Collecting data on patient experience is not enough: they must be used to improve care.
about
A short generic patient experience questionnaire: howRwe development and validationFactors that shape the patient's hospital experience and satisfaction with lower limb arthroplasty: an exploratory thematic analysisWhat does the literature tell us about health workers' experiences of task-shifting projects in sub-Saharan Africa? A systematic, qualitative reviewPatient involvement in clinical research: why, when, and howCapturing patients' experiences to change Parkinson's disease care delivery: a multicenter studyAn Association of Cancer Physicians' strategy for improving services and outcomes for cancer patientsStandardized Outcome Measurement for Patients With Coronary Artery Disease: Consensus From the International Consortium for Health Outcomes Measurement (ICHOM)The use of patient experience survey data by out-of-hours primary care services: a qualitative interview study.Systematic review of approaches to using patient experience data for quality improvement in healthcare settings.Doctors' engagements with patient experience surveys in primary and secondary care: a qualitative study.Patients' use and views of real-time feedback technology in general practice.Improving the quality of mental health services using patient outcome data: making the most of HoNOSShould health care providers be accountable for patients' care experiences?Patient and professional user experiences of simple telehealth for hypertension, medication reminders and smoking cessation: a service evaluationThe CORE study protocol: a stepped wedge cluster randomised controlled trial to test a co-design technique to optimise psychosocial recovery outcomes for people affected by mental illness in the community mental health settingPerspectives from health, social care and policy stakeholders on the value of a single self-report outcome measure across long-term conditions: a qualitative study.Patient Experience Shows Little Relationship with Hospital Quality Management StrategiesPerson-centred healthcare and medicine paradigm: it's time to clarify.Development and validation of a new patient experience tool in patients with serious illnessTaking data seriously: the value of actor-network theory in rethinking patient experience dataWhat do pharmaceutical industry professionals in Europe believe about involving patients and the public in research and development of medicines? A qualitative interview studyAchieving Research Impact Through Co-creation in Community-Based Health Services: Literature Review and Case Study"My cancer is not my deepest concern": life course disruption influencing patient pathways and health care needs among persons living with colorectal cancerElectroconvulsive Therapy - What Do Patients Think Of Their Treatment?Investigation of the degree of organisational influence on patient experience scores in acute medical admission units in all acute hospitals in England using multilevel hierarchical regression modelling.Development and Validation of an Instrument for Assessing Patient Experience of Chronic Illness Care.The Patient Feedback Response Framework - Understanding why UK hospital staff find it difficult to make improvements based on patient feedback: A qualitative study.A qualitative formative evaluation of a patient-centred patient safety intervention delivered in collaboration with hospital volunteers.From the closest observers of patient care: a thematic analysis of online narrative reviews of hospitals.Patients' expectations and solutions for improving primary diabetes care.Exploring how ward staff engage with the implementation of a patient safety intervention: a UK-based qualitative process evaluationClosing the patient experience chasm: A two-level validation of the Consumer Quality Index Inpatient Hospital Care.Integrating patients' perceptions into clinical practice guidelines for the management of rheumatoid arthritis in Japan.On the Brink of Genuinely Collaborative Care: Experience-Based Co-Design in Mental Health.The power of symbolic capital in patient and public involvement in health researchPReSaFe: A model of barriers and facilitators to patients providing feedback on experiences of safety.Associations between hospital characteristics and patient satisfaction in Germany.A Standard Set of Outcome Measures for the Comprehensive Appraisal of Cleft Care.Helping Hospitals Improve Patient Centeredness: Assessing the Impact of Feedback Following a Best Practices Workshop.Designing quality of care--contributions from parents: Parents' experiences of care processes in paediatric care and their contribution to improvements of the care process in collaboration with healthcare professionals.
P2860
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P2860
Collecting data on patient experience is not enough: they must be used to improve care.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մարտին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Collecting data on patient experience is not enough: they must be used to improve care.
@ast
Collecting data on patient experience is not enough: they must be used to improve care.
@en
type
label
Collecting data on patient experience is not enough: they must be used to improve care.
@ast
Collecting data on patient experience is not enough: they must be used to improve care.
@en
prefLabel
Collecting data on patient experience is not enough: they must be used to improve care.
@ast
Collecting data on patient experience is not enough: they must be used to improve care.
@en
P2093
P356
P1433
P1476
Collecting data on patient experience is not enough: they must be used to improve care.
@en
P2093
Joe Calabrese
Louise Locock
Sue Ziebland
P356
10.1136/BMJ.G2225
P407
P577
2014-03-26T00:00:00Z