4.8 Article

Approach to the Management of Recently Diagnosed Inflammatory Bowel Disease Patients: A User's Guide for Adult and Pediatric Gastroenterologists

期刊

GASTROENTEROLOGY
卷 161, 期 1, 页码 47-65

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.gastro.2021.04.063

关键词

Inflammatory Bowel Disease; Crohn's Disease; Ulcerative Colitis; Early Diagnosis; Early Therapy; Personalized Therapy; Adult

资金

  1. Dickler Family Fund
  2. Helmsley Charitable Trust Fund
  3. National Institutes of Health T32 [5T32GM082773-13]
  4. NY Crohn's Foundation
  5. Goldsmith Family Fund
  6. National Institutes of Health K23 Career Development Award [K23KD111995-01A1]
  7. New York Community Trust

向作者/读者索取更多资源

Inflammatory bowel diseases, including Crohn's disease and ulcerative colitis, are chronic, progressive, immune-mediated diseases of adults and children with no cure. Delay in diagnosis is common and associated with adverse outcomes, highlighting the importance of early diagnosis and prompt treatment. Risk stratification based on clinical, demographic, and serologic markers can guide selection of first-line therapy in personalized medicine.
Inflammatory bowel diseases (IBDs), including Crohn's disease and ulcerative colitis, are chronic, progressive, immune-mediated diseases of adults and children that have no cure. IBD can cause significant morbidity and lead to complications such as strictures, fistulas, infections, and cancer. In children, IBD can also result in growth impairment and pubertal delays. IBD is highly heterogenous, with severity ranging from mild to severe and symptoms ranging from mild to debilitating. Delay in IBD diagnosis, especially in Crohn's disease, is common and associated with adverse outcomes. Early diagnosis and prompt institution of treatment are the cornerstones for improving outcomes and maximizing health. Early diagnosis requires a low threshold of suspicion and red flags to guide early specialist referral at the primary provider level. Although the armamentarium of IBD medications is growing, many patients will not respond to treatment, and the selection of first-line therapy is critical. Risk stratification of disease severity, based on clinical, demographic, and serologic markers, can help guide selection of first-line therapy. Clinical decision support tools, genomics, and other biomarkers of response to therapy and risk of adverse events are the future of personalized medicine. After starting appropriate therapy, it is important to confirm remission using objective end points (treat to target) with continued control of inflammation with adjustment of therapy using surrogate biomarkers (tight control). Lastly, IBD therapy extends far beyond medications, and other aspects of the overall health and wellbeing of the patient are critical. These include preventive health, nutrition, and psychobehavioral support addressing patients' concerns around complementary therapy and medication adherence, prevention of disability, and ensuring open communication.

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