Evidence-based clinical practice guidelines for inflammatory bowel disease
- PMID: 29429045
- PMCID: PMC5847182
- DOI: 10.1007/s00535-018-1439-1
Evidence-based clinical practice guidelines for inflammatory bowel disease
Abstract
Inflammatory bowel disease (IBD) is a chronic disorder involving mainly the intestinal tract, but possibly other gastrointestinal and extraintestinal organs. Although etiology is still uncertain, recent knowledge in pathogenesis has accumulated, and novel diagnostic and therapeutic modalities have become available for clinical use. Therefore, the previous guidelines were urged to be updated. In 2016, the Japanese Society of Gastroenterology revised the previous versions of evidence-based clinical practice guidelines for ulcerative colitis (UC) and Crohn's disease (CD) in Japanese. A total of 59 clinical questions for 9 categories (1. clinical features of IBD; 2. diagnosis; 3. general consideration in treatment; 4. therapeutic interventions for IBD; 5. treatment of UC; 6. treatment of CD; 7. extraintestinal complications; 8. cancer surveillance; 9. IBD in special situation) were selected, and a literature search was performed for the clinical questions with use of the MEDLINE, Cochrane, and Igaku Chuo Zasshi databases. The guidelines were developed with the basic concept of the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) system. Recommendations were made using Delphi rounds. This English version was produced and edited based on the existing updated guidelines in Japanese.
Keywords: Consensus; Crohn’s disease; Evidence; Guidelines; Inflammatory bowel disease; Ulcerative colitis.
Conflict of interest statement
Any financial relationship with enterprises, businesses, or academic institutions in the subject matter or materials discussed in the manuscript are listed as follows: (1) those from which the authors have received individually any income, honoraria or any other types of remuneration; Abbvie Inc., EA Pharma Co., Ltd., Eisai Co., Ltd., IGAKU-SHOIN Ltd, Yakult Honsha Co., Ltd, Mitsubishi Tanabe Pharma Corporation; and (2) those from which the academic institutions of the authors received support (commercial/academic cooperation); Asahi Kasei Medical Co., Ltd., Astellas Pharma Inc., AstraZeneca K.K., Abbvie Inc., EA Pharma Co., Ltd., Eisai Co., Ltd., Eidia Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., GlaxoSmithKline K.K., JIMRO Co., Ltd., Zeria Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., Taiho Pharmaceutical Co., Ltd., Takeda Pharmaceutical Company Limited., Mitsubishi Tanabe Pharma Corporation, Chugai Pharmaceutical Co., Ltd., Biofermin Seiyaku Co., Ltd., Pfizer Inc. Bristol-Myers Squibb Company, Merck Serono Co., Ltd. Mochida Pharmaceutical Co., Ltd. Yakult Honsha Co., Ltd., Janssen Pharmaceutical K.K.
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