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Disability in Patients with Inflammatory Bowel Disease: Correlations with Quality of Life and Patient's Characteristics

BACKGROUND: Inflammatory bowel diseases may cause significant disability. However, little is known regarding the life domains where patients encounter most limitations. OBJECTIVES: To assess patients' overall disability and determine the life domains where most restrictions were applied. Second...

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Autores principales: Argyriou, Konstantinos, Kapsoritakis, Andreas, Oikonomou, Konstantinos, Manolakis, Anastassios, Tsakiridou, Eirini, Potamianos, Spyridon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467285/
https://www.ncbi.nlm.nih.gov/pubmed/28634576
http://dx.doi.org/10.1155/2017/6138105
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author Argyriou, Konstantinos
Kapsoritakis, Andreas
Oikonomou, Konstantinos
Manolakis, Anastassios
Tsakiridou, Eirini
Potamianos, Spyridon
author_facet Argyriou, Konstantinos
Kapsoritakis, Andreas
Oikonomou, Konstantinos
Manolakis, Anastassios
Tsakiridou, Eirini
Potamianos, Spyridon
author_sort Argyriou, Konstantinos
collection PubMed
description BACKGROUND: Inflammatory bowel diseases may cause significant disability. However, little is known regarding the life domains where patients encounter most limitations. OBJECTIVES: To assess patients' overall disability and determine the life domains where most restrictions were applied. Secondarily, we sought for possible relationships among disability, quality of life (HRQoL), and population characteristics. METHOD: The study lasted for two years (2013–2015) and included 200 patients [52%  ulcerative  colitis  (UC)] from a referral centre. Disability was evaluated using the 36-item version of WHODAS 2.0 questionnaire. The influence of population characteristics on overall disability was assessed with linear regression. RESULTS: Crohn's disease (CD) patients showed greater overall disability compared to UC (19.22 versus 15.01, p = 0.001), with higher scores in the domains of relationships, life activities, and participation. Disability was negatively associated with HRQoL (p < 0.001). Long activity, extensive disease, rural residence, and employment independently influenced the overall disability in both groups. Additionally, significant influence was recorded for lower education in the UC and for operation and celibacy in the CD group. CONCLUSIONS: CD patients were facing more limitations compared to those with UC, especially in the domains of relationships, activities, and participation. Other than clinical factors, sociodemographic characteristics were also associated with increased disability.
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spelling pubmed-54672852017-06-20 Disability in Patients with Inflammatory Bowel Disease: Correlations with Quality of Life and Patient's Characteristics Argyriou, Konstantinos Kapsoritakis, Andreas Oikonomou, Konstantinos Manolakis, Anastassios Tsakiridou, Eirini Potamianos, Spyridon Can J Gastroenterol Hepatol Research Article BACKGROUND: Inflammatory bowel diseases may cause significant disability. However, little is known regarding the life domains where patients encounter most limitations. OBJECTIVES: To assess patients' overall disability and determine the life domains where most restrictions were applied. Secondarily, we sought for possible relationships among disability, quality of life (HRQoL), and population characteristics. METHOD: The study lasted for two years (2013–2015) and included 200 patients [52%  ulcerative  colitis  (UC)] from a referral centre. Disability was evaluated using the 36-item version of WHODAS 2.0 questionnaire. The influence of population characteristics on overall disability was assessed with linear regression. RESULTS: Crohn's disease (CD) patients showed greater overall disability compared to UC (19.22 versus 15.01, p = 0.001), with higher scores in the domains of relationships, life activities, and participation. Disability was negatively associated with HRQoL (p < 0.001). Long activity, extensive disease, rural residence, and employment independently influenced the overall disability in both groups. Additionally, significant influence was recorded for lower education in the UC and for operation and celibacy in the CD group. CONCLUSIONS: CD patients were facing more limitations compared to those with UC, especially in the domains of relationships, activities, and participation. Other than clinical factors, sociodemographic characteristics were also associated with increased disability. Hindawi 2017 2017-05-29 /pmc/articles/PMC5467285/ /pubmed/28634576 http://dx.doi.org/10.1155/2017/6138105 Text en Copyright © 2017 Konstantinos Argyriou et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Argyriou, Konstantinos
Kapsoritakis, Andreas
Oikonomou, Konstantinos
Manolakis, Anastassios
Tsakiridou, Eirini
Potamianos, Spyridon
Disability in Patients with Inflammatory Bowel Disease: Correlations with Quality of Life and Patient's Characteristics
title Disability in Patients with Inflammatory Bowel Disease: Correlations with Quality of Life and Patient's Characteristics
title_full Disability in Patients with Inflammatory Bowel Disease: Correlations with Quality of Life and Patient's Characteristics
title_fullStr Disability in Patients with Inflammatory Bowel Disease: Correlations with Quality of Life and Patient's Characteristics
title_full_unstemmed Disability in Patients with Inflammatory Bowel Disease: Correlations with Quality of Life and Patient's Characteristics
title_short Disability in Patients with Inflammatory Bowel Disease: Correlations with Quality of Life and Patient's Characteristics
title_sort disability in patients with inflammatory bowel disease: correlations with quality of life and patient's characteristics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467285/
https://www.ncbi.nlm.nih.gov/pubmed/28634576
http://dx.doi.org/10.1155/2017/6138105
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