The epidemiology of Wegener's granulomatosis and microscopic polyangiitis in a Southern Hemisphere region

Objective . To determine the prevalence of Wegener's granulomatosis (WG) and microscopic polyangiitis (MPA) in the province of Canterbury, New Zealand. Method . Three hospital clinical databases and the immunology laboratory database were searched and case notes reviewed for patients fulfilling...

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Published in:Rheumatology
Main Authors: Gibson, A., Stamp, L. K., Chapman, P. T., O'Donnell, J. L.
Format: Text
Language:English
Published: Oxford University Press 2005
Subjects:
Online Access:http://rheumatology.oxfordjournals.org/cgi/content/short/kei259v1
https://doi.org/10.1093/rheumatology/kei259
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spelling fthighwire:oai:open-archive.highwire.org:rheumatology:kei259v1 2023-05-15T17:43:37+02:00 The epidemiology of Wegener's granulomatosis and microscopic polyangiitis in a Southern Hemisphere region Gibson, A. Stamp, L. K. Chapman, P. T. O'Donnell, J. L. 2005-12-20 06:58:06.0 text/html http://rheumatology.oxfordjournals.org/cgi/content/short/kei259v1 https://doi.org/10.1093/rheumatology/kei259 en eng Oxford University Press http://rheumatology.oxfordjournals.org/cgi/content/short/kei259v1 http://dx.doi.org/10.1093/rheumatology/kei259 Copyright (C) 2005, British Society for Rheumatology Original Papers TEXT 2005 fthighwire https://doi.org/10.1093/rheumatology/kei259 2007-06-24T13:09:16Z Objective . To determine the prevalence of Wegener's granulomatosis (WG) and microscopic polyangiitis (MPA) in the province of Canterbury, New Zealand. Method . Three hospital clinical databases and the immunology laboratory database were searched and case notes reviewed for patients fulfilling either the 1990 American College of Rheumatology (ACR) criteria for WG or a modification of those criteria that allowed for antineutrophil cytoplasmic antibody (ANCA) positivity in the absence of granulomatous vasculitis. MPA was defined by the Chapel Hill consensus definition; however, in the absence of histological evidence of pauci-immune glomerulonephritis, ANCA positivity in association with evidence of active glomerular disease was included as a criterion. The point prevalence at 31 December 2003 and the 5-yr period prevalence for the interval 1 January 1999 to 31 December 2003 were calculated. Results . Seventy-three patients with WG and 28 patients with MPA fulfilled the inclusion criteria. A 5-yr period prevalence of 152 WG cases/million [95% confidence interval (CI) 117-186] and 58 MPA cases/million (95% CI 37-80) was calculated using 2001 census data as denominator. Nineteen patients with WG died and 10 patients with MPA died during the study period, resulting in a point prevalence for survivors at 31 December 2003 of 112 cases/million (95% CI 82-142) and 37 cases/million (95% CI 20-55), respectively. Using unmodified ACR criteria the 5-yr period and point prevalence for WG were 131/million (95% CI 99-163) and 93.5/million (95% CI 66-121), respectively. Apart from respiratory tract involvement, which formed part of the case definition of WG, organ involvement was similar in both diseases. Conclusion. The prevalence of WG and MPA in Canterbury is the highest reported to date. Restricting the case definition of WG to the ACR classification criteria we found a prevalence equivalent to that described in northern Norway. The clinical severity and serological characteristics were similar to descriptions in other WG ... Text Northern Norway HighWire Press (Stanford University) Chapel Hill ENVELOPE(-57.976,-57.976,-63.685,-63.685) New Zealand Norway Rheumatology 45 5 624 628
institution Open Polar
collection HighWire Press (Stanford University)
op_collection_id fthighwire
language English
topic Original Papers
spellingShingle Original Papers
Gibson, A.
Stamp, L. K.
Chapman, P. T.
O'Donnell, J. L.
The epidemiology of Wegener's granulomatosis and microscopic polyangiitis in a Southern Hemisphere region
topic_facet Original Papers
description Objective . To determine the prevalence of Wegener's granulomatosis (WG) and microscopic polyangiitis (MPA) in the province of Canterbury, New Zealand. Method . Three hospital clinical databases and the immunology laboratory database were searched and case notes reviewed for patients fulfilling either the 1990 American College of Rheumatology (ACR) criteria for WG or a modification of those criteria that allowed for antineutrophil cytoplasmic antibody (ANCA) positivity in the absence of granulomatous vasculitis. MPA was defined by the Chapel Hill consensus definition; however, in the absence of histological evidence of pauci-immune glomerulonephritis, ANCA positivity in association with evidence of active glomerular disease was included as a criterion. The point prevalence at 31 December 2003 and the 5-yr period prevalence for the interval 1 January 1999 to 31 December 2003 were calculated. Results . Seventy-three patients with WG and 28 patients with MPA fulfilled the inclusion criteria. A 5-yr period prevalence of 152 WG cases/million [95% confidence interval (CI) 117-186] and 58 MPA cases/million (95% CI 37-80) was calculated using 2001 census data as denominator. Nineteen patients with WG died and 10 patients with MPA died during the study period, resulting in a point prevalence for survivors at 31 December 2003 of 112 cases/million (95% CI 82-142) and 37 cases/million (95% CI 20-55), respectively. Using unmodified ACR criteria the 5-yr period and point prevalence for WG were 131/million (95% CI 99-163) and 93.5/million (95% CI 66-121), respectively. Apart from respiratory tract involvement, which formed part of the case definition of WG, organ involvement was similar in both diseases. Conclusion. The prevalence of WG and MPA in Canterbury is the highest reported to date. Restricting the case definition of WG to the ACR classification criteria we found a prevalence equivalent to that described in northern Norway. The clinical severity and serological characteristics were similar to descriptions in other WG ...
format Text
author Gibson, A.
Stamp, L. K.
Chapman, P. T.
O'Donnell, J. L.
author_facet Gibson, A.
Stamp, L. K.
Chapman, P. T.
O'Donnell, J. L.
author_sort Gibson, A.
title The epidemiology of Wegener's granulomatosis and microscopic polyangiitis in a Southern Hemisphere region
title_short The epidemiology of Wegener's granulomatosis and microscopic polyangiitis in a Southern Hemisphere region
title_full The epidemiology of Wegener's granulomatosis and microscopic polyangiitis in a Southern Hemisphere region
title_fullStr The epidemiology of Wegener's granulomatosis and microscopic polyangiitis in a Southern Hemisphere region
title_full_unstemmed The epidemiology of Wegener's granulomatosis and microscopic polyangiitis in a Southern Hemisphere region
title_sort epidemiology of wegener's granulomatosis and microscopic polyangiitis in a southern hemisphere region
publisher Oxford University Press
publishDate 2005
url http://rheumatology.oxfordjournals.org/cgi/content/short/kei259v1
https://doi.org/10.1093/rheumatology/kei259
long_lat ENVELOPE(-57.976,-57.976,-63.685,-63.685)
geographic Chapel Hill
New Zealand
Norway
geographic_facet Chapel Hill
New Zealand
Norway
genre Northern Norway
genre_facet Northern Norway
op_relation http://rheumatology.oxfordjournals.org/cgi/content/short/kei259v1
http://dx.doi.org/10.1093/rheumatology/kei259
op_rights Copyright (C) 2005, British Society for Rheumatology
op_doi https://doi.org/10.1093/rheumatology/kei259
container_title Rheumatology
container_volume 45
container_issue 5
container_start_page 624
op_container_end_page 628
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