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Systematic review: The placebo effect of psychological interventions in the treatment of irritable bowel syndrome

机译:系统评价:心理干预对肠易激综合征的安慰剂作用

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AIM To determine the placebo response rate associated with different types of placebo interventions used in psychological intervention studies for irritable bowel syndrome. METHODS Randomized controlled trials comparing psychological interventions (stress management/relaxation therapy (cognitive) behavioral therapy, short-term psychodynamic therapy, and hypnotherapy) for the treatment of adult patients with irritable bowel syndrome (IBS) diagnosed with the Manning or Rome criteria with an adequate placebo control treatment and reporting data on IBS symptom severity were identified by searching PubMed, Embase, the Cochrane Library, CINAHL and PsycINFO databases. Full-text articles that were written in English and published between 1966 and February 2016 in peer-reviewed journals were selected for the present review. Placebo interventions were considered to be adequate if the number of sessions and the amount of time spent with the therapist were the same as in the active treatment. The placebo response rate (PRR) was computed for IBS symptom severity (primary outcome measure) as well as for anxiety, depression and quality of life (secondary outcome measures). RESULTS Six studies, with a total of 555 patients met the inclusion criteria. Four studies used an educational intervention, whereas two studies used a form of supportive therapy as the placebo intervention. The PRR for IBS symptom severity ranged from 25% to 59%, with a pooled mean of 41.4%. The relative PRR for the secondary outcome measures ranged from 0% to 267% for anxiety, 6% to 52% for depression 20% to 125% for quality of life. The PRR associated with pharmacological treatments, treatment with dietary bran and complementary medicine ranged from 37.5% to 47%. Contrary to our expectations, the PRR in studies on psychological interventions was comparable to that in studies on pharmacological, dietary and alternative medical interventions. CONCLUSION The PRR is probably determined to a larger extent by patient-related factors, such as expectations and desire for the treatment to be effective, than the content of the placebo intervention.
机译:目的确定用于肠易激综合征的心理干预研究中与不同类型的安慰剂干预措施相关的安慰剂缓解率。方法随机对照试验比较心理干预(压力管理/放松疗法(认知)行为疗法,短期心理动力疗法和催眠疗法)用于治疗以曼宁或罗马标准诊断为肠易激综合征(IBS)的成年患者,通过搜索PubMed,Embase,Cochrane库,CINAHL和PsycINFO数据库,可以确定适当的安慰剂对照治疗和有关IBS症状严重程度的报告数据。本文以英语撰写的全文文章发表于1966年至2016年2月之间,并在同行评审期刊上发表。如果治疗师的治疗次数和所花费的时间与积极治疗中的相同,则认为安慰剂干预是足够的。计算IBS症状严重程度(主要结局指标)以及焦虑,抑郁和生活质量(第二结局指标)的安慰剂反应率(PRR)。结果六项研究共555名患者符合入选标准。四项研究使用了教育干预措施,而两项研究使用了一种支持疗法作为安慰剂干预措施。 IBS症状严重程度的PRR为25%至59%,合并平均值为41.4%。二级结局指标的相对PRR为0%至267%(焦虑),6%至52%(抑郁),20%至125%(生活质量)。与药理治疗,饮食麸皮和辅助药物治疗相关的PRR为37.5%至47%。与我们的预期相反,心理干预研究中的PRR与药理,饮食和替代医学干预研究中的PRR相当。结论与安慰剂干预的内容相比,PRR可能在更大程度上取决于患者相关因素,例如对治疗有效的期望和期望。

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