Development of the Diabetes Technology Society Blood Glucose Monitor System Surveillance Protocol

Author:

Klonoff David C.1,Lias Courtney2,Beck Stayce2,Parkes Joan Lee3,Kovatchev Boris4,Vigersky Robert A.5,Arreaza-Rubin Guillermo6,Burk Robert D.7,Kowalski Aaron8,Little Randie9,Nichols James10,Petersen Matt11,Rawlings Kelly11,Sacks David B.6,Sampson Eric12,Scott Steve13,Seley Jane Jeffrie14,Slingerland Robbert15,Vesper Hubert W.16

Affiliation:

1. Mills-Peninsula Health Services, San Mateo, CA, USA

2. US Food and Drug Administration, Silver Spring, MD, USA

3. Joan Lee Parkes Consulting Inc, Bristol, IN, USA

4. University of Virginia, Center for Diabetes Technology, Charlottesville, VA, USA

5. Walter Reed National Military Medical Center, Bethesda, MD, USA

6. National Institutes of Health, Bethesda, MD, USA

7. Albert Einstein College of Medicine, Bronx, NY, USA

8. JDRF, New York, NY, USA

9. University of Missouri, School of Medicine, Columbia, MO, USA

10. Vanderbilt University, School of Medicine, Nashville, TN, USA

11. American Diabetes Association, Alexandria, VA, USA

12. Sampson Consulting Inc, Washington, DC

13. Abbott Diabetes Care, Alameda, CA, USA

14. New York-Presbyterian Hospital/Weill Cornell Medical College, New York, NY, USA

15. Isala, Zwolle, the Netherlands

16. Centers for Disease Control and Prevention, Atlanta, GA, USA

Abstract

Background: Inaccurate blood glucsoe monitoring systems (BGMSs) can lead to adverse health effects. The Diabetes Technology Society (DTS) Surveillance Program for cleared BGMSs is intended to protect people with diabetes from inaccurate, unreliable BGMS products that are currently on the market in the United States. The Surveillance Program will provide an independent assessment of the analytical performance of cleared BGMSs. Methods: The DTS BGMS Surveillance Program Steering Committee included experts in glucose monitoring, surveillance testing, and regulatory science. Over one year, the committee engaged in meetings and teleconferences aiming to describe how to conduct BGMS surveillance studies in a scientifically sound manner that is in compliance with good clinical practice and all relevant regulations. Results: A clinical surveillance protocol was created that contains performance targets and analytical accuracy-testing studies with marketed BGMS products conducted by qualified clinical and laboratory sites. This protocol entitled “Protocol for the Diabetes Technology Society Blood Glucose Monitor System Surveillance Program” is attached as supplementary material. Conclusion: This program is needed because currently once a BGMS product has been cleared for use by the FDA, no systematic postmarket Surveillance Program exists that can monitor analytical performance and detect potential problems. This protocol will allow identification of inaccurate and unreliable BGMSs currently available on the US market. The DTS Surveillance Program will provide BGMS manufacturers a benchmark to understand the postmarket analytical performance of their products. Furthermore, patients, health care professionals, payers, and regulatory agencies will be able to use the results of the study to make informed decisions to, respectively, select, prescribe, finance, and regulate BGMSs on the market.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Bioengineering,Endocrinology, Diabetes and Metabolism,Internal Medicine

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