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喹硫平治疗急性躁狂症:有效治疗的目标剂量

Quetiapine in the treatment of acute mania: target dose for efficacious treatment.

作者信息

Vieta Eduard, Goldberg Joseph F, Mullen Jamie, Vågerö Mårten, Paulsson Björn

机构信息

Clinical Institute of Neuroscience, Hospital Clinic, University of Barcelona, IDIBAPS, Barcelona, Spain.

出版信息

J Affect Disord. 2007;100 Suppl 1:S23-31. doi: 10.1016/j.jad.2007.02.009. Epub 2007 Mar 26.

Abstract

OBJECTIVE

To analyze the available evidence from randomized clinical trials regarding the effective dose range and optimal dose of quetiapine when treating bipolar I disorder patients with acute mania.

METHODS

Patients with acute mania were treated with quetiapine as monotherapy (for 12 weeks) or in combination with lithium (mean serum concentration 0.76 mEq/L) or divalproex (mean serum concentration 69.5 microg/mL) (Li/DVP) (for 3-6 weeks) in four double-blind, placebo-controlled studies according to a predetermined dosing schedule. Guidance for the dosing of quetiapine involved increasing the first day's dose (100 mg/day) by 100 mg on a daily basis until Day 4 (400 mg/day), then adjusting the dose up to 600 mg/day at Day 5, and up to 800 mg/day thereafter. Pooled data from the two monotherapy studies and the two combination therapy studies have been used to evaluate the effective quetiapine dose range. As the dose was flexible, effective dose was estimated by the mean last-week dose among responders. The mean last-week dose was defined as the median dose during the 7 days before the last available Young Mania Rating Scale (YMRS) assessment. Patients who achieved a > or = 50% decrease in the YMRS total score from baseline to end of treatment with quetiapine were considered responders. Tolerability was assessed from direct patient reports.

RESULTS

According to randomized clinical trials, administration of quetiapine compared with placebo achieved a statistically significant improvement in change from baseline YMRS score within the first week and onward, as monotherapy or in combination with Li/DVP. The average quetiapine dose (+/-SD) in responders during the last week of treatment was 575 (+/-175) at Day 21 and 598 (+/-198) mg/day at Day 84 for monotherapy, and 584+/-208 mg/day at Day 21 for combination therapy, with most responders receiving doses within the range of 400-800 mg/day. Dose escalation was rapid, with 92% of patients treated with monotherapy and 80% of patients treated with combination therapy reaching doses of 400 mg/day by Day 4, in accordance with protocol-defined dosing guidance. This dose administration schedule was generally well tolerated.

CONCLUSIONS

The mean last-week median dose among responders suggests that 600 mg/day of quetiapine is an effective target dose in acute mania.

摘要

目的

分析随机临床试验中有关喹硫平治疗双相I型障碍急性躁狂发作患者的有效剂量范围和最佳剂量的现有证据。

方法

在四项双盲、安慰剂对照研究中,根据预先确定的给药方案,急性躁狂发作患者接受喹硫平单药治疗(为期12周)或与锂盐(平均血清浓度0.76 mEq/L)或丙戊酸(平均血清浓度69.5 μg/mL)联合治疗(为期3 - 6周)。喹硫平给药指导包括第一天剂量(100 mg/天)每天增加100 mg直至第4天(400 mg/天),然后在第5天将剂量调整至600 mg/天,此后调整至800 mg/天。两项单药治疗研究和两项联合治疗研究的汇总数据用于评估喹硫平的有效剂量范围。由于剂量是灵活的,有效剂量通过反应者中最后一周的平均剂量来估计。最后一周的平均剂量定义为最后一次可用的青年躁狂评定量表(YMRS)评估前7天内的中位剂量。从基线到喹硫平治疗结束时YMRS总分下降≥50%的患者被视为反应者。耐受性通过患者的直接报告进行评估。

结果

根据随机临床试验,与安慰剂相比,喹硫平单药治疗或与锂盐/丙戊酸联合治疗在治疗第一周及之后,从基线YMRS评分的变化上取得了统计学上显著的改善。单药治疗时,治疗最后一周反应者的喹硫平平均剂量(±标准差)在第21天为575(±175)mg/天,在第84天为598(±198)mg/天;联合治疗在第21天为584 ± 208 mg/天,大多数反应者接受的剂量在400 - 800 mg/天范围内。剂量增加迅速,按照方案定义的给药指导,单药治疗的患者中有92%、联合治疗的患者中有80%在第4天达到400 mg/天的剂量。这种给药方案总体耐受性良好。

结论

反应者中最后一周的平均中位剂量表明,600 mg/天的喹硫平是急性躁狂发作的有效目标剂量。

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