Early Continuous Glucose Monitor Use in Children and Adolescents With Type 1 Diabetes: Rates of Initiation and Impact on Glycemic Outcomes

Author:

Mann Elizabeth A.1ORCID,Rompicherla Saketh2,Miyazaki Brian3,Rioles Nicole2,Hardison Holly2,Golden Lauren4,Sarhis Jennifer5,Akturk Halis K.6,Lee Joyce7,DeSalvo Daniel J.8,Gomez Patricia9,Ebekozien Osagie210,Prahalad Priya11

Affiliation:

1. 1School of Medicine and Public Health, University of Wisconsin, Madison, WI

2. 2T1D Exchange, Boston, MA

3. 3Children’s Hospital, Los Angeles, CA

4. 4NYU Langone Health, New York, NY

5. 5Cohen Children’s Medical Center, Queens, NY

6. 6Barbara Davis Center, Aurora, CO

7. 7Susan B. Meister Child Health Evaluation and Research Center, C.S. Mott Children’s Hospital, Ann Arbor, MI

8. 8Texas Children’s Hospital, Baylor College of Medicine, Houston, TX

9. 9Miller School of Medicine, University of Miami, Miami, FL

10. 10University of Mississippi School of Population Health, Jackson, MS

11. 11Stanford University, Stanford, CA

Abstract

OBJECTIVE Early initiation of continuous glucose monitor (CGM) after type 1 diabetes (T1D) diagnosis has been associated with lower hemoglobin A1C (HbA1c) in single-institution studies. This multicenter study evaluated the association between the timing of CGM initiation and HbA1c at 3 years postdiagnosis. RESEARCH DESIGN AND METHODS Data were obtained from the T1D Exchange Quality Improvement Collaborative (T1DX-QI) electronic health record database from 25 pediatric centers and included children and adolescents ≤18 years old diagnosed with T1D in 2019 and 2020. CGM initiation and glycemic outcomes were followed for 3 years after diagnosis. Locally estimated scatterplot smoothing plots evaluated the relationship between timing of CGM initiation and HbA1c over time, and logistic regression models were used to adjust for potential confounders. RESULTS There were 4,164 people included in this analysis, mean age was 12.6 (SD 3.5) years, and 37% had public health insurance. Of the 93% (n = 3,877) who initiated CGM within 3 years of T1D diagnosis, 21% did so at 0–3 months, 14% at 3–6 months, 14% at 6–12 months, and 51% after 12 months. Median HbA1c at 3 years postdiagnosis was lower for the 0–3 and 3–6 months groups compared with the 6–12 months and non-CGM user groups (7.9%, 7.9%, 8.4%, and 9.5%, respectively). Adjusted odds of HbA1c >9% were lowest for the 0–3 months group followed by the 3–6 months group. CONCLUSIONS In summary, early initiation of CGM within the first 6 months of diagnosis is associated with improved HbA1c outcomes at 3 years postdiagnosis.

Funder

Helmsley Charitable Trust

T1D Exchange QI Collaborative

Publisher

American Diabetes Association

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