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AGA 技术评论:中重度肠腔和肛旁瘘管型克罗恩病的医学管理

AGA Technical Review on the Medical Management of Moderate to Severe Luminal and Perianal Fistulizing Crohn's Disease.

机构信息

Division of Gastroenterology and Division of Biomedical Informatics, Department of Medicine, University of California, San Diego, La Jolla, California.

Division of Gastroenterology, Department of Medicine, Yale School of Medicine, New Haven, Connecticut.

出版信息

Gastroenterology. 2021 Jun;160(7):2512-2556.e9. doi: 10.1053/j.gastro.2021.04.023.

Abstract

The incidence and prevalence of Crohn's disease (CD) is rising globally. Patients with moderate to severe CD are at high risk for needing surgery and hospitalization and for developing disease-related complications, corticosteroid dependence, and serious infections. Optimal management of outpatients with moderate to severe luminal and/or fistulizing (including perianal) CD often requires the use of immunomodulator (thiopurines, methotrexate) and/or biologic therapies, including tumor necrosis factor-α antagonists, vedolizumab, or ustekinumab, either as monotherapy or in combination (with immunomodulators) to mitigate these risks. Decisions about optimal drug therapy in moderate to severe CD are complex, with limited guidance on comparative efficacy and safety of different treatments, leading to considerable practice variability. Since the last iteration of these guidelines published in 2013, significant advances have been made in the field, including the regulatory approval of 2 new biologic agents, vedolizumab and ustekinumab. Therefore, the American Gastroenterological Association prioritized updating clinical guidelines on this topic. To inform the clinical guidelines, this technical review was completed in accordance with the GRADE (Grading of Recommendations Assessment, Development and Evaluation) framework. The review addressed the following focused questions (in adult outpatients with moderate to severe luminal CD): overall and comparative efficacy of different medications for induction and maintenance of remission in patients with or without prior exposure to tumor necrosis factor-α antagonists, comparative efficacy and safety of biologic monotherapy vs combination therapy with immunomodulators, comparative efficacy of a top-down (upfront use of biologics and/or immunomodulator therapy) vs step-up treatment strategy (acceleration to biologic and/or immunomodulator therapy only after failure of mesalamine), and the role of corticosteroids and mesalamine for induction and/or maintenance of remission. Finally, in adult outpatients with moderate to severe fistulizing CD, this review addressed the efficacy of pharmacologic interventions for achieving fistula and the role of adjunctive antibiotics without clear evidence of active infection.

摘要

克罗恩病(CD)的发病率和患病率在全球范围内呈上升趋势。中重度 CD 患者有很高的手术和住院风险,并且有发展为与疾病相关的并发症、皮质类固醇依赖和严重感染的风险。中重度腔型和/或瘘管型(包括肛周)CD 患者的最佳门诊管理通常需要使用免疫调节剂(硫嘌呤、甲氨蝶呤)和/或生物疗法,包括肿瘤坏死因子-α拮抗剂、vedolizumab 或 ustekinumab,无论是单药治疗还是联合治疗(与免疫调节剂联合),以降低这些风险。中重度 CD 中最佳药物治疗的决策较为复杂,关于不同治疗方法的相对疗效和安全性的指导有限,导致实践差异较大。自 2013 年发表上一版指南以来,该领域取得了重大进展,包括 2 种新的生物制剂 vedolizumab 和 ustekinumab 的监管批准。因此,美国胃肠病学会优先更新了这一主题的临床指南。为了为临床指南提供信息,按照 GRADE(推荐评估、制定与评价)框架完成了这项技术审查。该审查针对以下重点问题(中重度腔型 CD 的成年门诊患者):不同药物用于诱导和维持缓解的总体和相对疗效,包括有和无肿瘤坏死因子-α拮抗剂暴露史的患者;生物单药治疗与免疫调节剂联合治疗的相对疗效和安全性;自上而下(优先使用生物制剂和/或免疫调节剂治疗)与逐步治疗策略(仅在柳氮磺胺吡啶治疗失败后加速使用生物制剂和/或免疫调节剂治疗)的相对疗效;以及皮质类固醇和柳氮磺胺吡啶在诱导和/或维持缓解中的作用。最后,在中重度瘘管型 CD 的成年门诊患者中,这项审查针对实现瘘管缓解的药物干预的疗效以及在无明确活动性感染证据的情况下辅助使用抗生素的作用。

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