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Decreased health-related quality of life in angiodysplasia patients: A cross-sectional cohort

Gastrointestinal angiodysplasias may cause anemia. Quality of life (QoL) is a valid patient reported outcome and improvement of QoL represents an important treatment goal. There is a paucity of data on the effect of angiodysplasias on QoL. Therefore, we aim to evaluate QoL and fatigue in angiodyspla...

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Autores principales: Grooteman, Karina V., Matheeuwsen, Mijntje, van Geenen, Erwin J. M., Drenth, Joost P. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446116/
https://www.ncbi.nlm.nih.gov/pubmed/28552982
http://dx.doi.org/10.1371/journal.pone.0177522
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author Grooteman, Karina V.
Matheeuwsen, Mijntje
van Geenen, Erwin J. M.
Drenth, Joost P. H.
author_facet Grooteman, Karina V.
Matheeuwsen, Mijntje
van Geenen, Erwin J. M.
Drenth, Joost P. H.
author_sort Grooteman, Karina V.
collection PubMed
description Gastrointestinal angiodysplasias may cause anemia. Quality of life (QoL) is a valid patient reported outcome and improvement of QoL represents an important treatment goal. There is a paucity of data on the effect of angiodysplasias on QoL. Therefore, we aim to evaluate QoL and fatigue in angiodysplasia patients. We performed a cross-sectional patient-reported outcome study. We included patients with endoscopy proven angiodysplasias and measured QoL with Short Form-36 and level of fatigue using Multi Fatigue Inventory-20. We distinguished three subgroups of patients according to disease severity: 1) with treatment for angiodysplasias, 2) without treatment for angiodysplasias and 3) without recent hospital visits. The primary outcome was the physical component summary (PCS) score on the SF-36. Multivariate regression analysis were performed to correct for differences at baseline. A total of 144 patients completed the questionnaires (response rate = 62%; mean age 68 years; 65% men). Angiodysplasia patients have a significant lower PCS compared to the age-matched general population (respectively 41.0 vs. 43.3, p = 0.01). Disease severity is independently associated with a negative outcome on QoL (ß -4.6, 95% CI -7.8–-1.3). Similarly patients score lower on multiple QoL subdomains, i.e. role limitations due to physical health problems (40.8 vs. 44.0, p<0.01), general health (39.7 vs. 47.3, p<0.01). Angiodysplasia patients are more fatigued compared to the general population (male 56.1 vs. 48.5, p<0.01, female 59.2 vs. 51.5, p = 0.01). In conclusion, angiodysplasias are independently associated with clinically significant impairments in multiple domains of health-related QoL, especially in measures of functional limitation.
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spelling pubmed-54461162017-06-12 Decreased health-related quality of life in angiodysplasia patients: A cross-sectional cohort Grooteman, Karina V. Matheeuwsen, Mijntje van Geenen, Erwin J. M. Drenth, Joost P. H. PLoS One Research Article Gastrointestinal angiodysplasias may cause anemia. Quality of life (QoL) is a valid patient reported outcome and improvement of QoL represents an important treatment goal. There is a paucity of data on the effect of angiodysplasias on QoL. Therefore, we aim to evaluate QoL and fatigue in angiodysplasia patients. We performed a cross-sectional patient-reported outcome study. We included patients with endoscopy proven angiodysplasias and measured QoL with Short Form-36 and level of fatigue using Multi Fatigue Inventory-20. We distinguished three subgroups of patients according to disease severity: 1) with treatment for angiodysplasias, 2) without treatment for angiodysplasias and 3) without recent hospital visits. The primary outcome was the physical component summary (PCS) score on the SF-36. Multivariate regression analysis were performed to correct for differences at baseline. A total of 144 patients completed the questionnaires (response rate = 62%; mean age 68 years; 65% men). Angiodysplasia patients have a significant lower PCS compared to the age-matched general population (respectively 41.0 vs. 43.3, p = 0.01). Disease severity is independently associated with a negative outcome on QoL (ß -4.6, 95% CI -7.8–-1.3). Similarly patients score lower on multiple QoL subdomains, i.e. role limitations due to physical health problems (40.8 vs. 44.0, p<0.01), general health (39.7 vs. 47.3, p<0.01). Angiodysplasia patients are more fatigued compared to the general population (male 56.1 vs. 48.5, p<0.01, female 59.2 vs. 51.5, p = 0.01). In conclusion, angiodysplasias are independently associated with clinically significant impairments in multiple domains of health-related QoL, especially in measures of functional limitation. Public Library of Science 2017-05-26 /pmc/articles/PMC5446116/ /pubmed/28552982 http://dx.doi.org/10.1371/journal.pone.0177522 Text en © 2017 Grooteman et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Grooteman, Karina V.
Matheeuwsen, Mijntje
van Geenen, Erwin J. M.
Drenth, Joost P. H.
Decreased health-related quality of life in angiodysplasia patients: A cross-sectional cohort
title Decreased health-related quality of life in angiodysplasia patients: A cross-sectional cohort
title_full Decreased health-related quality of life in angiodysplasia patients: A cross-sectional cohort
title_fullStr Decreased health-related quality of life in angiodysplasia patients: A cross-sectional cohort
title_full_unstemmed Decreased health-related quality of life in angiodysplasia patients: A cross-sectional cohort
title_short Decreased health-related quality of life in angiodysplasia patients: A cross-sectional cohort
title_sort decreased health-related quality of life in angiodysplasia patients: a cross-sectional cohort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446116/
https://www.ncbi.nlm.nih.gov/pubmed/28552982
http://dx.doi.org/10.1371/journal.pone.0177522
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