European consensus-based recommendations for diagnosis and treatment of immunoglobulin A vasculitis—the SHARE initiative

Abstract Objectives 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. Accordin...

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Published inRheumatology (Oxford, England) Vol. 58; no. 9; pp. 1607 - 1616
Main Authors Ozen, Seza, Marks, Stephen D., Brogan, Paul, Groot, Noortje, de Graeff, Nienke, Avcin, Tadej, Bader-Meunier, Brigitte, Dolezalova, Pavla, Feldman, Brian M., Kone-Paut, Isabelle, Lahdenne, Pekka, McCann, Liza, Pilkington, Clarissa, Ravelli, Angelo, van Royen, Annet, Uziel, Yosef, Vastert, Bas, Wulffraat, Nico, Kamphuis, Sylvia, Beresford, Michael W.
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.09.2019
Oxford Publishing Limited (England)
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Abstract Abstract Objectives 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. Methods 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. Results 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. Conclusion The SHARE initiative provides international, evidence-based recommendations for the diagnosis and treatment of IgAV that will facilitate improvement and uniformity of care.
AbstractList 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.
Abstract Objectives 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. Methods 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. Results 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. Conclusion The SHARE initiative provides international, evidence-based recommendations for the diagnosis and treatment of IgAV that will facilitate improvement and uniformity of care.
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.OBJECTIVESIgA 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.METHODSRecommendations 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.RESULTSIn 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.CONCLUSIONThe SHARE initiative provides international, evidence-based recommendations for the diagnosis and treatment of IgAV that will facilitate improvement and uniformity of care.
Objectives 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. Methods 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. Results 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. Conclusion The SHARE initiative provides international, evidence-based recommendations for the diagnosis and treatment of IgAV that will facilitate improvement and uniformity of care.
Author Uziel, Yosef
Marks, Stephen D.
Kamphuis, Sylvia
Vastert, Bas
Bader-Meunier, Brigitte
Ozen, Seza
Wulffraat, Nico
Avcin, Tadej
de Graeff, Nienke
Dolezalova, Pavla
Lahdenne, Pekka
Pilkington, Clarissa
Brogan, Paul
Groot, Noortje
Ravelli, Angelo
Kone-Paut, Isabelle
Feldman, Brian M.
McCann, Liza
van Royen, Annet
Beresford, Michael W.
Author_xml – sequence: 1
  givenname: Seza
  surname: Ozen
  fullname: Ozen, Seza
  organization: Department of Paediatrics, Hacettepe University, Ankara, Turkey
– sequence: 2
  givenname: Stephen D.
  surname: Marks
  fullname: Marks, Stephen D.
  organization: Great Ormond Street Hospital for Children NHS Foundation Trust, University College London Great Ormond Street Institute of Child Health, London, UK
– sequence: 3
  givenname: Paul
  surname: Brogan
  fullname: Brogan, Paul
  organization: Great Ormond Street Hospital for Children NHS Foundation Trust, University College London Great Ormond Street Institute of Child Health, London, UK
– sequence: 4
  givenname: Noortje
  orcidid: 0000-0002-4711-0472
  surname: Groot
  fullname: Groot, Noortje
  organization: Wilhelmina Children’s Hospital, University Medical Center, Utrecht
– sequence: 5
  givenname: Nienke
  surname: de Graeff
  fullname: de Graeff, Nienke
  organization: Wilhelmina Children’s Hospital, University Medical Center, Utrecht
– sequence: 6
  givenname: Tadej
  surname: Avcin
  fullname: Avcin, Tadej
  organization: Department of Paediatric Rheumatology, University Children’s Hospital Ljubljana, Ljubljana, Slovenia
– sequence: 7
  givenname: Brigitte
  surname: Bader-Meunier
  fullname: Bader-Meunier, Brigitte
  organization: Necker Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France
– sequence: 8
  givenname: Pavla
  surname: Dolezalova
  fullname: Dolezalova, Pavla
  organization: General University Hospital and 1st Faculty of Medicine, Charles University, Prague, Czech Republic
– sequence: 9
  givenname: Brian M.
  surname: Feldman
  fullname: Feldman, Brian M.
