Control-IQ Technology Positively Impacts Patient Reported Outcome Measures and Glycemic Control in Youth with Type 1 Diabetes in a Real-World Setting

Author:

Zuijdwijk Caroline123ORCID,Courtney Jennilea2,Mitsakakis Nicholas2ORCID,Hayawi Lamia2ORCID,Sutherland Stephanie2ORCID,Newhook Dennis2ORCID,Ahmet Alexandra123ORCID,Goldbloom Ellen B.123ORCID,Khatchadourian Karine123ORCID,Lawrence Sarah123ORCID

Affiliation:

1. Division of Endocrinology and Metabolism, Children’s Hospital of Eastern Ontario, Ottawa, Ontario, Canada

2. CHEO Research Institute, Ottawa, Ontario, Canada

3. University of Ottawa, Faculty of Medicine, Ottawa, Ontario, Canada

Abstract

Objective. To determine the impact of the t:slim X2 insulin pump with Control-IQ technology on the quality of life and glycemic control in youth with type 1 diabetes (T1D) and their parents in a real-world setting. Research Design and Methods. We conducted a single-center, prospective study on pediatric patients (6–18 years old) with T1D using a Tandem t:slim X2 pump and initiating Control-IQ technology as part of routine care. Youth (≥8 years) and parents completed validated patient-reported outcome measures (PROMs) at baseline and the end of the study (16 weeks). Glycemic control measures were recorded at baseline and every 4 weeks until the end of the study. Results. Fifty-nine youth participated; the median (IQR) age was 13.8 (11.1, 15.7) years, and T1D duration was 6.3 (3.1, 8.4) years. INSPIRE scores (evaluating expectations (baseline) and impact (post) of Control-IQ technology) were favorable, unchanged at the end of the study for youth, and lower for parents ( p = 0.04 ). Other PROM scores improved by the end of the study with mean (95% CI) differences for youth and parents, respectively, as follows: Diabetes Impact and Device Satisfaction (DIDS) Scale Diabetes Impact −1.08 (−1.51, −0.64) ( p < 0.001 ) and −1.41 (−1.96, −0.87) ( p < 0.001 ); DIDS Scale Device Satisfaction +0.43 (0.11, 0.74) ( p = 0.01 ) and +0.58 (0.31, 0.85) ( p < 0.001 ); Hypoglycemia Fear Survey −4.41 (−7.65, −1.17) ( p = 0.01 ) and −7.64 (−11.66, −3.62) ( p < 0.001 ); and WHO-5 Well-Being Index +5.10 (−1.40, 11.6) ( p = 0.12 ) and +9.60 (3.40, 15.8) ( p = 0.003 ). The mean time in range increased from 52.6% at baseline to 62.6% ( p < 0.001 ) at 4 weeks, sustained to 16 weeks. Conclusions. Initiation of Control-IQ technology in a real-world setting significantly reduced the impact of diabetes on daily life while simultaneously improving glycemic control. Trial Registration. This trial is registered with ClinicalTrials.gov Identifier NCT04838561 (https://www.clinicaltrials.gov/ct2/show/NCT04838561?term=Control-IQ&cond=Type+1+Diabetes&cntry=CA&draw=2&rank=1).

Funder

Tandem Diabetes Care

Publisher

Hindawi Limited

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health,Internal Medicine

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