首页> 外文期刊>The annals of pharmacotherapy >Effect of Tumor Necrosis Factor-α Inhibitors on Drug-Induced Pancreatitis in Inflammatory Bowel Disease
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Effect of Tumor Necrosis Factor-α Inhibitors on Drug-Induced Pancreatitis in Inflammatory Bowel Disease

机译:肿瘤坏死因子-α抑制剂对炎性肠病药物诱导的胰腺炎的影响

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Background: Mesalamine and thiopurines (6-mercaptopurine and azathioprine) have been shown to increase the risk of developing acute pancreatitis in inflammatory bowel disease (IBD) patients. Tumor necrosis factor-α (TNF-α) inhibitors have been shown to protect against pancreatitis in animal models. Objective: To determine the risk of pancreatitis when comparing thiopurine monotherapy, mesalamine monotherapy, and thiopurine and mesalamine dual therapy to identical treatments but with the addition of a TNF-α inhibitor. Methods: Using a case-control design, the Food and Drug Administration Adverse Event Reporting System was queried for cases of pancreatitis and control reactions in IBD patients on a thiopurine or mesalamine. The proportional reporting ratio method was used to compare the different therapy regimens with the same regimen combined with a TNF-α inhibitor. Results: In all, 549 cases and controls were identified. When comparing thiopurine monotherapy with thiopurines combined with a TNF-α inhibitor, the odds of pancreatitis were lower in those on combination therapy (odds ratio [OR] = 0.04; 95% CI = 0.01-0.12). A similar trend was seen when comparing mesalamine monotherapy to mesalamine combined with a TNF-α inhibitor (OR = 0.08; 95% CI = 0.04-0.14) and when comparing those on both a thiopurine and mesalamine with those on all 3 therapies (OR = 0.04; 95% CI = 0.01-0.16). Conclusions: Combination therapy with TNF-α inhibitors appears to be associated with a lower risk of pancreatitis in IBD patients on mesalamine, thiopurines, or a combination of both. Physicians should consider using TNF-α inhibitors in those with the greatest risk of pancreatitis, although prospective studies are needed.
机译:背景:美沙明胺和硫代嘌呤(6-巯基嘌呤和硫唑嘌呤)已显示出增加了炎症性肠病(IBD)患者发生急性胰腺炎的风险。在动物模型中,肿瘤坏死因子-α(TNF-α)抑制剂已被证明可预防胰腺炎。目的:通过比较硫嘌呤单药治疗,美沙拉敏单药治疗以及硫嘌呤和美沙拉敏双重疗法与相同治疗方法(但添加TNF-α抑制剂)的比较来确定胰腺炎的风险。方法:使用病例对照设计,查询食品和药物管理局不良事件报告系统,以了解IBD患者对硫嘌呤或美沙拉敏的胰腺炎和对照反应情况。使用比例报告比率法比较了相同TNF-α抑制剂治疗方案的不同治疗方案。结果:总共鉴定出549例病例和对照。当比较硫嘌呤单药治疗与硫嘌呤与TNF-α抑制剂联合治疗时,与联合治疗相比,胰腺炎的几率更低(几率[OR] = 0.04; 95%CI = 0.01-0.12)。当比较美沙拉敏单一疗法与美沙拉敏联合TNF-α抑制剂(OR = 0.08; 95%CI = 0.04-0.14)以及将硫嘌呤和美沙拉敏两者与所有3种疗法(OR = 0.04; 95%CI = 0.01-0.16)。结论:与美沙明胺,硫代嘌呤或两者合用的IBD患者,与TNF-α抑制剂联合治疗似乎与降低胰腺炎的风险有关。尽管需要前瞻性研究,但医师应考虑在胰腺炎风险最高的人群中使用TNF-α抑制剂。

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