Use of family proxies in quality of life research for cancer patients at the end of life: a literature review.
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Effectiveness and cost-effectiveness of home palliative care services for adults with advanced illness and their caregiversSystematic review of caregiver responses for patient health-related quality of life in adult cancer careDo nurses provide holistic care to cancer patients?The attitudes of brain cancer patients and their caregivers towards death and dying: a qualitative studyDesign, implementation and reporting strategies to reduce the instance and impact of missing patient-reported outcome (PRO) data: a systematic review.Late-stage HIV/AIDS patients' and their familial caregivers' agreement on the palliative care outcome scale.Bereaved family member perceptions of patient-focused family-centred care during the last 30 days of life using a mortality follow-back survey: does location matter?Benefits and challenges in use of a standardized symptom assessment instrument in hospice.Tailoring traditional interviewing techniques for qualitative research with seriously ill patients about the end-of-life: a primer.Trends in Advance Care Planning in Patients With Cancer: Results From a National Longitudinal Survey.Sensitivity analysis for nonignorable missingness and outcome misclassification from proxy reports.Symptom burden, palliative care need and predictors of physical and psychological discomfort in two UK hospitalsSpecialized palliative care services are associated with improved short- and long-term caregiver outcomes.Caregiver assessment of patients with advanced cancer: concordance with patients, effect of burden and positivity.How do proxy responses and proxy-assisted responses differ from what Medicare beneficiaries might have reported about their health care?Proxy perspectives regarding end-of-life care for persons with cancer.An eHealth system supporting palliative care for patients with non-small cell lung cancer: a randomized trialCaregivers for people with end-stage lung disease: characteristics and unmet needs in the whole population.Promoting the consumer voice in palliative care: exploring the possibility of using consumer impact statements.A 'pain-free' death.The selection and use of outcome measures in palliative and end-of-life care research: the MORECare International Consensus Workshop.Mixed methods research in the development and evaluation of complex interventions in palliative and end-of-life care: report on the MORECare consensus exercise.Using QALYs in cancer: a review of the methodological limitations.The EORTC QLQ-BN20 for assessment of quality of life in patients receiving treatment or prophylaxis for brain metastases: a literature review.Agreement between self-report and medical records on signs and symptoms of respiratory illness.The care experiences of patients who die in residential hospice: A qualitative analysis of the last three months of life from the views of bereaved caregivers.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.Qualitative analysis of cancer patients' experiences using donated human milk.Measuring healthcare integration: Operationalization of a framework for a systems evaluation of palliative care structures, processes, and outcomes.Living with skin diseases and topical treatment: patients' and providers' perspectives and priorities.Crossed views of burden and emotional distress of cancer patients and family caregivers during palliative care.The Views of Informal Carers' Evaluation of Services (VOICES): Toward an adaptation for the New Zealand bicultural context.A survey of patients' experience of pain and other symptoms while receiving care from palliative care services.Specialist palliative care needs of whole populations: a feasibility study using a novel approach.Are Disagreements in Caregiver and Patient Assessment of Patient Health Associated with Increased Caregiver Burden in Caregivers of Older Adults with Cancer?Perceived breathlessness and psychological distress among patients with chronic obstructive pulmonary disease and their spouses.Defining distinct caregiver subpopulations by intensity of end-of-life care provided.Proxy and patient reports of health-related quality of life in a national cancer survey.Measuring the quality of end-of-life care: Development, testing, and cultural validation of the Danish version of Views of Informal Carers' Evaluation of Services-Short Form.Differences in perception of hearing handicap between cochlear implant users and their spouses.
P2860
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P2860
Use of family proxies in quality of life research for cancer patients at the end of life: a literature review.
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Use of family proxies in quali ...... of life: a literature review.
@ast
Use of family proxies in quali ...... of life: a literature review.
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type
label
Use of family proxies in quali ...... of life: a literature review.
@ast
Use of family proxies in quali ...... of life: a literature review.
@en
prefLabel
Use of family proxies in quali ...... of life: a literature review.
@ast
Use of family proxies in quali ...... of life: a literature review.
@en
P2860
P356
P1433
P1476
Use of family proxies in quali ...... of life: a literature review.
@en
P2093
Ruth McCorkle
Siew Tzuh Tang
P2860
P304
P356
10.1081/CNV-120005928
P577
2002-01-01T00:00:00Z