RE-CODE DCM (REsearch Objectives and Common Data Elements for Degenerative Cervical Myelopathy): A Consensus Process to Improve Research Efficiency in DCM, Through Establishment of a Standardized Dataset for Clinical Research and the Definition of the Research Priorities

Author:

Davies Benjamin M.1,Khan Danyal Z.1,Mowforth Oliver D.1,McNair Angus G. K.2,Gronlund Toto3,Kolias Angelos G.1,Tetreault Lindsay4,Starkey Michelle L.1,Sadler Iwan5,Sarewitz Ellen6,Houlton Delphine5,Carter Julia5,Kalsi-Ryan Sukhvinder7,Aarabi Bizhan8,Kwon Brian K.9,Kurpad Shekar N.10,Harrop James11,Wilson Jefferson R.12,Grossman Robert13,Curt Armin14,Fehlings Michael G.4,Kotter Mark R. N.115

Affiliation:

1. Academic Neurosurgery Unit, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK

2. University of Bristol, Bristol, UK

3. James Lind Alliance, National Institute for Health Research, Southampton, UK

4. Toronto Western Hospital, University Health Network, University of Toronto, Toronto, Ontario, Canada

5. Myelopathy.org, Cambridge, UK

6. Goffin Consultancy, Kent, UK

7. Toronto Rehabilitation Institute-LC, University Health Network, Toronto, Ontario, Canada

8. University of Maryland, Baltimore, MD, USA

9. Vancouver General Hospital, University of British Columbia, Vancouver, British Columbia, Canada

10. Medical College of Wisconsin, Milwaukee, WI, USA

11. Thomas Jefferson University Hospital, Philadelphia, PA, USA

12. University of Toronto, Toronto, Ontario, Canada

13. Houston Methodist Hospital, Houston, TX, USA

14. Balgrist University Hospital, Zurich, Switzerland

15. Wellcome Trust & MRC Cambridge Stem Cell Institute, Cambridge, UK

Abstract

Study Design: Mixed-method consensus process. Objectives: Degenerative cervical myelopathy (DCM) is a common and disabling condition that arises when mechanical stress damages the spinal cord as a result of degenerative changes in the surrounding spinal structures. RECODE-DCM ( REsearch Objectives and Common Data Elements for Degenerative Cervical Myelopathy) aims to improve efficient use of health care resources within the field of DCM by using a multi-stakeholder partnership to define the DCM research priorities, to develop a minimum dataset for DCM clinical studies, and confirm a definition of DCM. Methods: This requires a multi-stakeholder partnership and multiple parallel consensus development processes. It will be conducted via 4 phases, adhering to the guidance set out by the COMET (Core Outcomes in Effectiveness Trials) and JLA (James Lind Alliance) initiatives. Phase 1 will consist of preliminary work to inform online Delphi processes (Phase 2) and a consensus meeting (Phase 3). Following the findings of the consensus meeting, a synthesis of relevant measurement instruments will be compiled and assessed as per the COSMIN (Consensus-based Standards for the Selection of Health Measurement Instruments) criteria, to allow recommendations to be made on how to measure agreed data points. Phase 4 will monitor and promote the use of eventual recommendations. Conclusions: RECODE-DCM sets out to establish for the first time an index term, minimum dataset, and research priorities together. Our aim is to reduce waste of health care resources in the future by using patient priorities to inform the scope of future DCM research activities. The consistent use of a standard dataset in DCM clinical studies, audit, and clinical surveillance will facilitate pooled analysis of future data and, ultimately, a deeper understanding of DCM.

Publisher

SAGE Publications

Subject

Neurology (clinical),Orthopedics and Sports Medicine,Surgery

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