Safety and Glycemic Outcomes During the MiniMed™ Advanced Hybrid Closed-Loop System Pivotal Trial in Children and Adolescents with Type 1 Diabetes

被引:6
|
作者
Pihoker, Catherine [1 ,15 ]
Shulman, Dorothy I. [2 ]
Forlenza, Gregory P. [3 ]
Kaiserman, Kevin B. [4 ]
Sherr, Jennifer L. [5 ]
Thrasher, James R. [6 ]
Buckingham, Bruce A. [7 ]
Kipnes, Mark S. [8 ]
Bode, Bruce W. [9 ]
Carlson, Anders L. [10 ]
Lee, Scott W. [11 ]
Latif, Kashif [12 ]
Liljenquist, David R. [13 ]
Slover, Robert H. [3 ]
Dai, Zheng [14 ]
Niu, Fang [14 ]
Shin, John [14 ]
Jonkers, Richard A. M. [14 ]
Roy, Anirban [14 ]
Grosman, Benyamin [14 ]
Vella, Melissa [14 ]
Cordero, Toni L. [14 ]
Mcvean, Jennifer [14 ]
Rhinehart, Andrew S. [14 ]
Vigersky, Robert A. [14 ]
MiniMedTM AHCL Study Grp [14 ]
机构
[1] Univ Washington, Dept Pediat, Seattle, WA USA
[2] Univ S Florida, Pediat Diabet & Endocrinol, Tampa, FL USA
[3] Barbara Davis Ctr Childhood Diabet, Dept Pediat, Aurora, CO USA
[4] SoCal Diabet, Torrance, CA USA
[5] Yale Univ, Sch Med, Dept Pediat, New Haven, CT USA
[6] Arkansas Diabet & Endocrinol Ctr, Little Rock, AR USA
[7] Stanford Univ, Sch Med, Pediat Diabet & Endocrinol, Stanford, CA USA
[8] Diabet & Glandular Dis Clin, San Antonio, TX USA
[9] Atlanta Diabet Associates, Atlanta, GA USA
[10] HealthPartners Inst, Int Diabet Ctr, Minneapolis, MN USA
[11] Loma Linda Univ, Dept Endocrinol, Loma Linda, CA USA
[12] AM Diabet & Endocrinol Ctr, Bartlett, TN USA
[13] Rocky Mt Diabet & Osteoporosis Ctr, Idaho Falls, ID USA
[14] Medtronic, Northridge, CA USA
[15] Univ Washington, Dept Pediat, Box 359300,OC7 820, Seattle, WA 98105 USA
关键词
Type; 1; diabetes; Advanced hybrid closed loop; A1C; Time-in-range; Glucose target; Active insulin time; Pediatric; ADULTS;
D O I
10.1089/dia.2023.0255
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: During MiniMed (TM) advanced hybrid closed-loop (AHCL) use by adolescents and adults in the pivotal trial, glycated hemoglobin (A1C) was significantly reduced, time spent in range (TIR) was significantly increased, and there were no episodes of severe hypoglycemia or diabetic ketoacidosis (DKA). The present study investigated the same primary safety and effectiveness endpoints during AHCL use by a younger cohort with type 1 diabetes (T1D).Methods: An intention-to-treat population (N = 160, aged 7-17 years) with T1D was enrolled in a single-arm study at 13 investigational centers. There was a run-in period (similar to 25 days) using HCL or sensor-augmented pump with/without predictive low-glucose management, followed by a 3-month study period with AHCL activated at two glucose targets (GTs; 100 and 120 mg/dL) for similar to 45 days each. The mean +/- standard deviation values of A1C, TIR, mean sensor glucose (SG), coefficient of variation (CV) of SG, time at SG ranges, and insulin delivered between run-in and study were analyzed (Wilcoxon signed-rank test or t-test).Results: Compared with baseline, AHCL use was associated with reduced A1C from 7.9 +/- 0.9% (N = 160) to 7.4 +/- 0.7% (N = 136) (P < 0.001) and overall TIR increased from the run-in 59.4 +/- 11.8% to 70.3 +/- 6.5% by end of study (P < 0.001), without change in CV, time spent below range (TBR) <70 mg/dL, or TBR <54 mg/dL. Relative to longer active insulin time (AIT) settings (N = 52), an AIT of 2 h (N = 19) with the 100 mg/dL GT increased mean TIR to 73.4%, reduced TBR <70 mg/dL from 3.5% to 2.2%, and reduced time spent above range (TAR) >180 mg/dL from 28.7% to 24.4%. During AHCL use, there was no severe hypoglycemia or DKA.Conclusions: In children and adolescents with T1D, MiniMed AHCL system use was safe, A1C was lower, and TIR was increased. The lowest GT and shortest AIT were associated with the highest TIR and lowest TBR and TAR, all of which met consensus-recommended glycemic targets.
引用
收藏
页码:755 / 764
页数:10
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