Skip to main content
  • More from ADA
    • Diabetes
    • Clinical Diabetes
    • Diabetes Spectrum
    • ADA Standards of Medical Care
    • ADA Scientific Sessions Abstracts
    • BMJ Open Diabetes Research & Care
  • Subscribe
  • Log in
  • Log out
  • My Cart
  • Follow ada on Twitter
  • RSS
  • Visit ada on Facebook
Diabetes Care

Advanced Search

Main menu

  • Home
  • Current
    • Current Issue
    • Online Ahead of Print
    • Special Article Collections
    • ADA Standards of Medical Care
  • Browse
    • By Topic
    • Issue Archive
    • Saved Searches
    • Special Article Collections
    • ADA Standards of Medical Care
  • Info
    • About the Journal
    • About the Editors
    • ADA Journal Policies
    • Instructions for Authors
    • Guidance for Reviewers
  • Reprints/Reuse
  • Advertising
  • Subscriptions
    • Individual Subscriptions
    • Institutional Subscriptions and Site Licenses
    • Access Institutional Usage Reports
    • Purchase Single Issues
  • Alerts
    • E­mail Alerts
    • RSS Feeds
  • Podcasts
    • Diabetes Core Update
    • Special Podcast Series: Therapeutic Inertia
    • Special Podcast Series: Influenza Podcasts
    • Special Podcast Series: SGLT2 Inhibitors
    • Special Podcast Series: COVID-19
  • Submit
    • Submit a Manuscript
    • Journal Policies
    • Instructions for Authors
    • ADA Peer Review
  • More from ADA
    • Diabetes
    • Clinical Diabetes
    • Diabetes Spectrum
    • ADA Standards of Medical Care
    • ADA Scientific Sessions Abstracts
    • BMJ Open Diabetes Research & Care

User menu

  • Subscribe
  • Log in
  • Log out
  • My Cart

Search

  • Advanced search
Diabetes Care
  • Home
  • Current
    • Current Issue
    • Online Ahead of Print
    • Special Article Collections
    • ADA Standards of Medical Care
  • Browse
    • By Topic
    • Issue Archive
    • Saved Searches
    • Special Article Collections
    • ADA Standards of Medical Care
  • Info
    • About the Journal
    • About the Editors
    • ADA Journal Policies
    • Instructions for Authors
    • Guidance for Reviewers
  • Reprints/Reuse
  • Advertising
  • Subscriptions
    • Individual Subscriptions
    • Institutional Subscriptions and Site Licenses
    • Access Institutional Usage Reports
    • Purchase Single Issues
  • Alerts
    • E­mail Alerts
    • RSS Feeds
  • Podcasts
    • Diabetes Core Update
    • Special Podcast Series: Therapeutic Inertia
    • Special Podcast Series: Influenza Podcasts
    • Special Podcast Series: SGLT2 Inhibitors
    • Special Podcast Series: COVID-19
  • Submit
    • Submit a Manuscript
    • Journal Policies
    • Instructions for Authors
    • ADA Peer Review
Emerging Treatments and Technologies

Improved Glycemic Control in Poorly Controlled Patients with Type 1 Diabetes Using Real-Time Continuous Glucose Monitoring

  1. Dorothee Deiss, MD1,
  2. Jan Bolinder, MD, PHD2,
  3. Jean-Pierre Riveline, MD3,
  4. Tadej Battelino, MD, PHD4,
  5. Emanuele Bosi, MD, PHD5,
  6. Nadia Tubiana-Rufi, MD6,
  7. David Kerr, MD7 and
  8. Moshe Phillip, MD8
  1. 1Children’s Hospital Charité, Humboldt-University, Berlin, Germany
  2. 2Karolinska University Hospital Huddinge, Stockholm, Sweden
  3. 3Sud-Francilien Hospital, Corbeil-Essonnes, France
  4. 4University Children’s Hospital, Ljubljana, Slovenia
  5. 5Vita-Salute San Raffaele University Hospital, Milan, Italy
  6. 6Robert Debré Hospital, Paris, France
  7. 7Royal Bournemouth Hospital, Bournemouth, U.K.
  8. 8Schneider Children Centre, Petah-Tikva, Israel
  1. Address correspondence and reprint requests to Prof. Jan Bolinder, Department of Medicine, M54, Karolinska University Hospital Huddinge, S-141 86 Stockholm, Sweden. E-mail: jan.bolinder{at}ki.se
Diabetes Care 2006 Dec; 29(12): 2730-2732. https://doi.org/10.2337/dc06-1134
PreviousNext
  • Article
  • Figures & Tables
  • Info & Metrics
  • PDF
Loading
  • CGM, continuous glucose monitoring
  • SMBG, self-monitoring of blood glucose.

