BMC Palliative Care

Papers
(The TQCC of BMC Palliative Care is 7. 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 2020-05-01 to 2024-05-01.)
ArticleCitations
Family experiences with palliative care for children at home: a systematic literature review46
How views of oncologists and haematologists impacts palliative care referral: a systematic review46
Patients’ experiences of eHealth in palliative care: an integrative review41
Using the technology acceptance model to explore health provider and administrator perceptions of the usefulness and ease of using technology in palliative care38
Equity and the financial costs of informal caregiving in palliative care: a critical debate36
Compassion in healthcare: an updated scoping review of the literature36
Nurses’ knowledge and attitudes towards palliative care and death: a learning intervention32
Caregiver burden among informal caregivers in the largest specialized palliative care unit in Malaysia: a cross sectional study31
Examining public knowledge, attitudes and perceptions towards palliative care: a mixed method sequential study31
Knowledge, attitude, confidence, and educational needs of palliative care in nurses caring for non-cancer patients: a cross-sectional, descriptive study30
Burnout and resilience among Canadian palliative care physicians28
Parental bereavement – impact of death of neonates and children under 12 years on personhood of parents: a systematic scoping review26
Barriers to advance care planning: a qualitative study of seriously ill Chinese patients and their families26
What makes palliative care needs “complex”? A multisite sequential explanatory mixed methods study of patients referred for specialist palliative care25
Effect of palliative care training on perceived self-efficacy of the nurses23
Evidence on the economic value of end-of-life and palliative care interventions: a narrative review of reviews23
Physicians’ clinical prediction of survival in head and neck cancer patients in the palliative phase22
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 workers22
How nurses support family caregivers in the complex context of end-of-life home care: a qualitative study21
Factors influencing the integration of a palliative approach in intensive care units: a systematic mixed-methods review21
What do you mean by “palliative sedation”?21
Two faces of the same coin: a qualitative study of patients’ and carers’ coexistence with chronic breathlessness associated with chronic obstructive pulmonary disease (COPD)21
Ethical challenges in family caregivers of patients with advanced cancer – a qualitative study21
Barthel Index is a valid and reliable tool to measure the functional independence of cancer patients in palliative care20
Prospective cohort study of patients with advanced cancer and their relatives on the experienced quality of care and life (eQuiPe study): a study protocol20
Advance care planning conversations in primary care: a quality improvement project using the Serious Illness Care Program20
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 spouses19
Priorities and opportunities for palliative and end of life care in United Kingdom health policies: a national documentary analysis19
Quality indicators for the evaluation of end-of-life care in Germany – a retrospective cross-sectional analysis of statutory health insurance data19
Exploring the relationship between spiritual well-being and death anxiety in patients with gynecological cancer: a cross-section study19
Virtual reality video promotes effectiveness in advance care planning19
A qualitative study of bereaved family caregivers: feeling of security, facilitators and barriers for rural home care and death for persons with advanced cancer18
Compassion fatigue and compassion satisfaction among palliative care health providers: a scoping review18
Better quality of end-of-life care for persons with advanced dementia in nursing homes compared to hospitals: a Swedish national register study17
Advanced care planning during the COVID-19 pandemic: ceiling of care decisions and their implications for observational data17
Communicating with patients and families about illness progression and end of life: a review of studies using direct observation of clinical practice17
Health and intention to leave the profession of nursing - which individual, social and organisational resources buffer the impact of quantitative demands? A cross-sectional study17
Validation and cultural adaptation of the Integrated Palliative care Outcome Scale (IPOS) for the Portuguese population17
Stakeholder perspectives and requirements to guide the development of digital technology for palliative cancer services: a multi-country, cross-sectional, qualitative study in Nigeria, Uganda and Zimb16
Complementary music therapy for cancer patients in at-home palliative care and their caregivers: protocol for a multicentre randomised controlled trial16
How can we improve the experiences of patients and families who request medical assistance in dying? A multi-centre qualitative study16
Palliative Performance Scale and survival in patients with cancer and non-cancer diagnoses needing a palliative care consultation: a retrospective cohort study16
Developing a family-reported measure of experiences with home-based pediatric palliative and hospice care: a multi-method, multi-stakeholder approach16
A systematic scoping review on patients’ perceptions of dignity16
Higher levels of unmet support needs in spouses are associated with poorer quality of life – a descriptive cross-sectional study in the context of palliative home care15
What’s suffering got to do with it? A qualitative study of suffering in the context of Medical Assistance in Dying (MAID)15
