Palliative & Supportive Care

Article	Citations
PAX volume 20 issue 6 Cover and Front matter	111
Would compassion be able to intervene?	62
A qualitative exploration of the impact of healthcare pre- and post-death on bereavement experiences	61
A little rain	28
The final beeps of the final beats	28
Decisions about treatment with targeted therapies in a palliative care unit: A case series	24
Matter	23
Validation of the Mexican version of the Schedule of Attitudes Toward Hastened Death in patients undergoing palliative care in Mexico	22
End of life distress as an economic issue: The case for psychedelic-assisted therapy	21
Reliability and validity of the Self-Efficacy in Palliative Care Scale among nurses	20
The silk road	20
“Rapid tele-psychotherapy” with single-session music therapy in the metaverse: An alternative solution for mental health services in the future	20
An exploratory qualitative study on factors influencing the level of agreement in symptom reports in child–caregiver dyads	19
Adverse COVID-19 experiences and physical and psychological outcomes in patients with lung cancer	19
Self-compassion training in palliative care during COVID-19: A pilot study	18
Methodological considerations in the combined methylphenidate and physical activity trial for cancer-related fatigue in immunotherapy patients	17
Scrambler therapy for chemotherapy-induced peripheral neuropathy: A case report	17
When and how to discuss about palliative care and advance care planning with cancer patients: A mixed-methods study	16
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 perspective	16
Spiritual care interventions for palliative care patients: A scoping review	16
Beyond emotional regulation: Expanding the existential dimensions of emotional labor in end-of-life care	15
Increased preparedness for caregiving among family caregivers in specialized home care by using the Carer Support Needs Assessment Tool Intervention	15
The longitudinal effects of faith and meaning on quality of life in US women with breast cancer undergoing chemotherapy	15
Inclusive palliative care for LGBTQIA+ individuals: A socioecological perspective on barriers and enablers	15
Utilization of medical interventions in hospitalized Mexican adults with cancer at the end of life in a referral hospital: The importance of early palliative care	15

Burden and anticipatory grief in caregivers of family members with Alzheimer’s disease and other dementias	14
Vacancies	14
Development and evaluation of a Hospice Foundation of Taiwan Bereavement Assessment Scale: A psychometric properties test	13
Inevitable changes	13
Impact of consultation-based hospice palliative care team on self-determination respect rates	13
End-of-life dreams and visions in a patient with delirium: A Brazilian case report and narrative review	13
Providing care for siblings of children on hospice	13
Emotion dysregulation and family functioning moderate family caregiving burden during the pandemic	13
Anthropology and its aftermath: Humanity in medical training	13
Nursing students’ willingness to discuss hospice and palliative care with family and associated factors: A cross-sectional study	12
He was only thirty one	12
Tongue edema as an adverse drug reaction to low-dose olanzapine in a cancer patient receiving palliative care	12
Making space for grief: The impact of remembrance programs for pediatric healthcare providers	12
Emotional ecosystems: Understanding the relationship between family interactions and anxiety among cancer caregivers	12
Integration of the geriatric palliative care in oncological care of elderly patient with cancer	12
Relationship between death anxiety, spiritual well-being, and social support in patients with gynecologic cancer	11
Nurse-led tele-palliative care for symptom management and family support: A hybrid umbrella review of reviews and primary studies	11
Scar tissue	11
Patient beliefs associated with medication hesitancy in palliative care: A systematic review using the theory of planned behavior	11
The relationship between moral distress, individual and professional values in oncology nurses: A structural equation study	11
Talking about dying and death: Essentials of communicating about approaching death from the perspective of major stakeholders	11
Motivations for choosing “home” as one’s preferred place of death: A scoping review	10
Compassion fatigue and palliative care in neonatal nurses	10
Validation of the Spanish translation Sheffield Profile for Assessment and Referral for Care (SPARC-Sp) at the Hospital Universitario San Jose of Popayan, Colombia	10
Died with compassion	10
Digging deeper: A critique of the mediation study of spirituality in ALS patients	10
The first reader: Montaigne and the body’s particularity	10
Nurses’ experiences of suicide attempts in palliative care	10
Concomitant use of hydroxyzine and haloperidol did not worsen delirium in patients with cancer: A multicenter, retrospective, observational study	10
