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一项关于喹硫平作为锂盐或丙戊酸辅助治疗双相躁狂症的双盲、随机、安慰剂对照试验。

A double blind, randomized, placebo-controlled trial of quetiapine as an add-on therapy to lithium or divalproex for the treatment of bipolar mania.

作者信息

Yatham Lakshmi N, Vieta Eduard, Young Allan H, Möller Hans-Jürgen, Paulsson Björn, Vågerö Mårten

机构信息

Division of Mood Disorders, University of British Columbia, UBC Hospital, Vancouver, British Columbia, Canada.

出版信息

Int Clin Psychopharmacol. 2007 Jul;22(4):212-20. doi: 10.1097/YIC.0b013e328080ca57.

Abstract

The aim of this study was to evaluate the efficacy and tolerability of quetiapine combined with lithium or divalproex in the treatment of bipolar mania. Patients were randomized to 6 weeks of quetiapine (up to 800 mg/day) and lithium/divalproex (Li/DVP) (target trough serum concentrations of 0.7-1.0 mEq/L and 50-100 microg/mL, respectively) or placebo and lithium/divalproex. Quetiapine+lithium/divalproex treatment (n=104) showed a 2.0-point greater improvement on the primary outcome (change from baseline in Young Mania Rating Scale total score at day 21) compared with placebo+lithium/divalproex (n=96), and a 2.8-point greater difference by day 42, but the differences between groups were not statistically significant. Other efficacy measures, however, did show a statistically significant advantage in favor of quetiapine+lithium/divalproex over lithium/divalproex monotherapy at day 42. Improvement of mean Young Mania Rating Scale scores with quetiapine+lithium/divalproex was numerically but not statistically significantly greater than lithium/divalproex monotherapy in the treatment of bipolar mania. Potential reasons for the failure of quetiapine+lithium/divalproex to differentiate from placebo+lithium/divalproex treatment on the primary outcome measure and the implications of this for the treatment of mania and future studies are discussed. Overall, the combination of quetiapine with lithium or divalproex was well tolerated.

摘要

本研究的目的是评估喹硫平联合锂盐或丙戊酸治疗双相躁狂症的疗效和耐受性。患者被随机分为接受6周的喹硫平(最高800毫克/天)和锂盐/丙戊酸(Li/DVP)(目标血清谷浓度分别为0.7 - 1.0毫当量/升和50 - 100微克/毫升)或安慰剂与锂盐/丙戊酸治疗。与安慰剂 + 锂盐/丙戊酸组(n = 96)相比,喹硫平 + 锂盐/丙戊酸治疗组(n = 104)在主要结局指标(第21天青年躁狂评定量表总分相对于基线的变化)上改善幅度大2.0分,到第42天差异大2.8分,但组间差异无统计学意义。然而,在第42天,其他疗效指标确实显示喹硫平 + 锂盐/丙戊酸组相对于锂盐/丙戊酸单药治疗具有统计学显著优势。在双相躁狂症治疗中,喹硫平 + 锂盐/丙戊酸组平均青年躁狂评定量表评分的改善在数值上高于锂盐/丙戊酸单药治疗,但无统计学显著差异。讨论了喹硫平 + 锂盐/丙戊酸在主要结局指标上未能与安慰剂 + 锂盐/丙戊酸治疗区分开来的潜在原因及其对躁狂症治疗和未来研究的意义。总体而言,喹硫平与锂盐或丙戊酸联合使用耐受性良好。

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