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Rheumatology 2008 47(4):530-534; doi:10.1093/rheumatology/ken035
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© The Author 2008. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Venous thromboembolism in ANCA-associated vasculitis—incidence and risk factors

P. M. Stassen1,*, R. P. H. Derks2,*, C. G. M. Kallenberg2 and C. A. Stegeman3

1Department of Internal Medicine, Medisch Spectrum Twente, Enschede, 2Department of Clinical Immunology, University Medical Center Groningen, University of Groningen and 3Department of Nephrology, University Medical Center Groningen, University of Groningen, The Netherlands.

Correspondence to: P. M. Stassen, Department of Internal Medicine, Medisch Spectrum Twente, PO box 50000, 7500 KA Enschede, The Netherlands. E-mail: p.m.stassen{at}int.umcg.nl; pstassen{at}home.nl


   Abstract

Objectives. In patients with ANCA-associated vasculitis (AAV), an increased incidence of venous thromboembolism (VTE), mainly during active disease, has been described. In a large cohort of AAV patients, we assessed the incidence of VTE and its relation with disease activity and classic risk factors for VTE.

Methods. Patients newly diagnosed with AAV between 1990 and 2005 and treated with cyclophosphamide and corticosteroids were included. Data were retrospectively retrieved from charts and by questionnaire. The incidence of VTE associated with and following a diagnosis of AAV was calculated (VTE/100 person-years) and related to periods with active disease.

Results. One hundred and ninety-eight patients with AAV were followed for 6.1 (0.2–17.6) yrs. In 23 patients (12%), 25 VTEs (17 deep venous thromboses, 3 pulmonary emboli, 5 both) occurred in association with AAV, of which 52% occurred during active disease, defined as 3 months before and after diagnosis or relapse of AAV. Overall, VTE incidence was 1.8/100 person-years, increasing to 6.7/100 during active disease. VTEs occurred significantly less frequently in patients with WG than in patients with microscopic polyangiitis and renal limited vasculitis. Classic risk factors were present in most patients at some moment during follow-up. There were no significant differences in classic risk factors between patients with and without AAV-associated VTE.

Conclusions. Patients with AAV have an increased risk of developing VTEs, especially when AAV is active. This finding could not be explained by classic risk factors, but is probably related to endothelial changes and hypercoagulability induced by AAV and its therapy.

KEY WORDS: ANCA-associated vasculitis, Venous thromboembolism, Incidence, Risk factors


*PM Stassen and RPH Derks equally contributed to this work.

Submitted 13 October 2007; revised version accepted 14 January 2008.
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