BMC Palliative Care

Papers
(The H4-Index of BMC Palliative Care is 21. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-11-01 to 2024-11-01.)
ArticleCitations
Compassion in healthcare: an updated scoping review of the literature61
How views of oncologists and haematologists impacts palliative care referral: a systematic review53
Nurses’ knowledge and attitudes towards palliative care and death: a learning intervention39
Examining public knowledge, attitudes and perceptions towards palliative care: a mixed method sequential study38
Caregiver burden among informal caregivers in the largest specialized palliative care unit in Malaysia: a cross sectional study34
Evidence on the economic value of end-of-life and palliative care interventions: a narrative review of reviews33
Burnout and resilience among Canadian palliative care physicians32
Parental bereavement – impact of death of neonates and children under 12 years on personhood of parents: a systematic scoping review30
How nurses support family caregivers in the complex context of end-of-life home care: a qualitative study30
What makes palliative care needs “complex”? A multisite sequential explanatory mixed methods study of patients referred for specialist palliative care27
Decision making in the end-of-life care of patients who are terminally ill with cancer – a qualitative descriptive study with a phenomenological approach from the experience of healthcare workers27
Advance care planning conversations in primary care: a quality improvement project using the Serious Illness Care Program26
Barthel Index is a valid and reliable tool to measure the functional independence of cancer patients in palliative care25
Communicating with patients and families about illness progression and end of life: a review of studies using direct observation of clinical practice25
A qualitative study of bereaved family caregivers: feeling of security, facilitators and barriers for rural home care and death for persons with advanced cancer24
Compassion fatigue and compassion satisfaction among palliative care health providers: a scoping review24
Priorities and opportunities for palliative and end of life care in United Kingdom health policies: a national documentary analysis24
Physicians’ clinical prediction of survival in head and neck cancer patients in the palliative phase24
Caregiver’s burden at the end of life of their loved one: insights from a longitudinal qualitative study among working family caregivers22
Talking about death and dying in a hospital setting - a qualitative study of the wishes for end-of-life conversations from the perspective of patients and spouses21
Quality indicators for the evaluation of end-of-life care in Germany – a retrospective cross-sectional analysis of statutory health insurance data21
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