Building dignity at the bedside: A reflective clinical model for clinical encounters	10
Sharing the burden: The experiences of HIV psychiatrists delivering primary palliative care	10
Stigma as a mediator in the impact of cancer-related symptoms on social relationships in survivors	10
Moral distress in healthcare professionals working with motor neuron disease	10
Homing instinct	10
Redefining caregiver strain for family caregivers in end-of-life care in Hong Kong – CORRIGENDUM	10
Exploring the landscape of palliative care provision for black patients with hematologic cancers: A scoping review	10
A cognitive behavioral therapy–based intervention to address body image in patients with facial cancers: Results from a randomized controlled trial	10
Afterlife matters	9
Examining the development of information needs assessment tools for use in the cancer context: A scoping and critical review	9
Adapting to the emotional complexity of palliative care communication: Palliative care clinicians’ experiences	9
Life meaning constructed from dignity therapy in traditional Chinese culture: A qualitative analysis of dignity therapy generativity documents	9
Dignity-related distress and recall among alert, non-delirious critically ill patients	9
Comprehensive psychosocial and spiritual care of people with advanced chronic conditions: The experience of La Caixa foundation program at 15 years – CORRIGENDUM	9
Meaning and Purpose (MaP) therapy I: Therapeutic processes and themes in advanced cancer – CORRIGENDUM	9
Spiritual embrace: A source of strength for caregivers in a mental health crisis	9
Virtual reality and neurofeedback as a supportive approach to managing cancer symptoms for patients receiving treatment: A brief report of a feasibility trial	9
The place of the relative at the time of the announcement of cancer progression: BABEL – a mixed-methods study	9
The relationship between cancer patients’ spiritual needs, quality of life and depression levels: A correlational study	9
Psychological symptom burden associated with malignant wounds: Secondary analysis of a prospective cohort study	9
Palliative care providers’ roles in medical assistance in dying decision-making triads with patients and families: A qualitative analysis	9

“With compliment from...”: A critical reflection on the function and use of compliment letters addressed to hospital staff	9
Are specialist-provided end-of-life scenarios key to initiation of advance care planning in primary care? A mixed-methods study	9
Be a burden	9
Healing across cultures	8
Palliative and end-of-life nursing care in Saudi Arabia: A systematic review of nursing practices, challenges, and patient–family outcomes	8
There is nothing informal about caregiving	8
A virtual program to teach pain coping skills to dyads of caregivers and Veterans with dementia or mild cognitive impairment: Preliminary quantitative and qualitative findings	8
Assessment of psychometric properties of the Persian version of the spiritual care competency self-assessment tool	8
The caregiver’s journey: A qualitative study on the integration of family caregivers of advanced cancer patients in outpatient settings in Germany	8
“It seemed I was having a conversation with him”: Posthumous Dignity Therapy case series	8
Experiences and attitudes of nurses with the legislation on assisted suicide in Austria	8
Interventions for unpaid carers of people living with breathlessness due to chronic respiratory diseases: Scoping review	7
What are family caregivers’ experiences of coordinating end-of-life care at home? A narrative review	7
Prognostic utility of Palliative Prognostic Index in advanced cancer: A systematic review and meta-analysis	7
I Am More	7
Strategies to prepare hospice providers to interact with adolescents with a parent in hospice	7
The effects of illness perception on death anxiety and satisfaction with life in patients with advanced gastrointestinal cancer	7
Feasibility of implementing Dignity Therapy in Dutch nursing homes: A pre–post study exploring potential effects on dignity, depression, and self-esteem	7
Knowledge, goals, and misperceptions about palliative care in adults with chronic disease or cancer	7
Disrespectful and inadequate palliative care to lesbian, gay, and bisexual patients	7
Improving palliative care in Nepal through virtual education	7
Families’ experiences of end-of-life care in an acute private hospital: A qualitative study	7
Medical Assistance in Dying (MAiD) in Canada: Why Coelho and colleagues are incorrect to suggest the MAiD framework is in significant distress	7
The communication experiences of persons referred to specialist palliative care services and their carers: A descriptive phenomenological study	7
Access to palliative and supportive care in the Philippines: A call to action	7
Identifying patients in need of palliative care: Adaptation of the Necesidades Paliativas CCOMS-ICO© (NECPAL) screening tool for use in Israel	7
