Palliative Medicine

Article	Citations
A tribute to Derek Doyle and Cynthia Goh	408
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	97
Facilitators and barriers in using comics to support family caregivers of patients receiving palliative care at home: A qualitative study	62
Neuropalliative care for progressive neurological diseases: A scoping review on models of care and priorities for future research	59
Posttraumatic growth in palliative care settings: A scoping review of prevalence, characteristics and interventions	57
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	53
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	52
Resilience in advanced cancer caregiving. A systematic review and meta-synthesis	44
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	41
‘Saying goodbye’. . . A systematic integrative review of palliative caregiving in intergenerational living contexts	40
Preserving the integrity of personhood in people with advanced cancer: An in-depth qualitative study among patients, relatives, and care professionals	37
The experiences, perceptions, and support needs among family caregivers of patients with advanced cancer and eating problems: An integrative review	36
Effect of continuous deep sedation on survival in the last days of life of cancer patients: A multicenter prospective cohort study	34
“Walk me through the final day”: A thematic analysis study on the family caregiver experience of the Medical Assistance in Dying procedure day	33
Palliative care volunteering: Pressing challenges in research	33
Maybe for unbearable suffering: Diverse racial, ethnic and cultural perspectives of assisted dying. A scoping review	31
Living experiences of people with advance cancer with low socioeconomic status: A systematic review of qualitative evidence	29
Corrigendum to Updating international consensus on best practice in care of the dying: A Delphi study	28
Facilitating equitable access to hospice care in socially deprived areas: A mixed methods multiple case study	28
Mixed methods process evaluation of an advance care planning intervention among nursing home staff	28
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	27
The 13th World Research Congress of the European Association for Palliative Care	27
The experience of nurses when providing care across acts that may be perceived as death hastening: A qualitative evidence synthesis	27
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
What is the role of paramedics in palliative and end of life care?	26

A rapid review of end-of-life needs in the LGBTQ+ community and recommendations for clinicians	26
‘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	25
Parents’ experiences of being involved in medical decision-making for their child with a life-limiting condition: A systematic review with narrative synthesis	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	23
Utilizing intricate care networks: An ethnography of patients and families navigating palliative care in a resource-limited setting	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
Support from healthcare professionals in empowering family carers to discuss advance care planning: A population-based survey	22
The management of absolute iron deficiency anaemia in the palliative care population: A reply to Neoh et al.	21
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	21
A peripherally acting μ-opioid receptor antagonist for treating opioid-associated tinnitus: A case report	21
An emergency department nurse led intervention to facilitate serious illness conversations among seriously ill older adults: A feasibility study	20
Education modalities for serious illness communication training: A scoping review on the impact on clinician behavior and patient outcomes	20
How much information is ‘reasonable’? A qualitative interview study of the prescribing practices of palliative care professionals	20
C-reactive protein and white blood cell count are adverse prognostic markers for patients with advanced cancer on parenteral nutrition in a palliative care unit setting: A retrospective cohort study	20
Delirium prevention in hospices: Opportunities and limitations – A focused ethnography	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	19
Bridging cultures in palliative care: A qualitative study of the care of Indigenous Australians with advanced illness	19
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	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
“ I think that she would have wanted. . .” : Qualitative interviews with bereaved caregivers reveal complexity in measuring goal-concordant care at the end of life	19
Implementation of an acute palliative care unit for COVID-19 patients in a tertiary hospital: Qualitative data on clinician perspectives	18
Integrating lived experiences of out-of-hours health services for people with palliative and end-of-life care needs with national datasets for people dying in Scotland in 2016: A mixed methods, multi-	18
Prevalence, risk factors and management of pressure injuries and their implications for palliative care: A rapid overview of reviews	18
Re: Tan et al., Subcutaneous sodium valproate in palliative care: A systematic review	18
‘How long do you think?’ Unresponsive dying patients in a specialist palliative care service: A consecutive cohort study	17
Factors associated with hospitalisations of patients with chronic heart failure approaching the end of life: A systematic review	17
Exploring “good days” with advanced cancer: A pilot daily diary study	16
The 19th World Congress of the European Association for Palliative Care 29 – 31 May 2025 Helsinki, Finland	16
Engagement of specialized palliative care services with the general public: A population-level survey in three European countries	16
Impact of expected parental death on the health of adolescent and young adult children: A systematic review of the literature	16
Enhancing the wellbeing of refugees living with advanced life-limiting illness in high-income resettlement countries: A systematic review	16
Effectiveness of and implementation requirements for telehealth in palliative care patients with advanced cancer: A systematic review and meta-analysis	16
Health care professional recruitment of patients and family carers to palliative care randomised controlled trials: A qualitative multiple case study	16
Hypertonic packs to reverse blindness caused by facial lymphoedema in the setting of head and neck cancer – A case report	16
