Palliative & Supportive Care

Papers
(The TQCC of Palliative & Supportive Care is 3. 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 2020-11-01 to 2024-11-01.)
ArticleCitations
The impact of COVID-19 on palliative care workers across the world: A qualitative analysis of responses to open-ended questions38
Impact of home-based palliative care on health care costs and hospital use: A systematic review34
Navigating the terrain of moral distress: Experiences of pediatric end-of-life care and bereavement during COVID-1933
“When the first session may be the last!”: A case report of the implementation of “rapid tele-psychotherapy” with single-session music therapy in the COVID-19 outbreak22
Virtual reality for improving pain and pain-related symptoms in patients with advanced stage colorectal cancer: A pilot trial to test feasibility and acceptability22
Voicing their choices: Advance care planning with adolescents and young adults with cancer and other serious conditions21
Increasing our understanding of nonphysical suffering within palliative care: A scoping review17
The realities of Medical Assistance in Dying in Canada16
Hope in end-of-life cancer patients: A cross-sectional analysis16
A lifespan approach to understanding family caregiver experiences of a blood cancer diagnosis15
Delirium is associated with an increased morbidity and in-hospital mortality in cancer patients: Results from a prospective cohort study14
Impact of educational programs on nurses’ knowledge and attitude toward pediatric palliative care14
Culturally sensitive palliative care in humanitarian action: Lessons from a critical interpretive synthesis of culture in palliative care literature14
Managing Anxiety from Cancer (MAC): A pilot randomized controlled trial of an anxiety intervention for older adults with cancer and their caregivers13
The experiences of health professionals, patients, and families with truth disclosure when breaking bad news in palliative care: A qualitative meta-synthesis12
Parents’ views on what facilitated or complicated their grief after losing a child to cancer12
Nurses’ involvement in end-of-life discussions with incurable cancer patients and family caregivers: An integrative review12
Impact of palliative care on end-of-life care and place of death in children, adolescents, and young adults with life-limiting conditions: A systematic review12
Effective communication in palliative care from the perspectives of patients and relatives: A systematic review11
Cardiovascular disease and meaning in life: A systematic literature review and conceptual model11
Death anxiety in patients with primary brain tumor: Measurement, prevalence, and determinants11
Evaluation of the Interprofessional Spiritual Care Education Curriculum in Australia: Online11
Palliative care nurses’ experiences of stress, anxiety, and burnout: A thematic synthesis11
Quality of life, anxiety, depression, and distress in patients with advanced and metastatic lung cancer10
Distress experienced by lung cancer patients and their family caregivers in the first year of their cancer journey10
Evaluation of care burden and preparedness of caregivers who provide care to palliative care patients10
Adapting the serious illness conversation guide for use in the emergency department by social workers10
Educational intervention to improve palliative care knowledge among informal caregivers of cognitively impaired older adults10
Posttraumatic growth in palliative care patients and its associations with psychological distress and quality of life10
Development and preliminary evaluation of EMPOWER for surrogate decision-makers of critically ill patients10
Does voluntary assisted dying cause public stigma for the bereaved? A vignette-based experiment10
But parents need help! Pathways to caregiver mental health care in pediatric hospital settings10
Description of a training protocol to improve research reproducibility for dignity therapy: an interview-based intervention9
Correlations among spiritual care competence, spiritual care perceptions and spiritual health of Chinese nurses: A cross-sectional correlational study9
The psychological experience of pediatric oncology patients facing life-threatening situations: A systematic review with narrative synthesis9
A qualitative exploration of the feasibility and acceptability of Meaning-Centered Psychotherapy for Cancer Caregivers9
Effect of virtual reality-based exercise intervention on sleep quality in children with acute lymphoblastic leukemia and healthy siblings: A randomized controlled trial9
Mapping end-of-life and anticipatory medications in palliative care patients using a longitudinal general practice database8
Australian perspectives on spiritual care training in healthcare: A Delphi study8
Determining the informational needs of family caregivers of people with intellectual disability who require palliative care: A qualitative study8
“The surprise questions” using variable time frames in hospitalized patients with advanced cancer8
Complexity of desire for hastened death in terminally ill cancer patients: A cluster analysis8
Development and evaluation of the feasibility, validity, and reliability of a screening tool for determining distress and supportive care needs of adolescents and young adults with cancer in Japan8
Advancing interprofessional education in communication8
Cultural implications for disclosure of diagnosis and prognosis toward terminally ill cancer patients in China: A literature review8
End of life communication among caregivers of children with cancer: A qualitative approach to understanding support desired by families8
