BMC Palliative Care

Article	Citations
Compassion in healthcare: an updated scoping review of the literature	61
How views of oncologists and haematologists impacts palliative care referral: a systematic review	53
Nurses’ knowledge and attitudes towards palliative care and death: a learning intervention	39
Examining public knowledge, attitudes and perceptions towards palliative care: a mixed method sequential study	38
Caregiver burden among informal caregivers in the largest specialized palliative care unit in Malaysia: a cross sectional study	34
Evidence on the economic value of end-of-life and palliative care interventions: a narrative review of reviews	33
Burnout and resilience among Canadian palliative care physicians	32
Parental bereavement – impact of death of neonates and children under 12 years on personhood of parents: a systematic scoping review	30
How nurses support family caregivers in the complex context of end-of-life home care: a qualitative study	30
What makes palliative care needs “complex”? A multisite sequential explanatory mixed methods study of patients referred for specialist palliative care	27
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 workers	27
Advance care planning conversations in primary care: a quality improvement project using the Serious Illness Care Program	26
Barthel Index is a valid and reliable tool to measure the functional independence of cancer patients in palliative care	25
Communicating with patients and families about illness progression and end of life: a review of studies using direct observation of clinical practice	25
A qualitative study of bereaved family caregivers: feeling of security, facilitators and barriers for rural home care and death for persons with advanced cancer	24
Compassion fatigue and compassion satisfaction among palliative care health providers: a scoping review	24
Priorities and opportunities for palliative and end of life care in United Kingdom health policies: a national documentary analysis	24
Physicians’ clinical prediction of survival in head and neck cancer patients in the palliative phase	24
Caregiver’s burden at the end of life of their loved one: insights from a longitudinal qualitative study among working family caregivers	22
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 spouses	21
Quality indicators for the evaluation of end-of-life care in Germany – a retrospective cross-sectional analysis of statutory health insurance data	21
“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 study	20
Exploring the relationship between spiritual well-being and death anxiety in patients with gynecological cancer: a cross-section study	20
How can we improve the experiences of patients and families who request medical assistance in dying? A multi-centre qualitative study	20
What’s suffering got to do with it? A qualitative study of suffering in the context of Medical Assistance in Dying (MAID)	20

Palliative Performance Scale and survival in patients with cancer and non-cancer diagnoses needing a palliative care consultation: a retrospective cohort study	19
Advanced care planning during the COVID-19 pandemic: ceiling of care decisions and their implications for observational data	19
Developing a family-reported measure of experiences with home-based pediatric palliative and hospice care: a multi-method, multi-stakeholder approach	18
Palliative care providers’ use of digital health and perspectives on technological innovation: a national study	18
Predictors of the final place of care of patients with advanced cancer receiving integrated home-based palliative care: a retrospective cohort study	17
How compassionate communities are implemented and evaluated in practice: a scoping review	17
Experiences of bereaved family caregivers with shared decision making in palliative cancer treatment: a qualitative interview study	17
A systematic scoping review on patients’ perceptions of dignity	17
Assessing professional identity formation (PIF) amongst medical students in Oncology and Palliative Medicine postings: a SEBA guided scoping review	17
The influence of symptom severity of palliative care patients on their family caregivers	17
Conceptualising effective symptom management in palliative care: a novel model derived from qualitative data	17
Validation and cultural adaptation of the Integrated Palliative care Outcome Scale (IPOS) for the Portuguese population	17
An integrative review to identify how nurses practicing in inpatient specialist palliative care units uphold the values of nursing	16
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 care	16
Preferences for home care to enable home death among adult patients with cancer in late palliative phase – a grounded theory study	16
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 Zimb	16
Documentation of older people’s end-of-life care in the context of specialised palliative care: a retrospective review of patient records	16
Learning to care for the spirit of dying patients: the impact of spiritual care training in a hospice-setting	16
