Burns T, Bale R
Department of Psychiatry, St George's Hospital Medical School, London, UK.
J Int Med Res. 2001 Nov-Dec;29(6):451-66. doi: 10.1177/147323000102900601.
Five studies have been conducted with the atypical anti-psychotic amisulpride (100-1200 mg/day) involving 1358 patients with acute exacerbations of schizophrenia; four studies were short-term (4-8 weeks), double-blind studies and one was a 12-month, open, randomized comparison. Amisulpride improved positive symptoms consistently, and changes were more pronounced than with haloperidol, flupenthixol and risperidone; amisulpride showed a more rapid onset of action compared to haloperidol, and improvement in negative symptoms was more effective than with any comparator. An optimum response was obtained with amisulpride doses 400-800 mg/day. The long-term study confirmed the usefulness of amisulpride for maintenance treatment in schizophrenia, with a clear advantage over haloperidol, leading to better functioning and quality of life. Amisulpride caused fewer neurological side-effects than conventional anti-psychotics and less weight gain than risperidone, both of which are crucial factors for long-term compliance.
针对非典型抗精神病药物氨磺必利(每日100 - 1200毫克)开展了五项研究,涉及1358例精神分裂症急性加重患者;四项研究为短期(4 - 8周)双盲研究,一项为12个月的开放性随机对照研究。氨磺必利持续改善阳性症状,且变化比氟哌啶醇、三氟噻吨和利培酮更显著;与氟哌啶醇相比,氨磺必利起效更快,改善阴性症状比任何对照药物更有效。氨磺必利每日剂量400 - 800毫克时可获得最佳疗效。长期研究证实氨磺必利对精神分裂症维持治疗有效,明显优于氟哌啶醇,能带来更好的功能状态和生活质量。与传统抗精神病药物相比,氨磺必利引起的神经副作用更少,与利培酮相比体重增加更少,这两个因素对长期依从性都至关重要。