Yatham Laksami N, Grossman Fred, Augustyns Ilse, Vieta Eduard, Ravindran Arun
University of British Columbia, Vancouver, Canada.
Br J Psychiatry. 2003 Feb;182:141-7. doi: 10.1192/bjp.182.2.141.
Few double-blind trials have examined the efficacy of a combination of a mood stabiliser and an atypical antipsychotic in acute mania.
To determine the efficacy of risperidone in combination with a mood stabiliser in acute mania.
Patients taking a mood stabiliser were randomised to 3 weeks' treatment with risperidone (n=75) or placebo (n=76).
Young Mania Rating Scale (YMRS) scores improved rapidly with significantly greater reductions at week 1 in the risperidone group compared with the placebo group. At end-point YMRS scores decreased by 14.5 and 10.3 points in the risperidone and placebo groups, respectively. Significant improvements v. placebo (P<0.05) were noted in the risperidone group on several other clinically meaningful measures. Additionally, a post hoc analysis excluding carbamazepine-treated patients (plasma concentrations of risperidone active moiety were 40% lower in this group) revealed significantly greater reductions (P=0.047) in YMRS scores in the risperidone group than in the placebo group. Incidence of adverse events was similar in both groups.
Risperidone is superior to placebo when used in combination with lithium or divalproex in acute mania.
很少有双盲试验研究心境稳定剂与非典型抗精神病药物联合治疗急性躁狂症的疗效。
确定利培酮与心境稳定剂联合治疗急性躁狂症的疗效。
正在服用心境稳定剂的患者被随机分为两组,分别接受为期3周的利培酮治疗(n = 75)或安慰剂治疗(n = 76)。
青年躁狂评定量表(YMRS)评分迅速改善,与安慰剂组相比,利培酮组在第1周时的评分显著降低。在研究终点,利培酮组和安慰剂组的YMRS评分分别下降了14.5分和10.3分。在其他几个具有临床意义的指标上,利培酮组与安慰剂组相比有显著改善(P<0.05)。此外,一项排除接受卡马西平治疗患者的事后分析(该组利培酮活性部分的血浆浓度低40%)显示,利培酮组的YMRS评分降低幅度显著大于安慰剂组(P = 0.047)。两组不良事件的发生率相似。
在急性躁狂症中,利培酮与锂盐或丙戊酸联合使用时优于安慰剂。