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用二丙酸倍氯米松或美沙拉嗪局部治疗远端活动性溃疡性结肠炎:一项单盲随机对照试验。

Topical treatment of distal active ulcerative colitis with beclomethasone dipropionate or mesalamine: a single-blind randomized controlled trial.

作者信息

Gionchetti Paolo, D'Arienzo Agesilao, Rizzello Fernando, Manguso Francesco, Maieron Roberto, Lecis Pier Enrico, Valpiani Daniela, Iaquinto Gaetano, Annese Vito, Balzano Antonio, Varoli Guido, Campieri Massimo

机构信息

Institute of Clinical Medicine, S. Orsola-Malpighi Hospital, University of Bologna, Italy.

出版信息

J Clin Gastroenterol. 2005 Apr;39(4):291-7. doi: 10.1097/01.mcg.0000155124.74548.61.

Abstract

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.

摘要

目标

活动性溃疡性结肠炎(UC)的治疗通常涉及使用皮质类固醇(CS)的直肠制剂,其特点是存在与全身类固醇相关的不良反应风险。

背景

比较局部作用的CS二丙酸倍氯米松(BDP)与美沙拉嗪(5-ASA)治疗活动性UC的疗效和安全性。

研究

在一项单盲、多中心、平行组对照研究中,将轻度至中度远端活动性UC患者随机分为两组,一组接受为期6周的每日一次3 mg BDP灌肠治疗,另一组接受每日一次1 g 5-ASA灌肠治疗。主要疗效变量为疾病活动指数(DAI)评分的降低。安全性变量包括肾上腺功能、不良事件监测、生命体征和实验室参数。

结果

共有217例患者入组并接受BDP(n = 111)或5-ASA(n = 106)治疗。两个治疗组的DAI评分均显著降低(P < 0.05),BDP组的临床缓解率为36.7%,5-ASA组为29.2%。两种治疗的耐受性均良好。BDP组早晨皮质醇水平与基线相比无变化。

结论

在为期6周的治疗期间,以直肠灌肠方式给予BDP对活动性UC患者有效且安全,不影响垂体肾上腺轴。

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