Palliative Medicine

Article	Citations
Facilitators and barriers in using comics to support family caregivers of patients receiving palliative care at home: A qualitative study	129
A tribute to Derek Doyle and Cynthia Goh	70
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	68
Posttraumatic growth in palliative care settings: A scoping review of prevalence, characteristics and interventions	54
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	54
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	48
Neuropalliative care for progressive neurological diseases: A scoping review on models of care and priorities for future research	48
Resilience in advanced cancer caregiving. A systematic review and meta-synthesis	48
Use of long term aprepitant as a treatment for refractory nausea following oesophageal stent insertion – a case report	47
Preserving the integrity of personhood in people with advanced cancer: An in-depth qualitative study among patients, relatives, and care professionals	47
Mixed methods process evaluation of an advance care planning intervention among nursing home staff	47
Prevalence of grief disorders in bereaved families of cancer patients: A meta-analysis	47
The COVID-19 pandemic: A tipping point for advance care planning? Experiences of general practitioners	44
Trends in quality of care and dying perceived by family caregivers of nursing home residents with dementia 2005–2019	41
Living experiences of people with advance cancer with low socioeconomic status: A systematic review of qualitative evidence	40
Impact of the COVID-19 pandemic on end of life care delivery in care homes: A mixed method systematic review	38
Effect of continuous deep sedation on survival in the last days of life of cancer patients: A multicenter prospective cohort study	36
“Walk me through the final day”: A thematic analysis study on the family caregiver experience of the Medical Assistance in Dying procedure day	36
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	36
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	34
Association between religious beliefs and discussions regarding advance care planning: A nationwide survey	34
Palliative care volunteering: Pressing challenges in research	32
Maybe for unbearable suffering: Diverse racial, ethnic and cultural perspectives of assisted dying. A scoping review	30
The experiences, perceptions, and support needs among family caregivers of patients with advanced cancer and eating problems: An integrative review	29
Parents’ experiences of being involved in medical decision-making for their child with a life-limiting condition: A systematic review with narrative synthesis	28

The utility of the surprise question: A useful tool for identifying patients nearing the last phase of life? A systematic review and meta-analysis	27
Adaptation and continuous learning: integrative review of coping strategies of palliative care professionals	27
A rapid review of end-of-life needs in the LGBTQ+ community and recommendations for clinicians	25
What is the role of paramedics in palliative and end of life care?	25
‘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
Utilizing intricate care networks: An ethnography of patients and families navigating palliative care in a resource-limited setting	25
Organizational and individual barriers and facilitators to the integration of pediatric palliative care for children: A grounded theory study	24
The 13th World Research Congress of the European Association for Palliative Care	24
Corrigendum to Updating international consensus on best practice in care of the dying: A Delphi study	23
Facilitating equitable access to hospice care in socially deprived areas: A mixed methods multiple case study	23
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	23
Conserving dignity and facilitating adaptation to dependency with intimate hygiene for people with advanced disease: A qualitative study	23
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	22
Differences in palliative care needs between cancer patients and non-cancer patients at the start of specialized palliative care: A nationwide register-based study	21
Defining end of life in dementia: A systematic review	21
The problems of using migration background as a conceptual framework in palliative care research	21
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	20
Using the Delphi technique to achieve consensus on bereavement care in palliative care in Europe: An EAPC White Paper	20
How doctors actually (do not) involve families in decisions to continue or discontinue life-sustaining treatment in neonatal, pediatric, and adult intensive care: A qualitative study	20
Support from healthcare professionals in empowering family carers to discuss advance care planning: A population-based survey	20
The experience of nurses when providing care across acts that may be perceived as death hastening: A qualitative evidence synthesis	20
An emergency department nurse led intervention to facilitate serious illness conversations among seriously ill older adults: A feasibility study	19
A peripherally acting μ-opioid receptor antagonist for treating opioid-associated tinnitus: A case report	19
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	18
How much information is ‘reasonable’? A qualitative interview study of the prescribing practices of palliative care professionals	18
Delirium prevention in hospices: Opportunities and limitations – A focused ethnography	17
