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 2021-06-01 to 2025-06-01.)
ArticleCitations
Leaving a lasting legacy: A scoping review of ethical wills35
PAX volume 20 issue 6 Cover and Front matter32
Would compassion be able to intervene?31
Validation of the Mexican version of the Schedule of Attitudes Toward Hastened Death in patients undergoing palliative care in Mexico29
The silk road27
An exploratory qualitative study on factors influencing the level of agreement in symptom reports in child–caregiver dyads25
A little rain24
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 perspective22
Utilization of medical interventions in hospitalized Mexican adults with cancer at the end of life in a referral hospital: The importance of early palliative care22
Reliability and validity of the Self-Efficacy in Palliative Care Scale among nurses18
The final beeps of the final beats18
Decisions about treatment with targeted therapies in a palliative care unit: A case series16
Increased preparedness for caregiving among family caregivers in specialized home care by using the Carer Support Needs Assessment Tool Intervention15
Self-compassion training in palliative care during COVID-19: A pilot study15
“Rapid tele-psychotherapy” with single-session music therapy in the metaverse: An alternative solution for mental health services in the future14
What if Beethoven had been given an SSRI with a benzodiazepine chaser?14
Matter14
Burden and anticipatory grief in caregivers of family members with Alzheimer’s disease and other dementias14
Impact of educational programs on nurses’ knowledge and attitude toward pediatric palliative care13
Translation, cultural adaptation, and validation of the mindful self-care scale among Brazilian palliative care providers12
Virtual reality for improving pain and pain-related symptoms in patients with advanced stage colorectal cancer: A pilot trial to test feasibility and acceptability12
When and how to discuss about palliative care and advance care planning with cancer patients: A mixed-methods study12
Reflecting on meaning in an existential-reorientation group psychotherapy approach for cancer patients: A qualitative thematic analysis12
Providing home hospice care for LGBTQ+ patients and caregivers: Perceptions and opinions of hospice interdisciplinary care team providers11
Inevitable changes11
Tongue edema as an adverse drug reaction to low-dose olanzapine in a cancer patient receiving palliative care11
Emotional ecosystems: Understanding the relationship between family interactions and anxiety among cancer caregivers11
Talking about dying and death: Essentials of communicating about approaching death from the perspective of major stakeholders11
Spiritual care interventions for palliative care patients: A scoping review11
Motivations for choosing “home” as one’s preferred place of death: A scoping review10
Development and evaluation of a Hospice Foundation of Taiwan Bereavement Assessment Scale: A psychometric properties test10
The 2nd Annual US Celebration of World Hospice and Palliative Care Day: A virtual coming together to support equity in palliative care access10
Patient beliefs associated with medication hesitancy in palliative care: A systematic review using the theory of planned behavior10
A cognitive behavioral therapy–based intervention to address body image in patients with facial cancers: Results from a randomized controlled trial10
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?10
Making space for grief: The impact of remembrance programs for pediatric healthcare providers10
Emotion dysregulation and family functioning moderate family caregiving burden during the pandemic9
Anthropology and its aftermath: Humanity in medical training9
Shores of acceptance9
Unsolved problems and unwanted decision-making in the last year of life: A qualitative analysis of comments from bereaved caregivers9
Vacancies9
Integration of the geriatric palliative care in oncological care of elderly patient with cancer9
The relationship between moral distress, individual and professional values in oncology nurses: A structural equation study9
Providing care for siblings of children on hospice9
Autonomy and control in the wish to die in terminally ill patients: A systematic integrative review9
Compassion fatigue and palliative care in neonatal nurses9
Nurses’ experiences of suicide attempts in palliative care8
Digging deeper: A critique of the mediation study of spirituality in ALS patients8
Psychometric validation and cross-cultural adaptation of the Integrated Palliative care Outcome Scale in Polish (IPOS-Pol)8
Wernicke encephalopathy in a caregiver: A serious physical issue resulting from stress in a family member caring for an advanced cancer patient8
Palliative care providers’ roles in medical assistance in dying decision-making triads with patients and families: A qualitative analysis8
Exploring the landscape of palliative care provision for black patients with hematologic cancers: A scoping review8
