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The 2023 ACR/EULAR Classification Criteria for Calcium Pyrophosphate Deposition Disease.
Abhishek, Abhishek; Tedeschi, Sara K; Pascart, Tristan; Latourte, Augustin; Dalbeth, Nicola; Neogi, Tuhina; Fuller, Amy; Rosenthal, Ann; Becce, Fabio; Bardin, Thomas; Ea, Hang Korng; Filippou, Georgios; FitzGerald, John; Iagnocco, AnnaMaria; Lioté, Frédéric; McCarthy, Geraldine M; Ramonda, Roberta; Richette, Pascal; Sivera, Francisca; Andres, Mariano; Cipolletta, Edoardo; Doherty, Michael; Pascual, Eliseo; Perez-Ruiz, Fernando; So, Alexander; Jansen, Tim L; Kohler, Minna J; Stamp, Lisa K; Yinh, Janeth; Adinolfi, Antonella; Arad, Uri; Aung, Thanda; Benillouche, Eva; Bortoluzzi, Alessandra; Dau, Jonathan; Maningding, Ernest; Fang, Meika A; Figus, Fabiana A; Filippucci, Emilio; Haslett, Janine; Janssen, Matthijs; Kaldas, Marian; Kimoto, Maryann; Leamy, Kelly; Navarro, Geraldine M; Sarzi-Puttini, Piercarlo; Scirè, Carlo; Silvagni, Ettore; Sirotti, Silvia; Stack, John R.
Affiliation
  • Abhishek A; Academic Rheumatology, University of Nottingham, Nottingham, UK.
  • Tedeschi SK; Division of Rheumatology, Inflammation and Immunity, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts.
  • Pascart T; Department of Rheumatology, Lille Catholic University, Saint-Philibert Hospital, Lille, France.
  • Latourte A; Université de Paris, INSERM, UMR-S 1132 BIOSCAR, and Service de Rhumatologie, AP-HP, Lariboisière Hospital, Paris, France.
  • Dalbeth N; Department of Medicine, University of Auckland, Auckland, New Zealand.
  • Neogi T; Department of Medicine, Section of Rheumatology, Boston University School of Medicine, Boston, Massachusetts.
  • Fuller A; Academic Rheumatology, University of Nottingham, Nottingham, UK.
  • Rosenthal A; Department of Medicine, Medical College of Wisconsin, Milwaukee.
  • Becce F; Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
  • Bardin T; Université de Paris, INSERM, UMR-S 1132 BIOSCAR, and Service de Rhumatologie, AP-HP, Lariboisière Hospital, Paris, France.
  • Ea HK; Université de Paris, INSERM, UMR-S 1132 BIOSCAR, and Service de Rhumatologie, AP-HP, Lariboisière Hospital, Paris, France.
  • Filippou G; Rheumatology Department, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.
  • FitzGerald J; David Geffen School of Medicine, University of California, and Veterans Administration for Greater Los Angeles, Los Angeles, California.
  • Iagnocco A; Academic Rheumatology Center, Università degli Studi di Torino, Turin, Italy.
  • Lioté F; Université de Paris, INSERM, UMR-S 1132 BIOSCAR, Service de Rhumatologie, AP-HP, Lariboisière Hospital, and Université Paris Cité, Faculté de Santé, Paris, France.
  • McCarthy GM; School of Medicine and Medical Science, University College Dublin, and Mater Misericordiae University Hospital, Dublin, Ireland.
  • Ramonda R; Rheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.
  • Richette P; Université de Paris, INSERM, UMR-S 1132 BIOSCAR, and Service de Rhumatologie, AP-HP, Lariboisière Hospital, Paris, France.
  • Sivera F; Department of Rheumatology, Hospital General Universitario Elda, Elda, Spain, and Department of Clinical Medicine, Universidad Miguel Hernandez, Elche, Spain.
  • Andres M; Department of Medicine, Rheumatology Section, Hospital General Universitario de Alicante, Universidad Miguel Hernández, Alicante, Spain.
  • Cipolletta E; Rheumatology Unit, Department of Clinical and Molecular Sciences, Polytechnic University of Marche, Ancona, Italy.
  • Doherty M; Academic Rheumatology, University of Nottingham, Nottingham, UK.
  • Pascual E; Rheumatology Division, Cruces University Hospital, Bilbao, Spain.
  • Perez-Ruiz F; Arthritis Investigation Group, Biocruces-Bizkaia Health Research Institute, Spain, Department of Medicine, Medicine and Nursing School, University of the Basque Country, and Basque Country Rheumatology Society, Bilbao, Spain.
  • So A; Lausanne University Hospital, Lausanne, Switzerland.
  • Jansen TL; VieCuri Medical Centre, Venlo, The Netherlands, and Medical Cell BioPhysics Group, University of Twente, Enschede, The Netherlands.
  • Kohler MJ; Department of Medicine, Rheumatology Unit, Massachusetts General Hospital, and Harvard Medical School, Boston, Massachusetts.
  • Stamp LK; Department of Medicine, University of Otago, Christchurch, New Zealand.
  • Yinh J; Department of Medicine, Rheumatology Unit, Massachusetts General Hospital, and Harvard Medical School, Boston, Massachusetts.
  • Adinolfi A; Rheumatology Unit, Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Arad U; Department of Rheumatology, Te Whatu Ora-Health New Zealand Waikato, Hamilton, New Zealand.
  • Aung T; Division of Rheumatology, University of California, Los Angeles.
  • Benillouche E; Department of Rheumatology, Lausanne University Hospital, Lausanne, Switzerland.
  • Bortoluzzi A; Section of Rheumatology, Department of Medical Sciences, University of Ferrara, Ferrara, Italy, and Azienda Ospedaliera-Universitaria di Ferrara, Cona (FE), Italy.
  • Dau J; Department of Medicine, Rheumatology Unit, Massachusetts General Hospital, Boston.
  • Maningding E; Highland Hospital, Oakland, California.
  • Fang MA; David Geffen School of Medicine, University of California, and Veterans Administration for Greater Los Angeles, Los Angeles, California.
  • Figus FA; Rheumatology Division, Local Health Unit (ASL), Turin-3, Collegno and Pinerolo, Italy.
  • Filippucci E; Rheumatology Unit, Department of Clinical and Molecular Sciences, Polytechnic University of Marche, Ancona, Italy.
  • Haslett J; Department of Medicine, University of Otago, Christchurch, New Zealand.
  • Janssen M; VieCuri Medical Centre, Venlo, The Netherlands.
  • Kaldas M; David Geffen School of Medicine, University of California, Los Angeles.
  • Kimoto M; David Geffen School of Medicine, University of California, Los Angeles.
  • Leamy K; Mater Misericordiae University Hospital, Dublin, Ireland.
  • Navarro GM; Division of Rheumatology, University of California, Los Angeles, California.
  • Sarzi-Puttini P; Department of Rheumatology, IRCCS Galeazzi-Sant'Ambrogio Hospital, Milan, Italy.
  • Scirè C; Epidemiology Unit, Italian Society for Rheumatology, Milan, Italy.
  • Silvagni E; Section of Rheumatology, Department of Medical Sciences, University of Ferrara, Ferrara, Italy, and Azienda Ospedaliera-Universitaria di Ferrara, Cona (FE), Italy.
  • Sirotti S; Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy.
  • Stack JR; School of Medicine and Medical Science, University College Dublin, and Mater Misericordiae University Hospital, Dublin, Ireland.
Arthritis Rheumatol ; 75(10): 1703-1713, 2023 10.
Article in En | MEDLINE | ID: mdl-37494275
ABSTRACT

