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临床里程碑可预测重度抑郁症(MDD)患者6个月以上的症状缓解情况及治疗选择。

Clinical milestones predict symptom remission over 6-month and choice of treatment of patients with major depressive disorder (MDD).

作者信息

Wade A G, Schlaepfer T E, Andersen H F, Kilts C D

机构信息

CPS Clinical Research Centre, Glasgow, United Kingdom.

出版信息

J Psychiatr Res. 2009 Feb;43(5):568-75. doi: 10.1016/j.jpsychires.2008.09.008. Epub 2008 Oct 26.

Abstract

BACKGROUND

It is uncertain as to what short-term outcomes predict long-term treatment compliance and outcomes in patients with MDD.

AIMS

To determine what treatment milestones predict symptom remission with long-term treatment with antidepressant medication.

METHOD

Pooled analysis of four randomised, double-blind, active comparator, 6-month trials in MDD.

RESULTS

Patients received double-blind treatment with escitalopram (N=699) or a comparator (citalopram, duloxetine, or paroxetine) (N=699). Onset of effect at week 2 was correlated with response at week 8, and response at week 8 with completion of 6-month treatment. Week 8 response was associated with a greater probability of achieving later remission. Week 24 remission (MADRS>or=10) was significantly (p<0.01) higher for patients treated with escitalopram (70.7%) than for the pooled comparators (64.7%). Week 24 complete remission (MADRS<or=5) was significantly (p<0.01) higher for escitalopram (51.7%) than for the pooled comparators (45.6%). Fewer patients discontinued treatment with escitalopram (15.9%) than with the pooled comparators (23.9%) (p<0.001).

CONCLUSION

A higher probability of achieving remission is associated with responding after 8 weeks and with completing 6 months of treatment.

摘要

背景

对于重度抑郁症(MDD)患者而言,哪些短期结果能够预测长期治疗依从性和治疗结果尚不确定。

目的

确定哪些治疗节点能够预测抗抑郁药物长期治疗后的症状缓解情况。

方法

对四项针对MDD患者的为期6个月的随机、双盲、活性对照试验进行汇总分析。

结果

患者接受艾司西酞普兰(N = 699)或对照药物(西酞普兰、度洛西汀或帕罗西汀)(N = 699)的双盲治疗。第2周起效与第8周的反应相关,第8周的反应与6个月治疗的完成情况相关。第8周的反应与后期实现缓解的可能性更大相关。接受艾司西酞普兰治疗的患者在第24周缓解(蒙哥马利-艾斯伯格抑郁量表>MADRS≥10)的比例(70.7%)显著高于(p<0.01)合并的对照药物组(64.7%)。艾司西酞普兰组在第24周完全缓解(MADRS≤5)的比例(51.7%)显著高于(p<0.01)合并的对照药物组(45.6%)。与合并的对照药物组(23.9%)相比,艾司西酞普兰组停药的患者更少(15.9%)(p<0.001)。

结论

实现缓解的较高概率与8周后出现反应以及完成6个月治疗相关。

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