Palliative Medicine

Papers
(The median citation count of Palliative Medicine is 4. 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 2020-10-01 to 2024-10-01.)
ArticleCitations
A qualitative study of bereaved relatives’ end of life experiences during the COVID-19 pandemic105
Estimating the current and future prevalence of life-limiting conditions in children in England86
‘Necessity is the mother of invention’: Specialist palliative care service innovation and practice change in response to COVID-19. Results from a multinational survey (CovPall)68
Health and social care professionals’ experiences of providing end of life care during the COVID-19 pandemic: A qualitative study64
Prevalence of burnout in healthcare professionals providing palliative care and the effect of interventions to reduce symptoms: A systematic literature review59
Sadness, despair and anger when a patient dies alone from COVID-19: A thematic content analysis of Twitter data from bereaved family members and friends49
Revised recommendations on standards and norms for palliative care in Europe from the European Association for Palliative Care (EAPC): A Delphi study46
Are public health measures and individualised care compatible in the face of a pandemic? A national observational study of bereaved relatives’ experiences during the COVID-19 pandemic44
Dying in times of the coronavirus: An online survey among healthcare professionals about end-of-life care for patients dying with and without COVID-19 (the CO-LIVE study)43
Changes in mortality patterns and place of death during the COVID-19 pandemic: A descriptive analysis of mortality data across four nations43
Missing the human connection: A rapid appraisal of healthcare workers’ perceptions and experiences of providing palliative care during the COVID-19 pandemic40
Defining end of life in dementia: A systematic review40
Risk factors associated with poorer experiences of end-of-life care and challenges in early bereavement: Results of a national online survey of people bereaved during the COVID-19 pandemic38
The support needs of parent caregivers of children with a life-limiting illness and approaches used to meet their needs: A scoping review37
Impact of Medical Assistance in Dying on palliative care: A qualitative study37
Understanding and addressing challenges for advance care planning in the COVID-19 pandemic: An analysis of the UK CovPall survey data from specialist palliative care services37
Asian patients’ perspectives on advance care planning: A mixed-method systematic review and conceptual framework36
‘Saying goodbye’ during the COVID-19 pandemic: A document analysis of online newspapers with implications for end of life care35
Lessons from the COVID-19 pandemic for improving outpatient neuropalliative care: A qualitative study of patient and caregiver perspectives35
Family involvement in advance care planning for people living with advanced cancer: A systematic mixed-methods review32
The role, impact, and support of informal caregivers in the delivery of palliative care for patients with advanced cancer: A multi-country qualitative study32
The utility of the surprise question: A useful tool for identifying patients nearing the last phase of life? A systematic review and meta-analysis31
Home palliative care professionals perception of challenges during the Covid-19 outbreak: A qualitative study31
The palliative care needs and experiences of people with advanced head and neck cancer: A scoping review31
Support needs and barriers to accessing support: Baseline results of a mixed-methods national survey of people bereaved during the COVID-19 pandemic31
Resilience in advanced cancer caregiving. A systematic review and meta-synthesis31
Implementing person-centred outcome measures in palliative care: An exploratory qualitative study using Normalisation Process Theory to understand processes and context30
Toward a socio-spiritual approach? A mixed-methods systematic review on the social and spiritual needs of patients in the palliative phase of their illness30
A systematic review of classifications systems to determine complexity of patient care needs in palliative care29
Legacy perceptions and interventions for adults and children receiving palliative care: A systematic review28
Mutual support between patients and family caregivers in palliative care: A systematic review and narrative synthesis28
Assessing the impact of COVID-19 on healthcare staff at a combined elderly care and specialist palliative care facility: A cross-sectional study27
Impact of the COVID-19 pandemic on end of life care delivery in care homes: A mixed method systematic review27
The importance of living well now and relationships: A qualitative study of the barriers and enablers to engaging frail elders with advance care planning26
Virtual models of care for people with palliative care needs living in their own home: A systematic meta-review and narrative synthesis26
Early, integrated palliative rehabilitation improves quality of life of patients with newly diagnosed advanced cancer: The Pal-Rehab randomized controlled trial26
Area-Based Compassionate Communities: A systematic integrative review of existing initiatives worldwide25
Invited Editorials25
Paramedics delivering palliative and end-of-life care in community-based settings: A systematic integrative review with thematic synthesis25
Dexmedetomidine for hyperactive delirium at the end of life: An open-label single arm pilot study with dose escalation in adult patients admitted to an inpatient palliative care unit25
The COVID-19 pandemic: A tipping point for advance care planning? Experiences of general practitioners23
