Palliative Medicine

Article	Citations
A qualitative study of bereaved relatives’ end of life experiences during the COVID-19 pandemic	105
Estimating the current and future prevalence of life-limiting conditions in children in England	88
‘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)	70
Health and social care professionals’ experiences of providing end of life care during the COVID-19 pandemic: A qualitative study	65
Sadness, despair and anger when a patient dies alone from COVID-19: A thematic content analysis of Twitter data from bereaved family members and friends	49
Revised recommendations on standards and norms for palliative care in Europe from the European Association for Palliative Care (EAPC): A Delphi study	48
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 pandemic	44
Changes in mortality patterns and place of death during the COVID-19 pandemic: A descriptive analysis of mortality data across four nations	43
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
Defining end of life in dementia: A systematic review	41
Missing the human connection: A rapid appraisal of healthcare workers’ perceptions and experiences of providing palliative care during the COVID-19 pandemic	40
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 pandemic	38
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 services	37
Asian patients’ perspectives on advance care planning: A mixed-method systematic review and conceptual framework	36
‘Saying goodbye’ during the COVID-19 pandemic: A document analysis of online newspapers with implications for end of life care	35
Lessons from the COVID-19 pandemic for improving outpatient neuropalliative care: A qualitative study of patient and caregiver perspectives	35
The role, impact, and support of informal caregivers in the delivery of palliative care for patients with advanced cancer: A multi-country qualitative study	34
Resilience in advanced cancer caregiving. A systematic review and meta-synthesis	33
Family involvement in advance care planning for people living with advanced cancer: A systematic mixed-methods review	33
Support needs and barriers to accessing support: Baseline results of a mixed-methods national survey of people bereaved during the COVID-19 pandemic	31
The utility of the surprise question: A useful tool for identifying patients nearing the last phase of life? A systematic review and meta-analysis	31
Home palliative care professionals perception of challenges during the Covid-19 outbreak: A qualitative study	31
Toward a socio-spiritual approach? A mixed-methods systematic review on the social and spiritual needs of patients in the palliative phase of their illness	30
Implementing person-centred outcome measures in palliative care: An exploratory qualitative study using Normalisation Process Theory to understand processes and context	30
Mutual support between patients and family caregivers in palliative care: A systematic review and narrative synthesis	29

A systematic review of classifications systems to determine complexity of patient care needs in palliative care	29
Legacy perceptions and interventions for adults and children receiving palliative care: A systematic review	28
Impact of the COVID-19 pandemic on end of life care delivery in care homes: A mixed method systematic review	28
Early, integrated palliative rehabilitation improves quality of life of patients with newly diagnosed advanced cancer: The Pal-Rehab randomized controlled trial	27
Assessing the impact of COVID-19 on healthcare staff at a combined elderly care and specialist palliative care facility: A cross-sectional study	27
Virtual models of care for people with palliative care needs living in their own home: A systematic meta-review and narrative synthesis	26
Paramedics delivering palliative and end-of-life care in community-based settings: A systematic integrative review with thematic synthesis	26
The importance of living well now and relationships: A qualitative study of the barriers and enablers to engaging frail elders with advance care planning	26
Invited Editorials	26
Area-Based Compassionate Communities: A systematic integrative review of existing initiatives worldwide	25
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 unit	25
How to measure the effects and potential adverse events of palliative sedation? An integrative review	23
Web and mobile-based symptom management interventions for physical symptoms of people with advanced cancer: A systematic review and meta-analysis	23
The COVID-19 pandemic: A tipping point for advance care planning? Experiences of general practitioners	23
How effective is virtual reality technology in palliative care? A systematic review and meta-analysis	22
The perspectives of children and young people affected by parental life-limiting illness: An integrative review and thematic synthesis	21
Real-world ethics in palliative care: A systematic review of the ethical challenges reported by specialist palliative care practitioners in their clinical practice	21
Video-based online interviews for palliative care research: A new normal in COVID-19?	21
Effectiveness and implementation of palliative care interventions for patients with chronic obstructive pulmonary disease: A systematic review	20
The effectiveness of hope-fostering interventions in palliative care: A systematic review and meta-analysis	20
Disparities in access to palliative care facilities for patients with and without cancer: A retrospective review	19
Efficacy of medicinal cannabis for appetite-related symptoms in people with cancer: A systematic review	19
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 study	19
The impact of public health palliative care interventions on health system outcomes: A systematic review	19
Preplanned participation of paramedics in end-of-life care at home: A retrospective cohort study	19