OBJECTIVE:

Calcium pyrophosphate deposition (CPPD) disease is prevalent and has diverse presentations, but there are no validated classification criteria for this symptomatic arthritis. The American College of Rheumatology (ACR) and EULAR have developed the first-ever validated classification criteria for symptomatic CPPD disease.

METHODS:

Supported by the ACR and EULAR, a multinational group of investigators followed established methodology to develop these disease classification criteria. The group generated lists of candidate items and refined their definitions, collected de-identified patient profiles, evaluated strengths of associations between candidate items and CPPD disease, developed a classification criteria framework, and used multi-criterion decision analysis to define criteria weights and a classification threshold score. The criteria were validated in an independent cohort.

RESULTS:

Among patients with joint pain, swelling, or tenderness (entry criterion) whose symptoms are not fully explained by an alternative disease (exclusion criterion), the presence of crowned dens syndrome or calcium pyrophosphate crystals in synovial fluid are sufficient to classify a patient as having CPPD disease. In the absence of these findings, a score >56 points using weighted criteria, comprising clinical features, associated metabolic disorders, and results of laboratory and imaging investigations, can be used to classify as CPPD disease. These criteria had a sensitivity of 92.2% and specificity of 87.9% in the derivation cohort (190 CPPD cases, 148 mimickers), whereas sensitivity was 99.2% and specificity was 92.5% in the validation cohort (251 CPPD cases, 162 mimickers).

CONCLUSION:

The 2023 ACR/EULAR CPPD disease classification criteria have excellent performance characteristics and will facilitate research in this field.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rheumatology / Calcinosis / Calcium Pyrophosphate / Chondrocalcinosis Type of study: Prognostic_studies Limits: Humans Country/Region as subject: America do norte Language: En Journal: Arthritis Rheumatol Year: 2023 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rheumatology / Calcinosis / Calcium Pyrophosphate / Chondrocalcinosis Type of study: Prognostic_studies Limits: Humans Country/Region as subject: America do norte Language: En Journal: Arthritis Rheumatol Year: 2023 Document type: Article Affiliation country: United kingdom