Characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study

Author:

Sarica Shifa H1,Dhaun Neeraj2ORCID,Sznajd Jan3,Harvie John3,McLaren John4,McGeoch Lucy5,Kumar Vinod6,Amft Nicole7,Erwig Lars7,Marks Angharad8,Black Corri1,Basu Neil9

Affiliation:

1. Aberdeen Centre for Health Data Science, University of Aberdeen, Aberdeen, UK

2. Queen’s Medical Research Institute, University/British Heart Foundation Centre of Research Excellence, University of Edinburgh, Edinburgh, UK

3. Department of Rheumatology, Raigmore Hospital, Inverness, UK

4. Fife Rheumatic Diseases Unit, Whyteman’s Brae Hospital, Kirkcaldy, UK

5. Centre for Rheumatic Diseases, Glasgow Royal Infirmary, Glasgow, UK

6. Rheumatology Department, Ninewells Hospital, Dundee, UK

7. GlaxoSmithKline, Medicines Research Centre, Stevenage, UK

8. Morriston Hospital Renal Unit, Abertawe Bro Morgannwg University Health Board, Swansea, UK

9. Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK

Abstract

AbstractObjectivesInfection exerts a major burden in ANCA-associated vasculitis (AAV), however, its precise extent and nature remains unclear. In this national study we aimed to longitudinally quantify, characterize and contextualize infection risk in AAV.MethodsWe conducted a multicentre matched cohort study of AAV. Complementary data on infections were retrieved via data linkage with the population-based Scottish microbiological laboratory, hospitalization and primary care prescribing registries.ResultsA total of 379 AAV patients and 1859 controls were followed up for a median of 3.5 years (interquartile range 1.9–5.7). During follow-up, the proportions of AAV patients with at least one laboratory-confirmed infection, severe infection and primary care antibiotic prescription were 55.4%, 35.6% and 74.6%, respectively. The risk of infection was higher in AAV than in matched controls {laboratory-confirmed infections: incidence rate ratio [IRR] 7.3 [95% confidence interval (CI) 5.6, 9.6]; severe infections: IRR 4.4 [95% CI 3.3, 5.7]; antibiotic prescriptions: IRR 2.2 [95% CI 1.9, 2.6]}. Temporal trend analysis showed that AAV patients remained at a higher risk of infections throughout the follow-up period, especially year 1. Although the Escherichia genus was the most commonly identified pathogen (16.6% of AAV, 5.5% of controls; P < 0.0001), AAV patients had the highest risk for Herpes [IRR 12.5 (95% CI 3.7, 42.6)] and Candida [IRR 11.4 (95% CI 2.4, 55.4)].ConclusionAAV patients have up to seven times higher risk of infection than the general population and the overall risk remains significant after 8 years of follow-up. The testing of enhanced short- to medium-term prophylactic antibiotic regimes should be considered.

Funder

Aberdeen Development Trust

Farr Institute of Health Informatics Research

British Heart Foundation

Economic and Social Research Council

Engineering and Physical Sciences Research Council

Medical Research Council, the National Institute of Health Research

National Institute for Social Care and Health Research

Chief Scientist Office

Scottish Government Health Directorates

Wellcome Trust

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Reference37 articles.

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