Cargando…
Characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study
OBJECTIVES: Infection 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. METHODS: We conducted a multicentre matched cohor...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7516107/ https://www.ncbi.nlm.nih.gov/pubmed/32159801 http://dx.doi.org/10.1093/rheumatology/keaa070 |
_version_ | 1783586937027690496 |
---|---|
author | Sarica, Shifa H Dhaun, Neeraj Sznajd, Jan Harvie, John McLaren, John McGeoch, Lucy Kumar, Vinod Amft, Nicole Erwig, Lars Marks, Angharad Black, Corri Basu, Neil |
author_facet | Sarica, Shifa H Dhaun, Neeraj Sznajd, Jan Harvie, John McLaren, John McGeoch, Lucy Kumar, Vinod Amft, Nicole Erwig, Lars Marks, Angharad Black, Corri Basu, Neil |
author_sort | Sarica, Shifa H |
collection | PubMed |
description | OBJECTIVES: Infection 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. METHODS: We 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. RESULTS: A 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)]. CONCLUSION: AAV 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. |
format | Online Article Text |
id | pubmed-7516107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75161072020-09-30 Characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study Sarica, Shifa H Dhaun, Neeraj Sznajd, Jan Harvie, John McLaren, John McGeoch, Lucy Kumar, Vinod Amft, Nicole Erwig, Lars Marks, Angharad Black, Corri Basu, Neil Rheumatology (Oxford) Clinical Science OBJECTIVES: Infection 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. METHODS: We 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. RESULTS: A 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)]. CONCLUSION: AAV 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. Oxford University Press 2020-03-11 /pmc/articles/PMC7516107/ /pubmed/32159801 http://dx.doi.org/10.1093/rheumatology/keaa070 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Rheumatology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Science Sarica, Shifa H Dhaun, Neeraj Sznajd, Jan Harvie, John McLaren, John McGeoch, Lucy Kumar, Vinod Amft, Nicole Erwig, Lars Marks, Angharad Black, Corri Basu, Neil Characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study |
title | Characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study |
title_full | Characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study |
title_fullStr | Characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study |
title_full_unstemmed | Characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study |
title_short | Characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study |
title_sort | characterizing infection in anti-neutrophil cytoplasmic antibody–associated vasculitis: results from a longitudinal, matched-cohort data linkage study |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7516107/ https://www.ncbi.nlm.nih.gov/pubmed/32159801 http://dx.doi.org/10.1093/rheumatology/keaa070 |
work_keys_str_mv | AT saricashifah characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT dhaunneeraj characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT sznajdjan characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT harviejohn characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT mclarenjohn characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT mcgeochlucy characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT kumarvinod characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT amftnicole characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT erwiglars characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT marksangharad characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT blackcorri characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy AT basuneil characterizinginfectioninantineutrophilcytoplasmicantibodyassociatedvasculitisresultsfromalongitudinalmatchedcohortdatalinkagestudy |