The management of absolute iron deficiency anaemia in the palliative care population: A reply to Neoh et al.	17
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	17
Improving palliative care for people with intellectual disabilities: Communication is key	17
Machine learning models to detect social distress, spiritual pain, and severe physical psychological symptoms in terminally ill patients with cancer from unstructured text data in electronic medical r	16
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	16
Re: Tan et al., Subcutaneous sodium valproate in palliative care: A systematic review	16
Sadness, despair and anger when a patient dies alone from COVID-19: A thematic content analysis of Twitter data from bereaved family members and friends	16
Education modalities for serious illness communication training: A scoping review on the impact on clinician behavior and patient outcomes	16
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-	16
Palliative care integration for patients with advanced chronic obstructive pulmonary disease (COPD): Identifying essential components using participatory action research	16
Implementation of an acute palliative care unit for COVID-19 patients in a tertiary hospital: Qualitative data on clinician perspectives	15
Caring toward end of life through acute hospital and community partnerships: A scoping review	15
‘How long do you think?’ Unresponsive dying patients in a specialist palliative care service: A consecutive cohort study	15
“I think that she would have wanted. . .”: Qualitative interviews with bereaved caregivers reveal complexity in measuring goal-concordant care at the end of life	15
Bridging cultures in palliative care: A qualitative study of the care of Indigenous Australians with advanced illness	15
Factors associated with hospitalisations of patients with chronic heart failure approaching the end of life: A systematic review	15
Capturing what matters: A retrospective observational study of advance care planning documentation at an academic medical center during the COVID-19 pandemic	15
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	15
Using advance and emergency care plans during transfer decisions: A grounded theory interview study with care home staff	15
EAPC2023 Abstract Book	14
Hypertonic packs to reverse blindness caused by facial lymphoedema in the setting of head and neck cancer – A case report	14
Impact of expected parental death on the health of adolescent and young adult children: A systematic review of the literature	14
Pharmacological treatment of pain, dyspnea, death rattle, fever, nausea, and vomiting in the last days of life in older people: A systematic review	14
Nurse perspectives on the psychosocial care of patients with urinary incontinence in home hospice: A qualitative study	14

Bereaved relatives’ quality of life before and during the COVID-19 pandemic: Results of the prospective, multicenter, observational eQuiPe study	14
Engagement of specialized palliative care services with the general public: A population-level survey in three European countries	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	13
Healthy siblings’ perspectives about paediatric palliative care: A qualitative systematic review and meta-synthesis	13
Health care professional recruitment of patients and family carers to palliative care randomised controlled trials: A qualitative multiple case study	13
Exploring “good days” with advanced cancer: A pilot daily diary study	13
International consensus on occupational therapy interventions for people with palliative care needs: A European Association for Palliative Care Group Concept Mapping study	13
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
Exercise interventions for advanced cancer palliative care patients: A systematic literature review and descriptive evidence synthesis of randomized controlled trials	13
Systematic review of conceptual and theoretical frameworks used in palliative care and end-of-life care research studies	13
Measurement equivalence of the paper-based and electronic version of the Integrated Palliative care Outcome Scale (IPOS): A randomised crossover trial	13
A systematic review on the impact of financial insecurity on the physical and psychological well-being for people living with terminal illness	13
Thanks to Reviewers	13
Deaths at home, area-based deprivation and the effect of the Covid-19 pandemic: An analysis of mortality data across four nations	13
‘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	13
Effectiveness of transmural team-based palliative care in prevention of hospitalizations in patients at the end of life: A systematic review and meta-analysis	13
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	13
What can patient safety science do for palliative care? Bridging the gap	12
Motor neurone disease: A point-prevalence study of patient reported symptom prevalence, severity and palliative care needs	12
Advance care planning and quality of life: A qualitative interview study in people with young-onset dementia and their family caregivers	12
Where to for core outcome sets for best care for the dying person?	12
End of life skin care – Research informing theory to traverse between Scylla and Charybdis?	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 and end-of-life care needs, experiences, and preferences of LGBTQ+ individuals with serious illness: A systematic mixed-methods review	12
