BMC Palliative Care

(The median citation count of BMC Palliative Care is 3. 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 2020-06-01 to 2024-06-01.)
Family experiences with palliative care for children at home: a systematic literature review51
How views of oncologists and haematologists impacts palliative care referral: a systematic review49
Patients’ experiences of eHealth in palliative care: an integrative review43
Compassion in healthcare: an updated scoping review of the literature42
Using the technology acceptance model to explore health provider and administrator perceptions of the usefulness and ease of using technology in palliative care40
Nurses’ knowledge and attitudes towards palliative care and death: a learning intervention36
Examining public knowledge, attitudes and perceptions towards palliative care: a mixed method sequential study34
Caregiver burden among informal caregivers in the largest specialized palliative care unit in Malaysia: a cross sectional study32
Knowledge, attitude, confidence, and educational needs of palliative care in nurses caring for non-cancer patients: a cross-sectional, descriptive study32
Burnout and resilience among Canadian palliative care physicians30
Barriers to advance care planning: a qualitative study of seriously ill Chinese patients and their families28
Parental bereavement – impact of death of neonates and children under 12 years on personhood of parents: a systematic scoping review26
Evidence on the economic value of end-of-life and palliative care interventions: a narrative review of reviews26
What makes palliative care needs “complex”? A multisite sequential explanatory mixed methods study of patients referred for specialist palliative care25
How nurses support family caregivers in the complex context of end-of-life home care: a qualitative study23
Physicians’ clinical prediction of survival in head and neck cancer patients in the palliative phase23
Advance care planning conversations in primary care: a quality improvement project using the Serious Illness Care Program22
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
A qualitative study of bereaved family caregivers: feeling of security, facilitators and barriers for rural home care and death for persons with advanced cancer21
Barthel Index is a valid and reliable tool to measure the functional independence of cancer patients in palliative care21
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
Communicating with patients and families about illness progression and end of life: a review of studies using direct observation of clinical practice20
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 spouses20
Priorities and opportunities for palliative and end of life care in United Kingdom health policies: a national documentary analysis20
Exploring the relationship between spiritual well-being and death anxiety in patients with gynecological cancer: a cross-section study20
Quality indicators for the evaluation of end-of-life care in Germany – a retrospective cross-sectional analysis of statutory health insurance data20
Compassion fatigue and compassion satisfaction among palliative care health providers: a scoping review20
Prospective cohort study of patients with advanced cancer and their relatives on the experienced quality of care and life (eQuiPe study): a study protocol20
Virtual reality video promotes effectiveness in advance care planning20
Health and intention to leave the profession of nursing - which individual, social and organisational resources buffer the impact of quantitative demands? A cross-sectional study18
Validation and cultural adaptation of the Integrated Palliative care Outcome Scale (IPOS) for the Portuguese population17
Caregiver’s burden at the end of life of their loved one: insights from a longitudinal qualitative study among working family caregivers17
Advanced care planning during the COVID-19 pandemic: ceiling of care decisions and their implications for observational data17
Better quality of end-of-life care for persons with advanced dementia in nursing homes compared to hospitals: a Swedish national register study17
Developing a family-reported measure of experiences with home-based pediatric palliative and hospice care: a multi-method, multi-stakeholder approach16
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 care16
What’s suffering got to do with it? A qualitative study of suffering in the context of Medical Assistance in Dying (MAID)16
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
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
A systematic scoping review on patients’ perceptions of dignity16
Palliative care providers’ use of digital health and perspectives on technological innovation: a national study16
Learning to care for the spirit of dying patients: the impact of spiritual care training in a hospice-setting15
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
Factors influencing GPs’ perception of specialised palliative homecare (SPHC) importance – results of a cross-sectional study15
Experiences of bereaved family caregivers with shared decision making in palliative cancer treatment: a qualitative interview study15
Views of advanced cancer patients, families, and oncologists on initiating and engaging in advance care planning: a qualitative study15
Supportive and palliative care indicators tool (SPICT™): content validity, feasibility and pre-test of the Italian version15
“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
