Abstract
Application of continuous glucose monitoring (CGM) has moved diabetes care from a reactive to a proactive process, in which a person with diabetes can prevent episodes of hypoglycemia or hyperglycemia, rather than taking action only once low and high glucose are detected. Consequently, CGM devices are now seen as the standard of care for people with type 1 diabetes mellitus (T1DM). Evidence now supports the use of CGM in people with type 2 diabetes mellitus (T2DM) on any treatment regimen, not just for those on insulin therapy. Expanding the application of CGM to include all people with T1DM or T2DM can support effective intensification of therapies to reduce glucose exposure and lower the risk of complications and hospital admissions, which are associated with high healthcare costs. All of this can be achieved while minimizing the risk of hypoglycemia and improving quality of life for people with diabetes. Wider application of CGM can also bring considerable benefits for women with diabetes during pregnancy and their children, as well as providing support for acute care of hospital inpatients who experience the adverse effects of hyperglycemia following admission and surgical procedures, as a consequence of treatment-related insulin resistance or reduced insulin secretion. By tailoring the application of CGM for daily or intermittent use, depending on the patient profile and their needs, one can ensure the cost-effectiveness of CGM in each setting. In this article we discuss the evidence-based benefits of expanding the use of CGM technology to include all people with diabetes, along with a diverse population of people with non-diabetic glycemic dysregulation.
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; Czupryniak, Leszek 2 ; Dzida, Grzegorz 3 ; Fichna, Piotr 4 ; Jarosz-Chobot, Przemyslawa 5 ; Gumprecht, Janusz 6 ; Mysliwiec, Malgorzata 7 ; Szadkowska, Agnieszka 8 ; Bomba-Opon, Dorota 9 ; Czajkowski, Krzysztof 10 ; Malecki, Maciej T. 1 ; Zozulinska-Ziolkiewicz, Dorota A. 11 1 Jagiellonian University Medical College, Department of Metabolic Diseases, Krakow, Poland (GRID:grid.5522.0) (ISNI:0000 0001 2162 9631)
2 Medical University of Warsaw, Department of Diabetology and Internal Medicine, Warsaw, Poland (GRID:grid.13339.3b) (ISNI:0000000113287408)
3 Medical University of Lublin, Department of Internal Diseases, Lublin, Poland (GRID:grid.411484.c) (ISNI:0000 0001 1033 7158)
4 Poznan University of Medical Sciences, Department of Pediatric Diabetes and Obesity, Poznan, Poland (GRID:grid.22254.33) (ISNI:0000 0001 2205 0971)
5 Medical University of Silesia, Department of Children’s Diabetology, Katowice, Poland (GRID:grid.411728.9) (ISNI:0000 0001 2198 0923)
6 Medical University of Silesia, Department of Internal Medicine, Diabetology and Nephrology, Katowice, Poland (GRID:grid.411728.9) (ISNI:0000 0001 2198 0923)
7 Medical University of Gdansk, Department of Pediatrics, Diabetology and Endocrinology, Gdansk, Poland (GRID:grid.11451.30) (ISNI:0000 0001 0531 3426)
8 Medical University of Lodz, Department of Pediatrics, Diabetology, Endocrinology and Nephrology, Lodz, Poland (GRID:grid.8267.b) (ISNI:0000 0001 2165 3025)
9 Medical University of Warsaw, 1st Department of Obstetrics and Gynecology, Warsaw, Poland (GRID:grid.13339.3b) (ISNI:0000000113287408)
10 Medical University of Warsaw, 2nd Department of Obstetrics and Gynecology, Warsaw, Poland (GRID:grid.13339.3b) (ISNI:0000000113287408)
11 Poznan University of Medical Science, Department of Internal Medicine and Diabetology, Poznan, Poland (GRID:grid.22254.33) (ISNI:0000 0001 2205 0971)





