首页> 外文期刊>Journal of Crohn’s & colitis >The association of psoriasiform rash with anti-tumor necrosis factor (anti-TNF) therapy in inflammatory bowel disease: A single academic center case series
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The association of psoriasiform rash with anti-tumor necrosis factor (anti-TNF) therapy in inflammatory bowel disease: A single academic center case series

机译:牛皮癣样皮疹与抗肿瘤坏死因子(TNF)治疗在炎症性肠病中的关联:一个学术中心案例系列

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Background & Aims: Anti-tumor necrosis factors (anti-TNF) including infliximab, adalimumab and certolizumab pegol are used to treat Crohn's disease (CD) and ulcerative colitis (UC). Paradoxically, while also indicated for the treatment of psoriasis, anti-TNF therapy has been associated with development of psoriasiform lesions in IBD patients and can compel discontinuation of therapy. We aim to investigate IBD patient, clinical characteristics, and frequency for the development of and outcomes associated with anti-TNF induced psoriasiform rash. Methods: We identify IBD patients on anti-TNFs with an onset of a psoriasiform rash. Patient characteristics, duration of anti-TNF, concomitant immunosuppressants, lesion distribution, and outcomes of rash are described. Results: Of 1004 IBD patients with exposure to anti-TNF therapy, 27 patients (2.7%) developed psoriasiform lesions. Psoriasiform rash cases stratified by biologic use were 1.3% for infliximab, 4.1% for adalimumab, and 6.4% for certolizumab. Average time on treatment (206.3. weeks) and time on treatment until onset of psoriasiform lesions (126.9. weeks) was significantly higher in the infliximab group. The adalimumab group had the highest need for treatment discontinuation (60%). The majority (59.3%) of patients were able to maintain on anti-TNFs despite rash onset. Among patients that required discontinuation (40.7%), the majority experienced improvement with a subsequent anti-TNF (66.7%). Conclusion: 27 cases of anti-TNF associated psoriasiform lesions are reported. Discontinuation of anti-TNF treatment is unnecessary in the majority. Dermatologic improvement was achieved in the majority with a subsequent anti-TNF, suggesting anti-TNF induced psoriasiform rash is not necessarily a class effect.
机译:背景与目的:包括英夫利昔单抗,阿达木单抗和塞妥珠单抗聚乙二醇乙二醇酯在内的抗肿瘤坏死因子(抗TNF)可用于治疗克罗恩病(CD)和溃疡性结肠炎(UC)。矛盾的是,尽管抗肿瘤坏死因子疗法也已被证明可用于牛皮癣的治疗,但它与IBD患者牛皮癣样病变的发展有关,并可能迫使中止治疗。我们的目的是调查IBD患者,临床特征以及抗TNF诱导的牛皮癣样皮疹的发展和相关结果的频率。方法:我们确定抗TNFs的IBD患者出现银屑病皮疹。描述患者的特征,抗TNF的持续时间,伴随的免疫抑制剂,病变分布和皮疹的结局。结果:在1004名接受抗TNF治疗的IBD患者中,有27名患者(2.7%)出现了牛皮癣样病变。按生物学用途分层的银屑病皮疹病例:英夫利昔单抗为1.3%,阿达木单抗为4.1%,赛妥珠单抗为6.4%。英夫利昔单抗组的平均治疗时间(206.3周)和直到银屑病皮损开始的治疗时间(126.9周)显着增加。阿达木单抗组中止治疗的需求最高(60%)。尽管有皮疹发作,但大多数(59.3%)患者仍能够维持抗TNFs。在需要停药的患者中(40.7%),大多数患者随后接受了抗TNF治疗(66.7%)。结论:报告了27例抗TNF相关的银屑病病灶。在大多数情况下,无需中止抗TNF治疗。皮肤疾病的改善在大多数患者中得到了改善,并随后出现了抗TNF,这表明抗TNF诱导的牛皮癣样皮疹不一定是一种类效应。

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