Long-term damage to the ENT system in Wegener's granulomatosis

Martinez Del Pero, Marcos, Walsh, Michael, Luqmani, Raashid, Flossmann, Oliver, Mukhtyar, Chetan ORCID: https://orcid.org/0000-0002-9771-6667, Jani, Piyush, Rasmussen, Niels and Jayne, David (2011) Long-term damage to the ENT system in Wegener's granulomatosis. European Archives of Oto-Rhino-Laryngology, 268 (5). pp. 733-739. ISSN 0937-4477

Full text not available from this repository. (Request a copy)

Abstract

The objectives of the study are to describe long-term ENT damage and assess risk factors in patients with newly diagnosed and treated Wegener's granulomatosis (WG) using the vasculitis damage index (VDI). Data from four randomised controlled trials carried out by the European Vasculitis Study Group was used. Patients newly diagnosed with WG with complete data at 5 years were included. Patients enrolled into the trials without 5-year data were excluded. Total and ENT VDI scores were recorded at 12 months and after at least 5 years. Logistic regression models were constructed to assess risk factors using total ENT and overall VDI score over the follow-up period, the proportion of patients with increased VDI score and the presence or absence of damage as the main outcomes. One hundred and thirty-eight patients were included. Ninety patients (65%) had long-term damage and 81% of these (73/90) developed some damage in the first 12 months. Positive ENT activity score (BVAS) at baseline and relapses were associated with higher ENT VDI scores long-term (OR = 6.90, 95% CI 2.01-23.75; OR = 2.65, 95% CI 1.20-5.82). Increasing BVAS score showed a trend towards lower VDI scores (OR = 0.93, 95% CI 0.88-0.99). Only ENT relapses and number of relapses were associated with an increase in VDI over time (OR = 8.38, 95% CI 3.10-22.68; OR = 1.79, 95% CI 1.24-2.58). In conclusion, most of the ENT damage in these patients was accrued within 12 months of diagnosis. We have shown an association between later ENT damage and the presence of ENT disease at baseline; lower initial BVAS and higher rate of disease relapse.

Item Type: Article
Additional Information: © Springer-Verlag 2010
Uncontrolled Keywords: adult,aged,female,complications,humans,male,middle aged,etiology,randomized controlled trials as topic,risk factors,young adult
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
Depositing User: LivePure Connector
Date Deposited: 27 Nov 2019 02:00
Last Modified: 22 Oct 2022 05:29
URI: https://ueaeprints.uea.ac.uk/id/eprint/73100
DOI: 10.1007/s00405-010-1421-x

Actions (login required)

View Item View Item