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 in | Rheumatology (Oxford, England) Vol. 58; no. 9; pp. 1607 - 1616 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Oxford University Press
01.09.2019
Oxford Publishing Limited (England) |
Subjects | |
Online Access | Get full text |
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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. |
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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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Cites_doi | 10.1136/ard.2006.055251 10.1016/0140-6736(92)91341-5 10.1186/1546-0096-11-5 10.1136/annrheumdis-2016-211001 10.1136/adc.2009.182394 10.1053/j.ackd.2017.09.011 10.1007/s00296-009-0853-3 10.1038/ki.2010.150 10.1136/ard.2009.116657 10.1007/s00467-009-1291-x 10.1016/j.jpeds.2012.09.012 10.1007/s00467-011-1919-5 10.1007/s00467-009-1317-4 10.1136/annrheumdis-2014-206844 10.1007/s00467-003-1315-x 10.1007/s00467-017-3846-6 10.1136/annrheumdis-2017-211898 10.1016/S0140-6736(02)09835-5 10.1371/journal.pone.0029512 10.1016/j.berh.2017.11.009 10.1053/j.ajkd.2006.02.178 10.1111/j.1440-172X.2012.02017.x 10.1681/ASN.2006040347 10.1093/rheumatology/key322 10.1136/annrheumdis-2016-209247 10.1007/s00467-018-4067-3 10.1136/annrheumdis-2016-210960 10.1007/5584_2016_231 10.1136/annrheumdis-2015-207546 10.7326/0003-4819-129-5-199809010-00013 10.1038/kisup.2012.24 10.1016/j.jpeds.2006.03.024 10.1136/ard.2006.055269 10.1136/adc.56.6.482 10.1136/ard.2004.023697 10.1371/journal.pone.0167346 10.1111/j.1651-2227.1988.tb10610.x 10.1002/art.1780330809 10.1007/s00467-011-2057-9 10.1093/med/9780198738756.001.0001 10.1016/j.jaad.2011.06.012 10.1007/s00467-017-3608-5 10.1007/s10620-007-0147-0 10.1002/art.37715 10.1136/archdischild-2013-303642 10.1080/03009740510026841 10.1046/j.1523-1755.1998.00915.x 10.2217/ijr.10.59 10.1159/000341914 10.1111/j.1651-2227.2006.00173.x 10.1186/1741-7015-2-7 10.1016/S0140-6736(02)11279-7 10.1136/adc.2005.074641 10.7326/0003-4819-140-3-200402030-00010 10.1007/s004670050446 10.1007/s00467-013-2550-4 10.1111/j.1651-2227.2009.01445.x 10.1155/2010/597648 10.1097/BOR.0b013e32835d8e2a 10.1177/0009922806298896 |
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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 2019 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. 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 |
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Keywords | systemic vasculitis childhood/paediatric diagnosis IgA vasculitis (Henoch–Schönlein purpura) management recommendations |
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References | Shin (2019091011584397900_kez041-B34) 2006; 35 Chen (2019091011584397900_kez041-B51) 2004; 27 Dougados (2019091011584397900_kez041-B19) 2004; 63 Ozen (2019091011584397900_kez041-B26) 2010; 69 Pillebout (2019091011584397900_kez041-B56) 2010; 78 Goldstein (2019091011584397900_kez041-B38) 1992; 339 Nielsen (2019091011584397900_kez041-B3) 1988; 77 Watson (2019091011584397900_kez041-B40) 2012; 7 Ha (2019091011584397900_kez041-B49) 2007; 96 Alvarez-Caro (2019091011584397900_kez041-B50) 2009; 29 Coppo (2019091011584397900_kez041-B55) 2007; 18 Whiting (2019091011584397900_kez041-B21) 2004; 140 Ebert (2019091011584397900_kez041-B45) 2008; 53 Salvador (2019091011584397900_kez041-B42) 2019; 34 Koskela (2019091011584397900_kez041-B44) 2017; 32 Davin (2019091011584397900_kez041-B65) 2013; 28 Groot (2019091011584397900_kez041-B16) 2017; 76 Gardner-Medwin (2019091011584397900_kez041-B2) 2002; 360 Linskey (2019091011584397900_kez041-B29) 2012; 66 Enders (2019091011584397900_kez041-B11) 2017; 76 Giancane (2019091011584397900_kez041-B12) 2015; 74 Du (2019091011584397900_kez041-B58) 