Palliative & Supportive Care

What do family caregivers know about palliative care? Results from a national survey.

Methods for overcoming barriers in palliative care for ethnic/racial minorities: a systematic review.

Exploring the associations between spiritual well-being, burden, and quality of life in family caregivers of cancer patients.

Meaning and Purpose (MaP) therapy II: Feasibility and acceptability from a pilot study in advanced cancer.

Liminality as a dimension of the experience of living with terminal cancer.

Addressing personal barriers to advance care planning: Qualitative investigation of a mindfulness-based intervention for adults with cancer and their family caregivers.

Attitudes toward assisted suicide requests in the context of severe and persistent mental illness: A survey of psychiatrists in Switzerland.

Fatigue in patients on oral targeted or chemotherapy for cancer and associations with anxiety, depression, and quality of life.

A systematic review of the integration of palliative care in dementia management.

Long-term prevalence and predictors of prolonged grief disorder amongst bereaved cancer caregivers: A cohort study.

Family caregiving for persons with advanced heart failure: An integrative review.

Adaptation and psychometric evaluation of the short version of Family Sense of Coherence Scale in a sample of persons with cancer in the palliative stage and their family members.

Meaning and Purpose (MaP) therapy I: Therapeutic processes and themes in advanced cancer.

The accuracy of measures in screening adults for spiritual suffering in health care settings: a systematic review.

Comparing the physical, psychological, social, and spiritual needs of patients with non-cancer and cancer diagnoses in a tertiary palliative care setting.

Patient autonomy and participation in end-of-life decision-making: An interpretive-systemic focus group study on perspectives of Asian healthcare professionals.

Spirituality in the continuing education of healthcare professionals: An approach to palliative care.

Biopsychosocial distress and clinical outcome in metastatic renal cell carcinoma.

Screening for delirium with the Intensive Care Delirium Screening Checklist (ICDSC): Symptom profile and utility of individual items in the identification of delirium dependent on the level of sedation.

The effects of the interventions on the DNR designation among cancer patients: A systematic review.

Evaluation of decision support tools for patients with advanced cancer: A systematic review of literature.

The utility of nursing instruments for daily screening for delirium: Delirium causes substantial functional impairment.

A systematic approach to family engagement: Feasibility pilot of a pediatric delirium management and prevention toolkit.

Palliative care knowledge, information sources, and beliefs: Results of a national survey of adults in the USA.

Preferences around the disclosure of dying: a vision from Portuguese society.

Ketamine as augmentation for the treatment of major depression and suicidal risk in advanced cancer: Case report.

Adapting the Portuguese dignity question framework for adolescents: ages 10-18.

Cross-cultural validation of the Brazilian version of the spiritual care competence scale.

Validation of the caregiver oncology quality of life questionnaire in Portuguese caregivers of myeloma patients.

Patterns of, and barriers to supportive care needs assessment and provision for Australian women with gynecological cancer and their caregivers: a mixed-methods study of clinical practice.

Association between palliative care and the rate of advanced care planning: A systematic review.

Caregiver burden and bereavement among family caregivers who lost terminally ill cancer patients.

Clinical management of delirium: The response depends on the subtypes. An observational cohort study in 602 patients.

Factors associated with caregiver burden for mothers of children undergoing Acute Lymphocytic Leukemia (ALL) treatment.

The deteriorating patient representative on a palliative care quality committee: Ethical and practical considerations.

Prevalence and predictors of major depressive disorder in bereaved caregivers at 6 and 13 months.

Comprehension and Acceptance of the Meaning-Centered Psychotherapy with a Puerto Rican Patient Diagnosed With Advanced Cancer: A Case Study.

Palliative care for older South Asian migrants: a systematic review.

Collusion in palliative care: an exploratory study with the Collusion Classification Grid.

Electronic medical orders for life-sustaining treatment in New York State: Length of stay, direct costs in an ICU setting.

Social support and psychosocial functioning in women after mastectomy.

Efficacy of a written prayer technique on the anxiety of mothers of children with cancer.

Reliability and validity of the Arabic translation of the palliative performance scale.

Translation, cultural adaptation, and validation of the Brazilian Portuguese version of the End-of-Life Professional Caregiver Survey.

Multidisciplinary staff perspectives on the integration of spiritual care in a new setting: Israel.

What makes one respond to acupuncture for insomnia? Perspectives of cancer survivors.

Pain-related distress among patients referred to a community-based palliative care program.