Palliative Medicine

Article	Citations
Response and role of palliative care during the COVID-19 pandemic: A national telephone survey of hospices in Italy	97
A qualitative study of bereaved relatives’ end of life experiences during the COVID-19 pandemic	91
‘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)	63
Estimating the current and future prevalence of life-limiting conditions in children in England	60
Health and social care professionals’ experiences of providing end of life care during the COVID-19 pandemic: A qualitative study	52
Prevalence of burnout in healthcare professionals providing palliative care and the effect of interventions to reduce symptoms: A systematic literature review	49
Identification of patients with potential palliative care needs: A systematic review of screening tools in primary care	48
Changing patterns of mortality during the COVID-19 pandemic: Population-based modelling to understand palliative care implications	47
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	45
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	42
Prioritising workforce wellbeing and resilience: What COVID-19 is reminding us about self-care and staff support	41
COVID-19 and Hospital Palliative Care – A service evaluation exploring the symptoms and outcomes of 186 patients and the impact of the pandemic on specialist Hospital Palliative Care	40
Nursing competencies across different levels of palliative care provision: A systematic integrative review with thematic synthesis	40
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)	38
What elements of a systems’ approach to bereavement are most effective in times of mass bereavement? A narrative systematic review with lessons for COVID-19	37
Changes in mortality patterns and place of death during the COVID-19 pandemic: A descriptive analysis of mortality data across four nations	37
The role and response of primary healthcare services in the delivery of palliative care in epidemics and pandemics: A rapid review to inform practice and service delivery during the COVID-19 pandemic	36
Missing the human connection: A rapid appraisal of healthcare workers’ perceptions and experiences of providing palliative care during the COVID-19 pandemic	34
Nursing education on palliative care across Europe: Results and recommendations from the EAPC Taskforce on preparation for practice in palliative care nursing across the EU based on an online-survey a	33
Lessons from the COVID-19 pandemic for improving outpatient neuropalliative care: A qualitative study of patient and caregiver perspectives	33
The support needs of parent caregivers of children with a life-limiting illness and approaches used to meet their needs: A scoping review	33
Asian patients’ perspectives on advance care planning: A mixed-method systematic review and conceptual framework	32
Specialist paediatric palliative care for children and young people with cancer: A mixed-methods systematic review	32
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	32
The burden of serious health-related suffering among cancer decedents: Global projections study to 2060	31

‘Saying goodbye’ during the COVID-19 pandemic: A document analysis of online newspapers with implications for end of life care	31
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	30
The impacts and effectiveness of support for people bereaved through advanced illness: A systematic review and thematic synthesis	30
Impact of Medical Assistance in Dying on palliative care: A qualitative study	29
Defining end of life in dementia: A systematic review	29
Nurses’ self-efficacy, rather than their knowledge, is associated with their engagement in advance care planning in nursing homes: A survey study	29
Home palliative care professionals perception of challenges during the Covid-19 outbreak: A qualitative study	28
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	27
Trends analysis of specialized palliative care services in 51 countries of the WHO European region in the last 14 years	27
‘My wife is my doctor at home’: A qualitative study exploring the challenges of home-based palliative care in a resource-poor setting	27
Revised recommendations on standards and norms for palliative care in Europe from the European Association for Palliative Care (EAPC): A Delphi study	27
An audit of end-of-life symptom control in patients with corona virus disease 2019 (COVID-19) dying in a hospital in the United Kingdom	26
The palliative care needs of adults with intellectual disabilities and their access to palliative care services: A systematic review	26
Hospital patients’ perspectives on what is essential to enable optimal palliative care: A qualitative study	25
Managing uncertainty and references to time in prognostic conversations with family members at the end of life: A conversation analytic study	25
Support needs and barriers to accessing support: Baseline results of a mixed-methods national survey of people bereaved during the COVID-19 pandemic	25
Terminal withdrawal of mechanical ventilation in adult intensive care units: A systematic review and narrative synthesis of perceptions, experiences and practices	25
Implementing person-centred outcome measures in palliative care: An exploratory qualitative study using Normalisation Process Theory to understand processes and context	24
Digitisation and the patient–professional relationship in palliative care	24
Are family carers part of the care team providing end-of-life care? A qualitative interview study on the collaboration between family and professional carers	24
The utility of the surprise question: A useful tool for identifying patients nearing the last phase of life? A systematic review and meta-analysis	24
A systematic review of classifications systems to determine complexity of patient care needs in palliative care	23