2012; 27 Chan (2019091011584397900_kez041-B30) 2016; 11 Dudley (2019091011584397900_kez041-B52) 2013; 98 de Graeff (2019091011584397900_kez041-B17) 2019 Foster (2019091011584397900_kez041-B43) 2018 Groot (2019091011584397900_kez041-B15) 2017; 76 Piram (2019091011584397900_kez041-B4) 2013; 25 Zhang (2019091011584397900_kez041-B23) 2006; 65 Kaku (2019091011584397900_kez041-B33) 1998; 53 ter Haar (2019091011584397900_kez041-B13) 2015; 74 Mills (2019091011584397900_kez041-B27) 1990; 33 Bogdanovic (2019091011584397900_kez041-B8) 2009; 98 Niaudet (2019091011584397900_kez041-B63) 1998; 12 Zhang (2019091011584397900_kez041-B22) 2006; 65 Ronkainen (2019091011584397900_kez041-B35) 2002; 360 Wulffraat (2019091011584397900_kez041-B10) 2013; 11 Groot (2019091011584397900_kez041-B14) 2017; 76 de Almeida (2019091011584397900_kez041-B32) 2007; 83 Jennette (2019091011584397900_kez041-B1) 2013; 65 Koskimies (2019091011584397900_kez041-B39) 1981; 56 de Graeff (2019091011584397900_kez041-B18) 2019; 58 Ren (2019091011584397900_kez041-B61) 2012; 36 Jauhola (2019091011584397900_kez041-B62) 2011; 26 Sohagia (2019091011584397900_kez041-B47) 2010; 2010 McMillan (2019091011584397900_kez041-B24) 2016; 38 Mian (2019091011584397900_kez041-B41) 2017; 24 Altugan (2019091011584397900_kez041-B7) 2009; 51 Coppo (2019091011584397900_kez041-B37) 2006; 47 Bayrakci (2019091011584397900_kez041-B9) 2010; 5 Jauhola (2019091011584397900_kez041-B31) 2010; 95 Baskin (2019091011584397900_kez041-B64) 2010; 25 (2019091011584397900_kez041-B54) 2012; 2 Butani (2019091011584397900_kez041-B36) 2007; 46 Ronkainen (2019091011584397900_kez041-B46) 2006; 149 Leclercq (2019091011584397900_kez041-B20) 2013; 162 Harvey (2019091011584397900_kez041-B25) 2012; 18 Narchi (2019091011584397900_kez041-B6) 2005; 90 Hackl (2019091011584397900_kez041-B59) 2018; 33 Tarshish (2019091011584397900_kez041-B57) 2004; 19 Huber (2019091011584397900_kez041-B53) 2004; 2 Sag (2019091011584397900_kez041-B48) 2017; 31 Mizerska-Wasiak (2019091011584397900_kez041-B60) 2016; 912 Brogan (2019091011584397900_kez041-B5) 2010; 25 Hunder (2019091011584397900_kez041-B28) 1998; 129 31243449 - Rheumatology (Oxford). 2019 Sep 1;58(9):1697 31170291 - Rheumatology (Oxford). 2019 Sep 1;58(9):1695-1697 |
References_xml | – volume: 65 start-page: 1301 year: 2006 ident: 2019091011584397900_kez041-B22 article-title: EULAR evidence based recommendations for gout. Part I: diagnosis. Report of a task force of the Standing Committee for International Clinical Studies Including Therapeutics (ESCISIT) publication-title: Ann Rheum Dis doi: 10.1136/ard.2006.055251 – volume: 339 start-page: 280 year: 1992 ident: 2019091011584397900_kez041-B38 article-title: Long-term follow-up of childhood Henoch-Schönlein nephritis publication-title: Lancet doi: 10.1016/0140-6736(92)91341-5 – volume: 11 start-page: 5 year: 2013 ident: 2019091011584397900_kez041-B10 article-title: Time to share publication-title: Pediatr Rheumatol Online J doi: 10.1186/1546-0096-11-5 – volume: 76 start-page: 1637 year: 2017 ident: 2019091011584397900_kez041-B14 article-title: European evidence-based recommendations for diagnosis and treatment of paediatric antiphospholipid syndrome: the SHARE initiative publication-title: Ann Rheum Dis doi: 10.1136/annrheumdis-2016-211001 – volume: 95 start-page: 877 year: 2010 ident: 2019091011584397900_kez041-B31 article-title: Renal manifestations of Henoch-Schonlein purpura in a 6-month prospective study of 223 children publication-title: Arch Dis Child doi: 10.1136/adc.2009.182394 – volume: 24 start-page: 348 year: 2017 ident: 2019091011584397900_kez041-B41 article-title: Measurement and estimation of glomerular filtration rate in children publication-title: Adv Chronic