Palliative Medicine

Papers
(The median citation count of Palliative Medicine is 4. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-02-01 to 2025-02-01.)
ArticleCitations
Nationwide evaluation of palliative care (Q-PAC study) provided by specialized palliative care teams using quality indicators : Large variations in quality of care113
Neuropalliative care for progressive neurological diseases: A scoping review on models of care and priorities for future research70
The importance of methodology to palliative care research: A new article type for Palliative Medicine68
Definition and recommendations of advance care planning: A Delphi study in five Asian sectors61
Development of a palliative paramedicine framework to standardise best practice: A Delphi study57
A qualitative service evaluation of patient and caregiver experiences of CAR-T therapy: Recommendations for service development and implications for palliative care teams51
The experiences of family members witnessing the diminishing drinking of a dying relative in hospital: A narrative inquiry47
A good death in the child with life shortening illness: A qualitative multiple-case study46
Components of home-based palliative and supportive care for adults with heart failure: A scoping review45
Co-production in practice: A qualitative study of the development of advance care planning workshops for South Asian elders44
Facilitators and barriers in using comics to support family caregivers of patients receiving palliative care at home: A qualitative study44
The effectiveness of hope-fostering interventions in palliative care: A systematic review and meta-analysis44
Integration of primary care and palliative care services to improve equality and equity at the end-of-life: Findings from realist stakeholder workshops44
The cost of providing care by family and friends (informal care) in the last year of life: A population observational study42
Palliative care consultation in patients with Staphylococcus aureus bacteremia40
Subcutaneous sodium valproate in palliative care: A systematic review40
Dexmedetomidine for hyperactive delirium at the end of life: An open-label single arm pilot study with dose escalation in adult patients admitted to an inpatient palliative care unit39
Outcomes and measures of delirium interventional studies in palliative care to inform a core outcome set: A systematic review39
‘It feels it’s wasting whatever time I’ve got left’: A qualitative study of living with treatable but not curable cancer during the COVID-19 pandemic38
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 relatives38
A therapist-supported internet-based intervention for bereaved siblings: A randomized controlled trial38
Development of the TIFFIN recommendations for co-producing palliative and end-of-life care research with individuals with lived experience of homelessness: A qualitative study32
It was like taking an inner bath’: A qualitative evaluation of a collaborative advance care planning-approach31
‘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 ant31
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 pain30
Revised European Association for Palliative Care (EAPC) recommended framework on palliative sedation: An international Delphi study30
Self-care towards the end of life: A systematic review and narrative synthesis on access, quality and cost29
Applying evidence-based symptomatic treatments from other clinical disciplines to palliative care29
Dying in times of COVID-19: Experiences in different care settings – An online questionnaire study among bereaved relatives (the CO-LIVE study)29
The spiritual dimension of parenting a child with a life-limiting or life-threatening condition: A mixed-methods systematic review28
Palliative and end-of-life care needs, experiences, and preferences of LGBTQ+ individuals with serious illness: A systematic mixed-methods review28
Prospective case series of neuropathic cancer pain in patients treated with an EGFR-inhibitor27
Combining realist evaluation and transformative evaluation to advance research in palliative care: The case of end of life companionship27
Translation and cross-cultural adaptation of the Integrated Palliative Care Outcome Scale in Hindi: Toward capturing palliative needs and concerns in Hindi speaking patients25
Variation in end-of-life care and hospital palliative care among hospitals and local authorities: A preliminary contribution of big data25
LGBT+ partner bereavement and appraisal of the Acceptance-Disclosure Model of LGBT+ bereavement: A qualitative interview study23
Call for emergency action to limit global temperature increases, restore biodiversity, and protect health: Wealthy nations must do much more, much faster23
Exercise interventions for advanced cancer palliative care patients: A systematic literature review and descriptive evidence synthesis of randomized controlled trials22
What do we do with all the evidence for symptoms in palliative care?22
A tribute to Derek Doyle and Cynthia Goh22
