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 2021-08-01 to 2025-08-01.)
ArticleCitations
Leaving a lasting legacy: A scoping review of ethical wills37
PAX volume 20 issue 6 Cover and Front matter34
Would compassion be able to intervene?33
The silk road32
Increased preparedness for caregiving among family caregivers in specialized home care by using the Carer Support Needs Assessment Tool Intervention32
An exploratory qualitative study on factors influencing the level of agreement in symptom reports in child–caregiver dyads31
Spiritual care interventions for palliative care patients: A scoping review27
Self-compassion training in palliative care during COVID-19: A pilot study23
A little rain20
Virtual reality for improving pain and pain-related symptoms in patients with advanced stage colorectal cancer: A pilot trial to test feasibility and acceptability20
“Rapid tele-psychotherapy” with single-session music therapy in the metaverse: An alternative solution for mental health services in the future20
Family caregivers’ experience of communication with nursing home staff from admission to end of life during the COVID-19 pandemic: A qualitative study employing a transitional perspective17
Utilization of medical interventions in hospitalized Mexican adults with cancer at the end of life in a referral hospital: The importance of early palliative care16
Validation of the Mexican version of the Schedule of Attitudes Toward Hastened Death in patients undergoing palliative care in Mexico15
The final beeps of the final beats15
Reliability and validity of the Self-Efficacy in Palliative Care Scale among nurses14
Matter14
Decisions about treatment with targeted therapies in a palliative care unit: A case series14
When and how to discuss about palliative care and advance care planning with cancer patients: A mixed-methods study13
Burden and anticipatory grief in caregivers of family members with Alzheimer’s disease and other dementias13
Translation, cultural adaptation, and validation of the mindful self-care scale among Brazilian palliative care providers12
Inevitable changes12
Impact of educational programs on nurses’ knowledge and attitude toward pediatric palliative care12
Emotional ecosystems: Understanding the relationship between family interactions and anxiety among cancer caregivers12
Tongue edema as an adverse drug reaction to low-dose olanzapine in a cancer patient receiving palliative care11
Providing home hospice care for LGBTQ+ patients and caregivers: Perceptions and opinions of hospice interdisciplinary care team providers11
Wernicke encephalopathy in a caregiver: A serious physical issue resulting from stress in a family member caring for an advanced cancer patient11
Talking about dying and death: Essentials of communicating about approaching death from the perspective of major stakeholders11
The 2nd Annual US Celebration of World Hospice and Palliative Care Day: A virtual coming together to support equity in palliative care access11
A cognitive behavioral therapy–based intervention to address body image in patients with facial cancers: Results from a randomized controlled trial11
Motivations for choosing “home” as one’s preferred place of death: A scoping review11
Which has more influence on a family's assessment of the quality of dying of their long-term care resident with dementia: Frequency of symptoms or quality of communication with healthcare team?11
Making space for grief: The impact of remembrance programs for pediatric healthcare providers10
Emotion dysregulation and family functioning moderate family caregiving burden during the pandemic10
Development and evaluation of a Hospice Foundation of Taiwan Bereavement Assessment Scale: A psychometric properties test10
Patient beliefs associated with medication hesitancy in palliative care: A systematic review using the theory of planned behavior10
Shores of acceptance9
Redefining caregiver strain for family caregivers in end-of-life care in Hong Kong – CORRIGENDUM9
The relationship between moral distress, individual and professional values in oncology nurses: A structural equation study9
Anthropology and its aftermath: Humanity in medical training9
Unsolved problems and unwanted decision-making in the last year of life: A qualitative analysis of comments from bereaved caregivers9
Nurses’ experiences of suicide attempts in palliative care9
Vacancies9
Integration of the geriatric palliative care in oncological care of elderly patient with cancer9
Compassion fatigue and palliative care in neonatal nurses9
Digging deeper: A critique of the mediation study of spirituality in ALS patients9
Providing care for siblings of children on hospice9
Building dignity at the bedside: A reflective clinical model for clinical encounters8
Fighting racism in research8
Eye movement desensitization and reprocessing (EMDR) and mediative behavioral therapy for the treatment of suffocation related post-traumatic stress disorder (PTSD) in amyotrophic lateral sclerosis (A8
Good death and bereavement in a lung cancer patient following meaning-centered couples psychotherapy by a cancer nursing specialist8
Psychometric validation and cross-cultural adaptation of the Integrated Palliative care Outcome Scale in Polish (IPOS-Pol)8