“It’s given me confidence”: a pragmatic qualitative evaluation exploring the perceived benefits of online end‐of‐life education on clinical care	15
Support received by family members before, at and after an ill person’s death	14
Analysis of the unmet needs of Palestinian advanced cancer patients and their relationship to emotional distress: results from a cross-sectional study	14
The hospice as a learning space: a death education intervention with a group of adolescents	14
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 project	14
Health-related quality of life in patients with colorectal cancer in the palliative phase: a systematic review and meta-analysis	14
Navigating a newly diagnosed cancer through clinician-facilitated discussions of health-related patient values: a qualitative analysis	14
Specialist palliative care teams and characteristics related to referral rate: a national cross-sectional survey among hospitals in the Netherlands	14
Introducing cross-cultural education in palliative care: focus groups with experts on practical strategies	14
Palliative care for rural growth and wellbeing: identifying perceived barriers and facilitators in access to palliative care in rural Indiana, USA	14
Palliative care provider attitudes toward existential distress and treatment with psychedelic-assisted therapies	14
Prescription trends at the end of life in a palliative care unit: observational study	14
Trend analysis of palliative care consultation service for terminally ill non-cancer patients in Taiwan: a 9-year observational study	13
Systematic adaptation of the Thai version of the supportive and palliative care indicators tool for low-income setting (SPICT-LIS)	13
Oral health plays second fiddle in palliative care: an interview study with registered nurses in home healthcare	13
Challenges faced by Chinese community nurses when providing home-based hospice and palliative care: a descriptive qualitative study	13
Hospice care self-efficacy among clinical medical staff working in the coronavirus disease 2019 (COVID-19) isolation wards of designated hospitals: a cross–sectional study	13
Continuous subcutaneous infusion for pain control in dying patients: experiences from a tertiary palliative care center	13
Validity and reliability of the English and translated Chinese versions of the Integrated Palliative care Outcome Scale (IPOS) in Singapore	13
To hydrate or not to hydrate? The effect of hydration on survival, symptoms and quality of dying among terminally ill cancer patients	13
Bereavement interventions to support informal caregivers in the intensive care unit: a systematic review	13
How does ethnicity affect presence of advance care planning in care records for individuals with advanced disease? A mixed-methods systematic review	13
A scoping review of the evidence for community-based dementia palliative care services and their related service activities	13
Chemotherapy during the last 30 days of life and the role of palliative care referral, a single center experience	12
Perceptions, knowledge and attitudes towards the concept and approach of palliative care amongst caregivers: a cross-sectional survey in Karachi, Pakistan	12
Advance care planning preferences in Chinese nursing home residents: results from two cross-sectional studies in Hong Kong and Taiwan	12
How well do documented goals-of-care discussions for patients with stage IV cancer reflect communication best practices?	12
A qualitative exploration of the unmet information needs of Chinese advanced cancer patients and their informal caregivers	12
“No thanks, I don’t want to see snakes again”: a qualitative study of pain management versus preservation of cognition in palliative care patients	12
Managing clinical uncertainty in older people towards the end of life: a systematic review of person-centred tools	12
Is progress being made on Canada’s palliative care framework and action plan? A survey of stakeholder perspectives	12
Quality of online self-management resources for adults living with primary brain cancer, and their carers: a systematic environmental scan	12

Association between attitude towards death and spiritual care competence of Chinese oncology nurses: a cross-sectional study	12
Finnish nursing students’ perceptions of the development needs in palliative care education and factors influencing learning in undergraduate nursing studies – a qualitative study	12
Effectiveness and cost effectiveness of palliative care interventions in people with chronic heart failure and their caregivers: a systematic review	12
Enhanced home palliative care could reduce emergency department visits due to non-organic dyspnea among cancer patients: a retrospective cohort study	12
Virtual reality reduces pain in palliative care–A feasibility trial	12
A qualitative study on continuous deep sedation until death as an alternative to assisted suicide in Switzerland	12
Opportunities and challenges for advance care planning in strongly religious family-centric societies: a Focus group study of Indonesian cancer-care professionals	12
