Lawrence Sally J, Sadarangani Manish, Jacobson Kevan
Department of Pediatric Gastroenterology, Hepatology and Nutrition, BC Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
Vaccine Evaluation Center, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada.
Front Pediatr. 2017 Jul 24;5:161. doi: 10.3389/fped.2017.00161. eCollection 2017.
Immunosuppressive therapy is a known risk factor for opportunistic infections. We report the first case of severe infection requiring intensive care in a pediatric patient with inflammatory bowel disease (IBD). The literature was reviewed and there were 92 reported cases of pneumonia (PCP) in patients with IBD. Most sources were case reports and there was likely reporting bias toward patients receiving immunomodulators, anti-tumor necrosis factor (anti-TNF) therapy, and those who died. Overall, 56% of patients were males and 58% had Crohn's disease. The median age was 45 years (interquartile range 30-68, range 8-78) and 86% of patients were lymphopenic. The case-fatality rate was 23%. Corticosteroids were used as IBD treatment in 88% of patients who subsequently developed PCP, 42% received thiopurines, 44% used anti-TNF therapy, and 15% received either cyclosporine or tacrolimus. Rates of mono, dual, triple, and quadruple immunosuppression therapy were 35, 35, 29, and 2%, respectively. This report highlights the importance of considering PCP in immunosuppressed lymphopenic pediatric IBD patients who present with unusual symptoms. Moreover, it should give gastroenterologists the impetus to limit immunosuppressive therapy to its minimal effective dose and consider options such as exclusive enteral nutrition wherever possible. Although there is no place for global PCP prophylaxis in IBD given the low incidence, in an era when there is increasing use of biologic agents with combination immunosuppressive therapy, the risk-benefit profile of PCP chemoprophylaxis should be revisited in selected cohorts such as patients on triple immunosuppression with corticosteroids, thiopurines, and a biological agent or calcineurin inhibitor, especially in lymphopenic individuals.
免疫抑制治疗是机会性感染的已知危险因素。我们报告了首例患有炎症性肠病(IBD)的儿科患者发生需要重症监护的严重感染病例。我们对文献进行了回顾,IBD患者中有92例报告的肺炎(肺孢子菌肺炎)病例。大多数资料来源为病例报告,且可能存在对接受免疫调节剂、抗肿瘤坏死因子(抗TNF)治疗的患者以及死亡患者的报告偏倚。总体而言,56%的患者为男性,58%患有克罗恩病。中位年龄为45岁(四分位间距30 - 68岁,范围8 - 78岁),86%的患者淋巴细胞减少。病死率为23%。在随后发生肺孢子菌肺炎的患者中,88%使用皮质类固醇作为IBD治疗,42%接受硫唑嘌呤治疗,44%使用抗TNF治疗,15%接受环孢素或他克莫司治疗。单一、双重、三重和四重免疫抑制治疗的比例分别为35%、35%、29%和2%。本报告强调了在出现异常症状的免疫抑制淋巴细胞减少的儿科IBD患者中考虑肺孢子菌肺炎的重要性。此外,这应促使胃肠病学家将免疫抑制治疗限制在最低有效剂量,并尽可能考虑诸如全肠内营养等选择。尽管鉴于发病率低,在IBD中没有全球预防性使用肺孢子菌肺炎药物的空间,但在生物制剂与联合免疫抑制治疗使用日益增加的时代,对于选定的队列,如接受皮质类固醇、硫唑嘌呤和生物制剂或钙调神经磷酸酶抑制剂三重免疫抑制治疗的患者,尤其是淋巴细胞减少的个体,应重新审视肺孢子菌肺炎化学预防的风险效益情况。