Palliative Medicine

Article	Citations
Where to for core outcome sets for best care for the dying person?	108
Assessing the suitability of the Carer Support Needs Assessment Tool (CSNAT-Paediatric) for use with parents of children with a life-limiting condition: A qualitative secondary analysis	70
Palliative care for teenagers and young adults - the need for more evidence	61
WITHDRAWAL – Administrative Duplicate Publication: Tribute to Derek Doyle and Cynthia Goh	51
A therapist-supported internet-based intervention for bereaved siblings: A randomized controlled trial	50
Practice review: Evidence-based and effective management of fatigue in patients with advanced cancer	48
Inequities of palliative care availability and access to opioids in low- and middle-income countries	47
Over a third of palliative medicine physicians meet burnout criteria: Results from a survey study during the COVID-19 pandemic	46
Motor neurone disease: A point-prevalence study of patient reported symptom prevalence, severity and palliative care needs	46
A tribute to Derek Doyle and Cynthia Goh	46
Development of a palliative paramedicine framework to standardise best practice: A Delphi study	45
Recognising dying in motor neurone disease: A scoping review	45
Translation and cross-cultural adaptation of the Integrated Palliative Care Outcome Scale in Hindi: Toward capturing palliative needs and concerns in Hindi speaking patients	45
A good death in the child with life shortening illness: A qualitative multiple-case study	42
Effects of advance care planning in care dependent community-dwelling older persons (STADPLAN): A cluster-randomised controlled trial	40
Evaluation of the integration of palliative care in a fragile setting amongst host and refugee communities: Using consecutive rapid participatory appraisals	39
Integration of primary care and palliative care services to improve equality and equity at the end-of-life: Findings from realist stakeholder workshops	39
Combining realist evaluation and transformative evaluation to advance research in palliative care: The case of end of life companionship	38
The potential of experience sampling methods in palliative care	34
End of life skin care – Research informing theory to traverse between Scylla and Charybdis?	33
Perceptions and experiences of clinicians and correctional officers facilitating palliative care for people in prison: A systematic review and meta-synthesis	32
Health professionals’ experiences of rapport during telehealth encounters in community palliative care: An interpretive description study	32
Variation in end-of-life care and hospital palliative care among hospitals and local authorities: A preliminary contribution of big data	32
Telehealth requires improved evidence to achieve its full potential in palliative care	30
Components of home-based palliative and supportive care for adults with heart failure: A scoping review	29

‘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	29
The cost of providing care by family and friends (informal care) in the last year of life: A population observational study	28
Prognostic performance of the Karnofsky Performance Status for predicting in-hospital mortality among unselected patients who receive palliative care consultations	28
Subcutaneous sodium valproate in palliative care: A systematic review	28
‘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	27
Healthy siblings’ perspectives about paediatric palliative care: A qualitative systematic review and meta-synthesis	27
Applied patient-level palliative care interventions designed to meet the needs of sexual and gender minorities: A scoping review and qualitative content analysis of how to support sexual and gender mi	26
Call for emergency action to limit global temperature increases, restore biodiversity, and protect health: Wealthy nations must do much more, much faster	25
More than 3 years of teleconsultations: A retrospective cohort study in specialized outpatient palliative care	24
Development of a research-based classification of approaches to paediatric palliative medicine service provision within children’s and young adults’ hospices: A mixed methods study	23
Neuropalliative care for progressive neurological diseases: A scoping review on models of care and priorities for future research	23
Interpersonal energy: New and bold directions in palliative care health professions education research	23
Changes and predictors of resilience among wife and husband caregivers of patients with advanced cancer: A longitudinal study	23
Prospective case series of neuropathic cancer pain in patients treated with an EGFR-inhibitor	22
Thanks to Reviewers: 2022	22
What can patient safety science do for palliative care? Bridging the gap	21
Nationwide evaluation of palliative care (Q-PAC study) provided by specialized palliative care teams using quality indicators : Large variations in quality of care	21
Re: Liu et al., Effectiveness and safety of opioids on breathlessness and exercise endurance in patients with chronic obstructive pulmonary disease: A systematic review and meta-analysis of randomised	20
