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Published in: Pediatric Rheumatology 1/2011

Open Access 01-12-2011 | Research

Long- term outcome of paediatric patients with ANCA vasculitis

Authors: Nishkantha Arulkumaran, Susan Jawad, Stuart W Smith, Lorraine Harper, Paul Brogan, Charles D Pusey, Alan D Salama

Published in: Pediatric Rheumatology | Issue 1/2011

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Abstract

Background

Primary systemic vasculitis presenting in childhood is an uncommon but serious condition. As these patients transfer to adult clinics for continuing care, defining long term outcomes with emphasis on disease and treatment- related morbidity and mortality is important. The aim of this study is to describe the long- term clinical course of paediatric patients with ANCA vasculitis.

Methods

The adult patients in our vasculitis clinics who had presented in childhood, with a follow up time of greater than 10 years were included. We also reviewed the literature for articles describing the clinical outcome of paediatric patients with ANCA vasculitis.

Results

We describe the clinical course of 8 adults who presented in childhood with ANCA vasculitis. 7 patients had Wegener's granulomatosis and 1 had microscopic polyangiitis. The median age at presentation was 11.5 years, and follow up time ranged form 11 to 30 years. Induction therapy for all patients was steroids and/or cyclophosphamide. Maintenance therapy was with azathioprine or mycophenolate mofetil. Biological agents were used in 3 patients for relapsed disease in adulthood only.
Seven patients achieved complete remission. All patients experienced disease relapse, with a median of 4 episodes. Kidney function was generally well preserved, with median eGFR 76 ml/min. Only one patient developed end-stage renal failure and one patient died after 25 years of disease. Treatment-related morbidity rates were high; 7 suffered from infections, 4 were infertile, 2 had skeletal complications, and 1 developed malignancy.