The effect of neuropalliative care on quality of life and satisfaction with quality of care in patients with progressive neurological disease and their family caregivers: an interventional control stu15
Experiences of bereaved family caregivers with shared decision making in palliative cancer treatment: a qualitative interview study15
Caregiver’s burden at the end of life of their loved one: insights from a longitudinal qualitative study among working family caregivers15
Palliative care providers’ use of digital health and perspectives on technological innovation: a national study15
Supportive and palliative care indicators tool (SPICT™): content validity, feasibility and pre-test of the Italian version14
“It’s given me confidence”: a pragmatic qualitative evaluation exploring the perceived benefits of online end‐of‐life education on clinical care14
Views of advanced cancer patients, families, and oncologists on initiating and engaging in advance care planning: a qualitative study14
The required competencies of physicians within palliative care from the perspectives of multi-professional expert groups: a qualitative study14
Factors influencing GPs’ perception of specialised palliative homecare (SPHC) importance – results of a cross-sectional study14
Instrumental and affective communication with patients with limited health literacy in the palliative phase of cancer or COPD14
Learning to care for the spirit of dying patients: the impact of spiritual care training in a hospice-setting14
“I want to get myself as fit as I can and not die just yet” – Perceptions of exercise in people with advanced cancer and cachexia: a qualitative study14
Peer support to maintain psychological wellbeing in people with advanced cancer: findings from a feasibility study for a randomised controlled trial14
How compassionate communities are implemented and evaluated in practice: a scoping review14
Hospice care self-efficacy among clinical medical staff working in the coronavirus disease 2019 (COVID-19) isolation wards of designated hospitals: a cross–sectional study13
Attitudes of registered nurses about the end – of – life care in multi-profile hospitals: a cross sectional survey13
Predictors of the final place of care of patients with advanced cancer receiving integrated home-based palliative care: a retrospective cohort study13
Assessing professional identity formation (PIF) amongst medical students in Oncology and Palliative Medicine postings: a SEBA guided scoping review13
Standard Operating Procedures (SOPs) for Palliative Care in German Comprehensive Cancer Centers - an evaluation of the implementation status13
National strategy for palliative care of severely ill and dying people and their relatives in pandemics (PallPan) in Germany - study protocol of a mixed-methods project13
South African paramedic perspectives on prehospital palliative care13
Perception of cancer in patients diagnosed with the most common gastrointestinal cancers12
Health-related quality of life in patients with colorectal cancer in the palliative phase: a systematic review and meta-analysis12
Supporting patient access to medicines in community palliative care: on-line survey of health professionals’ practice, perceived effectiveness and influencing factors12
Development and usability testing of Understanding Stroke, a tailored life-sustaining treatment decision support tool for stroke surrogate decision makers12
A qualitative study on continuous deep sedation until death as an alternative to assisted suicide in Switzerland12
A qualitative exploration of the unmet information needs of Chinese advanced cancer patients and their informal caregivers12
Palliative care in its own discourse: a focused ethnography of professional messaging in palliative care12
Spirituality alleviates the burden on family members caring for patients receiving palliative care exclusively12
Bereavement interventions to support informal caregivers in the intensive care unit: a systematic review12
Place of death associated with types of long-term care services near the end-of-life for home-dwelling older people in Japan: a pooled cross-sectional study12
Systematic symptom and problem assessment at admission to the palliative care ward – perspectives and prognostic impacts12
Conceptualising effective symptom management in palliative care: a novel model derived from qualitative data11
Opportunities and challenges for advance care planning in strongly religious family-centric societies: a Focus group study of Indonesian cancer-care professionals11
Challenges faced by Chinese community nurses when providing home-based hospice and palliative care: a descriptive qualitative study11
The hospice as a learning space: a death education intervention with a group of adolescents11
Access to and adequacy of psychological services for adult patients in UK hospices: a national, cross-sectional survey11
To hydrate or not to hydrate? The effect of hydration on survival, symptoms and quality of dying among terminally ill cancer patients11
Exploration of the acceptability and usability of advance care planning tools in long term care homes11
Documentation of older people’s end-of-life care in the context of specialised palliative care: a retrospective review of patient records11
End-of-life care in a pediatric intensive care unit: the impact of the development of a palliative care unit11
Palliative care provider attitudes toward existential distress and treatment with psychedelic-assisted therapies11
Perceptions, knowledge and attitudes towards the concept and approach of palliative care amongst caregivers: a cross-sectional survey in Karachi, Pakistan11
