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柳氮磺胺吡啶治疗溃疡性结肠炎的长期疗效及安全性观察

Long-term efficacy and safety of azathioprine in ulcerative colitis.

出版信息

J Crohns Colitis. 2015 Feb;9(2):191-7. doi: 10.1093/ecco-jcc/jju010.

DOI:10.1093/ecco-jcc/jju010
PMID:25518053
Abstract

BACKGROUND AND AIMS

Azathioprine (AZA) is an established treatment for ulcerative colitis (UC).However, controversy exists regarding its efficacy in inducing and maintaining clinical remission, and long-term data are lacking. We studied the effectiveness of AZA in a large cohort of UC patients treated in a single center.

METHODS

All UC patients treated with AZA were identified from a prospective electronic database. We assessed response to therapy at 4 months and sustained clinical benefit at the last point of follow-up. We also examined predictors of response and sustained clinical benefit, as well as outcomes in those treated with AZA for >5 years.

RESULTS

The study included 255 patients. At 4 months, 207 (81.2%) of 255 patients were still on AZA and 163 (63.9%) had responded to therapy. At the last point of follow-up 164 (64.3%) patients were still receiving AZA, of whom 154 (60.4%) achieved sustained clinical benefit. This effect was durable among 71 patients who received AZA for >5 years, with 61 (85.9%) considered to have achieved sustained clinical benefit. Twenty-six patients required admission to hospital for an exacerbation during AZA treatment, 20 patients ultimately required biologic therapy, and 21 underwent colectomy. Only two (2.8%) of 71 patients receiving AZA for >5 years needed to escalate to a biologic therapy, and only one (1.4%) required a colectomy.

CONCLUSIONS

AZA is a safe and effective therapy in UC patients who fail 5-aminosalisylates in both the short and long term. Escalation to a biologic therapy or colectomy was unlikely among patients who were able to continue AZA therapy beyond 5 years.

摘要

背景与目的

巯嘌呤(AZA)是溃疡性结肠炎(UC)的既定治疗方法。然而,其在诱导和维持临床缓解方面的疗效存在争议,且缺乏长期数据。我们在单中心治疗的 UC 患者大队列中研究了 AZA 的疗效。

方法

从前瞻性电子数据库中确定接受 AZA 治疗的所有 UC 患者。我们评估了 4 个月时的治疗反应和最后一次随访时的持续临床获益。我们还检查了反应和持续临床获益的预测因素,以及接受 AZA 治疗>5 年的患者的结局。

结果

该研究纳入了 255 例患者。在 4 个月时,255 例患者中有 207 例(81.2%)仍在接受 AZA 治疗,163 例(63.9%)对治疗有反应。在最后一次随访时,164 例(64.3%)患者仍在接受 AZA 治疗,其中 154 例(60.4%)达到持续临床缓解。在接受 AZA 治疗>5 年的 71 例患者中,这一效果是持久的,其中 61 例(85.9%)被认为达到了持续临床缓解。26 例患者在 AZA 治疗期间因病情加重需要住院治疗,20 例患者最终需要接受生物治疗,21 例患者接受了结肠切除术。在接受 AZA 治疗>5 年的 71 例患者中,只有 2 例(2.8%)需要升级为生物治疗,只有 1 例(1.4%)需要结肠切除术。

结论

AZA 是对 5-氨基水杨酸治疗失败的 UC 患者的一种安全有效的治疗方法,无论是短期还是长期。对于能够继续接受 AZA 治疗>5 年的患者,升级为生物治疗或结肠切除术的可能性不大。

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