Telehealth in outpatient delivery of palliative care: A qualitative study of patient and physician views8
Acceptability of a Serious Illness Conversation Guide to Black Americans: Results from a focus group and oncology pilot study8
End-of-life dreams and visions as perceived by palliative care professionals: A qualitative study8
Palliative and hospice social workers’ moral distress during the COVID-19 pandemic8
Systematic review of cancer-related fatigue instruments in breast cancer patients8
How does spirituality manifest in family caregivers of terminally ill cancer patients? A qualitative secondary analysis8
European interprofessional postgraduate curriculum in palliative care: A narrative synthesis of field interviews in the region of Middle, Eastern, and Southeastern Europe and Central and West Asia8
Effects of dignity therapy on palliative patients’ family members: A systematic review8
Comparison between patient-reported and clinician-reported outcomes: Validation of the Japanese version of the Integrated Palliative care Outcome Scale for staff8
Spiritual well-being, self-transcendence, and spiritual practices among Filipino women with breast cancer8
A cross-sectional study of the first two years of mandatory training for doctors participating in voluntary assisted dying7
A third of dying patients do not have end-of-life discussions with a physician: A nationwide registry study7
Psychological well-being of palliative care professionals: Who cares?7
Compassion fatigue in pediatric hematology, oncology, and bone marrow transplant healthcare providers: An integrative review7
Becoming an older caregiver: A study of gender differences in family caregiving at the end of life7
Tracheostomy decision-making for children with medical complexity: What supports and resources do caregivers need?7
Exploring the use of games in palliative care: A scoping review7
Professional experiences of formal healthcare providers in the provision of medical assistance in dying (MAiD): A scoping review7
Assessment of professional bereavement: The development and validation of the Professional Bereavement Scale7
A decision tree prediction model for a short-term outcome of delirium in patients with advanced cancer receiving pharmacological interventions: A secondary analysis of a multicenter and prospective ob7
Toward holistic care: Including substance use in mental health-palliative care integration7
Prevalence and factors associated with demoralization in palliative care patients: A cross-sectional study from Hong Kong7
Effects of end-of-life care on medical health professionals: A dialectical approach7
Objective burden, caregiver psychological distress, and patient religion and quality of life are associated with high-intensity burden of care among caregivers of advanced cancer patients in a Latino 7
Identifying practical clinical problems in active euthanasia: A systematic literature review of the findings in countries where euthanasia is legal7
A scoping review of studies exploring leisure-time physical activity in adults diagnosed with advanced cancer7
Needs for nurses to provide spiritual care and their associated influencing factors among elderly inpatients with stroke in China: A cross-sectional quantitative study6
Preparedness for family caregiving prior to allogeneic hematopoietic stem cell transplantation6
Providing home hospice care for LGBTQ+ patients and caregivers: Perceptions and opinions of hospice interdisciplinary care team providers6
Palliative care in the emergency department: A qualitative study exploring barriers, facilitators, desired clinician qualities, and future directions6
Assessing the need for a question prompt list that encourages end-of-life discussions between patients with advanced cancer and their physicians: A focus group interview study6
Examining public stigma and expectations of grief following medical aid and dying in the US: A vignette-based experiment6
Experiences and views of nurses about unmet needs of older cancer patients receiving chemotherapy: A qualitative study6
Associated factors of distress in patients with advanced cancer: A retrospective study6
Future provision of home end-of-life care: Family carers’ willingness for caregiving and needs for support6
A Portuguese trial using dignity therapy for adults who have a life-threatening disease: Qualitative analysis of generativity documents6
Cancer care reform in South Africa: A case for cancer care coordination: A narrative review6
Communicating is analogous to caring: A systematic review and thematic synthesis of the patient–clinician communication experiences of individuals with ovarian cancer6
A cognitive behavioral therapy–based intervention to address body image in patients with facial cancers: Results from a randomized controlled trial6
An exploration of financial toxicity among low-income patients with cancer in Central Texas: A mixed methods analysis6
Translation, cultural adaptation, and validation of the mindful self-care scale among Brazilian palliative care providers6
Dignity therapy in Mexican lung cancer patients with emotional distress: Impact on psychological symptoms and quality of life5
“Rapid tele-psychotherapy” with single-session music therapy in the metaverse: An alternative solution for mental health services in the future5
Current measures of distress may not account for what's most important in existential care interventions: Results of the outlook trial5
“A kaleidoscope of relationships” — cervical cancer survivors’ perspectives on their intimate relationships: A qualitative study5
Availability as key determinant in the palliative home care setting from the patients’ and family caregivers’ perspectives: A quantitative-qualitative-content analysis approach5
