Published in BMC Palliat Care on November 04, 2013
Factors associated with the designation of a health care proxy and writing advance directives for patients suffering from haematological malignancies. BMC Palliat Care (2014) 0.76
Death and the Oldest Old: Attitudes and Preferences for End-of-Life Care - Qualitative Research within a Population-Based Cohort Study. PLoS One (2016) 0.75
Associations between end-of-life discussions, patient mental health, medical care near death, and caregiver bereavement adjustment. JAMA (2008) 11.32
Factors considered important at the end of life by patients, family, physicians, and other care providers. JAMA (2000) 10.43
Patterns of functional decline at the end of life. JAMA (2003) 7.79
Advance directives and outcomes of surrogate decision making before death. N Engl J Med (2010) 7.09
The impact of advance care planning on end of life care in elderly patients: randomised controlled trial. BMJ (2010) 5.88
Association between advance directives and quality of end-of-life care: a national study. J Am Geriatr Soc (2007) 4.60
In search of a good death: observations of patients, families, and providers. Ann Intern Med (2000) 3.41
Brief communication: the relationship between having a living will and dying in place. Ann Intern Med (2004) 3.35
Preparing for the end of life: preferences of patients, families, physicians, and other care providers. J Pain Symptom Manage (2001) 2.79
Advance care planning and the quality of end-of-life care in older adults. J Am Geriatr Soc (2013) 2.49
Appraising the evidence: reviewing disparate data systematically. Qual Health Res (2002) 2.41
Complicated grief and bereavement-related depression as distinct disorders: preliminary empirical validation in elderly bereaved spouses. Am J Psychiatry (1995) 2.23
Older adults' attitudes to death, palliative treatment and hospice care. Palliat Med (2005) 2.17
Preferences for place of death if faced with advanced cancer: a population survey in England, Flanders, Germany, Italy, the Netherlands, Portugal and Spain. Ann Oncol (2012) 2.07
Planning for the end of life: the views of older people about advance care statements. Soc Sci Med (2004) 1.94
types of stressful life event and the onset of anxiety and depressive disorders. Psychol Med (1981) 1.68
'I don't want to talk about it.' Raising public awareness of end-of-life care planning in your locality. Int J Palliat Nurs (2012) 1.41
Barriers to advance care planning in chronic obstructive pulmonary disease. Palliat Med (2009) 1.37
End-of-life conversations: evolving practice and theory. JAMA (2000) 1.20
"At the foot of a very long ladder": discussing the end of life with older people and informal caregivers. J Pain Symptom Manage (2010) 1.16
Development of a peer education programme for advance end-of-life care planning. Int J Palliat Nurs (2006) 1.12
Preferences of the Dutch general public for a good death and associations with attitudes towards end-of-life decision-making. Palliat Med (2006) 1.09
An uncertain future: the unchanging views of care home residents about living and dying. Palliat Med (2011) 1.08
Planning for end of life care within lay-led chronic illness self-management training: the significance of 'death awareness' and biographical context in participant accounts. Soc Sci Med (2007) 1.06
End of life is a public health issue. Am J Prev Med (2002) 1.02
Denying the dying. Advance directives and dialysis discontinuation. Psychosomatics (1997) 1.02
The end of life: a qualitative study of the perceptions of people over the age of 80 on issues surrounding death and dying. J Pain Symptom Manage (2007) 0.99
Peer education for advance care planning: volunteers' perspectives on training and community engagement activities. Health Expect (2011) 0.96
Perspectives of healthy elders on advance care planning. J Am Acad Nurse Pract (2009) 0.96
Discussions by elders and adult children about end-of-life preparation and preferences. Prev Chronic Dis (2007) 0.91
Are we a 'death-denying' society? a sociological review. Soc Sci Med (1984) 0.88
Irish views on death and dying: a national survey. J Med Ethics (2010) 0.83
The long-term effect of a population-based educational intervention focusing on end-of-life home care, life-prolongation treatment, and knowledge about palliative care. J Palliat Care (2009) 0.82