Fighting racism in research8
Redefining caregiver strain for family caregivers in end-of-life care in Hong Kong – CORRIGENDUM8
Validation of the Spanish translation Sheffield Profile for Assessment and Referral for Care (SPARC-Sp) at the Hospital Universitario San Jose of Popayan, Colombia8
For Silvia8
Building dignity at the bedside: A reflective clinical model for clinical encounters8
Improving palliative care in Nepal through virtual education7
Assessment of psychometric properties of the Persian version of the spiritual care competency self-assessment tool7
Knowledge, goals, and misperceptions about palliative care in adults with chronic disease or cancer7
Race and prevalence of percutaneous endoscopic gastrostomy tubes in patients with advanced dementia7
Sharing the burden: The experiences of HIV psychiatrists delivering primary palliative care7
Examining the development of information needs assessment tools for use in the cancer context: A scoping and critical review7
Good death and bereavement in a lung cancer patient following meaning-centered couples psychotherapy by a cancer nursing specialist7
Equal palliative care for foreign-born patients: A national quality register study7
Life meaning constructed from dignity therapy in traditional Chinese culture: A qualitative analysis of dignity therapy generativity documents7
Be a burden7
Prognostic utility of Palliative Prognostic Index in advanced cancer: A systematic review and meta-analysis7
Died with compassion7
Psychological symptom burden associated with malignant wounds: Secondary analysis of a prospective cohort study7
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 (A7
“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
Fighting racism in research – CORRIGENDUM7
Concomitant use of hydroxyzine and haloperidol did not worsen delirium in patients with cancer: A multicenter, retrospective, observational study7
BRS: The Becker-Rank Syndrome7
Adapting to the emotional complexity of palliative care communication: Palliative care clinicians’ experiences7
Unscripted6
Experiences and attitudes of nurses with the legislation on assisted suicide in Austria6
Dignity-related distress and recall among alert, non-delirious critically ill patients6
“What it is like to be human”: The existential dimension of care as perceived by professionals caring for people approaching death6
What I Will Miss and What I Will Not Miss When I Am Near Death: A List Poem6
Virtual reality and neurofeedback as a supportive approach to managing cancer symptoms for patients receiving treatment: A brief report of a feasibility trial6
Evaluation of the Interprofessional Spiritual Care Education Curriculum in Australia: Online6
The communication experiences of persons referred to specialist palliative care services and their carers: A descriptive phenomenological study6
The place of the relative at the time of the announcement of cancer progression: BABEL – a mixed-methods study6
Are specialist-provided end-of-life scenarios key to initiation of advance care planning in primary care? A mixed-methods study6
Effect of a multidisciplinary ward-based intervention on end-of-life care for general medicine patients6
Identifying patients in need of palliative care: Adaptation of the Necesidades Paliativas CCOMS-ICO© (NECPAL) screening tool for use in Israel6
Voicing their choices: Advance care planning with adolescents and young adults with cancer and other serious conditions6
Access to palliative and supportive care in the Philippines: A call to action6
“It seemed I was having a conversation with him”: Posthumous Dignity Therapy case series6
There is nothing informal about caregiving6
Spiritual embrace: A source of strength for caregivers in a mental health crisis6
Cross-Cover6
Healing across cultures6
Disrespectful and inadequate palliative care to lesbian, gay, and bisexual patients6
The effects of illness perception on death anxiety and satisfaction with life in patients with advanced gastrointestinal cancer6
The efficacy of “rapid tele-psychotherapy” with single-session music therapy: A personal reflection as a founder6
Rights and obligations6
Qualitative analysis of expressions used in the end-of-life discussions and their associated factors5
Compassion fatigue and psychological resilience levels of nursing final students: A descriptive, cross-sectional, and relational study5
The fragility of trust between patients and oncologists: A multiple case study5
What we learnt from parents’ death experience: A cross-sectional study of death literacy and parent’s death quality among adult children in China5
Bereavement guilt among young adults impacted by caregivers’ cancer: Associations with attachment style, experiential avoidance, and psychological flexibility5
A third of dying patients do not have end-of-life discussions with a physician: A nationwide registry study5
A commentary on “Spirituality moderates the relationship between cancer caregiver burden and depression” (La. I.S, 2023)5