Effects of advance care planning in care dependent community-dwelling older persons (STADPLAN): A cluster-randomised controlled trial	12
Telehealth requires improved evidence to achieve its full potential in palliative care	12
The spiritual dimension of parenting a child with a life-limiting or life-threatening condition: A mixed-methods systematic review	12
Definition and recommendations of advance care planning: A Delphi study in five Asian sectors	12
Tensions in advance care planning with dementia: Time for a good-enough laid-back approach?	11
Palliative care and neuro-oncological care: Better integration is needed	11
The ideal path to a good death: An international meta-synthesis of rural residents’ perspectives	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
A rapid review of the evidence for online interventions for bereavement support	11
The spiritual care intervention “In dialogue with your life story”: Results of a longitudinal study on palliative clients’ spiritual wellbeing	11
Peer review and Palliative Medicine : Guiding reviewers’ contributions to ensuring high quality publications	11
A peripheral opioid antagonist for treating urinary retention induced by opioids: A case report	11
Moral distress amongst palliative care doctors working during the COVID-19 pandemic: A narrative-focussed interview study	11
The development of the ADO-SQ model to predict 1-year mortality in patients with COPD	11
Closing the health equity gap in palliative care: The time for action is now	11
End of life care for people with severe mental illness: Mixed methods systematic review and thematic synthesis (the MENLOC study)	11
Strategies and checklist for designing and conducting palliative care research with family carers: EAPC international expert elicitation study	10
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	10
Iatrogenic suffering at the end of life: An ethnographic study	10
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	10
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	10
Implementation of clinical guidelines in specialized palliative care—results from a national improvement project: A national register-based study	10
Revised recommendations on standards and norms for palliative care in Europe from the European Association for Palliative Care (EAPC): A Delphi study	10
The impact on emotional well-being of being a palliative care volunteer: An interpretative phenomenological analysis	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
Risk factors for delirium in adult patients receiving specialist palliative care: A systematic review and meta-analysis	10
COVID-19 in pediatric palliative care patients: Multicenter, retrospective cohort study	10
Practice review: Evidence-based and effective management of anaemia in palliative care patients	10
Loneliness, its effect on mental and physical health, and the dying	10
Intranasal dexmedetomidine: Procedural sedation in palliative care: A case report	10
Pharmacovigilance in hospice/palliative care: Net effect of amitriptyline or nortriptyline on neuropathic pain: UTS/IMPACCT Rapid programme international consecutive cohort	10
‘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	10
Paramedics delivering palliative and end-of-life care in community-based settings: A systematic integrative review with thematic synthesis	9
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	9
An easier way to die?—A qualitative interview study on specialist palliative care team members’ views on dying under sedation	9
A feasibility study of a decision aid to support family carers of people with severe dementia or those towards the end-of-life	9
Investigating the benefits and harms of hypodermoclysis of patients in palliative care: A consecutive cohort study	9
Preferences of patients with palliative care needs and their families for engagement with service improvement work within the hospital setting: A qualitative study	9
‘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	9
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	9
Palliative paramedicine: An interrupted time series analysis of pre-hospital guideline efficacy	9
Serious health-related suffering experienced by children with disability and their families living in Bangladesh: A scoping review	9
Do learners implement what they learn? Commitment-to-change following an interprofessional palliative care course	9
Co-designing a culturally-sensitive theory-driven advance care planning game with Chinese older adults and healthcare providers	9
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	9
Clinicians’ delirium treatment practice, practice change, and influences: A national online survey	9
More than the sum of its parts—A constructivist grounded-theory study on specialist palliative care during crises like the COVID pandemic	9
Understanding parent experiences of end-of-life care for children: A systematic review and qualitative evidence synthesis	9
The connections of physical and psychosocial symptoms among patients with terminal illnesses: A network analysis	8
Measuring the quality of patient-provider relationships in serious illness: A scoping review	8
‘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	8
Comparison of healthcare utilization and life-sustaining interventions between patients with glioblastoma receiving palliative care or not: A population-based study	8
