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Severe infections remain common in a real-world rheumatoid arthritis cohort: A simple clinical model to predict infection risk
OBJECTIVE: This study aimed to investigate the incidence of severe infections in patients of a dedicated rheumatoid arthritis (RA) clinic, identify the associated risk factors, and derive an infection risk screening tool. METHODS: Between January and July 2019, 263 eligible patients with a diagnosis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medical Research and Education Association
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9770411/ https://www.ncbi.nlm.nih.gov/pubmed/33372891 http://dx.doi.org/10.5152/eurjrheum.2020.20172 |
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author | Wang, Dorothy Yeo, Ai Li Dendle, Claire Morton, Susan Morand, Eric Leech, Michelle |
author_facet | Wang, Dorothy Yeo, Ai Li Dendle, Claire Morton, Susan Morand, Eric Leech, Michelle |
author_sort | Wang, Dorothy |
collection | PubMed |
description | OBJECTIVE: This study aimed to investigate the incidence of severe infections in patients of a dedicated rheumatoid arthritis (RA) clinic, identify the associated risk factors, and derive an infection risk screening tool. METHODS: Between January and July 2019, 263 eligible patients with a diagnosis of RA were recruited retrospectively and consecutively from an RA clinic of an Australian tertiary hospital. The primary outcome was severe infection (requiring hospital admission) between January 2018 and July 2019. We collected data from medical records and pathology results. We used validated scores, such as the disease activity score of 28 joints (DAS28) and the Charlson comorbidity index, to assess the disease activity and comorbidity burden. Multivariable logistic regression was used for statistical analysis. RESULTS: A total of 45 severe infection episodes occurred in 34 (13%) patients, corresponding to 10.8 infections per 100 patient-years. Respiratory (53%) and urinary (13%) tract infections were the most common. In the multivariable analysis, significant risk factors included low lymphocyte count (odds ratio [OR], 4.08; 95% confidence interval [CI], 1.16–14.29), severe infection in the past 3 years (OR, 3.58; 95% CI, 1.28–9.97), Charlson comorbidity index >2 (OR, 2.69; 95% CI, 1.03–7.00), and higher DAS28 (OR, 1.35/0.5-unit increment; 95% CI, 1.10–1.67). A model incorporating these factors and age had an area under receiver operating characteristic curve of 0.82. CONCLUSION: To the best of our knowledge, this was one of the first Australian studies to evaluate severe infection rates in a real-world RA cohort. The rates remained high and comparable with those of the older studies. Lymphopenia, disease activity, comorbidity burden, and previous severe infection were the independent risk factors for infection. A model comprising easily assessable clinical and biological parameters has an excellent predictive potential for severe infection. Once validated, it may be developed into a screening tool to help clinicians rapidly identify the high-risk patients and inform the tailored clinical decision making. |
format | Online Article Text |
id | pubmed-9770411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Medical Research and Education Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-97704112022-12-28 Severe infections remain common in a real-world rheumatoid arthritis cohort: A simple clinical model to predict infection risk Wang, Dorothy Yeo, Ai Li Dendle, Claire Morton, Susan Morand, Eric Leech, Michelle Eur J Rheumatol Original Article OBJECTIVE: This study aimed to investigate the incidence of severe infections in patients of a dedicated rheumatoid arthritis (RA) clinic, identify the associated risk factors, and derive an infection risk screening tool. METHODS: Between January and July 2019, 263 eligible patients with a diagnosis of RA were recruited retrospectively and consecutively from an RA clinic of an Australian tertiary hospital. The primary outcome was severe infection (requiring hospital admission) between January 2018 and July 2019. We collected data from medical records and pathology results. We used validated scores, such as the disease activity score of 28 joints (DAS28) and the Charlson comorbidity index, to assess the disease activity and comorbidity burden. Multivariable logistic regression was used for statistical analysis. RESULTS: A total of 45 severe infection episodes occurred in 34 (13%) patients, corresponding to 10.8 infections per 100 patient-years. Respiratory (53%) and urinary (13%) tract infections were the most common. In the multivariable analysis, significant risk factors included low lymphocyte count (odds ratio [OR], 4.08; 95% confidence interval [CI], 1.16–14.29), severe infection in the past 3 years (OR, 3.58; 95% CI, 1.28–9.97), Charlson comorbidity index >2 (OR, 2.69; 95% CI, 1.03–7.00), and higher DAS28 (OR, 1.35/0.5-unit increment; 95% CI, 1.10–1.67). A model incorporating these factors and age had an area under receiver operating characteristic curve of 0.82. CONCLUSION: To the best of our knowledge, this was one of the first Australian studies to evaluate severe infection rates in a real-world RA cohort. The rates remained high and comparable with those of the older studies. Lymphopenia, disease activity, comorbidity burden, and previous severe infection were the independent risk factors for infection. A model comprising easily assessable clinical and biological parameters has an excellent predictive potential for severe infection. Once validated, it may be developed into a screening tool to help clinicians rapidly identify the high-risk patients and inform the tailored clinical decision making. Medical Research and Education Association 2021-07 2020-12-28 /pmc/articles/PMC9770411/ /pubmed/33372891 http://dx.doi.org/10.5152/eurjrheum.2020.20172 Text en Copyright © 2021 European Journal of Rheumatology https://creativecommons.org/licenses/by-nc/4.0/Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
spellingShingle | Original Article Wang, Dorothy Yeo, Ai Li Dendle, Claire Morton, Susan Morand, Eric Leech, Michelle Severe infections remain common in a real-world rheumatoid arthritis cohort: A simple clinical model to predict infection risk |
title | Severe infections remain common in a real-world rheumatoid arthritis cohort: A simple clinical model to predict infection risk |
title_full | Severe infections remain common in a real-world rheumatoid arthritis cohort: A simple clinical model to predict infection risk |
title_fullStr | Severe infections remain common in a real-world rheumatoid arthritis cohort: A simple clinical model to predict infection risk |
title_full_unstemmed | Severe infections remain common in a real-world rheumatoid arthritis cohort: A simple clinical model to predict infection risk |
title_short | Severe infections remain common in a real-world rheumatoid arthritis cohort: A simple clinical model to predict infection risk |
title_sort | severe infections remain common in a real-world rheumatoid arthritis cohort: a simple clinical model to predict infection risk |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9770411/ https://www.ncbi.nlm.nih.gov/pubmed/33372891 http://dx.doi.org/10.5152/eurjrheum.2020.20172 |
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