美沙拉明治疗克罗恩病患儿的自然病史

Denise D. Young, Sharon Perry, Sindhoosha Malay, Thomas J. Sferra, Michael Finkler, Jonathan Moses
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摘要

背景:5-氨基水杨酸盐(5-ASA)用于治疗轻至中度溃疡性结肠炎。尽管它们在克罗恩病(CD)中缺乏疗效,但它们仍然在现实世界的实践中使用。此外,当患者病情进展时,他们可能会升级到生物治疗,这时5-ASA可能会或可能不会停药。目的:本研究的目的是评估开始使用5-ASA治疗儿科CD的患者的临床结果。次要目的是评估那些继续使用5-ASA的患者和那些在生物升级后停止使用5-ASA的患者的结果。方法:我们对2010年至2019年最初接受5-ASA治疗的儿科CD患者进行了单中心回顾性图表回顾。收集了人口统计、药物和实验室数据以及临床疾病活动。结果:61例患者纳入研究;多数为炎性乳糜泻并累及回肠结肠。24例患者同时服用免疫调节剂。大多数患者(85.2%)需要升级到生物制剂。32例(61.5%)升级到生物治疗的患者继续使用5-ASA。80%的患者在1年后达到临床缓解,在生物开始时继续使用5-ASA的患者与未继续使用药物的患者之间没有差异。停用5-ASA的患者平均每年节省费用6741美元。结论:5-ASA不是治疗儿童CD的持久单一疗法。需要从5-ASA升级到生物治疗的患者并不能从伴随的5-ASA治疗中获益。需要进一步的前瞻性研究来证实这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural History of Pediatric Patients With Crohn’s Disease Treated With Mesalamine Therapy
Background: 5-aminosalicylates (5-ASA) are used to treat mild to moderate ulcerative colitis. Despite their lack of efficacy in Crohn disease (CD), they are still used in real-world practice. Additionally, when patients have progressive disease, they may escalate to biologic therapy, at which time 5-ASA may or may not be discontinued. Objectives: The aim of this study is to assess the clinical outcomes of patients started on 5-ASA for the treatment of pediatric CD. The secondary aims were to evaluate the outcomes of those who continue 5-ASA to those who discontinue 5-ASA upon biologic escalation. Methods: We performed a single-center retrospective chart review of pediatric CD patients from 2010 to 2019 who were initially treated with 5-ASA. Demographics, medication and laboratory data, and clinical disease activity were collected. Results: Sixty-one patients were included in the study; the majority had inflammatory CD with ileocolonic involvement. Twenty-four patients were on a concomitant immunomodulator. The majority of patients (85.2%) required escalation to biologics. Thirty-two patients (61.5%) who escalated to biologic therapy continued on 5-ASA. Eighty percent of patients achieved clinical remission at 1 year, and there was no difference between those who continued 5-ASA at time of biologic initiation compared to those who did not continue the medication. Patients who discontinued 5-ASA had an average annual cost savings of $6741. Conclusion: 5-ASA is not a durable monotherapy for the treatment of pediatric CD. Patients who require escalation from 5-ASA to biologic therapy do not benefit from concomitant 5-ASA therapy. Further prospective studies are needed to confirm these findings.
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