Is it feasible and desirable to collect voluntarily quality and outcome data nationally in palliative oncology care?
about
The value of data collection within a palliative care programImproving national hospice/palliative care service symptom outcomes systematically through point-of-care data collection, structured feedback and benchmarking.How many children and young people with life-limiting conditions are clinically unstable? A national data linkage study.Implementing patient reported outcome measures (PROMs) in palliative care--users' cry for help.Increased access to palliative care and hospice services: opportunities to improve value in health care.Palliative care needs of patients with cancer living in the communityRegistration in a quality register: a method to improve end-of-life care--a cross-sectional study.The selection and use of outcome measures in palliative and end-of-life care research: the MORECare International Consensus Workshop.Are we heading in the same direction? European and African doctors' and nurses' views and experiences regarding outcome measurement in palliative care.Implementing patient-reported outcome measures in palliative care clinical practice: a systematic review of facilitators and barriers.EAPC White Paper on outcome measurement in palliative care: Improving practice, attaining outcomes and delivering quality services - Recommendations from the European Association for Palliative Care (EAPC) Task Force on Outcome Measurement.Together we can: experiences from 7 years of cross-sectional studies in a Swedish palliative care clinical research network.Designing and conducting randomized controlled trials in palliative care: A summary of discussions from the 2010 clinical research forum of the Australian Palliative Care Clinical Studies Collaborative.Variations in process and outcome in inpatient palliative care services in Korea.Do patients and carers find separate palliative care clinic consultations acceptable? A pilot study.Developing a national quality register in end-of-life care: the Swedish experience.The Impact of Measuring Patient-Reported Outcome Measures on Quality of and Access to Palliative Care.The Impact of Measuring Patient-Reported Outcome Measures on Quality of and Access to Palliative Care.Reliability testing of the FAMCARE-2 scale: measuring family carer satisfaction with palliative care.
P2860
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P2860
Is it feasible and desirable to collect voluntarily quality and outcome data nationally in palliative oncology care?
description
2008 nî lūn-bûn
@nan
2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Is it feasible and desirable t ...... y in palliative oncology care?
@ast
Is it feasible and desirable t ...... y in palliative oncology care?
@en
type
label
Is it feasible and desirable t ...... y in palliative oncology care?
@ast
Is it feasible and desirable t ...... y in palliative oncology care?
@en
prefLabel
Is it feasible and desirable t ...... y in palliative oncology care?
@ast
Is it feasible and desirable t ...... y in palliative oncology care?
@en
P2093
P356
P1476
Is it feasible and desirable t ...... y in palliative oncology care?
@en
P2093
Dave Fildes
Kathy Eagar
Linda J Kristjanson
Samar Aoun
P304
P356
10.1200/JCO.2008.16.5761
P407
P577
2008-08-01T00:00:00Z