Barriers to advance care planning among patients with advanced serious illnesses: A national survey of health-care professionals in Singapore5
Experiences with health information among caregivers of people with cancer from culturally and linguistically diverse backgrounds: A qualitative study5
Ketamine subcutaneous continuous infusion for depressive symptoms at home: A case report beyond pain use5
Perceived organizational support moderates the effect of job demands on outcomes: Testing the JD-R model in Italian oncology nurses5
Strategies to prepare hospice providers to interact with adolescents with a parent in hospice5
The impact of caregiver burden and associated factors on trait anger levels and anger expression styles in family caregivers of palliative care patients5
Advance care planning discussions – Perspectives from oncology patients with advanced-stage disease5
Families’ experiences of end-of-life care in an acute private hospital: A qualitative study5
A survey of statistical methods utilized for analysis of randomized controlled trials of behavioral interventions5
Integrating ACP into Nigeria’s culture and healthcare system for improved end-of-life care5
But parents need help! Pathways to caregiver mental health care in pediatric hospital settings5
Exploring unmet concerns in home hospice cancer care: Perspectives of patients, informal caregivers, palliative care providers, and family physicians5
Peaceful acceptance and struggle with terminal cancer: The role of mindfulness, self-compassion, and body image distress5
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
Memento mori5
Volunteers’ spiritual care competence and its relationship with attitudes toward palliative care: A cross-sectional study5
I Am More5
Factors influencing nurse spiritual care practices at the end of life: A systematic review5
Validity and reliability of the Turkish version of the Patient Dignity Inventory5
Wheelchair Song5
The Palliative Story Exchange: An innovative storytelling intervention to build community, foster shared meaning, and improve sustainability5
Relationship between the depression levels and nutritional statuses of advanced stage cancer patients5
Palliative care physicians’ decision-making about palliative sedation for existential suffering: A Belgian nationwide qualitative study5
Translation and validation of the Chinese version of Palliative Care Self-Efficacy Scale4
Palliative care is more than a “p” value4
Danse Macabre in W.H. Auden’s “Death’s Echo”4
Deathbed experiences and meaning-making: Perspectives of family caregivers of patients who received cancer palliative care4
Dyadic sleep intervention for adult patients with cancer and their sleep-partner caregivers: A feasibility study4
Factors associated with caregiver strain among mothers and fathers of children with advanced cancer4
Communicating about the end of life: The path of prognostic awareness4
Effective communication in palliative care from the perspectives of patients and relatives: A systematic review4
Embracing goodbye: A personal reflection on virtual reality intervention in palliative care4
Spiritual care perceptions and empathy of Chinese nursing students: The mediating roles of spiritual well-being4
Psychometric properties of the Turkish version of the Palliative Nursing Care Quality Scale4
Palliative care in pediatric patients with central nervous system cancer: Descriptive and comparative study4
Wernicke encephalopathy with active hallucinations during lung cancer treatment and hemodialysis: A case report4
Ogilvie's syndrome presented with delirium in an older lady with corticobasal syndrome4
An interpretative qualitative case study of a Compassionate Cities initiative in the United Kingdom: Lessons for implementation in other settings4
A review of clinical trials of advance care planning interventions adapted for limited health literacy4
Translation and cross-cultural adaptation of the Posthumous Dignity Therapy Schedule of Questions to Brazilian Portuguese – CORRIGENDUM4
“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 care4
Factors associated with surrogate families’ life-sustaining treatment preferences for patients at home or in a geriatric health service facility: A cross-sectional study4
Hemichorea–hemiballismus associated with a case of cerebral toxoplasmosis in a hematopoietic stem cell transplant recipient4
The effectiveness of pretreatment video-based psychoeducation for patients with breast cancer4
The experiences of families of children with cancer during the COVID-19 pandemic: A qualitative exploration4
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
An award from the Indonesian World-Records Museum (MURI) for “rapid tele-psychotherapy” theory: The most prestigious achievement in my life4
Moral and philosophical frameworks for discussing Voluntary Assisted Dying (VAD)4
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
Non-curative care options for patients with advanced-stage head and neck cancer: Current state of the science and future opportunities4
