234 results on '"Elliott, Meghan J."'
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2. Integrating the patient voice: patient-centred and equitable clinical risk prediction for kidney health and disease
3. Storytelling for impact: the creation of a storytelling program for patient partners in research
4. “You need a team”: perspectives on interdisciplinary symptom management using patient-reported outcome measures in hemodialysis care—a qualitative study
5. The effect of goal-directed fluid therapy on delayed graft function in kidney transplant recipients: A systematic review and meta-analysis
6. Nephroprotective Effects of Cilastatin in People at Risk of Acute Kidney Injury: A Systematic Review and Meta-analysis
7. Sex differences in COVID-19 symptoms and outcomes in people with kidney failure treated with dialysis: a prospective cohort study
8. Impaired Renal Function and Major Cardiovascular Events in Young Adults
9. Healthcare provider perspectives on integrating peer support in non-dialysis-dependent chronic kidney disease care: a mixed methods study
10. Deciding to Attend the Emergency Department: Experiences of Patients With Inflammatory Arthritis.
11. Emergency Department Use Among Adults Receiving Dialysis
12. Patient preferences and priorities for the design of an acute kidney injury prevention trial: Findings from a consensus workshop
13. Description of a Multi-faceted COVID-19 Pandemic Physician Workforce Plan at a Multi-site Academic Health System
14. Exploring the prospective acceptability of a healthy food incentive program from the perspective of people with type 2 diabetes and experiences of household food insecurity in Alberta, Canada
15. Online clinical pathway for chronic kidney disease management in primary care: a retrospective cohort study
16. A Web-Based Self-Management Support Prototype for Adults With Chronic Kidney Disease (My Kidneys My Health): Co-Design and Usability Testing
17. A cluster randomized controlled trial for the Evaluation of routinely Measured PATient reported outcomes in HemodialYsis care (EMPATHY): a study protocol
18. Priorities for peer support delivery among adults living with chronic kidney disease: a patient-oriented consensus workshop
19. Associations between modest reductions in kidney function and adverse outcomes in young adults: retrospective, population based cohort study
20. Alignment Among Patient, Caregiver, and Health Care Provider Perspectives on Hemodialysis Vascular Access Decision-Making: A Qualitative Study.
21. The dynamic nature of patient engagement within a Canadian patient‐oriented kidney health research network: Perspectives of researchers and patient partners
22. Patient and Clinician Perspectives on Shared Decision Making in Vascular Access Selection: A Qualitative Study
23. Progression of Chronic Kidney Disease
24. A Qualitative Content Analysis of Comments on Press Articles on Deemed Consent for Organ Donation in Canada
25. Sex differences in COVID-19 symptoms and outcomes in people with kidney failure treated with dialysis: a prospective cohort study
26. Moving patient-oriented research forward: thoughts from the next generation of knowledge translation researchers
27. An eHealth self-management intervention for adults with chronic kidney disease, My Kidneys My Health: a mixed-methods study
28. ‘It’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study
29. Additional file 6 of Healthcare provider perspectives on integrating peer support in non-dialysis-dependent chronic kidney disease care: a mixed methods study
30. sj-docx-1-cjk-10.1177_20543581221139025 – Supplemental material for The Diagnostic Journey of Childhood Idiopathic Nephrotic Syndrome: Perspectives of Children and Their Caregivers
31. Additional file 2 of Healthcare provider perspectives on integrating peer support in non-dialysis-dependent chronic kidney disease care: a mixed methods study
32. Additional file 4 of Healthcare provider perspectives on integrating peer support in non-dialysis-dependent chronic kidney disease care: a mixed methods study
33. Additional file 3 of Healthcare provider perspectives on integrating peer support in non-dialysis-dependent chronic kidney disease care: a mixed methods study
34. Additional file 1 of Healthcare provider perspectives on integrating peer support in non-dialysis-dependent chronic kidney disease care: a mixed methods study
35. The Diagnostic Journey of Childhood Idiopathic Nephrotic Syndrome: Perspectives of Children and Their Caregivers
36. Training clinicians in a problem‐solving fatigue programme for patients receiving maintenance haemodialysis.
37. Accounting for Age in the Definition of Chronic Kidney Disease
38. Training clinicians in a problem‐solving fatigue programme for patients receiving maintenance haemodialysis
39. sj-docx-1-cjk-10.1177_20543581211055001 ��� Supplemental material for Mainstreaming Genetic Testing for Adult Patients With Autosomal Dominant Polycystic Kidney Disease
40. sj-docx-2-cjk-10.1177_20543581211055001 ��� Supplemental material for Mainstreaming Genetic Testing for Adult Patients With Autosomal Dominant Polycystic Kidney Disease
41. sj-pdf-1-cjk-10.1177_20543581211004803 – Supplemental material for Defining the Scope of Knowledge Translation Within a National, Patient-Oriented Kidney Research Network
42. sj-docx-1-cjk-10.1177_20543581211063984 ��� Supplemental material for Evaluation of the Cost of a High-Dose Intravenous Iron Protocol in a Regional Hemodialysis Program: Research Letter
43. Additional file 1 of Online clinical pathway for chronic kidney disease management in primary care: a retrospective cohort study
44. Albuminuria, proteinuria, and dipsticks: novel relationships and utility in risk prediction
45. CJKHD_Supplemental_Material_-_Appendix_1-3_Revised_Clean_Copy_-_June_29_2020_1 – Supplemental material for Derivation and Internal Validation of a Clinical Risk Prediction Tool for Hyperkalemia-Related Emergency Department Encounters Among Hemodialysis Patients
46. Warfarin Anticoagulation in Hemodialysis Patients: A Systematic Review of Bleeding Rates
47. The Association Between Estimated Glomerular Filtration Rate and Hospitalization for Fatigue: A Population-Based Cohort Study
48. Mainstreaming Genetic Testing for Adult Patients With Autosomal Dominant Polycystic Kidney Disease
49. Defining the Scope of Knowledge Translation Within a National, Patient-Oriented Kidney Research Network
50. Evaluation of the Cost of a High-Dose Intravenous Iron Protocol in a Regional Hemodialysis Program: Research Letter
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