“Song of Life”: Results of a multicenter randomized trial on the effects of biographical music therapy in palliative care	18
‘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 study	18
‘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 study	18
Understanding the palliative care needs and experiences of people with mesothelioma and their family carers: An integrative systematic review	17
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 r	17
Civic engagement in serious illness, death, and loss: A systematic mixed-methods review	17
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 review	17
Bereavement outcomes in family members of those who died in acute care hospitals before and during the first wave of COVID-19: A cohort study	17
End-of-life communication strategies for healthcare professionals: A scoping review	16
Gamification for promoting advance care planning: A mixed-method systematic review and meta-analysis	16
Acceptance and commitment therapy for patient fatigue interference and caregiver burden in advanced gastrointestinal cancer: Results of a pilot randomized trial	16
Home or hospital as the place of end-of-life care and death: A grounded theory study of parents’ decision-making	16
Virtual reality for pain management in advanced heart failure: A randomized controlled study	16
Factors associated with health professionals decision to initiate paediatric advance care planning: A systematic integrative review	15
Inclusion of palliative care in health care policy for older people: A directed documentary analysis in 13 of the most rapidly ageing countries worldwide	15
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	15
Single early palliative care intervention added to usual oncology care for patients with advanced cancer: A randomized controlled trial (SENS Trial)	15
Risk factors for delirium in adult patients receiving specialist palliative care: A systematic review and meta-analysis	15
Moral distress amongst palliative care doctors working during the COVID-19 pandemic: A narrative-focussed interview study	15
Caregiver-guided pain coping skills training for patients with advanced cancer: Results from a randomized clinical trial	15
A qualitative study with people with young-onset dementia and their family caregivers on advance care planning: A holistic, flexible, and relational approach is recommended	15
Prevalence of grief disorders in bereaved families of cancer patients: A meta-analysis	15
What is the role of paramedics in palliative and end of life care?	14
End of life care for people with severe mental illness: Mixed methods systematic review and thematic synthesis (the MENLOC study)	14
Interventions to support family caregivers of people with advanced dementia at the end of life in nursing homes: A mixed-methods systematic review	14

Using the Delphi technique to achieve consensus on bereavement care in palliative care in Europe: An EAPC White Paper	14
Identifying barriers and facilitators to palliative care integration in the management of hospitalized patients with COVID-19: A qualitative study	14
Practice review: Evidence-based quality use of corticosteroids in the palliative care of patients with advanced cancer	14
The experience of delirium in palliative care settings for patients, family, clinicians and volunteers: A qualitative systematic review and thematic synthesis	14
Virtual home-based palliative care during COVID-19: A qualitative exploration of the patient, caregiver, and healthcare provider experience	14
Effectiveness of two types of palliative home care in cancer and non-cancer patients: A retrospective population-based study using claims data	14
Researching minoritised communities in palliative care: An agenda for change	13
Identifying older adults with frailty approaching end-of-life: A systematic review	13
Service change and innovation in community end-of-life care during the COVID-19 pandemic: Qualitative analysis of a nationwide primary care survey	13
Association between religious beliefs and discussions regarding advance care planning: A nationwide survey	13
Timely identification of patients in need of palliative care using the Double Surprise Question: A prospective study on outpatients with cancer	13
“Hanging in a balance”: A qualitative study exploring clinicians’ experiences of providing care at the end of life in the burn unit	13
Understanding the impact of the Covid-19 pandemic on delivery of rehabilitation in specialist palliative care services: An analysis of the CovPall-Rehab survey data	13
Adaptation and continuous learning: integrative review of coping strategies of palliative care professionals	13
Dying in times of COVID-19: Experiences in different care settings – An online questionnaire study among bereaved relatives (the CO-LIVE study)	13
Supporting best practice in reflexive thematic analysis reporting in Palliative Medicine: A review of published research and introduction to the Reflexive Thematic Analysis Reporting Guideli	13
Death doulas as supportive companions in end-of-life care: A scoping review	13
It’s like standing in front of a prison fence – Dying during the SARS-CoV2 pandemic: A qualitative study of bereaved relatives’ experiences	13
What defines the comprehensive assessment of needs in palliative care? An integrative systematic review	13
Symptom burden and lived experiences of patients, caregivers and healthcare professionals on the management of malignant bowel obstruction: A qualitative systematic review	13
A qualitative service evaluation of patient and caregiver experiences of CAR-T therapy: Recommendations for service development and implications for palliative care teams	12
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 review	12
Palliative care for adolescents and young adults with advanced illness: A scoping review	12