Predictors of the final place of care of patients with advanced cancer receiving integrated home-based palliative care: a retrospective cohort study14
“It’s given me confidence”: a pragmatic qualitative evaluation exploring the perceived benefits of online end‐of‐life education on clinical care14
Spirituality alleviates the burden on family members caring for patients receiving palliative care exclusively14
How compassionate communities are implemented and evaluated in practice: a scoping review14
Instrumental and affective communication with patients with limited health literacy in the palliative phase of cancer or COPD14
South African paramedic perspectives on prehospital palliative care13
Attitudes of registered nurses about the end – of – life care in multi-profile hospitals: a cross sectional survey13
Development and usability testing of Understanding Stroke, a tailored life-sustaining treatment decision support tool for stroke surrogate decision makers13
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
Assessing professional identity formation (PIF) amongst medical students in Oncology and Palliative Medicine postings: a SEBA guided scoping review13
Challenges faced by Chinese community nurses when providing home-based hospice and palliative care: a descriptive qualitative study13
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
Preferences for home care to enable home death among adult patients with cancer in late palliative phase – a grounded theory study13
To hydrate or not to hydrate? The effect of hydration on survival, symptoms and quality of dying among terminally ill cancer patients12
Perception of cancer in patients diagnosed with the most common gastrointestinal cancers12
A qualitative study on continuous deep sedation until death as an alternative to assisted suicide in Switzerland12
Analysis of the unmet needs of Palestinian advanced cancer patients and their relationship to emotional distress: results from a cross-sectional study12
Documentation of older people’s end-of-life care in the context of specialised palliative care: a retrospective review of patient records12
Supporting patient access to medicines in community palliative care: on-line survey of health professionals’ practice, perceived effectiveness and influencing factors12
Perceptions, knowledge and attitudes towards the concept and approach of palliative care amongst caregivers: a cross-sectional survey in Karachi, Pakistan12
Randomized control trial of advanced cancer patients at a private hospital in Kenya and the impact of dignity therapy on quality of life12
The influence of symptom severity of palliative care patients on their family caregivers12
Health-related quality of life in patients with colorectal cancer in the palliative phase: a systematic review and meta-analysis12
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 Hangzhou12
Opportunities and challenges for advance care planning in strongly religious family-centric societies: a Focus group study of Indonesian cancer-care professionals12
A scoping review of the evidence for community-based dementia palliative care services and their related service activities12
Trend analysis of palliative care consultation service for terminally ill non-cancer patients in Taiwan: a 9-year observational study12
Bereavement interventions to support informal caregivers in the intensive care unit: a systematic review12
A qualitative exploration of the unmet information needs of Chinese advanced cancer patients and their informal caregivers12
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
Palliative care in its own discourse: a focused ethnography of professional messaging in palliative care12
Palliative care provider attitudes toward existential distress and treatment with psychedelic-assisted therapies12
Enhanced home palliative care could reduce emergency department visits due to non-organic dyspnea among cancer patients: a retrospective cohort study11
Access to and adequacy of psychological services for adult patients in UK hospices: a national, cross-sectional survey11
Perceptions of palliative care in a South Asian community: findings from an observational study11
Navigating a newly diagnosed cancer through clinician-facilitated discussions of health-related patient values: a qualitative analysis11
“No thanks, I don’t want to see snakes again”: a qualitative study of pain management versus preservation of cognition in palliative care patients11
The hospice as a learning space: a death education intervention with a group of adolescents11
How well do documented goals-of-care discussions for patients with stage IV cancer reflect communication best practices?11
Palliative care for rural growth and wellbeing: identifying perceived barriers and facilitators in access to palliative care in rural Indiana, USA11
Symptoms, symptom relief and support in COVID-19 patients dying in hospitals during the first pandemic wave11
Comparison of the experience of caregiving at end of life or in hastened death: a narrative synthesis review11
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
Exploration of the acceptability and usability of advance care planning tools in long term care homes11
Conceptualising effective symptom management in palliative care: a novel model derived from qualitative data11
Advance care planning preferences in Chinese nursing home residents: results from two cross-sectional studies in Hong Kong and Taiwan10
