Palliative Medicine

Article	Citations
A tribute to Derek Doyle and Cynthia Goh	613
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	76
Facilitators and barriers in using comics to support family caregivers of patients receiving palliative care at home: A qualitative study	58
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	50
Neuropalliative care for progressive neurological diseases: A scoping review on models of care and priorities for future research	47
Posttraumatic growth in palliative care settings: A scoping review of prevalence, characteristics and interventions	46
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	39
“Walk me through the final day”: A thematic analysis study on the family caregiver experience of the Medical Assistance in Dying procedure day	38
Preserving the integrity of personhood in people with advanced cancer: An in-depth qualitative study among patients, relatives, and care professionals	37
Living experiences of people with advance cancer with low socioeconomic status: A systematic review of qualitative evidence	34
‘Saying goodbye’. . . A systematic integrative review of palliative caregiving in intergenerational living contexts	33
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	32
Mixed methods process evaluation of an advance care planning intervention among nursing home staff	32
REstoring Sleep and Energy using a mulTimodal non-pharmacological intervention in advanced Cancer: A feasibility study (RESET-C)	30
Maybe for unbearable suffering: Diverse racial, ethnic and cultural perspectives of assisted dying. A scoping review	30
The 13th World Research Congress of the European Association for Palliative Care	29
Parents’ experiences of being involved in medical decision-making for their child with a life-limiting condition: A systematic review with narrative synthesis	29
The utility of the surprise question: A useful tool for identifying patients nearing the last phase of life? A systematic review and meta-analysis	28
The experience of nurses when providing care across acts that may be perceived as death hastening: A qualitative evidence synthesis	28
‘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	28
Differences in palliative care needs between cancer patients and non-cancer patients at the start of specialized palliative care: A nationwide register-based study	27
End-of-life experience patterns among older adults and their association with pain near death: A population-based study	25
Utilizing intricate care networks: An ethnography of patients and families navigating palliative care in a resource-limited setting	25
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	24
The management of absolute iron deficiency anaemia in the palliative care population: A reply to Neoh et al.	23

Education modalities for serious illness communication training: A scoping review on the impact on clinician behavior and patient outcomes	23
Facilitating equitable access to hospice care in socially deprived areas: A mixed methods multiple case study	23
Enhancing identification of potential palliative care needs in older adults: An umbrella review of screening instruments	23
Corrigendum to Updating international consensus on best practice in care of the dying: A Delphi study	23
How best to capture the impact of complementary therapies in palliative care: A systematic review to identify and assess the appropriateness and validity of multi-domain tools	22
A peripherally acting μ-opioid receptor antagonist for treating opioid-associated tinnitus: A case report	21
Delirium prevention in hospices: Opportunities and limitations – A focused ethnography	20
What outcomes do studies use to measure the impact of prognostication on people with advanced cancer? Findings from a systematic review of quantitative and qualitative studies	20
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	20
How much information is ‘reasonable’? A qualitative interview study of the prescribing practices of palliative care professionals	20
Re: Tan et al., Subcutaneous sodium valproate in palliative care: A systematic review	19
‘How long do you think?’ Unresponsive dying patients in a specialist palliative care service: A consecutive cohort study	19
Support from healthcare professionals in empowering family carers to discuss advance care planning: A population-based survey	19
Effectiveness of and implementation requirements for telehealth in palliative care patients with advanced cancer: A systematic review and meta-analysis	19
An emergency department nurse led intervention to facilitate serious illness conversations among seriously ill older adults: A feasibility study	19
Prevalence, risk factors and management of pressure injuries and their implications for palliative care: A rapid overview of reviews	19
Barriers and facilitators influencing referral and access to palliative care for children and young people with life-limiting and life-threatening conditions: a scoping review of the evidence	19
Trauma-informed palliative care: A systematic scoping review of evidence sources describing concepts relevant to an emerging field of practice	18
Economic evaluations in the palliative and end-of-life care settings: A systematic review of existing evidence, methods and quality	18
Bridging cultures in palliative care: A qualitative study of the care of Indigenous Australians with advanced illness	18
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	17
The 19th World Congress of the European Association for Palliative Care 29 – 31 May 2025 Helsinki, Finland	17
Factors associated with hospitalisations of patients with chronic heart failure approaching the end of life: A systematic review	17
International consensus on occupational therapy interventions for people with palliative care needs: A European Association for Palliative Care Group Concept Mapping study	17
Enhancing the wellbeing of refugees living with advanced life-limiting illness in high-income resettlement countries: A systematic review	17