Conclusion

Close long- term follow up of paediatric patients with ANCA vasculitis is imperative, as this patient cohort is likely to live long enough to develop significant treatment and disease- related morbidities. Prospective cohort studies with novel therapies including paediatric patients are crucial to help us determine the best approach to managing this complex group of patients. In addition, although not yet observed in our series, late cardiovascular morbidity remains a major longer-term potential concern for adult survivors of paediatric vasculitis.
Literature
1.
go back to reference Jennette JC, Falk RJ: Small-vessel vasculitis. N Engl J Med. 1997, 337: 1512-23. 10.1056/NEJM199711203372106.CrossRefPubMed Jennette JC, Falk RJ: Small-vessel vasculitis. N Engl J Med. 1997, 337: 1512-23. 10.1056/NEJM199711203372106.CrossRefPubMed
2.
go back to reference Ozen S, Anton J, Arisoy N, Bakkaloglu A, Besbas N, Brogan P: Juvenile polyarteritis: Results of a multicenter survey of 110 children. J Pediatr. 2004, 145: 517-22. 10.1016/j.jpeds.2004.06.046.CrossRefPubMed Ozen S, Anton J, Arisoy N, Bakkaloglu A, Besbas N, Brogan P: Juvenile polyarteritis: Results of a multicenter survey of 110 children. J Pediatr. 2004, 145: 517-22. 10.1016/j.jpeds.2004.06.046.CrossRefPubMed
3.
go back to reference Rottem M, Fauci AS, Hallahan CW, Kerr GS, Lebovics R, Leavitt RY: Wegener granulomatosis in children and adolescents: Clinical presentation and outcome. J Pediatr. 1993, 122: 26-31. 10.1016/S0022-3476(05)83482-1.CrossRefPubMed Rottem M, Fauci AS, Hallahan CW, Kerr GS, Lebovics R, Leavitt RY: Wegener granulomatosis in children and adolescents: Clinical presentation and outcome. J Pediatr. 1993, 122: 26-31. 10.1016/S0022-3476(05)83482-1.CrossRefPubMed
4.
go back to reference Gardner-Medwin JM, Dolezalova P, Cummins C, Southwood TR: Incidence of henoch-schonlein purpura, kawasaki disease, and rare vasculitides in children of different ethnic origins. Lancet. 2002, 360: 1197-202. 10.1016/S0140-6736(02)11279-7.CrossRefPubMed Gardner-Medwin JM, Dolezalova P, Cummins C, Southwood TR: Incidence of henoch-schonlein purpura, kawasaki disease, and rare vasculitides in children of different ethnic origins. Lancet. 2002, 360: 1197-202. 10.1016/S0140-6736(02)11279-7.CrossRefPubMed
5.
go back to reference Harnden A, Alves B, Sheikh A: Rising incidence of kawasaki disease in england: Analysis of hospital admission data. BMJ. 2002, 324: 1424-5. 10.1136/bmj.324.7351.1424.PubMedCentralCrossRefPubMed Harnden A, Alves B, Sheikh A: Rising incidence of kawasaki disease in england: Analysis of hospital admission data. BMJ. 2002, 324: 1424-5. 10.1136/bmj.324.7351.1424.PubMedCentralCrossRefPubMed
6.
go back to reference Stegmayr BG, Gothefors L, Malmer B, Muller Wiefel DE, Nilsson K, Sundelin B: Wegener granulomatosis in children and young adults. A case study of ten patients. Pediatr Nephrol. 2000, 14: 208-13. 10.1007/s004670050043.CrossRefPubMed Stegmayr BG, Gothefors L, Malmer B, Muller Wiefel DE, Nilsson K, Sundelin B: Wegener granulomatosis in children and young adults. A case study of ten patients. Pediatr Nephrol. 2000, 14: 208-13. 10.1007/s004670050043.CrossRefPubMed
7.
go back to reference Ozen S, Ruperto N, Dillon MJ, Bagga A, Barron K, Davin JC: Eular/pres endorsed consensus criteria for the classification of childhood vasculitides. Ann Rheum Dis. 2006, 65: 936-41.PubMedCentralCrossRefPubMed Ozen S, Ruperto N, Dillon MJ, Bagga A, Barron K, Davin JC: Eular/pres endorsed consensus criteria for the classification of childhood vasculitides. Ann Rheum Dis. 2006, 65: 936-41.PubMedCentralCrossRefPubMed
8.
go back to reference Basu N, Watts R, Bajema I, Baslund B, Bley T, Boers M: Eular points to consider in the development of classification and diagnostic criteria in systemic vasculitis. Ann Rheum Dis. 2010, 69 (10): 1744-50. 10.1136/ard.2009.119032. Epub 2010 May 6CrossRefPubMed Basu N, Watts R, Bajema I, Baslund B, Bley T, Boers M: Eular points to consider in the development of classification and diagnostic criteria in systemic vasculitis. Ann Rheum Dis. 2010, 69 (10): 1744-50. 10.1136/ard.2009.119032. Epub 2010 May 6CrossRefPubMed
9.
go back to reference Belostotsky VM, Shah V, Dillon MJ: Clinical features in 17 paediatric patients with wegener granulomatosis. Pediatr Nephrol. 2002, 17: 754-61. 10.1007/s00467-002-0914-2.CrossRefPubMed Belostotsky VM, Shah V, Dillon MJ: Clinical features in 17 paediatric patients with wegener granulomatosis. Pediatr Nephrol. 2002, 17: 754-61. 10.1007/s00467-002-0914-2.CrossRefPubMed
10.
11.
go back to reference Peco-Antic A, Bonaci-Nikolic B, Basta-Jovanovic G, Kostic M, Markovic-Lipkovski J, Nikolic M: Childhood microscopic polyangiitis associated with mpo-anca. Pediatr Nephrol. 2006, 21: 46-53. 10.1007/s00467-005-2063-x.CrossRefPubMed Peco-Antic A, Bonaci-Nikolic B, Basta-Jovanovic G, Kostic M, Markovic-Lipkovski J, Nikolic M: Childhood microscopic polyangiitis associated with mpo-anca. Pediatr Nephrol. 2006, 21: 46-53. 10.1007/s00467-005-2063-x.CrossRefPubMed
12.
go back to reference Bakkaloglu A, Ozen S, Baskin E, Besbas N, Gur-Guven A, Kasapcopur O: The significance of antineutrophil cytoplasmic antibody in microscopic polyangitis and classic polyarteritis nodosa. Arch Dis Child. 2001, 85: 427-30. 10.1136/adc.85.5.427.PubMedCentralCrossRefPubMed Bakkaloglu A, Ozen S, Baskin E, Besbas N, Gur-Guven A, Kasapcopur O: The significance of antineutrophil cytoplasmic antibody in microscopic polyangitis and classic polyarteritis nodosa. Arch Dis Child. 2001, 85: 427-30. 10.1136/adc.85.5.427.PubMedCentralCrossRefPubMed
13.
go back to reference Valentini RP, Smoyer WE, Sedman AB, Kershaw DB, Gregory MJ, Bunchman TE: Outcome of antineutrophil cytoplasmic autoantibodies-positive glomerulonephritis and vasculitis in children: A single-center experience. J Pediatr. 1998, 132: 325-8. 10.1016/S0022-3476(98)70453-6.CrossRefPubMed Valentini RP, Smoyer WE, Sedman AB, Kershaw DB, Gregory MJ, Bunchman TE: Outcome of antineutrophil cytoplasmic autoantibodies-positive glomerulonephritis and vasculitis in children: A single-center experience. J Pediatr. 1998, 132: 325-8. 10.1016/S0022-3476(98)70453-6.CrossRefPubMed
14.
go back to reference Eleftheriou D, Melo M, Marks SD, Tullus K, Sills J, Cleary G: Biologic therapy in primary systemic vasculitis of the young. Rheumatology (Oxford). 2009, 48: 978-86. 10.1093/rheumatology/kep148.CrossRef Eleftheriou D, Melo M, Marks SD, Tullus K, Sills J, Cleary G: Biologic therapy in primary systemic vasculitis of the young. Rheumatology (Oxford). 2009, 48: 978-86. 10.1093/rheumatology/kep148.CrossRef
Metadata
Title
Long- term outcome of paediatric patients with ANCA vasculitis
Authors
Nishkantha Arulkumaran
Susan Jawad
Stuart W Smith
Lorraine Harper
Paul Brogan
Charles D Pusey
Alan D Salama
Publication date
01-12-2011
Publisher
BioMed Central
Published in
Pediatric Rheumatology / Issue 1/2011
Electronic ISSN: 1546-0096
DOI
https://doi.org/10.1186/1546-0096-9-12

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