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


Autoria(s): 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; PRINTO
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

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.

EULAR/PRINTO/PRES

Identificador

ANNALS OF THE RHEUMATIC DISEASES, v.69, n.5, p.798-806, 2010

0003-4967

http://producao.usp.br/handle/BDPI/21158

10.1136/ard.2009.116657

http://dx.doi.org/10.1136/ard.2009.116657

Idioma(s)

eng

Publicador

B M J PUBLISHING GROUP

Relação

Annals of the Rheumatic Diseases

Direitos

restrictedAccess

Copyright B M J PUBLISHING GROUP

Palavras-Chave #RHEUMATOLOGY 1990 CRITERIA #VASCULITIDES #Rheumatology
Tipo

article

original article

publishedVersion