A narrow view of palliative care and assisted dying	16
Deaths at home, area-based deprivation and the effect of the Covid-19 pandemic: An analysis of mortality data across four nations	16
EAPC2023 Abstract Book	16
Effectiveness of transmural team-based palliative care in prevention of hospitalizations in patients at the end of life: A systematic review and meta-analysis	16
Systematic review of conceptual and theoretical frameworks used in palliative care and end-of-life care research studies	16
Pharmacological treatment of pain, dyspnea, death rattle, fever, nausea, and vomiting in the last days of life in older people: A systematic review	16
Exploring “good days” with advanced cancer: A pilot daily diary study	16
Memory-making interventions for children with life-threatening or life-limiting conditions and their families: A systematic review of evidence and implications for practice	16
Impact of expected parental death on the health of adolescent and young adult children: A systematic review of the literature	15
A systematic review on the impact of financial insecurity on the physical and psychological well-being for people living with terminal illness	15
Models, components and outcomes of palliative and end-of-life care provided to adults living at home: A systematic umbrella review of reviews	15
Thanks to Reviewers	15
Health care professional recruitment of patients and family carers to palliative care randomised controlled trials: A qualitative multiple case study	15
‘So being here is. . . I feel like I’m being a social worker again, at the hospice’: Using interpretative phenomenological analysis to explore social workers’ experiences of hospice work	15
‘Adrift in a sea of just absolute unknowableness’: A multimethod qualitative study exploring patient, carer and healthcare professional experiences of communicating about future uncertainty in multimo	15
The perspectives of people with dementia and their supporters on advance care planning: A qualitative study with the European Working Group of People with Dementia	15
What can patient safety science do for palliative care? Bridging the gap	15
Caring toward end of life through acute hospital and community partnerships: A scoping review	15
Measurement equivalence of the paper-based and electronic version of the Integrated Palliative care Outcome Scale (IPOS): A randomised crossover trial	15
Supporting best practice in reflexive thematic analysis reporting in Palliative Medicine : A review of published research and introduction to the	15
The spiritual dimension of parenting a child with a life-limiting or life-threatening condition: A mixed-methods systematic review	15
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	14
Coming to terms with dying: Advance care planning as a conduit between clinicians, patients, and conversations about death and dying – a qualitative interview study	14
Motor neurone disease: A point-prevalence study of patient reported symptom prevalence, severity and palliative care needs	14
Effects of advance care planning in care dependent community-dwelling older persons (STADPLAN): A cluster-randomised controlled trial	14

The value of rehabilitation specialists to team-based palliative care	14
Palliative and end-of-life care needs, experiences, and preferences of LGBTQ+ individuals with serious illness: A systematic mixed-methods review	14
Where to for core outcome sets for best care for the dying person?	14
Healthy siblings’ perspectives about paediatric palliative care: A qualitative systematic review and meta-synthesis	14
Response to letters about “Palliative care and assisted dying: Uneasy bedfellows”	14
Specialist palliative care improves patient experience, reduces bed days and saves money: An economic modelling study of home- and hospital-based care	14
Reducing unnecessary hospital admissions for end-of-life patients in lower and middle-income countries	14
Masculinity and ethnicity in intersection: Implications for men’s health and palliative care services	13
Exercise interventions for advanced cancer palliative care patients: A systematic literature review and descriptive evidence synthesis of randomized controlled trials	13
Closing the health equity gap in palliative care: The time for action is now	13
Palliative care and neuro-oncological care: Better integration is needed	13
A peripheral opioid antagonist for treating urinary retention induced by opioids: A case report	13
Telehealth requires improved evidence to achieve its full potential in palliative care	13
Advance care planning and quality of life: A qualitative interview study in people with young-onset dementia and their family caregivers	13
Strategies and checklist for designing and conducting palliative care research with family carers: EAPC international expert elicitation study	13
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	13
Peer review and Palliative Medicine : Guiding reviewers’ contributions to ensuring high quality publications	13
Definition and recommendations of advance care planning: A Delphi study in five Asian sectors	13
The ideal path to a good death: An international meta-synthesis of rural residents’ perspectives	13
Memory making during bereavement care following the death of a child: A survey exploring parental experiences	13
A rapid review of the evidence for online interventions for bereavement support	13
How and in what circumstances does facilitation work for residential aged care staff in the implementation of palliative care interventions? A realist review	12
The spiritual care intervention “In dialogue with your life story”: Results of a longitudinal study on palliative clients’ spiritual wellbeing	12
Loneliness, its effect on mental and physical health, and the dying	12
COVID-19 in pediatric palliative care patients: Multicenter, retrospective cohort study	12
An easier way to die?—A qualitative interview study on specialist palliative care team members’ views on dying under sedation	12
