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Comparative safety of infliximab and etanercept on the risk of serious infections: does the association vary by patient characteristics?

机译:英夫利昔单抗和依赖伊斯坦普对严重感染风险的比较安全性:协会是否因患者特征而变化?

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Infliximab, a chimeric monoclonal anti-TNFα antibody, has been found to increase the risk of serious infections compared with the TNF receptor fusion protein etanercept in some studies. It is unclear whether the risk varies by patient characteristics. We conducted a study to address this question.We identified members of Kaiser Permanente Northern California who initiated infliximab (n = 793) or etanercept (n = 2692) in 1997-2007. Using a Cox model, we estimated the propensity-score-adjusted hazard ratio (HR) and 95% confidence interval (CI) of serious infections requiring hospitalization or opportunistic infections comparing infliximab initiators to etanercept initiators. We tested whether the adjusted HR differed by age, sex, race/ethnicity, body mass index, and smoking status.The crude incidence rate of serious infections per 100 person-years was 5.4 (95%CI: 3.8, 7.5) in patients <65 years and 16.0 (95%CI: 10.4, 23.4) in patients ≥ 65 years during the first 3 months following treatment initiation. Compared with etanercept, the adjusted HR during this period was elevated for infliximab in patients <65 years (HR: 3.01; 95%CI: 1.49, 6.07), but not in those ≥ 65 years (HR 0.94; 95%CI: 0.41, 2.13). Findings did not suggest that the HR varied by the other patient characteristics examined.An increased risk of serious infections associated with infliximab relative to etanercept did not appear to be modified by patients' sex, race/ethnicity, body mass index, or smoking status. There was an indication that the increased risk might be limited to patients <65 years. Additional studies are warranted to verify or refute this finding.
机译:已发现嵌合单克隆抗TNFα抗体的英夫利昔单抗,与一些研究中的TNF受体融合蛋白Etanercept相比,增加了严重感染的风险。目前尚不清楚风险是否因患者特征而变化。我们进行了一项研究,解决了这个问题。我们在1997 - 2007年开始了北加州北加州北加州北加州的成员。使用COX模型,我们估计了需要住院或机会感染的严重感染的倾向评分调整的危险比(HR)和95%置信区间(CI),这些感染与依赖昔单抗引发剂与依赖替昔替斯科特兴奋剂相比。我们测试了调整后的人力资源是否依靠年龄,性别,种族/种族,体重指数和吸烟状态。每100人的严重感染的原始发病率为5.4(95%CI:3.8,7.5)< 65岁和16.0(95%CI:10.4,23.4)患者≥65岁,在治疗开始后的前3个月内。与Etanercept相比,在此期间的调整后的HR为患者的英夫利昔单抗升高(HR:3.01; 95%CI:1.49,6.07),但不在≥65岁(HR 0.94; 95%CI:0.41 2.13)。研究结果并没有表明其他患者特征所不同的人力资源.AN相对于乙酸葡萄球菌的严重感染风险增加并未被患者的性,种族/种族,体重指数或吸烟地位进行修改。表明增加的风险可能限于患者<65岁。需要额外的研究来核实或反驳这一发现。

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