Dying in times of COVID-19: Experiences in different care settings – An online questionnaire study among bereaved relatives (the CO-LIVE study)	20
Psychological health in Palliative Care: Thematic analysis of a psychiatrist’s and an art therapist’s clinical reflexive journals	20
Facilitators and barriers in using comics to support family caregivers of patients receiving palliative care at home: A qualitative study	20
Parenting through grief: A cross-sectional study of recently bereaved adults with minor children	20
Good medicines management: From describing problems to a vision for change	19
Views on advance care planning of family members of older adults with Turkish and Moroccan backgrounds: An exploratory interview study	19
Updating international consensus on best practice in care of the dying: A Delphi study	18
‘It was like taking an inner bath’: A qualitative evaluation of a collaborative advance care planning-approach	18
Thanks to Reviewers	18
What do we do with all the evidence for symptoms in palliative care?	18
Coming to terms with dying: Advance care planning as a conduit between clinicians, patients, and conversations about death and dying – a qualitative interview study	18
Self-care towards the end of life: A systematic review and narrative synthesis on access, quality and cost	18
When a dying patient is asked to participate in a double-blind, placebo-controlled clinical trial on symptom control: The decision-making process and experiences of relatives	17
Co-production in practice: A qualitative study of the development of advance care planning workshops for South Asian elders	17
Outcomes and measures of delirium interventional studies in palliative care to inform a core outcome set: A systematic review	16
Posttraumatic growth in palliative care settings: A scoping review of prevalence, characteristics and interventions	16
The spiritual dimension of parenting a child with a life-limiting or life-threatening condition: A mixed-methods systematic review	16
Symptom burden and lived experiences of patients, caregivers and healthcare professionals on the management of malignant bowel obstruction: A qualitative systematic review	16
The health of mothers of children with a life-limiting condition: A qualitative interview study	15
Motivations and experiences of patients with advanced cancer participating in Phase 1 clinical trials: A qualitative study	15
Advance care planning and quality of life: A qualitative interview study in people with young-onset dementia and their family caregivers	15
Complexity and function of family involvement in advance care planning: A qualitative study of perspectives from people living with advanced cancer, family members and healthcare professionals	15
Revised European Association for Palliative Care (EAPC) recommended framework on palliative sedation: An international Delphi study	15
Development of the TIFFIN recommendations for co-producing palliative and end-of-life care research with individuals with lived experience of homelessness: A qualitative study	15
Systematic adaptation of public health palliative care interventions across settings using ADAPT guidance: Methodological learnings from the EU NAVIGATE project	15
Creating ‘safe spaces’: A qualitative study to explore enablers and barriers to culturally safe end-of-life care	15
More time in a community setting: A service evaluation of the impact of intrathecal drug delivery systems on place of care of patients with cancer pain	15
The effect of an integrated palliative care intervention on quality of life and acute healthcare use in patients with COPD: Results of the COMPASSION cluster randomized controlled trial	15
Patient perspectives on states worse than death: A qualitative study with implications for patient-centered outcomes and values elicitation	15
Exercise interventions for advanced cancer palliative care patients: A systematic literature review and descriptive evidence synthesis of randomized controlled trials	15
COP27 Climate Change Conference: Urgent action needed for Africa and the world	14
What does effective end-of-life care at home for children look like? A qualitative interview study exploring the perspectives of bereaved parents	14

How palliative care professionals develop coping competence through their career: A grounded theory	14
Models of care for people with dementia approaching end of life: A rapid review	14
The experiences of family members witnessing the diminishing drinking of a dying relative in hospital: A narrative inquiry	14
The importance of methodology to palliative care research: A new article type for Palliative Medicine	14
Efficacy of medicinal cannabis for appetite-related symptoms in people with cancer: A systematic review	14
Opportunities for computational tools in palliative care: Supporting patient needs and lowering burden	14
Palliative care referral criteria and application in pediatric illness care: A scoping review	13