Moral distress amongst palliative care doctors working during the COVID-19 pandemic: A narrative-focussed interview study	12
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	12
Iatrogenic suffering at the end of life: An ethnographic study	12
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	12
Tensions in advance care planning with dementia: Time for a good-enough laid-back approach?	12
Reducing inequity in the provision of children’s palliative care in low- and middle- income countries: A focus on education and research	12
Implementation of clinical guidelines in specialized palliative care—results from a national improvement project: A national register-based study	12
Feeling groovy? The present and future of psychedelic research in palliative care	12
‘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	11
Digital patient-reported outcome measures in palliative home care: A feasibility study	11
More than the sum of its parts—A constructivist grounded-theory study on specialist palliative care during crises like the COVID pandemic	11
‘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	11
Co-designing a culturally-sensitive theory-driven advance care planning game with Chinese older adults and healthcare providers	11
Sexual health at the end of life in patients with advanced cancer and their partners. Results of a Dutch prospective longitudinal study (eQuiPe)	11
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	11
‘That just doesn’t feel right at times’ – lone working practices, support and educational needs of newly employed Healthcare Assistants providing 24/7 palliative care in the community: A qualitative i	11
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	11
Serious health-related suffering experienced by children with disability and their families living in Bangladesh: A scoping review	10
Lived experiences of family caregivers of those with advanced illnesses: A secondary qualitative data analysis	10
Patients’ dignity in palliative care: An integrative review of lived experiences and family perspectives across cultures	10
Measuring the quality of patient-provider relationships in serious illness: A scoping review	10
Exploring older people’s end-of-life care preferences over time: A scoping review	10
Shared decision-making in palliative cancer care: A systematic review and metasynthesis	10
Investigating the benefits and harms of hypodermoclysis of patients in palliative care: A consecutive cohort study	10
A feasibility study of a decision aid to support family carers of people with severe dementia or those towards the end-of-life	10
Challenges of regional hospice and palliative care networks: A group discussion study with coordinators and network experts	10
“Never waste a good crisis”: A qualitative study of the impact of COVID-19 on palliative care in seven hospitals using the Dynamic Sustainability Framework	10
Developing a Theory of Change and Implementation Plan to implement a novel child- and family-centred outcome measure in paediatric palliative care	10
Understanding parent experiences of end-of-life care for children: A systematic review and qualitative evidence synthesis	10
Palliative paramedicine: An interrupted time series analysis of pre-hospital guideline efficacy	10
Practice review: Pharmacological management of severe chronic breathlessness in adults with advanced life-limiting diseases	10
Preferences of patients with palliative care needs and their families for engagement with service improvement work within the hospital setting: A qualitative study	10
Unrepresented, unheard and discriminated against: A qualitative exploration of relatives’ and professionals’ views of palliative care experiences of people of African and Caribbean descent during the	9
Defining patients living long-term with incurable cancer: A modified hybrid Delphi study	9
When should palliative care be introduced for people with progressive fibrotic interstitial lung disease? A meta-ethnography of the experiences of people with end-stage interstitial lung disease and t	9
‘Thank goodness you’re here’. Exploring the impact on patients, family carers and staff of enhanced 7-day specialist palliative care services: A mixed methods study	9
Psilocybin-assisted therapy for individuals with palliative care needs: A systematic review of safety and efficacy	9
Comparison of healthcare utilization and life-sustaining interventions between patients with glioblastoma receiving palliative care or not: A population-based study	9
What are the symptoms and concerns of young adults living with life-limiting conditions and how well are they captured by patient reported outcome measures? A mixed-methods systematic review and frame	9
Working with people living with motor neurone disease and the impact on professionals’ emotional and psychological well-being: A scoping review	9
The connections of physical and psychosocial symptoms among patients with terminal illnesses: A network analysis	9
Evaluating the measurement properties of patient-reported outcome measures for young adults with life-limiting conditions: A systematic review	9
A randomized controlled clinical trial of intranasal versus subcutaneous midazolam for agitation in terminal illness (MinTU study)	9
Loading phenobarbital in paediatric home-based terminal care: A case series	9
Mutual support between patients and family caregivers in palliative care: A qualitative study	9
Cancer pain: Results of a prospective study on prognostic indicators of pain intensity including pain syndromes assessment	9
Training programs in communication skills for healthcare professionals caring for children with life-limiting and life-threatening conditions and their families: A systematic review of healthcare prof	9
Feasibility and acceptability of the brief patient-reported experience measure consideRATE within the hospital setting for patients with palliative care needs, their families/carers and clinicians	9
