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2016 American College of Rheumatology/European League Against Rheumatism Criteria for Minimal, Moderate, and Major Clinical Response in Juvenile Dermatomyositis: An International Myositis Assessment and Clinical Studies Group/Paediatric Rheumatology International Trials Organisation Collaborative Initiative.
Rider, Lisa G; Aggarwal, Rohit; Pistorio, Angela; Bayat, Nastaran; Erman, Brian; Feldman, Brian M; Huber, Adam M; Cimaz, Rolando; Cuttica, Rubén J; de Oliveira, Sheila Knupp; Lindsley, Carol B; Pilkington, Clarissa A; Punaro, Marilynn; Ravelli, Angelo; Reed, Ann M; Rouster-Stevens, Kelly; van Royen-Kerkhof, Annet; Dressler, Frank; Saad Magalhaes, Claudia; Constantin, Tamás; Davidson, Joyce E; Magnusson, Bo; Russo, Ricardo; Villa, Luca; Rinaldi, Mariangela; Rockette, Howard; Lachenbruch, Peter A; Miller, Frederick W; Vencovsky, Jiri; Ruperto, Nicolino.
Afiliação
  • Rider LG; NIEHS, NIH, Bethesda, Maryland, USA.
  • Aggarwal R; University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Pistorio A; Istituto Giannina Gaslini, Servizio di Epidemiologia e Biostatistica, Genoa, Italy.
  • Bayat N; NIEHS, NIH, Bethesda, Maryland, USA.
  • Erman B; Social and Scientific Systems, Inc., Durham, North Carolina, USA.
  • Feldman BM; The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Huber AM; IWK Health Centre, Halifax, Nova Scotia, Canada.
  • Cimaz R; University of Firenze, Florence, Italy.
  • Cuttica RJ; Hospital de Niños Pedro de Elizalde, University of Buenos Aires, Buenos Aires, Argentina.
  • de Oliveira SK; Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Lindsley CB; University of Kansas City Medical Center, Kansas City, Kansas, USA.
  • Pilkington CA; Great Ormond Street Hospital for Children NHS Trust, London, UK.
  • Punaro M; University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Ravelli A; Istituto Giannina Gaslini, Pediatria II - Reumatologia, and Università degli Studi di Genova, Genoa, Italy.
  • Reed AM; Duke University, Durham, North Carolina, USA.
  • Rouster-Stevens K; Emory University School of Medicine, Atlanta, Georgia, USA.
  • van Royen-Kerkhof A; University Medical Centre Utrecht, Wilhelmina Children's Hospital, Utrecht, The Netherlands.
  • Dressler F; Hannover Medical School, Hannover, Germany.
  • Saad Magalhaes C; Universidade Estadual Paulista Júlio de Mesquita Filho, Botucatu, Saõ Paulo, Brazil.
  • Constantin T; Semmelweis University, Budapest, Hungary.
  • Davidson JE; Royal Hospital for Sick Children, Glasgow, UK.
  • Magnusson B; Royal Hospital for Sick Children, Edinburgh, UK.
  • Russo R; Karolinska University Hospital, Stockholm, Sweden.
  • Villa L; Hospital de Pediatría Garrahan, Buenos Aires, Argentina.
  • Rinaldi M; Istituto Giannina Gaslini, Pediatria II - Reumatologia, PRINTO, Genoa, Italy.
  • Rockette H; Istituto Giannina Gaslini, Pediatria II - Reumatologia, PRINTO, Genoa, Italy.
  • Lachenbruch PA; University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Miller FW; NIEHS, NIH, Bethesda, Maryland, USA.
  • Vencovsky J; NIEHS, NIH, Bethesda, Maryland, USA.
  • Ruperto N; Charles University, Prague, Czech Republic.
Ann Rheum Dis ; 76(5): 782-791, 2017 May.
Article em En | MEDLINE | ID: mdl-28385804
To develop response criteria for juvenile dermatomyositis (DM). We analysed the performance of 312 definitions that used core set measures from either the International Myositis Assessment and Clinical Studies Group (IMACS) or the Paediatric Rheumatology International Trials Organisation (PRINTO) and were derived from natural history data and a conjoint analysis survey. They were further validated using data from the PRINTO trial of prednisone alone compared to prednisone with methotrexate or cyclosporine and the Rituximab in Myositis (RIM) trial. At a consensus conference, experts considered 14 top candidate criteria based on their performance characteristics and clinical face validity, using nominal group technique. Consensus was reached for a conjoint analysis-based continuous model with a total improvement score of 0-100, using absolute per cent change in core set measures of minimal (≥30), moderate (≥45), and major (≥70) improvement. The same criteria were chosen for adult DM/polymyositis, with differing thresholds for improvement. The sensitivity and specificity were 89% and 91-98% for minimal improvement, 92-94% and 94-99% for moderate improvement, and 91-98% and 85-86% for major improvement, respectively, in juvenile DM patient cohorts using the IMACS and PRINTO core set measures. These criteria were validated in the PRINTO trial for differentiating between treatment arms for minimal and moderate improvement (p=0.009-0.057) and in the RIM trial for significantly differentiating the physician's rating for improvement (p<0.006). The response criteria for juvenile DM consisted of a conjoint analysis-based model using a continuous improvement score based on absolute per cent change in core set measures, with thresholds for minimal, moderate, and major improvement.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Índice de Gravidade de Doença / Avaliação de Resultados em Cuidados de Saúde / Dermatomiosite Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Índice de Gravidade de Doença / Avaliação de Resultados em Cuidados de Saúde / Dermatomiosite Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos