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

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          Abstract

          We aim to provide guidance for medical treatment of luminal Crohn's disease in children.

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          Most cited references156

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          Ustekinumab induction and maintenance therapy in refractory Crohn's disease.

          In patients with Crohn's disease, the efficacy of ustekinumab, a human monoclonal antibody against interleukin-12 and interleukin-23, is unknown. We evaluated ustekinumab in adults with moderate-to-severe Crohn's disease that was resistant to anti-tumor necrosis factor (TNF) treatment. During induction, 526 patients were randomly assigned to receive intravenous ustekinumab (at a dose of 1, 3, or 6 mg per kilogram of body weight) or placebo at week 0. During the maintenance phase, 145 patients who had a response to ustekinumab at 6 weeks underwent a second randomization to receive subcutaneous injections of ustekinumab (90 mg) or placebo at weeks 8 and 16. The primary end point was a clinical response at 6 weeks. The proportions of patients who reached the primary end point were 36.6%, 34.1%, and 39.7% for 1, 3, and 6 mg of ustekinumab per kilogram, respectively, as compared with 23.5% for placebo (P=0.005 for the comparison with the 6-mg group). The rate of clinical remission with the 6-mg dose did not differ significantly from the rate with placebo at 6 weeks. Maintenance therapy with ustekinumab, as compared with placebo, resulted in significantly increased rates of clinical remission (41.7% vs. 27.4%, P=0.03) and response (69.4% vs. 42.5%, P<0.001) at 22 weeks. Serious infections occurred in 7 patients (6 receiving ustekinumab) during induction and 11 patients (4 receiving ustekinumab) during maintenance. Basal-cell carcinoma developed in 1 patient receiving ustekinumab. Patients with moderate-to-severe Crohn's disease that was resistant to TNF antagonists had an increased rate of response to induction with ustekinumab, as compared with placebo. Patients with an initial response to ustekinumab had significantly increased rates of response and remission with ustekinumab as maintenance therapy. (Funded by Janssen Research and Development; CERTIFI ClinicalTrials.gov number, NCT00771667.).
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            The Toronto Consensus for the Treatment of Helicobacter pylori Infection in Adults.

            Helicobacter pylori infection is increasingly difficult to treat. The purpose of these consensus statements is to provide a review of the literature and specific, updated recommendations for eradication therapy in adults.
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              Mucosal healing in inflammatory bowel diseases: a systematic review.

              Recent studies have identified mucosal healing on endoscopy as a key prognostic parameter in the management of inflammatory bowel diseases (IBD), thus highlighting the role of endoscopy for monitoring of disease activity in IBD. In fact, mucosal healing has emerged as a key treatment goal in IBD that predicts sustained clinical remission and resection-free survival of patients. The structural basis of mucosal healing is an intact barrier function of the gut epithelium that prevents translocation of commensal bacteria into the mucosa and submucosa with subsequent immune cell activation. Thus, mucosal healing should be considered as an initial event in the suppression of inflammation of deeper layers of the bowel wall, rather than as a sign of complete healing of gut inflammation. In this systematic review, the clinical studies on mucosal healing are summarised and the effects of anti-inflammatory or immunosuppressive drugs such as 5-aminosalicylates, corticosteroids, azathioprine, ciclosporin and anti-TNF antibodies (adalimumab, certolizumab pegol, infliximab) on mucosal healing are discussed. Finally, the implications of mucosal healing for subsequent clinical management in patients with IBD are highlighted.
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                Author and article information

                Journal
                J Can Assoc Gastroenterol
                Journal of the Canadian Association of Gastroenterology
                Oxford University Press (OUP)
                2515-2092
                2515-2084
                Aug 2019
                : 2
                : 3
                Affiliations
                [1 ] Children's Hospital of Eastern Ontario Inflammatory Bowel Disease Centre, Division of Gastroenterology, Hepatology and Nutrition, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
                [2 ] Department of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada.
                [3 ] Ch.I.L.D. Foundation Canadian Children IBD Network, Vancouver, British Columbia, Canada.
                [4 ] School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
                [5 ] Faculty of Medicine, Memorial University, St John's, Newfoundland and Labrador, Canada.
                [6 ] Section of Pediatric Gastroenterology, Department of Pediatrics, Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada.
                [7 ] Division of Gastroenterology and Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
                [8 ] IBD Centre, Department of Paediatrics, SickKids Hospital, University of Toronto, Toronto, Ontario, Canada.
                [9 ] Department of Pediatric Gastroenterology, Hepatology, and Nutrition, Centre Hospitalier Universitaire, Sainte-Justine, Montréal, Quebec, Canada.
                [10 ] Section of Pediatric Gastroenterology, Department of Pediatrics, Health Sciences Centre, Winnipeg, Manitoba, Canada.
                [11 ] Department of Pediatrics (Gastroenterology), Stollery Children's Hospital, Edmonton, Alberta, Canada.
                [12 ] Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
                [13 ] Division of Gastroenterology and Nutrition, IWK Health Centre, Halifax, Nova Scotia, Canada.
                [14 ] Division of Pediatric Gastroenterology, McMaster University, Hamilton, Ontario, Canada.
                [15 ] Division of Pediatric Gastroenterology, University of North Carolina, Hospital-Children's Specialty Clinic, Chapel Hill, North Carolina.
                [16 ] Division of Gastroenterology, Royal Alexandra Hospital, Edmonton, Alberta, Canada.
                Article
                gwz018
                10.1093/jcag/gwz018
                6619414
                31294379
                72893099-f28b-4282-8e34-2a00785d4ede
                History

                GRADE,IBD,Inflammatory Bowel Diseases,TNF
                GRADE, IBD, Inflammatory Bowel Diseases, TNF

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