Health professionals’ experiences of rapport during telehealth encounters in community palliative care: An interpretive description study21
The effect of an integrated palliative care intervention on quality of life and acute healthcare use in patients with COPD: Results of the COMPASSION cluster randomized controlled trial21
Evaluation of the integration of palliative care in a fragile setting amongst host and refugee communities: Using consecutive rapid participatory appraisals21
What can patient safety science do for palliative care? Bridging the gap20
How palliative care professionals develop coping competence through their career: A grounded theory20
Eliciting the educational needs and priorities of home care workers on end-of-life care for patients with heart failure using nominal group technique20
Palliative care for teenagers and young adults - the need for more evidence19
Patient perspectives on states worse than death: A qualitative study with implications for patient-centered outcomes and values elicitation19
What does effective end-of-life care at home for children look like? A qualitative interview study exploring the perspectives of bereaved parents19
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 mi18
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 analysis18
Parenting through grief: A cross-sectional study of recently bereaved adults with minor children18
Prognostic performance of the Karnofsky Performance Status for predicting in-hospital mortality among unselected patients who receive palliative care consultations18
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 study18
Updating international consensus on best practice in care of the dying: A Delphi study18
The health of mothers of children with a life-limiting condition: A qualitative interview study18
WITHDRAWAL – Administrative Duplicate Publication: Tribute to Derek Doyle and Cynthia Goh18
Bereavement outcomes in family members of those who died in acute care hospitals before and during the first wave of COVID-19: A cohort study18
Psychological health in Palliative Care: Thematic analysis of a psychiatrist’s and an art therapist’s clinical reflexive journals17
Motor neurone disease: A point-prevalence study of patient reported symptom prevalence, severity and palliative care needs17
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 professionals17
Thanks to Reviewers17
Opportunities for computational tools in palliative care: Supporting patient needs and lowering burden16
Over a third of palliative medicine physicians meet burnout criteria: Results from a survey study during the COVID-19 pandemic16
Willingness and concerns of transfusion-dependent hematological patients toward the option of home transfusion therapy16
Effects of advance care planning in care dependent community-dwelling older persons (STADPLAN): A cluster-randomised controlled trial16
Models of care for people with dementia approaching end of life: A rapid review16
Creating ‘safe spaces’: A qualitative study to explore enablers and barriers to culturally safe end-of-life care16
Symptom burden and lived experiences of patients, caregivers and healthcare professionals on the management of malignant bowel obstruction: A qualitative systematic review15
Identifying barriers and facilitators to palliative care integration in the management of hospitalized patients with COVID-19: A qualitative study15
Resilience in advanced cancer caregiving. A systematic review and meta-synthesis15
Healthy siblings’ perspectives about paediatric palliative care: A qualitative systematic review and meta-synthesis15
Inequities of palliative care availability and access to opioids in low- and middle-income countries15
Good medicines management: From describing problems to a vision for change15
End of life skin care – Research informing theory to traverse between Scylla and Charybdis?15
Development of a research-based classification of approaches to paediatric palliative medicine service provision within children’s and young adults’ hospices: A mixed methods study14
COP27 Climate Change Conference: Urgent action needed for Africa and the world14
Posttraumatic growth in palliative care settings: A scoping review of prevalence, characteristics and interventions14
Perceptions and experiences of clinicians and correctional officers facilitating palliative care for people in prison: A systematic review and meta-synthesis14
Delirium screening tools validated in the context of palliative care: A systematic review14
Interpersonal energy: New and bold directions in palliative care health professions education research14
Thanks to Reviewers: 202214
Efficacy of medicinal cannabis for appetite-related symptoms in people with cancer: A systematic review14
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 randomised13
Recognising dying in motor neurone disease: A scoping review13
Sexual health and closeness in couples coping with advanced cancer: Results of a multicenter observational study (eQuiPe)13
Palliative care for people who use drugs during communicable disease epidemics and pandemics: A scoping review on access, policies, and programs and guidelines13
