Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20087
Title: Systematic Review and Meta-analysis: Optimal Salvage Therapy in Acute Severe Ulcerative Colitis.
Austin Authors: Choy, Matthew C ;Seah, Dean ;Faleck, David M;Shah, Shailja C;Chao, Che-Yung;An, Yoon-Kyo;Radford-Smith, Graham;Bessissow, Talat;Dubinsky, Marla C;Ford, Alexander C;Churilov, Leonid ;Yeomans, Neville D ;De Cruz, Peter P 
Affiliation: Division of Gastroenterology, McGill University, Montreal, Canada
Medicine (University of Melbourne)
The Dr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, New York
Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia
Gastroenterology and Hepatology
The Florey Institute of Neuroscience and Mental Health
Department of Gastroenterology, Royal Brisbane and Women's Hospital, Brisbane Australia
Division of Gastroenterology, McGill University, Montreal, Canada
Leeds Gastroenterology Institute, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom
Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia
Division of Gastroenterology, Hepatology and Nutrition, Vanderbilt University Medical Center, Nashville, Tennessee
Leeds Institute of Biomedical and Clinical Sciences, University of Leeds, Leeds, United Kingdom
Issue Date: 2019
Date: 2019-01-03
Publication information: Inflammatory Bowel Diseases 2019; 25(7): 1169-1186
Abstract: Infliximab is an effective salvage therapy in acute severe ulcerative colitis; however, the optimal dosing strategy is unknown. We performed a systematic review and meta-analysis to examine the impact of infliximab dosage and intensification on colectomy-free survival in acute severe ulcerative colitis. Studies reporting outcomes of hospitalized steroid-refractory acute severe ulcerative colitis treated with infliximab salvage were identified. Infliximab use was categorized by dose, dose number, and schedule. The primary outcome was colectomy-free survival at 3 months. Pooled proportions and odds ratios with 95% confidence intervals were reported. Forty-one cohorts (n = 2158 cases) were included. Overall colectomy-free survival with infliximab salvage was 79.7% (95% confidence interval [CI], 75.48% to 83.6%) at 3 months and 69.8% (95% CI, 65.7% to 73.7%) at 12 months. Colectomy-free survival at 3 months was superior with 5-mg/kg multiple (≥2) doses compared with single-dose induction (odds ratio [OR], 4.24; 95% CI, 2.44 to 7.36; P < 0.001). However, dose intensification with either high-dose or accelerated strategies was not significantly different to 5-mg/kg standard induction at 3 months (OR, 0.70; 95% CI, 0.39 to 1.27; P = 0.24) despite being utilized in patients with a significantly higher mean C-reactive protein and lower albumin levels. In acute severe ulcerative colitis, multiple 5-mg/kg infliximab doses are superior to single-dose salvage. Dose-intensified induction outcomes were not significantly different compared to standard induction and were more often used in patients with increased disease severity, which may have confounded the results. This meta-analysis highlights the marked variability in the management of infliximab salvage therapy and the need for further studies to determine the optimal dose strategy.
URI: https://ahro.austin.org.au/austinjspui/handle/1/20087
DOI: 10.1093/ibd/izy383
ORCID: 0000-0001-5206-0097
0000-0001-9870-832X
0000-0002-3399-7236
Journal: Inflammatory Bowel Diseases
PubMed URL: 30605549
Type: Journal Article
Appears in Collections:Journal articles

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