  organization: The Hospital for Sick Children, University of Toronto, Toronto, Canada
– sequence: 10
  givenname: Isabelle
  surname: Kone-Paut
  fullname: Kone-Paut, Isabelle
  organization: Department of Paediatric Rheumatology, Bicêtre University Hospital, Paris, France
– sequence: 11
  givenname: Pekka
  surname: Lahdenne
  fullname: Lahdenne, Pekka
  organization: Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland
– sequence: 12
  givenname: Liza
  surname: McCann
  fullname: McCann, Liza
  organization: Department of Paediatric Rheumatology, Alder Hey Children’s NHS Foundation Trust, Liverpool, UK
– sequence: 13
  givenname: Clarissa
  surname: Pilkington
  fullname: Pilkington, Clarissa
  organization: Great Ormond Street Hospital for Children NHS Foundation Trust, University College London Great Ormond Street Institute of Child Health, London, UK
– sequence: 14
  givenname: Angelo
  surname: Ravelli
  fullname: Ravelli, Angelo
  organization: Gaslini Children’s Hospital, Genoa, Italy
– sequence: 15
  givenname: Annet
  surname: van Royen
  fullname: van Royen, Annet
  organization: Wilhelmina Children’s Hospital, University Medical Center, Utrecht
– sequence: 16
  givenname: Yosef
  surname: Uziel
  fullname: Uziel, Yosef
  organization: Meir Medical Centre, Tel Aviv University, Tel Aviv, Israel
– sequence: 17
  givenname: Bas
  surname: Vastert
  fullname: Vastert, Bas
  organization: Wilhelmina Children’s Hospital, University Medical Center, Utrecht
– sequence: 18
  givenname: Nico
  surname: Wulffraat
  fullname: Wulffraat, Nico
  organization: Wilhelmina Children’s Hospital, University Medical Center, Utrecht
– sequence: 19
  givenname: Sylvia
  surname: Kamphuis
  fullname: Kamphuis, Sylvia
  organization: Sophia Children’s Hospital, Erasmus University Medical Centre, Rotterdam, The Netherlands
– sequence: 20
  givenname: Michael W.
  orcidid: 0000-0002-5400-9911
  surname: Beresford
  fullname: Beresford, Michael W.
  email: m.w.beresford@liverpool.ac.uk
  organization: Department of Paediatric Rheumatology, Alder Hey Children’s NHS Foundation Trust, Liverpool, UK
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30879080$$D View this record in MEDLINE/PubMed
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Keywords systemic vasculitis
childhood/paediatric
diagnosis
IgA vasculitis (Henoch–Schönlein purpura)
management
recommendations
Language English
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Snippet Abstract Objectives IgA vasculitis (IgAV, formerly known as Henoch–Schönlein purpura) is the most common cause of systemic vasculitis in childhood. To date,...
IgA vasculitis (IgAV, formerly known as Henoch-Schönlein purpura) is the most common cause of systemic vasculitis in childhood. To date, there are no...
Objectives IgA vasculitis (IgAV, formerly known as Henoch–Schönlein purpura) is the most common cause of systemic vasculitis in childhood. To date, there are...
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SubjectTerms Analgesia
Analgesia - methods
Angiotensin-converting enzyme inhibitors
Angiotensin-Converting Enzyme Inhibitors - therapeutic use
Biopsy
Child
Children
Diagnosis
Enzymes
Evidence-Based Medicine - methods
Gastrointestinal Diseases - diagnosis
Gastrointestinal Diseases - etiology
Glomerulonephritis, IGA - diagnosis
Glomerulonephritis, IGA - drug therapy
Glomerulonephritis, IGA - etiology
Glomerulonephritis, IGA - pathology
Glucocorticoids - therapeutic use
Humans
Immunoglobulin A
Immunoglobulin A - analysis
Kidney - pathology
Kidneys
Literature reviews
Medical diagnosis
Nephritis
Pain perception
Pediatrics
Peptidyl-dipeptidase A
Purpura, Schoenlein-Henoch - complications
Purpura, Schoenlein-Henoch - diagnosis
Purpura, Schoenlein-Henoch - drug therapy
Purpura, Schoenlein-Henoch - pathology
Rheumatology
Schonlein-Henoch purpura
Severity of Illness Index
Skin - pathology
Systemic vasculitis
Title European consensus-based recommendations for diagnosis and treatment of immunoglobulin A vasculitis—the SHARE initiative
URI https://www.ncbi.nlm.nih.gov/pubmed/30879080
https://www.proquest.com/docview/2474941560
https://www.proquest.com/docview/2193607964
Volume 58
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