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苏格兰中部认知行为疗法临床试验的长期结果。

Long-term outcome of cognitive behaviour therapy clinical trials in central Scotland.

作者信息

Durham R C, Chambers J A, Power K G, Sharp D M, Macdonald R R, Major K A, Dow M Gt, Gumley A I

机构信息

Psychiatry and Behavioural Sciences, Division of Pathology and Neuroscience, University of Dundee, Scotland, UK.

出版信息

Health Technol Assess. 2005 Nov;9(42):1-174. doi: 10.3310/hta9420.

Abstract

OBJECTIVES

To establish the long-term outcome of participants in clinical trials of cognitive behaviour therapy (CBT) for anxiety disorders and psychosis, examining the effectiveness and cost-effectiveness associated with receiving CBT in comparison with alternative treatments.

DESIGN

An attempt was made to contact and interview all of the participants in eight randomised, controlled, clinical trials of CBT for anxiety disorders and two randomised, controlled, clinical trials of CBT for schizophrenia conducted between 1985 and 2001. Case note reviews of healthcare resources used in the 2 years prior to entering the trials and the 2 years prior to follow-up interview were undertaken.

SETTING

Mixed rural and urban settings in five localities in central Scotland. Anxiety disorder trials were conducted mainly in primary care and included three with generalised anxiety disorder, four with panic disorder and one with post-traumatic stress disorder (PTSD). The psychosis studies (one on relapse prevention and one with chronic disorder) were conducted in secondary care.

PARTICIPANTS

Of the 1071 entrants to the 10 studies, 489 agreed to participate (46% of original entrants, 52% of those available to contact).

INTERVENTIONS

Follow-up interviews took place between 1999 and 2003, 2-14 years after the original treatment. Interviews for Trials 1-8 were conducted by a research psychologist blind to original treatment condition. Interviews for Trials 9 and 10 were conducted by community psychiatric nurses also blind to treatment condition. Case note reviews were completed following the interview.

MAIN OUTCOME MEASURES

For Trials 1-8 the main interview-based outcome measures were: Anxiety Disorders Interview Schedule-DSM-IV for diagnosis and co-morbidity, Clinical Global Severity (0-8) and the Hamilton Anxiety Rating Scale. The main patient-rated measures were: Brief Symptom Inventory, SF-36 II, Clinical Global Improvement (1-7), and the Positive and Negative Affect Scale. For Trials 9 and 10 the primary outcome measure was the interview-based Positive and Negative Syndrome Scale (PANSS).

RESULTS

For the anxiety disorder studies (Trials 1-8), over half of the participants (52%) had at least one diagnosis at long-term follow-up, with significant levels of co-morbidity and health status scores comparable to the lowest 10% of the general population. Only 36% reported receiving no interim treatment for anxiety over the follow-up period with 19% receiving almost constant treatment. Patients with PTSD did particularly poorly. There was a 40% real increase in healthcare costs over the two time periods, mainly due to an increase in prescribing. A close relationship was found between poor mental and physical health for those with a chronic anxiety disorder. Treatment with CBT was associated with a better long-term outcome than non-CBT in terms of overall symptom severity but not with regard to diagnostic status. The positive effects of CBT found in the original trials were eroded over longer time periods. No evidence was found for an association between more intensive therapy and more enduring effects of CBT. Long-term outcome was found to be most strongly predicted by the complexity and severity of presenting problems at the time of referral, by completion of treatment irrespective of modality and by the amount of interim treatment during the follow-up period. The quality of the therapeutic alliance, measured in two of the studies, was not related to long-term outcome but was related to short-term outcome. The cost-effectiveness analysis showed no advantages of CBT over non-CBT. The cost of providing CBT in the original trials was only a very small proportion (6.4%) of the overall costs of healthcare for this population, which are high for both physical and mental health problems. In the psychosis studies (Trials 9 and 10), outcome was generally poor with only 10% achieving a 25% reduction in total PANSS scores from pretreatment to long-term follow-up, also cost-effectiveness analysis showed no advantages of CBT over non-CBT, although healthcare costs fell over the two time periods mainly owing to a reduction in inpatient costs.