The influence of symptom severity of palliative care patients on their family caregivers11
Trend analysis of palliative care consultation service for terminally ill non-cancer patients in Taiwan: a 9-year observational study11
Investigation of the awareness of and demand for hospice care and attitudes towards life-sustaining treatment at the end of life among community residents in Hangzhou11
Symptoms, symptom relief and support in COVID-19 patients dying in hospitals during the first pandemic wave11
“No thanks, I don’t want to see snakes again”: a qualitative study of pain management versus preservation of cognition in palliative care patients11
Preferences for home care to enable home death among adult patients with cancer in late palliative phase – a grounded theory study11
Enhanced home palliative care could reduce emergency department visits due to non-organic dyspnea among cancer patients: a retrospective cohort study11
Specialist palliative care teams and characteristics related to referral rate: a national cross-sectional survey among hospitals in the Netherlands11
Support received by family members before, at and after an ill person’s death11
Randomized control trial of advanced cancer patients at a private hospital in Kenya and the impact of dignity therapy on quality of life11
Dignity of patients with palliative needs in the Middle East: an integrative review10
Parental perspectives on the grief and support needs of children and young people bereaved during the COVID-19 pandemic: qualitative findings from a national survey10
Validation of the Palliative Prognostic Index, Performance Status–Based Palliative Prognostic Index and Chinese Prognostic Scale in a home palliative care setting for patients with advanced cancer in 10
Finnish nursing students’ perceptions of the development needs in palliative care education and factors influencing learning in undergraduate nursing studies – a qualitative study10
Home hospitalization for palliative cancer care: factors associated with unplanned hospital admissions and death in hospital10
Oral health plays second fiddle in palliative care: an interview study with registered nurses in home healthcare10
Implementing volunteer-navigation for older persons with advanced chronic illness (Nav-CARE): a knowledge to action study10
Chemotherapy during the last 30 days of life and the role of palliative care referral, a single center experience10
Introducing cross-cultural education in palliative care: focus groups with experts on practical strategies10
An explorative analysis of the differences in levels of happiness between cancer patients, informal caregivers and the general population10
How well do documented goals-of-care discussions for patients with stage IV cancer reflect communication best practices?10
Perceptions of palliative care in a South Asian community: findings from an observational study10
Continuous subcutaneous infusion for pain control in dying patients: experiences from a tertiary palliative care center10
Validity and reliability of the English and translated Chinese versions of the Integrated Palliative care Outcome Scale (IPOS) in Singapore10
“Transition from children’s to adult services for adolescents/young adults with life-limiting conditions: developing realist programme theory through an international comparison”10
Comparison of the experience of caregiving at end of life or in hastened death: a narrative synthesis review10
Advance care planning preferences in Chinese nursing home residents: results from two cross-sectional studies in Hong Kong and Taiwan10
Association between attitude towards death and spiritual care competence of Chinese oncology nurses: a cross-sectional study10
Palliative care for rural growth and wellbeing: identifying perceived barriers and facilitators in access to palliative care in rural Indiana, USA10
Analysis of the unmet needs of Palestinian advanced cancer patients and their relationship to emotional distress: results from a cross-sectional study10
Navigating a newly diagnosed cancer through clinician-facilitated discussions of health-related patient values: a qualitative analysis10
Second opinions in medical oncology10
A scoping review of the evidence for community-based dementia palliative care services and their related service activities10
“Teach for ethics in palliative care”: a mixed-method evaluation of a medical ethics training programme10
Providing dignity therapy to patients with advanced cancer: a feasibility study within the setting of a hospital palliative care unit9
Brief Engagement and Acceptance Coaching for Hospice Settings (the BEACHeS study): results from a Phase I study of acceptability and initial effectiveness in people with non-curative cancer9
Challenges for palliative care day services: a focus group study9
Patients and family caregivers report high treatment expectations during palliative chemotherapy: a longitudinal prospective study9
Paediatric palliative screening scale as a useful tool for clinicians’ assessment of palliative care needs of pediatric patients: a retrospective cohort study9
Prescription trends at the end of life in a palliative care unit: observational study9
Development of an international Core Outcome Set (COS) for best care for the dying person: study protocol9
The impact of uncertainty on bereaved family’s experiences of care at the end of life: a thematic analysis of free text survey data9
Hospice care providers experiences of grappling with medical assistance in dying in a hospice setting: a qualitative descriptive study9
Co-construction of the family-focused support conversation: a participatory learning and action research study to implement support for family members whose relatives are being discharged for end-of-l9