Resilience in advanced cancer caregiving. A systematic review and meta-synthesis	23
Assessing the impact of COVID-19 on healthcare staff at a combined elderly care and specialist palliative care facility: A cross-sectional study	23
Learning a palliative care approach during the COVID-19 pandemic: A case study in an Infectious Diseases Unit	23
Impact of the COVID-19 pandemic on end of life care delivery in care homes: A mixed method systematic review	22
The palliative care needs and experiences of people with advanced head and neck cancer: A scoping review	22
The role, impact, and support of informal caregivers in the delivery of palliative care for patients with advanced cancer: A multi-country qualitative study	21
The need for early referral to palliative care especially for Black, Asian and minority ethnic groups in a COVID-19 pandemic: Findings from a service evaluation	21
Legacy perceptions and interventions for adults and children receiving palliative care: A systematic review	21
Paramedics delivering palliative and end-of-life care in community-based settings: A systematic integrative review with thematic synthesis	21
Invited Editorials	21
Patients’ preferences and factors influencing initial advance care planning discussions’ timing: A cross-cultural mixed-methods study	21
End-of-life care in COVID-19: An audit of pharmacological management in hospital inpatients	21
How to measure the effects and potential adverse events of palliative sedation? An integrative review	20
Family involvement in advance care planning for people living with advanced cancer: A systematic mixed-methods review	20
Early, integrated palliative rehabilitation improves quality of life of patients with newly diagnosed advanced cancer: The Pal-Rehab randomized controlled trial	19
The perspectives of children and young people affected by parental life-limiting illness: An integrative review and thematic synthesis	19
Bereavement care interventions for children under the age of 18 following the death of a sibling: a systematic review	19
Caregiving at the margins: An ethnographic exploration of family caregivers experiences providing care for structurally vulnerable populations at the end-of-life	19
Patient and public involvement in palliative care research: What works, and why? A qualitative evaluation	19
Real-world ethics in palliative care: A systematic review of the ethical challenges reported by specialist palliative care practitioners in their clinical practice	19
A mixed-methods systematic review and meta-analysis of barriers and facilitators to paediatric symptom management at end of life	19
Virtual models of care for people with palliative care needs living in their own home: A systematic meta-review and narrative synthesis	18
The importance of living well now and relationships: A qualitative study of the barriers and enablers to engaging frail elders with advance care planning	18
Video-based online interviews for palliative care research: A new normal in COVID-19?	18
Mutual support between patients and family caregivers in palliative care: A systematic review and narrative synthesis	18
Validation of the Distress Thermometer in patients with advanced cancer receiving specialist palliative care in a hospice setting	17
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	17
Web and mobile-based symptom management interventions for physical symptoms of people with advanced cancer: A systematic review and meta-analysis	17

Comparison of end-of-life care in people with chronic obstructive pulmonary disease or lung cancer: A systematic review	17
The COVID-19 pandemic: A tipping point for advance care planning? Experiences of general practitioners	17
Preplanned participation of paramedics in end-of-life care at home: A retrospective cohort study	16
The Palliative Performance Scale predicts mortality in hospitalized patients with COVID-19	16
The impact of public health palliative care interventions on health system outcomes: A systematic review	16
‘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	16
Tools to help healthcare professionals recognize palliative care needs in patients with advanced heart failure: A systematic review	15
Healthcare professionals’ experiences of inter-professional collaboration during patient’s transfers between care settings in palliative care: A focus group study	15
How effective is virtual reality technology in palliative care? A systematic review and meta-analysis	15
‘This is your golden time. You enjoy it and you’ve plenty time for crying after’: How dysphagia impacts family caregivers of people with amyotrophic lateral sclerosis – A qualitative study	15
Palliative care transitions from acute care to community-based care: A qualitative systematic review of the experiences and perspectives of health care providers	15
Effectiveness and implementation of palliative care interventions for patients with chronic obstructive pulmonary disease: A systematic review	14
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	14
Disparities in access to palliative care facilities for patients with and without cancer: A retrospective review	14
The effectiveness of hope-fostering interventions in palliative care: A systematic review and meta-analysis	14
The experiences of, and need for, palliative care for people with motor neurone disease and their informal caregivers: A qualitative systematic review	14
Home or hospital as the place of end-of-life care and death: A grounded theory study of parents’ decision-making	14
‘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	14
A systematic review and meta-analysis of studies comparing burden from lung cancer and chronic obstructive pulmonary disease	13
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	13
