Safety and Performance of the Tandem t:slim X2 with Control-IQ Automated Insulin Delivery System in Toddlers and Preschoolers

被引:38
作者
Ekhlaspour, Laya [1 ,2 ]
Schoelwer, Melissa J. [3 ,4 ]
Forlenza, Gregory P. [5 ]
Deboer, Mark D. [3 ,4 ]
Norlander, Lisa [1 ]
Hsu, Liana [1 ]
Kingman, Ryan [1 ]
Boranian, Emily [5 ]
Berget, Cari [5 ]
Emory, Emma [3 ]
Buckingham, Bruce A. [1 ,2 ]
Breton, Marc D. [3 ]
Wadwa, R. Paul [5 ]
机构
[1] Stanford Univ, Dept Pediat, Div Endocrinol & Diabet, Palo Alto, CA 94304 USA
[2] Stanford Diabet Res Ctr, Stanford, CA USA
[3] Univ Virginia, Ctr Diabet Technol, Charlottesville, VA USA
[4] Univ Virginia, Dept Pediat, Charlottesville, VA USA
[5] Univ Colorado, Barbara Davis Ctr Diabet, Anschutz Med Campus, Aurora, CO USA
关键词
Type; 1; diabetes; Closed loop; Artificial pancreas; Pediatrics; ARTIFICIAL PANCREAS SYSTEM; YOUNG-CHILDREN; DIABETIC-KETOACIDOSIS; SEVERE HYPOGLYCEMIA; TYPE-1; ASSOCIATION; YOUTH;
D O I
10.1089/dia.2020.0507
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Glycemic control is particularly challenging for toddlers and preschoolers with type 1 diabetes (T1D), and data on the use of closed-loop systems in this age range are limited. Materials and Methods: We studied use of a modified investigational version of the Tandem t:slim X2 Control-IQ system in children aged 2 to 5 years during 48 h in an outpatient supervised hotel (SH) setting followed by 3 days of home use to examine the safety of this system in young children. Meals and snacks were not restricted and boluses were estimated per parents' usual routine. At least 30 min of daily exercise was required during the SH phase. All participants were remotely monitored by study staff while on closed-loop in addition to monitoring by at least one parent throughout the study. Results: Twelve participants diagnosed with T1D for at least 3 months with mean age 4.7 +/- 1.0 years (range 2.0-5.8 years) and hemoglobin A1c of 7.3% +/- 0.8% were enrolled at three sites. With use of Control-IQ, the percentage of participants meeting our prespecified goals of less than 6% time below 70 mg/dL and less than 40% time above 180 mg/dL increased from 33% to 83%. Control-IQ use significantly improved percent time in range (70-180 mg/dL) compared to baseline (71.3 +/- 12.5 vs. 63.7 +/- 15.1, P = 0.016). All participants completed the study with no adverse events. Conclusions: In this brief pilot study, use of the modified Control-IQ system was safe in 2-5-year-old children with T1D and improved glycemic control.
引用
收藏
页码:384 / 391
页数:8
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