Peter C. Grayson
2022 American College of Rheumatology/European Alliance of Associations for Rheumatology classification criteria for eosinophilic granulomatosis with polyangiitis
Grayson, Peter C.; Ponte, Cristina; Suppiah, Ravi; Robson, Joanna C.; Craven, Anthea; Judge, Andrew; Khalid, Sara; Hutchings, Andrew; Luqmani, Raashid A.; Watts, Richard A.; Merkel, Peter A.
Authors
Cristina Ponte
Ravi Suppiah
Jo Robson Jo.Robson@uwe.ac.uk
Consultant Associate Professor in Rheumatology
Anthea Craven
Andrew Judge
Sara Khalid
Andrew Hutchings
Raashid A. Luqmani
Richard A. Watts
Peter A. Merkel
Abstract
Objective To develop and validate revised classification criteria for eosinophilic granulomatosis with polyangiitis (EGPA).
Methods Patients with vasculitis or comparator diseases were recruited into an international cohort. The study proceeded in five phases: (1) identification of candidate criteria items using consensus methodology, (2) prospective collection of candidate items present at the time of diagnosis, (3) data-driven reduction of the number of candidate items, (4) expert panel review of cases to define the reference diagnosis and (5) derivation of a points-based risk score for disease classification in a development set using least absolute shrinkage and selection operator logistic regression, with subsequent validation of performance characteristics in an independent set of cases and comparators.
Results The development set for EGPA consisted of 107 cases of EGPA and 450 comparators. The validation set consisted of an additional 119 cases of EGPA and 437 comparators. From 91 candidate items, regression analysis identified 11 items for EPGA, 7 of which were retained. The final criteria and their weights were as follows: maximum eosinophil count ≥1×109/L (+5), obstructive airway disease (+3), nasal polyps (+3), cytoplasmic antineutrophil cytoplasmic antibody (ANCA) or anti-proteinase 3–ANCA positivity (−3), extravascular eosinophilic predominant inflammation (+2), mononeuritis multiplex/motor neuropathy not due to radiculopathy (+1) and haematuria (−1). After excluding mimics of vasculitis, a patient with a diagnosis of small- or medium-vessel vasculitis could be classified as having EGPA if the cumulative score was ≥6 points. When these criteria were tested in the validation data set, the sensitivity was 85% (95% CI 77% to 91%) and the specificity was 99% (95% CI 98% to 100%).
Conclusion The 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology Classification Criteria for Eosinophilic Granulomatosis with Polyangiitis demonstrate strong performance characteristics and are validated for use in research.
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 4, 2021 |
Online Publication Date | Feb 2, 2022 |
Publication Date | Feb 14, 2022 |
Deposit Date | Feb 2, 2022 |
Journal | Annals of the rheumatic diseases |
Print ISSN | 0003-4967 |
Electronic ISSN | 1468-2060 |
Publisher | BMJ Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 81 |
Issue | 3 |
Pages | 309-314 |
DOI | https://doi.org/10.1136/annrheumdis-2021-221794 |
Public URL | https://uwe-repository.worktribe.com/output/8186344 |
You might also like
The OMERACT emerging leaders program: The good, the bad, and the future
(2019)
Journal Article
Update on outcome measure development in large-vessel vasculitis: Report from OMERACT 2018
(2019)
Journal Article
Downloadable Citations
About UWE Bristol Research Repository
Administrator e-mail: repository@uwe.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2025
Advanced Search