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dc.contributor.author Enders FB
dc.contributor.author Bader-Meunier B
dc.contributor.author Baildam E
dc.contributor.author Constantin, Tamás
dc.contributor.author Dolezalova P
dc.contributor.author Feldman BM
dc.contributor.author Lahdenne P
dc.contributor.author Magnusson B
dc.contributor.author Nistala K
dc.contributor.author Ozen S
dc.contributor.author Pilkington C
dc.contributor.author Ravelli A
dc.contributor.author Russo R
dc.contributor.author Uziel Y
dc.contributor.author van Brussel M
dc.contributor.author van der Net J
dc.contributor.author Vastert S
dc.contributor.author Wedderburn LR
dc.contributor.author Wulffraat N
dc.contributor.author McCann LJ
dc.contributor.author van Royen-Kerkhof A
dc.date.accessioned 2017-01-18T14:40:56Z
dc.date.available 2017-01-18T14:40:56Z
dc.date.issued 2017
dc.identifier.citation pagination=329-340; journalVolume=76; journalIssueNumber=2; journalTitle=ANNALS OF THE RHEUMATIC DISEASES;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3954
dc.identifier.uri doi:10.1136/annrheumdis-2016-209247
dc.description.abstract BACKGROUND: In 2012, a European initiative called Single Hub and Access point for pediatric Rheumatology in Europe (SHARE) was launched to optimise and disseminate diagnostic and management regimens in Europe for children and young adults with rheumatic diseases. Juvenile dermatomyositis (JDM) is a rare disease within the group of paediatric rheumatic diseases (PRDs) and can lead to significant morbidity. Evidence-based guidelines are sparse and management is mostly based on physicians' experience. Consequently, treatment regimens differ throughout Europe. OBJECTIVES: To provide recommendations for diagnosis and treatment of JDM. METHODS: Recommendations were developed by an evidence-informed consensus process using the European League Against Rheumatism standard operating procedures. A committee was constituted, consisting of 19 experienced paediatric rheumatologists and 2 experts in paediatric exercise physiology and physical therapy, mainly from Europe. Recommendations derived from a validated systematic literature review were evaluated by an online survey and subsequently discussed at two consensus meetings using nominal group technique. Recommendations were accepted if >80% agreement was reached. RESULTS: In total, 7 overarching principles, 33 recommendations on diagnosis and 19 recommendations on therapy were accepted with >80% agreement among experts. Topics covered include assessment of skin, muscle and major organ involvement and suggested treatment pathways. CONCLUSIONS: The SHARE initiative aims to identify best practices for treatment of patients suffering from PRD. Within this remit, recommendations for the diagnosis and treatment of JDM have been formulated by an evidence-informed consensus process to produce a standard of care for patients with JDM throughout Europe.
dc.relation.ispartof urn:issn:0003-4967
dc.title Consensus-based recommendations for the management of juvenile dermatomyositis
dc.type Journal Article
dc.date.updated 2016-12-28T11:54:24Z
dc.language.rfc3066 en
dc.identifier.mtmt 3146614
dc.identifier.pubmed 27515057
dc.contributor.department SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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