How to measure the effects and potential adverse events of palliative sedation? An integrative review23
Web and mobile-based symptom management interventions for physical symptoms of people with advanced cancer: A systematic review and meta-analysis23
How effective is virtual reality technology in palliative care? A systematic review and meta-analysis22
Video-based online interviews for palliative care research: A new normal in COVID-19?21
Real-world ethics in palliative care: A systematic review of the ethical challenges reported by specialist palliative care practitioners in their clinical practice21
The perspectives of children and young people affected by parental life-limiting illness: An integrative review and thematic synthesis21
The effectiveness of hope-fostering interventions in palliative care: A systematic review and meta-analysis20
Effectiveness and implementation of palliative care interventions for patients with chronic obstructive pulmonary disease: A systematic review20
How doctors actually (do not) involve families in decisions to continue or discontinue life-sustaining treatment in neonatal, pediatric, and adult intensive care: A qualitative study19
The impact of public health palliative care interventions on health system outcomes: A systematic review19
Preplanned participation of paramedics in end-of-life care at home: A retrospective cohort study19
Disparities in access to palliative care facilities for patients with and without cancer: A retrospective review19
Efficacy of medicinal cannabis for appetite-related symptoms in people with cancer: A systematic review19
Tools to help healthcare professionals recognize palliative care needs in patients with advanced heart failure: A systematic review18
‘Living in parallel worlds’ – bereaved parents’ experience of family life when a parent with dependent children is at end of life from cancer: A qualitative study18
“Song of Life”: Results of a multicenter randomized trial on the effects of biographical music therapy in palliative care17
It’s almost superstition: If I don’t think about it, it won’t happen’. Public knowledge and attitudes towards advance care planning: A sequential mixed methods study17
Understanding the palliative care needs and experiences of people with mesothelioma and their family carers: An integrative systematic review17
Healthcare professionals’ experiences of inter-professional collaboration during patient’s transfers between care settings in palliative care: A focus group study17
Attitudes and preferences towards palliative and end of life care in patients with advanced illness and their family caregivers in Latin America: A mixed studies systematic review17
Civic engagement in serious illness, death, and loss: A systematic mixed-methods review17
Acceptance and commitment therapy for patient fatigue interference and caregiver burden in advanced gastrointestinal cancer: Results of a pilot randomized trial16
Home or hospital as the place of end-of-life care and death: A grounded theory study of parents’ decision-making16
Gamification for promoting advance care planning: A mixed-method systematic review and meta-analysis16
Machine learning models to detect social distress, spiritual pain, and severe physical psychological symptoms in terminally ill patients with cancer from unstructured text data in electronic medical r16
Bereavement outcomes in family members of those who died in acute care hospitals before and during the first wave of COVID-19: A cohort study16
Inclusion of palliative care in health care policy for older people: A directed documentary analysis in 13 of the most rapidly ageing countries worldwide15
Prevalence of grief disorders in bereaved families of cancer patients: A meta-analysis15
Caregiver-guided pain coping skills training for patients with advanced cancer: Results from a randomized clinical trial15
End-of-life communication strategies for healthcare professionals: A scoping review15
A qualitative study with people with young-onset dementia and their family caregivers on advance care planning: A holistic, flexible, and relational approach is recommended15
Factors associated with health professionals decision to initiate paediatric advance care planning: A systematic integrative review15
Virtual reality for pain management in advanced heart failure: A randomized controlled study15
Single early palliative care intervention added to usual oncology care for patients with advanced cancer: A randomized controlled trial (SENS Trial)15
Effectiveness of two types of palliative home care in cancer and non-cancer patients: A retrospective population-based study using claims data14
Moral distress amongst palliative care doctors working during the COVID-19 pandemic: A narrative-focussed interview study14
Risk factors for delirium in adult patients receiving specialist palliative care: A systematic review and meta-analysis14
Practice review: Evidence-based quality use of corticosteroids in the palliative care of patients with advanced cancer14
End of life care for people with severe mental illness: Mixed methods systematic review and thematic synthesis (the MENLOC study)14
Death doulas as supportive companions in end-of-life care: A scoping review13
Interventions to support family caregivers of people with advanced dementia at the end of life in nursing homes: A mixed-methods systematic review13
Using the Delphi technique to achieve consensus on bereavement care in palliative care in Europe: An EAPC White Paper13
What is the role of paramedics in palliative and end of life care?13
