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首页> 外文期刊>Alimentary pharmacology & therapeutics. >Review article: delivery and efficacy of topical 5-aminosalicylic acid (mesalazine) therapy in the treatment of ulcerative colitis.
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Review article: delivery and efficacy of topical 5-aminosalicylic acid (mesalazine) therapy in the treatment of ulcerative colitis.

机译:综述文章:局部5-氨基水杨酸(美沙拉嗪)治疗溃疡性结肠炎的疗效和递送。

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BACKGROUND: The use of topical therapy in the treatment of ulcerative colitis has declined in recent years despite evidence of good efficacy. AIMS: To review US prescription trends for 5-aminosalicylic acid (5-ASA) since the US approval of Asacol extended-release oral mesalazine (mesalamine) in 1992; to estimate the optimal level of 5-ASA exposure in the distal colon; to determine factors influencing distal colonic exposures; and to compare the effectiveness of different 5-ASA formulations (oral, topical suspension, foam, suppositories) in clinical trials. METHODS: Review of clinical trials, physiologic studies and prescription trends of various mesalazine formulations for treatment of distal ulcerative colitis. RESULTS: Between 1992 and 2009, prescriptions for oral mesalazine increased sixfold, whereas topical suspensions declined by 10%. In clinical trials, topical therapy resulted in higher remission and clinical response rates than oral therapy, with trends to earlier improvement. The mucosal concentrations of 5-ASA achieved by topical agents in the distal colon were up to 200-fold higher than those achieved by oral administration alone. Despite active colitis, over 40% of a topically administered 4 g 5-ASA suspension (equal to 1.6 g) reached the sigmoid colon. This likely represents a therapeutic exposure of 5-ASA. Although topical therapies are less convenient than oral medications, treatment algorithms have failed to take into account quality of life improvements resulting from more rapid and complete treatment response. CONCLUSIONS: Topical mesalazine therapy is superior to oral therapy in distal ulcerative colitis for both therapeutic response and drug delivery. Practice patterns should be re-evaluated in light of this information.
机译:背景:尽管有很好的疗效证据,近年来局部治疗溃疡性结肠炎的使用有所减少。目的:回顾自1992年美国批准Asacol缓释口服美沙拉嗪(美沙拉敏)以来,美国5-氨基水杨酸(5-ASA)的处方趋势;评估远端结肠中5-ASA暴露的最佳水平;确定影响远端结肠暴露的因素;并比较不同5-ASA制剂(口服,局部混悬剂,泡沫剂,栓剂)在临床试验中的有效性。方法:回顾了各种美沙拉嗪制剂治疗远端溃疡性结肠炎的临床试验,生理研究和处方趋势。结果:1992年至2009年间,口服美沙拉嗪的处方量增加了六倍,而局部混悬液的处方量下降了10%。在临床试验中,局部治疗比口服治疗可带来更高的缓解和临床反应率,并且有改善的趋势。通过局部药物在远端结肠中获得的5-ASA的粘膜浓度比仅口服给药所获得的粘膜浓度高200倍。尽管有活动性结肠炎,但超过40%的局部用药4 g 5-ASA悬浮液(相当于1.6 g)到达了乙状结肠。这可能代表5-ASA的治疗性暴露。尽管局部治疗不如口服药物方便,但治疗算法未能考虑到因更快,更全面的治疗反应而导致的生活质量改善。结论:局部美沙拉嗪治疗在远端溃疡性结肠炎中在治疗反应和药物输送方面均优于口服治疗。应根据此信息重新评估练习模式。

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