The impact of COVID-19 on palliative care workers across the world and measures to support their coping capacity5
Effectiveness of a cognitive–behavioral group therapy for complicated grief in relatives of patients with cancer: A randomized clinical trial5
Measuring and understanding death anxiety in caregivers of patients with primary brain tumor5
Prevalence and factors associated with depressive symptoms among family caregivers of palliative care patients at Hospice Africa Uganda5
Effect of a social network-based supportive program (WhatsApp) on the sexual self-concept of women with breast cancer: A single-blind-randomized controlled trial5
Effects of prolonged interruption of rehabilitation routines in amyotrophic lateral sclerosis patients5
The perceptions of cancer health-care practitioners in New Zealand and the USA toward psychedelic-assisted therapy with cancer patients: A cross-sectional survey5
What are the digitally enabled psychosocial interventions delivered by trained practitioners being offered to adults with life-shortening illnesses and palliative care needs and their informal and pro5
What do we know about experiencing end-of-life in burn intensive care units? A scoping review5
Psychosocial well-being among patients with malignant pleural mesothelioma5
Existential distress and meaning making among female breast cancer patients with cancer-related fertility concerns5
Barriers to advance care planning among patients with advanced serious illnesses: A national survey of health-care professionals in Singapore5
The burden in palliative care assistance: A comparison of psychosocial risks and burnout between inpatient hospice and home care services workers5
Meaning-centered group psychotherapy in Portuguese cancer patients: A pilot exploratory trial5
The inaugural United States World Hospice and Palliative Care Day Celebration: A virtual coming together5
Psychometric evaluation of the Persian version of the spiritual well-being scale (SWBS) in Iranian patients with cancer5
End-of-life dreams and visions: A systematic integrative review5
Screening for distress in cancer care: How to overcome barriers after unsuccessful implementation?5
“The education is a mirror of where palliative care stands in Israel today”: An exploration of palliative care undergraduate education at medical schools in Israel5
The conscious state of the dying patient: An integrative review5
Predictors and moderators of outcomes in mindfulness-based cognitive therapy intervention for early breast cancer patients5
Utilization of inpatient palliative care services among adolescents and young adults with cancer: Evidence from National Inpatient Sample 2016–20195
What should be measured to assess the quality of community-based palliative care? Results from a collaborative expert workshop5
Rural Hispanic/Latino cancer patients’ perspectives on facilitators, barriers, and suggestions for advance care planning: A qualitative study4
Palliative care among adult cancer survivors: Knowledge, attitudes, and correlates4
Fighting racism in research4
Religious–spiritual experiences of family members and caregivers of children and adolescents with cancer4
Family functioning and psychosocial symptoms among Latinx patients coping with advanced cancer4
Burden and anticipatory grief in caregivers of family members with Alzheimer’s disease and other dementias4
Palliative care and aggressive interventions after falling: A Nationwide Inpatient Sample analysis4
Feasibility and acceptability of cognitive behavioral therapy for insomnia (CBT-I) or acupuncture for insomnia and related distress among cancer caregivers4
Psychometric properties of the PG-13-R scale to assess prolonged grief disorder among bereaved Iranian adults4
An adaptation of meaning-centered psychotherapy integrating “essential care”: A pilot study4
Breaking the silence about illness and death: Potential effects of a pilot study of the family talk intervention when a parent with dependent children receives specialized palliative home care4
From “surviving to thriving”: Mood Lifters – a wellness program for parents of medically complex children4
Factors influencing nurse spiritual care practices at the end of life: A systematic review4
The prevalence rates and sequelae of delirium at age older than 90 years4
Attitudes toward death and death acceptance among hemato-oncologists: An Israeli sample4
Race and prevalence of percutaneous endoscopic gastrostomy tubes in patients with advanced dementia4
Cervical cancer survivors: The experiences of the journey4
Hospital, hospice, or home: A scoping review of the importance of place in pediatric palliative care4
An ethical conundrum: Palliative care in the COVID-19 pandemic4
Empathic communication in dignity therapy: Feasibility of measurement and descriptive findings4
Voice your values, a tailored advance care planning intervention in persons living with mild dementia: A pilot study4
A review of clinical trials of advance care planning interventions adapted for limited health literacy4
Spiritual care needs and their associated influencing factors among elderly patients with moderate-to-severe chronic heart failure in China: A cross-sectional study4
There is nothing informal about caregiving4
Cancer-related fatigue: Systematic reviews and meta-analyses of mind–body intervention4
The effectiveness of compassion-based interventions among cancer patients: A systematic review and meta-analysis4
Advance care planning among African Americans: A review and synthesis of theory application4
