首页> 外文期刊>JAMA: the Journal of the American Medical Association >Delivery of evidence-based treatment for multiple anxiety disorders in primary care: a randomized controlled trial.
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Delivery of evidence-based treatment for multiple anxiety disorders in primary care: a randomized controlled trial.

机译:为初级保健中的多种焦虑症提供循证治疗:一项随机对照试验。

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CONTEXT: Improving the quality of mental health care requires moving clinical interventions from controlled research settings into real-world practice settings. Although such advances have been made for depression, little work has been performed for anxiety disorders. OBJECTIVE: To determine whether a flexible treatment-delivery model for multiple primary care anxiety disorders (panic, generalized anxiety, social anxiety, and posttraumatic stress disorders) would be better than usual care (UC). DESIGN, SETTING, AND PATIENTS: A randomized controlled effectiveness trial of Coordinated Anxiety Learning and Management (CALM) compared with UC in 17 primary care clinics in 4 US cities. Between June 2006 and April 2008, 1004 patients with anxiety disorders (with or without major depression), aged 18 to 75 years, English- or Spanish-speaking, were enrolled and subsequently received treatment for 3 to 12 months. Blinded follow-up assessments at 6, 12, and 18 months after baseline were completed in October 2009. INTERVENTION: CALM allowed choice of cognitive behavioral therapy (CBT), medication, or both; included real-time Web-based outcomes monitoring to optimize treatment decisions; and a computer-assisted program to optimize delivery of CBT by nonexpert care managers who also assisted primary care clinicians in promoting adherence and optimizing medications. MAIN OUTCOME MEASURES: Twelve-item Brief Symptom Inventory (BSI-12) anxiety and somatic symptoms score. Secondary outcomes included proportion of responders (> or = 50% reduction from pretreatment BSI-12 score) and remitters (total BSI-12 score < 6). RESULTS: A significantly greater improvement for CALM vs UC in global anxiety symptoms was found (BSI-12 group mean differences of -2.49 [95% confidence interval {CI}, -3.59 to -1.40], -2.63 [95% CI, -3.73 to -1.54], and -1.63 [95% CI, -2.73 to -0.53] at 6, 12, and 18 months, respectively). At 12 months, response and remission rates (CALM vs UC) were 63.66% (95% CI, 58.95%-68.37%) vs 44.68% (95% CI, 39.76%-49.59%), and 51.49% (95% CI, 46.60%-56.38%) vs 33.28% (95% CI, 28.62%-37.93%), with a number needed to treat of 5.27 (95% CI, 4.18-7.13) for response and 5.50 (95% CI, 4.32-7.55) for remission. CONCLUSION: For patients with anxiety disorders treated in primary care clinics, CALM compared with UC resulted in greater improvement in anxiety symptoms, depression symptoms, functional disability, and quality of care during 18 months of follow-up. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT00347269.
机译:背景:提高精神卫生保健的质量需要将临床干预措施从受控的研究环境转移到现实的实践环境中。尽管对于抑郁症已经取得了这样的进步,但是对于焦虑症几乎没有进行任何工作。目的:确定针对多种初级保健焦虑症(恐慌症,全身性焦虑症,社交焦虑症和创伤后应激障碍)的灵活治疗分娩模型是否比常规护理(UC)更好。设计,地点和患者:在美国4个城市的17家初级护理诊所中,进行了一项协调性焦虑学习与管理(CALM)与UC对比的随机对照有效性试验。在2006年6月至2008年4月之间,招募了1004名年龄在18至75岁,讲英语或西班牙语的焦虑症患者(有或没有严重抑郁),并接受了3到12个月的治疗。在基线于2009年10月完成后的第6、12和18个月,进行了盲人随访评估。干预:CALM允许选择认知行为疗法(CBT),药物或两者兼而有之。包括基于网络的实时结果监测,以优化治疗决策;以及一个计算机辅助程序,以优化非专家护理经理的CBT递送,他们还协助初级保健临床医生促进依从性和优化药物治疗。主要观察指标:十二项简短症状量表(BSI-12)焦虑和躯体症状评分。次要结果包括缓解者的比例(比治疗前BSI-12评分降低>或= 50%)和缓解者(总BSI-12评分<6)。结果:发现CALM与UC在整体焦虑症状方面有显着改善(BSI-12组的平均差异为-2.49 [95%置信区间{CI},-3.59至-1.40],-2.63 [95%CI,- 3.73至-1.54]和-1.63 [95%CI,-2.73至-0.53]分别在6、12和18个月时)。在12个月时,缓解率(CALM vs UC)为63.66%(95%CI,58.95%-68.37%)对44.68%(95%CI,39.76%-49.59%)和51.49%(95%CI, 46.60%-56.38%)vs 33.28%(95%CI,28.62%-37.93%),需要治疗的数字为5.27(95%CI,4.18-7.13)和5.50(95%CI,4.32-7.55) )的缓解。结论:对于在初级保健诊所接受治疗的焦虑症患者,在随访的18个月中,CALM与UC相比可显着改善焦虑症状,抑郁症状,功能障碍和护理质量。试验注册:clinicaltrials.gov标识符:NCT00347269。

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