Exploring the landscape of palliative care provision for black patients with hematologic cancers: A scoping review8
Concomitant use of hydroxyzine and haloperidol did not worsen delirium in patients with cancer: A multicenter, retrospective, observational study8
Psychological symptom burden associated with malignant wounds: Secondary analysis of a prospective cohort study8
Palliative care providers’ roles in medical assistance in dying decision-making triads with patients and families: A qualitative analysis8
For Silvia8
BRS: The Becker-Rank Syndrome8
Examining the development of information needs assessment tools for use in the cancer context: A scoping and critical review8
Validation of the Spanish translation Sheffield Profile for Assessment and Referral for Care (SPARC-Sp) at the Hospital Universitario San Jose of Popayan, Colombia7
Assessment of psychometric properties of the Persian version of the spiritual care competency self-assessment tool7
Fighting racism in research – CORRIGENDUM7
“It seemed I was having a conversation with him”: Posthumous Dignity Therapy case series7
The place of the relative at the time of the announcement of cancer progression: BABEL – a mixed-methods study7
Improving palliative care in Nepal through virtual education7
Adapting to the emotional complexity of palliative care communication: Palliative care clinicians’ experiences7
Race and prevalence of percutaneous endoscopic gastrostomy tubes in patients with advanced dementia7
Died with compassion7
Prognostic utility of Palliative Prognostic Index in advanced cancer: A systematic review and meta-analysis7
Are specialist-provided end-of-life scenarios key to initiation of advance care planning in primary care? A mixed-methods study7
Spiritual embrace: A source of strength for caregivers in a mental health crisis7
Be a burden7
“A Wanderer's Tale”: The development of a virtual reality application for pain and quality of life in Australian burns and oncology patients7
The last time I saw mother7
What are family caregivers’ experiences of coordinating end-of-life care at home? A narrative review7
The effects of illness perception on death anxiety and satisfaction with life in patients with advanced gastrointestinal cancer7
Dignity-related distress and recall among alert, non-delirious critically ill patients7
Experiences and attitudes of nurses with the legislation on assisted suicide in Austria7
Sharing the burden: The experiences of HIV psychiatrists delivering primary palliative care7
Identifying patients in need of palliative care: Adaptation of the Necesidades Paliativas CCOMS-ICO© (NECPAL) screening tool for use in Israel6
“What it is like to be human”: The existential dimension of care as perceived by professionals caring for people approaching death6
The communication experiences of persons referred to specialist palliative care services and their carers: A descriptive phenomenological study6
Voicing their choices: Advance care planning with adolescents and young adults with cancer and other serious conditions6
There is nothing informal about caregiving6
Families’ experiences of end-of-life care in an acute private hospital: A qualitative study6
Perceived organizational support moderates the effect of job demands on outcomes: Testing the JD-R model in Italian oncology nurses6
Life meaning constructed from dignity therapy in traditional Chinese culture: A qualitative analysis of dignity therapy generativity documents6
Disrespectful and inadequate palliative care to lesbian, gay, and bisexual patients6
What I Will Miss and What I Will Not Miss When I Am Near Death: A List Poem6
Evaluation of the Interprofessional Spiritual Care Education Curriculum in Australia: Online6
The efficacy of “rapid tele-psychotherapy” with single-session music therapy: A personal reflection as a founder6
Effect of a multidisciplinary ward-based intervention on end-of-life care for general medicine patients6
Compassion fatigue and psychological resilience levels of nursing final students: A descriptive, cross-sectional, and relational study6
Bereavement guilt among young adults impacted by caregivers’ cancer: Associations with attachment style, experiential avoidance, and psychological flexibility6
A survey of statistical methods utilized for analysis of randomized controlled trials of behavioral interventions6
Virtual reality and neurofeedback as a supportive approach to managing cancer symptoms for patients receiving treatment: A brief report of a feasibility trial6
Healing across cultures6
Access to palliative and supportive care in the Philippines: A call to action6
Knowledge, goals, and misperceptions about palliative care in adults with chronic disease or cancer6
Factors influencing nurse spiritual care practices at the end of life: A systematic review6
I Am More6
Integrating ACP into Nigeria’s culture and healthcare system for improved end-of-life care6
Relationship between the depression levels and nutritional statuses of advanced stage cancer patients6
Ketamine subcutaneous continuous infusion for depressive symptoms at home: A case report beyond pain use5
