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首页> 外文期刊>Journal of gastroenterology and hepatology >Serious infections in patients with inflammatory bowel disease receiving anti-tumor-necrosis-factor-alpha therapy: an Australian and New Zealand experience.
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Serious infections in patients with inflammatory bowel disease receiving anti-tumor-necrosis-factor-alpha therapy: an Australian and New Zealand experience.

机译:接受抗肿瘤坏死因子-α治疗的炎性肠病患者的严重感染:澳大利亚和新西兰的经验。

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摘要

BACKGROUND AND AIM: Anti-tumor-necrosis-factor-alpha (anti-TNF-alpha) medications are effective in inflammatory bowel disease (IBD), but have an increased risk of tuberculosis (TB) and serious infections. The aim of this study was to examine the Australian/New Zealand experience of serious infections and TB in IBD patients receiving anti-TNF-alpha therapy from 1999-2009. METHODS: Serious infections, defined as 'requiring hospital admission' and TB cases in patients receiving, or within 3 months following, anti-TNF-alpha therapy were analyzed across Australia and New Zealand. Patient demographics, IBD medications, duration of anti-TNF-alpha therapy, and infection details were collected. RESULTS: A total of 5562 IBD patients were managed across the centers. Of these, 489 (16.8%) Crohn's disease and 137 (5.2%) ulcerative colitis patients received anti-TNF-alpha therapy. There were three cases of latent TB that received prophylaxis prior to anti-TNF-alpha therapy. No cases of active TB were reported. Fourteen (2.2%) serious infections occurred. Seven occurred in patients receiving anti-TNF-alpha therapy for less than 6 months, including two cases of primary Varicella zoster (VZV), two cases of Pneumocystis jiroveci pneumonia, two cases of Staphylococcus aureus bacteremia, and one severe flu-like illness. Six patients were taking additional immunosuppressive medications. The other seven infections occurred after 6 months (mean 32.6 +/- 24.3 months) and included one case of primary VZV, one flu-like illness, and five bacterial infections. All infections resolved with treatment. CONCLUSION: TB is a very rare complication of anti-TNF-alpha therapy in Australia and New Zealand. Serious infections are uncommon but early opportunistic infections with Pneumocystis jiroveci pneumonia suggest a need for vigilance in patients on multiple immunosuppressive medications. VZV vaccination prior to immunosuppressive therapy should be considered in VZV-naive patients.
机译:背景与目的:抗肿瘤坏死因子-α(anti-TNF-alpha)药物可有效治疗炎症性肠病(IBD),但增加了患结核病(TB)和严重感染的风险。这项研究的目的是调查澳大利亚/新西兰从1999年至2009年接受抗TNF-α治疗的IBD患者的严重感染和结核病的经历。方法:在澳大利亚和新西兰,对接受抗TNF-α治疗的患者或接受治疗后3个月内的严重感染(定义为“需要入院”)和结核病病例进行了分析。收集患者的人口统计资料,IBD药物,抗TNF-α治疗的持续时间以及感染的详细信息。结果:各中心共治疗5562名IBD患者。在这些患者中,有489名(16.8%)克罗恩氏病和137名(5.2%)溃疡性结肠炎患者接受了抗TNF-α治疗。有3例潜在的TB患者在接受抗TNF-α治疗之前接受了预防。没有活动性结核病例的报道。发生了十四例(2.2%)严重感染。接受抗TNF-α治疗的少于6个月的患者中有7例发生,其中包括2例原发性水痘带状疱疹(VZV),2例初级肺炎杆状肺炎,2例金黄色葡萄球菌菌血症和1例严重的流感样疾病。六名患者正在接受其他免疫抑制药物。其他7例感染发生在6个月后(平均32.6 +/- 24.3个月),包括1例原发性VZV,1例流感样疾病和5例细菌感染。所有感染均可通过治疗解决。结论:在澳大利亚和新西兰,结核病是一种非常罕见的抗TNF-α疗法。严重感染并不常见,但早期罗氏肺孢子虫肺炎的机会性感染提示需要对多种免疫抑制药物的患者保持警惕。对于未经VZV感染的患者,应考虑在免疫抑制治疗之前进行VZV疫苗接种。

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