Intensive self-management with frequent self-monitoring of blood glucose (SMBG) is important in type 1 diabetes to achieve good metabolic control (1–3). Nevertheless, many patients still experience episodes of unrecognized hypo- and hyperglycemia (4). Novel technologies for continuous glucose monitoring (CGM) that provide information about glucose excursions are now available. Previous studies reported the benefits of retrospective evaluation of CGM data (5–11), but few assessed effects on glycemic control (5,12–14), and only one showed improvements compared with SMBG (14). We evaluated the effect of a new real-time glucose monitor on glycemic control in patients with poorly controlled type 1 diabetes. The device, Guardian RT (Medtronic MiniMed, Northridge, CA), allows users to see glucose readings and set hypo- and hyperglycemic alarms and provides trend information on changing glucose values.

RESEARCH DESIGN AND METHODS—

The study included 81 children (median age 14.4 years [range 8.0–18.9]) and 81 adults (age 39.1 years [19.0–59.5]) with stable type 1 diabetes. All had adhered to intensified insulin treatment (continuous subcutaneous insulin infusion, n = 78; multiple daily injection, n = 84) but had HbA1c (A1C) levels ≥8.1%. Informed consent was obtained from patients regularly attending the eight participating centers.

Subjects were randomly assigned 1:1:1 for 3 months to Guardian RT continuously (arm 1) or biweekly for 3-day periods every 2 weeks (arm 2) or to continue conventional SMBG (control). Treatment adjustments made by physicians and patients were based on SMBG profiles in control subjects and on real-time glucose profiles in arms 1 and 2. Patients were instructed to perform confirmatory SMBG measurements before therapeutical interventions or corrective action if hypo- or hyperglycemic alarms or symptoms occurred. A1C was measured centrally after 1 and 3 months.

The Guardian RT continuously displays real-time interstitial glucose values and is calibrated prospectively using SMBG reference values. High/low alert thresholds were set at 50–80 mg/dl for hypoglycemia and 170–250 mg/dl for hyperglycemia with the upper alarm lowering to 200 mg/dl after the first 10 days. Settings could be readjusted during the study.

A repeated-measures ANOVA model was used to analyze changes from baseline across groups and visits (PROC MIXED using SAS, version 9.1). Fisher’s least significant differences test was used to assess statistical significance (P ≤ 0.05) between groups. Data were analyzed by intention-to-treat approach using last value carried forward for missing end points and adjusted for age-group (< or ≥19 years) as patients were randomized within age-groups.

RESULTS—

In total, 156 patients completed the evaluation. One discontinued before the start of intervention. Four discontinued arm 1, and one discontinued arm 2 due to difficulties with continuous sensor use and/or alarms.

Baseline values in arms 1 and 2 and the control arm for A1C were (means ± SD) 9.5 ± 1.1, 9.6 ± 1.2, and 9.7 ± 1.3%, respectively. Real-time CGM was associated with reductions from baseline in A1C in arm 1 versus control (Fig. 1) at 1 month (0.6 ± 0.8 vs. 0.2 ± 0.8%, P = 0.008) and 3 months (1.0 ± 1.1 vs. 0.4 ± 1.0%, P = 0.003). In arm 2 (1 month 0.4 ± 0.9%, 3 months 0.7 ± 1.3%), there was no difference versus control or arm 1. At 3 months, 50% of the patients in arm 1 had A1C reductions ≥1% (37% in arm 2 and 15% in control arm) and 26% had reductions ≥2% (9% in arm 2 and 4% in control arm).

Average baseline SMBG per day were 4.6 ± 1.4, 5.0 ± 1.5, and 5.1 ± 1.8, respectively. A mean reduction in SMBG per day from baseline was observed at 1 and 3 months in arm 1 (0.9 ± 1.8 and 1.4 ± 1.7, respectively) but was not statistically significant compared with arm 2 (0.5 ± 1.9 and 0.4 ± 2.1) or control subjects (0.5 ± 1.5 and 0.7 ± 1.8).