The experiences, perceptions, and support needs among family caregivers of patients with advanced cancer and eating problems: An integrative 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	13
LGBT+ partner bereavement and appraisal of the Acceptance-Disclosure Model of LGBT+ bereavement: A qualitative interview study	13
Strategies and checklist for designing and conducting palliative care research with family carers: EAPC international expert elicitation study	13
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	13
Resilience in advanced cancer caregiving. A systematic review and meta-synthesis	13
Palliative and end-of-life care needs, experiences, and preferences of LGBTQ+ individuals with serious illness: A systematic mixed-methods review	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
‘Constipation’: One word, many meanings amongst persons with cancer: An observational study	13
The impact of COVID-19 on palliative care social work: An online survey by a European Association of Palliative Care Task Force	13
Identifying barriers and facilitators to palliative care integration in the management of hospitalized patients with COVID-19: A qualitative study	13
Safety of subcutaneous plastic cannulas in patients with severe thrombocytopenia: Findings from a retrospective analysis	13
What are we planning, exactly? The perspectives of people with intellectual disabilities, their carers and professionals on end-of-life care planning: A focus group study	13
Definition and recommendations of advance care planning: A Delphi study in five Asian sectors	13
The impact of digital health interventions on the psychological outcomes of patients and families receiving paediatric palliative care: A systematic review and narrative synthesis	12
Improving family grief outcomes: A scoping review of family-based interventions before and after the death of a child	12
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	12
Palliative care for people who use drugs during communicable disease epidemics and pandemics: A scoping review on access, policies, and programs and guidelines	12
Views of patients with progressive illness and carers about the role of digital advance care planning systems to record and share information: A qualitative study	12
Perceptions of prognosis and end-of-life care outcomes in patients with advanced lung and gastrointestinal cancer	12
Associations between physicians’ personal preferences for end-of-life decisions and their own clinical practice: PROPEL survey study in Europe, North America, and Australia	12
Understanding the role and deployment of volunteers within specialist palliative care services and organisations as they have adjusted to the COVID-19 pandemic: A multi-national EAPC volunteer taskfor	12
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	12
Arts engagement facilitated by artists with individuals with life-limiting illness: A systematic integrative review of the literature	11
Culture in the spotlight—cultural adaptation and content validity of the integrated palliative care outcome scale for dementia: A cognitive interview study	11
Effect of continuous deep sedation on survival in the last days of life of cancer patients: A multicenter prospective cohort study	11
Perspectives of inpatients with palliative care needs, their families, clinicians and key stakeholders on measuring quality of hospital care via patient experience measures: A qualitative study	11
Strategies for recruiting the dependent children of patients with a life-limiting illness as research participants	11
Role and response of primary healthcare services in community end-of-life care during COVID-19: Qualitative study and recommendations for primary palliative care delivery	11
Cannabinoids for the treatment of refractory neuropathic pruritus in amyotrophic lateral sclerosis: A case report	11
Validating the socio-spiritual items of the Utrecht Symptom Diary—4 Dimensional: Content and construct validity	11
Non-steroidal anti-inflammatory drugs (NSAIDs) in cancer pain: A database analysis to determine recruitment feasibility for a clinical trial	11
Serious illness care quality during COVID-19: Identifying improvement opportunities in narrative reports from a National Bereaved Family Survey	11
Understanding the experiences of mothers receiving perinatal palliative care: A qualitative study	11
“They were here, and they still matter”: A qualitative study of bereaved parents legacy experiences and perceptions	10
How do people in prison access palliative care? A scoping review of models of palliative care delivery for people in prison in high-income countries	10
Closing the health equity gap in palliative care: The time for action is now	10
End of life care for people with severe mental illness: Mixed methods systematic review and thematic synthesis (the MENLOC study)	10
Area-Based Compassionate Communities: A systematic integrative review of existing initiatives worldwide	10
