BMC Palliative Care

Papers
(The median citation count of BMC Palliative Care is 2. 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 2021-06-01 to 2025-06-01.)
ArticleCitations
Do surrogates predict patient preferences more accurately after a physician-led discussion about advance directives? A randomized controlled trial98
Palliative care needs of Jordanian women’s experience of living with stroke: a descriptive phenomenological study53
Preference for initiation of end-of-life care discussion in Indonesia: a quantitative study44
Communication about incurable illness and remaining life between spouses and patients with incurable illness receiving specialized home care: effects of a family caregiver-targeted web-based psycho-ed42
Use of palliative radiotherapy among patients with metastatic non-small-cell lung cancer in Puerto Rico38
Comparison of actigraphy with a sleep protocol maintained by professional caregivers and questionnaire-based parental judgment in children and adolescents with life-limiting conditions38
A specific role of village doctors in reducing disparities: a quantile regression analysis of end-of-life medical care35
Correction: Oncologists’ palliative care referral behaviour: testing utility of social exchange theory as an explanatory framework35
Palliative care training in medical undergraduate education: a survey among the faculty32
Correction: Improving Palliative Care Knowledge of nurses caring for heart failure patients31
Experiences and perceptions of palliative care patients receiving virtual reality therapy: a meta-synthesis of qualitative studies31
Personal positioning of oncology patients in palliative care: a mixed-methods study31
Bereaved parents’ perceptions of memory making: a qualitative meta-synthesis30
The impact of the COVID-19 pandemic on processes, resource use and cost in palliative care30
Experiences of bereaved family caregivers with shared decision making in palliative cancer treatment: a qualitative interview study27
"Nebulized lidocaine for intractable cough in hospice care: a comprehensive review of efficacy, safety, and future perspectives"27
Palliative care needs of patients with multiple sclerosis in southeast Iran27
Exploring spirituality, religion and life philosophy among parents of children receiving palliative care: a qualitative study25
Eye donation in hospice and hospital palliative care settings: perceptions, practice, and service development needs – findings from a national survey24
Differences in end-of-life care patterns between types of hospice used for cancer patients: a retrospective cohort study24
Prescription trends at the end of life in a palliative care unit: observational study24
Factors related to advance directives completion among cancer patients: a systematic review24
Implementation of a hospital-based end-of-life and bereavement care program in a latin American middle-income country. A source of light and compassion in the midst of cloudy times24
Cross-referencing French hematology teams’ knowledge and perception of end-of-life situations: a national mixed-methods survey23
Resuscitation, yes or no ? the criteria for transferring patients with hematological malignancies to intensive care. A qualitative study23
Interdisciplinary staff perceptions of advance care planning in long-term care homes: a qualitative study22
Current status of academic palliative medicine in Poland: a nationwide study21
Palliative care provider attitudes toward existential distress and treatment with psychedelic-assisted therapies20
Characterizing uncertainty in goals-of-care discussions among black and white patients: a qualitative study20
Control in patients with advanced cancer: an interpretative phenomenological study20
Bicentre, randomized, parallel-arm, sham-controlled trial of transcranial direct-current stimulation (tDCS) in the treatment of palliative care patients with refractory cancer pain20
Carer preferences of route of administration of transmucosal diamorphine and willingness to take part in a randomised controlled trial: an interview study (DIPPER)20
Protocol for the promoting resilience in stress management (PRISM) intervention: a multi-site randomized controlled trial for adolescents and young adults with advanced cancer19
Increasing access to palliative care for patients with advanced cancer of African and Latin American descent: a patient-oriented community-based study protocol19
Regional and age differences in specialised palliative care for patients with pancreatic cancer19
Adapting the serious illness conversation guide for unhoused older adults: a rapid qualitative study19
Assessing the relationship between the distress levels in patients with irreversible terminal delirium and the good quality of death from the perspective of bereaved family19
Effectiveness of the “Living with Cancer” peer self-management support program for persons with advanced cancer and their relatives: study protocol of a non-randomized stepped wedge study19
Validity and reliability of the spiritual care competency scale for oncology nurses in Taiwan19
Filling gaps in experiences religious understanding of people living with cancer in palliative care: a phenomenological qualitative study19
Correction: “The patient as teacher” - thematic analysis of undergraduate medical students’ experiences with an experiential learning project in palliative care19
