Page 135 - Glucose Monitoring Devices
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136    CHAPTER 7 Clinical impact of CGM use




                            The turn of the 21st century saw the first clinically approved continuous glucose
                         monitoring (CGM) device using a subcutaneously sited sensor to measure changes
                         in interstitial fluid glucose concentrations. Glucose levels are derived from propor-
                         tionally produced electric currents and are automatically measured and accessible to
                         users at 5-min intervals. The evolution of CGM over the last decade has seen devices
                         become smaller with fewer required calibrations and longer sensor change intervals.
                         The addition of mobile Bluetooth technology has also allowed wireless data transfer
                         and integration of smartphone technology to display results on purpose-designed
                         applications. This chapter will address the current and future benefits, limitations,
                         and clinical applications of CGM technology.



                         Parameters of glucose control and risk association
                         HbA1c
                         The association between prolonged exposure to hyperglycemia and increased risk of
                         diabetes-associated micro- and macrovascular is well documented [1e4]. Signifi-
                         cant outcomes include the fourfold increased risk of coronary heart disease [5]
                         and cardiovascular disease being responsible for a quarter of diabetes deaths [6].
                         The Diabetes Control and Complications Trial (DCCT) and the United Kingdom
                         Prospective Diabetes Study revealed a reduced risk of microvascular complications
                         in participants with type 1 (T1DM) and type 2 (T2DM) diabetes following intensive
                         glycemic control, respectively [1,2]. These benefits extended long beyond the dura-
                         tion of the trial “legacy effect” with lower rates of microvascular disease persisting
                         despite HbA1c rebounding to levels seen in the standard care groups [7e10].
                         Furthermore, the curvilinear relationship between HbA1c and vascular risk suggests
                         that the greatest risk reduction is achieved when glycemic control is successfully
                         improved from hyper- to normoglycemia with minimal benefit to be gained from
                         further glucose reduction [3,11]. HbA1c levels above 6%e7% have been shown
                         to significantly increase microvascular and cardiovascular risk in diabetes popula-
                         tions. However, many trials including ACCORD and VADT have failed to identify
                         significant cardiovascular risk reduction with intensive glucose control and, in fact,
                         highlight the importance of balancing glucose reduction with the increased risk of
                         hypoglycemia.


                         Hypoglycemia
                         Despite pharmaceutical advances in the preparation and delivery of insulin
                         replacement, hypoglycemia remains a common complication among insulin-
                         requiring individuals with diabetes. Errors in mismatching insulin dose to ingested
                         carbohydrates and the nonphysiological pharmacokinetics and pharmacodynamics
                         of exogenous insulin are among various factors responsible for iatrogenic hypogly-
                         cemia. As established in the DCCT, hypoglycemia risk is further increased in
                         attempts to diminish vascular risk by implementing intensive insulin therapy.
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