“Walk me through the final day”: A thematic analysis study on the family caregiver experience of the Medical Assistance in Dying procedure day	10
Primary palliative care in low- and middle-income countries: A systematic review and thematic synthesis of the evidence for models and outcomes	10
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	10
Use of long term aprepitant as a treatment for refractory nausea following oesophageal stent insertion – a case report	10
The double awareness of the wish to hasten death and the will to live: A secondary analysis of outlier patients from a mixed-methods study	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
Professionals’, patients’ and families’ views on the use of opioids for chronic breathlessness: A systematic review using the framework method and pillar process	10
Pain assessment tools in paediatric palliative care: A systematic review of psychometric properties and recommendations for clinical practice	10
‘Life became slow down’: A descriptive qualitative study of the experiences of cancer-related fatigue amongst people with advanced lung cancer	10
Time estimates in prognostic discussions: A conversation analytic study of hospice multidisciplinary team meetings	10
Co-design and prototype development of the ‘Ayzot App’: A mobile phone based remote monitoring system for palliative care	9
Virtual home-based palliative care during COVID-19: A qualitative exploration of the patient, caregiver, and healthcare provider experience	9
Trends in quality of care and dying perceived by family caregivers of nursing home residents with dementia 2005–2019	9
What does ‘good’ palliative care look like for children and young people? A qualitative study of parents’ experiences and perspectives	9
Implementation of clinical guidelines in specialized palliative care—results from a national improvement project: A national register-based study	9
Moral distress amongst palliative care doctors working during the COVID-19 pandemic: A narrative-focussed interview study	9
‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium	9
Facilitating family needs and support at the end of life in hospital: A descriptive study	9
A peripheral opioid antagonist for treating urinary retention induced by opioids: A case report	9
Understanding advance care planning in care homes throughout the COVID-19 pandemic: A critical realist review and synthesis	9
Palliative care volunteering: Pressing challenges in research	9
Mixed methods process evaluation of an advance care planning intervention among nursing home staff	9
Prevalence of grief disorders in bereaved families of cancer patients: A meta-analysis	9
Preserving the integrity of personhood in people with advanced cancer: An in-depth qualitative study among patients, relatives, and care professionals	9
How to enhance advance care planning research?	9
A rapid review of the evidence for online interventions for bereavement support	9
Measuring quality of dying, death and end-of-life care for children and young people: A scoping review of available tools	9
An electronic pre-visit agenda-setting questionnaire in ambulatory palliative care is feasible and acceptable to patients, care partners, and clinicians: A mixed methods evaluation	9
Sexual health and closeness in couples coping with advanced cancer: Results of a multicenter observational study (eQuiPe)	8
Association between religious beliefs and discussions regarding advance care planning: A nationwide survey	8
Civic engagement in serious illness, death, and loss: A systematic mixed-methods review	8
‘A good ending but not the end’: Exploring family preparations surrounding a relative’s death and the Afterlife – A qualitative study	8
The ideal path to a good death: An international meta-synthesis of rural residents’ perspectives	8
Revised recommendations on standards and norms for palliative care in Europe from the European Association for Palliative Care (EAPC): A Delphi study	8

Maybe for unbearable suffering: Diverse racial, ethnic and cultural perspectives of assisted dying. A scoping review	8
The spiritual care intervention “In dialogue with your life story”: Results of a longitudinal study on palliative clients’ spiritual wellbeing	8
Efficacy of spiritual interventions in palliative care: An umbrella review of systematic reviews	8
The impact of regular, low-dose, sustained-release morphine for chronic breathlessness on caregiver burden: An exploratory analysis of the BEAMS trial	8
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
Virtual reality for pain management in advanced heart failure: A randomized controlled study	8
Palliative care and neuro-oncological care: Better integration is needed	8
Loneliness, its effect on mental and physical health, and the dying	8
“By the time she got sick it was just kind of too late”: A qualitative study on advanced care planning among bereaved lesbian, gay, and bisexual older women	8
‘There’s something about admitting that you are lonely’ – prevalence, impact and solutions to loneliness in terminal illness: An explanatory sequential multi-methods study	8