Palliative care and new technologies. The use of smart sensor technologies and its impact on the Total Care principle18
Trajectories of Health-related quality of life in patients with Advanced Cancer during the Last Year of Life: findings from the COMPASS study18
Enhancing equity and diversity in palliative care clinical practice, research and education18
Frequency and predictors of palliative sedation among patients with cancer who died in a specialist inpatient palliative care unit: a retrospective study18
Physician-patient boundaries in palliative care18
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 study18
“I didn’t know it was going to be like this.”: unprepared for end-of-Life care, the experiences of care aides care in long-term care17
Use of the supportive and palliative care indicators tool (SPICT™) for end-of-life discussions: a scoping review17
Perspectives from patients with chronic lung disease on a telehealth-facilitated integrated palliative care model: a qualitative content analysis study17
Impact of an outpatient palliative care consultation and symptom clusters in terminal patients at a tertiary care center in Pakistan17
Barriers and facilitators to palliative care for patients with non-curable cancer in Colombia: perspectives of allied health and social care professionals17
“You like to be in control of your own destiny to a degree, don't you?”: conscientious autonomy and planning for future care with dementia17
The state of undergraduate palliative care education at Austrian medical schools – a mixed methods study17
Compassion fatigue and compassion satisfaction among palliative care health providers: a scoping review17
Exploring the relationship between spiritual well-being and death anxiety in patients with gynecological cancer: a cross-section study17
Attitude of nurses towards palliative care and its associated factors in Ethiopia, systematic review and meta-analysis16
Communication of palliative care needs in discharge letters from hospice providers to primary care: a multisite sequential explanatory mixed methods study16
Unmet supportive care needs in patients with advanced cancer and its impact on distress16
End-of-life medical decisions in French overseas departments: results of a retrospective survey16
Factors influencing the spiritual needs of patients with terminal cancer: a multicenter study in southern China16
Cross-cultural adaptation and validation of the Chinese version of the quality of communication questionnaire15
Building a programme theory of a specialist paediatric palliative and hospice care programme: development process and methodological reflection15
Correction: 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 interv15
Healthcare professionals’ perspectives on assessing selected patient-reported outcome measures in specialist palliative care institutions: a multi-country mixed-methods study15
Quality of dying in hospital general wards: a cross-sectional study about the end-of-life care15
Divergent patterns of confrontation with death using the Anticipated Farewell to Existence Questionnaire (AFEQT): a cross-sectional comparative study of four samples with increasing proximity to death15
Challenges and coping strategies among caregivers of children with cancer receiving care at a national referral hospital in Kenya15
Factors influencing the survival time of patients with advanced cancer at the end of life: a retrospective study15
A nationwide neurosurgical inter-disciplinary service for cancer-related refractory pain15
Communication strategies for adults in palliative care: the speech-language therapists’ perspective15
Behaviors and influencing factors of Chinese oncology nurses towards hospice care: a cross-sectional study based on social cognitive theory in 202214
Perceptions of healthcare professionals towards palliative care in internal medicine wards: a cross-sectional survey14
Acknowledgement and use of advance care directives and goals of care by emergency department staff: a mixed method post intervention study14
Advance care planning in primary care: a retrospective medical record study among patients with different illness trajectories14
Correction: Translation and cultural adaptation of the Greek integrated palliative care outcome scale (IPOS): challenges in a six-phase process14
Early experiences of the End of Life Choice Act 2019 amongst assisted dying practitioners in Aotearoa New Zealand14
Priorities and opportunities for palliative and end of life care in United Kingdom health policies: a national documentary analysis14
Interrater agreement of multi-professional case review as reference standard for specialist palliative care need: a mixed-methods study14
Conceptualising effective symptom management in palliative care: a novel model derived from qualitative data13
Caregiver burden among family caregivers of incurable cancer patients in two eastern Mediterranean countries13
End-of-life care in rural China: the crucial role and challenges of village doctors13
Psychosocial functioning in individuals with advanced oesophago-gastric cancer: a mixed methods systematic review13
Development and validation of impact of early integration of palliative care and oncology(IEI PCO) questionnaire: a survey for medical oncologists and nurses13
Analyzing the use of specialized palliative care in intensive care unit patients in Germany: a cross-sectional study13
A 15-year experience in pediatric palliative care: a retrospective hospital-based study13
Designing and psychometric properties of the hospitalized patients’ spiritual needs questionnaire (HPSNQ) in the medical-surgical hospital setting13
How do navigation programs address the needs of those living in the community with advanced, life-limiting Illness? A realist evaluation of programs in Canada13
The prevalence of perceived stigma and self-blame and their associations with depression, emotional well-being and social well-being among advanced cancer patients: evidence from the APPROACH cross-se13
Effect of motivational interviewing to promote advance care planning among palliative care patients in ambulatory care setting: a randomized controlled trial13
My virtual home: needs of patients in palliative cancer care and content effects of individualized virtual reality – a mixed methods study protocol13
Overview of spiritual care instruments and its domains: a scoping review13
Physicians’ decreased tendency to choose palliative care for patients with advanced dementia between 1999 and 201513
The APSY-SED study: protocol of an observational, longitudinal, mixed methods and multicenter study exploring the psychological adjustment of relatives and healthcare providers of patients with cancer13
Comparison of the sociodemographic and clinical profiles of cancer patients admitted to a tertiary palliative care unit before and during the COVID-19 pandemic13
Looking back: Identifying supportive care and unmet needs of parents of children receiving specialist paediatric palliative care from the bereavement perspective12
The meaning of culture in nursing at the end of life – an interview study with nurses in specialized palliative care12
Spiritual well-being and attitudes toward caring for dying patients: a cross-sectional study in Iranian nursing students12
Learning from experience: does providing end-of-life care support for relatives boost personal end-of-life health literacy?12
Perceived risk of death among patients with advanced cancer: a qualitative directed content analysis12
Uncertainty and probability in neonatal end-of-life decision-making: analysing real-time conversations between healthcare professionals and families of critically ill newborns12
The knowledge, attitude and behavior on the palliative care among neonatal nurses: what can we do12
How compassionate communities are implemented and evaluated in practice: a scoping review12
Unaddressed palliative care needs of ischemic stroke patients treated with reperfusion therapies after age 8012
Documentation of older people’s end-of-life care in the context of specialised palliative care: a retrospective review of patient records12
Meta-aggregation of facilitators and barriers to home-based palliative care12
“Discussion or silent accompaniment: a grounded theory study about voluntary stopping of eating and drinking in Switzerland”12
Analysis of the unmet needs of Palestinian advanced cancer patients and their relationship to emotional distress: results from a cross-sectional study12
Supportive and palliative care indicators tool (SPICT™) in a Danish healthcare context: translation, cross-cultural adaptation, and content validation12
A qualitative exploration of “empathic labor” in Chinese hospice nurses11
Contribution of Eastern Mediterranean Region countries to palliative care journals from 1991 to 2020 and its relationship to the development of palliative care11
Oncologist responses to advanced cancer patients’ lived illness experiences and effects: an applied conversation analysis study11
Reply to “A better interpretation of data regarding the opioid switching to methadone”11
Experiences of pain and pain management in advanced disease and serious illness for people from South Asian communities in Leeds and Bradford: a qualitative interview study11
Integrating palliative care education in pulmonary rehabilitation: a randomized controlled study protocol11
Primary data on symptom burden and quality of life among elderly patients at risk of dying during unplanned admissions to an NHS hospital: a cohort study using EuroQoL and the integrated palliative ca11
Implementation of a palliative care intervention for patients with COPD – a mixed methods process evaluation of the COMPASSION study11
The CAREPAL-8: a short screening tool for multidimensional family caregiver burden in palliative care11
Evaluation of palliative care needs rounds in residential aged care homes in South Australia: a qualitative study11
Palliative sedation at the end of life: prevalence, characteristics and possible determinants11
“The patient as teacher” - thematic analysis of undergraduate medical students’ experiences with an experiential learning project in palliative care11
A systematic scoping review on patients’ perceptions of dignity11
Natural language processing and network analysis in patients withdrawing from life-sustaining treatments: a retrospective cohort study11
Barriers to recruitment into emergency department-initiated palliative care: a sub-study of a multi-site, randomized controlled trial11
State-wide implementation of patient-reported outcome measures (PROMs) in specialized outpatient palliative care teams (ELSAH): A mixed-methods evaluation and implications for their sustainable use11
Palliative care as a digital working world (PALLADiUM) - A mixed-method research protocol11
