Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2025
Medical Therapy for Acute Severe Ulcerative Colitis: A Systematic Review With Meta-analysis.
СтатьяСистематический обзорМетаанализНазвание и аннотация: Перевод в очереди
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Vuyyuru Sudheer K, Shaban Nader, Yuan Yuhong, Honap Sailish, Alphonsus Lotus, De Silva Theshani Amalka, Alajmi Abdulaziz, MacDonald John K, Ma Christopher, Dulai Parambir S, Peyrin Biroulet Laurent, Jairath Vipul
Аннотация
BACKGROUND & AIMS: Acute severe ulcerative colitis (ASUC) is a medical emergency associated with high morbidity and mortality. We aimed to assess the efficacy and safety of medical treatments for ASUC.
METHODS: MEDLINE, EMBASE, and CENTRAL were searched to November 14, 2024 for randomized controlled trials (placebo or active comparator), and comparative cohort studies that evaluated medical therapies for hospitalized adults with ASUC. Primary outcomes were colectomy rate at discharge and at 3 and 12 months. Safety outcomes included adverse events, serious adverse events, and infections. Pooled risk ratios (RR) and 95% confidence intervals (CI) were calculated.
RESULTS: Forty-four studies (18 randomized controlled trials, and 26 cohort studies) assessing 22 different comparisons were included. Low certainty evidence suggests that infliximab (IFX) was significantly superior to cyclosporine A for reducing the risk of colectomy at discharge (RR, 0.56; 95% CI, 0.38-0.81; I2 = 30%), 3 months (RR, 0.67; 95% CI, 0.48-0.92; I2 = 36%), and 12 months (RR, 0.56; 95% CI, 0.42-0.75; I2 = 46%). IFX patients were significantly more likely than cyclosporine A patients to develop an infection (RR, 2.38; 95% CI, 1.27-4.47; I2 = 15%). There was no significant difference between accelerated and standard dosing regimens of IFX for colectomy at discharge or at 3 months. Tofacitinib in combination with intravenous corticosteroids was significantly superior to intravenous corticosteroids alone for induction of clinical response at Day 7; however, there was no difference in colectomy rate or infections at 3 months.
CONCLUSIONS: IFX may be more efficacious than cyclosporine A for the treatment of ASUC. Janus kinase inhibitors are promising treatment options in select individuals. Future studies should explore the efficacy of other advanced therapies.
METHODS: MEDLINE, EMBASE, and CENTRAL were searched to November 14, 2024 for randomized controlled trials (placebo or active comparator), and comparative cohort studies that evaluated medical therapies for hospitalized adults with ASUC. Primary outcomes were colectomy rate at discharge and at 3 and 12 months. Safety outcomes included adverse events, serious adverse events, and infections. Pooled risk ratios (RR) and 95% confidence intervals (CI) were calculated.
RESULTS: Forty-four studies (18 randomized controlled trials, and 26 cohort studies) assessing 22 different comparisons were included. Low certainty evidence suggests that infliximab (IFX) was significantly superior to cyclosporine A for reducing the risk of colectomy at discharge (RR, 0.56; 95% CI, 0.38-0.81; I2 = 30%), 3 months (RR, 0.67; 95% CI, 0.48-0.92; I2 = 36%), and 12 months (RR, 0.56; 95% CI, 0.42-0.75; I2 = 46%). IFX patients were significantly more likely than cyclosporine A patients to develop an infection (RR, 2.38; 95% CI, 1.27-4.47; I2 = 15%). There was no significant difference between accelerated and standard dosing regimens of IFX for colectomy at discharge or at 3 months. Tofacitinib in combination with intravenous corticosteroids was significantly superior to intravenous corticosteroids alone for induction of clinical response at Day 7; however, there was no difference in colectomy rate or infections at 3 months.
CONCLUSIONS: IFX may be more efficacious than cyclosporine A for the treatment of ASUC. Janus kinase inhibitors are promising treatment options in select individuals. Future studies should explore the efficacy of other advanced therapies.