Access to and adequacy of psychological services for adult patients in UK hospices: a national, cross-sectional survey	11
Exploration of the acceptability and usability of advance care planning tools in long term care homes	11
Symptoms, symptom relief and support in COVID-19 patients dying in hospitals during the first pandemic wave	11
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 study	11
Verbalizing spiritual needs in palliative care: a qualitative interview study on verbal and non-verbal communication in two Danish hospices	11
The relationship between anticipatory grief and illness uncertainty among Chinese family caregivers of patients with advanced lung cancer: a cross-sectional study	11
Home hospitalization for palliative cancer care: factors associated with unplanned hospital admissions and death in hospital	11
The training effects of a continuing education program on nurses’ knowledge and attitudes to palliative care: a cross sectional study	11
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 evaluati	11
Where would Canadians prefer to die? Variation by situational severity, support for family obligations, and age in a national study	11
Challenges for palliative care day services: a focus group study	11
Looking back: Identifying supportive care and unmet needs of parents of children receiving specialist paediatric palliative care from the bereavement perspective	11
Spirituality in palliative care	11
Delphi consensus on strategies in the management of opioid-induced constipation in cancer patients	11
Advancing pediatric palliative care in a low-middle income country: an implementation study, a challenging but not impossible task	10
Views of general practitioners on end-of-life care learning preferences: a systematic review	10
Feasibility, use and benefits of patient-reported outcome measures in palliative care units: a multicentre observational study	10
Evaluating satisfaction with the quality and provision of end-of-life care for patients from diverse ethnocultural backgrounds	10
The impact of uncertainty on bereaved family’s experiences of care at the end of life: a thematic analysis of free text survey data	10
Supportive and palliative care indicators tool (SPICT™) in a Danish healthcare context: translation, cross-cultural adaptation, and content validation	10
Paediatric palliative screening scale as a useful tool for clinicians’ assessment of palliative care needs of pediatric patients: a retrospective cohort study	10
Patient participation and associated factors in the discussions on do-not-attempt-resuscitation and end-of-life disclosure: a retrospective chart review study	10
Knowledge of end-of-life wishes by physicians and family caregivers in cancer patients	10
Professional oral care in end-of-life patients with advanced cancers in a hospice ward: improvement of oral conditions	10
Dignity of patients with palliative needs in the Middle East: an integrative review	10
Parental perspectives on the grief and support needs of children and young people bereaved during the COVID-19 pandemic: qualitative findings from a national survey	10
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 cancer	10
Palliative care nurse champions’ views on their role and impact: a qualitative interview study among hospital and home care nurses	10
Changes in decision-making process for life-sustaining treatment in patients with advanced cancer after the life-sustaining treatment decisions-making act	10
Simulation-based learning in palliative care in postgraduate nursing education: a scoping review	10
Nurses’ perceptions of barriers and supportive behaviors in end-of-life care in the intensive care unit: a cross-sectional study	10
Psychosocial distress and the quality of life of cancer patients in two health facilities in Cameroon	10
The Promoting Resilience in Stress Management (PRISM) intervention for adolescents and young adults receiving hematopoietic cell transplantation: a randomized controlled trial protocol	10
Healthcare professionals’ perspectives of patient and family preferences of patient place of death: a qualitative study	10
Psychosocial factors affecting the bereavement experience of relatives of palliative-stage cancer patients: a systematic review	10
A prognostic model using the neutrophil-albumin ratio and PG-SGA to predict overall survival in advanced palliative lung cancer	10
Patients and family caregivers report high treatment expectations during palliative chemotherapy: a longitudinal prospective study	10
Health care needs of elderly patients with lung, liver, or colon cancer in Taiwan	9
Developing an integrated model of community-based palliative care into the primary health care (PHC) for terminally ill cancer patients in Iran	9
The level of knowledge about palliative care in Iranian patients with cancer	9
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 databases	9
Caring for depression in the dying is complex and challenging – survey of palliative physicians	9