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	8
Multiple points of system failure underpin continuous subcutaneous infusion safety incidents in palliative care: A mixed methods analysis	8
Peer review and Palliative Medicine: Guiding reviewers’ contributions to ensuring high quality publications	8
Iatrogenic suffering at the end of life: An ethnographic study	8
Palliative and end-of-life care for patients with pleural mesothelioma: A cohort study	8
Waking up from fatigue: The hidden burden of fatigue	8
Acceptance and Commitment Therapy (ACT) for people with advanced progressive illness, their caregivers and staff involved in their care: A scoping review	8
A palliative care goals model for people with dementia and their family: Consensus achieved in an international Delphi study	8
Living experiences of people with advance cancer with low socioeconomic status: A systematic review of qualitative evidence	8
A core outcome set for best care for the dying person: Results of an international Delphi study and consensus meeting	7
The COVID-19 pandemic: A tipping point for advance care planning? Experiences of general practitioners	7
Navigating the caregiving abyss: A metasynthesis of how family caregivers manage end-of-life care for older adults at home	7
‘You can’t feel what we feel’: Multifaceted dyspnoea invisibility in advanced chronic obstructive pulmonary disease examined through interpretative phenomenological analysis	7
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	7
Factors facilitating positive outcomes in community-based end-of-life care: A cross-sectional qualitative study of patients and family caregivers	7
Evaluation of a WeChat-based Dyadic Life Review Program for people with advanced cancer and family caregivers: A mixed-method feasibility study	7
Invited Editorials	7
Impact of the COVID-19 pandemic on end of life care delivery in care homes: A mixed method systematic review	7
Why patients in specialist palliative care in-patient settings are at high risk of falls and falls-related harm: A realist synthesis	7
Which factors influence the quality of end-of-life care in interstitial lung disease? A systematic review with narrative synthesis	7
Practice review: Evidence-based and effective management of anaemia in palliative care patients	7
Abstracts from the 17th World Congress of the EAPC 2021	7
The effects of confronting one’s own end of life on older individuals and those with a life-threatening disease: A systematic literature review	7
The development of the ADO-SQ model to predict 1-year mortality in patients with COPD	7
Tensions in advance care planning with dementia: Time for a good-enough laid-back approach?	7
Trauma-informed palliative care is needed: A call for implementation and research	7
Palliative care for adolescents and young adults with advanced illness: A scoping review	7
Cognitive Authority Theory: Reframing health inequity, disadvantage and privilege in palliative and end-of-life care	7
A feasibility and acceptability pilot for the longitudinal measurement of inspiratory and expiratory pressures in people with advanced pancreatic cancer	7
‘My life is a mess but I cope’: An analysis of the language children and young people use to describe their own life-limiting or life-threatening condition	7
Using the Delphi technique to achieve consensus on bereavement care in palliative care in Europe: An EAPC White Paper	6
Long-term 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	6
Co-designing a culturally-sensitive theory-driven advance care planning game with Chinese older adults and healthcare providers	6
What are the triggers for palliative care referral in burn intensive care units? Results from a qualitative study based on healthcare professionals’ views, clinical experiences and practices	6
Corrigendum to Updating international consensus on best practice in care of the dying: A Delphi study	6
A task service and a talking service: A qualitative exploration of bereaved family perceptions of community nursing care at the end of life	6
Adaptation and continuous learning: integrative review of coping strategies of palliative care professionals	6
Effectiveness and safety of opioids on breathlessness and exercise endurance in patients with chronic obstructive pulmonary disease: A systematic review and meta-analysis of randomised controlled tria	6
Applying the community readiness model to identify and address inequity in end-of-life care in South Asian communities	6
‘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	6
Risk factors for delirium in adult patients receiving specialist palliative care: A systematic review and meta-analysis	6
Spiritual, religious, and existential concerns of children and young people with life-limiting and life-threatening conditions: A qualitative interview study	6
The financial costs of anticipatory prescribing: A retrospective observational study of prescribed, administered and wasted medications using community clinical records	6