Pharmacological treatment of pain, dyspnea, death rattle, fever, nausea, and vomiting in the last days of life in older people: A systematic review	15
Memory-making interventions for children with life-threatening or life-limiting conditions and their families: A systematic review of evidence and implications for practice	15
Systematic review of conceptual and theoretical frameworks used in palliative care and end-of-life care research studies	15
Measurement equivalence of the paper-based and electronic version of the Integrated Palliative care Outcome Scale (IPOS): A randomised crossover trial	14
‘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	14
Thanks to Reviewers	14
A narrow view of palliative care and assisted dying	14
Effectiveness of transmural team-based palliative care in prevention of hospitalizations in patients at the end of life: A systematic review and meta-analysis	14
International consensus on occupational therapy interventions for people with palliative care needs: A European Association for Palliative Care Group Concept Mapping study	14
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	14
Supporting best practice in reflexive thematic analysis reporting in Palliative Medicine: A review of published research and introduction to the Reflexive Thematic Analysis Reporting Guideli	14
EAPC2023 Abstract Book	14
Caring toward end of life through acute hospital and community partnerships: A scoping review	14
Deaths at home, area-based deprivation and the effect of the Covid-19 pandemic: An analysis of mortality data across four nations	14
‘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	14
A systematic review on the impact of financial insecurity on the physical and psychological well-being for people living with terminal illness	14

Models, components and outcomes of palliative and end-of-life care provided to adults living at home: A systematic umbrella review of reviews	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	13
Effects of advance care planning in care dependent community-dwelling older persons (STADPLAN): A cluster-randomised controlled trial	13
Advance care planning and quality of life: A qualitative interview study in people with young-onset dementia and their family caregivers	13
Where to for core outcome sets for best care for the dying person?	13
Healthy siblings’ perspectives about paediatric palliative care: A qualitative systematic review and meta-synthesis	13
Exercise interventions for advanced cancer palliative care patients: A systematic literature review and descriptive evidence synthesis of randomized controlled trials	13
What can patient safety science do for palliative care? Bridging the gap	13
Reducing unnecessary hospital admissions for end-of-life patients in lower and middle-income countries	13
The spiritual dimension of parenting a child with a life-limiting or life-threatening condition: A mixed-methods systematic review	13
A peripheral opioid antagonist for treating urinary retention induced by opioids: A case report	12
Practice review: Evidence-based and effective management of anaemia in palliative care patients	12
A rapid review of the evidence for online interventions for bereavement support	12
Telehealth requires improved evidence to achieve its full potential in palliative care	12
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	12
Palliative care and neuro-oncological care: Better integration is needed	12
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	12
Closing the health equity gap in palliative care: The time for action is now	12
The development of the ADO-SQ model to predict 1-year mortality in patients with COPD	12
The ideal path to a good death: An international meta-synthesis of rural residents’ perspectives	12
Definition and recommendations of advance care planning: A Delphi study in five Asian sectors	12
Reducing inequity in the provision of children’s palliative care in low- and middle- income countries: A focus on education and research	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
Strategies and checklist for designing and conducting palliative care research with family carers: EAPC international expert elicitation study	12
Iatrogenic suffering at the end of life: An ethnographic study	12
Masculinity and ethnicity in intersection: Implications for men’s health and palliative care services	12
Motor neurone disease: A point-prevalence study of patient reported symptom prevalence, severity and palliative care needs	12
Response to letters about “Palliative care and assisted dying: Uneasy bedfellows”	12
Palliative and end-of-life care needs, experiences, and preferences of LGBTQ+ individuals with serious illness: A systematic mixed-methods review	12
Memory making during bereavement care following the death of a child: A survey exploring parental experiences	12
Tensions in advance care planning with dementia: Time for a good-enough laid-back approach?	11
COVID-19 in pediatric palliative care patients: Multicenter, retrospective cohort study	11
Revised recommendations on standards and norms for palliative care in Europe from the European Association for Palliative Care (EAPC): A Delphi study	11
An easier way to die?—A qualitative interview study on specialist palliative care team members’ views on dying under sedation	11
Pharmacovigilance in hospice/palliative care: Net effect of amitriptyline or nortriptyline on neuropathic pain: UTS/IMPACCT Rapid programme international consecutive cohort	11
Implementation of clinical guidelines in specialized palliative care—results from a national improvement project: A national register-based study	11
Peer review and Palliative Medicine : Guiding reviewers’ contributions to ensuring high quality publications	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
‘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
Sexual health at the end of life in patients with advanced cancer and their partners. Results of a Dutch prospective longitudinal study (eQuiPe)	11
Feeling groovy? The present and future of psychedelic research in palliative care	11
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	11
Moral distress amongst palliative care doctors working during the COVID-19 pandemic: A narrative-focussed interview study	11
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	11
Co-designing a culturally-sensitive theory-driven advance care planning game with Chinese older adults and healthcare providers	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
