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dc.contributor.authorOzen, Seza
dc.contributor.authorPistorio, Angela
dc.contributor.authorIusan, Silvia M.
dc.contributor.authorBakkaloglu, Aysin
dc.contributor.authorHerlin, Troels
dc.contributor.authorBrik, Riva
dc.contributor.authorBuoncompagni, Antonella
dc.contributor.authorLazar, Calin
dc.contributor.authorBilge, Ilmay
dc.contributor.authorUziel, Yosef
dc.contributor.authorRigante, Donato
dc.contributor.authorCantarini, Luca
dc.contributor.authorHilario, Maria Odete
dc.contributor.authorSilva, Clovis A.
dc.contributor.authorAlegria, Mauricio
dc.contributor.authorNorambuena, Ximena
dc.contributor.authorBelot, Alexandre
dc.contributor.authorBerkun, Yackov
dc.contributor.authorEstrella, Amparo Ibanez
dc.contributor.authorOlivieri, Alma Nunzia
dc.contributor.authorAlpigiani, Maria Giannina
dc.contributor.authorRumba, Ingrida
dc.contributor.authorSztajnbok, Flavio
dc.contributor.authorTambic-Bukovac, Lana
dc.contributor.authorBreda, Luciana
dc.contributor.authorAl-Mayouf, Sulaiman
dc.contributor.authorMihaylova, Dimitrina
dc.contributor.authorChasnyk, Vyacheslav
dc.contributor.authorSengler, Claudia
dc.contributor.authorKlein-Gitelman, Maria
dc.contributor.authorDjeddi, Djamal
dc.contributor.authorNuno, Laura
dc.contributor.authorPruunsild, Chris
dc.contributor.authorBrunner, Jurgen
dc.contributor.authorKondi, Anuela
dc.contributor.authorPagava, Karaman
dc.contributor.authorPederzoli, Silvia
dc.contributor.authorMartini, Alberto
dc.contributor.authorRuperto, Nicolino
dc.date.accessioned2019-12-10T10:36:48Z
dc.date.available2019-12-10T10:36:48Z
dc.date.issued2010
dc.identifier.issn0003-4967
dc.identifier.urihttps://doi.org/10.1136/ard.2009.116657
dc.identifier.urihttp://hdl.handle.net/11655/13969
dc.description.abstractObjectives 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.
dc.language.isoen
dc.publisherBMJ
dc.relation.isversionof10.1136/ard.2009.116657
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectRheumatology
dc.titleEular/Printo/Pres Criteria For Henoch-Schonlein Purpura, Childhood Polyarteritis Nodosa, Childhood Wegener Granulomatosis And Childhood Takayasu Arteritis: Ankara 2008. Part Ii: Final Classification Criteria
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalAnnals Of The Rheumatic Diseases
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume69
dc.identifier.issue5
dc.identifier.startpage798
dc.identifier.endpage806
dc.description.indexWoS
dc.description.indexScopus


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