CONCLUSIONS

Psychological therapy services need to recognise that anxiety disorders tend to follow a chronic course and that good outcomes with CBT over the short term are no guarantee of good outcomes over the longer term. Clinicians who go beyond standard treatment protocols of about 10 sessions over a 6-month period are unlikely to bring about greater improvement. Poor outcomes over the long term are related to greater complexity and severity of presenting problems at the time of referral, failure to complete treatment irrespective of modality and the amount of interim treatment during the follow-up period. The relative gains of CBT are greater in anxiety disorders than in psychosis. Longitudinal research designs over extended periods of time (2-5 years), with large numbers of participants (500+), are required to investigate the relative importance of patient characteristics, therapeutic alliance and therapist expertise in determining the cost-effectiveness of CBT in the longer term.

摘要

目的

确定焦虑症和精神病认知行为疗法(CBT)临床试验参与者的长期预后,研究与接受CBT相比,其他替代治疗的有效性和成本效益。

设计

试图联系并访谈1985年至2001年间进行的八项焦虑症CBT随机对照临床试验以及两项精神分裂症CBT随机对照临床试验的所有参与者。对进入试验前2年和随访访谈前2年使用的医疗资源进行病例记录回顾。

地点

苏格兰中部五个地区的城乡混合环境。焦虑症试验主要在初级保健机构进行,包括三项广泛性焦虑症试验、四项惊恐障碍试验和一项创伤后应激障碍(PTSD)试验。精神病研究(一项预防复发研究和一项慢性疾病研究)在二级保健机构进行。

参与者

10项研究的1071名参与者中,489人同意参与(占原始参与者的46%,可联系参与者的52%)。

干预措施

随访访谈在1999年至2003年进行,即原始治疗后2至14年。试验1 - 8的访谈由对原始治疗情况不知情的研究心理学家进行。试验9和10的访谈由同样对治疗情况不知情的社区精神科护士进行。访谈后完成病例记录回顾。

主要结局指标

试验1 - 8基于访谈的主要结局指标为:用于诊断和共病的《焦虑症访谈量表 - DSM - IV》、临床总体严重程度(0 - 8)和汉密尔顿焦虑量表。主要的患者自评指标为:简明症状量表、SF - 36 II、临床总体改善情况(1 - 7)以及正负性情绪量表。试验9和10的主要结局指标是基于访谈的阳性和阴性症状量表(PANSS)。

结果

对于焦虑症研究(试验1 - 8),超过一半的参与者(52%)在长期随访中有至少一种诊断,共病水平显著,健康状况得分与普通人群中最低的10%相当。只有36%的参与者报告在随访期间未接受焦虑症的临时治疗,19%的参与者几乎持续接受治疗。PTSD患者的情况尤其不佳。两个时间段内医疗保健成本实际增加了40%,主要是由于处方量增加。发现慢性焦虑症患者的身心健康状况不佳之间存在密切关系。就总体症状严重程度而言,CBT治疗的长期预后优于非CBT治疗,但在诊断状况方面并非如此。原始试验中发现的CBT的积极效果在更长时间段内逐渐减弱。没有证据表明强化治疗与CBT更持久的效果之间存在关联。发现长期预后最强烈地由转诊时呈现问题的复杂性和严重程度、无论治疗方式如何的治疗完成情况以及随访期间的临时治疗量所预测。两项研究中测量的治疗联盟质量与长期预后无关,但与短期预后有关。成本效益分析显示CBT相对于非CBT没有优势。原始试验中提供CBT的成本仅占该人群总体医疗保健成本的极小比例(6.4%),该人群的身心健康问题成本都很高。在精神病研究(试验9和10)中,预后总体较差,只有10%的参与者从治疗前到长期随访时PANSS总分降低了25%,成本效益分析也显示CBT相对于非CBT没有优势,尽管两个时间段内医疗保健成本下降,主要是由于住院成本降低。

结论

心理治疗服务需要认识到焦虑症往往呈慢性病程,短期内CBT取得良好效果并不能保证长期也有良好效果。超出约6个月10次标准治疗方案的临床医生不太可能带来更大改善。长期预后不佳与转诊时呈现问题的更大复杂性和严重程度、无论治疗方式如何未完成治疗以及随访期间的临时治疗量有关。CBT在焦虑症中的相对获益大于精神病。需要进行长时间(2 - 5年)、大量参与者(500人以上)的纵向研究设计,以调查患者特征、治疗联盟和治疗师专业知识在长期确定CBT成本效益方面的相对重要性。

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