EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria

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Date
2010-05-01Author
Ozen, Seza
Pistorio, Angela
Iusan, Silvia M.
Bakkaloglu, Aysin
Herlin, Troels
Brik, Riva
Buoncompagni, Antonella
Lazar, Calin
Bilge, Ilmay
Uziel, Yosef
Rigante, Donato
Cantarini, Luca
Hilario, Maria Odete [UNIFESP]
Silva, Clovis A.
Alegria, Mauricio
Norambuena, Ximena
Belot, Alexandre
Berkun, Yackov
Estrella, Amparo Ibanez
Olivieri, Alma Nunzia
Alpigiani, Maria Giannina
Rumba, Ingrida
Sztajnbok, Flavio
Tambic-Bukovac, Lana
Breda, Luciana
Al-Mayouf, Sulaiman
Mihaylova, Dimitrina
Chasnyk, Vyacheslav
Sengler, Claudia
Klein-Gitelman, Maria
Djeddi, Djamal
Nuno, Laura
Pruunsild, Chris
Brunner, Jurgen
Kondi, Anuela
Pagava, Karaman
Pederzoli, Silvia
Martini, Alberto
Ruperto, Nicolino
PRINTO
Type
ArtigoISSN
0003-4967Is part of
Annals of the Rheumatic DiseasesDOI
10.1136/ard.2009.116657Metadata
Show full item recordAbstract
Objectives To validate the previously proposed classification criteria for Henoch-Schonlein purpura (HSP), childhood polyarteritis nodosa (c-PAN), c-Wegener granulomatosis (c-WG) and c-Takayasu arteritis (c-TA).Methods Step 1: retrospective/prospective webdata collection for children with HSP, c-PAN, c-WG and c-TA with age at diagnosis <= 18 years. Step 2: blinded classification by consensus panel of a representative sample of 280 cases. Step 3: statistical (sensitivity, specificity, area under the curve and.-agreement) and nominal group technique consensus evaluations.Results 827 patients with HSP, 150 with c-PAN, 60 with c-WG, 87 with c-TA and 52 with c-other were compared with each other. A patient was classified as HSP in the presence of purpura or petechiae (mandatory) with lower limb predominance plus one of four criteria: (1) abdominal pain; (2) histopathology (IgA); (3) arthritis or arthralgia; (4) renal involvement. Classification of c-PAN required a systemic inflammatory disease with evidence of necrotising vasculitis OR angiographic abnormalities of medium-/small-sized arteries (mandatory criterion) plus one of five criteria: (1) skin involvement; (2) myalgia/muscle tenderness; (3) hypertension; (4) peripheral neuropathy; (5) renal involvement. Classification of c-WG required three of six criteria: (1) histopathological evidence of granulomatous inflammation; (2) upper airway involvement; (3) laryngo-tracheo-bronchial involvement; (4) pulmonary involvement (x-ray/CT); (5) antineutrophilic cytoplasmic antibody positivity; (6) renal involvement. Classification of c-TA required typical angiographic abnormalities of the aorta or its main branches and pulmonary arteries (mandatory criterion) plus one of five criteria: (1) pulse deficit or claudication; (2) blood pressure discrepancy in any limb; (3) bruits; (4) hypertension; (5) elevated acute phase reactant.Conclusion European League Against Rheumatism/Paediatric Rheumatology International Trials Organisation/Paediatric Rheumatology European Society propose validated classification criteria for HSP, c-PAN, c-WG and c-TA with high sensitivity/specificity.
Citation
Annals of the Rheumatic Diseases. London: B M J Publishing Group, v. 69, n. 5, p. 798-806, 2010.Sponsorship
EULAR/PRINTO/PRESCollections
- EPM - Artigos [17709]