Systematic adaptation of the Thai version of the supportive and palliative care indicators tool for low-income setting (SPICT-LIS)10
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
Paediatric palliative screening scale as a useful tool for clinicians’ assessment of palliative care needs of pediatric patients: a retrospective cohort study10
Chemotherapy during the last 30 days of life and the role of palliative care referral, a single center experience10
Prescription trends at the end of life in a palliative care unit: observational study10
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
An explorative analysis of the differences in levels of happiness between cancer patients, informal caregivers and the general population10
Continuous subcutaneous infusion for pain control in dying patients: experiences from a tertiary palliative care center10
How does ethnicity affect presence of advance care planning in care records for individuals with advanced disease? A mixed-methods systematic review10
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
“Teach for ethics in palliative care”: a mixed-method evaluation of a medical ethics training programme10
Introducing cross-cultural education in palliative care: focus groups with experts on practical strategies10
Challenges for palliative care day services: a focus group study10
Association between attitude towards death and spiritual care competence of Chinese oncology nurses: a cross-sectional 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
Second opinions in medical oncology10
Knowledge of end-of-life wishes by physicians and family caregivers in cancer patients10
Caring for depression in the dying is complex and challenging – survey of palliative physicians9
Providing dignity therapy to patients with advanced cancer: a feasibility study within the setting of a hospital palliative care unit9
The impact of uncertainty on bereaved family’s experiences of care at the end of life: a thematic analysis of free text survey data9
Virtual reality reduces pain in palliative care–A feasibility trial9
Patient participation and associated factors in the discussions on do-not-attempt-resuscitation and end-of-life disclosure: a retrospective chart review 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
Managing clinical uncertainty in older people towards the end of life: a systematic review of person-centred tools9
Is progress being made on Canada’s palliative care framework and action plan? A survey of stakeholder perspectives9
The relationship between anticipatory grief and illness uncertainty among Chinese family caregivers of patients with advanced lung cancer: a cross-sectional study9
Development of an international Core Outcome Set (COS) for best care for the dying person: study protocol9
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
Supportive and palliative care indicators tool (SPICT™) in a Danish healthcare context: translation, cross-cultural adaptation, and content validation9
Collaborative advance care planning in advanced cancer patients: col-ACP –study – study protocol of a randomised controlled trial9
The training effects of a continuing education program on nurses’ knowledge and attitudes to palliative care: a cross sectional study9
Factors influencing length of survival in ambulatory palliative care - a cross sectional study based on secondary data9
Verbalizing spiritual needs in palliative care: a qualitative interview study on verbal and non-verbal communication in two Danish hospices9
Evaluating satisfaction with the quality and provision of end-of-life care for patients from diverse ethnocultural backgrounds9
Quality of online self-management resources for adults living with primary brain cancer, and their carers: a systematic environmental scan9
Psychosocial distress and the quality of life of cancer patients in two health facilities in Cameroon9
Palliative care for nursing home patients with dementia: service evaluation and risk factors of mortality9
Hospice care providers experiences of grappling with medical assistance in dying in a hospice setting: a qualitative descriptive study9
Changes in decision-making process for life-sustaining treatment in patients with advanced cancer after the life-sustaining treatment decisions-making act9
Patients and family caregivers report high treatment expectations during palliative chemotherapy: a longitudinal prospective study9
Simulation-based learning in palliative care in postgraduate nursing education: a scoping review9
Where would Canadians prefer to die? Variation by situational severity, support for family obligations, and age in a national study9
Effectiveness and cost effectiveness of palliative care interventions in people with chronic heart failure and their caregivers: a systematic review8
Nurses’ perceptions of barriers and supportive behaviors in end-of-life care in the intensive care unit: a cross-sectional study8
Exploring socioeconomic inequities in access to palliative and end-of-life care in the UK: a narrative synthesis8
Impact on place of death in cancer patients: a causal exploration in southern Switzerland8
Factors affecting quality of end-of-life hospital care - a qualitative analysis of free text comments from the i-CODE survey in Norway8
Designing a Mission statement Mobile app for palliative care: an innovation project utilizing design-thinking methodology8
Perceptions and practices of spiritual care among hospice physicians and nurses in a Taiwanese tertiary hospital: a qualitative study8
