Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/181862
Title: Quality of life and disease experience in patients with heart failure with reduced ejection fraction in Spain: a mixed-methods study
Author: Rubio, Raül
Palacios, Beatriz
Varela, Luis
Fernández, Raquel
Camargo Correa, Selene
Estupiñan, María Fernanda
Calvo, Elena
José, Nuria
Ruiz Muñoz, Marta
Yun, Sergi
Jiménez Marrero, Santiago
Alcoberro, Lídia
Garay, Alberto
Moliner, Pedro
Sánchez Fernández, Lydia
Soria Gómez, María Teresa
Hidalgo, Encarna
Enjuanes, Cristina
Calero Molina, Esther
Rueda, Yolanda
San Saturnino, Maite
Garcimartín Cerezo, Paloma
López Ibor, Jorge V.
Segovia Cubero, Javier
Comin Colet, Josep
Keywords: Insuficiència cardíaca
Qualitat de vida
Heart failure
Quality of life
Issue Date: 1-Dec-2021
Publisher: BMJ
Abstract: Objectives: To gather insights on the disease experience of patients with heart failure (HF) with reduced ejection fraction (HFrEF), and assess how patients' experiences and narratives related to the disease complement data collected through standardised patient-reported outcome measures (PROMs). Also, to explore new ways of evaluating the burden experienced by patients and caregivers. Design: Observational, descriptive, multicentre, cross-sectional, mixed-methods study. Setting: Secondary care, patient's homes. Participants: Twenty patients with HFrEF (New York Heart Association (NYHA) classification I-III) aged 38-85 years. Measures: PROMs EuroQoL 5D-5L (EQ-5D-5L) and Kansas City Cardiomyopathy Questionnaire and patient interview and observation. Results: A total of 20 patients with HFrEF participated in the study. The patients' mean (SD) age was 72.5 (11.4) years, 65% were male and were classified inNYHA functional classes I (n=4), II (n=7) and III (n=9). The study showed a strong impact of HF in the patients' quality of life (QoL) and disease experience, as revealed by the standardised PROMs (EQ-5D-5L global index=0.64 (0.36); Kansas City Cardiomyopathy Questionnaire total symptom score=71.56 (20.55)) and the in-depth interviews. Patients and caregivers often disagreed describing and evaluating perceived QoL, as patients downplayed their limitations and caregivers overemphasised the poor QoL of the patients. Patients related current QoL to distant life experiences or to critical moments in their disease, such as hospitalisations. Anxiety over the disease progression is apparent in both patients and caregivers, suggesting that caregiver-specific tools should be developed. Conclusions: PROMs are an effective way of assessing symptoms over the most recent time period. However, especially in chronic diseases such as HFrEF, PROM scores could be complemented with additional tools to gain a better understanding of the patient's status. New PROMs designed to evaluate and compare specific points in the life of the patient could be clinically more useful to assess changes in health status.
Note: Reproducció del document publicat a: https://doi.org/10.1136/bmjopen-2021-053216
It is part of: BMJ Open, 2021, vol. 11, num. 12
URI: http://hdl.handle.net/2445/181862
Related resource: https://doi.org/10.1136/bmjopen-2021-053216
ISSN: 2044-6055
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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