Exploring unmet concerns in home hospice cancer care: Perspectives of patients, informal caregivers, palliative care providers, and family physicians5
Wheelchair Song5
What we learnt from parents’ death experience: A cross-sectional study of death literacy and parent’s death quality among adult children in China5
Memento mori5
A commentary on “Spirituality moderates the relationship between cancer caregiver burden and depression” (La. I.S, 2023)5
Qualitative analysis of expressions used in the end-of-life discussions and their associated factors5
Hemichorea–hemiballismus associated with a case of cerebral toxoplasmosis in a hematopoietic stem cell transplant recipient5
Life/time/d - Is the life shortened, a shortened life?5
Peaceful acceptance and struggle with terminal cancer: The role of mindfulness, self-compassion, and body image distress5
The Palliative Story Exchange: An innovative storytelling intervention to build community, foster shared meaning, and improve sustainability5
Strategies to prepare hospice providers to interact with adolescents with a parent in hospice5
But parents need help! Pathways to caregiver mental health care in pediatric hospital settings5
The fragility of trust between patients and oncologists: A multiple case study5
Volunteers’ spiritual care competence and its relationship with attitudes toward palliative care: A cross-sectional study5
Barriers to advance care planning among patients with advanced serious illnesses: A national survey of health-care professionals in Singapore5
Social injustice is moral suffering5
Factors associated with surrogate families’ life-sustaining treatment preferences for patients at home or in a geriatric health service facility: A cross-sectional study5
“You’re the only thing he comes out [of his room] for”: A qualitative study of engagement between Laughter Care Specialists and families of people with dementia in long-term care5
Dyadic sleep intervention for adult patients with cancer and their sleep-partner caregivers: A feasibility study5
Palliative care physicians’ decision-making about palliative sedation for existential suffering: A Belgian nationwide qualitative study5
End-of-life care for Filipino patients with cancer5
Medical Assistance in Dying (MAiD) in Canada: Why Coelho and colleagues are incorrect to suggest the MAiD framework is in significant distress5
Advance care planning discussions – Perspectives from oncology patients with advanced-stage disease5
The impact of caregiver burden and associated factors on trait anger levels and anger expression styles in family caregivers of palliative care patients5
Experiences with health information among caregivers of people with cancer from culturally and linguistically diverse backgrounds: A qualitative study5
Deathbed experiences and meaning-making: Perspectives of family caregivers of patients who received cancer palliative care5
Psychometric properties of the Turkish version of the Palliative Nursing Care Quality Scale5
Non-curative care options for patients with advanced-stage head and neck cancer: Current state of the science and future opportunities4
Mystery prevails over absurdity4
Oh happy fault!4
Danse Macabre in W.H. Auden’s “Death’s Echo”4
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 study4
Translation and validation of the Chinese version of Palliative Care Self-Efficacy Scale4
Situations in which caregivers and patients are likely to collude: Perspectives from caregivers of advanced cancer patients in Bangladesh– ERRATUM4
The effectiveness of pretreatment video-based psychoeducation for patients with breast cancer4
A review of clinical trials of advance care planning interventions adapted for limited health literacy4
Identifying the active content of interventions targeting the psychological well-being of carers of people with motor neuron disease: A systematic review4
Acceptability of a Serious Illness Conversation Guide to Black Americans: Results from a focus group and oncology pilot study4
Palliative care in pediatric patients with central nervous system cancer: Descriptive and comparative study4
An award from the Indonesian World-Records Museum (MURI) for “rapid tele-psychotherapy” theory: The most prestigious achievement in my life4
What do health professionals think about implementing psilocybin-assisted therapy in palliative care for existential distress? A World Café qualitative study4
Moral and philosophical frameworks for discussing Voluntary Assisted Dying (VAD)4
Spiritual care perceptions and empathy of Chinese nursing students: The mediating roles of spiritual well-being4
An interpretative qualitative case study of a Compassionate Cities initiative in the United Kingdom: Lessons for implementation in other settings4
Pancreatic cancer, depression, and spirituality in therapy: “Unio Mystica” and “Achrayut,” 2 case reports4
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 Japan4
The Pediatric Serious Illness Conversation Program: Understanding challenges and experiences for clinicians after advance care planning training4
The experiences of families of children with cancer during the COVID-19 pandemic: A qualitative exploration4
Communicating about the end of life: The path of prognostic awareness4
