TY - JOUR
T1 - Approach to the Management of Recently Diagnosed Inflammatory Bowel Disease Patients
T2 - A User's Guide for Adult and Pediatric Gastroenterologists
AU - Agrawal, Manasi
AU - Spencer, Elizabeth A.
AU - Colombel, Jean Frederic
AU - Ungaro, Ryan C.
N1 - Funding Information:
Funding Manasi Agrawal receives research support from the Dickler Family Fund, New York Community Trust, and the Helmsley Charitable Trust Fund for SECURE-IBD. Elizabeth A. Spencer receives research support from an National Institutes of Health T32 ( 5T32GM082773-13 ), NY Crohn’s Foundation, and the Goldsmith Family Fund. Ryan C. Ungaro is supported by an National Institutes of Health K23 Career Development Award ( K23KD111995-01A1 ).
Funding Information:
Conflicts of interest These authors disclose the following: Jean-Frederic Colombel has received research grants from AbbVie, Janssen Pharmaceuticals and Takeda; has received payment for lectures from AbbVie, Amgen, Allergan, Bristol-Myers Squibb Company, Ferring Pharmaceuticals, Shire, Takeda and Tillots; has received consulting fees from AbbVie, Amgen, Arena Pharmaceuticals, Boehringer Ingelheim, Bristol-Myers Squibb Company, Celgene Corporation, Celltrion, Eli Lilly, Enterome, Ferring Pharmaceuticals, Genentech, Gilead, Iterative Scopes, Ipsen, Immunic, lmtbio, Inotrem, Janssen Pharmaceuticals, Landos, LimmaTech Biologics AG, Medimmune, Merck, Novartis, O Mass, Otsuka, Pfizer, Shire, Takeda, Tigenix, Viela bio; and hold stock options in Intestinal Biotech Development. Ryan C. Ungaro has served as a consultant and/or advisory board member for Bristol Myers Squibb, Eli Lilly, Janssen, Pfizer, and Takeda. He has received research support from AbbVie, Boehringer Ingelheim, and Pfizer. The remaining authors disclose no conflicts.Funding Manasi Agrawal receives research support from the Dickler Family Fund, New York Community Trust, and the Helmsley Charitable Trust Fund for SECURE-IBD. Elizabeth A. Spencer receives research support from an National Institutes of Health T32 (5T32GM082773-13), NY Crohn's Foundation, and the Goldsmith Family Fund. Ryan C. Ungaro is supported by an National Institutes of Health K23 Career Development Award (K23KD111995-01A1).
Publisher Copyright:
© 2021 AGA Institute
PY - 2021/7
Y1 - 2021/7
N2 - 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.
AB - 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.
KW - Adult
KW - Crohn's Disease
KW - Early Diagnosis
KW - Early Therapy
KW - Inflammatory Bowel Disease
KW - Pediatric
KW - Personalized Therapy
KW - Ulcerative Colitis
UR - http://www.scopus.com/inward/record.url?scp=85108440965&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2021.04.063
DO - 10.1053/j.gastro.2021.04.063
M3 - Review article
C2 - 33940007
AN - SCOPUS:85108440965
SN - 0016-5085
VL - 161
SP - 47
EP - 65
JO - Gastroenterology
JF - Gastroenterology
IS - 1
ER -