A thematic analysis of hospital medical records of patients with advanced illness experiencing incarceration in the last 3 months of life	8
Demographic and clinical characteristics, practices, and outcomes of continuous palliative sedation: A multi-setting, province-wide retrospective cohort study	8
Electronic symptom monitoring for home-based palliative care: A systematic review	8
The use of natural language processing in palliative care research: A scoping review	8
A think-aloud study of the feasibility of patients with end-stage organ failure completing the ICECAP-SCM	8
Employment and family caregiving in palliative care: An international qualitative study	8

Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item	8
Public health palliative care: Reframing death, dying, loss and caregiving	8
The emotional effects on professional interpreters of interpreting palliative care conversations for adult patients: A rapid review	8
Writing for the world: Enhancing engagement and connection with an international audience	8
The ICaRAS randomised controlled trial: Intravenous iron to treat anaemia in people with advanced cancer – feasibility of recruitment, intervention and delivery	8
Translation and cross-cultural adaptation of the Integrated Palliative Care Outcome Scale in Hindi: Toward capturing palliative needs and concerns in Hindi speaking patients	7
Components of home-based palliative and supportive care for adults with heart failure: A scoping review	7
Quality in specialist palliative care for patients with pre-existing severe mental disorders: A retrospective cohort study	7
Views on advance care planning of family members of older adults with Turkish and Moroccan backgrounds: An exploratory interview study	7
Interpersonal energy: New and bold directions in palliative care health professions education research	7
‘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	7
‘A good ending but not the end’: Exploring family preparations surrounding a relative’s death and the Afterlife – A qualitative study	7
Multiple points of system failure underpin continuous subcutaneous infusion safety incidents in palliative care: A mixed methods analysis	7
Palliative care for people who use drugs during communicable disease epidemics and pandemics: A scoping review on access, policies, and programs and guidelines	7
Motivations and experiences of patients with advanced cancer participating in Phase 1 clinical trials: A qualitative study	7
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	7
Recognising dying in motor neurone disease: A scoping review	7
A qualitative service evaluation of patient and caregiver experiences of CAR-T therapy: Recommendations for service development and implications for palliative care teams	7
The effectiveness of nurse-led telehealth interventions in palliative care for patients with cancer and their family caregivers: A systematic review and meta-analysis	7
Time estimates in prognostic discussions: A conversation analytic study of hospice multidisciplinary team meetings	7
Mapping potential cultural and religious tensions in end-of-life care for Muslim patients: A scoping review	7
Characteristics and population estimates of unpaid end of life carers: An observational study	7
Over a third of palliative medicine physicians meet burnout criteria: Results from a survey study during the COVID-19 pandemic	7
The impact of regular, low-dose, sustained-release morphine for chronic breathlessness on caregiver burden: An exploratory analysis of the BEAMS trial	7
A therapist-supported internet-based intervention for bereaved siblings: A randomized controlled trial	7
The cost of providing care by family and friends (informal care) in the last year of life: A population observational study	7
Prospective case series of neuropathic cancer pain in patients treated with an EGFR-inhibitor	7
Co-production in practice: A qualitative study of the development of advance care planning workshops for South Asian elders	7
Thanks to Reviewers: 2022	7
Primary palliative care in low- and middle-income countries: A systematic review and thematic synthesis of the evidence for models and outcomes	7
The experiences of family members witnessing the diminishing drinking of a dying relative in hospital: A narrative inquiry	7
Bringing up the end of life and euthanasia. A mixed method study on consultations with people with dementia and their families in the hospital setting	6
Palliative care referral criteria and application in pediatric illness care: A scoping 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
Improving family grief outcomes: A scoping review of family-based interventions before and after the death of a child	6
A pragmatic approach to selecting a grading system for clinical practice recommendations in palliative care	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
A systematic practice review: Providing palliative care for people with Parkinson’s disease and their caregivers	6
Understanding the experiences of mothers receiving perinatal palliative care: A qualitative study	6
‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium	6
How do primary care clinicians approach hospital admission decisions for people in the final year of life? A systematic review and narrative synthesis	6
‘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	6
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	6
Too vulnerable? Successful practices for conducting research with children and young people who have life-limiting or life-threatening illness	6
Corrigendum	6
The financial costs of anticipatory prescribing: A retrospective observational study of prescribed, administered and wasted medications using community clinical records	6
Non-steroidal anti-inflammatory drugs (NSAIDs) in cancer pain: A database analysis to determine recruitment feasibility for a clinical trial	6