Associations of health literacy, personality traits, and pro-individualism with the willingness to complete advance directives in Taiwan11
Together but still alone - A qualitative study exploring how family members of persons with incurable oesophageal or gastric cancer manage everyday life11
Health-related quality of life in patients with colorectal cancer in the palliative phase: a systematic review and meta-analysis11
Adaptation of the Australian Palliative Care Phase concept to the German palliative care context: a mixed-methods approach using cognitive interviews and cross-sectional data11
The experiences of clinical nurses coping with patient death in the context of rising hospital deaths in China: a qualitative study11
Palliative care needs and quality of life among adults with advanced chronic illnesses in low-income communities of Bangladesh11
Characteristics and outcomes of patients with do-not-resuscitate and physician orders for life-sustaining treatment in a medical intensive care unit: a retrospective cohort study10
Bereaved family members’ perspectives on quality of death in deceased acute cardiovascular disease patients compared with cancer patients – a comparison of the J-HOPE3 study and the quality of palliat10
Effect of chocolate on older patients with cancer in palliative care: a randomised controlled study10
A better interpretation of data regarding the opioid switching to methadone10
The impact of covid-19 on out-of-hours adult hospice care: an online survey10
Caring for depression in the dying is complex and challenging – survey of palliative physicians10
A palliative care approach for adult non-cancer patients with life-limiting illnesses is cost-saving or cost-neutral: a systematic review of RCTs10
Exploring the challenges and roles of nurses in delivering palliative care for cancer patients and co-morbidities in Ghana10
The meaning of dignity in care during the COVID-19 pandemic: a qualitative study in acute and intensive care10
Parental bereavement – impact of death of neonates and children under 12 years on personhood of parents: a systematic scoping review10
Pattern of admissions and needs assessment for palliative care services among in-patients in a tertiary health facility in South-Western Nigeria10
Development of palliative care clinical practice guidelines and referral care pathways for primary care practitioners in Pakistan10
The experience of hope in dyads living with advanced chronic illness in Portugal: a longitudinal mixed-methods study10
Benefits, for patients with late stage chronic obstructive pulmonary disease, of being cared for in specialized palliative care compared to hospital. A nationwide register study10
Family caregivers’ administration of medications at the end-of-life in China: a qualitative study10
Advance care planning conversations in primary care: a quality improvement project using the Serious Illness Care Program10
Experiences of patients with advanced cancer coping with chronic pain: a qualitative analysis10
Factors influencing terminal cancer patients’ autonomous DNR decision: a longitudinal statutory document and clinical database study10
Development, validation and reliability testing of the hospice care environment scale10
The effect of a single session of 30-min mindful breathing in reducing fatigue among patients with haematological cancer – a randomised controlled trial10
Symptom- and function-based trajectories of patients with dementia in hospital and community palliative care settings in the last two weeks of life: a retrospective cohort study10
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 project10
Perception of diagnosis by family caregivers in severe brain injury patients in China10
Discussing patient preferences for levels of life-sustaining treatment: development and pilot testing of a Danish POLST form10
When cultural values meets professional values: a qualitative study of chinese nurses’ attitudes and experiences concerning death10
Caring for persons with Dementia: a qualitative study of the needs of carers following care recipient discharge from hospital10
Home care nurses facilitating planned home deaths. A focused ethnography9
Monitoring the clinical practice of palliative sedation (PALSED) in patients with advanced cancer: an international, multicentre, non-experimental prospective observational study protocol9
Palliative care symptoms, concerns and well-being of older people with frailty and complex care needs upon hospital discharge: a cross-sectional study9
Expert survey on coverage and characteristics of pediatric palliative care in Europe – a focus on home care9
Prediction model for delirium in advanced cancer patients receiving palliative care: development and validation9
Understanding barriers and facilitators to palliative and end-of-life care research: a mixed method study of generalist and specialist health, social care, and research professionals9
Hospitalizations and re-hospitalizations at the end-of-life among cancer patients; a retrospective register data study9
Knowledge and awareness of undergraduate medical students regarding palliative care in Pakistan: a cross-sectional study9
Correction: Palliative care progress in Benin: a situation analysis using the WHO development indicators9
Increasing palliative care capacity in primary care: study protocol of a cluster randomized controlled trial of the CAPACITI training program9