Adaptation and continuous learning: integrative review of coping strategies of palliative care professionals13
Association between religious beliefs and discussions regarding advance care planning: A nationwide survey13
Identifying barriers and facilitators to palliative care integration in the management of hospitalized patients with COVID-19: A qualitative study13
“Hanging in a balance”: A qualitative study exploring clinicians’ experiences of providing care at the end of life in the burn unit13
Understanding the impact of the Covid-19 pandemic on delivery of rehabilitation in specialist palliative care services: An analysis of the CovPall-Rehab survey data13
It’s like standing in front of a prison fence – Dying during the SARS-CoV2 pandemic: A qualitative study of bereaved relatives’ experiences13
Service change and innovation in community end-of-life care during the COVID-19 pandemic: Qualitative analysis of a nationwide primary care survey13
Experiences of transitioning between settings of care from the perspectives of patients with advanced illness receiving specialist palliative care and their family caregivers: A qualitative interview 13
Timely identification of patients in need of palliative care using the Double Surprise Question: A prospective study on outpatients with cancer13
Symptom burden and lived experiences of patients, caregivers and healthcare professionals on the management of malignant bowel obstruction: A qualitative systematic review13
Supporting best practice in reflexive thematic analysis reporting in Palliative Medicine: A review of published research and introduction to the Reflexive Thematic Analysis Reporting Guideli13
Researching minoritised communities in palliative care: An agenda for change13
The experience of delirium in palliative care settings for patients, family, clinicians and volunteers: A qualitative systematic review and thematic synthesis13
What defines the comprehensive assessment of needs in palliative care? An integrative systematic review13
Perceptions and experiences of laws and regulations governing access to opioids in South, Southeast, East and Central Asia: A systematic review, critical interpretative synthesis and development of a 13
Dying in times of COVID-19: Experiences in different care settings – An online questionnaire study among bereaved relatives (the CO-LIVE study)13
Identification of palliative care needs among people with dementia and its association with acute hospital care and community service use at the end-of-life: A retrospective cohort study using linked 12
Virtual home-based palliative care during COVID-19: A qualitative exploration of the patient, caregiver, and healthcare provider experience12
Public health palliative care: Reframing death, dying, loss and caregiving12
Existential suffering in the day to day lives of those living with palliative care needs arising from chronic obstructive pulmonary disease (COPD): A systematic integrative literature review12
Effect of continuous deep sedation on survival in the last days of life of cancer patients: A multicenter prospective cohort study12
Palliative and end-of-life care needs, experiences, and preferences of LGBTQ+ individuals with serious illness: A systematic mixed-methods review12
Is trained communication about desire to die harmful for patients receiving palliative care? A cohort study12
Palliative care for adolescents and young adults with advanced illness: A scoping review12
Navigating the caregiving abyss: A metasynthesis of how family caregivers manage end-of-life care for older adults at home12
Identifying older adults with frailty approaching end-of-life: A systematic review12
End-of-life care after the legal introduction of advance directives: A qualitative study involving healthcare professionals and family caregivers of patients with amyotrophic lateral sclerosis11
An examination and proposed definitions of family members’ grief prior to the death of individuals with a life-limiting illness: A systematic review11
Fatigue in advanced disease associated with palliative care: A systematic review of non-pharmacological treatments11
How can we ensure the success of specialised palliative home-care? A qualitative study (ELSAH) identifying key issues from the perspective of patients, relatives and health professionals11
Do family meetings for hospitalised palliative care patients improve outcomes and reduce health care costs? A cluster randomised trial11
What constitutes a palliative care need in people with serious illnesses across Africa? A mixed-methods systematic review of the concept and evidence11
Smiles behind the masks: A systematic review and narrative synthesis exploring how family members of seriously ill or dying patients are supported during infectious disease outbreaks11
A qualitative service evaluation of patient and caregiver experiences of CAR-T therapy: Recommendations for service development and implications for palliative care teams11
‘Traversing difficult terrain’. Advance care planning in residential aged care through multidisciplinary case conferences: A qualitative interview study exploring the experiences of families, staff an11
The benefits and challenges of embedding specialist palliative care teams within homeless hostels to enhance support and learning: Perspectives from palliative care teams and hostel staff11
Culture in the spotlight—cultural adaptation and content validity of the integrated palliative care outcome scale for dementia: A cognitive interview study11
COP27 Climate Change Conference: Urgent action needed for Africa and the world11
The promise of big data for palliative and end-of-life care research10
