Feeling like a burden: exploring the perspectives of patients at the end of life.
about
Protocol for a longitudinal qualitative interview study: maintaining psychological well-being in advanced cancer--what can we learn from patients' and carers' own coping strategies?"You don't want to burden them": older adults' views on family involvement in care.A qualitative investigation of the roles and perspectives of older patients with advanced cancer and their family caregivers in managing pain in the home.Older adults' preferences for independent or delegated end-of-life medical decision makingCan comprehensive specialised end-of-life care be provided at home? Lessons from a study of an innovative consultant-led community service in the UK.Feeling like a burden to others: a systematic review focusing on the end of life.Vengeance, HIV disclosure, and perceived HIV transmission to othersPatients' Experiences of Being a Burden on Family in Terminal Illness.Caregivers for people with end-stage lung disease: characteristics and unmet needs in the whole population.Self-perceived burden in chronic pain: relevance, prevalence, and predictorsSuffering and distress at the end-of-life.Clinical considerations for working with patients with advanced cancer.The end of life and the family: hospice patients' views on dying as relational.Gendered Processes in Hospice Palliative Home Care for Seniors With Cancer and Their Family Caregivers.A revised model for coping with advanced cancer. Mapping concepts from a longitudinal qualitative study of patients and carers coping with advanced cancer onto Folkman and Greer's theoretical model of appraisal and coping.Lived-through past, experienced present, anticipated future: Understanding "existential loss" in the context of life-limiting illness.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.Structural impact on gendered expectations and exemptions for family caregivers in hospice palliative home care.Supporting shared decisions when clinical evidence is low.Self-perceived burden as a mediator of depression symptoms amongst individuals living with a movement disorder."I hate being a burden": The patient perspective on carer burden in amyotrophic lateral sclerosis.Crossed views of burden and emotional distress of cancer patients and family caregivers during palliative care.Dignity and the essence of medicine: the A, B, C, and D of dignity conserving care.Attachment theory and spirituality: two threads converging in palliative care?End-of-life concerns and care preferences: congruence among terminally ill elders and their family caregivers.Palliative respite services using nursing staff reduces hospitalization of patients and improves acceptance among carers.A separate structured conversation with relatives of patients enrolled for advanced palliative home care: a care development project.Exploring family relationships through associations of comfort, relatedness states, and life closure in hospice patients: A pilot study.Positive emotion communication: Fostering well-being at end of life.Between Two Worlds: Liminality and Late-Stage Cancer-Directed Therapy.Living with suffering as voiced by Thai patients with terminal advanced cancer.Patients' self-perceived burden, caregivers' burden and quality of life for amyotrophic lateral sclerosis patients: a cross-sectional study.Factors associated with self-perceived burden to the primary caregiver in older patients with hematologic malignancies: an exploratory study.Health Care Communication and Agreement and Disagreement About Symptoms Within the Context of Multimorbidity.Trajectory and predictors of quality of life during the dying process: roles of perceived sense of burden to others and posttraumatic growth.The experiences of suffering of palliative care patients in Malaysia: a thematic analysis.On euthanasia, resistance, and redemption: the moralities and politics of a hospice.Patients' experiences of care and support at home after a family member's participation in an intervention during palliative care.On the meanings and experiences of living and dying in an Australian hospice.Knowledge, beliefs, and concerns about opioids, palliative care, and homecare of advanced cancer patients: a nationwide survey in Japan.
P2860
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P2860
Feeling like a burden: exploring the perspectives of patients at the end of life.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Feeling like a burden: exploring the perspectives of patients at the end of life.
@en
type
label
Feeling like a burden: exploring the perspectives of patients at the end of life.
@en
prefLabel
Feeling like a burden: exploring the perspectives of patients at the end of life.
@en
P2093
P1476
Feeling like a burden: exploring the perspectives of patients at the end of life.
@en
P2093
Christine J McPherson
Keith G Wilson
Mary Ann Murray
P304
P356
10.1016/J.SOCSCIMED.2006.09.013
P407
P577
2006-10-27T00:00:00Z