Challenges of regional hospice and palliative care networks: A group discussion study with coordinators and network experts	8
Working with people living with motor neurone disease and the impact on professionals’ emotional and psychological well-being: A scoping review	8
Exploring older people’s end-of-life care preferences over time: A scoping review	8
An online international comparison of palliative care identification in primary care using the Surprise Question	8

A thematic analysis of hospital medical records of patients with advanced illness experiencing incarceration in the last 3 months of life	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
Practice review: Pharmacological management of severe chronic breathlessness in adults with advanced life-limiting diseases	8
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	8
Unwelcome memento mori or best clinical practice? Community end of life anticipatory medication prescribing practice: A mixed methods observational study	8
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	8
Cancer pain: Results of a prospective study on prognostic indicators of pain intensity including pain syndromes assessment	8
Is trained communication about desire to die harmful for patients receiving palliative care? A cohort study	8
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	8
Writing for the world: Enhancing engagement and connection with an international audience	8
A think-aloud study of the feasibility of patients with end-stage organ failure completing the ICECAP-SCM	8
Assessment tools for problematic opioid use in palliative care: A scoping review	8
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	8
Operationalizing legal rights in end-of- life decision-making: A qualitative study	8
The association between ethnicity, socioeconomic deprivation and receipt of hospital-based palliative care for people with Covid-19: A dual centre service evaluation	8
“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	8
Shared decision-making in palliative cancer care: A systematic review and metasynthesis	8
Perspectives of board-certified healthcare chaplains on challenges and adaptations in delivery of spiritual care in the COVID-19 era: Findings from an online survey	8
The emotional effects on professional interpreters of interpreting palliative care conversations for adult patients: A rapid review	8
Electronic symptom monitoring for home-based palliative care: A systematic review	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
Care practices of specialized outpatient pediatric palliative care teams in collaboration with parents: Results of participatory observations	8
Mutual support between patients and family caregivers in palliative care: A qualitative study	8
‘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
Employment and family caregiving in palliative care: An international qualitative study	7
Effectiveness of two types of palliative home care in cancer and non-cancer patients: A retrospective population-based study using claims data	7
Palliative care for teenagers and young adults - the need for more evidence	7
Co-production in practice: A qualitative study of the development of advance care planning workshops for South Asian elders	7
Over a third of palliative medicine physicians meet burnout criteria: Results from a survey study during the COVID-19 pandemic	7
The ‘work’ of managing medications when someone is seriously ill and dying at home: A longitudinal qualitative case study of patient and family perspectives’	7
The importance of living well now and relationships: A qualitative study of the barriers and enablers to engaging frail elders with advance care planning	7
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	7
Prospective case series of neuropathic cancer pain in patients treated with an EGFR-inhibitor	7
Thanks to Reviewers: 2022	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 ICaRAS randomised controlled trial: Intravenous iron to treat anaemia in people with advanced cancer – feasibility of recruitment, intervention and delivery	7
The use of natural language processing in palliative care research: A scoping review	7
Public health palliative care: Reframing death, dying, loss and caregiving	7
Interpersonal energy: New and bold directions in palliative care health professions education research	7
Motivations and experiences of patients with advanced cancer participating in Phase 1 clinical trials: A qualitative study	6
The impact of COVID-19 on palliative care social work: An online survey by a European Association of Palliative Care Task Force	6
Corrigendum	6
Paramedics’ experiences and educational needs when participating end-of-life care at home: A mixed method study	6
Time estimates in prognostic discussions: A conversation analytic study of hospice multidisciplinary team meetings	6
Palliative care for people who use drugs during communicable disease epidemics and pandemics: A scoping review on access, policies, and programs and guidelines	6
‘A good ending but not the end’: Exploring family preparations surrounding a relative’s death and the Afterlife – A qualitative study	6
Recognising dying in motor neurone disease: A scoping review	6
‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium	6
The experiences of family members witnessing the diminishing drinking of a dying relative in hospital: A narrative inquiry	6
