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首页> 外文期刊>Pharmacoepidemiology and drug safety >Comparative safety of infliximab and etanercept on the risk of serious infections: does the association vary by patient characteristics?
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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:英夫利昔单抗和依那西普对严重感染风险的比较安全性:关联因患者特征而异吗?

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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:在一些研究中,英夫利昔单抗是一种嵌合的单克隆抗TNFα抗体,与TNF受体融合蛋白etanercept相比,发现增加了严重感染的风险。目前尚不清楚该风险是否因患者特征而异。我们进行了一项研究来解决这个问题。我们确定了北加州Kaiser Permanente的成员,他们在1997-2007年期间启动了英夫利昔单抗(n = 793)或依那西普(n = 2692)。使用Cox模型,我们将英夫利昔单抗引发剂与依那西普引发剂相比,估计了需要住院或机会性感染的严重感染的倾向得分调整后的危险比(HR)和95%置信区间(CI)。我们测试了调整后的HR是否随年龄,性别,种族/民族,体重指数和吸烟状况的不同而不同。患者每100人年的严重感染的粗略发生率为5.4(95%CI:3.8,7.5)<在治疗开始后的头三个月内,≥65岁的患者为65岁和16.0(95%CI:10.4,23.4)。与依那西普相比,英夫利昔单抗在65岁以下患者中的调整后HR升高(HR:3.01; 95%CI:1.49,6.07),但在≥65岁的患者中未调整(HR 0.94; 95%CI:0.41, 2.13)。研究结果并未显示出HR随其他患者特征而异。英夫利昔单抗相对于依那西普的严重感染风险增加似乎并未因患者的性别,种族/民族,体重指数或吸烟状况而改变。有迹象表明,增加的风险可能仅限于<65岁的患者。需进行其他研究以证实或驳斥此发现。

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