Nagpal Ria, Ulaganathan Hemnaath, Khan Khushal, Egan Brian
Department of Gastroenterology, Mayo University Hospital, Castlebar, County Mayo, Ireland.
J Med Cases. 2023 May;14(5):155-161. doi: 10.14740/jmc4041. Epub 2023 May 31.
Anti-tumor necrosis factor (TNF) biologics have revolutionized the management of inflammatory bowel diseases (IBDs) by promoting mucosal healing and delaying surgical intervention in ulcerative colitis (UC). However, biologics can potentiate the risk of opportunistic infections alongside the use of other immunomodulators in IBD. As recommended by the European Crohn's and Colitis Organisation (ECCO), anti-TNF-α therapy should be suspended in the setting of a potentially life-threatening infection. The objective of this case report was to highlight how the practice of appropriately discontinuing immunosuppression can exacerbate underlying colitis. We need to maintain a high index of suspicion for complications of anti-TNF therapy, so that we can intervene early and prevent potential adverse sequelae. In this report, a 62-year-old female presented to the emergency department with non-specific symptoms including fever, diarrhea and confusion on a background of known UC. She had been commenced on infliximab (INFLECTRA) 4 weeks earlier. Inflammatory markers were elevated, and was identified on both blood cultures and cerebrospinal fluid (CSF) polymerase chain reaction (PCR). The patient improved clinically and completed a 21-day course of amoxicillin advised by microbiology. After a multidisciplinary discussion, the team planned to switch her from infliximab to vedolizumab (ENTYVIO). Unfortunately, the patient re-presented to hospital with acute severe UC. Left-sided colonoscopy demonstrated modified Mayo endoscopic score 3 colitis. She has had recurrent hospital admissions over the past 2 years for acute flares of UC, ultimately culminating in colectomy. To our knowledge, our case-based review is unique in unpacking the dilemma of holding immunosuppression at the risk of IBD worsening.
抗肿瘤坏死因子(TNF)生物制剂通过促进黏膜愈合和延缓溃疡性结肠炎(UC)的手术干预,彻底改变了炎症性肠病(IBD)的治疗方式。然而,在IBD中,生物制剂与其他免疫调节剂联合使用时会增加机会性感染的风险。根据欧洲克罗恩病和结肠炎组织(ECCO)的建议,在出现可能危及生命的感染时,应停用抗TNF-α治疗。本病例报告的目的是强调适当停用免疫抑制治疗的做法如何会加重潜在的结肠炎。我们需要对抗TNF治疗的并发症保持高度警惕,以便能够早期干预并预防潜在的不良后果。在本报告中,一名62岁女性因已知患有UC,出现包括发热、腹泻和意识模糊等非特异性症状而就诊于急诊科。她在4周前开始使用英夫利昔单抗(INFLECTRA)。炎症指标升高,血液培养和脑脊液(CSF)聚合酶链反应(PCR)均检测到[具体病原体未给出]。患者临床症状改善,并完成了微生物学建议的21天阿莫西林疗程。经过多学科讨论,团队计划将她从英夫利昔单抗换为维多珠单抗(ENTYVIO)。不幸的是,患者因急性重症UC再次入院。左侧结肠镜检查显示改良梅奥内镜评分3级结肠炎。在过去2年中,她因UC急性发作多次住院,最终接受了结肠切除术。据我们所知,我们基于病例的综述在剖析因担心IBD恶化而停用免疫抑制治疗的困境方面具有独特性。