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Caregivers of Patients with Heart Failure: Burden and the Determinants of Health-Related Quality of Life

PURPOSE: To assess the burden among caregivers of patients with heart failure (HF) with left ventricular ejection fraction (LVEF) ≤60%. The burden by New York Heart Association (NYHA) functional class was also characterized. PATIENTS AND METHODS: A cross-sectional study was conducted in France, Germ...

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Autores principales: Lahoz, Raquel, Proudfoot, Clare, Fonseca, Ana Filipa, Loefroth, Emil, Corda, Stefano, Jackson, James, Cotton, Sarah, Studer, Rachel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165301/
https://www.ncbi.nlm.nih.gov/pubmed/34079236
http://dx.doi.org/10.2147/PPA.S297816
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author Lahoz, Raquel
Proudfoot, Clare
Fonseca, Ana Filipa
Loefroth, Emil
Corda, Stefano
Jackson, James
Cotton, Sarah
Studer, Rachel
author_facet Lahoz, Raquel
Proudfoot, Clare
Fonseca, Ana Filipa
Loefroth, Emil
Corda, Stefano
Jackson, James
Cotton, Sarah
Studer, Rachel
author_sort Lahoz, Raquel
collection PubMed
description PURPOSE: To assess the burden among caregivers of patients with heart failure (HF) with left ventricular ejection fraction (LVEF) ≤60%. The burden by New York Heart Association (NYHA) functional class was also characterized. PATIENTS AND METHODS: A cross-sectional study was conducted in France, Germany, Italy, Spain, and UK from June to November 2019. Patient record forms were completed by 257 cardiologists and 158 general practitioners for consecutive HF patients. Caregivers who accompanied the patient to their consultation completed a caregiver self-completion survey voluntarily, which included the Family Caregiver Quality of Life Questionnaire (FAMQOL) and 5-level 5-dimension EuroQol questionnaire (EQ-5D-5L). RESULTS: We analyzed 361 caregivers of patients with HF (NYHA class I, n=41; II, n=212; III IV, n=108). Mean age of caregivers was 58.8 years (NYHA I/II/III–IV: 59.1/60.8/54.6 years; p=0.0029), with majority being females (73.1%). Caregivers spent on average 19.8 hours/week caring for a HF patient, which increased with increase in NYHA class (I/II/III–IV: 11.8/18.1/25.9 hours/week; p=0.0094). Caregivers (24.1%) reported providing emotional support/encouragement to patients as the most troublesome/inconvenient caregiving activity (no significant difference across NYHA class). Nearly one-third of caregivers experienced stress (NYHA I/II/III–IV: 17.1%/28.8%/40.7%; p=0.0111) and anxiety (26.8%/24.1%/39.8%; p=0.0127) due to caregiving burden. The overall FAMQOL mean score decreased significantly (poorer QoL) with increase in NYHA class (I/II/III–IV: 58.1/56.3/52.2; p=0.0069). A trend of decreasing scores with increasing NYHA class was observed across physical, emotional, and social domains (each p≤0.012). CONCLUSION: Caregivers of HF patients with LVEF ≤60% experienced a significant burden, which was higher among caregivers of patients with more severe and symptomatic disease.
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spelling pubmed-81653012021-06-01 Caregivers of Patients with Heart Failure: Burden and the Determinants of Health-Related Quality of Life Lahoz, Raquel Proudfoot, Clare Fonseca, Ana Filipa Loefroth, Emil Corda, Stefano Jackson, James Cotton, Sarah Studer, Rachel Patient Prefer Adherence Original Research PURPOSE: To assess the burden among caregivers of patients with heart failure (HF) with left ventricular ejection fraction (LVEF) ≤60%. The burden by New York Heart Association (NYHA) functional class was also characterized. PATIENTS AND METHODS: A cross-sectional study was conducted in France, Germany, Italy, Spain, and UK from June to November 2019. Patient record forms were completed by 257 cardiologists and 158 general practitioners for consecutive HF patients. Caregivers who accompanied the patient to their consultation completed a caregiver self-completion survey voluntarily, which included the Family Caregiver Quality of Life Questionnaire (FAMQOL) and 5-level 5-dimension EuroQol questionnaire (EQ-5D-5L). RESULTS: We analyzed 361 caregivers of patients with HF (NYHA class I, n=41; II, n=212; III IV, n=108). Mean age of caregivers was 58.8 years (NYHA I/II/III–IV: 59.1/60.8/54.6 years; p=0.0029), with majority being females (73.1%). Caregivers spent on average 19.8 hours/week caring for a HF patient, which increased with increase in NYHA class (I/II/III–IV: 11.8/18.1/25.9 hours/week; p=0.0094). Caregivers (24.1%) reported providing emotional support/encouragement to patients as the most troublesome/inconvenient caregiving activity (no significant difference across NYHA class). Nearly one-third of caregivers experienced stress (NYHA I/II/III–IV: 17.1%/28.8%/40.7%; p=0.0111) and anxiety (26.8%/24.1%/39.8%; p=0.0127) due to caregiving burden. The overall FAMQOL mean score decreased significantly (poorer QoL) with increase in NYHA class (I/II/III–IV: 58.1/56.3/52.2; p=0.0069). A trend of decreasing scores with increasing NYHA class was observed across physical, emotional, and social domains (each p≤0.012). CONCLUSION: Caregivers of HF patients with LVEF ≤60% experienced a significant burden, which was higher among caregivers of patients with more severe and symptomatic disease. Dove 2021-05-26 /pmc/articles/PMC8165301/ /pubmed/34079236 http://dx.doi.org/10.2147/PPA.S297816 Text en © 2021 Lahoz et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Lahoz, Raquel
Proudfoot, Clare
Fonseca, Ana Filipa
Loefroth, Emil
Corda, Stefano
Jackson, James
Cotton, Sarah
Studer, Rachel
Caregivers of Patients with Heart Failure: Burden and the Determinants of Health-Related Quality of Life
title Caregivers of Patients with Heart Failure: Burden and the Determinants of Health-Related Quality of Life
title_full Caregivers of Patients with Heart Failure: Burden and the Determinants of Health-Related Quality of Life
title_fullStr Caregivers of Patients with Heart Failure: Burden and the Determinants of Health-Related Quality of Life
title_full_unstemmed Caregivers of Patients with Heart Failure: Burden and the Determinants of Health-Related Quality of Life
title_short Caregivers of Patients with Heart Failure: Burden and the Determinants of Health-Related Quality of Life
title_sort caregivers of patients with heart failure: burden and the determinants of health-related quality of life
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165301/
https://www.ncbi.nlm.nih.gov/pubmed/34079236
http://dx.doi.org/10.2147/PPA.S297816
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