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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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  • معلومة اضافية
    • Contributors:
      Hacettepe Univ; IRCCS G Gaslini; PRINTO; Aarhus Univ Hosp; Rambam Med Ctr; Clin Pediat 1; Istanbul Univ; Meir Med Ctr; Univ Cattolica Sacro Cuore; Med Clin & Sci Immunol Ist; Universidade Federal de São Paulo (UNIFESP); Universidade de São Paulo (USP); Hosp Ninos Benjamin Bloom; Hosp Dr Exequiel Gonzalez Cortes; Hop Femme Mere Enfant; Safra Childrens Hosp; Inst Salud Nino; Univ Naples 2; IRCCS Ist G Gaslini; Latvian State Univ; Hosp Univ Pedro Ernesto; Univ Zagreb; Univ G dAnnunzio; King Faisal Specialist Hosp & Res Ctr; Univ Children Hosp; Hosp Paediat Dept; Charite; Childrens Mem Hosp; Dept Pediat; Hosp Gen Univ La Paz; Tartu Univ Hosp; Med Univ; Tblisi State Med Univ; Univ Genoa
    • بيانات النشر:
      B M J Publishing Group
    • الموضوع:
      2010
    • Collection:
      Universidade Federal de São Paulo (UNIFESP): Repositório Institucional
    • نبذة مختصرة :
      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 ...
    • File Description:
      798-806; application/pdf
    • ISSN:
      0003-4967
    • Relation:
      Annals of the Rheumatic Diseases; http://dx.doi.org/10.1136/ard.2009.116657; Annals of the Rheumatic Diseases. London: B M J Publishing Group, v. 69, n. 5, p. 798-806, 2010.; http://repositorio.unifesp.br/handle/11600/32490; WOS000276982300004.pdf; WOS:000276982300004
    • الرقم المعرف:
      10.1136/ard.2009.116657
    • الدخول الالكتروني :
      http://repositorio.unifesp.br/handle/11600/32490
      https://doi.org/10.1136/ard.2009.116657
    • Rights:
      Acesso aberto
    • الرقم المعرف:
      edsbas.36D26D73