Motivations and experiences of patients with advanced cancer participating in Phase 1 clinical trials: A qualitative study13
Views on advance care planning of family members of older adults with Turkish and Moroccan backgrounds: An exploratory interview study13
The experiences, perceptions, and support needs among family caregivers of patients with advanced cancer and eating problems: An integrative review13
The impact of digital health interventions on the psychological outcomes of patients and families receiving paediatric palliative care: A systematic review and narrative synthesis13
Acceptance and Commitment Therapy (ACT) for people with advanced progressive illness, their caregivers and staff involved in their care: A scoping review13
Telehealth requires improved evidence to achieve its full potential in palliative care13
The potential of experience sampling methods in palliative care13
Facilitating family needs and support at the end of life in hospital: A descriptive study13
Practice review: Evidence-based and effective management of fatigue in patients with advanced cancer13
Understanding the role and deployment of volunteers within specialist palliative care services and organisations as they have adjusted to the COVID-19 pandemic: A multi-national EAPC volunteer taskfor13
‘A good ending but not the end’: Exploring family preparations surrounding a relative’s death and the Afterlife – A qualitative study12
Palliative care and neuro-oncological care: Better integration is needed12
‘There’s something about admitting that you are lonely’ – prevalence, impact and solutions to loneliness in terminal illness: An explanatory sequential multi-methods study12
The impact of regular, low-dose, sustained-release morphine for chronic breathlessness on caregiver burden: An exploratory analysis of the BEAMS trial12
“By the time she got sick it was just kind of too late”: A qualitative study on advanced care planning among bereaved lesbian, gay, and bisexual older women12
Primary palliative care in low- and middle-income countries: A systematic review and thematic synthesis of the evidence for models and outcomes12
Moral distress amongst palliative care doctors working during the COVID-19 pandemic: A narrative-focussed interview study12
Inadequate human resources, equipment and training: A qualitative assessment of the objectives of the NUHELP end-of-life care programme in the context of the COVID-19 pandemic12
Loneliness, its effect on mental and physical health, and the dying12
Living experiences of people with advance cancer with low socioeconomic status: A systematic review of qualitative evidence12
Association between religious beliefs and discussions regarding advance care planning: A nationwide survey12
Navigating the caregiving abyss: A metasynthesis of how family caregivers manage end-of-life care for older adults at home11
Serious illness care quality during COVID-19: Identifying improvement opportunities in narrative reports from a National Bereaved Family Survey11
A core outcome set for best care for the dying person: Results of an international Delphi study and consensus meeting11
End-of-life cost trajectories and the trade-off between treatment costs and life-extension: Findings from the Cost and Medical Care of Patients with Advanced Serious Illness (COMPASS) cohort study11
Perceptions of prognosis and end-of-life care outcomes in patients with advanced lung and gastrointestinal cancer11
Culture in the spotlight—cultural adaptation and content validity of the integrated palliative care outcome scale for dementia: A cognitive interview study11
Efficacy of spiritual interventions in palliative care: An umbrella review of systematic reviews11
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 professionals11
Multiple points of system failure underpin continuous subcutaneous infusion safety incidents in palliative care: A mixed methods analysis11
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’ perspectives11
Prevalence of grief disorders in bereaved families of cancer patients: A meta-analysis10
Waking up from fatigue: The hidden burden of fatigue10
Description of patient reported experience measures (PREMs) for hospitalised patients with palliative care needs and their families, and how these map to noted areas of importance for quality care: A 10
The double awareness of the wish to hasten death and the will to live: A secondary analysis of outlier patients from a mixed-methods study10
Pain assessment tools in paediatric palliative care: A systematic review of psychometric properties and recommendations for clinical practice10
Arts engagement facilitated by artists with individuals with life-limiting illness: A systematic integrative review of the literature10
Impact of the COVID-19 pandemic on end of life care delivery in care homes: A mixed method systematic review10
Understanding advance care planning in care homes throughout the COVID-19 pandemic: A critical realist review and synthesis10
Invited Editorials10