Navigating the caregiving abyss: A metasynthesis of how family caregivers manage end-of-life care for older adults at home	12
Palliative and end-of-life care needs, experiences, and preferences of LGBTQ+ individuals with serious illness: A systematic mixed-methods review	12
Public health palliative care: Reframing death, dying, loss and caregiving	12
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 staff	12
Culture in the spotlight—cultural adaptation and content validity of the integrated palliative care outcome scale for dementia: A cognitive interview study	12
Effect of continuous deep sedation on survival in the last days of life of cancer patients: A multicenter prospective cohort study	12
Is trained communication about desire to die harmful for patients receiving palliative care? A cohort study	12
What constitutes a palliative care need in people with serious illnesses across Africa? A mixed-methods systematic review of the concept and evidence	12
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
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 review	11
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 outbreaks	11
COP27 Climate Change Conference: Urgent action needed for Africa and the world	11
‘Traversing difficult terrain’. Advance care planning in residential aged care through multidisciplinary case conferences: A qualitative interview study exploring the experiences of families, staff an	11
An examination and proposed definitions of family members’ grief prior to the death of individuals with a life-limiting illness: A systematic review	11
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 professionals	11
Assessment tools for problematic opioid use in palliative care: A scoping review	11
Fatigue in advanced disease associated with palliative care: A systematic review of non-pharmacological treatments	11
Practice review: Evidence-based and effective management of fatigue in patients with advanced cancer	11
The promise of big data for palliative and end-of-life care research	10
The Me in We dyadic communication intervention is feasible and acceptable among advanced cancer patients and their family caregivers	10
Spiritual, religious, and existential concerns of children and young people with life-limiting and life-threatening conditions: A qualitative interview study	10
Determining massage dose-response to improve cancer-related symptom cluster of pain, fatigue, and sleep disturbance: A 7-arm randomized trial in palliative cancer care	10
Patient perspectives on states worse than death: A qualitative study with implications for patient-centered outcomes and values elicitation	10
Using advance and emergency care plans during transfer decisions: A grounded theory interview study with care home staff	10
Pharmacological strategies used to manage symptoms of patients dying of COVID-19: A rapid systematic review	10
The impact on emotional well-being of being a palliative care volunteer: An interpretative phenomenological analysis	10
‘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 pandemic	10
The use of natural language processing in palliative care research: A scoping review	10
Identifying, exploring and integrating the spiritual dimension in proactive care planning: A mixed methods evaluation of a communication training intervention for multidisciplinary palliative care tea	10
Organizational and individual barriers and facilitators to the integration of pediatric palliative care for children: A grounded theory study	10
LGBT+ partner bereavement and appraisal of the Acceptance-Disclosure Model of LGBT+ bereavement: A qualitative interview study	10
Development and validation of a prediction model of poor performance status and severe symptoms over time in cancer patients (PROVIEW+)	9
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 interviews	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 survey	9
Palliative care needs and experiences of people in prison: A systematic review and meta-synthesis	9
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 cluste	9
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 study	9
Pain assessment tools in paediatric palliative care: A systematic review of psychometric properties and recommendations for clinical practice	9
Delirium screening tools validated in the context of palliative care: A systematic review	9
Care practices of specialized outpatient pediatric palliative care teams in collaboration with parents: Results of participatory observations	9
Compounded trauma: A qualitative study of the challenges for refugees living with advanced cancer	9
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 study	9
A rapid review of end-of-life needs in the LGBTQ+ community and recommendations for clinicians	9
‘You can’t feel what we feel’: Multifaceted dyspnoea invisibility in advanced chronic obstructive pulmonary disease examined through interpretative phenomenological analysis	9
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 study	9
Cannabinoids for the treatment of refractory neuropathic pruritus in amyotrophic lateral sclerosis: A case report	9
What does effective end-of-life care at home for children look like? A qualitative interview study exploring the perspectives of bereaved parents	9
Bereaved relatives’ quality of life before and during the COVID-19 pandemic: Results of the prospective, multicenter, observational eQuiPe study	9
Health care professionals’ perceptions of factors influencing the process of identifying patients for serious illness conversations: A qualitative study	9
Do learners implement what they learn? Commitment-to-change following an interprofessional palliative care course	9
Trends of concerns from diagnosis in patients with advanced lung cancer and their family caregivers: A 2-year longitudinal study	9
