4.4 Article

Gathering Global Perspectives to Establish the Research Priorities and Minimum Data Sets for Degenerative Cervical Myelopathy: Sampling Strategy of the First Round Consensus Surveys of AO Spine RECODE-DCM

Journal

GLOBAL SPINE JOURNAL
Volume 12, Issue 1_SUPPL, Pages 8S-18S

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/21925682211047546

Keywords

spinal cord diseases; cervical vertebrae; spondylosis; spinal osteophytosis; surveys and questionnaires

Funding

  1. AO Spine through the AO Spine Knowledge Forum Spinal Cord Injury
  2. AO Spine Research Department
  3. National Institute for Health Research (NIHR) Clinician Scientists Fellowship award [NIHR CS-2017-17-010]
  4. NIHR Biomedical Research Centre (BRC) at University Hospitals Bristol
  5. Weston NHS Foundation Trust
  6. University of Bristol [BRC-1215-20011]
  7. National Institute for Health Research (NIHR) Brain Injury MedTech Cooperative based at Cambridge University Hospitals NHS Foundation Trust
  8. University of Cambridge
  9. BMD a NIHR Clinical Doctoral Research Fellowship

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The AO Spine RECODE-DCM initiative aimed to accelerate knowledge discovery and improve outcomes by developing a consensus framework through a survey involving perspectives from spinal surgeons, healthcare professionals, and individuals with degenerative cervical myelopathy (DCM). The survey engaged a diverse group of participants from 76 countries and successfully combined priority setting and minimum dataset processes for the first time.
Study Design: Survey. Introduction: AO Spine Research Objectives and Common Data Elements for Degenerative Cervical Myelopathy (RECODEDCM) is an international initiative that aims to accelerate knowledge discovery and improve outcomes by developing a consensus framework for research. This includes defining the top research priorities, an index term and a minimum data set (core outcome set and core data elements set - core outcome set (COS)/core data elements (CDE)). Objective: To describe how perspectives were gathered and report the detailed sampling characteristics. Methods: A two-stage, electronic survey was used to gather and seek initial consensus. Perspectives were sought from spinal surgeons, other healthcare professionals and people with degenerative cervical myelopathy (DCM). Participants were allocated to one of two parallel streams: (1) priority setting or (2) minimum dataset. An email campaign was developed to advertise the survey to relevant global stakeholder individuals and organisations. People with DCM were recruited using the international DCM charity Myelopathy.org and its social media channels. A network of global partners was recruited to act as project ambassadors. Data from Google Analytics, MailChimp and Calibrum helped optimise survey dissemination. Results: Survey engagement was high amongst the three stakeholder groups: 208 people with DCM, 389 spinal surgeons and 157 other healthcare professionals. Individuals from 76 different countries participated; the United States, United Kingdom and Canada were the most common countries of participants. Conclusion: AO Spine RECODE-DCM recruited a diverse and sufficient number of participants for an international PSP and COS/CDE process. Whilst PSP and COS/CDE have been undertaken in other fields, to our knowledge, this is the first time they have been combined in one process.

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