Improving end-of-life care for patients with chronic heart failure: "Let's hope it'll get better, when I know in my heart of hearts it won't"

TY - JOUR

T1 - Improving end-of-life care for patients with chronic heart failure: "Let's hope it'll get better, when I know in my heart of hearts it won't"

AU - Selman, Lucy

AU - Harding, R

AU - Beynon, T

AU - Hodson, F

AU - Coady, E

AU - Hazeldine, C

AU - Walton, M

AU - Gibbs, L

AU - Higginson, I J

PY - 2007/8

Y1 - 2007/8

N2 - Background: Although chronic heart failure (CHF) has a high mortality rate and symptom burden, and clinical guidance stipulates palliative care intervention, there is a lack of evidence to guide clinical practice for patients approaching the end of life. Aims: (1) To formulate guidance and recommendations for improving end- of- life care in CHF; (2) to generate data on patients' and carers' preferences regarding future treatment modalities, and to investigate communication between staff, patients and carers on end-of-life issues. Design: Semistructured qualitative interviews were conducted with 20 patients with CHF (New York Heart Association functional classification III - IV), 11 family carers, 6 palliative care clinicians and 6 cardiology clinicians. Setting: A tertiary hospital in London, UK. Results: Patients and families reported a wide range of end-of-life care preferences. None had discussed these with their clinicians, and none was aware of choices or alternatives in future care modalities, such as adopting a palliative approach. Patients and carers live with fear and anxiety, and are uninformed about the implications of their diagnosis. Cardiac staff confirmed that they rarely raise such issues with patients. Disease- and specialism-specific barriers to improving end-of-life care were identified. Conclusions: The novel, integrated data presented here provide three recommendations for improving care in line with policy directives: sensitive provision of information and discussion of end-of-life issues with patients and families; mutual education of cardiology and palliative care staff; and mutually agreed palliative care referral criteria and care pathways for patients with CHF

AB - Background: Although chronic heart failure (CHF) has a high mortality rate and symptom burden, and clinical guidance stipulates palliative care intervention, there is a lack of evidence to guide clinical practice for patients approaching the end of life. Aims: (1) To formulate guidance and recommendations for improving end- of- life care in CHF; (2) to generate data on patients' and carers' preferences regarding future treatment modalities, and to investigate communication between staff, patients and carers on end-of-life issues. Design: Semistructured qualitative interviews were conducted with 20 patients with CHF (New York Heart Association functional classification III - IV), 11 family carers, 6 palliative care clinicians and 6 cardiology clinicians. Setting: A tertiary hospital in London, UK. Results: Patients and families reported a wide range of end-of-life care preferences. None had discussed these with their clinicians, and none was aware of choices or alternatives in future care modalities, such as adopting a palliative approach. Patients and carers live with fear and anxiety, and are uninformed about the implications of their diagnosis. Cardiac staff confirmed that they rarely raise such issues with patients. Disease- and specialism-specific barriers to improving end-of-life care were identified. Conclusions: The novel, integrated data presented here provide three recommendations for improving care in line with policy directives: sensitive provision of information and discussion of end-of-life issues with patients and families; mutual education of cardiology and palliative care staff; and mutually agreed palliative care referral criteria and care pathways for patients with CHF

KW - Advance Care Planning

KW - Aged

KW - Aged, 80 and over

KW - Cardiology

KW - Communication

KW - Heart Failure

KW - Humans

KW - Interviews as Topic

KW - Middle Aged

KW - Nurse's Role

KW - Palliative Care

KW - Patient Participation

KW - Quality of Life

KW - Terminal Care

U2 - 10.1136/hrt.2006.106518

DO - 10.1136/hrt.2006.106518

M3 - Article

C2 - 17309905

SN - 1468-201X

VL - 93

SP - 963

EP - 967

JO - Heart

JF - Heart

IS - 8

ER -