Existential experiences and perceptions of death among children with terminal cancer: An interpretative qualitative study	6
‘It was like an airbag, it cushioned the blow’: A multi-site qualitative study of bereaved parents’ experiences of using cooling facilities	6
A grounded theory of interdependence between specialist and generalist palliative care teams across healthcare settings	6
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	6
Paramedics’ experiences and educational needs when participating end-of-life care at home: A mixed method study	6
Evaluating parent and public involvement activities within a paediatric palliative care research centre: Route map to impactful and meaningful engagement	6
The impact on emotional well-being of being a palliative care volunteer: An interpretative phenomenological analysis	6
A pragmatic approach to selecting a grading system for clinical practice recommendations in palliative care	6
Predictors to forgo resuscitative effort during Covid-19 critical illness at the height of the pandemic : A retrospective cohort study	6
Prescribing and deprescribing in older people with life-limiting illnesses receiving hospice care at the end of life: A longitudinal, retrospective cohort study	6
‘People don’t realise how much their past experiences affect them in adulthood’: A qualitative study of adult siblings’ experiences of growing-up with a sister/brother with a childhood life-lim	6
Exploring expanded interdisciplinary roles in goals of care conversations in a national goals of care initiative: A qualitative approach	6
Differences in palliative care needs between cancer patients and non-cancer patients at the start of specialized palliative care: A nationwide register-based study	6
‘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	6
An easier way to die?—A qualitative interview study on specialist palliative care team members’ views on dying under sedation	6
Parents’ experiences of being involved in medical decision-making for their child with a life-limiting condition: A systematic review with narrative synthesis	5
How do primary care clinicians approach hospital admission decisions for people in the final year of life? A systematic review and narrative synthesis	5
Intranasal dexmedetomidine: Procedural sedation in palliative care: A case report	5
“Collateral beauty.” Experiences and needs of professionals caring for parents continuing pregnancy after a life-limiting prenatal diagnosis: A grounded theory study	5
Shoulder pain in a patient with renal cell carcinoma? Suprascapular neuropathy caused by bone metastasis of renal cell carcinoma: A case report	5
‘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	5
Palliative paramedicine: Comparing clinical practice through guideline quality appraisal and qualitative content analysis	5
Corrigendum	5
The problems of using migration background as a conceptual framework in palliative care research	5
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	5
Defining end of life in dementia: A systematic review	5
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	5
The 13th World Research Congress of the European Association for Palliative Care	5
Feasibility of prospective error reporting in home palliative care: A mixed methods study	5
‘There’s this big fear around palliative care because it’s connected to death and dying’: A qualitative exploration of the perspectives of undergraduate students on the role of the speech and language	5
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	5
Feasibility and effectiveness of a two-tiered intervention involving training and a new consultation model for patients with palliative care needs in primary care: A before-after study	5
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	5
Performance status and trial site-level factors are associated with missing data in palliative care trials: An individual participant-level data analysis of 10 phase 3 trials	5
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	5
‘I couldn’t live without hope’: A qualitative study using reflexive thematic analysis on approaches to hope and prognostic awareness among people with advanced disease	5
Facilitating equitable access to hospice care in socially deprived areas: A mixed methods multiple case study	5
Factors influencing deprescribing in primary care for those towards the end of life: A qualitative interview study with patients and healthcare practitioners	5
Palliative care needs and experiences of people in prison: A systematic review and meta-synthesis	5
‘Saying goodbye’ during the COVID-19 pandemic: A document analysis of online newspapers with implications for end of life care	5
Conserving dignity and facilitating adaptation to dependency with intimate hygiene for people with advanced disease: A qualitative study	5
It’s like standing in front of a prison fence – Dying during the SARS-CoV2 pandemic: A qualitative study of bereaved relatives’ experiences	5