Kidney Dis doi: 10.1053/j.ackd.2017.09.011 – volume: 29 start-page: 1491 year: 2009 ident: 2019091011584397900_kez041-B50 article-title: Massive lower gastrointestinal haemorrhage, successfully treated with corticosteroids, as main symptom of Schönlein-Henoch purpura publication-title: Rheumatol Int doi: 10.1007/s00296-009-0853-3 – volume: 78 start-page: 495 year: 2010 ident: 2019091011584397900_kez041-B56 article-title: Addition of cyclophosphamide to steroids provides no benefit compared with steroids alone in treating adult patients with severe Henoch Schonlein Purpura publication-title: Kidney Int doi: 10.1038/ki.2010.150 – volume: 69 start-page: 798 year: 2010 ident: 2019091011584397900_kez041-B26 article-title: EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: final classification criteria publication-title: Ann Rheum Dis doi: 10.1136/ard.2009.116657 – volume: 25 start-page: 111 year: 2010 ident: 2019091011584397900_kez041-B64 article-title: The use of low-dose cyclophosphamide followed by AZA/MMF treatment in childhood lupus nephritis publication-title: Pediatr Nephrol doi: 10.1007/s00467-009-1291-x – volume: 162 start-page: 629 year: 2013 ident: 2019091011584397900_kez041-B20 article-title: Validation of search filters for identifying pediatric studies in PubMed publication-title: J Pediatr doi: 10.1016/j.jpeds.2012.09.012 – volume: 26 start-page: 2159 year: 2011 ident: 2019091011584397900_kez041-B62 article-title: Cyclosporine A vs. methylprednisolone for Henoch-Schönlein nephritis: a randomized trial publication-title: Pediatr Nephrol doi: 10.1007/s00467-011-1919-5 – volume: 25 start-page: 1025 year: 2010 ident: 2019091011584397900_kez041-B5 article-title: Small vessel vasculitis publication-title: Pediatr Nephrol doi: 10.1007/s00467-009-1317-4 – volume: 74 start-page: 635 year: 2015 ident: 2019091011584397900_kez041-B12 article-title: Evidence-based recommendations for genetic diagnosis of familial Mediterranean fever publication-title: Ann Rheum Dis doi: 10.1136/annrheumdis-2014-206844 – volume: 19 start-page: 51 year: 2004 ident: 2019091011584397900_kez041-B57 article-title: Henoch-Schönlein purpura nephritis: course of disease and efficacy of cyclophosphamide publication-title: Pediatr Nephrol doi: 10.1007/s00467-003-1315-x – volume: 83 start-page: 259 year: 2007 ident: 2019091011584397900_kez041-B32 article-title: Renal involvement in Henoch-Schönlein purpura: a multivariate analysis of initial prognostic factors publication-title: J Pediatr (Rio J) – volume: 33 start-page: 619 year: 2018 ident: 2019091011584397900_kez041-B59 article-title: Mycophenolate mofetil following glucocorticoid treatment in Henoch-Schönlein purpura nephritis: the role of early initiation and therapeutic drug monitoring publication-title: Pediatr Nephrol doi: 10.1007/s00467-017-3846-6 – volume: 76 start-page: 1965 year: 2017 ident: 2019091011584397900_kez041-B16 article-title: European evidence-based recommendations for the diagnosis and treatment of childhood-onset lupus nephritis: the SHARE initiative publication-title: Ann Rheum Dis doi: 10.1136/annrheumdis-2017-211898 – volume: 360 start-page: 666 year: 2002 ident: 2019091011584397900_kez041-B35 article-title: The adult kidney 24 years after childhood Henoch-Schönlein purpura: a retrospective cohort study publication-title: Lancet doi: 10.1016/S0140-6736(02)09835-5 – volume: 7 start-page: e29512 year: 2012 ident: 2019091011584397900_kez041-B40 article-title: Henoch schonlein purpura–a 5-year review and proposed pathway publication-title: PLoS One doi: 10.1371/journal.pone.0029512 – volume: 31 start-page: 558 year: 2017 ident: 2019091011584397900_kez041-B48 article-title: Childhood systemic vasculitis publication-title: Best Pract Res