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Osteoarthritis and risk of hospitalization for ambulatory care-sensitive conditions: a general population-based cohort study

OBJECTIVE: To determine the association between OA and risk of hospitalization for ambulatory care-sensitive conditions (HACSCs). METHODS: We included all individuals aged 40–85 years who resided in Skåne, Sweden on 31 December 2005 with at least one healthcare consultation during 1998–2005 (n = 515...

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Autores principales: Kiadaliri, Ali, Englund, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410004/
https://www.ncbi.nlm.nih.gov/pubmed/33590848
http://dx.doi.org/10.1093/rheumatology/keab161
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author Kiadaliri, Ali
Englund, Martin
author_facet Kiadaliri, Ali
Englund, Martin
author_sort Kiadaliri, Ali
collection PubMed
description OBJECTIVE: To determine the association between OA and risk of hospitalization for ambulatory care-sensitive conditions (HACSCs). METHODS: We included all individuals aged 40–85 years who resided in Skåne, Sweden on 31 December 2005 with at least one healthcare consultation during 1998–2005 (n = 515 256). We identified those with a main diagnosis of OA between 1 January 1998 and 31 December 2016. People were followed from 1 January 2006 until an HACSC, death, relocation outside Skåne, or 31 December 2016 (whichever occurred first). OA status was treated as a time-varying covariate (those diagnosed before 1 January 2006 considered as exposed for whole study period). We assessed relative [hazard ratios (HRs) using Cox proportional hazard model] and absolute (hazard difference using additive hazard model) effects of OA on HACSCs adjusted for potential confounders. RESULTS: Crude incidence rates of HACSCs were 239 (95% CI: 235, 242) and 151 (150, 152) per 10 000 person-years among OA and non-OA persons, respectively. The OA persons had an increased risk of HACSCs [HR (95% CI) 1.11 (1.09, 1.13)] and its subcategories of medical conditions except chronic obstructive pulmonary disease [HR (95% CI) 0.86 (0.81, 0.90)]. There were 20 (95% CI: 16, 24) more HACSCs per 10 000 person-years in OA compared with non-OA persons. While HRs for knee and hip OA were generally comparable, only knee OA was associated with increased risk of hospitalization for diabetes. CONCLUSION: OA is associated with an increased risk of HACSCs, highlighting the urgent need to improve outpatient care for OA patients.
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spelling pubmed-84100042021-09-02 Osteoarthritis and risk of hospitalization for ambulatory care-sensitive conditions: a general population-based cohort study Kiadaliri, Ali Englund, Martin Rheumatology (Oxford) Clinical Science OBJECTIVE: To determine the association between OA and risk of hospitalization for ambulatory care-sensitive conditions (HACSCs). METHODS: We included all individuals aged 40–85 years who resided in Skåne, Sweden on 31 December 2005 with at least one healthcare consultation during 1998–2005 (n = 515 256). We identified those with a main diagnosis of OA between 1 January 1998 and 31 December 2016. People were followed from 1 January 2006 until an HACSC, death, relocation outside Skåne, or 31 December 2016 (whichever occurred first). OA status was treated as a time-varying covariate (those diagnosed before 1 January 2006 considered as exposed for whole study period). We assessed relative [hazard ratios (HRs) using Cox proportional hazard model] and absolute (hazard difference using additive hazard model) effects of OA on HACSCs adjusted for potential confounders. RESULTS: Crude incidence rates of HACSCs were 239 (95% CI: 235, 242) and 151 (150, 152) per 10 000 person-years among OA and non-OA persons, respectively. The OA persons had an increased risk of HACSCs [HR (95% CI) 1.11 (1.09, 1.13)] and its subcategories of medical conditions except chronic obstructive pulmonary disease [HR (95% CI) 0.86 (0.81, 0.90)]. There were 20 (95% CI: 16, 24) more HACSCs per 10 000 person-years in OA compared with non-OA persons. While HRs for knee and hip OA were generally comparable, only knee OA was associated with increased risk of hospitalization for diabetes. CONCLUSION: OA is associated with an increased risk of HACSCs, highlighting the urgent need to improve outpatient care for OA patients. Oxford University Press 2021-02-16 /pmc/articles/PMC8410004/ /pubmed/33590848 http://dx.doi.org/10.1093/rheumatology/keab161 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Science
Kiadaliri, Ali
Englund, Martin
Osteoarthritis and risk of hospitalization for ambulatory care-sensitive conditions: a general population-based cohort study
title Osteoarthritis and risk of hospitalization for ambulatory care-sensitive conditions: a general population-based cohort study
title_full Osteoarthritis and risk of hospitalization for ambulatory care-sensitive conditions: a general population-based cohort study
title_fullStr Osteoarthritis and risk of hospitalization for ambulatory care-sensitive conditions: a general population-based cohort study
title_full_unstemmed Osteoarthritis and risk of hospitalization for ambulatory care-sensitive conditions: a general population-based cohort study
title_short Osteoarthritis and risk of hospitalization for ambulatory care-sensitive conditions: a general population-based cohort study
title_sort osteoarthritis and risk of hospitalization for ambulatory care-sensitive conditions: a general population-based cohort study
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410004/
https://www.ncbi.nlm.nih.gov/pubmed/33590848
http://dx.doi.org/10.1093/rheumatology/keab161
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