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首页> 外文期刊>Psychosomatic Medicine: Journal of the American Psychosomatic Society >Efficacy, tolerability, and safety of hypnosis in adult irritable bowel syndrome: Systematic review and meta-analysis
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Efficacy, tolerability, and safety of hypnosis in adult irritable bowel syndrome: Systematic review and meta-analysis

机译:催眠治疗成人肠易激综合征的功效,耐受性和安全性:系统评价和荟萃分析

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摘要

OBJECTIVE: To assess the efficacy, tolerability, and safety of hypnosis in adult irritable bowel syndrome by a meta-analysis of randomized controlled trials. METHODS: Studies were identified by a literature search of the databases Allied and Complementary Medicine Database, Central Register of Controlled Trials, Cumulative Index to Nursing and Allied Health Literature, PubMed, PsycINFO, and Scopus (from inception to June 30, 2013). Primary outcomes were adequate symptom relief, global gastrointestinal score, and safety. Summary relative risks (RRs) with number needed to treat (NNT) and standardized mean differences (SMDs) with 95% confidence intervals (95% CIs) were calculated using random-effects models. RESULTS: Eight randomized controlled trials with a total of 464 patients and a median of 8.5 (7-12) hypnosis sessions over a median of 12 (5-12) weeks were included into the analysis. At the end of therapy, hypnosis was superior to control conditions in producing adequate symptom relief (RR, 1.69 [95% CI = 1.14-2.51]; NNT, 5 [3-10]) and in reducing global gastrointestinal score (SMD, 0.32 [95% CI =-0.56 to-0.08]). At long-term follow-up, hypnosis was superior to controls in adequate symptom relief (RR, 2.17 [95% CI = 1.22-3.87]; NNT, 3 [2-10]), but not in reducing global gastrointestinal score (SMD,-0.57 [-1.40 to 0.26]). One (0.4%) of 238 patients in the hypnosis group dropped out due to an adverse event (panic attack). CONCLUSION: This meta-analysis demonstrated that hypnosis was safe and provided long-term adequate symptom relief in 54% of patients with irritable bowel syndrome refractory to conventional therapy.
机译:目的:通过对随机对照试验的荟萃分析,评估催眠术对成人肠易激综合征的疗效,耐受性和安全性。方法:通过文献检索,对相关和补充医学数据库,对照试验中心登记册,护理和相关健康文献累积索引,PubMed,PsycINFO和Scopus(从成立到2013年6月30日)进行文献检索。主要结果是症状缓解,胃肠道总体评分和安全性。使用随机效应模型计算了具有95%置信区间(95%CI)的需要治疗的数量(NNT)和标准均数差(SMD)的摘要相对风险(RRs)。结果:八项随机对照试验共纳入464例患者,中位数为12(5-12)周,平均催眠时间为8.5(7-12)次。在治疗结束时,催眠在产生足够的症状缓解(RR,1.69 [95%CI = 1.14-2.51]; NNT,5 [3-10])和降低总体胃肠道评分(SMD,0.32)方面优于对照条件。 [95%CI = -0.56至-0.08]。在长期随访中,催眠在缓解症状方面优于对照组(RR,2.17 [95%CI = 1.22-3.87]; NNT,3 [2-10]),但在降低总体胃肠道得分(SMD)方面没有,-0.57 [-1.40至0.26])。催眠组的238名患者中有1名(0.4%)由于不良事件(惊恐发作)而退学。结论:这项荟萃分析表明,对于传统疗法难以治疗的肠易激综合征的54%的患者,催眠是安全的,可以长期缓解症状。

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