Perceptions of healthcare professionals towards palliative care in internal medicine wards: a cross-sectional survey8
A pilot evaluation of the Strengthening a Palliative Approach in Long-Term Care (SPA-LTC) program8
Professional oral care in end-of-life patients with advanced cancers in a hospice ward: improvement of oral conditions8
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 study8
Control in patients with advanced cancer: an interpretative phenomenological study8
Midazolam sedation in palliative medicine: retrospective study in a French center for cancer control8
Expanding the 3 Wishes Project for compassionate end-of-life care: a qualitative evaluation of local adaptations8
Healthcare providers’ perception of advance care planning for patients with critical illnesses in acute-care hospitals: a cross-sectional study8
Developing an integrated model of community-based palliative care into the primary health care (PHC) for terminally ill cancer patients in Iran8
Addressing challenges in information-provision: a qualitative study among oncologists and women with advanced breast cancer8
Chinese medical teachers’ cultural attitudes influence palliative care education: a qualitative study8
Palliative care nurse champions’ views on their role and impact: a qualitative interview study among hospital and home care nurses8
An integrative review to identify how nurses practicing in inpatient specialist palliative care units uphold the values of nursing8
Hypernatremia at admission predicts poor survival in patients with terminal cancer: a retrospective cohort study8
Factors influencing terminal cancer patients’ autonomous DNR decision: a longitudinal statutory document and clinical database study8
The level of knowledge about palliative care in Iranian patients with cancer8
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
Healthcare professionals’ perspectives of patient and family preferences of patient place of death: a qualitative study8
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
Community palliative care services on addressing physical and psychosocial needs in people with advanced illness: a prospective cohort study8
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
Need for additional professional psychosocial and spiritual support in patients with advanced diseases in the course of specialist palliative care – a longitudinal observational study8
Socioeconomy as a prognostic factor for location of death in Swedish palliative cancer patients8
The impact of covid-19 on out-of-hours adult hospice care: an online survey8
Living and dying with incurable cancer: a qualitative study on older patients’ life values and healthcare professionals’ responsivity8
A cross-sectional assessment of symptom burden among patients with advanced cervical cancer8
The end of life experiences of people living with socio-economic deprivation in the developed world: an integrative review8
Advance care planning in primary care: a retrospective medical record study among patients with different illness trajectories7
Cost-utility analysis of palliative care in patients with advanced cancer: a retrospective study7
Pain talk in hospice care: a conversation analysis7
The Promoting Resilience in Stress Management (PRISM) intervention for adolescents and young adults receiving hematopoietic cell transplantation: a randomized controlled trial protocol7
Quality of life of patients with metastatic pancreatic adenocarcinoma initiating first-line chemotherapy in routine practice7
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
Young adults understanding and readiness to engage with palliative care: extending the reach of palliative care through a public health approach: 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
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
Adapting ENABLE for patients with advanced cancer and their family caregivers in Singapore: a qualitative formative evaluation7
Subjective burdens among informal caregivers of critically ill patients: a cross-sectional study in rural Shandong, China7
Presuppositions, cost–benefit, collaboration, and competency impacts palliative care referral in paediatric oncology: a qualitative study7
Looking back: Identifying supportive care and unmet needs of parents of children receiving specialist paediatric palliative care from the bereavement perspective7
A survey of cancer care institutions in Nepal to inform design of a pain management mobile application7
Differences in perspectives of pediatricians on advance care planning: a cross-sectional survey7
A meaning-centered spiritual care training program for hospice palliative care teams in South Korea: development and preliminary evaluation7
Spiritual care practices in hospices in the Western cape, South Africa: the challenge of diversity7
A mixed-method evaluation of a volunteer navigation intervention for older persons living with chronic illness (Nav-CARE): findings from a knowledge translation study7
Nurse-led normalised advance care planning service in hospital and community health settings: a qualitative study7
Unmet needs in palliative care for patients with common non-cancer diseases: a cross-sectional study7
A prospective cohort study assessing aggressive interventions at the end-of-life among patients with solid metastatic cancer7
NUrsing Homes End of Life care Program (NUHELP): developing a complex intervention7
Psychological distress and resilience in patients with advanced cancer during the Covid-19 pandemic: the mediating role of spirituality7
