Systematic review: treatment pattern and clinical effectiveness and safety of pharmaceutical therapies for Crohn’s disease in Europe

IF 2.3 Q2 GASTROENTEROLOGY & HEPATOLOGY Clinical and Experimental Gastroenterology Pub Date : 2016-10-05 DOI:10.2147/CEG.S109696
F. Lelli, S. Nuhoho, X. Y. Lee, Weiwei Xu
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引用次数: 6

Abstract

Background Although many clinical trials have been conducted in treatments of Crohn’s disease (CD), whether the trial results were representative of daily practice needs to be supported by studies conducted in real-world settings. Aim This study aims to identify how CD is treated and what are the clinical effectiveness and safety of the pharmaceutical therapies of CD in real-world settings. Methods A systematic literature review was conducted based on Medline®, Embase®, and Cochrane. All publications were assessed for title/abstract and full-text according to a predefined study protocol. Data were extracted and reported. Results A total of 1,998 publications were identified. Fifty studies including six publications reporting treatment pattern and 44 studies reporting clinical effectiveness and safety of pharmaceutical therapies in CD management in Europe were included. 5-Aminosalicylic acid and corticosteroids were reported to be used among 14%–74% of CD patients. Immunomodulators were used by 14%–25% and 29%–31% of CD patients as an initial and follow-up treatment, respectively. Biological therapies were used by 25%–33% of CD patients. A trend toward an increasing use of immunomodulators and biological therapies in Europe has been reported in recent years. Approximately 50% of patients achieved remission on immunomodulator or biologic treatment, although a relapse rate of up to 23% has been reported. Conclusion There is a trend of treatment shift to immunomodulators and biologics in CD management. Clinical effectiveness of immunomodulators and biologics has been demonstrated, though with a lack of sustainability of the effectiveness.
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系统评价:欧洲克罗恩病药物治疗的治疗模式、临床有效性和安全性
虽然在克罗恩病(CD)治疗方面进行了许多临床试验,但试验结果是否能代表日常实践,还需要在现实环境中进行的研究来支持。目的本研究旨在确定在现实世界中如何治疗乳糜泻,以及乳糜泻药物治疗的临床有效性和安全性。方法基于Medline®、Embase®和Cochrane进行系统文献综述。根据预先确定的研究方案,对所有出版物的标题/摘要和全文进行评估。提取并报告数据。结果共检索到1998篇文献。纳入了50项研究,包括6篇报告治疗模式的出版物和44项报告药物治疗在欧洲乳糜泻管理中的临床有效性和安全性的研究。据报道,14%-74%的CD患者使用5-氨基水杨酸和皮质类固醇。分别有14%-25%和29%-31%的乳糜泻患者使用免疫调节剂作为初始和随访治疗。25%-33%的乳糜泻患者使用生物疗法。近年来,欧洲有越来越多地使用免疫调节剂和生物疗法的趋势。大约50%的患者通过免疫调节剂或生物治疗获得缓解,尽管据报道复发率高达23%。结论CD治疗有向免疫调节剂和生物制剂转移的趋势。免疫调节剂和生物制剂的临床有效性已得到证实,但其有效性缺乏可持续性。
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来源期刊
Clinical and Experimental Gastroenterology
Clinical and Experimental Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
5.10
自引率
0.00%
发文量
26
审稿时长
16 weeks
期刊最新文献
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