2020
DOI: 10.1177/0269216320917873
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Building trust and facilitating goals of care conversations: A qualitative study in people with heart failure receiving home hospice care

Abstract: Background: Despite a majority of persons receiving hospice care in their homes, there are gaps in understanding how to facilitate goals of care conversations between persons with heart failure and healthcare providers. Aim: To identify barriers and facilitators which shape goals of care conversations for persons with heart failure in the context of home hospice. D… Show more

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Cited by 15 publications
(5 citation statements)
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“…While patients on homecare might be reasonably presumed to prefer remaining at home, it was the patient's preference for home as a place of death that cognitively prepared the patient, proved to unveil perceived control over symptoms, and differentiated healthcare utilization. This finding has implications for improving documented clarity on a place of death and dying for more tailored interventions (Baik et al 2020). Studies showed that patient's endof-life wishes were often not discussed during hospitalization or at the time of referral to homecare, partly due to the lack of unwillingness among patients and caregivers (Hemsley et al 2019;Simon et al 2015).…”
Section: Discussionmentioning
confidence: 99%
“…While patients on homecare might be reasonably presumed to prefer remaining at home, it was the patient's preference for home as a place of death that cognitively prepared the patient, proved to unveil perceived control over symptoms, and differentiated healthcare utilization. This finding has implications for improving documented clarity on a place of death and dying for more tailored interventions (Baik et al 2020). Studies showed that patient's endof-life wishes were often not discussed during hospitalization or at the time of referral to homecare, partly due to the lack of unwillingness among patients and caregivers (Hemsley et al 2019;Simon et al 2015).…”
Section: Discussionmentioning
confidence: 99%
“…In the vast majority of articles that referenced care partners, the intent was not to examine or measure their inclusion in the health care team, but instead to better understand aspects of the care partner experience (burden, Bristol et al, 2020; improved preparedness, Aboumatar et al, 2017; prognostic awareness, Applebaum et al, 2018; etc.). In those few studies that examined caregiving behaviors—though not explicitly stated as contributing to the care team’s responsibilities—there was a focus on communication functions such as effective communication with clinicians (Aboumatar et al, 2017) or inclusion in care conversations (Baik et al, 2020). Accordingly, there are little to no studies examining interventions that seek to enhance care partner involvement in the care team, or to make them formal members of care teams (i.e., no boundaries being set, lack of communication processes).…”
Section: Discussionmentioning
confidence: 99%
“…Trust building activities should be planned accordingly. Such efforts could focus on participatory approaches to ensure sustainability such as longitudinal stepwise interventions or simple interventions where the focus is improving communication and the goals of care [60].…”
Section: Plos Onementioning
confidence: 99%