Current Application of Continuous Glucose Monitoring in the Treatment of Diabetes

PROS OF CGM

From the Diabetes Control and Complications Trial and the UK Prospective Diabetes Study, we learned that lowering HbA_1c reduces morbidity and mortality (11,12) and that tight glycemic control is associated with an increased rate of severe hypoglycemic episodes. We therefore should judge the pros of CGM by its HbA_1c-lowering potency and its influence on severe hypoglycemia rates. Table 1 summarizes all intervention trials that have been performed with real-time CGM regarding HbA_1c and the incidence of severe hypoglycemia.

The Juvenile Diabetes Research Foundation (JDRF) landmark study randomized 322 adults, adolescents, and children with type 1 diabetes at a baseline HbA_1c of 7.0–10.0% to CGM or self-monitoring of blood glucose (SMBG). CGM use for 26 weeks significantly reduced HbA_1c by 0.5% in adult patients (13). Although the intention-to-treat analyses did not show a significant HbA_1c reduction in children and adolescents, it was demonstrated among all age groups that there was a significant HbA_1c reduction in patients who used CGM for ≥6 days/week (14). The adolescents were the most infrequent users of CGM devices. In a follow-up study of the JDRF trial, patients initially randomized to the control group were put on CGM after the trial. Again, HbA_1c decrease was significantly associated with CGM use among all age groups (15). Previously, Deiss et al. (16) randomized type 1 diabetic patients with baseline HbA_1c of ≥8.1% to 3 months of continuous CGM use, biweekly CGM use, or intensive insulin treatment with SMBG. Continuous CGM use resulted in a significant HbA_1c reduction of 0.6% compared with conventional treatment, whereas biweekly use did not improve HbA_1c compared with conventional treatment. Thus, it seems that the frequency of CGM use is important. This is also evident from the Sensor-Augmented Pump Therapy for A1C Reduction 1 (STAR-1) trial and the RealTrend study (Table 1), in which the efficacy of CGM with CSII was investigated in CSII users and insulin pump–naive type 1 diabetic patients, respectively (17,18). Although there was no significant between-group difference in HbA_1c decrease in both studies, subanalyses showed that sensor use of at least 60–70% of the time did result in a significant HbA_1c decrease. The importance of frequency of CGM use is further substantiated by results from O’Connell et al. (19), who randomized 62 patients with well-controlled type 1 diabetes using CSII to intervention with CGM or conventional SMBG for 3 months. HbA_1c improved by 0.4% in favor of the intervention group, but within the intervention group, HbA_1c was 0.5% lower in patients using CGM ≥70% of the time compared with <70% use. Thus, CGM is effective in lowering HbA_1c in patients who actually use it. In daily practice, patients who are noncompliant are easy to identify by accessing downloaded data, and (dis)continuation of CGM treatment can be openly discussed.

In addition, initiating CGM treatment might even be more effective when combined with the initiation of CSII. This result is relevant, since most type 1 diabetic patients use multiple daily injection (MDI) therapy with SMBG as standard care, especially in Europe (3). In a multicenter randomized controlled trial (RCT) (the Eurythmics trial), adult type 1 diabetic patients (HbA_1c at entry ≥8.2%) on intensive treatment were allocated to CGM, augmented with CSII or continuation of their multiple daily injections and SMBG regimen (20). After 26 weeks, this regimen resulted in an HbA_1c decrease in the CGM-augmented CSII group of 1.2%. Recently, the STAR-3 trial was published with a design similar to the Eurythmics trial. HbA_1c decreased after 1 year in the CSII augmented with CGM group compared with continuation of injection treatment and SMBG in both children and adults (Table 1) (21). In the previously mentioned RealTrend study, initiating CGM-augmented CSII treatment was also superior to starting CSII treatment alone in the per-protocol analysis, indicated by an HbA_1c improvement of 0.4% in favor of the CGM-augmented CSII group (18).

It is important to emphasize that these reductions in HbA_1c with CGM was not associated with an increase in the number or severity of hypoglycemic episodes.

Next to its effects on HbA_1c, CGM seems to have a positive impact on patient-reported outcomes. Despite being confronted throughout the day with diabetes through CGM alarms and the discomfort of the device itself, results from an Internet survey administered to 162 patients using CGM-augmented CSII and 149 patients using CSII alone demonstrated that patients using CGM were more satisfied with their treatment and had better quality of life (22). In the Eurythmics trial, patients randomized to CGM-augmented CSII experienced significantly less problems with their diabetes and increased treatment satisfaction as measured by the Problem Area In Diabetes questionnaire and the Diabetes Treatment Satisfaction questionnaire (20,23,24).

Two other patient groups in which CGM might be of importance are pregnant women with diabetes and hospitalized patients (25,26). In an Australian RCT, 71 women with type 1 diabetes were randomized to antenatal care with CGM at 4- to- 6-week intervals during pregnancy or to standard antenatal care (27). Patients who were allocated to CGM had lower HbA_1c levels at the end of pregnancy and an odds ratio for macrosomia of 0.36 (95% CI 0.13–0.98).

For hospitalized patients, the application of CGM is being investigated, especially with regard to tight glycemic control in the intensive care unit (28). Although concerns exist about the accuracy of sensors in this setting, a recent trial showed that CGMs may prevent hypoglycemia in the intensive care unit (29).

