Feeling like a burden to others: a systematic review focusing on the end of life. - Wikidata - awgldk - TriplyDB

Feeling like a burden to others: a systematic review focusing on the end of life.

Feeling like a burden to others: a systematic review focusing on the end of life.

http://www.wikidata.org/entity/Q36753967

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A lines-of-defense model for managing health threats: a review Is the Evaluation of Quality of Life in NSCLC Trials Important? Are the Results to be Trusted?Thwarted belongingness and perceived burdensomeness: construct validity and psychometric properties of the Interpersonal Needs Questionnaire Are the data on quality of life and patient reported outcomes from clinical trials of metastatic non-small-cell lung cancer important?Distress in older patients with cancer Change in suicidal ideation after interdisciplinary treatment of chronic pain EMPOWER: an intervention to address barriers to pain management in hospice.End-of-Life Treatment Preferences Among Older Adults: An Assessment of Psychosocial Influences.Reasoning in the capacity to make medical decisions: the consideration of values Older adults' preferences for independent or delegated end-of-life medical decision making Constructing understandings of end-of-life care in Europe: a qualitative study involving cognitive interviewing with implications for cross-national surveys.The interpersonal needs questionnaire with a shortened response scale for oral administration with older adults.Do personality traits moderate the impact of care receipt on end-of-life care planning?Associations between advanced cancer patients' survival and family caregiver presence and burden.Legacy activities as interventions approaching the end of life The Legacy Project Intervention to Enhance Meaningful Family Interactions: Case Examples The preferences and perspectives of family caregivers towards place of care for their relatives at the end-of-life. A systematic review and thematic synthesis of the qualitative evidence.Chronic pain and the interpersonal theory of suicide.Self-perceived burden in chronic pain: relevance, prevalence, and predictors Suffering and distress at the end-of-life.A Patient with Cancer and Her Family in Caring Partnership Based on Margaret Newman's Theory of Health as Expanding Consciousness.Preparation for the end of life and life completion during late-stage lung cancer: An exploratory analysis.Impact of high self-perceived burden to others with preferences for end-of-life care and its determinants for terminally ill cancer patients: a prospective cohort study.A scoping research literature review to assess the state of existing evidence on the "bad" death.Suffering and euthanasia: a qualitative study of dying cancer patients' perspectives.The relationship between hope and pain in a sample of hospitalized oncology patients.Crossed views of burden and emotional distress of cancer patients and family caregivers during palliative care.Financial burden among US households affected by cancer at the end of life.Caregiver burden, patients' self-perceived burden, and preference for palliative care among cancer patients and caregivers.Suffering and dying well: on the proper aim of palliative care Navigating assisted death and end-of-life care.Construction of health preferences: a comparison of direct value assessment and personal narratives.The reluctance to burden others as a value in end-of-life decision making: a source of inaccuracy in substituted judgment.Can't live with you, can't live without you: negative family exchanges and adaptation in end-stage renal disease patients.Family predictors of psychosocial outcomes among Hong Kong Chinese cancer patients in palliative care: living and dying with the "support paradox".End of life care preferences among people of advanced age: LiLACS NZ.Reported distress in patients living with advanced cancer: changes pre-post interdisciplinary palliative rehabilitation.Analysis of the psychometric properties of the Interpersonal Needs Questionnaire (INQ) among community-dwelling older adults.Detrimental social interactions predict loss of dignity among patients with cancer.The PERS(2) ON score for systemic assessment of symptomatology in palliative care: a pilot study.

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P2860

Feeling like a burden to others: a systematic review focusing on the end of life.

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Keith G Wilson

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P2860

In search of a good death: observations of patients, families, and providers.

Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers.

End-of-life decision making: a qualitative study of elderly individuals.

An integrative review of the concept of spirituality in the health sciences.

Structured interview assessment of symptoms and concerns in palliative care.

Place of care in advanced cancer: a qualitative systematic literature review of patient preferences.

Clinical applications of the interpersonal-psychological theory of attempted and completed suicide.

Perceptions of do-not-resuscitate orders.

Older people's views about home as a place of care at the end of life.

Characteristics of terminal cancer patients who committed suicide during a home palliative care program.

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