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Mesalazine granules 1.5 g once-daily maintain remission in patients with ulcerative colitis who switch from other 5-ASA formulations: A pooled analysis from two randomised controlled trials

机译:使用其他5-ASA制剂的溃疡性结肠炎患者每天服用美沙拉嗪颗粒1.5 g维持缓解:来自两项随机对照试验的汇总分析

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Background Mesalazine (mesalamine) granules (MG) were shown to be effective for the maintenance of remission of ulcerative colitis (UC) in two double-blind placebo-controlled trials. Aim To evaluate the efficacy of once-daily MG for maintenance of remission in patients with UC who switched from other 5-aminosalicylic acid (5-ASA) formulations. Methods Data from two independent multicenter, randomised, double-blind, placebo-controlled, 6-month trials evaluating patients with UC in remission were combined for analysis of a subpopulation of patients who switched from other 5-ASA formulations to MG 1.5 g or placebo upon randomisation. The primary endpoint was the percentage of patients who remained relapse-free at Month 6 or end of treatment. Relapse was defined as a Sutherland Disease Activity Index (SDAI) rectal bleeding score ≥1 and mucosal appearance score ≥2, a UC flare or medication used to treat a UC flare. Results Of the 487 patients who received 5-ASA maintenance therapy at enrolment, 322 were in the MG group and 165 were in the placebo group. The percentage of patients who remained relapse-free (based on Sutherland Disease Activity Index scores) after 6 months was significantly higher with MG than placebo (78.3% vs. 58.8%, P < 0.001). Rectal bleeding, stool frequency and the physician's rating of disease activity remained unchanged after 6 months in a higher percentage of patients using MG compared with those on placebo (P < 0.004 for each endpoint). Conclusion Mesalazine granules 1.5 g once-daily is effective for maintenance of remission in UC patients who switch from other 5-ASA formulations. identifiers NCT00744016, NCT00767728.
机译:背景在两项双盲安慰剂对照试验中,美沙拉嗪(美沙拉敏)颗粒(MG)被证明可有效维持溃疡性结肠炎(UC)缓解。目的评估每日一次MG对于从其他5-氨基水杨酸(5-ASA)制剂转用的UC患者维持缓解的疗效。方法结合来​​自两个独立的多中心,随机,双盲,安慰剂对照,为期6个月的评估UC缓解患者的试验数据,分析从其他5-ASA制剂转为MG 1.5 g或安慰剂的患者的亚群根据随机化。主要终点指标是在第6个月或治疗结束后保持无复发的患者百分比。复发定义为Sutherland疾病活动指数(SDAI)直肠出血评分≥1和粘膜外观评分≥2,UC耀斑或用于治疗UC耀斑的药物。结果入选5-ASA维持治疗的487例患者中,MG组322例,安慰剂组165例。 MG组6个月后仍无复发的患者百分比(基于Sutherland疾病活动指数评分)显着高于安慰剂组(分别为78.3%和58.8%,P <0.001)。与安慰剂组相比,使用MG的患者在6个月后的直肠出血,粪便频率和医师对疾病活动的评级保持不变(每个终点P <0.004)。结论美沙那嗪颗粒每天1.5 g可以有效维持从其他5-ASA制剂转用的UC患者的缓解。标识符NCT00744016,NCT00767728。

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