Clinicians' guide to the use of fecal calprotectin to identify and monitor disease activity in inflammatory bowel disease

被引:52
|
作者
Bressler, Brian [1 ]
Panaccione, Remo [2 ]
Fedorak, Richard N. [3 ]
Seidman, Ernest G. [4 ]
机构
[1] St Pauls Hosp, Div Gastroenterol, Dept Med, Vancouver, BC V6Z 1Y6, Canada
[2] Univ Calgary, Dept Med, Calgary, AB, Canada
[3] Univ Alberta, Div Gastroenterol, Edmonton, AB, Canada
[4] McGill Univ, Ctr Hlth, Div Gastroenterol, Montreal, PQ, Canada
来源
CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY | 2015年 / 29卷 / 07期
关键词
Disease activity; Fecal calprotectin; Inflammatory bowel disease; Monitoring; C-REACTIVE PROTEIN; ULCERATIVE-COLITIS; CROHNS-DISEASE; SURROGATE MARKERS; BLOOD LEUKOCYTES; INTESTINAL INFLAMMATION; ENDOSCOPIC ACTIVITY; PREDICTIVE MARKER; ACTIVITY INDEX; RELAPSE;
D O I
10.1155/2015/852723
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND: Objective monitoring of the severity of inflammation in patients with inflammatory bowel disease (IBD) is an essential part of disease management. However, repeat endoscopy to define extent and severity of inflammation is not practical. Fecal calprotectin (FC) is a biomarker that can be used as a surrogate test to distinguish inflammatory from noninflammatory gastrointestinal disease. METHODS: A targeted search of the literature regarding FC, focusing primarily on the past three years, was conducted to develop practical clinical guidance on the current utility of FC in the routine management of IBD patients. RESULTS: It is recommended that samples for FC testing be obtained from the first bowel excretion of the day. FC testing should be used as standard of care to accurately confirm inflammation and 'real-time' disease activity when a clinician suspects an IBD flare. Although FC is a reliable marker of inflammation, its role in routine monitoring in improving long-term outcomes has not yet been fully assessed. Based on available evidence, the authors suggest the following cut-off values and management strategies: when FC levels are <50 mu g/g to 100 mu g/g, quiescent disease is likely and therapy should be continued; when FC levels are >100 mu g/g to 250 mu g/g, inflammation is possible and further testing (eg, colonoscopy) is required to confirm inflammation; and when FC levels are >250 mu g/g, active inflammation is likely and strategies to control inflammation should be initiated (eg, optimizing current therapies or switching to an alternative therapy). DISCUSION: FC is a useful biomarker to accurately assess the degree of inflammation and should be incorporated into the management of patients with IBD.
引用
收藏
页码:369 / 372
页数:4
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