Using satisfaction to measure the quality of palliative care: a review of the literature.
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Training and supportive programs for palliative care volunteers in community settingsTraining and supportive programs for palliative care volunteers in community settingsLiverpool care pathway carers surveyThe National Tumor Association Foundation (ANT): A 30 year old model of home palliative care.Exploring patients' experience of receiving information about cancer: a comparison of interview and questionnaire methods of data collection.Decision-making capacity and communication about care of older people during their last three months of lifeSystematic review of interventions to improve the provision of information for adults with primary brain tumors and their caregivers.Patients still wish for key improvements after total knee arthroplastyQuality nursing care for hospitalized patients with advanced illness: concept development.The quality of medical care at the end-of-life in the USA: existing barriers and examples of process and outcome measures.Unpacking the concept of patient satisfaction: a feminist analysis.Dying at home or in an institution: perspectives of Dutch physicians and bereaved relatives.Development the Care Evaluation Scale Version 2.0: a modified version of a measure for bereaved family members to evaluate the structure and process of palliative care for cancer patientWorking conditions that support patient safety.Home care by general practitioners for cancer patients in the last 3 months of life: An epidemiological study of quality and associated factors.Chronic illness and patient satisfaction.Evaluation and ethical review of a tool to explore patient preferences for information and involvement in decision making.A patient and carer survey in a community clinical nurse specialist service.Patient expectation and satisfaction with nursing care in Turkey: a literature review.How well do current instruments using bereaved relatives' views evaluate care for dying patients?A comparison of palliative care outcome measures used to assess the quality of palliative care provided in long-term care facilities: a systematic review.Outcome assessment instruments in palliative and hospice care--a review of the literature."Don't get weak in your compassion": bereaved next of kin's suggestions for improving end-of-life care in Veterans Affairs Medical Centers.The communication experiences of patients with palliative care needs: A systematic review and meta-synthesis of qualitative findings.Validation Study for the Brief Measure of Quality of Life and Quality of Care: A Questionnaire for the National Random Sampling Hospital Survey.Psychometric Properties of the Patients' Satisfaction Instrument FAMCARE-P13 in a Palliative Care Unit.Palliative care quality indicators in Italy. What do we evaluate?Towards a culturally acceptable end-of-life survey questionnaire: a Bengali translation of VOICES.Patients' evaluations of the quality of care: influencing factors and the importance of engagement.Family presence and environmental factors at the time of a patient's death in an ICU.Improvements in patient satisfaction at an outpatient clinic for patients with breast cancer.Legitimising and rationalising in talk about satisfaction with formal healthcare among bereaved family members.Symptom pathways from referral to death: measuring palliative care outcomes.Connecting the voices of users, caregivers and providers on service quality: a study of home-care services.Environmental Design for End-of-Life Care: An Integrative Review on Improving the Quality of Life and Managing Symptoms for Patients in Institutional Settings.Satisfaction with oncology care among patients with advanced cancer and their caregivers.Experience of services as a key outcome in amyotrophic lateral sclerosis (ALS) care: the case for a better understanding of patient experiences.A comparison of the quality of care provided to cancer patients in the UK in the last three months of life in in-patient hospices compared with hospitals, from the perspective of bereaved relatives: results from a survey using the VOICES questionnaiPatient perspective: what do palliative care patients think about their care?Translation and Testing of the Italian Version of FAMCARE-2: Measuring Family Caregivers' Satisfaction With Palliative Care.
P2860
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P2860
Using satisfaction to measure the quality of palliative care: a review of the literature.
description
2003 nî lūn-bûn
@nan
2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Using satisfaction to measure the quality of palliative care: a review of the literature.
@ast
Using satisfaction to measure the quality of palliative care: a review of the literature.
@en
type
label
Using satisfaction to measure the quality of palliative care: a review of the literature.
@ast
Using satisfaction to measure the quality of palliative care: a review of the literature.
@en
prefLabel
Using satisfaction to measure the quality of palliative care: a review of the literature.
@ast
Using satisfaction to measure the quality of palliative care: a review of the literature.
@en
P2860
P1476
Using satisfaction to measure the quality of palliative care: a review of the literature
@en
P2093
Julia Addington-Hall
Rhidian Hughes
P2860
P304
P356
10.1046/J.1365-2648.2003.02624.X
P407
P577
2003-05-01T00:00:00Z