A qualitative service evaluation of patient and caregiver experiences of CAR-T therapy: Recommendations for service development and implications for palliative care teams	6
Non-steroidal anti-inflammatory drugs (NSAIDs) in cancer pain: A database analysis to determine recruitment feasibility for a clinical trial	6
Multiple points of system failure underpin continuous subcutaneous infusion safety incidents in palliative care: A mixed methods analysis	6
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	6
The effects of confronting one’s own end of life on older individuals and those with a life-threatening disease: A systematic literature review	6
Primary palliative care in low- and middle-income countries: A systematic review and thematic synthesis of the evidence for models and outcomes	6
A palliative care goals model for people with dementia and their family: Consensus achieved in an international Delphi study	6
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	6
Improving family grief outcomes: A scoping review of family-based interventions before and after the death of a child	6
Understanding the experiences of mothers receiving perinatal palliative care: A qualitative study	6
Components of home-based palliative and supportive care for adults with heart failure: A scoping review	6
Translation and cross-cultural adaptation of the Integrated Palliative Care Outcome Scale in Hindi: Toward capturing palliative needs and concerns in Hindi speaking patients	6
The cost of providing care by family and friends (informal care) in the last year of life: A population observational study	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
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
Exploring expanded interdisciplinary roles in goals of care conversations in a national goals of care initiative: A qualitative approach	6
Shoulder pain in a patient with renal cell carcinoma? Suprascapular neuropathy caused by bone metastasis of renal cell carcinoma: A case report	6
Facilitating family needs and support at the end of life in hospital: A descriptive study	6
Palliative care referral criteria and application in pediatric illness care: A scoping review	6
The impact of regular, low-dose, sustained-release morphine for chronic breathlessness on caregiver burden: An exploratory analysis of the BEAMS trial	6
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
A therapist-supported internet-based intervention for bereaved siblings: A randomized controlled trial	6
Views on advance care planning of family members of older adults with Turkish and Moroccan backgrounds: An exploratory interview study	6
Predictors to forgo resuscitative effort during Covid-19 critical illness at the height of the pandemic : A retrospective cohort study	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
Evaluating a partnership model of hospice enabled dementia care: A three-phased monitoring, focus group and interview study	5
Providing life-sustaining treatments at home for those with Motor Neurone Disease: A qualitative study of bereaved family members’ experiences of responsibility	5
Intersectoral collaboration in home-based end-of-life pediatric cancer care: A qualitative multiple-case study integrating families’ and professionals’ experiences	5
A rapid umbrella review of the literature surrounding the provision of patient-centred end-of-life care	5
A systematic practice review: Providing palliative care for people with Parkinson’s disease and their caregivers	5
A pragmatic approach to selecting a grading system for clinical practice recommendations in palliative care	5
A mixed methods exploration of the health and caregiving experiences of fathers of children with a life-limiting condition	5
The effectiveness of out-of-hours palliative care telephone advice lines: A rapid systematic review	5
What makes the palliative care initial encounter meaningful? A descriptive study with patients with cancer, family carers and palliative care professionals	5
Identifying older adults with frailty approaching end-of-life: A systematic review	5
The concept of holism applied in recent palliative care practice: A scoping review	5
Impact of compounded drugs on the caregivers’ burden of home therapy management in pediatric palliative care: A descriptive study	5
The financial costs of anticipatory prescribing: A retrospective observational study of prescribed, administered and wasted medications using community clinical records	5
Evaluating parent and public involvement activities within a paediatric palliative care research centre: Route map to impactful and meaningful engagement	5
Cognitive Authority Theory: Reframing health inequity, disadvantage and privilege in palliative and end-of-life care	5
Telephone advice lines for adults with advanced illness and their family carers: a qualitative analysis and novel practical framework	5
Death education interventions for people with advanced diseases and/or their family caregivers: A scoping review	5
Attitudes and preferences towards palliative and end of life care in patients with advanced illness and their family caregivers in Latin America: A mixed studies systematic review	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
Orally dissolving pilocarpine tablets for xerostomia in advanced cancer: A pilot N-of-1 feasibility study	5
Palliative care needs and models of care for people who use drugs and/or alcohol: A mixed methods systematic review	5