Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Division of Clinical Pharmacology and Toxicology, Department of Paediatrics, The Hospital for Sick Children, 555 University Ave, Toronto, ON, M5G 1X8, Canada.
Am J Clin Dermatol. 2024 Jul;25(4):609-621. doi: 10.1007/s40257-024-00867-y. Epub 2024 May 16.
Drug reaction with eosinophilia and systemic symptoms (DReSS) is known to cause mortality and long-term sequelae in the pediatric population, however there are no established clinical practice guidelines for the management of pediatric DReSS. We conducted a scoping review, according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, to summarize the currently available data on treatment, mortality, and long-term sequelae of DReSS in children (aged 0-18 years). Data from 644 individuals revealed that various treatment strategies are being used in the management of pediatric DReSS, and strategies were often used in combination. The diversity in treatment approaches cannot be solely attributed to age or disease severity and reflects the lack of evidence-based management guidelines for DReSS. Children are also at risk of developing autoimmune sequelae following DReSS, most commonly thyroid disease and type 1 diabetes mellitus. We found that the eventual development of autoimmune disease was more often associated with DReSS caused by antibiotics, especially minocycline and sulfamethoxazole, in comparison with individuals who did not develop sequelae. In this study, we identify strengths and weaknesses in the currently available literature and highlight that future prospective studies with structured and long-term follow-up of children with DReSS are needed to better understand potential risk factors for mortality and development of sequelae after DReSS.
药物反应伴嗜酸性粒细胞增多和全身性症状(DReSS)已知可导致儿科人群死亡和长期后遗症,但目前尚无针对儿科 DReSS 管理的既定临床实践指南。我们根据系统评价和荟萃分析的首选报告项目(PRISMA)指南进行了范围综述,以总结目前关于儿童(0-18 岁)DReSS 的治疗、死亡率和长期后遗症的数据。来自 644 个人的数据表明,正在使用各种治疗策略来管理儿科 DReSS,并且这些策略经常联合使用。治疗方法的多样性不能仅仅归因于年龄或疾病严重程度,这反映了缺乏针对 DReSS 的循证管理指南。儿童在 DReSS 后也有发生自身免疫后遗症的风险,最常见的是甲状腺疾病和 1 型糖尿病。我们发现,与没有发生后遗症的个体相比,抗生素引起的 DReSS,尤其是米诺环素和磺胺甲噁唑,更常导致自身免疫疾病的最终发展。在这项研究中,我们确定了现有文献的优缺点,并强调需要未来进行前瞻性研究,对 DReSS 患儿进行结构化和长期随访,以更好地了解 DReSS 后死亡率和后遗症发展的潜在风险因素。