“What it is like to be human”: The existential dimension of care as perceived by professionals caring for people approaching death	7
Methylphenidate and physical activity for cancer-related fatigue in immunotherapy patients: Response to letter to the editor	7
The burden of care: Health and wellbeing of informal caregivers of people with amyotrophic lateral sclerosis	7
Sexuality in the light of awareness of approaching mortality	7
Qualitative analysis of expressions used in the end-of-life discussions and their associated factors	6
Validation of an assessment of prolonged grief disorder among Mexican mourners	6
A commentary on “Spirituality moderates the relationship between cancer caregiver burden and depression” (La. I.S, 2023)	6
Alone	6
A survey of statistical methods utilized for analysis of randomized controlled trials of behavioral interventions	6
Danse Macabre in W.H. Auden’s “Death’s Echo”	6
Compassion fatigue and psychological resilience levels of nursing final students: A descriptive, cross-sectional, and relational study	6
But parents need help! Pathways to caregiver mental health care in pediatric hospital settings	6
End-of-life care for Filipino patients with cancer	6
Memento mori	6
Volunteers’ spiritual care competence and its relationship with attitudes toward palliative care: A cross-sectional study	6
Integrating ACP into Nigeria’s culture and healthcare system for improved end-of-life care	6
Relational–temporal dignity at the end of life: Ethical foundations for the DiRePal model in the algorithmic age	6
Hemichorea–hemiballismus associated with a case of cerebral toxoplasmosis in a hematopoietic stem cell transplant recipient	6
Exploring unmet concerns in home hospice cancer care: Perspectives of patients, informal caregivers, palliative care providers, and family physicians	6
Advance care planning discussions – Perspectives from oncology patients with advanced-stage disease	6
Impact of nurse-led advance care planning in a primary care setting	6
The impact of caregiver burden and associated factors on trait anger levels and anger expression styles in family caregivers of palliative care patients	6
What we learnt from parents’ death experience: A cross-sectional study of death literacy and parent’s death quality among adult children in China	6
Palliative care physicians’ decision-making about palliative sedation for existential suffering: A Belgian nationwide qualitative study	6
Bereavement guilt among young adults impacted by caregivers’ cancer: Associations with attachment style, experiential avoidance, and psychological flexibility	6
Life/time/d - Is the life shortened, a shortened life?	6
Perceived organizational support moderates the effect of job demands on outcomes: Testing the JD-R model in Italian oncology nurses	6
The dose divided	6
Translation and validation of the Chinese version of Palliative Care Self-Efficacy Scale	5
Deathbed experiences and meaning-making: Perspectives of family caregivers of patients who received cancer palliative care	5
Ketamine subcutaneous continuous infusion for depressive symptoms at home: A case report beyond pain use	5
The Palliative Story Exchange: An innovative storytelling intervention to build community, foster shared meaning, and improve sustainability	5
An existential perspective on physician-assisted dying in contemporary legislative debates	5
Factors associated with caregiver strain among mothers and fathers of children with advanced cancer	5
Psychometric properties of the Turkish version of the Palliative Nursing Care Quality Scale	5
From theory to compassion: Why duloxetine matters for chemotherapy-induced neuropathy in the Global South	5
Translation and cross-cultural adaptation of the Posthumous Dignity Therapy Schedule of Questions to Brazilian Portuguese – CORRIGENDUM	5
Mystery prevails over absurdity	5
Tendencies in the association between fatigue and quality of life in terminally ill patients with cancer admitted to a palliative care unit	5
Experiences with health information among caregivers of people with cancer from culturally and linguistically diverse backgrounds: A qualitative study	5
Peaceful acceptance and struggle with terminal cancer: The role of mindfulness, self-compassion, and body image distress	5
A name unasked	5
Eulogy	5
Post-biographical dignity in the age of artificial intelligence: Narrative, ePROMs and ethical challenges in end-of-life care	5
Moral and philosophical frameworks for discussing Voluntary Assisted Dying (VAD)	5
The 4th and 5th Annual U.S. World Hospice and Palliative Care Day conferences: Unifying the global palliative care community	5
Nurses’ stressful experiences in providing palliative and end-of-life care for children: A meta-synthesis	5
Pancreatic cancer, depression, and spirituality in therapy: “Unio Mystica” and “Achrayut,” 2 case reports	5
Dyadic sleep intervention for adult patients with cancer and their sleep-partner caregivers: A feasibility study	5