Evaluating the specialist palliative care clinical nurse specialist role in an acute hospital setting: a mixed methods sequential explanatory study9
The implementation of guidelines in palliative care – a scoping review9
Medical decision-making experiences of persons with dementia and their carepartners: a qualitative study9
Nurses’ perceptions of barriers and supportive behaviors in end-of-life care in the intensive care unit: a cross-sectional study9
Patient-centeredness and determinant factors of palliative care service for adult cancer patients in public hospitals of addis Ababa, Ethiopia, 2024: cross-sectional mixed method study9
When life is lived with dignity and decline: integration of rehabilitation and palliation in dementia care – a case report9
Physicians’ experiences and perceptions about withholding and withdrawal life-sustaining treatment in Chiang Mai University Hospital: a cross-sectional study9
Paediatric oncologists’ perspectives on Strategic solutions to develop Integrated Cancer Palliative Care: feedback intervention theory as an explanatory Framework9
Correction to: The impact of the COVID-19 pandemic on processes, resource use and cost in palliative care9
Palliative care education in undergraduate medical and nursing programs in Colombia: a cross-sectional analysis9
“Starting to think that way from the start”: approaching deprescribing decision-making for people accessing palliative care - a qualitative exploration of healthcare professionals views9
Death place and palliative outcome indicators in patients under palliative home care service: an observational study9
Preparing for the end-of-life: public attitudes towards advance directives and assisted suicide in Switzerland9
Evaluation of interactive web-based tools to stimulate reflection and communication about advance care planning with people with dementia and their family caregivers9
Home care nurses more positive about the palliative care that is provided and their own competence than hospital nurses: a nationwide survey9
Balancing pandemic public health restrictions and family support at the end of life: palliative care and bereavement experiences of parents whose child died during the COVID-19 pandemic9
Predicting place of death of patients with advanced cancer receiving home-based palliative care services in Iran9
Challenges in recognizing and discussing changes in a resident’s condition in the palliative phase: focus group discussions with nursing staff working in nursing homes about their experiences9
Telehealth adoption in palliative care: a systematic review of patient barriers and facilitators9
The impacts of the scope of benefits expansion on hospice care among adult decedents: a nationwide longitudinal observational study8
Validation of the advance care planning engagement survey in Singapore8
Accuracy of clinical predictions of prognosis at the end-of-life: evidence from routinely collected data in urgent care records8
Is aggressive care appropriate for patients with cancer complicated by pneumonia? A retrospective chart review in a tertiary hospital8
Translation and psychometric validation of the Persian version of palliative care attitudes scale in cancer patients8
Outpatient palliative care during the COVID-19 pandemic: a retrospective single centre analysis in Germany8
Correction to: Readiness for advance care planning and related factors in the general population: a cross sectional study in Iran8
Chinese and Belgian pediatricians’ perspectives toward pediatric palliative care: an online survey8
Barrier analysis for continuity of palliative care from health facility to household among adult cancer patients in Addis Ababa, Ethiopia8
Use of antithrombotics at the end of life: an in-depth chart review study8
Cost-utility analysis of palliative care in patients with advanced cancer: a retrospective study8
“My everyday life has returned to normal”- Experiences of patients and relatives with a palliative day care clinic: a qualitative evaluation study8
Chemotherapy during the last 30 days of life and the role of palliative care referral, a single center experience8
Adapting ENABLE for patients with advanced cancer and their family caregivers in Singapore: a qualitative formative evaluation8
Digital advance care planning with severe mental illness: a retrospective observational cohort analysis of the use of an electronic palliative care coordination system8
Inpatient generalist palliative care during the SARS-CoV-2 pandemic – experiences, challenges and potential solutions from the perspective of health care workers8
What’s suffering got to do with it? A qualitative study of suffering in the context of Medical Assistance in Dying (MAID)8
A realist evaluation of a home-based end of life care service for children and families: what works, for whom, how, in what circumstances and why?8
Challenges and coping strategies when caring for terminally ill persons with cancer: perspectives of family caregivers8
Implementation of the Richmond Agitation-Sedation Scale (palliative version) on an inpatient palliative care unit8
Towards a set of competencies in palliative care nursing in Spain: what’s getting in the way of consensus?8
Validating the self-competence in death work scale for end-of-life care volunteers7
Don’t assume, ask! A focus group study on end-of-life care planning with people with intellectual disabilities from minoritised ethnic groups7