Role of nurses in medication management at the end of life: a qualitative interview study9
Knowledge of end-of-life wishes by physicians and family caregivers in cancer patients9
The relationship between anticipatory grief and illness uncertainty among Chinese family caregivers of patients with advanced lung cancer: a cross-sectional study9
Systematic adaptation of the Thai version of the supportive and palliative care indicators tool for low-income setting (SPICT-LIS)9
How does ethnicity affect presence of advance care planning in care records for individuals with advanced disease? A mixed-methods systematic review9
The training effects of a continuing education program on nurses’ knowledge and attitudes to palliative care: a cross sectional study9
Where would Canadians prefer to die? Variation by situational severity, support for family obligations, and age in a national study9
Hypernatremia at admission predicts poor survival in patients with terminal cancer: a retrospective cohort study8
Factors influencing length of survival in ambulatory palliative care - a cross sectional study based on secondary data8
Simulation-based learning in palliative care in postgraduate nursing education: a scoping review8
Nurses’ perceptions of barriers and supportive behaviors in end-of-life care in the intensive care unit: a cross-sectional study8
Impact on place of death in cancer patients: a causal exploration in southern Switzerland8
An exploration of the experiences of professionals supporting patients approaching the end of life in medicines management at home. A qualitative study8
Palliative care for nursing home patients with dementia: service evaluation and risk factors of mortality8
Addressing challenges in information-provision: a qualitative study among oncologists and women with advanced breast cancer8
Community palliative care services on addressing physical and psychosocial needs in people with advanced illness: a prospective cohort study8
Professional oral care in end-of-life patients with advanced cancers in a hospice ward: improvement of oral conditions8
Factors affecting quality of end-of-life hospital care - a qualitative analysis of free text comments from the i-CODE survey in Norway8
Patient participation and associated factors in the discussions on do-not-attempt-resuscitation and end-of-life disclosure: a retrospective chart review study8
Living and dying with incurable cancer: a qualitative study on older patients’ life values and healthcare professionals’ responsivity8
A pilot evaluation of the Strengthening a Palliative Approach in Long-Term Care (SPA-LTC) program8
Control in patients with advanced cancer: an interpretative phenomenological study8
Facilitating advance care planning in the general practice setting for patients with a chronic, life-limiting illness: protocol for a phase-III cluster-randomized controlled trial and process evaluati8
Delphi consensus on strategies in the management of opioid-induced constipation in cancer patients8
Verbalizing spiritual needs in palliative care: a qualitative interview study on verbal and non-verbal communication in two Danish hospices8
Virtual reality reduces pain in palliative care–A feasibility trial8
Optimizing of a question prompt list to improve communication about the heart failure trajectory in patients, families, and health care professionals8
Building a telepalliative care strategy in nursing homes: a qualitative study with mobile palliative care teams8
Psychosocial distress and the quality of life of cancer patients in two health facilities in Cameroon8
Designing a Mission statement Mobile app for palliative care: an innovation project utilizing design-thinking methodology8
Translation, cultural adaptation and validation of the Chinese version of the Carer Support Needs Assessment Tool for family caregivers of cancer patients receiving home-based hospice care8
Collaborative advance care planning in advanced cancer patients: col-ACP –study – study protocol of a randomised controlled trial8
Socioeconomy as a prognostic factor for location of death in Swedish palliative cancer patients8
Changes in decision-making process for life-sustaining treatment in patients with advanced cancer after the life-sustaining treatment decisions-making act8
The level of knowledge about palliative care in Iranian patients with cancer8
Midazolam sedation in palliative medicine: retrospective study in a French center for cancer control8
Caring for depression in the dying is complex and challenging – survey of palliative physicians8
Is progress being made on Canada’s palliative care framework and action plan? A survey of stakeholder perspectives8
Expanding the 3 Wishes Project for compassionate end-of-life care: a qualitative evaluation of local adaptations8
Exploring socioeconomic inequities in access to palliative and end-of-life care in the UK: a narrative synthesis8
Healthcare providers’ perception of advance care planning for patients with critical illnesses in acute-care hospitals: a cross-sectional study8
Supportive and palliative care indicators tool (SPICT™) in a Danish healthcare context: translation, cross-cultural adaptation, and content validation8
Quality of online self-management resources for adults living with primary brain cancer, and their carers: a systematic environmental scan8
Perceptions and practices of spiritual care among hospice physicians and nurses in a Taiwanese tertiary hospital: a qualitative study8
Need for additional professional psychosocial and spiritual support in patients with advanced diseases in the course of specialist palliative care – a longitudinal observational study8
