136 results on '"Nelson, Eugene C."'
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2. Women’s experiences of maternity care in the United Kingdom during the COVID-19 pandemic: A follow-up systematic review and qualitative evidence synthesis
3. Better Patient and Population Outcome
4. ConnectShareCare builds connections among care partners of people with serious illness
5. ConnectShareCare builds connections among care partners of people with serious illness
6. A Web-Based Peer Support Network to Help Care Partners of People With Serious Illness: Co-Design Study (Preprint)
7. Harnessing the Collective Expertise of Patients, Care Partners, Clinical Teams, and Researchers Through a Coproduction Learning Health System
8. Enhancing Care Partnerships Using a Rheumatology Dashboard: Bringing Together What Matters Most to Both Patients and Clinicians
9. The Cystic Fibrosis Learning Network: A mixed methods evaluation of program goals, attributes, and impact
10. Patient-Reported Outcome Dashboards Within the Electronic Health Record to Support Shared Decision-making: Protocol for Co-design and Clinical Evaluation With Patients With Advanced Cancer and Chronic Kidney Disease
11. Utilization Patterns and Outcomes of People With Diabetes and COVID-19: Evidence From United States Medicare Beneficiaries in 2020
12. Eliciting patients’ healthcare goals and concerns: Do questions influence responses?
13. Impact of the COVID-19 pandemic: How our response is shaping the future of cystic fibrosis care
14. A ‘COVID Compass’ for navigating the pandemic
15. Policy, accreditation and leadership: creating the conditions for effective coproduction of health, healthcare and science
16. Point-of-care dashboards promote coproduction of healthcare services for patients with inflammatory bowel disease
17. International, national and local trends in the spread of COVID-19: a geographic view of COVID-19 spread and the role to be played by coproduction
18. Development of Balanced Whole System Value Measures for Inflammatory Bowel Disease Care in the IBD Qorus Collaborative Using a Modified Delphi Process
19. COproduction VALUE creation in healthcare service (CO-VALUE): an international multicentre protocol to describe the application of a model of value creation for use in systems of coproduced healthcare services and to evaluate the initial feasibility, utility and acceptability of associated system-level value creation assessment approaches
20. Formative evaluation of a dashboard to support coproduction of healthcare services in cystic fibrosis
21. Using Electronic Health Record Portals to Improve Patient Engagement: Research Priorities and Best Practices
22. A qualitative study of design stakeholders’ views of developing and implementing a registry-based learning health system
23. No date for the PROM: the association between patient-reported health events and clinical coding in primary care
24. Chronic Condition Measurement Requires Engagement, Not Measurement Alone
25. Turning Feed-forward and Feedback Processes on Patient-reported Data into Intelligent Action and Informed Decision-making
26. How social business innovates health care: two cases of social value creation leading to high-quality services
27. Design and Implementation of a Novel Electronic Health Record Tool to Enhance the Care of Individuals with Cystic Fibrosis: The Cystic Fibrosis Note Template
28. A Person-Centered, Registry-Based Learning Health System for Palliative Care: A Path to Coproducing Better Outcomes, Experience, Value, and Science
29. Evidence on the Validity of a Comprehensive Health Risk Index and Implications for Ambulatory Care and Population Health Management
30. Domains associated with successful quality improvement in healthcare – a nationwide case study
31. Using patient-reported outcome measurement to improve patient care
32. Fostering Collaboration Through Creation of an IBD Learning Health System
33. A14 Health care delivery in Enroll-HD and ehdn’s registry sites: an international survey
34. Measuring Adverse Events in Hospitalized Patients: An Administrative Method for Measuring Harm
35. Health Care Delivery Practices in Huntington’s Disease Specialty Clinics: An International Survey
36. Patient focused registries can improve health, care, and science
37. Validation of a new predictive risk model: measuring the impact of the major modifiable risks of death for patients and populations
38. Development and Validation of the CPO Scale, a New Instrument for Evaluation of Health Care Improvement Efforts
39. Using Patient-Reported Outcomes in Routine Practice
40. Patient reported outcome measures in practice
41. Mollie's Story
42. The SPORT Value Compass
43. Von Klinischen MikroSystemen lernen: Aufbau und Bedeutung einer ergiebigen Informationsumgebung
44. Highly Effective Cystic Fibrosis Clinical Research Teams: Critical Success Factors
45. Self-Care
46. Developing a Pathway for High-value, Patient-centered Total Joint Arthroplasty
47. Accelerating implementation of biomedical research advances: critical elements of a successful 10 year Cystic Fibrosis Foundation healthcare delivery improvement initiative
48. Coaching interprofessional health care improvement teams: the coachee, the coach and the leader perspectives
49. Validation of a new predictive risk model: measuring the impact of major modifiable risks of death for patients and populations
50. Validation of a new predictive risk model for mortality using Framingham Heart Study data
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