European consensus-based recommendations for the diagnosis and treatment of rare paediatric vasculitides - the SHARE initiative
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
30535249
DOI
10.1093/rheumatology/key322
PII: 5232680
Knihovny.cz E-zdroje
- Klíčová slova
- SHARE recommendations, Takayasu arteritis, childhood/paediatric, eosinophilic granulomatosis with polyangiitis, granulomatosis with polyangiitis, microscopic polyangiitis, polyarteritis nodosa, systemic vasculitis, treatment,
- MeSH
- dítě MeSH
- konsensus MeSH
- lidé MeSH
- medicína založená na důkazech normy MeSH
- pediatrie normy MeSH
- revmatologie normy MeSH
- směrnice pro lékařskou praxi jako téma normy MeSH
- systémová vaskulitida * MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Evropa MeSH
OBJECTIVES: The European initiative Single Hub and Access point for paediatric Rheumatology in Europe (SHARE) aimed to optimize care for children with rheumatic diseases. Systemic vasculitides are very rare in children. Consequently, despite recent advances, paediatric-specific information is sparse. The lack of evidence-based recommendations is an important, unmet need. This study aimed to provide recommendations for diagnosing and treating children with rare forms of childhood systemic vasculitis. METHODS: Recommendations were developed by a consensus process in accordance with the European League Against Rheumatism standard operating procedures. A systematic literature review informed the recommendations, which were devised and evaluated by a panel of experts via an online survey, and two consensus meetings using nominal group technique. Recommendations were accepted when ⩾ 80% of experts agreed. RESULTS: Ninety-three relevant articles were found, and 78 recommendations were accepted in the two consensus meetings. General, cross-cutting recommendations and disease-specific statements regarding the diagnosis and treatment of childhood-onset PAN, granulomatosis with polyangiitis, microscopic polyangiitis, eosinophilic granulomatosis with polyangiitis, and Takayasu arteritis are provided. CONCLUSION: These Single Hub and Access point for paediatric Rheumatology in Europe recommendations were formulated through an evidence-based consensus process to support uniform, high-quality standard of care for children with rare forms of paediatric systemic vasculitis.
1st Faculty of Medicine Charles University and General University Hospital Prague Czech Republic
Department of Paediatric Rheumatology Alder Hey Children's Hospital Liverpool
Department of Paediatric Rheumatology Gaslini Children's Hospital Genoa Italy
Department of Paediatric Rheumatology Hacettepe University Ankara Turkey
Department of Paediatric Rheumatology University Children's Hospital Ljubljana Ljubljana Slovenia
Department of Paediatric Rheumatology Wilhelmina Children's Hospital Utrecht
Institute of Translational Medicine University of Liverpool Liverpool UK
Meir Medical Center Kfar Saba Tel Aviv University Sackler School of Medicine Tel Aviv Israel
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