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首页> 外文期刊>Yonsei Medical Journal >Incidences of Serious Infections and Tuberculosis among Patients Receiving Anti-Tumor Necrosis Factor-α Therapy
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Incidences of Serious Infections and Tuberculosis among Patients Receiving Anti-Tumor Necrosis Factor-α Therapy

机译:接受抗肿瘤坏死因子-α治疗的患者中严重感染和结核病的发生率

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Purpose Anti-tumor necrosis factor-alpha (TNF-α) medications represent a major advancement in the management of chronic inflammatory diseases. However, these agents are associated with increased risks of tuberculosis (TB) and other serious infections. The aim of this study was to evaluate the incidences of such disease among tertiary hospitals in Korea. Materials and Methods We retrospectively studied patients who received anti-TNF-α therapy; we reviewed serious infections including TB that developed within 6 months after initiation of anti-TNF-α therapy. Data concerning patient demographics, types of anti-TNF-α agents, concomitant immunosuppressive drugs use, and infection details were collected. Results A total 175 patients treated with infliximab (n=72) or adalimumab (n=103) with the following conditions were enrolled: Crohn's disease, 34 (19.4%); ulcerative colitis, 20 (11.4%); ankylosing spondylitis, 82 (46.9%); and rheumatoid arthritis, 39 (22.2%). There were 18 cases (6.0%) of serious infections. The most common site of serious infection was the intra-abdomen (n=6), followed by TB (n=3), skin and soft tissue (n=3), bone and joints (n=2), ocular neurons (n=2), lower respiratory tract (n=1), and urinary tract (n=1). Of the 175 patients, only 3 cases showed development of TB. Furthermore, of all those who developed TB, none had taken anti-TB chemoprophylaxis prior to treatment with an anti-TNF agent due to negative screening results. Conclusion Serious infections with anti-TNF-α therapy were uncommon among tertiary hospitals in Korea; TB was the second most frequent infection. Nevertheless, there were no TB reactivations after anti-TB chemoprophylaxis. Accordingly, physicians should be aware of TB in subjects undergoing anti-TNF-α therapy, especially in countries with a high prevalence of TB.
机译:目的抗肿瘤坏死因子-α(TNF-α)药物代表了慢性炎性疾病管理的重大进步。但是,这些药物会增加结核病(TB)和其他严重感染的风险。这项研究的目的是评估韩国三级医院中这种疾病的发生率。材料和方法我们回顾性研究了接受抗TNF-α治疗的患者。我们回顾了在开始抗TNF-α治疗后6个月内发生的包括TB在内的严重感染。收集了有关患者人口统计学,抗TNF-α药物类型,伴随的免疫抑制药物使用以及感染细节的数据。结果共纳入175例接受英夫利昔单抗(n = 72)或阿达木单抗(n = 103)治疗的患者,这些患者具有以下状况:克罗恩病34例(19.4%);克罗恩病34例。溃疡性结肠炎20(11.4%);强直性脊柱炎,82(46.9%);类风湿关节炎39(22.2%)。严重感染者18例(6.0%)。严重感染的最常见部位是腹部内(n = 6),其次是TB(n = 3),皮肤和软组织(n = 3),骨骼和关节(n = 2),眼神经元(n = 2),下呼吸道(n = 1)和泌尿道(n = 1)。在175名患者中,只有3例显示出结核病的发展。此外,在所有患有结核病的患者中,由于筛选结果阴性,没有人在接受抗TNF药物治疗之前进行过抗结核药物的化学预防。结论在韩国三级医院中,抗TNF-α疗法引起的严重感染并不常见。结核病是第二常见的感染。尽管如此,抗结核化学预防后仍未出现结核再激活。因此,在接受抗TNF-α治疗的受试者中,尤其是在结核病高发国家,医生应意识到结核病。

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