Perceptions of the meaning of life among Korean patients with advanced cancer: A mixed-methods study4
Investigation of the validity and reliability of the Turkish version of the Functional Assessment of Cancer Therapy—Cognitive Function in cancer patients4
Adapting the collaborative care model to palliative care: Establishing mental health–serious illness care integration4
Perspectives in preparedness of family caregivers of patients with cancer providing end-of-life care in the home: A narrative review of qualitative studies4
How do trained palliative care providers experience open desire to die-conversations? An explorative thematic analysis4
Informal caregivers of older Muslims diagnosed with cancer: A portrait of depression, social support, and faith4
A qualitative study exploring family caregivers’ support needs in the context of medical assistance in dying4
Family caregiver grief and post-loss adjustment: A longitudinal cohort study4
Community perspectives on structural barriers to dying well at home in Canada4
Empowering families facing end-stage nonmalignant chronic diseases with a holistic, transdisciplinary, community-based intervention: 3 months outcome of the Life Rainbow Program4
National and international non-therapeutic recommendations for adult palliative and end-of-life care in times of pandemics: A scoping review4
The effect of time since reconstruction on breast cancer patients’ quality of life, self-esteem, shame, guilt, and pride3
Patient–physician conversations about life-sustaining treatment: Treatment preferences and participant assessments3
Assessing well-being in pediatric palliative care: A pilot study about views of children, parents and health professionals3
A COVID-19 Obituary3
Relationship between the depression levels and nutritional statuses of advanced stage cancer patients3
Unsolved problems and unwanted decision-making in the last year of life: A qualitative analysis of comments from bereaved caregivers3
Spiritual care perceptions and empathy of Chinese nursing students: The mediating roles of spiritual well-being3
Partnering to cope with pain: A pilot study of a caregiver-assisted pain coping skills intervention for patients with cognitive impairment and dementia3
Polarization in public attitudes toward end-of-life decisions in Israel – A cross-sectional study3
The efficacy of “rapid tele-psychotherapy” with single-session music therapy: A personal reflection as a founder3
Prevalence and associated factors of psychological distress among young adult cancer patients in Japan3
Preferences of quality delivery of palliative care among cancer patients in low- and middle-income countries: A review3
Compassion fatigue and psychological resilience levels of nursing final students: A descriptive, cross-sectional, and relational study3
Equal palliative care for foreign-born patients: A national quality register study3
Validity and reliability of the Turkish version of the Patient Dignity Inventory3
Integration between humor and music therapy to increase spirituality and meaning in palliative and supportive care3
Spiritual care needs among Chinese elders hospitalized for severe chronic heart failure: An observational study3
The Neonatal Palliative Care Attitude Scale: Psychometric properties for Portuguese neonatal nurses3
A feasibility study of a peer discussion group intervention for patients with pancreatobiliary cancer and their caregivers3
Changes in the palliative performance scale may be as important as the initial palliative performance scale for predicting survival in terminal cancer patients3
Measuring double awareness in patients with advanced cancer: A preliminary scale development study3
Arabic version of the Palliative Care Self-Efficacy Scale: Translation, adaptation, and validation3
Dementia caregiver burdens predict overnight hospitalization and hospice utilization3
Patients’ spiritual concerns and needs and how to address them during advance care planning conversations: Healthcare chaplains’ perspectives3
“A Wanderer's Tale”: The development of a virtual reality application for pain and quality of life in Australian burns and oncology patients3
Unmet mental health needs in patients with advanced B-cell lymphomas3
Family caregivers’ perceived communication self-efficacy with physicians3
Race-conscious serious illness communication: An interpersonal tool to dismantle racism in practice and research3
Factors associated with distress and the impact of distress on acute health-care service utilization among patients diagnosed with breast and gynecological cancers3
Disrespectful and inadequate palliative care to transgender persons3
Mourning in the time of coronavirus: Examining how grief differs in those who lost loved ones to COVID-19 vs. natural causes in Iran3
Increased preparedness for caregiving among family caregivers in specialized home care by using the Carer Support Needs Assessment Tool Intervention3
Reflecting on meaning in an existential-reorientation group psychotherapy approach for cancer patients: A qualitative thematic analysis3
Is there a relationship between end-of-life cancer patients’ dignity-related distress and caregivers’ distress? An exploratory study3
“What it is like to be human”: The existential dimension of care as perceived by professionals caring for people approaching death3
The effect of playing games with toys made with medical materials in children with cancer on pain during intravenous treatment3
The impact of caring on caregivers of patients with life-threatening organ failure3
Ketamine-assisted meaning-centered psychotherapy for a patient with severe suicidal behavior3
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