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Societal impact for patients with psoriasis: A nationwide Swedish register study
BACKGROUND: Psoriasis is an immune-mediated chronic inflammatory disease having a significant negative health impact. Psoriasis has societal impact; loss of productivity has been estimated at approximately 10% and it may influence the patient's financial status. Relationships between quality of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8362274/ https://www.ncbi.nlm.nih.gov/pubmed/34409373 http://dx.doi.org/10.1016/j.jdin.2021.02.003 |
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author | Häbel, Henrike Wettermark, Björn Hägg, David Villacorta, Reginald Wennerström, E.Christina M. Linder, Marie |
author_facet | Häbel, Henrike Wettermark, Björn Hägg, David Villacorta, Reginald Wennerström, E.Christina M. Linder, Marie |
author_sort | Häbel, Henrike |
collection | PubMed |
description | BACKGROUND: Psoriasis is an immune-mediated chronic inflammatory disease having a significant negative health impact. Psoriasis has societal impact; loss of productivity has been estimated at approximately 10% and it may influence the patient's financial status. Relationships between quality of life, disease severity, and cost of care need exploration. Understanding the disease burden is important for health policy and research allocation. Few studies address the research gaps in socioeconomics, comorbidity, and medication use. OBJECTIVE: Observing differences in education, income, employment status, marital status, health care consumption, and drug utilization between patients with psoriasis and matched controls. METHODS: Cohort study following socioeconomics and health care consumption for all psoriasis patients from the Swedish patient register. All individuals with a first diagnosis of psoriasis in outpatient or inpatient care from 2002 to 2013 were followed until death, emigration, or end of the study. RESULTS: Overall, 109,803 patients were included (mean age 51.2 years, 53% women) and matched with 1.08 million controls. The levels of education and income were similar, but the proportion employed was significantly lower for patients with psoriasis. There was a tendency for fewer patients with psoriasis to be married. LIMITATIONS: Generalizability, lack of primary care diagnoses, and lack of early treatments (available from 2005). CONCLUSION: Understanding of the socioeconomic impact of psoriasis is extended by showing reductions in employment. |
format | Online Article Text |
id | pubmed-8362274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83622742021-08-17 Societal impact for patients with psoriasis: A nationwide Swedish register study Häbel, Henrike Wettermark, Björn Hägg, David Villacorta, Reginald Wennerström, E.Christina M. Linder, Marie JAAD Int Original Article BACKGROUND: Psoriasis is an immune-mediated chronic inflammatory disease having a significant negative health impact. Psoriasis has societal impact; loss of productivity has been estimated at approximately 10% and it may influence the patient's financial status. Relationships between quality of life, disease severity, and cost of care need exploration. Understanding the disease burden is important for health policy and research allocation. Few studies address the research gaps in socioeconomics, comorbidity, and medication use. OBJECTIVE: Observing differences in education, income, employment status, marital status, health care consumption, and drug utilization between patients with psoriasis and matched controls. METHODS: Cohort study following socioeconomics and health care consumption for all psoriasis patients from the Swedish patient register. All individuals with a first diagnosis of psoriasis in outpatient or inpatient care from 2002 to 2013 were followed until death, emigration, or end of the study. RESULTS: Overall, 109,803 patients were included (mean age 51.2 years, 53% women) and matched with 1.08 million controls. The levels of education and income were similar, but the proportion employed was significantly lower for patients with psoriasis. There was a tendency for fewer patients with psoriasis to be married. LIMITATIONS: Generalizability, lack of primary care diagnoses, and lack of early treatments (available from 2005). CONCLUSION: Understanding of the socioeconomic impact of psoriasis is extended by showing reductions in employment. Elsevier 2021-03-30 /pmc/articles/PMC8362274/ /pubmed/34409373 http://dx.doi.org/10.1016/j.jdin.2021.02.003 Text en © 2021 by the American Academy of Dermatology, Inc. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Article Häbel, Henrike Wettermark, Björn Hägg, David Villacorta, Reginald Wennerström, E.Christina M. Linder, Marie Societal impact for patients with psoriasis: A nationwide Swedish register study |
title | Societal impact for patients with psoriasis: A nationwide Swedish register study |
title_full | Societal impact for patients with psoriasis: A nationwide Swedish register study |
title_fullStr | Societal impact for patients with psoriasis: A nationwide Swedish register study |
title_full_unstemmed | Societal impact for patients with psoriasis: A nationwide Swedish register study |
title_short | Societal impact for patients with psoriasis: A nationwide Swedish register study |
title_sort | societal impact for patients with psoriasis: a nationwide swedish register study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8362274/ https://www.ncbi.nlm.nih.gov/pubmed/34409373 http://dx.doi.org/10.1016/j.jdin.2021.02.003 |
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