Medical decision-making in hospices from the viewpoint of physicians: results from two qualitative studies7
Determining timeframes to death for imminently dying patients: a retrospective cohort study7
The influence of care home registration type and size on senior care leader’s confidence to provide palliative and end-of-life care: an explanatory sequential mixed methods study7
Patshitinikutau Natukunisha Tshishennuat Uitshuau (a place for Elders to spend their last days in life): a qualitative study about Innu perspectives on end-of-life care7
Socio-economic determinants for the place of last care: results from the acute palliative care unit of a large comprehensive cancer center in a high-income country in Europe7
Combining paid work and family care for a patient at the end of life at home: insights from a qualitative study among caregivers in the Netherlands7
Perspectives of clinicians on shared decision making in hospice care for advanced cancer patients in Nanjing: a descriptive qualitative study7
Provision and related factors of end-of-life care in elderly housing with care services in collaboration with home-visiting nurse agencies: a nationwide survey7
Unmet needs in palliative care for patients with common non-cancer diseases: a cross-sectional study7
Possible age-related differences in healthcare professionals’ perspectives on younger and older patients’ autonomy and decision-making in the context of sedation in specialised palliative care: explor7
Outcomes of delivery in patients with diagnosed life-limiting fetal condition and evaluation of perinatal palliative care program: a retrospective review of palliative care service over 7 years7
Status and predictors of medical students’ knowledge and attitude towards palliative care in Jordan: a cross-sectional study7
Barriers to healthcare professionals screening, recognizing, and managing delirium in the adult patients receiving specialist palliative care: a mixed-methods systematic review7
Decreased aggressive care at the end of life among advanced cancer patients in the Republic of Korea: a nationwide study from 2012 to 20187
Correction: Advanced care planning during the COVID-19 pandemic: ceiling of care decisions and their implications for observational data7
Dignity enhanced through faith & family support in palliative care: a qualitative study7
Interdisciplinary strategies for establishing a trusting relation as a pre-requisite for existential conversations in palliative care: a grounded theory study7
The end of life experiences of people living with socio-economic deprivation in the developed world: an integrative review7
What are the experiences and support needs of district nurses caring for terminally ill people with delirium at home? A qualitative study7
Eleven-year retrospective study characterizing patients with severe brain damage and poor neurological prognosis -role of physicians’ attitude toward life-sustaining treatment7
Facilitators and barriers of implementing end-of-life care volunteering in a hospital in five European countries: the iLIVE study7
Characteristics and place of death in home care recipients in Germany – an analysis of nationwide health insurance claims data7
Correction: Effect of motivational interviewing to promote advance care planning among palliative care patients in ambulatory care setting: a randomized controlled trial7
Using a self-directed workbook to support advance care planning with long term care home residents7
Dying in hospital in Germany – optimising care in the dying phase: study protocol for a multi-centre bottom-up intervention on ward level7
Managing cultural diversity in end-of-life care: a qualitative study7
Children with cancer at the end of life in a middle-income country: integrated pediatric palliative care improves outcomes6
Research attitudes, practice and literacy among Kenyan palliative care healthcare professionals: an observational, cross-sectional online survey6
Finding their place – general practitioners' experiences with palliative care—a Norwegian qualitative study6
Adaptation and validation of the Brazilian version of the Measure of Moral Distress for Healthcare Professionals (MMD-HP BR) in the context of palliative care6
Specialist perinatal palliative care: a retrospective review of antenatal referrals to a children’s palliative care service over 14 years6
Experiences of healthcare professionals providing palliative care in home settings - a scoping review6
Telehealth-facilitated palliative care enables more people to die at home: An analysis of clinical outcomes and service activity data6
Intensive end-of-life care in acute leukemia from a French national hospital database study (2017–2018)6
Exploring knowledge, attitude, and intention towards advance care planning, advance directive, and the patient self-determination act among hemodialysis patients6
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 internat6
The state of transience, and its influence on the wish to die of advanced disease patients: insights from a qualitative phenomenological study6
Impact of palliative care at end-of-life Covid-19 patients – a small-scale pioneering experience6
Health care utilization at the end of life in Parkinson’s disease: a population-based register study6
Drug landscape in patients receiving general outpatient palliative care in Germany: results from a retrospective analysis of 10,464 patients6
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