At 3 months, average total insulin dose per day was not significantly different from baseline in the three arms (about 0.8 units · kg−1 · day−1). Almost all patients (82% at 1 month and 95% at 3 months) in arms 1 and 2 reported making insulin, dietary, or lifestyle adjustments using the real-time information.

Severe hypoglycemia occurred once each in arms 1 and 2. The patient in arm 2 was not wearing the device at the time. The event during real-time CGM occurred despite a confirmatory low SMBG value and corrective carbohydrate intake.

CONCLUSIONS—

This is the first randomized controlled trial to demonstrate a clinically meaningful reduction in A1C using real-time CGM in type 1 diabetic patients. One previous study (15) showed real-time CGM decreased time spent in hypo- and hyperglycemia but was too short (9 days) to assess A1C. Another controlled trial used real-time CGM for 1–2 days/week over 6 months and found no improvement in overall metabolic control (16). In the present study, real-time CGM gradually improved glycemic control over 3 months, resulting in a reduction in A1C by at least 1% in half the patients and at least 2% in one-quarter. This was achieved in a broad population of children and adults with type 1 diabetes and in a setting translatable into current clinical practice. Study patients had poor metabolic control, despite intensive insulin treatment and frequent SMBG. These patients are the main target group for improving glycemic control (17). Notably, the control subjects performed, on average, more than five SMBG per day at baseline, consistent with acknowledged recommendations (18) and with no significant within-group decrease throughout the trial. In addition, a within-group reduction in SMBG frequency was observed in arm 1, possibly because the patients became more confident at interpreting the real-time glucose readings and trend information.

In this study, the patients did not register specific information about their self-management of diabetes therapy on a daily basis. Therefore, we cannot delineate in detail the link between the use of real-time CGM and the improvement in glycemic control. However, despite no overall change in total daily dose of insulin, almost all patients using real-time CGM reported making treatment adjustments and/or changes to their lifestyle and food intake. Thus, intermittent corrective adjustments of insulin administration, such as the number of boluses or the basal-to–total dose ratio, and food intake adjustments based on the real-time glucose display and alarm functions may have been carried out on an individual basis. Evidently, further investigations are needed to better define treatment guidelines when using real-time CGM to optimize the improvement in glycemic control observed in this study. Moreover, other aspects of this new technique, such as long-term efficacy, clinical feasibility in patients with more satisfactory glycemic control, and effect on the incidence of hypoglycemia, need to be investigated. Our findings strongly indicate that the use of real-time CGM has considerable potential for the management of patients with diabetes.

Figure 1—
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 1—

Change from baseline at 1 and 3 months of AIC. Values are means ± SE. P values correspond to the difference in change from baseline between the continuous and control groups. •, continuous group (arm 1); ▪, biweekly group (arm 2); ▴, control group.

Acknowledgments

This study was sponsored by Medtronic Europe Sàrl, Tolochenaz, Switzerland.

The authors thank the GuardControl Study coinvestigators and staff: Dr. O. Kordonouri, Dr. J. Hoeffe, and R. Hartmann, Germany; R. Nimri, H. Benzaquen, and R. Ofan, Israel; I. Bredenberg and M. Pihl, Sweden; Dr. G. Charpentier and Dr. D. Dardari, France; Dr. N. Ursic-Bratina and M. Avbelj, Slovenia; Dr. G. Galimberti, Dr. A. Laurenzi, and Dr. E. Meneghini, Italy; Prof. P. Czernichow, F. Thourer, and CIC nurses, France; M. Weiss and J. Ryder, U.K.; and Severine Liabat for her outstanding assistance to this project.

Footnotes

  • D.D., J.B., and N.T.-R. have received travel expenses from Medtronic. J.-P.R. has received honoraria and travel grants from Medtronic. T.B. has received consulting fees and honoraria from Medtronic and Abbott. D.K. has received honoraria from and served on advisory boards for Medtronic, Roche, and LifeScan. M.P. has served on advisory boards for Medtronic, Abbott, and D-Medical.