The effect of a single session of 30-min mindful breathing in reducing fatigue among patients with haematological cancer – a randomised controlled trial	9
Non-pharmacological interventions to manage psychological distress in patients living with cancer: a systematic review	9
A cross-sectional assessment of symptom burden among patients with advanced cervical cancer	9
Hospice care providers experiences of grappling with medical assistance in dying in a hospice setting: a qualitative descriptive study	9
Impact of interprofessional collaborative practice in palliative care on outcomes for advanced cancer inpatients in a resource-limited setting	9
Factors influencing length of survival in ambulatory palliative care - a cross sectional study based on secondary data	9
The end of life experiences of people living with socio-economic deprivation in the developed world: an integrative review	9
Palliative radiotherapy for gastric cancer bleeding: a multi-institutional retrospective study	9
Providing dignity therapy to patients with advanced cancer: a feasibility study within the setting of a hospital palliative care unit	9
Adaptation of the Australian Palliative Care Phase concept to the German palliative care context: a mixed-methods approach using cognitive interviews and cross-sectional data	9
A survey of hospice day services in the United Kingdom & Republic of Ireland : how did hospices offer social support to palliative care patients, pre-pandemic?	9
Addressing challenges in information-provision: a qualitative study among oncologists and women with advanced breast cancer	9
Why is hospice care important? An exploration of its benefits for patients with terminal cancer	9
Inpatient generalist palliative care during the SARS-CoV-2 pandemic – experiences, challenges and potential solutions from the perspective of health care workers	9
Presuppositions, cost–benefit, collaboration, and competency impacts palliative care referral in paediatric oncology: a qualitative study	9
The impact of covid-19 on out-of-hours adult hospice care: an online survey	9
Development of an international Core Outcome Set (COS) for best care for the dying person: study protocol	9
Healthcare providers’ perception of advance care planning for patients with critical illnesses in acute-care hospitals: a cross-sectional study	9
When cultural values meets professional values: a qualitative study of chinese nurses’ attitudes and experiences concerning death	8
Correlation between depression and intimacy in lung cancer patients and their family caregivers	8
Young adults understanding and readiness to engage with palliative care: extending the reach of palliative care through a public health approach: a qualitative study	8
Palliative care in the pre-hospital service in Brazil: experiences of health professionals	8
Exploring socioeconomic inequities in access to palliative and end-of-life care in the UK: a narrative synthesis	8
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 appro	8
Control in patients with advanced cancer: an interpretative phenomenological study	8
Unmet needs in palliative care for patients with common non-cancer diseases: a cross-sectional study	8
Physician decision-making process about withholding/withdrawing life-sustaining treatments in paediatric patients: a systematic review of qualitative evidence	8
Meeting ethical challenges with authenticity when engaging patients and families in end-of-life and palliative care research: a qualitative study	8
A meaning-centered spiritual care training program for hospice palliative care teams in South Korea: development and preliminary evaluation	8
Chinese medical teachers’ cultural attitudes influence palliative care education: a qualitative study	8
Community palliative care services on addressing physical and psychosocial needs in people with advanced illness: a prospective cohort study	8

A prospective cohort study assessing aggressive interventions at the end-of-life among patients with solid metastatic cancer	8
Quality of dying in hospital general wards: a cross-sectional study about the end-of-life care	8
Benefits, for patients with late stage chronic obstructive pulmonary disease, of being cared for in specialized palliative care compared to hospital. A nationwide register study	8
Socioeconomy as a prognostic factor for location of death in Swedish palliative cancer patients	8
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 internat	8
Evaluating the integration of palliative care in national health systems: an indicator rating process with EAPC task force members to measure advanced palliative care development	8
Psychological distress and resilience in patients with advanced cancer during the Covid-19 pandemic: the mediating role of spirituality	8
Before the 2020 Pandemic: an observational study exploring public knowledge, attitudes, plans, and preferences towards death and end of life care in Wales	8
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 intervention	8