Using advance and emergency care plans during transfer decisions: A grounded theory interview study with care home staff10
Organizational and individual barriers and facilitators to the integration of pediatric palliative care for children: A grounded theory study10
Identifying, exploring and integrating the spiritual dimension in proactive care planning: A mixed methods evaluation of a communication training intervention for multidisciplinary palliative care tea10
‘It feels it’s wasting whatever time I’ve got left’: A qualitative study of living with treatable but not curable cancer during the COVID-19 pandemic10
The Me in We dyadic communication intervention is feasible and acceptable among advanced cancer patients and their family caregivers10
Addressing inequity in palliative care provision for older people living with multimorbidity. Perspectives of community-dwelling older people on their palliative care needs: A scoping review10
The impact on emotional well-being of being a palliative care volunteer: An interpretative phenomenological analysis10
Determining massage dose-response to improve cancer-related symptom cluster of pain, fatigue, and sleep disturbance: A 7-arm randomized trial in palliative cancer care10
Practice review: Evidence-based and effective management of fatigue in patients with advanced cancer10
The use of natural language processing in palliative care research: A scoping review10
Assessment tools for problematic opioid use in palliative care: A scoping review10
Pharmacological strategies used to manage symptoms of patients dying of COVID-19: A rapid systematic review10
Spiritual, religious, and existential concerns of children and young people with life-limiting and life-threatening conditions: A qualitative interview study10
LGBT+ partner bereavement and appraisal of the Acceptance-Disclosure Model of LGBT+ bereavement: A qualitative interview study10
Patient perspectives on states worse than death: A qualitative study with implications for patient-centered outcomes and values elicitation10
Development and validation of a prediction model of poor performance status and severe symptoms over time in cancer patients (PROVIEW+)9
Perspectives of board-certified healthcare chaplains on challenges and adaptations in delivery of spiritual care in the COVID-19 era: Findings from an online survey9
Improved quality of care and reduced healthcare costs at the end-of-life among older people with dementia who received palliative home care: A nationwide propensity score-matched decedent cohort study9
A rapid review of end-of-life needs in the LGBTQ+ community and recommendations for clinicians9
‘You can’t feel what we feel’: Multifaceted dyspnoea invisibility in advanced chronic obstructive pulmonary disease examined through interpretative phenomenological analysis9
Practice review: Evidence-based and effective management of anaemia in palliative care patients9
Delirium screening tools validated in the context of palliative care: A systematic review9
Bereaved relatives’ quality of life before and during the COVID-19 pandemic: Results of the prospective, multicenter, observational eQuiPe study9
Specialist palliative care staff’s varying experiences of talking with people with intellectual disability about their dying and death: A thematic analysis of in-depth interviews9
Do learners implement what they learn? Commitment-to-change following an interprofessional palliative care course9
Cannabinoids for the treatment of refractory neuropathic pruritus in amyotrophic lateral sclerosis: A case report9
Hearing the voices of children diagnosed with a life-threatening or life-limiting illness and their parents’ accounts in a palliative care setting: A qualitative study9
What does effective end-of-life care at home for children look like? A qualitative interview study exploring the perspectives of bereaved parents9
Care practices of specialized outpatient pediatric palliative care teams in collaboration with parents: Results of participatory observations9
Health care professionals’ perceptions of factors influencing the process of identifying patients for serious illness conversations: A qualitative study9
Compounded trauma: A qualitative study of the challenges for refugees living with advanced cancer9
Palliative care needs and experiences of people in prison: A systematic review and meta-synthesis9
Pain assessment tools in paediatric palliative care: A systematic review of psychometric properties and recommendations for clinical practice9
End-of-life cost trajectories and the trade-off between treatment costs and life-extension: Findings from the Cost and Medical Care of Patients with Advanced Serious Illness (COMPASS) cohort study9
It was like taking an inner bath’: A qualitative evaluation of a collaborative advance care planning-approach9
‘Sadly I think we are sort of still quite white, middle-class really’ – Inequities in access to bereavement support: Findings from a mixed methods study8
Trends of concerns from diagnosis in patients with advanced lung cancer and their family caregivers: A 2-year longitudinal study8
Facilitating family needs and support at the end of life in hospital: A descriptive study8
Willingness and concerns of transfusion-dependent hematological patients toward the option of home transfusion therapy8
Development of guidelines to reduce, handle and report missing data in palliative care trials: A multi-stakeholder modified nominal group technique8
COVID-19: Challenges and solutions for the provision of care to seriously ill and dying people and their relatives during SARS-CoV-2 pandemic – perspectives of pandemic response team members: A qualit8