    A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    • Accepted September 1, 2006.
    • Received June 2, 2006.
  • DIABETES CARE

References

  1. ↵
    Diabetes Control and Complications Trial Research Group: The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med 329: 977–986, 1993
    OpenUrlCrossRefPubMedWeb of Science
  2. Haller MJ, Stalvey MS, Silverstein JH: Predictors of control of diabetes: monitoring may be the key. J Pediatr 144: 660–661, 2004
    OpenUrlCrossRefPubMedWeb of Science
  3. ↵
    Levine BS, Anderson BJ, Butler DA, Antisdel JE, Brackett J, Laffel LM: Predictors of glycemic control and short-term adverse outcomes in youth with type 1 diabetes. J Pediatr 139: 174–176, 2001
    OpenUrlCrossRefPubMed
  4. ↵
    Bolinder J, Hagstrom-Toft E, Ungerstedt U, Arner P: Self-monitoring of blood glucose in type 1 diabetic patients: comparison with continuous microdialysis measurements of glucose in subcutaneous adipose tissue during ordinary life conditions. Diabetes Care 20: 64–70, 1997
    OpenUrlAbstract/FREE Full Text
  5. ↵
    Chase HP, Kim LM, Owen SL, MacKenzie TA, Klingensmith GJ, Murtfeld R, Garg SK: Continuous subcutaneous glucose monitoring in children with type 1 diabetes. Pediatrics 107: 222–226, 2001
    OpenUrlAbstract/FREE Full Text
  6. Boland E, Monsod T, Delucia M, Brandt CA, Fernando S, Tamborlane WV: Limitations of conventional methods of self-monitoring of blood glucose: lessons learned from 3 days of continuous glucose sensing in pediatric patients with type 1 diabetes. Diabetes Care 24: 1858–1862, 2001
    OpenUrlAbstract/FREE Full Text
  7. Danne T, Deiss D, Hopfenmuller W, von Schutz W, Kordonouri O: Experience with insulin analogues in children. Horm Res 57(Suppl. 1): S46–S53, 2002
    OpenUrl
  8. Weintrop N, Schechter A, Benzaquen H, Shalitin S, Lilos P, Galatzer A, Phillip M: Glycemic patterns detected by continuous subcutaneous glucose sensing in children and adolescents with type 1 diabetes mellitus treated by multiple daily injections vs continuous subcutaneous insulin infusion. Arch Pediatr Adolesc Med 158: 677–684, 2004
    OpenUrlCrossRefPubMed
  9. Bolinder J, Ungerstedt U, Arner P: Long-term continuous monitoring with microdialysis in ambulatory insulin-dependent diabetic patients. Lancet 342: 1080–1085, 1993
    OpenUrlCrossRefPubMedWeb of Science
  10. Klonoff D: Continuous glucose monitoring: roadmap for the 21st century diabetes therapy. Diabetes Care 28: 1231–1239, 2005
    OpenUrlFREE Full Text
  11. ↵
    Deiss D, Kordonouri O, Meyer K, Danne T: Long hypoglycemic periods detected by subcutaneous continuous glucose monitoring in toddlers and pre-school children with diabetes mellitus. Diabet Med 18: 337–338, 2001
    OpenUrlCrossRefPubMed
  12. ↵
    Tanenberg R, Bode B, Lane W, Levetan C, Mestman J, Harmel AP, Tobian J, Gross T, Mastrototaro J: Use of the continuous glucose monitoring system to guide therapy in patients with insulin-treated diabetes: a randomized controlled trial. Mayo Clin Proc 79: 1521–1526, 2004
    OpenUrlCrossRefPubMedWeb of Science
  13. Chico A, Vidal-Rios P, Subira M, Novials A: The continuous glucose monitoring system is useful for detecting unrecognized hypoglycemias in patients with type 1 and type 2 diabetes but is not better than frequent capillary glucose measurements for improving metabolic control. Diabetes Care 26: 1153–1157, 2003
    OpenUrlAbstract/FREE Full Text
  14. ↵
    Ludvigsson J, Hanas R: Continuous subcutaneous glucose monitoring improved metabolic control in pediatric patients with type 1 diabetes: a controlled crossover study. Pediatrics 111: 933–938, 2003
    OpenUrlAbstract/FREE Full Text
  15. ↵
    Garg SK, Zisser H, Schwartz S, Bailey T, Kaplan R, Ellis S, Jovanovic L: Improvement in glycemic excursions with a transcutaneous, real-time continuous glucose sensor. Diabetes Care 29: 44–50, 2006
    OpenUrlAbstract/FREE Full Text
  16. ↵
    The Diabetes Research in Children Network (DirecNet) Study Group: Accuracy of the modified continuous glucose monitoring system (CGMS) sensor in an outpatient setting: results from a diabetes research in children network (DirecNet) study. Diabetes Technol Ther 7: 109–114, 2005
    OpenUrlCrossRefPubMed
  17. ↵
    Diabetes Control and Complications Trial Research Group: The relationship of glycemic exposure (HbA1c) to the risk of development and progression of retinopathy in the Diabetes Control and Complication Trial. Diabetes 44: 968–983, 1995
    OpenUrlAbstract/FREE Full Text
  18. ↵
    American Diabetes Association: Clinical practice recommendations. Diabetes Care 29(Suppl. 1): S1–S80, 2006
View Abstract
PreviousNext
Back to top
Diabetes Care: 29 (12)

