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A randomized controlled trial of imipramine in patients with irritable bowel syndrome

查看全文 作  者:Heitham Abdul-[1]Baki;Ihab I El [1]Hajj;Lara [1]ElZahabi;Cecilio [1]Azar;Elie [1]Aoun;Assaad [1]Skoury;Hani [1]Chaar;Ala I [1]Sharara 高影响力作者 机构地区:[1]Department of Internal Medicine, Division of Gastroenterology, American University of Beirut Medical Center, Riad El Solh 110 72020, Beirut, Lebanon高影响力机构 出  处:《World Journal of Gastroenterology》索引2009年第15卷第29期,共7页高影响力期刊 基  金:Supported by A Private Research Fund From the Division of Gastroenterology at the American University of Beirut Medical Center, Beirut, Lebanon 摘  要:AIM: To study the efficacy of low-dose imipramine in relieving symptoms associated with the irritable bowel syndrome (IBS). METHODS: A randomized, double-blind trial of 25 mg imipramine vs matched placebo for 12 wk was performed. Doubling the dose was allowed once at week 2 in case of an unsatisfactory early response. Primary efficacy variables were subjective global symptom relief and quality of life (QoL) using SF-36 at week 12. RESULTS: One hundred and seven patients were enrolled by advertisement or referral by general practitioners and 56 (31 imipramine: 25 placebo) completed the 16-wk study. Baseline characteristics were comparable. A high overall dropout rate was noted in the imipramine and placebo arms (47.5% vs 47.9%, P > 0.05), a mean of 25.0 and 37.4 d from enrollment, respectively (P < 0.05). At the end of 12 wk, there was a significant difference in global symptom relief with imipramine over placebo (per-protocol: 80.6% vs48.0%, P = 0.01) and a trend on intent-to-treat (ITT) analysis (42.4% vs 25.0%, P = 0.06). This improvement was evident early and persisted to week 16 (P = 0.024 and 0.053 by per-protocol and ITT analyses, respectively). Mean cumulative and componentspecific SF-36 scores improved in the imipramine group only (per-protocol, P < 0.01). Drug-related adverse events leading to patient dropout were more common in the imipramine group (25.4% vs 12.5%, P > 0.05). CONCLUSION: Imipramine may be effective in the treatment of IBS patients and is associated with improved QoL. Careful patient selection, initiation of a low dose with gradual escalation and monitoring for side effects may result in an improved therapeutic response. 关 键 词:对照试验 综合征 患者 随机
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