Preferences of patients with palliative care needs and their families for engagement with service improvement work within the hospital setting: A qualitative study	10
How and in what circumstances does facilitation work for residential aged care staff in the implementation of palliative care interventions? A realist review	10
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	10
Do learners implement what they learn? Commitment-to-change following an interprofessional palliative care course	10
More than the sum of its parts—A constructivist grounded-theory study on specialist palliative care during crises like the COVID pandemic	10
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	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
Investigating the benefits and harms of hypodermoclysis of patients in palliative care: A consecutive cohort study	10
‘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	10
Serious health-related suffering experienced by children with disability and their families living in Bangladesh: A scoping review	10
Developing a Theory of Change and Implementation Plan to implement a novel child- and family-centred outcome measure in paediatric palliative care	10
Measuring the quality of patient-provider relationships in serious illness: A scoping review	9
Understanding parent experiences of end-of-life care for children: A systematic review and qualitative evidence synthesis	9
Lived experiences of family caregivers of those with advanced illnesses: A secondary qualitative data analysis	9
Exploring older people’s end-of-life care preferences over time: A scoping review	9
Cancer pain: Results of a prospective study on prognostic indicators of pain intensity including pain syndromes assessment	9
Mutual support between patients and family caregivers in palliative care: A qualitative study	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
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
‘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
Shared decision-making in palliative cancer care: A systematic review and metasynthesis	9
Challenges of regional hospice and palliative care networks: A group discussion study with coordinators and network experts	9
“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	9
Loading phenobarbital in paediatric home-based terminal care: A case series	9
The connections of physical and psychosocial symptoms among patients with terminal illnesses: A network analysis	9
Trapped in a double cage: How patients’ partners experience the diagnosis of advanced cancer in times of the COVID-19 pandemic: An interpretative phenomenological analysis	9
Palliative paramedicine: An interrupted time series analysis of pre-hospital guideline efficacy	9
Working with people living with motor neurone disease and the impact on professionals’ emotional and psychological well-being: A scoping review	9
Practice review: Pharmacological management of severe chronic breathlessness in adults with advanced life-limiting diseases	9
Comparison of healthcare utilization and life-sustaining interventions between patients with glioblastoma receiving palliative care or not: A population-based 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
Defining patients living long-term with incurable cancer: A modified hybrid Delphi study	9
Electronic symptom monitoring for home-based palliative care: A systematic review	8

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	8
Employment and family caregiving in palliative care: An international qualitative study	8
A think-aloud study of the feasibility of patients with end-stage organ failure completing the ICECAP-SCM	8
Writing for the world: Enhancing engagement and connection with an international audience	8
The use of natural language processing in palliative care research: A scoping review	8
Thanks to Reviewers: 2022	8
Components of home-based palliative and supportive care for adults with heart failure: A scoping review	8
Psilocybin-assisted therapy for individuals with palliative care needs: A systematic review of safety and efficacy	8
The ICaRAS randomised controlled trial: Intravenous iron to treat anaemia in people with advanced cancer – feasibility of recruitment, intervention and delivery	8
Evaluating the measurement properties of patient-reported outcome measures for young adults with life-limiting conditions: A systematic review	8
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	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	8
Views on advance care planning of family members of older adults with Turkish and Moroccan backgrounds: An exploratory interview study	8
Recognising dying in motor neurone disease: A scoping review	8
A thematic analysis of hospital medical records of patients with advanced illness experiencing incarceration in the last 3 months of life	8
Public health palliative care: Reframing death, dying, loss and caregiving	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
The emotional effects on professional interpreters of interpreting palliative care conversations for adult patients: A rapid review	8
Interpersonal energy: New and bold directions in palliative care health professions education research	8
The experiences of family members witnessing the diminishing drinking of a dying relative in hospital: A narrative inquiry	8
The cost of providing care by family and friends (informal care) in the last year of life: A population observational study	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
‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium	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
Time estimates in prognostic discussions: A conversation analytic study of hospice multidisciplinary team meetings	7
Characteristics and population estimates of unpaid end of life carers: An observational study	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
Co-production in practice: A qualitative study of the development of advance care planning workshops for South Asian elders	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
Non-steroidal anti-inflammatory drugs (NSAIDs) in cancer pain: A database analysis to determine recruitment feasibility for a clinical trial	7
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	7
The impact of COVID-19 on palliative care social work: An online survey by a European Association of Palliative Care Task Force	7
Improving family grief outcomes: A scoping review of family-based interventions before and after the death of a child	7
