首页> 外文期刊>The Journal of investigative dermatology. >Risk of Serious Infection in Patients with Psoriasis Receiving Biologic Therapies: A Prospective Cohort Study from the British Association of Dermatologists Biologic Interventions Register (BADBIR)
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Risk of Serious Infection in Patients with Psoriasis Receiving Biologic Therapies: A Prospective Cohort Study from the British Association of Dermatologists Biologic Interventions Register (BADBIR)

机译:接受生物疗法牛皮癣患者严重感染的风险:英国皮肤科医师生物干预率注册(BADBIR)的前瞻性队列研究

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摘要

Serious infection is a concern for patients with psoriasis receiving biologic therapies. We assessed the risk of serious infections for biologics used to treat psoriasis by comparison with a cohort receiving non-biologic systemic therapies in a propensity score-weighted Cox proportional hazards model using data from the British Association of Dermatologists Biologic Interventions Register. Overall, 1,352; 3,271; and 994 participants were included in the etanercept, adalimumab, ustekinumab cohorts, respectively, and 3,421 participants were in the non-biologic cohort. A total of 283 patients had a serious infection; the incidence rates with 95% confidence intervals (CI) per 1,000 person-years were as follows: non-biologic, 14.2 (11.5-17.4); etanercept, 15.3 (11.6-20.1); adalimumab, 13.9 (11.4-16.6); and ustekinumab, 15.1 (10.8-21.1). No significant increases in the risk of serious infection were observed for etanercept (hazard ratio [HR] = 1.10, 95% CI = 0.75-1.60), adalimumab (HR = 0.93, 95% CI = 0.69-1.26), or ustekinumab (HR = 0.92, 95% CI = 0.60-1.41) compared with non-biologic systemic therapies or methotrexate-only (etanercept: HR = 1.47, 95% CI = 0.95-2.28; adalimumab: HR = 1.26, 95% CI = 0.86-1.84; ustekinumab: HR = 1.22, 95% CI = 0.75-1.99). The risk of serious infection should not be a key discriminator for patients and clinicians when choosing between non-biologic systemic therapies, etanercept, adalimumab, and ustekinumab for the treatment of psoriasis.
机译:严重的感染是对牛皮癣接受生物疗法的患者的关注。我们评估了用于治疗牛皮癣的生物学感染的严重感染的风险,所述群体通过来自英国皮肤科生物学干预率登记的数据的倾向评分加权的Cox比例危害模型进行了促进的评分重量的Cox比例危害模型。总体而言,1,352; 3,271;和994名参与者分别包含在涅累普,达塔洛单抗,Ustekumab队列中,3,421名参与者处于非生物队列中。共有283名患者发生严重感染;每1,000人置信度(CI)的发病率为95% - 年份如下:非生物学,14.2(11.5-17.4);依托西普,15.3(11.6-20.1); Adalimumab,13.9(11.4-16.6);和Ustekinumab,15.1(10.8-21.1)。对于依那西(危害比[HR] = 1.10,95%CI = 0.75-1.60),Adalimalab(HR = 0.93,95%CI = 0.69-1.26),或Ustekinub(HR),无明显增加严重感染的风险与非生物全身疗法或仅甲氨蝶呤(Etanercept:Hr = 1.47,95%Ci = 0.95-2.28; Adalimalab:HR = 1.26,95%Ci = 0.86-1.84 ; Ustekinumab:HR = 1.22,95%CI = 0.75-1.99)。 The risk of serious infection should not be a key discriminator for patients and clinicians when choosing between non-biologic systemic therapies, etanercept, adalimumab, and ustekinumab for the treatment of psoriasis.

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