A rapid review of the evidence for online interventions for bereavement support10
A peripheral opioid antagonist for treating urinary retention induced by opioids: A case report10
Understanding the experiences of mothers receiving perinatal palliative care: A qualitative study10
Time estimates in prognostic discussions: A conversation analytic study of hospice multidisciplinary team meetings10
Views of patients with progressive illness and carers about the role of digital advance care planning systems to record and share information: A qualitative study10
‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium10
Preserving the integrity of personhood in people with advanced cancer: An in-depth qualitative study among patients, relatives, and care professionals10
Civic engagement in serious illness, death, and loss: A systematic mixed-methods review10
The COVID-19 pandemic: A tipping point for advance care planning? Experiences of general practitioners9
Professionals’, patients’ and families’ views on the use of opioids for chronic breathlessness: A systematic review using the framework method and pillar process9
Maybe for unbearable suffering: Diverse racial, ethnic and cultural perspectives of assisted dying. A scoping review9
‘Life became slow down’: A descriptive qualitative study of the experiences of cancer-related fatigue amongst people with advanced lung cancer9
Mixed methods process evaluation of an advance care planning intervention among nursing home staff9
Iatrogenic suffering at the end of life: An ethnographic study9
Hearing the voices of children diagnosed with a life-threatening or life-limiting illness and their parents’ accounts in a palliative care setting: A qualitative study9
“Walk me through the final day”: A thematic analysis study on the family caregiver experience of the Medical Assistance in Dying procedure day9
Determining massage dose-response to improve cancer-related symptom cluster of pain, fatigue, and sleep disturbance: A 7-arm randomized trial in palliative cancer care9
Strategies for recruiting the dependent children of patients with a life-limiting illness as research participants9
Virtual home-based palliative care during COVID-19: A qualitative exploration of the patient, caregiver, and healthcare provider experience9
“They were here, and they still matter”: A qualitative study of bereaved parents legacy experiences and perceptions9
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 9
Implementation of clinical guidelines in specialized palliative care—results from a national improvement project: A national register-based study9
A palliative care goals model for people with dementia and their family: Consensus achieved in an international Delphi study9
Gamification for promoting advance care planning: A mixed-method systematic review and meta-analysis8
Palliative care referral criteria and application in pediatric illness care: A scoping review8
Why patients in specialist palliative care in-patient settings are at high risk of falls and falls-related harm: A realist synthesis8
What does ‘good’ palliative care look like for children and young people? A qualitative study of parents’ experiences and perspectives8
Measuring quality of dying, death and end-of-life care for children and young people: A scoping review of available tools8
Use of long term aprepitant as a treatment for refractory nausea following oesophageal stent insertion – a case report8
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 study8
‘You can’t feel what we feel’: Multifaceted dyspnoea invisibility in advanced chronic obstructive pulmonary disease examined through interpretative phenomenological analysis8
Strategies and checklist for designing and conducting palliative care research with family carers: EAPC international expert elicitation study8
Area-Based Compassionate Communities: A systematic integrative review of existing initiatives worldwide8
Identification of palliative care needs among people with dementia and its association with acute hospital care and community service use at the end-of-life: A retrospective cohort study using linked 8
Cannabinoids for the treatment of refractory neuropathic pruritus in amyotrophic lateral sclerosis: A case report8
The ideal path to a good death: An international meta-synthesis of rural residents’ perspectives8
Closing the health equity gap in palliative care: The time for action is now8
Effect of continuous deep sedation on survival in the last days of life of cancer patients: A multicenter prospective cohort study8
Which factors influence the quality of end-of-life care in interstitial lung disease? A systematic review with narrative synthesis8
Improving family grief outcomes: A scoping review of family-based interventions before and after the death of a child8
Practice review: Evidence-based and effective management of anaemia in palliative care patients8
The development of the ADO-SQ model to predict 1-year mortality in patients with COPD8
Virtual reality for pain management in advanced heart failure: A randomized controlled study8