Motivations and experiences of patients with advanced cancer participating in Phase 1 clinical trials: A qualitative study	7
A therapist-supported internet-based intervention for bereaved siblings: A randomized controlled trial	7
Prospective case series of neuropathic cancer pain in patients treated with an EGFR-inhibitor	7
Symptom burden and lived experiences of patients, caregivers and healthcare professionals on the management of malignant bowel obstruction: A qualitative systematic review	7
The impact of regular, low-dose, sustained-release morphine for chronic breathlessness on caregiver burden: An exploratory analysis of the BEAMS trial	7
Multiple points of system failure underpin continuous subcutaneous infusion safety incidents in palliative care: A mixed methods analysis	7
Understanding the experiences of mothers receiving perinatal palliative care: A qualitative study	7
Palliative care referral criteria and application in pediatric illness care: A scoping review	7
Over a third of palliative medicine physicians meet burnout criteria: Results from a survey study during the COVID-19 pandemic	7
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
How do primary care clinicians approach hospital admission decisions for people in the final year of life? A systematic review and narrative synthesis	6
Evaluating parent and public involvement activities within a paediatric palliative care research centre: Route map to impactful and meaningful engagement	6
Paramedics’ experiences and educational needs when participating end-of-life care at home: A mixed method study	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
Too vulnerable? Successful practices for conducting research with children and young people who have life-limiting or life-threatening illness	6
A palliative care goals model for people with dementia and their family: Consensus achieved in an international Delphi study	6
The financial costs of anticipatory prescribing: A retrospective observational study of prescribed, administered and wasted medications using community clinical records	6
Cognitive Authority Theory: Reframing health inequity, disadvantage and privilege in palliative and end-of-life care	6
A systematic practice review: Providing palliative care for people with Parkinson’s disease and their caregivers	6
Palliative care needs and models of care for people who use drugs and/or alcohol: A mixed methods systematic review	6
Orally dissolving pilocarpine tablets for xerostomia in advanced cancer: A pilot N-of-1 feasibility study	6
Primary palliative care in low- and middle-income countries: A systematic review and thematic synthesis of the evidence for models and outcomes	6
Corrigendum	6
‘A good ending but not the end’: Exploring family preparations surrounding a relative’s death and the Afterlife – A qualitative study	6
A pragmatic approach to selecting a grading system for clinical practice recommendations in palliative 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
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	6
Social acceptability of psilocybin-assisted therapy for existential distress at the end of life: A population-based survey	5
Death doulas as supportive companions in end-of-life care: A scoping review	5
An evidence-base for the implementation of hospital-based palliative care programs in routine cancer practice: A systematic review	5
Impact of compounded drugs on the caregivers’ burden of home therapy management in pediatric palliative care: A descriptive study	5
Intersectoral collaboration in home-based end-of-life pediatric cancer care: A qualitative multiple-case study integrating families’ and professionals’ experiences	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 mixed methods exploration of the health and caregiving experiences of fathers of children with a life-limiting condition	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
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
A rapid umbrella review of the literature surrounding the provision of patient-centred end-of-life care	5
The effectiveness of out-of-hours palliative care telephone advice lines: A rapid systematic review	5
The concept of holism applied in recent palliative care practice: A scoping review	5
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
Oxycodone/naloxone PR versus oxycodone PR in advanced cancer: A multi-centre randomised trial (ENhANCE trial)	5
Evaluating a partnership model of hospice enabled dementia care: A three-phased monitoring, focus group and interview study	5
What makes the palliative care initial encounter meaningful? A descriptive study with patients with cancer, family carers and palliative care professionals	5
Death education interventions for people with advanced diseases and/or their family caregivers: A scoping 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
The range and suitability of outcome measures used in the assessment of palliative treatment for inoperable malignant bowel obstruction: A systematic review	5
A qualitative study exploring the perceptions and understandings of advance care planning by people with treatable but not curable cancer	4
More than 3 years of teleconsultations: A retrospective cohort study in specialized outpatient palliative care	4
What do we do with all the evidence for symptoms in palliative care?	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
Integration of primary care and palliative care services to improve equality and equity at the end-of-life: Findings from realist stakeholder workshops	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
Creating ‘safe spaces’: A qualitative study to explore enablers and barriers to culturally safe end-of-life care	4
Ethnic inequality in place of death: Analysis using ‘gold standard’ self-reported ethnicity data from the Census Longitudinal Study	4
Systematic adaptation of public health palliative care interventions across settings using ADAPT guidance: Methodological learnings from the EU NAVIGATE project	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
‘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
Subcutaneous sodium valproate in palliative care: A systematic review	4
Unpaid care, time taken off work and healthcare costs before and after partner bereavement among same-gender and different-gender partners: A national population-based study	4
Disparity in health care in end-of-life among patients with lung cancer and pre-existing mental disorders: A nationwide cohort study	4
Good medicines management: From describing problems to a vision for change	4