Translational Autoinflammatory Diseases Section, National Institutes of Health, Bethesda, Maryland, USA.
Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center and University of Cincinnati, Cincinnati, Ohio, USA.
Ann Rheum Dis. 2023 Oct;82(10):1271-1285. doi: 10.1136/ard-2023-224123. Epub 2023 Jul 24.
Haemophagocytic lymphohistiocytosis (HLH) and macrophage activation syndrome (MAS) are life-threatening systemic hyperinflammatory syndromes that can develop in most inflammatory contexts. They can progress rapidly, and early identification and management are critical for preventing organ failure and mortality. This effort aimed to develop evidence-based and consensus-based points to consider to assist clinicians in optimising decision-making in the of diagnosis, treatment and monitoring of HLH/MAS.
A multinational, multidisciplinary task force of physician experts, including adult and paediatric rheumatologists, haematologist/oncologists, immunologists, infectious disease specialists, intensivists, allied healthcare professionals and patients/parents, formulated relevant research questions and conducted a systematic literature review (SLR). Delphi methodology, informed by SLR results and questionnaires of experts, was used to generate statements aimed at assisting early decision-making and optimising the initial care of patients with HLH/MAS.
The task force developed 6 overarching statements and 24 specific points to consider relevant to early recognition of HLH/MAS, diagnostic approaches, initial management and monitoring of HLH/MAS. Major themes included the simultaneous need for prompt syndrome recognition, systematic evaluation of underlying contributors, early intervention targeting both hyperinflammation and likely contributors, careful monitoring for progression/complications and expert multidisciplinary assistance.
These 2022 EULAR/American College of Rheumatology points to consider provide up-to-date guidance, based on the best available published data and expert opinion. They are meant to help guide the initial evaluation, management and monitoring of patients with HLH/MAS in order to halt disease progression and prevent life-threatening immunopathology.
噬血细胞性淋巴组织细胞增生症(HLH)和巨噬细胞活化综合征(MAS)是危及生命的全身性炎症过度活跃综合征,可在大多数炎症情况下发生。这些疾病可能迅速进展,早期识别和管理对于防止器官衰竭和死亡至关重要。本研究旨在制定基于循证医学和共识的考虑要点,以协助临床医生优化 HLH/MAS 的诊断、治疗和监测决策。
一个由医师专家组成的多学科、多国家的工作组,包括成人和儿科风湿病学家、血液科医生/肿瘤学家、免疫学家、传染病专家、重症监护医生、辅助医疗专业人员以及患者/家长,制定了相关的研究问题,并进行了系统文献回顾(SLR)。德尔菲方法(Delphi method),由 SLR 结果和专家问卷提供信息,用于生成有助于早期决策和优化 HLH/MAS 患者初始治疗的陈述。
工作组制定了 6 项总体陈述和 24 项具体考虑要点,涉及 HLH/MAS 的早期识别、诊断方法、初始管理和监测。主要主题包括同时需要迅速识别综合征、系统评估潜在诱因、针对炎症过度活跃和潜在诱因的早期干预、仔细监测进展/并发症以及多学科专家协助。
这些 2022 年 EULAR/美国风湿病学会的考虑要点提供了基于现有最佳发表数据和专家意见的最新指南。它们旨在帮助指导 HLH/MAS 患者的初始评估、管理和监测,以阻止疾病进展并预防危及生命的免疫病理学。