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February 25, 2026European Journal of Cardiovascular Nursing2 citations

Understanding Heart Failure Patients’ Beliefs and Social Representations of Palliative Care and Advance Directives

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NRNathalie Vionnet RouxbedatCentre Hospitalier Universitaire de BesançonLBLiesbet Van BulckAdult Congenital Heart DiseaseMGMathilde GiffardCentre Hospitalier Universitaire de Besançon

Key Result

Heart failure patients often misunderstand palliative care as imminent death and lack awareness of advance directives, highlighting the need for better patient education.

Key Points

  • The study aims to explore heart failure patients' beliefs and social representations regarding palliative care and advance directives.
  • Conducted a qualitative study with chronic heart failure patients
  • Performed in-depth, face-to-face interviews
  • Analyzed data using a thematic approach
  • Patients often misunderstood palliative care, associating it with imminent death
  • Many had not considered end-of-life issues or written advance directives
  • Personal experiences with end-of-life care positively influenced their views on palliative care and willingness to establish advance directives

Structured PICO

How do heart failure patients perceive palliative care and advance directives?

P
Population
Chronic heart failure patients (age ≥18 years, NYHA class II-IV, active follow-up) in a French university hospital.
I
Intervention
Qualitative in-depth face-to-face interviews exploring representations and beliefs associated with palliative care and advance directives.
O
Outcome
Representations and beliefs associated with palliative care and advance directives.patient reported

Heart failure patients often misunderstand palliative care as being only for imminent death and lack awareness of advance directives, highlighting a need for better patient education and early integration.

Abstract

Abstract Aim Currently, only a few heart failure patients receive Palliative Care (PC). This is partly because the point of view of heart failure patients on PC remains insufficiently understood. Understanding how these patients perceive PC may help identify the obstacles at play and improve PC provision. Therefore, the aim of this study was to explore representations and beliefs associated with PC in heart failure patients. Methods We performed a qualitative study with chronic heart failure patients in a French university hospital. Participants were eligible if they met the following criteria: (i) age ≥18 years; (ii) confirmed diagnosis of heart failure (HF) with a New York Heart Association (NYHA) functional classification of stage II, III, or IV; (iii) active follow-up for HF at the hospital. We conducted in-depth, face-to-face interviews with participants. The interviews were audio-recorded, anonymized, and transcribed verbatim. Data were analyzed using a thematic approach. Results Participants reported a misconstrued understanding of PC and often associated it with imminent death. Most had not anticipated end-of-life issues, and some did not feel concerned. Many were unaware of advance directives (AD) or did not have written AD. Personal experiences with end-of-life accompaniment appeared to be associated with a more positive view of PC and a greater willingness to establish AD. Conclusion The results of our study highlight the need to inform patients about the mission and scope of PC. Developing assessment and communication tools for healthcare workers may help improve early integration of PC

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Cite This Study

Rouxbedat et al. (2026) studied this question. Heart failure patients often misunderstand palliative care as imminent death and lack awareness of advance directives, highlighting the need for better patient education.

synapsesocial.com/papers/699e918df5123be5ed04f299https://doi.org/10.1093/eurjcn/zvag055
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