Effect of a population-based educational intervention focusing on end-of-life home care, life-prolonging treatment and knowledge about palliative care. Palliat Med (2008) 0.79
Family perceptions of worry, symptoms, and suffering in the dying. J Palliat Care (2004) 0.77
Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. Am J Hum Genet (2008) 1.79
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31. Brain (2008) 1.77
An evaluation of research capacity building from the Cancer Experiences Collaborative. BMJ Support Palliat Care (2012) 1.41
Breakthrough strong opioid analgesia prescription in patients using transdermal fentanyl admitted to a hospice. Am J Hosp Palliat Care (2003) 1.39
Researching the mental health needs of hard-to-reach groups: managing multiple sources of evidence. BMC Health Serv Res (2009) 1.29
How do palliative medicine physicians assess and manage depression. Palliat Med (2004) 1.19
How children cope when a parent has advanced cancer. Psychooncology (2009) 1.17
From personal challenge to technical fix: the risks of depersonalised care. Health Soc Care Community (2011) 0.99
Revisiting biographical disruption: exploring individual embodied illness experience in people with terminal cancer. Health (London) (2010) 0.95
Compassion in healthcare - lessons from a qualitative study of the end of life care of people with dementia. J R Soc Med (2013) 0.95
Depression assessment and classification in palliative cancer patients: a systematic literature review. Palliat Med (2009) 0.90
Linkage to a known gene but no mutation identified: comprehensive reanalysis of SPG4 HSP pedigrees reveals large deletions as the sole cause. Hum Mutat (2007) 0.87
Further evidence of dementia in SPG4-linked autosomal dominant hereditary spastic paraplegia. Neurology (2004) 0.86
Depression in advanced cancer. Eur J Oncol Nurs (2010) 0.85
The need for palliative care to remain primary care focused. Fam Pract (2002) 0.83
Information and communication when a parent has advanced cancer. J Affect Disord (2008) 0.83
A survey of the services provided by children's hospices in the United Kingdom. Support Care Cancer (2006) 0.81
The experience of cough in patients diagnosed with lung cancer. Support Care Cancer (2010) 0.81
Development and evaluation of culturally sensitive psychosocial interventions for under-served people in primary care. BMC Psychiatry (2014) 0.79
Clinical expert guidelines for the management of cough in lung cancer: report of a UK task group on cough. Cough (2010) 0.79
The long-term impact of early parental death: lessons from a narrative study. J R Soc Med (2013) 0.79
What can we learn about the spiritual needs of palliative care patients from the research literature? J Pain Symptom Manage (2012) 0.79
Depression in terminal illness: the need for primary care-specific research. Fam Pract (2007) 0.78
"Until the trial is complete you can't really say whether it helped you or not, can you?": exploring cancer patients' perceptions of taking part in a trial of acupressure wristbands. BMC Complement Altern Med (2013) 0.78
Benefits and challenges of collaborative research: lessons from supportive and palliative care. BMJ Support Palliat Care (2011) 0.78
Protocol for a longitudinal qualitative interview study: maintaining psychological well-being in advanced cancer--what can we learn from patients' and carers' own coping strategies? BMJ Open (2013) 0.78
In search of a good death: Medical education has important role in extending palliative care. BMJ (2003) 0.78
GPs' experiences of palliative care. Palliat Med (2003) 0.78
Out-of-hours medical cover in community hospitals: implications for palliative care. Int J Palliat Nurs (2006) 0.77
Understanding spirituality: a synoptic view. BMJ Support Palliat Care (2012) 0.76
Real life ethics. Br J Gen Pract (2008) 0.75
Specialist palliative care in dementia: patients with dementia are unable to access appropriate palliative care. BMJ (2005) 0.75
Perspectives on the impact of early parent loss in adulthood in the UK: narratives provide the way forward. Eur J Cancer Care (Engl) (2008) 0.75
The dragon and the snake: health practices among Chinese in the UK from an inter-disciplinary perspective. Ethn Health (2014) 0.75
A survey of continuing professional development (CPD) in palliative medicine. Clin Med (2005) 0.75