In this Issue

December 2006, 29(12)
  • Table of Contents
  • About the Cover
  • Index by Author
Sign up to receive current issue alerts
View Selected Citations (0)
Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word about Diabetes Care.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Improved Glycemic Control in Poorly Controlled Patients with Type 1 Diabetes Using Real-Time Continuous Glucose Monitoring
(Your Name) has forwarded a page to you from Diabetes Care
(Your Name) thought you would like to see this page from the Diabetes Care web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
Improved Glycemic Control in Poorly Controlled Patients with Type 1 Diabetes Using Real-Time Continuous Glucose Monitoring
Dorothee Deiss, Jan Bolinder, Jean-Pierre Riveline, Tadej Battelino, Emanuele Bosi, Nadia Tubiana-Rufi, David Kerr, Moshe Phillip
Diabetes Care Dec 2006, 29 (12) 2730-2732; DOI: 10.2337/dc06-1134

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Add to Selected Citations
Share

Improved Glycemic Control in Poorly Controlled Patients with Type 1 Diabetes Using Real-Time Continuous Glucose Monitoring
Dorothee Deiss, Jan Bolinder, Jean-Pierre Riveline, Tadej Battelino, Emanuele Bosi, Nadia Tubiana-Rufi, David Kerr, Moshe Phillip
Diabetes Care Dec 2006, 29 (12) 2730-2732; DOI: 10.2337/dc06-1134
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • RESEARCH DESIGN AND METHODS—
    • RESULTS—
    • CONCLUSIONS—
    • Acknowledgments
    • Footnotes
    • References
  • Figures & Tables
  • Info & Metrics
  • PDF

Related Articles

Cited By...

More in this TOC Section

  • Autologous Umbilical Cord Blood Transfusion in Young Children With Type 1 Diabetes Fails to Preserve C-Peptide
  • Effects of MK-0941, a Novel Glucokinase Activator, on Glycemic Control in Insulin-Treated Patients With Type 2 Diabetes
  • Diabetes Antibody Standardization Program
Show more Emerging Treatments and Technologies

Similar Articles

Navigate

  • Current Issue
  • Standards of Care Guidelines
  • Online Ahead of Print
  • Archives
  • Submit
  • Subscribe
  • Email Alerts
  • RSS Feeds

More Information

  • About the Journal
  • Instructions for Authors
  • Journal Policies
  • Reprints and Permissions
  • Advertising
  • Privacy Policy: ADA Journals
  • Copyright Notice/Public Access Policy
  • Contact Us

Other ADA Resources

  • Diabetes
  • Clinical Diabetes
  • Diabetes Spectrum
  • Scientific Sessions Abstracts
  • Standards of Medical Care in Diabetes
  • BMJ Open - Diabetes Research & Care
  • Professional Books
  • Diabetes Forecast

 

  • DiabetesJournals.org
  • Diabetes Core Update
  • ADA's DiabetesPro
  • ADA Member Directory
  • Diabetes.org

© 2021 by the American Diabetes Association. Diabetes Care Print ISSN: 0149-5992, Online ISSN: 1935-5548.