The impact of COVID-19 on palliative care social work: An online survey by a European Association of Palliative Care Task Force	6
A palliative care goals model for people with dementia and their family: Consensus achieved in an international Delphi study	6
Cognitive Authority Theory: Reframing health inequity, disadvantage and privilege in palliative and end-of-life care	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
PALLiative care in ONcology (PALLiON): A cluster-randomised trial investigating the effect of palliative care on the use of anticancer treatment at the end of life	5
The effectiveness of out-of-hours palliative care telephone advice lines: A rapid systematic review	5
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	5
Development of a national strategy with recommendations for the care of seriously ill and dying people and their relatives in pandemics: A modified Delphi study	5
Is paramedic palliative care different in rural compared to urban settings: A mixed methods study	5
Oxycodone/naloxone PR versus oxycodone PR in advanced cancer: A multi-centre randomised trial (ENhANCE trial)	5
Death education interventions for people with advanced diseases and/or their family caregivers: A scoping review	5
The concept of holism applied in recent palliative care practice: A scoping review	5
The range and suitability of outcome measures used in the assessment of palliative treatment for inoperable malignant bowel obstruction: A systematic review	5
Intersectoral collaboration in home-based end-of-life pediatric cancer care: A qualitative multiple-case study integrating families’ and professionals’ experiences	5
Impact of compounded drugs on the caregivers’ burden of home therapy management in pediatric palliative care: A descriptive study	5
Evaluating a partnership model of hospice enabled dementia care: A three-phased monitoring, focus group and interview study	5
What are the anticipated benefits, risks, barriers and facilitators to implementing person-centred outcome measures into routine care for children and young people with life-limiting and life-threaten	5
A mixed methods exploration of the health and caregiving experiences of fathers of children with a life-limiting condition	5
Telephone advice lines for adults with advanced illness and their family carers: a qualitative analysis and novel practical framework	5
Providing life-sustaining treatments at home for those with Motor Neurone Disease: A qualitative study of bereaved family members’ experiences of responsibility	5
A rapid umbrella review of the literature surrounding the provision of patient-centred end-of-life care	5
Social acceptability of psilocybin-assisted therapy for existential distress at the end of life: A population-based survey	5
Orally dissolving pilocarpine tablets for xerostomia in advanced cancer: A pilot N-of-1 feasibility study	5
Improving the Detection, Assessment, Management and Prevention of Delirium in Hospices (the DAMPen-D study): Feasibility study of a flexible and scalable implementat	5
What makes the palliative care initial encounter meaningful? A descriptive study with patients with cancer, family carers and palliative care professionals	5
Health and disability care providers’ experiences and perspectives on end-of-life care needs of individuals with long-standing physical disability: A qualitative interview study	5
The impact of advanced cancer on sexual health and relationships: A qualitative study on patient and partner perspectives	4
‘Regrets become a lasting source of pain’: A qualitative study on family caregivers’ experiences leading up to a relative’s death	4
‘It is easier to not allow them to see your disability straight away, to see you as a person’: An Interpretative Phenomenological Analysis of video gaming from the perspectives of men with Duchenne Mu	4
Off-label drug use in palliative medicine: Delphi study for the consensus of evidence-based treatment recommendations	4
Patient and family perspectives on rural palliative care models: A systematic review and meta-synthesis	4
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	4
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	4
Mapping primary and generalist palliative care: Taking a closer look at the base of the pyramid	4
Asian family members’ participation in advance care planning: An integrative review	4
Mapping palliative care for people living with advanced cancer in phase 1 clinical trials: A scoping review	4
Challenges and opportunities for improvement when people with an intellectual disability or serious mental illness also need palliative care: A qualitative meta-ethnography	4
Exploring engagement with a web-based self-directed psychoeducational program for advanced cancer patients and their caregivers (iFOCUS): A sub study analysis of the DIAdIC trial	4
‘Do I actually even need all these tablets?’ A qualitative study exploring deprescribing decision-making for people in receipt of palliative care and their family members	4
Integration of primary care and palliative care services to improve equality and equity at the end-of-life: Findings from realist stakeholder workshops	4
An evidence-base for the implementation of hospital-based palliative care programs in routine cancer practice: A systematic review	4
Exploring the hidden before the end: A phenomenological analysis of forgiveness at the end of life among spiritual caregivers	4
Reduction in potentially inappropriate end-of-life hospital care for cancer patients during the COVID-19 pandemic: A retrospective population-based study	4
Factors associated with the place of death of persons with advanced dementia: A systematic review of international literature with meta-analysis	4
Patient and families’ perspectives on telepalliative care: A systematic integrative review	4
A qualitative study exploring the perceptions and understandings of advance care planning by people with treatable but not curable cancer	4
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	4