Predictive validity of the ASAS classification criteria for axial and peripheral spondyloarthritis after follow-up in the ASAS cohort: a final analysis

To establish the predictive validity of the Assessment of SpondyloArthritis international Society (ASAS) spondyloarthritis (SpA) classification criteria. 22 centres (N=909 patients) from the initial 29 ASAS centres (N=975) participated in the ASAS-cohort follow-up study. Patients had either chronic...

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Published in:Annals of the rheumatic diseases Vol. 75; no. 6; p. 1034
Main Authors: Sepriano, Alexandre, Landewé, Robert, van der Heijde, Désirée, Sieper, Joachim, Akkoc, Nurullah, Brandt, Jan, Braun, Jürgen, Collantes-Estevez, Eduardo, Dougados, Maxime, Fitzgerald, Oliver, Huang, Feng, Gu, Jieruo, Kirazli, Yesim, Maksymowych, Walter P, Marzo-Ortega, Helena, Olivieri, Ignazio, Ozgocmen, Salih, Roussou, Euthalia, Scarpato, Salvatore, Sørensen, Inge J, Valle-Oñate, Rafael, Van den Bosch, Filip, van der Horst-Bruinsma, Irene, Weber, Ulrich, Wei, James, Rudwaleit, Martin
Format: Journal Article
Language:English
Published: England 01-06-2016
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Summary:To establish the predictive validity of the Assessment of SpondyloArthritis international Society (ASAS) spondyloarthritis (SpA) classification criteria. 22 centres (N=909 patients) from the initial 29 ASAS centres (N=975) participated in the ASAS-cohort follow-up study. Patients had either chronic (>3 months) back pain of unknown origin and age of onset below 45 years (N=658) or peripheral arthritis and/or enthesitis and/or dactylitis (N=251). At follow-up, information was obtained at a clinic visit or by telephone. The positive predictive value (PPV) of the baseline classification by the ASAS criteria was calculated using rheumatologist's diagnosis at follow-up as external standard. In total, 564 patients were assessed at follow-up (345 visits; 219 telephone) with a mean follow-up of 4.4 years (range: 1.9; 6.8) and 70.2% received a SpA diagnosis by the rheumatologist. 335 patients fulfilled the axial SpA (axSpA) or peripheral SpA (pSpA) criteria at baseline and of these, 309 were diagnosed SpA after follow-up (PPV SpA criteria: 92.2%). The PPV of the axSpA and pSpA criteria was 93.3% and 89.5%, respectively. The PPV for the 'clinical arm only' was 88.0% and for the 'clinical arm'±'imaging arm' 96.0%, for the 'imaging arm only' 86.2% and for the 'imaging arm'+/-'clinical arm' 94.7%. A series of sensitivity analyses yielded similar results (range: 85.1-98.2%). The PPV of the axSpA and pSpA criteria to forecast an expert's diagnosis of 'SpA' after more than 4 years is excellent. The 'imaging arm' and 'clinical arm' of the axSpA criteria have similar predictive validity and are truly complementary.
ISSN:1468-2060
DOI:10.1136/annrheumdis-2015-208730