Canadian Association of Gastroenterology Clinical Practice Guideline for the Management of Luminal Crohn's Disease.


Journal

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
ISSN: 1542-7714
Titre abrégé: Clin Gastroenterol Hepatol
Pays: United States
ID NLM: 101160775

Informations de publication

Date de publication:
08 2019
Historique:
received: 11 10 2018
revised: 21 02 2019
accepted: 25 02 2019
pubmed: 12 3 2019
medline: 28 10 2020
entrez: 12 3 2019
Statut: ppublish

Résumé

Crohn's disease (CD) is a lifelong illness with substantial morbidity, although new therapies and treatment paradigms have been developed. We provide guidance for treatment of ambulatory patients with mild to severe active luminal CD. We performed a systematic review to identify published studies of the management of CD. The quality of evidence and strength of recommendations were rated according to the Grading of Recommendation Assessment, Development and Evaluation (GRADE) approach. Statements were developed through an iterative online platform and then finalized and voted on by a group of specialists. The consensus includes 41 statements focused on 6 main drug classes: antibiotics, 5-aminosalicylate, corticosteroids, immunosuppressants, biologic therapies, and other therapies. The group suggested against the use of antibiotics or 5-aminosalicylate as induction or maintenance therapies. Corticosteroid therapies (including budesonide) can be used as induction, but not maintenance therapies. Among immunosuppressants, thiopurines should not be used for induction, but can be used for maintenance therapy for selected low-risk patients. Parenteral methotrexate was proposed for induction and maintenance therapy in patients with corticosteroid-dependent CD. Biologic agents, including tumor necrosis factor antagonists, vedolizumab, and ustekinumab, were recommended for patients failed by conventional induction therapies and as maintenance therapy. The consensus group was unable to clearly define the role of concomitant immunosuppressant therapies in initiation of treatment with a biologic agent. Optimal management of CD requires careful patient assessment, acknowledgement of patient preferences, evidence-based use of existing therapies, and thorough assessment to define treatment success.

Sections du résumé

BACKGROUND & AIMS
Crohn's disease (CD) is a lifelong illness with substantial morbidity, although new therapies and treatment paradigms have been developed. We provide guidance for treatment of ambulatory patients with mild to severe active luminal CD.
METHODS
We performed a systematic review to identify published studies of the management of CD. The quality of evidence and strength of recommendations were rated according to the Grading of Recommendation Assessment, Development and Evaluation (GRADE) approach. Statements were developed through an iterative online platform and then finalized and voted on by a group of specialists.
RESULTS
The consensus includes 41 statements focused on 6 main drug classes: antibiotics, 5-aminosalicylate, corticosteroids, immunosuppressants, biologic therapies, and other therapies. The group suggested against the use of antibiotics or 5-aminosalicylate as induction or maintenance therapies. Corticosteroid therapies (including budesonide) can be used as induction, but not maintenance therapies. Among immunosuppressants, thiopurines should not be used for induction, but can be used for maintenance therapy for selected low-risk patients. Parenteral methotrexate was proposed for induction and maintenance therapy in patients with corticosteroid-dependent CD. Biologic agents, including tumor necrosis factor antagonists, vedolizumab, and ustekinumab, were recommended for patients failed by conventional induction therapies and as maintenance therapy. The consensus group was unable to clearly define the role of concomitant immunosuppressant therapies in initiation of treatment with a biologic agent.
CONCLUSIONS
Optimal management of CD requires careful patient assessment, acknowledgement of patient preferences, evidence-based use of existing therapies, and thorough assessment to define treatment success.

Identifiants

pubmed: 30853616
pii: S1542-3565(19)30253-8
doi: 10.1016/j.cgh.2019.02.043
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Anti-Inflammatory Agents, Non-Steroidal 0
Antibodies, Monoclonal, Humanized 0
Gastrointestinal Agents 0
Glucocorticoids 0
Immunosuppressive Agents 0
Tumor Necrosis Factor Inhibitors 0
Sulfasalazine 3XC8GUZ6CB
Mesalamine 4Q81I59GXC
Budesonide 51333-22-3
Prednisolone 9PHQ9Y1OLM
vedolizumab 9RV78Q2002
Ustekinumab FU77B4U5Z0
Azathioprine MRK240IY2L
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article Practice Guideline Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1680-1713

Informations de copyright

Copyright © 2019 AGA Institute and the Canadian Association of Gastroenterology. Published by Elsevier Inc. All rights reserved.

Auteurs

Remo Panaccione (R)

Department of Medicine, University of Calgary, Calgary, Alberta, Canada. Electronic address: rpanacci@ucalgary.ca.

A Hillary Steinhart (AH)

Division of Gastroenterology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.

Brian Bressler (B)

Department of Medicine, Division of Gastroenterology, St Paul's Hospital, Vancouver, British Columbia, Canada.

Reena Khanna (R)

Department of Medicine, University of Western Ontario, London, Ontario, Canada.

John K Marshall (JK)

Division of Gastroenterology and Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Laura Targownik (L)

Section of Gastroenterology, University of Manitoba, Winnipeg, Manitoba, Canada.

Waqqas Afif (W)

Department of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.

Alain Bitton (A)

Department of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.

Mark Borgaonkar (M)

Faculty of Medicine, Memorial University, St John's, Newfoundland, Canada.

Usha Chauhan (U)

Hamilton Health Sciences, Hamilton, Ontario, Canada.

Brendan Halloran (B)

Division of Gastroenterology, University of Alberta, Edmonton, Alberta, Canada.

Jennifer Jones (J)

Department of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.

Erin Kennedy (E)

Division of General Surgery, Mount Sinai Hospital, Toronto, Ontario, Canada.

Grigorios I Leontiadis (GI)

Division of Gastroenterology and Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Edward V Loftus (EV)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.

Jonathan Meddings (J)

Department of Medicine, University of Calgary, Calgary, Alberta, Canada.

Paul Moayyedi (P)

Division of Gastroenterology and Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Sanjay Murthy (S)

Division of Gastroenterology, University of Ottawa, Ottawa, Ontario, Canada.

Sophie Plamondon (S)

Department of Medicine, University of Sherbrooke, Sherbrooke, Quebec, Canada.

Greg Rosenfeld (G)

Division of Gastroenterology, Pacific Gastroenterology Associates, Vancouver, British Columbia, Canada.

David Schwartz (D)

Inflammatory Bowel Disease Center, Vanderbilt University, Nashville, Tennessee.

Cynthia H Seow (CH)

Departments of Medicine and Community Health Sciences, University of Calgary, Calgary, Alberta, Canada.

Chadwick Williams (C)

Hilyard Place, Saint John, New Brunswick, Canada.

Charles N Bernstein (CN)

Section of Gastroenterology, University of Manitoba, Winnipeg, Manitoba, Canada.

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Classifications MeSH