Clin Rheumatol doi: 10.1016/j.berh.2017.11.009 – volume: 47 start-page: 993 year: 2006 ident: 2019091011584397900_kez041-B37 article-title: Predictors of outcome in Henoch-Schönlein nephritis in children and adults publication-title: Am J Kidney Dis doi: 10.1053/j.ajkd.2006.02.178 – volume: 18 start-page: 188 year: 2012 ident: 2019091011584397900_kez041-B25 article-title: Nominal group technique: an effective method for obtaining group consensus publication-title: Int J Nurs Pract doi: 10.1111/j.1440-172X.2012.02017.x – volume: 18 start-page: 1880 year: 2007 ident: 2019091011584397900_kez041-B55 article-title: IgACE: a placebo-controlled, randomized trial of angiotensin-converting enzyme inhibitors in children and young people with IgA nephropathy and moderate proteinuria publication-title: J Am Soc Nephrol doi: 10.1681/ASN.2006040347 – volume: 58 start-page: 656 year: 2019 ident: 2019091011584397900_kez041-B18 article-title: European consensus-based recommendations for the diagnosis and treatment of rare paediatric vasculitides – the SHARE initiative publication-title: Rheumatology doi: 10.1093/rheumatology/key322 – volume: 76 start-page: 329 year: 2017 ident: 2019091011584397900_kez041-B11 article-title: Consensus-based recommendations for the management of juvenile dermatomyositis publication-title: Ann Rheum Dis doi: 10.1136/annrheumdis-2016-209247 – volume: 34 start-page: 301 year: 2019 ident: 2019091011584397900_kez041-B42 article-title: Estimating glomerular filtration rate in children: evaluation of creatinine- and cystatin C-based equations publication-title: Pediatr Nephrol doi: 10.1007/s00467-018-4067-3 – volume: 76 start-page: 1788 year: 2017 ident: 2019091011584397900_kez041-B15 article-title: European evidence-based recommendations for diagnosis and treatment of childhood-onset systemic lupus erythematosus: the SHARE initiative publication-title: Ann Rheum Dis doi: 10.1136/annrheumdis-2016-210960 – volume: 912 start-page: 65 year: 2016 ident: 2019091011584397900_kez041-B60 article-title: Treatment outcomes in children with Henoch-Schönlein nephritis publication-title: Adv Exp Med Biol doi: 10.1007/5584_2016_231 – volume: 74 start-page: 1636 year: 2015 ident: 2019091011584397900_kez041-B13 article-title: Recommendations for the management of autoinflammatory diseases publication-title: Ann Rheum Dis doi: 10.1136/annrheumdis-2015-207546 – volume: 129 start-page: 417 year: 1998 ident: 2019091011584397900_kez041-B28 article-title: The use and misuse of classification and diagnostic criteria for complex diseases publication-title: Ann Intern Med doi: 10.7326/0003-4819-129-5-199809010-00013 – volume: 2 start-page: 218 year: 2012 ident: 2019091011584397900_kez041-B54 article-title: Chapter 11: Henoch-Schönlein purpura nephritis publication-title: Kidney Int Suppl (2011) doi: 10.1038/kisup.2012.24 – volume: 149 start-page: 241 year: 2006 ident: 2019091011584397900_kez041-B46 article-title: Early prednisone therapy in Henoch-Schönlein purpura: a randomized, double-blind, placebo-controlled trial publication-title: J Pediatr doi: 10.1016/j.jpeds.2006.03.024 – start-page: 672 year: 2019 ident: 2019091011584397900_kez041-B17 – volume: 65 start-page: 1312 year: 2006 ident: 2019091011584397900_kez041-B23 article-title: EULAR evidence based recommendations for gout. Part II: management. Report of a task force of the EULAR Standing Committee for International Clinical Studies Including Therapeutics (ESCISIT) publication-title: Ann Rheum Dis doi: 10.1136/ard.2006.055269 – volume: 56 start-page: 482 year: 1981 ident: 2019091011584397900_kez041-B39 article-title: Henoch-Schönlein nephritis: long-term prognosis of unselected patients publication-title: Arch Dis Child doi: 10.1136/adc.56.6.482 – volume: 63 start-page: 1172 year: 2004 ident: 2019091011584397900_kez041-B19 article-title: EULAR standardised operating procedures for the elaboration, evaluation, dissemination, and implementation of recommendations endorsed by the EULAR standing committees publication-title: Ann Rheum Dis doi: 10.1136/ard.2004.023697 – volume: 11 start-page: e0167346 year: 2016 ident: 2019091011584397900_kez041-B30 article-title: Risk factors associated with renal involvement in childhood Henoch-Schönlein purpura: a meta-analysis publication-title: PLoS One doi: 10.1371/journal.pone.0167346 – volume: 77 start-page: 125 year: 1988 ident: 2019091011584397900_kez041-B3 article-title: Epidemiology of Schönlein-Henoch purpura publication-title: Acta Paediatr Scand doi: 10.1111/j.1651-2227.1988.tb10610.x – volume: 33 start-page: 1114 year: 1990 ident: 2019091011584397900_kez041-B27 article-title: The American College of Rheumatology 1990 criteria for the classification of Henoch-Schönlein purpura publication-title: Arthritis Rheum doi: 10.1002/art.1780330809 – volume: 27 start-page: 765 year: 2012 ident: 2019091011584397900_kez041-B58 article-title: Treatment of children with Henoch-Schönlein purpura nephritis with mycophenolate mofetil publication-title: Pediatr Nephrol doi: 10.1007/s00467-011-2057-9 – volume-title: Oxford handbook of paediatric rheumatology year: 2018 ident: 2019091011584397900_kez041-B43 doi: 10.1093/med/9780198738756.001.0001 – volume: 66 start-page: 813 year: 2012 ident: 2019091011584397900_kez041-B29 article-title: Immunoglobulin-A-associated small-vessel vasculitis: a 10-year experience at the Massachusetts General Hospital publication-title: J Am Acad Dermatol doi: 10.1016/j.jaad.2011.06.012 – volume: 32 start-page: 1201 year: 2017 ident: 2019091011584397900_kez041-B44 article-title: The ISKDC classification and a new semiquantitative classification for predicting outcomes of Henoch-Schönlein purpura nephritis publication-title: Pediatr Nephrol doi: 10.1007/s00467-017-3608-5 – volume: 53 start-page: 2011 year: 2008 ident: 2019091011584397900_kez041-B45 article-title: Gastrointestinal manifestations of Henoch-Schonlein Purpura publication-title: Dig Dis Sci doi: 10.1007/s10620-007-0147-0 – volume: 65 start-page: 1 year: 2013 ident: 2019091011584397900_kez041-B1 article-title: 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides publication-title: Arthritis Rheum doi: 10.1002/art.37715 – volume: 98 start-page: 756 year: 2013 ident: 2019091011584397900_kez041-B52 article-title: Randomised, double-blind, placebo-controlled trial to determine whether steroids reduce the incidence and severity of nephropathy in Henoch-Schonlein Purpura (HSP) publication-title: Arch Dis Child doi: 10.1136/archdischild-2013-303642 – volume: 35 start-page: 56 year: 2006 ident: 2019091011584397900_kez041-B34 article-title: Predictive factors for nephritis, relapse, and significant proteinuria in childhood Henoch-Schönlein purpura publication-title: Scand J Rheumatol doi: 10.1080/03009740510026841 – volume: 53 start-page: 1755 year: 1998 ident: 2019091011584397900_kez041-B33 article-title: Renal involvement in Henoch-Schönlein purpura: a multivariate analysis of prognostic factors publication-title: Kidney Int doi: 10.1046/j.1523-1755.1998.00915.x – volume: 5 start-page: 669 year: 2010 ident: 2019091011584397900_kez041-B9 article-title: Treatment of Henoch Schönlein Purpura: what evidence do we have? publication-title: Int J Clin Rheumatol doi: 10.2217/ijr.10.59 – volume: 36 start-page: 271 year: 2012 ident: 2019091011584397900_kez041-B61 article-title: The combination of mycophenolate mofetil with corticosteroids induces remission of Henoch-Schönlein purpura nephritis publication-title: Am