A feasibility study of a decision aid to support family carers of people with severe dementia or those towards the end-of-life8
Comparing the effect of a consult model versus an integrated palliative care and medical oncology co-rounding model on health care utilization in an acute hospital – an open-label stepped-wedge cluste8
Intranasal dexmedetomidine: Procedural sedation in palliative care: A case report8
Exploring expanded interdisciplinary roles in goals of care conversations in a national goals of care initiative: A qualitative approach8
Making the best of multidisciplinary care for patients with malignant fungating wounds: A qualitative study of clinicians’ narratives8
Creating ‘safe spaces’: A qualitative study to explore enablers and barriers to culturally safe end-of-life care8
Medical communication and decision-making about assisted hydration in the last days of life: A qualitative study of doctors experienced with end of life care8
Exploring the prevalence, impact and experience of cardiac cachexia in patients with advanced heart failure and their caregivers: A sequential phased study8
Opportunities for public involvement in big data research in palliative and end-of-life care8
‘It’s not just all about the fancy words and the adults’: Recommendations for practice from a qualitative interview study with children and young people with a parent with a life-limiting illness8
Abstracts from the 17th World Congress of the EAPC 20218
Paramedics’ experiences and educational needs when participating end-of-life care at home: A mixed method study8
Measures of financial burden for families dealing with serious illness: A systematic review and analysis8
Communication in the context of glioblastoma treatment: A qualitative study of what matters most to patients, caregivers and health care professionals8
Implementation of an acute palliative care unit for COVID-19 patients in a tertiary hospital: Qualitative data on clinician perspectives8
Clinicians’ delirium treatment practice, practice change, and influences: A national online survey8
Timely short-term specialized palliative care service intervention for older people with frailty and their family carers in primary care: Development and modelling of the frailty+ intervention using t8
Co-designing Community Out-of-hours Palliative Care Services: A systematic literature search and review7
How is community based ‘out-of-hours’ care provided to patients with advanced illness near the end of life: A systematic review of care provision7
The impact of digital health interventions on the psychological outcomes of patients and families receiving paediatric palliative care: A systematic review and narrative synthesis7
Closing the health equity gap in palliative care: The time for action is now7
Over a third of palliative medicine physicians meet burnout criteria: Results from a survey study during the COVID-19 pandemic7
Monitoring nociception and awareness during palliative sedation: A systematic review7
‘Mum, I think we might ring the ambulance, okay?’ A qualitative exploration of bereaved family members’ experiences of emergency ambulance care at the end of life7
Preferences of patients with palliative care needs and their families for engagement with service improvement work within the hospital setting: A qualitative study7
Understanding advance care planning in care homes throughout the COVID-19 pandemic: A critical realist review and synthesis7
Revised European Association for Palliative Care (EAPC) recommended framework on palliative sedation: An international Delphi study7
A meta-ethnographic study of fathers’ experiences of caring for a child with a life-limiting illness7
Face and content validity, acceptability, feasibility, and implementability of a novel outcome measure for children with life-limiting or life-threatening illness in three sub-Saharan African countrie7
The monetary valuation of informal care to cancer decedents at end-of-life: Evidence from a national census survey7
Unwelcome memento mori or best clinical practice? Community end of life anticipatory medication prescribing practice: A mixed methods observational study7
Palliative paramedicine: Comparing clinical practice through guideline quality appraisal and qualitative content analysis7
Perspectives on COVID-19 and palliative care research7
Parenting through grief: A cross-sectional study of recently bereaved adults with minor children7
The ‘work’ of managing medications when someone is seriously ill and dying at home: A longitudinal qualitative case study of patient and family perspectives’7
Factors associated with hospitalisations of patients with chronic heart failure approaching the end of life: A systematic review6
Health and social care services for people with dementia at home at the end of life: A qualitative study of bereaved informal caregivers’ experiences6
The range and suitability of outcome measures used in the assessment of palliative treatment for inoperable malignant bowel obstruction: A systematic review6
‘It was like an airbag, it cushioned the blow’: A multi-site qualitative study of bereaved parents’ experiences of using cooling facilities6
Advance care planning and end-of-life care in patients with an implantable cardioverter defibrillator: The perspective of relatives6
‘Life became slow down’: A descriptive qualitative study of the experiences of cancer-related fatigue amongst people with advanced lung cancer6
Updating international consensus on best practice in care of the dying: A Delphi study6
‘You have a little human being kicking inside you and an unbearable pain of knowing there will be a void at the end’: A meta-ethnography exploring the experience of parents whose baby is diagnosed ant6
