2014
DOI: 10.1177/1474515114521746
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Communicating prognosis and end-of-life care to heart failure patients: A survey of heart failure nurses’ perspectives

Abstract: Although HF nurses feel competent discussing prognosis and end-of-life care with the HF patient, they are hesitant to have these conversations. This might be partly explained by the fact that they consider the physician to be responsible for such conversations, and by perceived barriers to communication. This implies a need for clinical policy and education for HF nurses to expand their knowledge and awareness of the patients' possible needs for palliative care.

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Cited by 48 publications
(70 citation statements)
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References 38 publications
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“…Moreover, most of these studies were conducted in an era before the widespread use of ICDs and focused largely upon HF patients in the outpatient general practice setting. The number of cardiology clinicians included in most studies was small, with little representation from the hospital setting 18, 19, 20, 21, 22, 23, 24, 25…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, most of these studies were conducted in an era before the widespread use of ICDs and focused largely upon HF patients in the outpatient general practice setting. The number of cardiology clinicians included in most studies was small, with little representation from the hospital setting 18, 19, 20, 21, 22, 23, 24, 25…”
Section: Discussionmentioning
confidence: 99%
“…285 A survey of HF nurses found that 67% felt it was a physician's role to initiate discussions about end-of-life care with patients, and 91% reported a need for more palliative training. 286 Additional barriers to the provision of palliative care services identified by healthcare providers included uncertainty about end of life because of its unpredictable trajectory, lack of need for end-of-life discussions in patients in New York Heart Association class II to III HF, and lack of time and resources to initiate discussions. [286][287][288] In qualitative reports, patients and families had misperceptions about being separated from familiar, trusted healthcare providers and not being hospitalized once they committed to palliative care.…”
Section: Palliative Care Use and Perceptions In Cardiovascular Practicementioning
confidence: 99%
“…286 Additional barriers to the provision of palliative care services identified by healthcare providers included uncertainty about end of life because of its unpredictable trajectory, lack of need for end-of-life discussions in patients in New York Heart Association class II to III HF, and lack of time and resources to initiate discussions. [286][287][288] In qualitative reports, patients and families had misperceptions about being separated from familiar, trusted healthcare providers and not being hospitalized once they committed to palliative care. Accordingly, it has been suggested that healthcare providers need to introduce palliative care as a philosophy of care rather than a strategy used at end of life.…”
Section: Palliative Care Use and Perceptions In Cardiovascular Practicementioning
confidence: 99%
“…A good relationship with the patient and family and repeated opportunities for discussion can greatly facilitate communication. 102 …”
Section: Patient and Caregiver Understanding Of Disease Treatment Amentioning
confidence: 99%