Barriers to the use of health status measures in clinical investigation, patient care, and policy research.
about
Measuring health-related quality of life in patients with chronic obstructive pulmonary disease in a routine hospital setting: feasibility and perceived valueA Wireless Health Outcomes Monitoring System (WHOMS): development and field testing with cancer patients using mobile phonesBrief assessment of priority symptoms in hormone refractory prostate cancer: the FACT Advanced Prostate Symptom Index (FAPSI)Role of health-related quality of life measures in the routine care of people with multiple sclerosisClinician adherence to a standardized assessment battery across settings and disciplines in a poststroke rehabilitation populationUsability of a computer-assisted interview system for the unaided self-entry of patient data in an urban rheumatology clinic.Satisfaction of hospitalized psychiatry patients: why should clinicians care?Evidence for validity of a health status measure in assessing short term outcomes of cholecystectomy.Health-related quality of life and hearing aids: a tutorial.Determinants of reduced health-related quality of life in pediatric inherited neuropathies.WHO's ICF and functional status information in health records.Predicting mortality and healthcare utilization with a single question.Health-related quality of life in children with hemifacial microsomia: parent and child perspectives.Validation of a computer-adaptive test to evaluate generic health-related quality of life.The linkage between pediatric quality of life and health conditions: establishing clinically meaningful cutoff scores for the PedsQLEffectiveness of a measurement feedback system on outcome in rheumatoid arthritis: a controlled clinical trial.Direct improvement of quality of life using a tailored quality of life diagnosis and therapy pathway: randomised trial in 200 women with breast cancerThe use of patient-reported outcomes becomes standard practice in the routine clinical care of lung-heart transplant patientsCancer clinical outcomes for minority ethnic groups.Logistic feasibility of health related quality of life measurement in clinical practice: results of a prospective study in a large population of chronic liver patientsComputer-based quality of life questionnaires may contribute to doctor-patient interactions in oncology.Is there value in routine administration of outcome questionnaires?Reporting on quality of life in RCTs. CONSORT guidelines should be expanded.Quality of life: what does it mean for general practice?Importance of sensitivity to change as a criterion for selecting health status measures.Development and validation of 11 symptom indexes to evaluate response to chemotherapy for advanced cancer.Patient-reported outcome measurements in clinical routine of trauma, spine and craniomaxillofacial surgeons: between expectations and reality: a survey among 1212 surgeons.
P2860
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P2860
Barriers to the use of health status measures in clinical investigation, patient care, and policy research.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Barriers to the use of health ...... ent care, and policy research.
@en
type
label
Barriers to the use of health ...... ent care, and policy research.
@en
prefLabel
Barriers to the use of health ...... ent care, and policy research.
@en
P1433
P1476
Barriers to the use of health ...... ent care, and policy research.
@en
P2093
P304
P433
P577
1989-03-01T00:00:00Z