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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

Peter C. Grayson

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.

Citation

Grayson, P. C., Ponte, C., Suppiah, R., Robson, J. C., Craven, A., Judge, A., …Merkel, P. A. (2022). 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology classification criteria for eosinophilic granulomatosis with polyangiitis. Annals of the Rheumatic Diseases, 81(3), 309-314. https://doi.org/10.1136/annrheumdis-2021-221794

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