Factors associated with health professionals decision to initiate paediatric advance care planning: A systematic integrative review	13
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	13
The preferences of patients with chronic obstructive pulmonary disease are to discuss palliative care plans with familiar respiratory clinicians, but to delay conversations until their condition deter	13
Clinical uncertainty and Covid-19: Embrace the questions and find solutions	13
Does the carer support needs assessment tool cover the established support needs of carers of patients with chronic obstructive pulmonary disease? A systematic literature search and narrative review	13
Association between religious beliefs and discussions regarding advance care planning: A nationwide survey	13
Caregiver-guided pain coping skills training for patients with advanced cancer: Results from a randomized clinical trial	13
Acceptance and commitment therapy for patient fatigue interference and caregiver burden in advanced gastrointestinal cancer: Results of a pilot randomized trial	13
Understanding the palliative care needs and experiences of people with mesothelioma and their family carers: An integrative systematic review	12
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	12
“Hanging in a balance”: A qualitative study exploring clinicians’ experiences of providing care at the end of life in the burn unit	12
Gamification for promoting advance care planning: A mixed-method systematic review and meta-analysis	12
Civic engagement in serious illness, death, and loss: A systematic mixed-methods review	12
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	12
Area-Based Compassionate Communities: A systematic integrative review of existing initiatives worldwide	12
Complementary therapy in palliative care: A synthesis of qualitative and quantitative systematic reviews	11
Persistent socioeconomic inequalities in location of death and receipt of palliative care: A population-based cohort study	11
What defines the comprehensive assessment of needs in palliative care? An integrative systematic review	11
Efficacy of medicinal cannabis for appetite-related symptoms in people with cancer: A systematic review	11
Identifying barriers and facilitators to palliative care integration in the management of hospitalized patients with COVID-19: A qualitative study	11
Palliative care and infection management at end of life in nursing homes: A descriptive survey	11
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	11
End of life care for people with severe mental illness: Mixed methods systematic review and thematic synthesis (the MENLOC study)	11
Dying in times of COVID-19: Experiences in different care settings – An online questionnaire study among bereaved relatives (the CO-LIVE study)	11
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	11
Single early palliative care intervention added to usual oncology care for patients with advanced cancer: A randomized controlled trial (SENS Trial)	11
Service change and innovation in community end-of-life care during the COVID-19 pandemic: Qualitative analysis of a nationwide primary care survey	11
Repeated subcutaneous esketamine administration for depressive symptoms and pain relief in a terminally ill cancer patient: A case report	11
Timely identification of patients in need of palliative care using the Double Surprise Question: A prospective study on outpatients with cancer	11
Effect of continuous deep sedation on survival in the last days of life of cancer patients: A multicenter prospective cohort study	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
Do family meetings for hospitalised palliative care patients improve outcomes and reduce health care costs? A cluster randomised trial	10
The pervasive relevance of COVID-19 within routine paediatric palliative care consultations during the pandemic: A conversation analytic study	10
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	10
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	10
Prevalence of grief disorders in bereaved families of cancer patients: A meta-analysis	10
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	10
Symptom burden and lived experiences of patients, caregivers and healthcare professionals on the management of malignant bowel obstruction: A qualitative systematic review	10
Practice review: Evidence-based quality use of corticosteroids in the palliative care of patients with advanced cancer	10
Death doulas as supportive companions in end-of-life care: A scoping review	10
The roles, responsibilities and practices of healthcare assistants in out-of-hours community palliative care: A systematic scoping review	10
What is the role of paramedics in palliative and end of life care?	10
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	10
Culture in the spotlight—cultural adaptation and content validity of the integrated palliative care outcome scale for dementia: A cognitive interview study	10
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 sclerosis	10
Opioid underuse in terminal care of long-term care facility residents with pain and/or dyspnoea: A cross-sectional PACE-survey in six European countries	10
Interventions to support family caregivers of people with advanced dementia at the end of life in nursing homes: A mixed-methods systematic review	10
Virtual reality for pain management in advanced heart failure: A randomized controlled study	10
Effectiveness of two types of palliative home care in cancer and non-cancer patients: A retrospective population-based study using claims data	9
Researching minoritised communities in palliative care: An agenda for change	9
“Song of Life”: Results of a multicenter randomized trial on the effects of biographical music therapy in palliative care	9