Trauma-informed palliative care is needed: A call for implementation and research8
Co-design and prototype development of the ‘Ayzot App’: A mobile phone based remote monitoring system for palliative care8
How do people in prison access palliative care? A scoping review of models of palliative care delivery for people in prison in high-income countries8
Trends in quality of care and dying perceived by family caregivers of nursing home residents with dementia 2005–20198
Palliative care volunteering: Pressing challenges in research8
The impact on emotional well-being of being a palliative care volunteer: An interpretative phenomenological analysis7
How to enhance advance care planning research?7
Using the Delphi technique to achieve consensus on bereavement care in palliative care in Europe: An EAPC White Paper7
End of life care for people with severe mental illness: Mixed methods systematic review and thematic synthesis (the MENLOC study)7
Comparing the effect of a consult model versus an integrated palliative care and medical oncology co-rounding model on health care utilization in an acute hospital – an open-label stepped-wedge cluste7
‘It was like an airbag, it cushioned the blow’: A multi-site qualitative study of bereaved parents’ experiences of using cooling facilities7
‘People don’t realise how much their past experiences affect them in adulthood’: A qualitative study of adult siblings’ experiences of growing-up with a sister/brother with a childhood life-lim7
Associations between physicians’ personal preferences for end-of-life decisions and their own clinical practice: PROPEL survey study in Europe, North America, and Australia7
Non-steroidal anti-inflammatory drugs (NSAIDs) in cancer pain: A database analysis to determine recruitment feasibility for a clinical trial7
Role and response of primary healthcare services in community end-of-life care during COVID-19: Qualitative study and recommendations for primary palliative care delivery7
Organizational and individual barriers and facilitators to the integration of pediatric palliative care for children: A grounded theory study7
Accelerated transcranial magnetic stimulation for psychological distress in advanced cancer: A phase 2a feasibility and preliminary efficacy clinical trial7
Differences in palliative care needs between cancer patients and non-cancer patients at the start of specialized palliative care: A nationwide register-based study7
Palliative and end-of-life care for patients with pleural mesothelioma: A cohort study7
The impact of COVID-19 on palliative care social work: An online survey by a European Association of Palliative Care Task Force7
Revised recommendations on standards and norms for palliative care in Europe from the European Association for Palliative Care (EAPC): A Delphi study7
A feasibility and acceptability pilot for the longitudinal measurement of inspiratory and expiratory pressures in people with advanced pancreatic cancer7
Advance care planning and end-of-life care in patients with an implantable cardioverter defibrillator: The perspective of relatives7
Assessing the impact of a health navigator on improving access to care and addressing the social needs of palliative care patients experiencing homelessness: A service evaluation7
Existential experiences and perceptions of death among children with terminal cancer: An interpretative qualitative study7
Estimating the escalating future need for palliative care among people living with dementia6
“Collateral beauty.” Experiences and needs of professionals caring for parents continuing pregnancy after a life-limiting prenatal diagnosis: A grounded theory study6
COVID-19 in pediatric palliative care patients: Multicenter, retrospective cohort study6
A grounded theory of interdependence between specialist and generalist palliative care teams across healthcare settings6
A task service and a talking service: A qualitative exploration of bereaved family perceptions of community nursing care at the end of life6
Utilizing intricate care networks: An ethnography of patients and families navigating palliative care in a resource-limited setting6
‘Saying goodbye’ during the COVID-19 pandemic: A document analysis of online newspapers with implications for end of life care6
Abstracts from the 17th World Congress of the EAPC 20216
Predictors to forgo resuscitative effort during Covid-19 critical illness at the height of the pandemic : A retrospective cohort study6
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 practices6
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 trials6
Fatigue in advanced disease associated with palliative care: A systematic review of non-pharmacological treatments6
‘It was never about me’: A qualitative inquiry into the experiences of psychological support and perceived support needs of family caregivers of people with high-grade glioma6
‘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 i6
Risk factors for delirium in adult patients receiving specialist palliative care: A systematic review and meta-analysis6
