The 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria

医学 抗磷脂综合征 内科学 狼疮抗凝剂 金标准(测试) 痹症科 队列 血栓形成
作者
Medha Barbhaiya,Stéphane Zuily,Ray Naden,Alison Hendry,Florian Manneville,Mary‐Carmen Amigo,Zahir Amoura,Danieli Andrade,Laura Andréoli,Bahar Artim‐Esen,Tatsuya Atsumi,Tadej Avčin,H. Michael Belmont,María Laura Bertolaccini,D. Ware Branch,Graziela Carvalheiras,Alessandro Casini,Ricard Cervera,Hannah Cohen,N. Costedoat‐Chalumeau,Mark Crowther,Guilherme Ramires de Jesús,Aurélien Delluc,Sheetal Desai,Maria De Sancho,Katrien Devreese,Reyhan Diz Küçükkaya,Alí Duarte‐García,Camille Françès,David García,Jean‐Christophe Gris,Natasha Jordan,Rebecca Karp Leaf,Nina Kello,Jason S. Knight,Carl A. Laskin,Alfred Ian Lee,Kimberly Legault,Steve Levine,Roger A. Levy,Maarten Limper,Michael D. Lockshin,K Mayer-Pickel,Jack Musial,Pier Luigi Meroni,Giovanni Orsolini,Thomas L. Ortel,Vittorio Pengo,Michelle Petri,Guillermo J. Pons‐Estel,José A. Gómez‐Puerta,Quentin Raimboug,Robert Roubey,Giovanni Sanna,Surya V. Seshan,Savino Sciascia,Maria G. Tektonidou,Anǵela Tincani,Denis Wahl,Rohan Willis,Cécile Yelnik,Catherine Zuily,Françis Guillemin,Karen H. Costenbader,Doruk Erkan
出处
期刊:Arthritis & rheumatology [Wiley]
卷期号:75 (10): 1687-1702 被引量:128
标识
DOI:10.1002/art.42624
摘要

To develop new antiphospholipid syndrome (APS) classification criteria with high specificity for use in observational studies and trials, jointly supported by the American College of Rheumatology (ACR) and EULAR.This international multidisciplinary initiative included 4 phases: 1) Phase I, criteria generation by surveys and literature review; 2) Phase II, criteria reduction by modified Delphi and nominal group technique exercises; 3) Phase III, criteria definition, further reduction with the guidance of real-world patient scenarios, and weighting via consensus-based multicriteria decision analysis, and threshold identification; and 4) Phase IV, validation using independent adjudicators' consensus as the gold standard.The 2023 ACR/EULAR APS classification criteria include an entry criterion of at least one positive antiphospholipid antibody (aPL) test within 3 years of identification of an aPL-associated clinical criterion, followed by additive weighted criteria (score range 1-7 points each) clustered into 6 clinical domains (macrovascular venous thromboembolism, macrovascular arterial thrombosis, microvascular, obstetric, cardiac valve, and hematologic) and 2 laboratory domains (lupus anticoagulant functional coagulation assays, and solid-phase enzyme-linked immunosorbent assays for IgG/IgM anticardiolipin and/or IgG/IgM anti-β2 -glycoprotein I antibodies). Patients accumulating at least 3 points each from the clinical and laboratory domains are classified as having APS. In the validation cohort, the new APS criteria versus the 2006 revised Sapporo classification criteria had a specificity of 99% versus 86%, and a sensitivity of 84% versus 99%.These new ACR/EULAR APS classification criteria were developed using rigorous methodology with multidisciplinary international input. Hierarchically clustered, weighted, and risk-stratified criteria reflect the current thinking about APS, providing high specificity and a strong foundation for future APS research.
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