Oh happy fault!4
Prevalence and associated factors of psychological distress among young adult cancer patients in Japan4
Mystery prevails over absurdity4
Social injustice is moral suffering4
Life/time/d - Is the life shortened, a shortened life?4
Preferences for end-of-life care settings among the healthy population in Israel—Related socio-demographic variables4
What do health professionals think about implementing psilocybin-assisted therapy in palliative care for existential distress? A World Café qualitative study4
Pancreatic cancer, depression, and spirituality in therapy: “Unio Mystica” and “Achrayut,” 2 case reports4
Situations in which caregivers and patients are likely to collude: Perspectives from caregivers of advanced cancer patients in Bangladesh4
A Portuguese trial using dignity therapy for adults who have a life-threatening disease: Qualitative analysis of generativity documents4
AD-LAST! An interdisciplinary clinical workshop to improve cultural and spiritual awareness in advance care planning skills4
End-of-life dreams and visions as perceived by palliative care professionals: A qualitative study4
A cross-sectional study of the first two years of mandatory training for doctors participating in voluntary assisted dying4
Preparedness for family caregiving prior to allogeneic hematopoietic stem cell transplantation3
When death is desired: A case of MAiD & the CL psychiatrist3
“The surprise questions” using variable time frames in hospitalized patients with advanced cancer3
Stigma in Mexican patients with Lung Cancer: Psychometric Properties of the Cataldo Lung Cancer Stigma Scale (CLCSS) - Brief version3
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
Identifying the active content of interventions targeting the psychological well-being of carers of people with motor neuron disease: A systematic review3
Delirium in supportive and palliative care3
Measuring compassion in end-of-life cancer patients: The Italian validation of the Sinclair Compassion Questionnaire (SCQit)3
The value of time3
Palliative team involvement in end-of-life care for Jewish and Muslim children in Jerusalem: A unique clinical and cultural context3
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
Caring for people who take care: What is already done?3
Development and preliminary evaluation of EMPOWER for surrogate decision-makers of critically ill patients3
Cervical cancer survivors: The experiences of the journey3
Balancing burden and benefit: Reflecting on interviews with individuals nearing the end of their lives3
Spirituality in the care of patients with cancer: What is the psychiatrist's role?3
Facial edema as an adverse drug reaction to olanzapine in a patient with cancer receiving palliative care3
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
A Christmas Carol — or how I learned to love visits from the dead3
Acceptability of a Serious Illness Conversation Guide to Black Americans: Results from a focus group and oncology pilot study3
The Pediatric Serious Illness Conversation Program: Understanding challenges and experiences for clinicians after advance care planning training3
Against our post-modern palliation3
Reiki intervention for supporting healthcare professional care behaviors in pediatric palliative care: A pilot study3
Identification of palliative care needs in hemodialysis patients: An update3
The realities of Medical Assistance in Dying in Canada – CORRIGENDUM3
The effectiveness of compassion-based interventions among cancer patients: A systematic review and meta-analysis3
Behind the scenes: Moral distress among psychosocial oncology clinical research staff during the COVID-19 pandemic3
Healthcare professionals’ discussion of loss and grief with parents of children with life-limiting severe neurological impairment: Findings from a scoping review3
Melodies and memories3
Validity and reliability of the Turkish version of the Spiritual Needs Assessment Scale of Patients with Cancer3
Effect of virtual reality-based exercise intervention on sleep quality in children with acute lymphoblastic leukemia and healthy siblings: A randomized controlled trial3
Precision medicine3
Prophylaxis and treatment of cancer-related dyspnea with pharmacologic agents: A systematic review and network meta-analysis3
“Optimizing empathic self-disclosures in dignity therapy: Improving the patient–provider relationship for more humanistic palliative care”3
Associations between Latino ethnicity and the use of emotional support and completion of advance directives3
Mourning, memories and moving forward3
Lessons from the Darkness3
Facing discrimination in research3
Posthumous dignity therapy: Challenges and opportunities in the Brazilian cultural context3
Resonance, self-reflection, and preparedness through a web-based intervention for family caregivers of patients with life-threatening illness receiving specialised home care3
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