4.7 Article

Improving the Clinical Value and Utility of CGM Systems: Issues and Recommendations: A Joint Statement of the European Association for the Study of Diabetes and the American Diabetes Association Diabetes Technology Working Group

Journal

DIABETES CARE
Volume 40, Issue 12, Pages 1614-1621

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/dci17-0043

Keywords

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Funding

  1. EASD
  2. ADA
  3. Medtronic/MiniMed Foundation
  4. Novo Nordisk
  5. Medtronic
  6. Roche Diagnostics
  7. Boehringer Ingelheim
  8. Eli Lilly

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The first systems for continuous glucose monitoring (CGM) became available over 15 years ago. Many then believed CGM would revolutionize the use of intensive insulin therapy in diabetes; however, progress toward that vision has been gradual. Although increasing, the proportion of individuals using CGM rather than conventional systems for self-monitoring of blood glucose on a daily basis is still low in most parts of the world. Barriers to uptake include cost, measurement reliability (particularly with earlier-generation systems), human factors issues, lack of a standardized format for displaying results, and uncertainty on how best to use CGM data to make therapeutic decisions. This Scientific Statement makes recommendations for systemic improvements in clinical use and regulatory (pre- and postmarketing) handling of CGM devices. The aim is to improve safety and efficacy in order to support the advancement of the technology in achieving its potential to improve quality of life and health outcomes for more people with diabetes.

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