Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20087
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dc.contributor.authorChoy, Matthew C-
dc.contributor.authorSeah, Dean-
dc.contributor.authorFaleck, David M-
dc.contributor.authorShah, Shailja C-
dc.contributor.authorChao, Che-Yung-
dc.contributor.authorAn, Yoon-Kyo-
dc.contributor.authorRadford-Smith, Graham-
dc.contributor.authorBessissow, Talat-
dc.contributor.authorDubinsky, Marla C-
dc.contributor.authorFord, Alexander C-
dc.contributor.authorChurilov, Leonid-
dc.contributor.authorYeomans, Neville D-
dc.contributor.authorDe Cruz, Peter P-
dc.date2019-01-03-
dc.date.accessioned2019-01-18T04:19:40Z-
dc.date.available2019-01-18T04:19:40Z-
dc.date.issued2019-
dc.identifier.citationInflammatory Bowel Diseases 2019; 25(7): 1169-1186en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20087-
dc.description.abstractInfliximab 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.en_US
dc.language.isoeng-
dc.titleSystematic Review and Meta-analysis: Optimal Salvage Therapy in Acute Severe Ulcerative Colitis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleInflammatory Bowel Diseasesen_US
dc.identifier.affiliationDivision of Gastroenterology, McGill University, Montreal, Canadaen_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationThe Dr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, New Yorken_US
dc.identifier.affiliationDepartment of Gastroenterology, St Vincent's Hospital, Melbourne, Australiaen_US
dc.identifier.affiliationGastroenterology and Hepatologyen_US
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen_US
dc.identifier.affiliationDepartment of Gastroenterology, Royal Brisbane and Women's Hospital, Brisbane Australiaen_US
dc.identifier.affiliationDivision of Gastroenterology, McGill University, Montreal, Canadaen_US
dc.identifier.affiliationLeeds Gastroenterology Institute, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdomen_US
dc.identifier.affiliationDepartment of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australiaen_US
dc.identifier.affiliationDivision of Gastroenterology, Hepatology and Nutrition, Vanderbilt University Medical Center, Nashville, Tennesseeen_US
dc.identifier.affiliationLeeds Institute of Biomedical and Clinical Sciences, University of Leeds, Leeds, United Kingdomen_US
dc.identifier.doi10.1093/ibd/izy383en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-5206-0097en_US
dc.identifier.orcid0000-0001-9870-832Xen_US
dc.identifier.orcid0000-0002-3399-7236en_US
dc.identifier.pubmedid30605549-
dc.type.austinJournal Article-
local.name.researcherChoy, Matthew C
item.languageiso639-1en-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptOffice for Research-
crisitem.author.deptGastroenterology and Hepatology-
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