It’s like standing in front of a prison fence – Dying during the SARS-CoV2 pandemic: A qualitative study of bereaved relatives’ experiences	9
Moral distress amongst palliative care doctors working during the COVID-19 pandemic: A narrative-focussed interview study	9
The Me in We dyadic communication intervention is feasible and acceptable among advanced cancer patients and their family caregivers	9
Compounded trauma: A qualitative study of the challenges for refugees living with advanced cancer	9
A cross-sectional gender-sensitive analysis of depressive symptoms in patients with advanced cancer	9
Adaptation and continuous learning: integrative review of coping strategies of palliative care professionals	9
Palliative care in the context of immune and targeted therapies: A qualitative study of bereaved carers’ experiences in metastatic melanoma	9
Using advance and emergency care plans during transfer decisions: A grounded theory interview study with care home staff	9
Public health palliative care: Reframing death, dying, loss and caregiving	9

Pharmacological strategies used to manage symptoms of patients dying of COVID-19: A rapid systematic review	9
The experience of delirium in palliative care settings for patients, family, clinicians and volunteers: A qualitative systematic review and thematic synthesis	9
Practice review: Evidence-based and effective management of anaemia in palliative care patients	9
Building organizational compassion among teams delivering end-of-life care in the intensive care unit: The 3 Wishes Project	9
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	8
Economic evaluation of a combined screening and stepped-care treatment program targeting psychological distress in patients with metastatic colorectal cancer: A cluster randomized controlled trial	8
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	8
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	8
Risk factors for delirium in adult patients receiving specialist palliative care: A systematic review and meta-analysis	8
Navigating the caregiving abyss: A metasynthesis of how family caregivers manage end-of-life care for older adults at home	8
What does effective end-of-life care at home for children look like? A qualitative interview study exploring the perspectives of bereaved parents	8
Development of guidelines to reduce, handle and report missing data in palliative care trials: A multi-stakeholder modified nominal group technique	8
Inclusion of palliative care in health care policy for older people: A directed documentary analysis in 13 of the most rapidly ageing countries worldwide	8
Identifying older adults with frailty approaching end-of-life: A systematic review	8
Abstracts from the 17th World Congress of the EAPC 2021	8
Poor physical and mental health predicts prolonged grief disorder: A prospective, population-based cohort study on caregivers of patients at the end of life	8
Assessment tools for problematic opioid use in palliative care: A scoping review	8
Is trained communication about desire to die harmful for patients receiving palliative care? A cohort study	8
End-of-life communication strategies for healthcare professionals: A scoping review	8
Fatigue in advanced disease associated with palliative care: A systematic review of non-pharmacological treatments	8
Trends of concerns from diagnosis in patients with advanced lung cancer and their family caregivers: A 2-year longitudinal study	8
Palliative and end-of-life care needs, experiences, and preferences of LGBTQ+ individuals with serious illness: A systematic mixed-methods 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
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	7
Using the Delphi technique to achieve consensus on bereavement care in palliative care in Europe: An EAPC White Paper	7
A rapid review of end-of-life needs in the LGBTQ+ community and recommendations for clinicians	7
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	7
Exploring the meaning of dignity at end of life for Chinese Canadians caregivers: A qualitative cross-cultural study	7
Perspectives on COVID-19 and palliative care research	7
‘It was like taking an inner bath’: A qualitative evaluation of a collaborative advance care planning-approach	7
A dignified last phase of life for patients with a migration background: A qualitative study	7
Implementation of an acute palliative care unit for COVID-19 patients in a tertiary hospital: Qualitative data on clinician perspectives	7
An examination and proposed definitions of family members’ grief prior to the death of individuals with a life-limiting illness: A systematic review	7
The impact on emotional well-being of being a palliative care volunteer: An interpretative phenomenological analysis	7
Intranasal dexmedetomidine: Procedural sedation in palliative care: A case report	7
Virtual home-based palliative care during COVID-19: A qualitative exploration of the patient, caregiver, and healthcare provider experience	7
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	7
A meta-ethnographic study of fathers’ experiences of caring for a child with a life-limiting illness	7
Willingness and concerns of transfusion-dependent hematological patients toward the option of home transfusion therapy	7
The promise of big data for palliative and end-of-life care research	7
Process evaluation of the Cancer Home-Life Intervention: What can we learn from it for future intervention studies?	7
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	7
Paramedics’ experiences and educational needs when participating end-of-life care at home: A mixed method study	7
The occurrence and timing of delirium in acute care hospitalizations in the last year of life: A population-based retrospective cohort study	7