Effectiveness of a nurse-delivered (FOCUS+) and a web-based (iFOCUS) psychoeducational intervention for people with advanced cancer and their family caregivers (DIAdIC): study protocol for an internat7
Advancing pediatric palliative care in a low-middle income country: an implementation study, a challenging but not impossible task7
The experiences of clinical nurses coping with patient death in the context of rising hospital deaths in China: a qualitative study7
Inpatient generalist palliative care during the SARS-CoV-2 pandemic – experiences, challenges and potential solutions from the perspective of health care workers7
Implementing welfare technology in palliative homecare for patients with cancer: a qualitative study of health-care professionals’ experiences7
Psychometric evaluation of the Chinese version of advance care planning self-efficacy scale among clinical nurses7
Why is hospice care important? An exploration of its benefits for patients with terminal cancer7
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
Health-related expectations of the chronically critically ill: a multi-perspective qualitative study7
Evaluating the integration of palliative care in national health systems: an indicator rating process with EAPC task force members to measure advanced palliative care development7
Sense of support within the family: a cross-sectional study of family members in palliative home care7
Palliative care in the pre-hospital service in Brazil: experiences of health professionals7
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
Video decision support tool promoting values conversations in advanced care planning in cancer: protocol of a randomised controlled trial7
Identifying palliative care needs of patients with non-communicable diseases in Indonesia using the SPICT tool: a descriptive cross-sectional study7
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
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
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
Exploring the status of and demand for palliative day-care clinics and day hospices in Germany: a protocol for a mixed-methods study7
Melatonin to prevent delirium in patients with advanced cancer: a double blind, parallel, randomized, controlled, feasibility trial7
Validation of the Japanese version of the barriers questionnaire II in cancer pain management: a cross-sectional study7
Spirituality in palliative care7
Health care needs of elderly patients with lung, liver, or colon cancer in Taiwan7
End-of-life care preferences among cancer patients in Southern Thailand: a university hospital-based cross-sectional survey7
Caregiver burden among family caregivers of incurable cancer patients in two eastern Mediterranean countries7
Impact of interprofessional collaborative practice in palliative care on outcomes for advanced cancer inpatients in a resource-limited setting7
Integrating patient- and caregiver-reported outcome measures into the daily care routines of specialised outpatient palliative care: a qualitative study (ELSAH) on feasibility, acceptability and appro7
“My life became more meaningful”: confronting one’s own end of life and its effects on well-being—a qualitative study6
Meeting ethical challenges with authenticity when engaging patients and families in end-of-life and palliative care research: a qualitative study6
Advance care planning for patients with cancer and family caregivers in Indonesia: a qualitative study6
Development of the palliative care referral system: proposal of a tool for the referral of cancer patients to specialized palliative care6
Physician decision-making process about withholding/withdrawing life-sustaining treatments in paediatric patients: a systematic review of qualitative evidence6
Acute and long-term grief reactions and experiences in parentally cancer-bereaved teenagers6
Improving serious illness communication: a qualitative study of clinical culture6
Charitably funded hospices and the challenges associated with the COVID-19 pandemic: a mixed-methods study (CovPall)6
Support practices by an interdisciplinary team in a palliative-care unit for relatives of patients in agonal phase6
A prognostic model using the neutrophil-albumin ratio and PG-SGA to predict overall survival in advanced palliative lung cancer6
General population-based study on preferences towards end-of-life care in Southern Thailand: a cross-sectional survey6
Regional and age differences in specialised palliative care for patients with pancreatic cancer6
The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study6
Palliative care symptoms, concerns and well-being of older people with frailty and complex care needs upon hospital discharge: a cross-sectional study6
Use of antithrombotics at the end of life: an in-depth chart review study6
Quality of dying in hospital general wards: a cross-sectional study about the end-of-life care6
The explorations of the awareness, contemplation, self-Efficacy, and readiness of advance care planning, and its predictors in Taiwanese patients while receiving hemodialysis treatment6
Correlation between depression and intimacy in lung cancer patients and their family caregivers6
What to consider when implementing a tool for timely recognition of palliative care needs in heart failure: a context-based qualitative study6
Medical Assistance in Dying in patients with advanced cancer and their caregivers: a mixed methods longitudinal study protocol6