Finally, CGM is an essential part in the development of the closed-loop or artificial pancreas. In the last years, much research has been performed to develop and improve closed-loop systems (30–32). In particular, algorithms are being developed that use the continuous stream of data to control insulin titration (33,34). In a recent publication by Hovorka et al. (2), the efficacy of a closed-loop format was investigated in a controlled trial. The closed-loop comprised different commercially available CGMs for data input, a control algorithm, and a nurse adjusting the insulin pump. Type 1 diabetic patients using CSII were studied overnight, after a meal and after exercise. During the application of the closed-loop system, glucose was significantly more often in the target range and less in the hypoglycemic range compared with the standard CSII regimen. These results are promising, and future studies will have to work toward investigating the closed loop in outpatient settings, most preferably at home.

CONS OF CGM

CGM is effective in specific patient groups with regard to HbA_1c lowering. First, and most evidently, poorly controlled type 1 diabetic patients seem to benefit from CGM when they use it frequently enough. This result reveals the first problem, because especially children and adolescents are noncompliant with CGM use, and its value in this patient group is therefore limited to only the most motivated patients (13,35). Second, there are many patients that do not tolerate the CGM devices. This scenario is illustrated by the higher dropout rates in the CGM arms of the RCTs (Table 1). Also, in the JDRF trial and the Eurythmics trial, patients were already exposed to (blinded) CGMs before inclusion or randomization to obtain a baseline CGM measurement for all patients (13,20). This resulted in 23 of 345 and 4 of 87 patients dropping out before randomization in the JDRF trial and Eurythmics trial, respectively—probably patients not tolerating the device. Clearly, CGM is not for everyone.

Furthermore, in most trials summarized in Table 1, patients were either already on CSII before randomization or were put on CSII during the trial. Consequently, we have to be cautious when extrapolating the RCT results to patients using CGM in combination with MDI therapy.

Now that the first substantial randomized controlled trials on CGM have been performed, another conclusion is that CGM does not seem to prevent severe hypoglycemia. This is in contrast with early expectations and current beliefs. Table 1 shows the incidences of severe hypoglycemia across several CGM trials that are mostly comparable in the intervention and control groups. In the STAR-1 trial, there were even significantly more severe hypoglycemic events in the CGM arm that in the control arm (17). There seem to be three possible explanations for the inability of CGM to prevent severe hypoglycemia. First, there is CGM inaccuracy. When compared with actual plasma glucose values, CGMs have an inaccuracy up to 21% (expressed as mean absolute difference, |CGM glucose − plasma glucose|/plasma glucose). This number is even higher in the hypoglycemic range or during rapid rise and fall of the plasma glucose (36). Probably a physiologic and instrumental delay, inherent to the current real-time CGMs, contribute to the inaccuracy of the devices (37).

Second, during severe hypoglycemia, there is a decline of cognitive function and patients are less adequate in responding to acoustic or vibration alarms (38). Third, during intensive sport activities, which bring along an increased risk of hypoglycemia, the CGM device is more likely to be put aside. However, we have to note that no trials so far were specifically designed and powered to investigate CGM in relation to prevention of severe hypoglycemia. One multicenter trial is underway and the results are eagerly awaited (NCT00843609). In an observational follow-up study from the JDRF-CGM study group, CGM use was associated with both HbA_1c reduction and reduction in severe hypoglycemia rate (15). This association indicates the need for controlled trials, perhaps with a longer duration than 6 months, to allow for the possibility that a longer user learning phase is needed to learn to avoid severe hypoglycemia. Such trials investigating the value of CGM in preventing severe hypoglycemia should be targeted to patients at high risk for severe hypoglycemia. This is also important for reimbursement of CGM in well-controlled type 1 diabetic patients. Because these patients have already achieved their HbA_1c targets without CGM, the incremental CGM value has to come from preventing hypoglycemia and gaining quality of life.

In addition, CGM is always discussed in the context of type 1 diabetes, whereas the vast majority of the diabetes population consists of type 2 diabetic patients. Blood glucose monitoring with SMBG is the standard of care, but its effectiveness is debated (39). Having this in mind, the evidence on CGM in the type 2 diabetic population is surprisingly scarce. Yoo et al. (40) performed an RCT in 65 patients with type 2 diabetes, comparing 12 weeks of intermittent real-time CGM use (3 days per month) with standard care using SMBG. In both groups, HbA_1c decreased, but it decreased significantly more (−0.5%, P = 0.004) in the CGM arm. To our knowledge, this is the only RCT that specifically assessed HbA_1c decrease by CGM in type 2 diabetes. Adequate powered trials with sufficient follow-up time are needed.

Finally, the costs of the CGM devices are a major con. Treatment with CGM costs about $4,930–7,120 per person-year compared with $550–2,740 for SMBG (41). It can be assumed that CGM would be cost-effective in poorly controlled type 1 diabetic patients because of the gain in long-term health benefits, as indicated by HbA_1c lowering. However, the cost-effectiveness of CGM in other patient groups or in preventing hypoglycemia is hard to assess because of the existing lack of evidence. This result is reflected in the current reimbursement status of CGMs. In the U.S., federal Medicare and most other health plans reimburse real-time CGM only for type 1 diabetic patients who are not meeting the ADA HbA_1c targets or experience severe hypoglycemic events. In Europe, real-time CGM is only reimbursed in Sweden and Slovenia. CSII-using patients in Sweden with two or more severe hypoglycemic episodes per year, patients with HbA_1c >10% while receiving intensive insulin therapy, and children who require at least 10 plasma glucose tests per 24 h are eligible for reimbursement. If CGM does not have the desired effect after 3 months, it should be discontinued. In Israel, real-time CGM is included in the National Health Basket and is reimbursed by the Sickness Funds. Children (aged 6–18 years) with type 1 diabetes and severe hypoglycemia unawareness, experiencing two severe episodes of hypoglycemia in the past 12 months (requiring ambulance assistance or emergency ward treatment), can apply for reimbursement.