J Nephrol doi: 10.1159/000341914 – volume: 38 start-page: 655 year: 2016 ident: 2019091011584397900_kez041-B24 article-title: How to use the nominal group and Delphi techniques publication-title: Int J Clin Pharm – volume: 96 start-page: 552 year: 2007 ident: 2019091011584397900_kez041-B49 article-title: Scrotal involvement in childhood Henoch-Schönlein purpura publication-title: Acta Paediatr doi: 10.1111/j.1651-2227.2006.00173.x – volume: 2 year: 2004 ident: 2019091011584397900_kez041-B53 article-title: A randomized, placebo-controlled trial of prednisone in early Henoch Schonlein Purpura [ISRCTN85109383] publication-title: BMC Med doi: 10.1186/1741-7015-2-7 – volume: 27 start-page: 175 year: 2004 ident: 2019091011584397900_kez041-B51 article-title: Gastrointestinal manifestations and complications of Henoch-Schonlein purpura publication-title: Chang Gung Med J – volume: 360 start-page: 1197 year: 2002 ident: 2019091011584397900_kez041-B2 article-title: Incidence of Henoch-Schönlein purpura, Kawasaki disease, and rare vasculitides in children of different ethnic origins publication-title: Lancet doi: 10.1016/S0140-6736(02)11279-7 – volume: 90 start-page: 916 year: 2005 ident: 2019091011584397900_kez041-B6 article-title: Risk of long term renal impairment and duration of follow up recommended for Henoch-Schonlein purpura with normal or minimal urinary findings: a systematic review publication-title: Arch Dis Child doi: 10.1136/adc.2005.074641 – volume: 140 start-page: 189 year: 2004 ident: 2019091011584397900_kez041-B21 article-title: Sources of variation and bias in studies of diagnostic accuracy: a systematic review publication-title: Ann Intern Med doi: 10.7326/0003-4819-140-3-200402030-00010 – volume: 12 start-page: 238 year: 1998 ident: 2019091011584397900_kez041-B63 article-title: Methylprednisolone pulse therapy in the treatment of severe forms of Schönlein-Henoch purpura nephritis publication-title: Pediatr Nephrol doi: 10.1007/s004670050446 – volume: 28 start-page: 1897 year: 2013 ident: 2019091011584397900_kez041-B65 article-title: Pitfalls in recommending evidence-based guidelines for a protean disease like Henoch-Schönlein purpura nephritis publication-title: Pediatr Nephrol doi: 10.1007/s00467-013-2550-4 – volume: 98 start-page: 1882 year: 2009 ident: 2019091011584397900_kez041-B8 article-title: Henoch-Schonlein purpura nephritis in children: risk factors, prevention and treatment publication-title: Acta Paediatr doi: 10.1111/j.1651-2227.2009.01445.x – volume: 2010 start-page: 597648 year: 2010 ident: 2019091011584397900_kez041-B47 article-title: Henoch-schonlein purpura-a case report and review of the literature publication-title: Gastroenterol Res Pract doi: 10.1155/2010/597648 – volume: 25 start-page: 171 year: 2013 ident: 2019091011584397900_kez041-B4 article-title: Epidemiology of immunoglobulin A vasculitis (Henoch-Schönlein): current state of knowledge publication-title: Curr Opin Rheumatol doi: 10.1097/BOR.0b013e32835d8e2a – volume: 51 start-page: 551 year: 2009 ident: 2019091011584397900_kez041-B7 article-title: Treatment of severe Henoch-Schönlein nephritis: justifying more immunosuppression publication-title: Turk J Pediatr – volume: 46 start-page: 505 year: 2007 ident: 2019091011584397900_kez041-B36 article-title: Long-term outcome in children after Henoch-Schönlein purpura nephritis publication-title: Clin Pediatr (Phila) doi: 10.1177/0009922806298896 – reference: 31243449 - Rheumatology (Oxford). 2019 Sep 1;58(9):1697 – reference: 31170291 - Rheumatology (Oxford). 2019 Sep 1;58(9):1695-1697 |
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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 |
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