Accuracy of clinical predictions of prognosis at the end-of-life: evidence from routinely collected data in urgent care records	8
SPICT as a predictive tool for risk of 1-year health degradation and death in older patients admitted to the emergency department: a bicentric cohort study in Belgium	8
End-of-life care preferences among cancer patients in Southern Thailand: a university hospital-based cross-sectional survey	8
Palliative care in Uganda: quantitative descriptive study of key palliative care indicators 2018-2020	8
Palliative care in the community – the role of the resource nurse, a qualitative study	8
Advance care planning in primary care: a retrospective medical record study among patients with different illness trajectories	8
Methadone switching for refractory cancer pain	8
Perceptions of healthcare professionals towards palliative care in internal medicine wards: a cross-sectional survey	8
Factors influencing terminal cancer patients’ autonomous DNR decision: a longitudinal statutory document and clinical database study	8
Need for additional professional psychosocial and spiritual support in patients with advanced diseases in the course of specialist palliative care – a longitudinal observational study	8
Subjective burdens among informal caregivers of critically ill patients: a cross-sectional study in rural Shandong, China	8
Development of the palliative care referral system: proposal of a tool for the referral of cancer patients to specialized palliative care	8
What to consider when implementing a tool for timely recognition of palliative care needs in heart failure: a context-based qualitative study	8
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 at	8
Identifying palliative care needs of patients with non-communicable diseases in Indonesia using the SPICT tool: a descriptive cross-sectional study	8
“My life became more meaningful”: confronting one’s own end of life and its effects on well-being—a qualitative study	8
The experiences of clinical nurses coping with patient death in the context of rising hospital deaths in China: a qualitative study	8
Improving serious illness communication: a qualitative study of clinical culture	8
Building a telepalliative care strategy in nursing homes: a qualitative study with mobile palliative care teams	8
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 care	8
Video decision support tool promoting values conversations in advanced care planning in cancer: protocol of a randomised controlled trial	8
Advance care planning for patients with cancer and family caregivers in Indonesia: a qualitative study	8
Unmet needs related to the quality of life of advanced cancer patients in Korea: a qualitative study	7
Structured implementation of the Supportive and Palliative Care Indicators Tool in general practice – A prospective interventional study with follow-up	7
Health-related expectations of the chronically critically ill: a multi-perspective qualitative study	7
Spiritual care practices in hospices in the Western cape, South Africa: the challenge of diversity	7
Nurse-led normalised advance care planning service in hospital and community health settings: a qualitative study	7
Acute and long-term grief reactions and experiences in parentally cancer-bereaved teenagers	7
Medical Assistance in Dying in patients with advanced cancer and their caregivers: a mixed methods longitudinal study protocol	7
A survey of cancer care institutions in Nepal to inform design of a pain management mobile application	7
No difference in effects of ‘PACE steps to success’ palliative care program for nursing home residents with and without dementia: a pre-planned subgroup analysis of the seven-country PACE trial	7
Factors influencing nurses’ intention to work in the oncology specialty: multi-institutional cross-sectional study	7
Public perceptions of advance care planning (ACP) from an international perspective: a scoping review	7
Implementing welfare technology in palliative homecare for patients with cancer: a qualitative study of health-care professionals’ experiences	7
Cost-utility analysis of palliative care in patients with advanced cancer: a retrospective study	7
Adapting ENABLE for patients with advanced cancer and their family caregivers in Singapore: a qualitative formative evaluation	7
Views of people living with dementia and their carers on their present and future: a qualitative study	7
Evaluating the specialist palliative care clinical nurse specialist role in an acute hospital setting: a mixed methods sequential explanatory study	7
Use of antithrombotics at the end of life: an in-depth chart review study	7
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 countries	7
Exploring the status of and demand for palliative day-care clinics and day hospices in Germany: a protocol for a mixed-methods study	7
A systematic review defining non-beneficial and inappropriate end-of-life treatment in patients with non-cancer diagnoses: theoretical development for multi-stakeholder intervention design in acute ca	7
