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The 2022 EULAR/ACR Points to Consider at the Early Stages of Diagnosis and Management of Suspected Haemophagocytic Lymphohistiocytosis/Macrophage Activation Syndrome (HLH/MAS).
Shakoory, Bita; Geerlinks, Ashley; Wilejto, Marta; Kernan, Kate; Hines, Melissa; Romano, Micol; Piskin, David; Ravelli, Angelo; Sinha, Rashmi; Aletaha, Daniel; Allen, Carl; Bassiri, Hamid; Behrens, Edward M; Carcillo, Joseph; Carl, Linda; Chatham, Winn; Cohen, Jeffrey I; Cron, Randy Q; Drewniak, Erik; Grom, Alexei A; Henderson, Lauren A; Horne, Annacarin; Jordan, Michael B; Nichols, Kim E; Schulert, Grant; Vastert, Sebastiaan; Demirkaya, Erkan; Goldbach-Mansky, Raphaela; de Benedetti, Fabrizio; Marsh, Rebecca A; Canna, Scott W.
Afiliação
  • Shakoory B; Translational Autoinflammatory Diseases Section, NIH, Bethesda, Maryland.
  • Geerlinks A; Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center and University of Cincinnati, Cincinnati, Ohio, and Hematology/Oncology, University of Western Ontario Schulich School of Medicine & Dentistry, London, Ontario, Canada.
  • Wilejto M; Hematology/Oncology, University of Western Ontario Schulich School of Medicine & Dentistry, London, Ontario, Canada.
  • Kernan K; Hematology/Oncology, University of Western Ontario Schulich School of Medicine & Dentistry, London, Ontario, Canada.
  • Hines M; Pediatric Critical Care Medicine, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
  • Romano M; Pediatric Critical Care Medicine, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Piskin D; Pediatrics, University of Western Ontario Schulich School of Medicine & Dentistry, London, Ontario, Canada.
  • Ravelli A; Department of Epidemiology and Biostatistics, Western University and Department of Paediatrics, Lawson Health Research Institute, London, Ontario, Canada.
  • Sinha R; Direzione Scientifica, IRCCS Istituto Giannina Gaslini, Genova, Italy.
  • Aletaha D; Systemic JIA Foundation, Cincinnati, Ohio.
  • Allen C; Department of Rheumatology, Medical University of Vienna, Vienna, Austria.
  • Bassiri H; Pediatric Oncology, Texas Children's Hospital, Houston.
  • Behrens EM; Pediatric Infectious Diseases, Children's Hospital of Philadelphia and University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
  • Carcillo J; Pediatric Rheumatology, Children's Hospital of Philadelphia and University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
  • Carl L; Pediatric Critical Care Medicine, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
  • Chatham W; Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center and University of Cincinnati, Cincinnati, Ohio.
  • Cohen JI; Rheumatology, University of Alabama at Birmingham.
  • Cron RQ; Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland.
  • Drewniak E; Pediatric Rheumatology, University of Alabama at Birmingham.
  • Grom AA; Autoinflammatory Alliance, San Francisco, California.
  • Henderson LA; Pediatric Rheumatology, Cincinnati Children's Hospital Medical Center and University of Cincinnati, Cincinnati, Ohio.
  • Horne A; Pediatric Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Jordan MB; Department of Women's and Children's Health, Karolinska Institutet Cancerforskning KI, Stockholm, Sweden.
  • Nichols KE; Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center and University of Cincinnati, Cincinnati, Ohio.
  • Schulert G; Division of Cancer Predisposition Department of Oncology, St. Jude Children's Research Hospital Department of Oncology, Memphis, Tennessee.
  • Vastert S; Pediatric Rheumatology, Cincinnati Children's Hospital Medical Center and University of Cincinnati, Cincinnati, Ohio.
  • Demirkaya E; Center for Translational Immunology Research, UMC Utrecht, Utrecht, The Netherlands.
  • Goldbach-Mansky R; Pediatrics, University of Western Ontario Schulich School of Medicine & Dentistry, London, Ontario, Canada.
  • de Benedetti F; Translational Autoinflammatory Diseases Section, NIH, Bethesda, Maryland.
  • Marsh RA; Division of Rheumatology, IRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy.
  • Canna SW; Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center and University of Cincinnati, Cincinnati, Ohio.
Arthritis Rheumatol ; 75(10): 1714-1732, 2023 10.
Article em En | MEDLINE | ID: mdl-37486733
ABSTRACT

OBJECTIVE:

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 early stages of diagnosis, treatment and monitoring of HLH/MAS.

METHODS:

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.

RESULTS:

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.

CONCLUSION:

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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Médicos / Linfo-Histiocitose Hemofagocítica / Síndrome de Ativação Macrofágica Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Limite: Adult / Child / Humans Idioma: En Revista: Arthritis Rheumatol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Médicos / Linfo-Histiocitose Hemofagocítica / Síndrome de Ativação Macrofágica Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Limite: Adult / Child / Humans Idioma: En Revista: Arthritis Rheumatol Ano de publicação: 2023 Tipo de documento: Article