Symptomatic Remission in Patients with Bipolar Mania: Results from a Double-Blind, Placebo-Controlled Trial of Risperidone Monotherapy

S. Gopal, J. Beyer, D. Steffens, M. Kramer
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引用次数: 2

Abstract

ABSTRACTBackground: The purpose of this analysis was to compare symptomatic remission rates between risperidone and placebo in a completed randomized controlled trial. Design and Methods: Two hundred ninety (290) adult patients who met DSM-IV criteria for Bipolar I Disorder Manic or Mixed episode were randomized to flexible doses of risperidone or placebo for 3 weeks. An entry Young Mania Rating Scale (YMRS) score of > 20 was required at trial screening and baseline. Time to first onset of remission (as defined as a YMRS score of < 8) was assessed using Cox proportional hazards. Persence or absence of sustained remission was analyzed using logistic regression. Sustained remission was defined as maintaining a YMRS < 8 for the remainder of the trial or until censor. Results: After adjusting for presence of psychosis, baseline YMRS, gender, number of mood cycles in the previous year and treatment,the odds of sustained remission for subjects on risperidone was 5.6 (p < 0.0001). Similarly the adjusted hazard or remission for subjects on rsiperidone was 4.0 (p < 0.0001). Interpretaion: A statistically significant proportion of manic patients receiving risperidone monotherapy achieved symptomatic remission within 3 weeks as compared to placebo.
双相躁狂症患者的症状缓解:利培酮单药治疗的双盲、安慰剂对照试验结果
摘要背景:本分析的目的是在一项完整的随机对照试验中比较利培酮和安慰剂的症状缓解率。设计和方法:290例符合DSM-IV双相I型躁狂症或混合性发作标准的成年患者随机接受灵活剂量的利培酮或安慰剂治疗3周。在试验筛选和基线时,要求青年躁狂症评定量表(YMRS)得分> 20。使用Cox比例风险评估到首次发作缓解的时间(定义为YMRS评分< 8)。使用逻辑回归分析是否存在持续缓解。持续缓解被定义为在试验剩余时间或直到审查前维持YMRS < 8。结果:在调整精神病的存在、基线YMRS、性别、前一年的情绪周期次数和治疗后,利培酮受试者持续缓解的几率为5.6 (p < 0.0001)。同样,利培酮治疗的调整后危险度或缓解度为4.0 (p < 0.0001)。解释:与安慰剂相比,接受利培酮单药治疗的躁狂患者在3周内症状缓解的比例具有统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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