Shoulder pain in a patient with renal cell carcinoma? Suprascapular neuropathy caused by bone metastasis of renal cell carcinoma: A case report6
Spiritual, religious, and existential concerns of children and young people with life-limiting and life-threatening conditions: A qualitative interview study6
Smiles behind the masks: A systematic review and narrative synthesis exploring how family members of seriously ill or dying patients are supported during infectious disease outbreaks6
Palliative care needs and models of care for people who use drugs and/or alcohol: A mixed methods systematic review6
‘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 illness6
General practitioners’ evaluations of optimal timing to initiate advance care planning for patients with cancer, organ failure, or multimorbidity: A health records survey study6
How do primary care clinicians approach hospital admission decisions for people in the final year of life? A systematic review and narrative synthesis6
Factors facilitating positive outcomes in community-based end-of-life care: A cross-sectional qualitative study of patients and family caregivers6
Understanding and addressing challenges for advance care planning in the COVID-19 pandemic: An analysis of the UK CovPall survey data from specialist palliative care services6
Prescribing and deprescribing in older people with life-limiting illnesses receiving hospice care at the end of life: A longitudinal, retrospective cohort study6
It’s almost superstition: If I don’t think about it, it won’t happen’. Public knowledge and attitudes towards advance care planning: A sequential mixed methods study6
Intranasal dexmedetomidine: Procedural sedation in palliative care: A case report6
The 13th World Research Congress of the European Association for Palliative Care6
A systematic practice review: Providing palliative care for people with Parkinson’s disease and their caregivers6
Palliative care needs and experiences of people in prison: A systematic review and meta-synthesis6
Applying the community readiness model to identify and address inequity in end-of-life care in South Asian communities6
Corrigendum5
Factors influencing deprescribing in primary care for those towards the end of life: A qualitative interview study with patients and healthcare practitioners5
Opportunities for public involvement in big data research in palliative and end-of-life care5
Palliative care for adolescents and young adults with advanced illness: A scoping review5
A pragmatic approach to selecting a grading system for clinical practice recommendations in palliative care5
A rapid review of end-of-life needs in the LGBTQ+ community and recommendations for clinicians5
It’s like standing in front of a prison fence – Dying during the SARS-CoV2 pandemic: A qualitative study of bereaved relatives’ experiences5
Parents’ experiences of being involved in medical decision-making for their child with a life-limiting condition: A systematic review with narrative synthesis5
What is the role of paramedics in palliative and end of life care?5
Exploring expanded interdisciplinary roles in goals of care conversations in a national goals of care initiative: A qualitative approach5
Evaluating parent and public involvement activities within a paediatric palliative care research centre: Route map to impactful and meaningful engagement5
Evaluation of a WeChat-based Dyadic Life Review Program for people with advanced cancer and family caregivers: A mixed-method feasibility study5
Palliative paramedicine: Comparing clinical practice through guideline quality appraisal and qualitative content analysis5
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 study5
The financial costs of anticipatory prescribing: A retrospective observational study of prescribed, administered and wasted medications using community clinical records5
How patients with advanced cancer conceptualize prognosis: A phenomenological qualitative inquiry5
Paracentesis for cancer-related ascites in palliative care: An international, prospective cohort study5
‘Sadly I think we are sort of still quite white, middle-class really’ – Inequities in access to bereavement support: Findings from a mixed methods study5
Paramedics’ experiences and educational needs when participating end-of-life care at home: A mixed method study5
Adaptation and continuous learning: integrative review of coping strategies of palliative care professionals5
Service change and innovation in community end-of-life care during the COVID-19 pandemic: Qualitative analysis of a nationwide primary care survey5
Trends of concerns from diagnosis in patients with advanced lung cancer and their family caregivers: A 2-year longitudinal study5
‘There’s this big fear around palliative care because it’s connected to death and dying’: A qualitative exploration of the perspectives of undergraduate students on the role of the speech and language5
The problems of using migration background as a conceptual framework in palliative care research5
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