Cannabinoids for the treatment of refractory neuropathic pruritus in amyotrophic lateral sclerosis: A case report	7
Facilitating family needs and support at the end of life in hospital: A descriptive study	7
Over a third of palliative medicine physicians meet burnout criteria: Results from a survey study during the COVID-19 pandemic	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
COP27 Climate Change Conference: Urgent action needed for Africa and the world	6
Education needed to improve antimicrobial use during end-of-life care of older adults with advanced cancer: A cross-sectional survey	6
Development and validation of a prediction model of poor performance status and severe symptoms over time in cancer patients (PROVIEW+)	6
Unwelcome memento mori or best clinical practice? Community end of life anticipatory medication prescribing practice: A mixed methods observational study	6
What constitutes a palliative care need in people with serious illnesses across Africa? A mixed-methods systematic review of the concept and evidence	6
Palliative care needs and experiences of people in prison: A systematic review and meta-synthesis	6
Opportunities for public involvement in big data research in palliative and end-of-life care	6
Understanding advance care planning in care homes throughout the COVID-19 pandemic: A critical realist review and synthesis	6
Which factors influence the quality of end-of-life care in interstitial lung disease? A systematic review with narrative synthesis	6
Pain assessment tools in paediatric palliative care: A systematic review of psychometric properties and recommendations for clinical practice	6
Measures of financial burden for families dealing with serious illness: A systematic review and analysis	6
Delirium screening tools validated in the context of palliative care: A systematic review	6
Caring precariously: An interpretive description of palliative care and welfare worker perspectives on end of life carers navigating social welfare	6
Care practices of specialized outpatient pediatric palliative care teams in collaboration with parents: Results of participatory observations	6
The use of natural language processing in palliative care research: A scoping review	6
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	6
Ethical and research governance approval across Europe: Experiences from three European palliative care studies	6
Palliative paramedicine: Comparing clinical practice through guideline quality appraisal and qualitative content analysis	6
Exploring expanded interdisciplinary roles in goals of care conversations in a national goals of care initiative: A qualitative approach	6
Patient-reported symptoms and problems at admission to specialized palliative care improved survival prediction in 30,969 cancer patients: A nationwide register-based study	6
Trends in quality of care and dying perceived by family caregivers of nursing home residents with dementia 2005–2019	6
LGBT+ partner bereavement and appraisal of the Acceptance-Disclosure Model of LGBT+ bereavement: A qualitative interview study	6
Parenting through grief: A cross-sectional study of recently bereaved adults with minor children	6
A qualitative service evaluation of patient and caregiver experiences of CAR-T therapy: Recommendations for service development and implications for palliative care teams	6
Making the best of multidisciplinary care for patients with malignant fungating wounds: A qualitative study of clinicians’ narratives	6
‘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	6
Monitoring nociception and awareness during palliative sedation: A systematic review	6
The monetary valuation of informal care to cancer decedents at end-of-life: Evidence from a national census survey	6
Do learners implement what they learn? Commitment-to-change following an interprofessional palliative care course	6
Organizational and individual barriers and facilitators to the integration of pediatric palliative care for children: A grounded theory study	6
Palliative care for adolescents and young adults with advanced illness: A scoping review	6
The impact of digital health interventions on the psychological outcomes of patients and families receiving paediatric palliative care: A systematic review and narrative synthesis	6
Building trust and facilitating goals of care conversations: A qualitative study in people with heart failure receiving home hospice care	6
Practice review: Evidence-based and effective management of fatigue in patients with advanced cancer	5
‘Cold bedrooms’ and other cooling facilities in UK children’s hospices, how they are used and why they are offered: A mixed methods study	5
Hoping for the best and preparing for the worst: a forgotten maxim in the immunotherapy era?	5
Measuring quality of dying, death and end-of-life care for children and young people: A scoping review of available tools	5
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	5
‘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	5
Patient perspectives on states worse than death: A qualitative study with implications for patient-centered outcomes and values elicitation	5
‘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	5
‘You can’t feel what we feel’: Multifaceted dyspnoea invisibility in advanced chronic obstructive pulmonary disease examined through interpretative phenomenological analysis	5
The health of mothers of children with a life-limiting condition: A qualitative interview study	5
Medication use in aged care residents in the last year of life: A scoping review	5
COVID-19: A personal perspective	5
National dementia plans to address escalating global palliative care needs	5
A mixed-methods pilot study of ‘LIFEView’ audiovisual technology: Virtual travel to support well-being and quality of life in palliative and end-of-life care patients	5