Palliative Care Experience in the Last 3 Months of Life: A Quantitative Comparison of Care Provided in Residential Hospices, Hospitals, and the Home From the Perspectives of Bereaved Caregivers.

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Palliative Care Experience in the Last 3 Months of Life: A Quantitative Comparison of Care Provided in Residential Hospices, Hospitals, and the Home From the Perspectives of Bereaved Caregivers.

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http://www.wikidata.org/entity/Q39154318

description

2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

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2017年论文

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2017年论文

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name

Palliative Care Experience in ...... ctives of Bereaved Caregivers.

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Palliative Care Experience in ...... ctives of Bereaved Caregivers.

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type

Item

label

Palliative Care Experience in ...... ctives of Bereaved Caregivers.

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Palliative Care Experience in ...... ctives of Bereaved Caregivers.

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prefLabel

Palliative Care Experience in ...... ctives of Bereaved Caregivers.

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Palliative Care Experience in ...... ctives of Bereaved Caregivers.

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P1476

Palliative Care Experience in ...... ectives of Bereaved Caregivers

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P2093

Hsien Seow

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Dying in the hospital setting: A systematic review of quantitative studies identifying the elements of end-of-life care that patients and their families rank as being most important

Heterogeneity and changes in preferences for dying at home: a systematic review.

Family evaluation of hospice care: results from voluntary submission of data via website.

Capturing the Palliative Home Care Experience From Bereaved Caregivers Through Qualitative Survey Data: Toward Informing Quality Improvement.

Research agenda for developing measures to examine quality of care and quality of life of patients diagnosed with life-limiting illness.

Hospice care delivered at home, in nursing homes and in dedicated hospice facilities: A systematic review of quantitative and qualitative evidence.

Variability in access to hospital palliative care in the United States

The challenges of uncertainty and interprofessional collaboration in palliative care for non-cancer patients in the community: a systematic review of views from patients, carers and health-care professionals

Measurement of quality of care and quality of life at the end of life.

Use of family proxies in quality of life research for cancer patients at the end of life: a literature review.

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456-463

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scholarly article

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10.1177/1049909117713497

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Daryl Bainbridge

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2017-06-14T00:00:00Z

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28610431

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5794103

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