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Identifying potential classification criteria for calcium pyrophosphate deposition disease (CPPD): Item generation and item reduction: Item Generation and Item Reduction

  • Sara K Tedeschi
  • , Tristan Pascart
  • , Augustin Latourte
  • , Cattleya Godsave
  • , Burak Kundakci
  • , Raymond P Naden
  • , William J Taylor
  • , Nicola Dalbeth
  • , Tuhina Neogi
  • , Fernando Perez-Ruiz
  • , Ann Rosenthal
  • , Fabio Becce
  • , Eliseo Pascual
  • , Mariano Andres
  • , Thomas Bardin
  • , Michael Doherty
  • , Hang-Korng Ea
  • , Georgios Filippou
  • , John FitzGerald
  • , Marwin Guitierrez
  • Annamaria Iagnocco, Tim L Jansen, Minna J Kohler, Frédéric Lioté, Mark Matza, Geraldine M McCarthy, Roberta Ramonda, Anthony M Reginato, Pascal Richette, Jasvinder A Singh, Francisca Sivera, Alexander So, Lisa K Stamp, Janeth Yinh, Chio Yokose, Robert Terkeltaub, Hyon Choi, Abhishek Abhishek
  • Brigham and Womens Hospital
  • Université Catholoique de Lille
  • Hôpital Lariboisière
  • Nottingham University Hospital NHS Trust
  • University of Otago
  • Auckland University of Technology
  • Boston University
  • Hospital Universitario Cruces
  • Medical College of Wisconsin
  • Lausanne University Hospital
  • Alicante Institute of Sanitary and Biomedical Research
  • Luigi Sacco University Hospital
  • Instituto Nacional de Rehabilitación
  • Universita Degli Studi di Torino
  • University of Twente
  • Massachusetts General Hospital
  • Mater Misericordiae University Hospital
  • Universita Degli Studi di Padova
  • Brown University
  • Birmingham Veterans Affairs Medical Center
  • Hospital General Universitario Elda
  • San Diego Veterans Administration Healthcare Service
  • University of California,San Diego
  • University of Alabama at Birmingham
  • Harvard Medical School
  • Hospital General Universitario de Alicante

Research output: Contribution to journalArticlepeer-review

Abstract

Abstract Objective Classification criteria for calcium pyrophosphate deposition disease (CPPD) will facilitate clinical research on this common crystalline arthritis. We report on the first two phases of a four-phase process for developing CPPD classification criteria. Methods CPPD classification criteria development is overseen by a 12-member Steering Committee. Item generation (Phase I) included a scoping literature review of five literature databases and contributions from a 35-member Combined Expert Committee and two Patient Research Partners. Item reduction and refinement (Phase II) involved a Combined Expert Committee meeting, discussions among Clinical, Imaging, and Laboratory Advisory Groups, and an item rating exercise to assess the influence of individual items toward classification. The Steering Committee reviewed the modal rating score for each item (range -3 [strongly pushes away from CPPD] to +3 [strongly pushes toward CPPD]) to determine items to retain for future phases of criteria development. Results Item generation yielded 420 items (312 from the literature, 108 from experts/patients). The Advisory Groups eliminated items they agreed were unlikely to distinguish between CPPD and other forms of arthritis, yielding 127 items for the item rating exercise. Fifty-six items, most of which had a modal rating of +/- 2 or 3, were retained for future phases. As numerous imaging items were rated +3, the Steering Committee recommended focusing on imaging of the knee, wrist, and one additional affected joint for calcification suggestive of CPP crystal deposition. Conclusion A data- and expert-driven process is underway to develop CPPD classification criteria. Candidate items comprise clinical, imaging, and laboratory features.
Original languageEnglish
JournalArthritis Care & Research
Early online date10 May 2021
DOIs
Publication statusPublished - 30 Jun 2021

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