“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 care	5
Social injustice is moral suffering	5
Situations in which caregivers and patients are likely to collude: Perspectives from caregivers of advanced cancer patients in Bangladesh– ERRATUM	5
The ethics of staying: Medicine at the limits of intervention	5
Barriers to advance care planning among patients with advanced serious illnesses: A national survey of health-care professionals in Singapore	5

The effectiveness of pretreatment video-based psychoeducation for patients with breast cancer	5
Lessons from the Darkness	4
The end of medicine	4
Measuring compassion in end-of-life cancer patients: The Italian validation of the Sinclair Compassion Questionnaire (SCQit)	4
Precision medicine	4
Structure of the spiritual pain of bereaved caregivers of cancer patients: A preliminary scale development	4
Facing death in care: Nurses’ lived experiences in the care of bedridden patients	4
The value of time	4
Associations between Latino ethnicity and the use of emotional support and completion of advance directives	4
Benefits of duloxetine may outweigh risks in a patient with hormone-positive breast cancer	4
Non-curative care options for patients with advanced-stage head and neck cancer: Current state of the science and future opportunities	4
Communicating about the end of life: The path of prognostic awareness	4
Wernicke encephalopathy with active hallucinations during lung cancer treatment and hemodialysis: A case report	4
The Pediatric Serious Illness Conversation Program: Understanding challenges and experiences for clinicians after advance care planning training	4
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 Asia	4
Embracing goodbye: A personal reflection on virtual reality intervention in palliative care	4
Healthcare professionals’ discussion of loss and grief with parents of children with life-limiting severe neurological impairment: Findings from a scoping review	4
Bridging the gaps in inclusive palliative care: Reflections on a socioecological perspective for LGBTQIA + populations	4
Reiki intervention for supporting healthcare professional care behaviors in pediatric palliative care: A pilot study	4
Remembrance programs in pediatric care: Transforming grief into community resilience	4
Practicing with what you left	4
Manic and hypomanic states in cancer patients: A systematic review	4
“Optimizing empathic self-disclosures in dignity therapy: Improving the patient–provider relationship for more humanistic palliative care”	4
When death is desired: A case of MAiD & the CL psychiatrist	4
The experiences of families of children with cancer during the COVID-19 pandemic: A qualitative exploration	4
Acceptability of a Serious Illness Conversation Guide to Black Americans: Results from a focus group and oncology pilot study	4
Palliative care in pediatric patients with central nervous system cancer: Descriptive and comparative study	4
Impact of home healthcare reform on place of death for people with dementia: A nationwide cohort study accounting for cultural factors of impending death discharge	4
Timely integration of palliative care into standard oncology care: An interview study with clinicians and patients with incurable cancer	4
Cross-cultural adaptation and validation of the Suffering Pictogram for Brazilian cancer patients	4
Capacity debt in palliative care: A case report illustrating longitudinal exhaustion following early engagement	4
Juana la Loca	4
Balancing burden and benefit: Reflecting on interviews with individuals nearing the end of their lives	4
Palliative team involvement in end-of-life care for Jewish and Muslim children in Jerusalem: A unique clinical and cultural context	4
Psychometric properties of the Patient Health Questionnaire-9 and the Generalized Anxiety Disorder-7 in Mexican cancer patients	4
Melodies and memories	4
When presence remains	4
Situations in which caregivers and patients are likely to collude: Perspectives from caregivers of advanced cancer patients in Bangladesh	4
AutoFOCUS: A mindfulness-based intervention for caregivers of autologous hematopoietic stem cell transplant recipients	4
Effective communication in palliative care from the perspectives of patients and relatives: A systematic review	4
Cervical cancer survivors: The experiences of the journey	4
Posthumous dignity therapy: Challenges and opportunities in the Brazilian cultural context	4
Learning to remain: Silence, suffering, and the hidden curriculum of care	4
Spiritual care perceptions and empathy of Chinese nursing students: The mediating roles of spiritual well-being	4
What do health professionals think about implementing psilocybin-assisted therapy in palliative care for existential distress? A World Café qualitative study	4
An interpretative qualitative case study of a Compassionate Cities initiative in the United Kingdom: Lessons for implementation in other settings	4
In the underbelly of grief	4
