Pujalte D, Bottaï T, Huë B, Alric R, Pouget R, Blayac J P, Petit P
Unité de Psychopharmacologie, Faculté de Médecine, Montpellier, France.
Clin Neuropharmacol. 1994 Jun;17(3):236-42. doi: 10.1097/00002826-199406000-00003.
The present study was designed to investigate the efficacy of clonazepam in neuroleptic-induced akathisia. Twelve patients were treated during 2 weeks with clonazepam or placebo in a double-blind randomized design. Akathisia was scored by an independent rater before and after treatment, as well as 1 week after medication withdrawal. Clonazepam (0.5-2.5 mg/day) induced a significantly higher reduction in the akathisia scores than placebo (p < 0.05). One week after stopping the drug, there was a partial but significant relapse in the treated group as compared with controls, in whom the symptoms remained stable. In addition, the clinical improvement was significantly correlated with the daily dose of clonazepam (rs = 0.827; p < 0.002). These results support the potential usefulness of clonazepam in the treatment of neuroleptic-induced akathisia and suggest an optimal daily dose in the range of 10-40 micrograms/kg.
本研究旨在调查氯硝西泮治疗抗精神病药物所致静坐不能的疗效。采用双盲随机设计,12例患者接受了为期2周的氯硝西泮或安慰剂治疗。在治疗前后以及停药1周后,由独立评估者对静坐不能进行评分。氯硝西泮(0.5 - 2.5毫克/天)导致的静坐不能评分降低显著高于安慰剂(p < 0.05)。停药1周后,与症状保持稳定的对照组相比,治疗组出现了部分但显著的复发。此外,临床改善与氯硝西泮的日剂量显著相关(rs = 0.827;p < 0.002)。这些结果支持氯硝西泮在治疗抗精神病药物所致静坐不能方面的潜在效用,并提示最佳日剂量范围为10 - 40微克/千克。