Efficacy and safety of tumor necrosis factor-α blockers for ulcerative colitis: A systematic review and meta-analysis of published randomized controlled trials
被引:11
作者:
论文数: 引用数:
h-index:
机构:
Song, Yun-Na
[1
]
Zheng, Ping
论文数: 0引用数: 0
h-index: 0
机构:
Tongji Univ, Shanghai East Hosp, Dept Gastroenterol, Shanghai 200120, Peoples R ChinaShanghai Jiao Tong Univ, Sch Med, Shanghai Peoples Hosp 1, Dept Gastroenterol, Shanghai 200080, Peoples R China
Zheng, Ping
[2
]
机构:
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Peoples Hosp 1, Dept Gastroenterol, Shanghai 200080, Peoples R China
[2] Tongji Univ, Shanghai East Hosp, Dept Gastroenterol, Shanghai 200120, Peoples R China
To evaluate the efficacy and safety of TNF-alpha blockers for ulcerative colitis. A systematic search for randomized controlled trials (RCTs) of TNF-alpha blockers for treatment of ulcerative colitis (UC) were performed in PubMed, Web of Science, Embase and cochrane clinical trial. We estimated Pooled estimates of the odds ratio (OR) and relevant 95% confidence interval (CI) using fixed effects model or random effects model as appropriate. Heterogeneity, publication bias, and subgroup analyses were conducted. Nine randomized controlled studies met the selection criteria with a total of 2518 patients. Five studies compared Infliximab with placebo. Two studies compared Infliximab to corticosteroids. Two studies compared Adalimumab to placebo. One study compared subcutaneous golimumab to placebo. Short-term response, short-term remission, long-term remission and mucosal healing were better in the TNF-alpha blocker group than in the control group (p <0.05). TNF-alpha blockers decreased the colectomy rate and serious adverse reactions (p <0.05). The TNF-alpha blockers were superior to controls in achieving short-term clinical response/remission, long-term remission and mucosal healing and decreased the colectomy rate and serious adverse reactions. Copyright (C) 2014, Food and Drug Administration, Taiwan. Published by Elsevier Taiwan LLC. All rights reserved.