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
Date
2010Author
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
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
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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.