A cross-sectional study of the first two years of mandatory training for doctors participating in voluntary assisted dying4
Translation and cross-cultural adaptation of the Posthumous Dignity Therapy Schedule of Questions to Brazilian Portuguese – CORRIGENDUM4
End-of-life dreams and visions as perceived by palliative care professionals: A qualitative study4
Factors associated with caregiver strain among mothers and fathers of children with advanced cancer4
Prevalence and associated factors of psychological distress among young adult cancer patients in Japan4
Wernicke encephalopathy with active hallucinations during lung cancer treatment and hemodialysis: A case report4
Palliative care is more than a “p” value4
“Optimizing empathic self-disclosures in dignity therapy: Improving the patient–provider relationship for more humanistic palliative care”4
Patient altruism at the end of life: A scoping review3
Emergency department use and responsiveness to the palliative care needs of patients with dementia at the end of life: A scoping review3
Preparedness for family caregiving prior to allogeneic hematopoietic stem cell transplantation3
Melodies and memories3
Stigma in Mexican patients with Lung Cancer: Psychometric Properties of the Cataldo Lung Cancer Stigma Scale (CLCSS) - Brief version3
Posthumous dignity therapy: Challenges and opportunities in the Brazilian cultural context3
The realities of Medical Assistance in Dying in Canada – CORRIGENDUM3
Embracing goodbye: A personal reflection on virtual reality intervention in palliative care3
Prophylaxis and treatment of cancer-related dyspnea with pharmacologic agents: A systematic review and network meta-analysis3
Associations between Latino ethnicity and the use of emotional support and completion of advance directives3
Against our post-modern palliation3
Effect of virtual reality-based exercise intervention on sleep quality in children with acute lymphoblastic leukemia and healthy siblings: A randomized controlled trial3
From “surviving to thriving”: Mood Lifters – a wellness program for parents of medically complex children3
Facial edema as an adverse drug reaction to olanzapine in a patient with cancer receiving palliative care3
The potential impact of proxy reports for symptom experience and care quality and experience in advanced cancer3
The relationship between nursing students’ compassion competencies and perceptions of spirituality and spiritual care3
Caring for people who take care: What is already done?3
Evaluating the effectiveness of psilocybin in alleviating distress among cancer patients: A systematic review3
Healthcare professionals’ discussion of loss and grief with parents of children with life-limiting severe neurological impairment: Findings from a scoping review3
Balancing burden and benefit: Reflecting on interviews with individuals nearing the end of their lives3
When death is desired: A case of MAiD & the CL psychiatrist3
Lessons from the Darkness3
The value of time3
AD-LAST! An interdisciplinary clinical workshop to improve cultural and spiritual awareness in advance care planning skills3
Cervical cancer survivors: The experiences of the journey3
A Christmas Carol — or how I learned to love visits from the dead3
Effective communication in palliative care from the perspectives of patients and relatives: A systematic review3
Potential and challenges of virtual reality in improving the quality of life of palliative care patients3
Irrevocably other: Narrative medicine and Jorge Luis Borges’ “The other death”3
Cosmology of belonging: The role of community in the therapeutic use of psychedelics3
Resonance, self-reflection, and preparedness through a web-based intervention for family caregivers of patients with life-threatening illness receiving specialised home care3
The effectiveness of compassion-based interventions among cancer patients: A systematic review and meta-analysis3
Exploring the experience of a cognitive rehabilitation intervention for cancer-related cognitive change in people living with cancer: An interpretative phenomenological analysis3
Behind the scenes: Moral distress among psychosocial oncology clinical research staff during the COVID-19 pandemic3
Spirituality in the care of patients with cancer: What is the psychiatrist's role?3
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 Asia3
Reiki intervention for supporting healthcare professional care behaviors in pediatric palliative care: A pilot study3
The need to be needed3
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 ob3
Situations in which caregivers and patients are likely to collude: Perspectives from caregivers of advanced cancer patients in Bangladesh3
Precision medicine3
Measuring compassion in end-of-life cancer patients: The Italian validation of the Sinclair Compassion Questionnaire (SCQit)3
Facing discrimination in research3
Comparing situational influences on differential healthcare utilization trajectories in patients on home palliative care: A qualitative study3
Palliative team involvement in end-of-life care for Jewish and Muslim children in Jerusalem: A unique clinical and cultural context3
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