European consensus-based recommendations for diagnosis and treatment of immunoglobulin A vasculitis-the SHARE initiative.
Analgesia
/ methods
Angiotensin-Converting Enzyme Inhibitors
/ therapeutic use
Biopsy
Child
Evidence-Based Medicine
/ methods
Gastrointestinal Diseases
/ diagnosis
Glomerulonephritis, IGA
/ diagnosis
Glucocorticoids
/ therapeutic use
Humans
IgA Vasculitis
/ complications
Immunoglobulin A
/ analysis
Kidney
/ pathology
Severity of Illness Index
Skin
/ pathology
IgA vasculitis (Henoch–Schönlein purpura)
childhood/paediatric
diagnosis
management
recommendations
systemic vasculitis
Journal
Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501
Informations de publication
Date de publication:
01 09 2019
01 09 2019
Historique:
received:
31
07
2018
revised:
09
01
2019
pubmed:
18
3
2019
medline:
21
3
2020
entrez:
18
3
2019
Statut:
ppublish
Résumé
IgA vasculitis (IgAV, formerly known as Henoch-Schönlein purpura) is the most common cause of systemic vasculitis in childhood. To date, there are no internationally agreed, evidence-based guidelines concerning the appropriate diagnosis and treatment of IgAV in children. Accordingly, treatment regimens differ widely. The European initiative SHARE (Single Hub and Access point for paediatric Rheumatology in Europe) aims to optimize care for children with rheumatic diseases. The aim therefore was to provide internationally agreed consensus recommendations for diagnosis and treatment for children with IgAV. Recommendations were developed by a consensus process in accordance with the EULAR standard operating procedures. An extensive systematic literature review was performed, and evidence-based recommendations were extrapolated from the included papers. These were evaluated by a panel of 16 international experts via online surveys and subsequent consensus meeting, using nominal group technique. Recommendations were accepted when ⩾80% of experts agreed. In total, 7 recommendations for diagnosis and 19 for treatment of paediatric IgAV were accepted. Diagnostic recommendations included: appropriate use of skin and renal biopsy, renal work-up and imaging. Treatment recommendations included: the importance of appropriate analgesia and angiotensin-converting enzyme inhibitor use and non-renal indications for CS use, as well as a structured approach to treating IgAV nephritis, including appropriate use of CS and second-line agents in mild, moderate and severe disease along with use of angiotensin-converting enzyme inhibitors and maintenance therapy. The SHARE initiative provides international, evidence-based recommendations for the diagnosis and treatment of IgAV that will facilitate improvement and uniformity of care.
Identifiants
pubmed: 30879080
pii: 5382174
doi: 10.1093/rheumatology/kez041
doi:
Substances chimiques
Angiotensin-Converting Enzyme Inhibitors
0
Glucocorticoids
0
Immunoglobulin A
0
Types de publication
Consensus Development Conference
Journal Article
Practice Guideline
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1607-1616Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn
Informations de copyright
© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.