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Long- term outcome of paediatric patients with ANCA vasculitis
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 stu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150312/ https://www.ncbi.nlm.nih.gov/pubmed/21682926 http://dx.doi.org/10.1186/1546-0096-9-12 |
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author | Arulkumaran, Nishkantha Jawad, Susan Smith, Stuart W Harper, Lorraine Brogan, Paul Pusey, Charles D Salama, Alan D |
author_facet | Arulkumaran, Nishkantha Jawad, Susan Smith, Stuart W Harper, Lorraine Brogan, Paul Pusey, Charles D Salama, Alan D |
author_sort | Arulkumaran, Nishkantha |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3150312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31503122011-08-05 Long- term outcome of paediatric patients with ANCA vasculitis Arulkumaran, Nishkantha Jawad, Susan Smith, Stuart W Harper, Lorraine Brogan, Paul Pusey, Charles D Salama, Alan D Pediatr Rheumatol Online J Research 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. BioMed Central 2011-06-19 /pmc/articles/PMC3150312/ /pubmed/21682926 http://dx.doi.org/10.1186/1546-0096-9-12 Text en Copyright ©2011 Arulkumaran et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Arulkumaran, Nishkantha Jawad, Susan Smith, Stuart W Harper, Lorraine Brogan, Paul Pusey, Charles D Salama, Alan D Long- term outcome of paediatric patients with ANCA vasculitis |
title | Long- term outcome of paediatric patients with ANCA vasculitis |
title_full | Long- term outcome of paediatric patients with ANCA vasculitis |
title_fullStr | Long- term outcome of paediatric patients with ANCA vasculitis |
title_full_unstemmed | Long- term outcome of paediatric patients with ANCA vasculitis |
title_short | Long- term outcome of paediatric patients with ANCA vasculitis |
title_sort | long- term outcome of paediatric patients with anca vasculitis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150312/ https://www.ncbi.nlm.nih.gov/pubmed/21682926 http://dx.doi.org/10.1186/1546-0096-9-12 |
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