Refractory symptoms and end of life midazolam use in cancer patients, a single center experience	4
Implementation of psycho-existential symptom distress screening among Italian healthcare providers	4
Identifying the active content of interventions targeting the psychological well-being of carers of people with motor neuron disease: A systematic review	4
Irrevocably other: Narrative medicine and Jorge Luis Borges’ “The other death”	4
Death comes	4
Spiritual wellbeing in psychedelic-assisted therapy with palliative care populations: An analysis of outcome measures	4
The realities of Medical Assistance in Dying in Canada – CORRIGENDUM	3
Children’s understanding of dying and death: A multinational grounded theory study	3
Healthcare professionals’ experiences in using a patient-reported outcome tool (PRO-Pall) to identify symptoms and problems in palliative care: A mixed-methods study	3
Perceptions about medical aid in dying among healthcare workers in Pakistan	3
Beyond the surface: Exploring differing aspects of wishes to hasten death in patients with amyotrophic lateral sclerosis	3
“Rapid counseling” with single-session music therapy in the workplace: An alternative treatment in increasing the constructiveness of destructive bystanders that promote resilience for caregivers	3
Burden of care and quality of life among informal caregivers to Alzheimer patients in Egypt	3
Potential and challenges of virtual reality in improving the quality of life of palliative care patients	3
Dress rehearsal	3
Sharing “off-script”: A qualitative analysis of providers’ empathic self-disclosures during dignity therapy	3
Benefit-finding in children with advanced cancer and their parents	3
Development and expert consensus validation of a technological resource to support the integration of palliative care from hospital to home: A Delphi study	3
Hope at the end of life: Can hope endure when life nears its end?	3
Caring with time and despite de time: Reflections on prognosis	3
Impact of a mental training program for pediatric cancer patients after allogeneic hematopoietic stem cell transplantation or high-dose chemotherapy – Results of a randomized controlled trial	3
Cosmology of belonging: The role of community in the therapeutic use of psychedelics	3
Evaluating the effectiveness of psilocybin in alleviating distress among cancer patients: A systematic review	3
Repeated exposure to trauma narratives and professional quality of life in palliative and end-of-life healthcare providers	3
Color without light	3
Triad of agency, mood, and meaning: A nursing perspective on patient activation, depression, and quality of life in older adults receiving palliative oncology care	3
Pandemic grief risk factors and prolonged grief disorder in bereaved young adults during COVID-19	3
Valued Outcomes in the Cancer Experience (VOICE)™: Development and validation of a multidimensional measure of perceived control	3
From “surviving to thriving”: Mood Lifters – a wellness program for parents of medically complex children	3
Identifying practical clinical problems in active euthanasia: A systematic literature review of the findings in countries where euthanasia is legal	3
Stigma in Mexican patients with Lung Cancer: Psychometric Properties of the Cataldo Lung Cancer Stigma Scale (CLCSS) - Brief version	3
In the fragile light of dawn	3
A whisper from dementia	3
Communicating cancer to children: Strategies and needs of parents with cancer. A qualitative study	3
Fulfilling end-of-life dreams: A scoping review of bucket lists in palliative and hospice care	3
Ivan Illich and convivial palliative care	3
Disrespectful and inadequate palliative care to transgender persons	3
“You think you got it down and then the moment comes”: The certainty of uncertainty in end-of-life decision making	3
Positive psychology and palliative care: A call for an integrative approach	3
“I’m not a physician, but i’m the expert for my child” experiences of parents caring for their child with a life-limiting condition in an inpatient setting – A qualitative study	3
Psychedelic medicines for end-of-life care: Pipeline clinical trial review 2022	3
From awareness to action: Reimagining cultural responsiveness in pediatric palliative care	3
Understanding the desire for hastened death in terminal cancer: Implications for whole-person palliative care	3
What is the current state of the research literature examining the impact of the motor neurone disease journey on the couple’s relationship? A scoping review	3
The effectiveness of compassion-based interventions among cancer patients: A systematic review and meta-analysis	3
The benefits of concurrent engagement in meaning-centered psychotherapy and meaning-centered psychotherapy for cancer caregivers: A case study	3
Enhancing psychosocial care at end of life: A novel simulation training program	3
A cognitive–behavioral model of dyspnea: Qualitative interviews with individuals with advanced lung cancer – ADDENDUM	3