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揭开药物反应伴嗜酸性粒细胞增多和全身症状(DRESS)的神秘面纱:文献复习与管理指南。

Demystifying drug reaction with eosinophilia and systemic symptoms (DRESS): a review of the literature and guidelines for management.

机构信息

Faculty of Health Sciences, University of the Fraser Valley, Chilliwack, BC, Canada.

出版信息

Arch Dermatol Res. 2024 Sep 26;316(9):644. doi: 10.1007/s00403-024-03389-z.

DOI:10.1007/s00403-024-03389-z
PMID:39325061
Abstract

Drug reaction with eosinophilia and systemic symptoms (DRESS) is a severe, adverse drug reaction that is notoriously complex in both its presentation and treatment. Although early diagnosis and cessation of the causative agent are universally accepted as the initial interventions for DRESS, the subsequent management lacks a standardized approach. Historically, systemic steroids have been used as first-line treatment, but there is debate about the optimal dosing and route of administration, and evidence persists on the long-term complications associated with steroid use. Novel treatment approaches with targeted therapy, cyclosporine, intravenous immunoglobulin, and plasmapheresis have been gaining interest as alternative mono- and adjuvant therapies, but their use has yet to be supported by clinical trials. This narrative review provides a summary of the current knowledge of DRESS, with a focus on clinical management. The various mono- and adjuvant therapy options are discussed, with literature-supported suggestions for their optimal use in clinical practice. The risks for relapses, viral reactivation, and long-term complications are also considered. The PubMed and Medline databases were searched for articles on DRESS, published between January 1, 2008, and May 1, 2023. 334 articles met the inclusion criteria. Based on the literature, a DRESS management tool with step-by-step guidance is provided. Further suggestions for management are woven throughout this review, giving clinicians a toolbelt of resources with which to approach diagnosis, treatment, and follow-up.

摘要

药物反应伴嗜酸性粒细胞增多和全身症状(DRESS)是一种严重的药物不良反应,其表现和治疗都非常复杂。虽然早期诊断和停用致病药物被普遍认为是 DRESS 的初始干预措施,但随后的管理缺乏标准化方法。历史上,全身性类固醇一直被用作一线治疗药物,但关于最佳剂量和给药途径仍存在争议,而且关于类固醇使用相关的长期并发症的证据仍然存在。新型靶向治疗、环孢素、静脉注射免疫球蛋白和血浆置换等治疗方法作为单一和辅助治疗的替代方法越来越受到关注,但它们的使用尚未得到临床试验的支持。本文综述了 DRESS 的现有知识,重点是临床管理。讨论了各种单一和辅助治疗选择,并根据文献提出了在临床实践中最佳使用的建议。还考虑了复发、病毒再激活和长期并发症的风险。在 PubMed 和 Medline 数据库中搜索了 2008 年 1 月 1 日至 2023 年 5 月 1 日期间发表的关于 DRESS 的文章,共有 334 篇文章符合纳入标准。基于文献,提供了一个具有逐步指导的 DRESS 管理工具。在本综述中还贯穿了进一步的管理建议,为临床医生提供了一个工具包,用于诊断、治疗和随访。

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Am J Emerg Med. 2022 Jun;56:1-6. doi: 10.1016/j.ajem.2022.03.024. Epub 2022 Mar 18.
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本文引用的文献

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Novel targeted inhibition of the IL-5 axis for drug reaction with eosinophilia and systemic symptoms syndrome.新型靶向抑制白细胞介素-5 轴治疗药物反应伴嗜酸性粒细胞增多和全身性症状综合征。
Front Immunol. 2023 Apr 28;14:1134178. doi: 10.3389/fimmu.2023.1134178. eCollection 2023.
2
Current understanding of genetic associations with delayed hypersensitivity reactions induced by antibiotics and anti-osteoporotic drugs.目前对抗生素和抗骨质疏松药物引起的迟发型超敏反应的遗传关联的认识。
Front Pharmacol. 2023 Apr 26;14:1183491. doi: 10.3389/fphar.2023.1183491. eCollection 2023.
3
Etanercept leads to a rapid recovery of a Dabrafenib-/Trametinib-associated toxic epidermal necrolysis-like severe skin reaction.
依那西普可使与达拉非尼/曲美替尼相关的中毒性表皮坏死松解症样严重皮肤反应迅速恢复。
Skin Health Dis. 2022 Nov 5;3(1):e185. doi: 10.1002/ski2.185. eCollection 2023 Feb.
4
Comparison of cyclosporine and systemic corticosteroid for treating drug reaction with eosinophilia and systemic symptoms syndrome: A retrospective 20-year single-centre study in South Korea.比较环孢素与全身皮质类固醇治疗药物反应伴嗜酸性粒细胞增多和全身症状综合征:韩国 20 年单中心回顾性研究。
Australas J Dermatol. 2023 Feb;64(1):50-57. doi: 10.1111/ajd.13982. Epub 2023 Jan 25.
5
Management and treatment outcome of DRESS patients in Europe: An international multicentre retrospective study of 141 cases.欧洲中毒性表皮坏死松解症伴嗜酸性粒细胞增多和全身症状患者的管理与治疗结果:一项对141例病例的国际多中心回顾性研究。
J Eur Acad Dermatol Venereol. 2023 Apr;37(4):753-762. doi: 10.1111/jdv.18808. Epub 2022 Dec 19.
6
Case report: Drug rash with eosinophilia and systemic symptoms syndrome in a patient with anti-interferon-γ autoantibody-associated immunodeficiency.病例报告:抗干扰素-γ自身抗体相关性免疫缺陷患者的药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征。
Front Immunol. 2022 Aug 22;13:969912. doi: 10.3389/fimmu.2022.969912. eCollection 2022.
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Biomedicines. 2022 Apr 26;10(5):999. doi: 10.3390/biomedicines10050999.
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