Facilitating family needs and support at the end of life in hospital: A descriptive study	9
Practice review: Evidence-based and effective management of anaemia in palliative care patients	9
‘It was like taking an inner bath’: A qualitative evaluation of a collaborative advance care planning-approach	9
Paramedics’ experiences and educational needs when participating end-of-life care at home: A mixed method study	8
Abstracts from the 17th World Congress of the EAPC 2021	8
Creating ‘safe spaces’: A qualitative study to explore enablers and barriers to culturally safe end-of-life care	8

Development of guidelines to reduce, handle and report missing data in palliative care trials: A multi-stakeholder modified nominal group technique	8
Medical communication and decision-making about assisted hydration in the last days of life: A qualitative study of doctors experienced with end of life care	8
Clinicians’ delirium treatment practice, practice change, and influences: A national online survey	8
‘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 illness	8
Opportunities for public involvement in big data research in palliative and end-of-life care	8
Exploring expanded interdisciplinary roles in goals of care conversations in a national goals of care initiative: A qualitative approach	8
Willingness and concerns of transfusion-dependent hematological patients toward the option of home transfusion therapy	8
Communication in the context of glioblastoma treatment: A qualitative study of what matters most to patients, caregivers and health care professionals	8
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 qualit	8
Exploring the prevalence, impact and experience of cardiac cachexia in patients with advanced heart failure and their caregivers: A sequential phased study	8
Palliative paramedicine: Comparing clinical practice through guideline quality appraisal and qualitative content analysis	8
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 t	8
Intranasal dexmedetomidine: Procedural sedation in palliative care: A case report	8
Measures of financial burden for families dealing with serious illness: A systematic review and analysis	8
Implementation of an acute palliative care unit for COVID-19 patients in a tertiary hospital: Qualitative data on clinician perspectives	8
A feasibility study of a decision aid to support family carers of people with severe dementia or those towards the end-of-life	8
‘Sadly I think we are sort of still quite white, middle-class really’ – Inequities in access to bereavement support: Findings from a mixed methods study	8
Understanding advance care planning in care homes throughout the COVID-19 pandemic: A critical realist review and synthesis	7
Monitoring nociception and awareness during palliative sedation: A systematic review	7
Revised European Association for Palliative Care (EAPC) recommended framework on palliative sedation: An international Delphi study	7
‘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 life	7
Co-designing Community Out-of-hours Palliative Care Services: A systematic literature search and review	7
Preferences of patients with palliative care needs and their families for engagement with service improvement work within the hospital setting: A qualitative study	7
Closing the health equity gap in palliative care: The time for action is now	7
The impact of digital health interventions on the psychological outcomes of patients and families receiving paediatric palliative care: A systematic review and narrative synthesis	7
Evidence-based management approaches for patients with severe chronic obstructive pulmonary disease (COPD): A practice review	7
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
Parenting through grief: A cross-sectional study of recently bereaved adults with minor children	7
The monetary valuation of informal care to cancer decedents at end-of-life: Evidence from a national census survey	7
How is community based ‘out-of-hours’ care provided to patients with advanced illness near the end of life: A systematic review of care provision	7
Researching Compassionate Communities: Identifying theoretical frameworks to evaluate the complex processes behind public health palliative care initiatives	7
Perspectives on COVID-19 and palliative care research	7
Over a third of palliative medicine physicians meet burnout criteria: Results from a survey study during the COVID-19 pandemic	7
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 countrie	7
Updating international consensus on best practice in care of the dying: A Delphi study	7
Factors associated with hospitalisations of patients with chronic heart failure approaching the end of life: A systematic review	7
A meta-ethnographic study of fathers’ experiences of caring for a child with a life-limiting illness	7
Unwelcome memento mori or best clinical practice? Community end of life anticipatory medication prescribing practice: A mixed methods observational study	7
Effects of a theory-based advance care planning intervention for nursing homes: A cluster randomized controlled trial	7
Advance care planning and end-of-life care in patients with an implantable cardioverter defibrillator: The perspective of relatives	7
‘It was like an airbag, it cushioned the blow’: A multi-site qualitative study of bereaved parents’ experiences of using cooling facilities	6
‘There’s something about admitting that you are lonely’ – prevalence, impact and solutions to loneliness in terminal illness: An explanatory sequential multi-methods study	6
Which factors influence the quality of end-of-life care in interstitial lung disease? A systematic review with narrative synthesis	6
‘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 ant	6
A good death in the child with life shortening illness: A qualitative multiple-case study	6
