组的缓解率同样较高(阿立哌唑组为77%;氟哌啶醇组为74%)。无论治疗类型如何,缓解者的总体临床评分显著高于未缓解者(p<0.0001)。与氟哌啶醇相比,阿立哌唑因不良事件(AE)导致的停药率显著更低(分别为8.0%和18.4%;p<0.001),同时用于锥体外系症状(EPS)的伴随药物使用也更少(分别为23%和57%;p<0.001)。
与氟哌啶醇治疗的患者相比,接受阿立哌唑治疗的急性精神分裂症患者在52周内症状缓解率显著更高。两个治疗组试验完成者的缓解率相似,加上阿立哌唑组与AE相关的停药较少且EPS药物使用较低表明,阿立哌唑更好的耐受性可能导致了更高的总体缓解率。