Caregiver burden among family caregivers of incurable cancer patients in two eastern Mediterranean countries	7
Enhancing equity and diversity in palliative care clinical practice, research and education	7
Regional and age differences in specialised palliative care for patients with pancreatic cancer	7
Cross-cultural conceptualization of a good end of life with dementia: a qualitative study	7
Psychometric evaluation of the Chinese version of advance care planning self-efficacy scale among clinical nurses	7
Implementation of advance care planning decision aids for patients undergoing high-risk surgery: a field-testing study	6
Palliative care symptoms, concerns and well-being of older people with frailty and complex care needs upon hospital discharge: a cross-sectional study	6
Psychometric validation of the death literacy index and benchmarking of death literacy level in a representative uk population sample	6
Support practices by an interdisciplinary team in a palliative-care unit for relatives of patients in agonal phase	6
Impact of ambulatory palliative care on symptoms and service outcomes in cancer patients: a retrospective cohort study	6
Being a safe place: a qualitative study exploring perceptions as to how a rural community hospice could respond to enactment of voluntary assisted dying legislation	6
Palliative care in home health care services and hospitals – the role of the resource nurse, a qualitative study	6
Towards cataloguing and characterising advance care planning and end-of-life care resources	6
Patient and physician perspectives on engaging in palliative and healthcare trials: a qualitative descriptive study	6
Acute healthcare utilization in end-of-life among Swedish brain tumor patients – a population based register study	6
Prevalence and clinical characteristics of patients with Advanced Chronic Illness and Palliative Care needs, identified with the NECPAL CCOMS-ICO© Tool at a Tertiary Care Hospital	6
Comparison of the health-related quality of life of end stage kidney disease patients on hemodialysis and non-hemodialysis management in Uganda	6
Muslim patients in the U.S. confronting challenges regarding end-of-life and palliative care: the experiences and roles of hospital chaplains	6
NUrsing Homes End of Life care Program (NUHELP): developing a complex intervention	6
Charitably funded hospices and the challenges associated with the COVID-19 pandemic: a mixed-methods study (CovPall)	6
Palliative care in day-hospital for advanced cancer patients: a study protocol for a multicentre randomized controlled trial	6
Experiences of family caregivers of children with cancer while receiving home-based pediatric palliative care in Indonesia: a qualitative study	6
Context and mechanisms that enable implementation of specialist palliative care Needs Rounds in care homes: results from a qualitative interview study	6
Finding their place – general practitioners' experiences with palliative care—a Norwegian qualitative study	6
Feeling called to care: a qualitative interview study on normativity in family caregivers’ experiences in Dutch home settings in a palliative care context	6
Challenges encountered by family caregivers of prostate cancer patients in Cape Coast, Ghana: a descriptive phenomenological study	6
The explorations of the awareness, contemplation, self-Efficacy, and readiness of advance care planning, and its predictors in Taiwanese patients while receiving hemodialysis treatment	6
General population-based study on preferences towards end-of-life care in Southern Thailand: a cross-sectional survey	6
Interdisciplinary staff perceptions of advance care planning in long-term care homes: a qualitative study	6
The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study	6
The pattern of change in opioid and adjuvant prescriptions for cancer pain before and after referral to a comprehensive program in the Palliative Care Center in Kuwait	6
How do cancer patients refuse treatment? A grounded theory study	6
Low rates of structured advance care planning documentation in electronic health records: results of a single-center observational study	6
The impact of death and dying on the personhood of senior nurses at the National Cancer Centre Singapore (NCCS): a qualitative study	6
Impact of a specialised palliative care intervention in patients with advanced soft tissue sarcoma – a single-centre retrospective analysis	6
Impact of resilience and social support on long-term grief in cancer-bereaved siblings: an exploratory study	6
Trends in specialized palliative care referrals at an oncology center from 2007 to 2019	6
Using natural language processing to explore heterogeneity in moral terminology in palliative care consultations	6
End of life care in UK care homes during the COVID-19 pandemic: a qualitative study	6
Advance directives among cognitively impaired persons who had an amyloid PET scan and their care partners: a mixed-methods study	6
Validity and reliability of the spiritual care competency scale for oncology nurses in Taiwan	6