Defining the patient population: one of the problems for palliative care research.
about
Physical activity in advanced cancer patients: a systematic review protocolSelection bias in family reports on end of life with dementia in nursing homesIssues using linkage of hospital records and death certificate data to determine the size of a potential palliative care populationHospitalisations at the end of life: using a sentinel surveillance network to study hospital use and associated patient, disease and healthcare factors.Nationwide monitoring of end-of-life care via the Sentinel Network of General Practitioners in Belgium: the research protocol of the SENTI-MELC study.Euthanasia and other end-of-life decisions: a mortality follow-back study in BelgiumPalliative inpatients in general hospitals: a one day observational study in Belgium.Burden on family carers and care-related financial strain at the end of life: a cross-national population-based studyGPs' recognition of death in the foreseeable future and diagnosis of a fatal condition: a national surveyPalliative care service use in four European countries: a cross-national retrospective study via representative networks of general practitioners.End-of-life care research with bereaved informal caregivers--analysis of recruitment strategy and participation rate from a multi-centre validation studyImportant treatment aims at the end of life: a nationwide study among GPs.Symptom Control Trials in Patients With Advanced Cancer: A Qualitative Study.GPs' awareness of patients' preference for place of death.Classification of pain in cancer patients--a systematic literature review.Which variables are associated with pain intensity and treatment response in advanced cancer patients?--Implications for a future classification system for cancer pain.Defining the palliative care patient: a systematic review.The European Association for Palliative Care basic dataset to describe a palliative care cancer population: Results from an international Delphi process.The Spectrum of Children's Palliative Care Needs: a classification framework for children with life-limiting or life-threatening conditions.What is the incidence of patients with palliative care needs presenting to the Emergency Department? a critical review.Conceptualising psychological distress in families in palliative care: Findings from a systematic review.Access to palliative care services in hospital: a matter of being in the right hospital. Hospital charts study in a Canadian city.Crossing over: transforming palliative care nursing services for the 21st century.Hospitalisations at the end of life in four European countries: a population-based study via epidemiological surveillance networks.Quality of care of older people living with advanced dementia in the community in Israel.
P2860
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P2860
Defining the patient population: one of the problems for palliative care research.
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
Defining the patient population: one of the problems for palliative care research.
@en
type
label
Defining the patient population: one of the problems for palliative care research.
@en
prefLabel
Defining the patient population: one of the problems for palliative care research.
@en
P2093
P2860
P1433
P1476
Defining the patient population: one of the problems for palliative care research.
@en
P2093
Anneke L Francke
Dick L Willems
Gerrit van der Wal
Jacques T M van Eijk
Sander D Borgsteede
Wim A B Stalman
P2860
P356
10.1191/0269216306PM1112OA
P577
2006-03-01T00:00:00Z