A therapist-supported internet-based intervention for bereaved siblings: A randomized controlled trial6
A good death in the child with life shortening illness: A qualitative multiple-case study6
Early resuscitation orders in hospitalized oldest-old with COVID-19: A multicenter cohort study6
Capturing what matters: A retrospective observational study of advance care planning documentation at an academic medical center during the COVID-19 pandemic6
Researching Compassionate Communities: Identifying theoretical frameworks to evaluate the complex processes behind public health palliative care initiatives6
Effects of a theory-based advance care planning intervention for nursing homes: A cluster randomized controlled trial6
A systematic review of quality improvement initiatives for continuous sedation until death6
Which factors influence the quality of end-of-life care in interstitial lung disease? A systematic review with narrative synthesis6
The most important components of out-of-hours community care for patients at the end of life: A Delphi study of healthcare professionals’ and patient and family carers’ perspectives6
The importance of methodology to palliative care research: A new article type for Palliative Medicine6
The health of mothers of children with a life-limiting condition: A qualitative interview study6
Caring precariously: An interpretive description of palliative care and welfare worker perspectives on end of life carers navigating social welfare6
Impact of physician-based palliative care delivery models on health care utilization outcomes: A population-based retrospective cohort study6
EAPC2023 Abstract Book6
Understanding parent experiences of end-of-life care for children: A systematic review and qualitative evidence synthesis6
Barriers and facilitators for parents in end-of-life decision-making for neonates at the Neonatal Intensive Care Unit: A qualitative study6
Investigating the benefits and harms of hypodermoclysis of patients in palliative care: A consecutive cohort study6
The effects of confronting one’s own end of life on older individuals and those with a life-threatening disease: A systematic literature review6
Description of patient reported experience measures (PREMs) for hospitalised patients with palliative care needs and their families, and how these map to noted areas of importance for quality care: A 6
Trends in quality of care and dying perceived by family caregivers of nursing home residents with dementia 2005–20196
‘Cold bedrooms’ and other cooling facilities in UK children’s hospices, how they are used and why they are offered: A mixed methods study6
Development and psychometric validation of the family-centered multidimensional outcome measure for pediatric palliative care targeted to children with severe neurological impairmentis—A multicenter p6
The spiritual dimension of parenting a child with a life-limiting or life-threatening condition: A mixed-methods systematic review6
Communication in palliative care during the COVID-19 pandemic: Lessons from rapidly changing, uncertain, complex, and high-stake interventions6
What makes the palliative care initial encounter meaningful? A descriptive study with patients with cancer, family carers and palliative care professionals5
Existential experiences and perceptions of death among children with terminal cancer: An interpretative qualitative study5
Palliative care needs and models of care for people who use drugs and/or alcohol: A mixed methods systematic review5
‘There’s something about admitting that you are lonely’ – prevalence, impact and solutions to loneliness in terminal illness: An explanatory sequential multi-methods study5
Palliative care volunteering: Pressing challenges in research5
Neuropalliative care for progressive neurological diseases: A scoping review on models of care and priorities for future research5
Opportunities for computational tools in palliative care: Supporting patient needs and lowering burden5
Sleeping-related distress in a palliative care population: A national, prospective, consecutive cohort5
Paracentesis for cancer-related ascites in palliative care: An international, prospective cohort study5
Caring, sharing, preparing and declaring: how do hospices support prisons to provide palliative and end of life care? A qualitative descriptive study using telephone interviews5
Measuring quality of dying, death and end-of-life care for children and young people: A scoping review of available tools5
How to enhance advance care planning research?5
Motivations and experiences of patients with advanced cancer participating in Phase 1 clinical trials: A qualitative study5
General practitioners’ evaluations of optimal timing to initiate advance care planning for patients with cancer, organ failure, or multimorbidity: A health records survey study5
Assessing the impact of a health navigator on improving access to care and addressing the social needs of palliative care patients experiencing homelessness: A service evaluation5
Sexual health and closeness in couples coping with advanced cancer: Results of a multicenter observational study (eQuiPe)5
Validation of the responding to urgency of need in palliative care (RUN-PC) triage tool5
Inadequate human resources, equipment and training: A qualitative assessment of the objectives of the NUHELP end-of-life care programme in the context of the COVID-19 pandemic5
Eliciting the educational needs and priorities of home care workers on end-of-life care for patients with heart failure using nominal group technique5
0.10625982284546