Eliciting the educational needs and priorities of home care workers on end-of-life care for patients with heart failure using nominal group technique	6
A grounded theory study exploring palliative care healthcare professionals’ experiences of managing digital legacy as part of advance care planning for people receiving palliative care	6
Communication in palliative care during the COVID-19 pandemic: Lessons from rapidly changing, uncertain, complex, and high-stake interventions	6
The association between ethnicity, socioeconomic deprivation and receipt of hospital-based palliative care for people with Covid-19: A dual centre service evaluation	6
Understanding parent experiences of end-of-life care for children: A systematic review and qualitative evidence synthesis	6
Health and social care services for people with dementia at home at the end of life: A qualitative study of bereaved informal caregivers’ experiences	6
The effects of confronting one’s own end of life on older individuals and those with a life-threatening disease: A systematic literature review	6
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’ perspectives	6
The importance of methodology to palliative care research: A new article type for Palliative Medicine	6
The health of mothers of children with a life-limiting condition: A qualitative interview study	6
‘Cold bedrooms’ and other cooling facilities in UK children’s hospices, how they are used and why they are offered: A mixed methods study	6
EAPC2023 Abstract Book	6
“Once you open that door, it’s a floodgate”: Exploring work-related grief among community service workers providing care for structurally vulnerable populations at the end of life through parti	6
Capturing what matters: A retrospective observational study of advance care planning documentation at an academic medical center during the COVID-19 pandemic	6
Investigating the benefits and harms of hypodermoclysis of patients in palliative care: A consecutive cohort study	6
A systematic review of quality improvement initiatives for continuous sedation until death	6
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 2005–2019	6
The spiritual dimension of parenting a child with a life-limiting or life-threatening condition: A mixed-methods systematic review	6
A therapist-supported internet-based intervention for bereaved siblings: A randomized controlled trial	6
Development and psychometric validation of the family-centered multidimensional outcome measure for pediatric palliative care targeted to children with severe neurological impairmentis—A multicenter p	6
Impact of physician-based palliative care delivery models on health care utilization outcomes: A population-based retrospective cohort study	6
Early resuscitation orders in hospitalized oldest-old with COVID-19: A multicenter cohort study	6
Examining the course of transitions from hospital to home-based palliative care: A mixed methods study	6
The range and suitability of outcome measures used in the assessment of palliative treatment for inoperable malignant bowel obstruction: A systematic review	6
Barriers and facilitators for parents in end-of-life decision-making for neonates at the Neonatal Intensive Care Unit: A qualitative study	6
Paracentesis for cancer-related ascites in palliative care: An international, prospective cohort study	5
Existential experiences and perceptions of death among children with terminal cancer: An interpretative qualitative study	5
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 pandemic	5
Implementation of clinical guidelines in specialized palliative care—results from a national improvement project: A national register-based study	5
Palliative care volunteering: Pressing challenges in research	5
Neuropalliative care for progressive neurological diseases: A scoping review on models of care and priorities for future research	5
The connections of physical and psychosocial symptoms among patients with terminal illnesses: A network analysis	5
What makes the palliative care initial encounter meaningful? A descriptive study with patients with cancer, family carers and palliative care professionals	5
General practitioners’ evaluations of optimal timing to initiate advance care planning for patients with cancer, organ failure, or multimorbidity: A health records survey study	5
Caring, sharing, preparing and declaring: how do hospices support prisons to provide palliative and end of life care? A qualitative descriptive study using telephone interviews	5
Measuring quality of dying, death and end-of-life care for children and young people: A scoping review of available tools	5
How to enhance advance care planning research?	5
Motivations and experiences of patients with advanced cancer participating in Phase 1 clinical trials: A qualitative study	5
Opportunities for computational tools in palliative care: Supporting patient needs and lowering burden	5
End of life care for long-term neurological conditions: A meta-ethnographic review of the experiences of informal carers	5
Turkish imams and their role in decision-making in palliative care: A Directed Content and Narrative analysis	5
Sleeping-related distress in a palliative care population: A national, prospective, consecutive cohort	5
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 evaluation	5
Palliative care needs and models of care for people who use drugs and/or alcohol: A mixed methods systematic review	5
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 tool	5
Health professionals’ experiences of rapport during telehealth encounters in community palliative care: An interpretive description study	5
Why does palliative care need to consider access and care for LGBTQ people?	5
“I think that she would have wanted. . .”: Qualitative interviews with bereaved caregivers reveal complexity in measuring goal-concordant care at the end of life	5