Development of a harmonised core outcome set for more personalised care of patients with diabetes: results of a multi-country Delphi study
- Porth, Ann-Kristin1
- Huberts, Anouk S.2
- Rogge, Alizé3
- Bénard, Angèle H.M.4
- Forbes, Angus5
- Strootker, Anja6
- Hurtado Del Pozo, Carmen7
- Kownatka, Dagmar8
- Hopkins, David9
- Nathanson, David10
- Soderberg, Jeanette7
- Eeg-Olofsson, Katarina11
- Hamilton, Kathryn5
- Delbecque, Laure12
- Ninov, Lyudmil13
- Due-Christensen, Mette5
- Leutner, Michael1
- Vikstrom-Greve, Sara10
- Rössner, Sophia10
- Seidler, Yuki14
- Hasler, Yvonne6
- Stamm, Tanja14
- Kautzky-Willer, Alexandra1
- 1. Divison of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University Vienna, Austria
- 2. Department of Quality and patientcare, Erasmus Medical Center, Rotterdam, Netherlands
- 3. Health Outcomes Research, Department of Psychosomatic Medicine, Center for Internal Medicine and Dermatology, Charité - Universitätsmedizin Berlin, Germany
- 4. Department of Information Systems and Decision Support, Vall d'Hebron Institute of Research (VHIR), Vall d'Hebron Barcelona Hospital Campus, Spain
- 5. Florence Nightingale Faculty of Nursing and Midwifery, Kings College London, UK
- 6. Medtronic International Trading Sàrl, Tolochenaz, Switzerland
- 7. JDRF International, New York, NY, USA
- 8. F. Hoffmann-La Roche Ltd, Basel, Switzerland
- 9. Department of Diabetes, King's College London, UK
- 10. Department of Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Sweden
- 11. Department of Molecular and Clinical Medicine, Institute of Medicine, University of Gothenburg, Sweden
- 12. Eli Lilly and Company, Indianapolis, IN, USA
- 13. European Patients' Forum (EPF), Brussels, Belgium
- 14. Section for Outcomes Research, Center for Medical Statistics, Informatics and Intelligent Systems, Medical University of Vienna, Austria
Description
Collecting patient-reported outcomes (PROs) in a standardised way and integrating them with clinical data can empower patients and support diabetes care. We sought to develop a patient-centred core outcome set (COS) to be used in routine diabetes care employing an international multi-stakeholder consensus process focusing on outcome relevance, feasibility and measurement frequency.
The three-round Delphi study and subsequent consensus meeting led to a comprehensive outcome set and recommendations for frequency of measurement for each included outcome.
The outcome set allows for collecting patient-reported and clinical data in a standardised way to sustainably support diabetes management on the international level and inform research and policy making.
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Additional details
References
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