Understanding family caregivers’ needs to support relatives with advanced progressive disease at home: an ethnographic study in rural Portugal8
A mixed-method evaluation of a volunteer navigation intervention for older persons living with chronic illness (Nav-CARE): findings from a knowledge translation study7
Spiritual care practices in hospices in the Western cape, South Africa: the challenge of diversity7
Evaluation of an advance care planning training program for practice professionals in Japan incorporating shared decision making skills training: a prospective study of a curricular intervention7
Unmet needs in palliative care for patients with common non-cancer diseases: a cross-sectional study7
The end of life experiences of people living with socio-economic deprivation in the developed world: an integrative review7
Does ethnicity affect pain management for people with advanced disease? A mixed methods cross-national systematic review of ‘very high’ Human Development Index English-speaking countries7
Psychological distress and resilience in patients with advanced cancer during the Covid-19 pandemic: the mediating role of spirituality7
NUrsing Homes End of Life care Program (NUHELP): developing a complex intervention7
Inpatient generalist palliative care during the SARS-CoV-2 pandemic – experiences, challenges and potential solutions from the perspective of health care workers7
Exploring the status of and demand for palliative day-care clinics and day hospices in Germany: a protocol for a mixed-methods study7
Exploring the costs, consequences and efficiency of three types of palliative care day services in the UK: a pragmatic before-and-after descriptive cohort study7
The experiences of clinical nurses coping with patient death in the context of rising hospital deaths in China: a qualitative study7
Palliative care nurse champions’ views on their role and impact: a qualitative interview study among hospital and home care nurses7
Health-related expectations of the chronically critically ill: a multi-perspective qualitative study7
Advance care planning in primary care: a retrospective medical record study among patients with different illness trajectories7
An integrative review to identify how nurses practicing in inpatient specialist palliative care units uphold the values of nursing7
Effectiveness and cost effectiveness of palliative care interventions in people with chronic heart failure and their caregivers: a systematic review7
Cancer patients spend more time at home and more often die at home with advance care planning conversations in primary health care: a retrospective observational cohort study7
Evaluating quality of care at the end of life and setting best practice performance standards: a population-based observational study using linked routinely collected administrative databases7
Factors influencing terminal cancer patients’ autonomous DNR decision: a longitudinal statutory document and clinical database study7
Melatonin to prevent delirium in patients with advanced cancer: a double blind, parallel, randomized, controlled, feasibility trial7
The Promoting Resilience in Stress Management (PRISM) intervention for adolescents and young adults receiving hematopoietic cell transplantation: a randomized controlled trial protocol7
End-of-life care preferences among cancer patients in Southern Thailand: a university hospital-based cross-sectional survey7
Adaptation of the Australian Palliative Care Phase concept to the German palliative care context: a mixed-methods approach using cognitive interviews and cross-sectional data7
Healthcare professionals’ perspectives of patient and family preferences of patient place of death: a qualitative study7
Caregiver burden among family caregivers of incurable cancer patients in two eastern Mediterranean countries7
Chinese medical teachers’ cultural attitudes influence palliative care education: a qualitative study7
Palliative care in the pre-hospital service in Brazil: experiences of health professionals7
Nurse-led normalised advance care planning service in hospital and community health settings: a qualitative study7
Before the 2020 Pandemic: an observational study exploring public knowledge, attitudes, plans, and preferences towards death and end of life care in Wales7
Engaging family caregivers and health system partners in exploring how multi-level contexts in primary care practices affect case management functions and outcomes of patients and family caregivers at7
A prospective cohort study assessing aggressive interventions at the end-of-life among patients with solid metastatic cancer7
Advancing pediatric palliative care in a low-middle income country: an implementation study, a challenging but not impossible task7
Quality of life of patients with metastatic pancreatic adenocarcinoma initiating first-line chemotherapy in routine practice7
Pain talk in hospice care: a conversation analysis7
Evaluating satisfaction with the quality and provision of end-of-life care for patients from diverse ethnocultural backgrounds7
A survey of cancer care institutions in Nepal to inform design of a pain management mobile application7
Differing needs of mothers and fathers during their child’s end-of-life care: secondary analysis of the “Paediatric end-of-life care needs” (PELICAN) study7
Subjective burdens among informal caregivers of critically ill patients: a cross-sectional study in rural Shandong, China7
A meaning-centered spiritual care training program for hospice palliative care teams in South Korea: development and preliminary evaluation7
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