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首页> 外文期刊>Journal of clinical gastroenterology >Topical treatment of distal active ulcerative colitis with beclomethasone dipropionate or mesalamine: a single-blind randomized controlled trial.
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Topical treatment of distal active ulcerative colitis with beclomethasone dipropionate or mesalamine: a single-blind randomized controlled trial.

机译:倍氯米松双丙酸酯或美沙拉敏局部治疗远端活动性溃疡性结肠炎:单盲随机对照试验。

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摘要

GOALS: Therapy for active ulcerative colitis (UC) usually involves rectal formulations of corticosteroids (CS), which are characterized by the risk of systemic steroid-related adverse effects. BACKGROUND: To compare the efficacy and safety of the topically acting CS beclomethasone dipropionate (BDP) versus mesalamine (5-ASA) in the treatment of active UC. STUDY: Patients with mild to moderate distal active UC were randomized to a 6-week treatment with BDP 3 mg enema o.d. or 5-ASA 1 g enema daily in a single-blind, multicenter, parallel-group, controlled study. The primary efficacy variable was the decrease in Disease Activity Index (DAI) score. Safety variables were adrenal function, monitoring of adverse events, vital signs, and laboratory parameters. RESULTS: A total of 217 patients were enrolled and treated with BDP (n = 111) or 5-ASA (n = 106). A significant decrease in the DAI score (P < 0.05) was observed in both treatment groups, with a clinical remission rate of 36.7% in the BDP group and of 29.2% in the 5-ASA group. Both treatments were well tolerated. No changes from baseline in morning cortisol levels were observed in the BDP group. CONCLUSIONS: BDP administered as a rectal enema over a 6-week treatment period was efficacious and safe in patients with active UC, without interference with pituitary adrenal axis.
机译:目标:活动性溃疡性结肠炎(UC)的治疗通常涉及皮质类固醇(CS)的直肠制剂,其特征在于存在与全身性类固醇相关的不良反应的风险。背景:为了比较局部作用的CS倍氯米松二丙酸酯(BDP)与美沙拉敏(5-ASA)在活动性UC中的疗效和安全性。研究:轻度至中度远端活动性UC患者被随机分配接受3个月BDP灌肠治疗6周。或单盲,多中心,平行组,对照研究中的每日5-ASA 1 g灌肠。主要功效变量是疾病活动指数(DAI)得分的降低。安全变量是肾上腺功能,不良事件监测,生命体征和实验室参数。结果:共有217名患者入组并接受BDP(n = 111)或5-ASA(n = 106)治疗。在两个治疗组中均观察到DAI评分显着降低(P <0.05),BDP组的临床缓解率为36.7%,而5-ASA组的临床缓解率为29.2%。两种治疗均耐受良好。 BDP组未观察到早晨皮质醇水平相对于基线的变化。结论:在活动性UC患者中,BDP在6周的治疗期内作为直肠灌肠剂有效且安全,且不干扰垂体肾上腺轴。

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