{"title":"ACG 2024","authors":"Bethany Gomersall","doi":"10.1016/s2468-1253(24)00402-3","DOIUrl":null,"url":null,"abstract":"<h2>Section snippets</h2><section><section><h2>Subcutaneous guselkumab for Crohn's disease</h2>Induction with subcutaneous guselkumab—a dual acting IL-23p19 subunit inhibitor—was safe and efficacious in patients with Crohn's disease according to the phase 3 GRAVITI study presented by Remo Panaccione (Calgary, AB, Canada). 347 patients with moderate-to-severe Crohn's disease with an inadequate response or intolerance to oral corticosteroids and advanced therapies were randomly assigned to subcutaneous guselkumab 400 mg at weeks 0, 4, and 8, then 200 mg every 4 weeks (n=115); subcutaneous</section></section><section><section><h2>Auxora in acute pancreatitis and SIRS</h2>In the phase 2b CARPO trial presented by Robert Sutton (Liverpool, UK), 216 patients with acute pancreatitis and at least two criteria for systemic inflammatory response syndrome (SIRS) were randomly assigned to receive, with standard of care, intravenous auxora (zegocractin)—a calcium release-activated calcium channel inhibitor—at a dose of 2 mg/kg (n=54), 1 mg/kg (n=54), or 0·5 mg/kg (n=54), or placebo (n=54), over 4 h for 3 days. Median time to solid food tolerance (the primary endpoint) in</section></section><section><section><h2>Biofeedback <em>vs</em> dextranomer–hyaluronate acid injection for faecal incontinence</h2>There was no difference in the efficacy of biofeedback therapy versus dextranomer–hyaluronate acid anal injection for the treatment of faecal incontinence, according to a trial presented by Adil Bharucha (Rochester, MN, USA). Adults with faecal incontinence who had not responded at 4 or 12 weeks of enhanced medical management, including bowel agents and pelvic floor exercises, were randomly assigned to receive biofeedback therapy (n=99) or injection (n=101). There was no difference in the</section></section><section><section><h2>Bezlotoxumab plus FMT for <em>Clostridiodes difficile</em> in IBD</h2>According to data presented by Jessica R Allegretti (Boston, MA, USA), the addition of bezlotoxumab did not enhance the efficacy of faecal microbiota transplantation (FMT) for the treatment of recurrent <em>Clostridioides difficile</em> infection in patients with inflammatory bowel disease (IBD). 61 patients with IBD who had had at least two episodes of <em>C difficile</em> infection were randomly assigned to receive a single bezlotoxumab infusion (n=30) or placebo (n=31) before receiving a single colonoscopic</section></section>","PeriodicalId":56028,"journal":{"name":"Lancet Gastroenterology & Hepatology","volume":"41 1","pages":""},"PeriodicalIF":30.9000,"publicationDate":"2024-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lancet Gastroenterology & Hepatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/s2468-1253(24)00402-3","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Section snippets
Subcutaneous guselkumab for Crohn's disease
Induction with subcutaneous guselkumab—a dual acting IL-23p19 subunit inhibitor—was safe and efficacious in patients with Crohn's disease according to the phase 3 GRAVITI study presented by Remo Panaccione (Calgary, AB, Canada). 347 patients with moderate-to-severe Crohn's disease with an inadequate response or intolerance to oral corticosteroids and advanced therapies were randomly assigned to subcutaneous guselkumab 400 mg at weeks 0, 4, and 8, then 200 mg every 4 weeks (n=115); subcutaneous
Auxora in acute pancreatitis and SIRS
In the phase 2b CARPO trial presented by Robert Sutton (Liverpool, UK), 216 patients with acute pancreatitis and at least two criteria for systemic inflammatory response syndrome (SIRS) were randomly assigned to receive, with standard of care, intravenous auxora (zegocractin)—a calcium release-activated calcium channel inhibitor—at a dose of 2 mg/kg (n=54), 1 mg/kg (n=54), or 0·5 mg/kg (n=54), or placebo (n=54), over 4 h for 3 days. Median time to solid food tolerance (the primary endpoint) in
Biofeedback vs dextranomer–hyaluronate acid injection for faecal incontinence
There was no difference in the efficacy of biofeedback therapy versus dextranomer–hyaluronate acid anal injection for the treatment of faecal incontinence, according to a trial presented by Adil Bharucha (Rochester, MN, USA). Adults with faecal incontinence who had not responded at 4 or 12 weeks of enhanced medical management, including bowel agents and pelvic floor exercises, were randomly assigned to receive biofeedback therapy (n=99) or injection (n=101). There was no difference in the
Bezlotoxumab plus FMT for Clostridiodes difficile in IBD
According to data presented by Jessica R Allegretti (Boston, MA, USA), the addition of bezlotoxumab did not enhance the efficacy of faecal microbiota transplantation (FMT) for the treatment of recurrent Clostridioides difficile infection in patients with inflammatory bowel disease (IBD). 61 patients with IBD who had had at least two episodes of C difficile infection were randomly assigned to receive a single bezlotoxumab infusion (n=30) or placebo (n=31) before receiving a single colonoscopic
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