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Published Online: 24 August 2022

Reduced Rate of Acute Diabetes Events with Flash Glucose Monitoring Is Sustained for 2 Years After Initiation: Extended Outcomes from the RELIEF Study

Publication: Diabetes Technology & Therapeutics
Volume 24, Issue Number 9

Abstract

Background: The RELIEF study has previously shown a fall in the rate of acute diabetes events (ADEs) in people living with type 1 diabetes (PwDT1) or people living with type 2 diabetes (PwDT2) in the 12 months after initiation of flash glucose monitoring (FLASH) in France. The 2-year follow-up has provided new insights on the frequency of ADEs, including severe hypoglycemia and diabetic ketoacidosis (DKA), during use of FLASH.
Methods: The RELIEF study included 31,446 PwDT1 and 41,027 PwDT2 with a first delivery of FreeStyle Libre (FSL) between August 1 and December 31, 2017. Hospitalizations for DKA, severe hypoglycemia, diabetes-related coma, and hyperglycemia were recorded for the 12 months before and 24 months after FSL initiation. Persistence of the FSL system use was estimated through a Kaplan–Meier survival curve. Change in usual blood glucose monitoring was estimated through acquisition of blood glucose test strips.
Results: In the 2 years after FSL initiation, hospitalizations for ADEs were reduced by 49% and by 48% in PwDT1 or PwDT2, respectively, driven by reductions in DKA. After 2 years, 88% of patients persisted with the system and estimated mean consumption of blood glucose test strips had fallen after 2 years by −82% and by −84% in type 1 diabetes mellitus and type 2 diabetes mellitus, respectively.
Conclusion: Use of FSL consistently reduces the rates of hospitalization for ADEs, mainly DKA, 2 years after initiation, confirming this is not a transitory effect. Use of FSL also results in a clear and progressive drop in use of blood glucose test strips over the 2-year period.

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Published In

cover image Diabetes Technology & Therapeutics
Diabetes Technology & Therapeutics
Volume 24Issue Number 9September 2022
Pages: 611 - 618
PubMed: 35604792

History

Published in print: September 2022
Published online: 24 August 2022
Published ahead of print: 11 July 2022
Published ahead of production: 23 May 2022

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Authors

Affiliations

Jean-Pierre Riveline [email protected]
Institut Necker Enfants Malades (INEM), INSERM U1151, CNRS UMR 8253, Université de Paris Cité, IMMEDIAB Laboratory, Paris, France.
Service of Diabetology, Endocrinology and Nutrition, Lariboisière Hospital, Féderation de Diabétologie, Assistance Publique - Hôpitaux de Paris, Paris, France.
Department of Diabetology and Endocrinology, Lariboisière Hospital, Paris, France.
Ronan Roussel
Institut Necker Enfants Malades (INEM), INSERM U1151, CNRS UMR 8253, Université de Paris Cité, IMMEDIAB Laboratory, Paris, France.
Department of Diabetology and Endocrinology, Lariboisière Hospital, Paris, France.
Department of Diabetology, Endocrinology, and Nutrition, Bichat-Claude Bernard Hospital, Paris, France.
Eric Vicaut
Clinical Research Unit, Fernand Vidal Hospital, Paris, France.
Gérard de Pouvourville
Department of Economics, ESSEC Business School, Cergy-Pontoise, France.
CEMKA, Bourg-la-Reine, France.
Corinne Emery
CEMKA, Bourg-la-Reine, France.
Fleur Levrat-Guillen
Abbott Laboratories, Maidenhead, Berkshire, United Kingdom.
Bruno Guerci
Department of Endocrinology, Diabetology, and Nutrition, Brabois Adult Hospital, University of Lorraine, Vandoeuvre-lès-Nancy, France.

Notes

We dedicate this study to our colleague Professor Ronan Roussel, who sadly passed away on January 29, 2022, before the publication of this article.
Address correspondence to: Jean-Pierre Riveline, MD, PhD, Service de Diabétologie, Endocrinologie, Nutrition, Centre Universitaire du Diabète et de ses Complications, Hôpital Lariboisière, 2, rue Ambroise Paré, 75475 Paris France 10 [email protected]

Authors' Contributions

J-P.R. is the guarantor of this study and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. R.R., E.V., G.d.P., F.L.G., and B.G. contributed to methodology, analyses, and article writing. B.D. and C.E. contributed to methodology, conducted statistical analyses, and contributed to article writing. Editorial assistance in the preparation of this article was provided by Dr Robert Brines of Bite Medical Consulting.

Author Disclosure Statement

J-P.R. is an advisory panel member for Sanofi, MSD, Eli Lilly, Novo Nordisk, AstraZeneca, Abbott, Dexcom, Alphadiab, and Medtronic, and has received research funding and provided research support to Abbott, Air liquide, Sanofi, and Novo Nordisk. R.R. is an advisory panel member for Abbott, Astra-Zeneca, Sanofi, MSD, Eli Lilly, Boehringer-Ingelheim, and Novo Nordisk, and has received research funding and provided research support to Diabnext, Sanofi, and Novo Nordisk; all honoraria were donated to the Foundation APHP for research. G.d.P. is health economist and an advisory board member for the following companies: Abbott, Amgen, Astra-Zeneca, Bayer, BMS, Boerhinger-Ingelheim, Janssen, MSD, Novartis, Novo Nordisk, Roche, and Sanofi. He has received research funding from Amgen, BMS, Boerhinger-Ingelheim, MSD, Novartis, Roche, and Sanofi. He has received honoraria for his participation to the RELIEF study advisory board. E.V. is consultant specializing in the methodology and statistical analysis of clinical trials for Abbott, Bristol-Myers Squibb, Celgene, Edwards, Novartis, Pfizer, and Sanofi. He has received honoraria for his participation. B.D. and C.E. are employees of CEMKA, a French Heathcare CRO. B.D has also received advisory board and lecture fees from Sanofi, MSD, Eli Lilly, Novo Nordisk, Pfizer, and Janssen. F.L-G. is employed by Abbott Diabetes Care. B.G. is an advisory board member for Sanofi, Eli Lilly, Novo Nordisk, Novartis, GSK, MSD, Boehringer Ingelheim, AstraZeneca, Abbott, Medtronic, and Roche Diagnostics. He is a clinical investigator for Sanofi, Eli Lilly, Novo Nordisk, GSK, BMS, AstraZeneca, Medtronic, Abbott, Roche Diagnostics, MSD, Novartis, Janssen, and Boehringer Ingelheim. He receives research support from Medtronic, Vitalaire, Sanofi, Eli Lilly, and Novo Nordisk.

Funding Information

The authors acknowledge funding support from Abbott Diabetes Care. The funding did not affect the collection, analysis, or presentation of the data.

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