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Cognitive behavioural therapy as an adjunct to pharmacotherapy for primary care based patients with treatment resistant depression: results of the CoBalT randomised controlled trial

机译:认知行为疗法作为基础药物治疗耐药性抑郁症患者药物治疗的辅助手段:CoBalT随机对照试验的结果

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Background Only a third of patients with depression respond fully to antidepressant medication but little evidence exists regarding the best next-step treatment for those whose symptoms are treatment resistant. The CoBalT trial aimed to examine the effectiveness of cognitive behavioural therapy (CBT) as an adjunct to usual care (including pharmacotherapy) for primary care patients with treatment resistant depression compared with usual care alone.Methods This two parallel-group multicentre randomised controlled trial recruited 469 patients aged 18-75 years with treatment resistant depression (on antidepressants for >6 weeks, Beck depression inventory [BDI] score >14 and international classification of diseases [ICDJ-10 criteria for depression) from 73 UK general practices. Participants were randomised, with a computer generated code (stratified by centre and minimised according to baseline BDI score, whether the general practice had a counsellor, previous treatment with antidepressants, and duration of present episode of depression) to one of two groups: usual care or CBT in addition to usual care, and were followed up for 12 months. Because of the nature of the intervention it was not possible to mask participants, general practitioners, CBT therapists, or researchers to the treatment allocation. Analyses were by intention to treat. The primary outcome was response, defined as at least 50% reduction in depressive symptoms (BDI score) at 6 months compared with baseline. This trial is registered, ISRCTN38231611.Findings Between Nov 4, 2008, and Sept 30, 2010, we assigned 235 patients to usual care, and 234 to CBT plus usual care. 422 participants (90%) were followed up at 6 months and 396 (84%) at 12 months, finishing on Oct 31, 2011. 95 participants (46%) in the intervention group met criteria for response at 6 months compared with 46 (22%) in the usual care group (odds ratio 3 ? 26, 95% CI 2 ? 10-5 ? 06, p<0 ? 001).Interpretation Before this study, no evidence from large-scale randomised controlled trials was available for the effectiveness of augmentation of antidepressant medication with CBT as a next-step for patients whose depression has not responded to pharmacotherapy. Our study has provided robust evidence that CBT as an adjunct to usual care that includes antidepressants is an effective treatment, reducing depressive symptoms in this population.Funding National Institute for Health Research Health Technology Assessment.
机译:背景技术只有三分之一的抑郁症患者对抗抑郁药完全反应,但是对于症状较难治疗的患者,最好的下一步治疗证据很少。 CoBalT试验旨在研究认知行为疗法(CBT)作为治疗顽固性抑郁症的初级护理患者与常规护理相比的常规护理(包括药物疗法)辅助疗法的有效性。方法这是两个平行组的多中心随机对照试验469例年龄在18-75岁的患有抗药性抑郁症的患者(抗抑郁药> 6周,贝克抑郁量表[BDI]得分> 14,国际疾病分类[ICDJ-10抑郁症标准])来自73个英国常规实践。将参与者随机分为两组:计算机生成的代码(按中心分层,并根据基线BDI分数最小化,根据惯例,是否有辅导员,以前接受过抗抑郁药治疗以及当前抑郁发作的持续时间),分为两组:常规护理除了常规护理外,还进行了CBT随访,随访时间为12个月。由于干预的性质,不可能掩盖参与者,全科医生,CBT治疗师或研究人员的治疗分配。分析是按意向进行的。主要结果是缓解,定义为与基线相比6个月时抑郁症状(BDI评分)降低至少50%。该试验的注册号为ISRCTN38231611。发现在2008年11月4日至2010年9月30日期间,我们为235名患者分配了常规护理,为234例CBT加常规护理。 422名参与者(90%)在6个月后得到了随访,而396名(84%)在12个月时得到了随访,于2011年10月31日结束。在干预组中,有95名参与者(46%)在6个月时达到了响应标准,而46名(常规护理组为22%(赔率3?26,95%CI 2?10-5?06,p <0?001)。解释在此研究之前,尚无大规模随机对照试验的证据可用于抑郁症对药物治疗无反应的患者,下一步使用CBT增强抗抑郁药的有效性。我们的研究提供了有力的证据,证明CBT可以作为包括抗抑郁药在内的常规护理的辅助手段,是一种有效的治疗方法,可以减轻该人群的抑郁症状。美国国立卫生研究院卫生技术评估基金会。

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