Autonomous and Continuous Adaptation of a Bihormonal Bionic Pancreas in Adults and Adolescents With Type 1 Diabetes

被引:80
作者
El-Khatib, Firas H. [1 ]
Russell, Steven J. [2 ,3 ,4 ]
Magyar, Kendra L. [2 ,3 ,4 ]
Sinha, Manasi [2 ,3 ,4 ]
McKeon, Katherine [1 ]
Nathan, David M. [2 ,3 ,4 ]
Damiano, Edward R. [1 ]
机构
[1] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[2] Massachusetts Gen Hosp, Diabet Unit, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
LOOP INSULIN DELIVERY; LOGIC ARTIFICIAL PANCREAS; GLUCOSE CONTROL; SEVERE HYPOGLYCEMIA; YOUNG-ADULTS; SYSTEM; KETOACIDOSIS; FEASIBILITY; YOUTH;
D O I
10.1210/jc.2013-4151
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: A challenge for automated glycemic control in type 1 diabetes (T1D) is the large variation in insulin needs between individuals and within individuals at different times in their lives. Objectives: The objectives of the study was to test the ability of a third-generation bihormonal bionic pancreas algorithm, initialized with only subject weight; to adapt automatically to the different insulin needs of adults and adolescents; and to evaluate the impact of optional, automatically adaptive meal-priming boluses. Design: This was a randomized controlled trial. Setting: The study was conducted at an inpatient clinical research center. Patients: Twelve adults and 12 adolescents with T1D participated in the study. Interventions: Subjects in each age group were randomized to automated glycemic control for 48 hours with or without automatically adaptive meal-priming boluses. Main Outcome Measures: Mean plasma glucose (PG), time with PG less than 60 mg/dL, and insulin total daily dose were measured. Results: The 48-hour mean PG values with and without adaptive meal-priming boluses were 132 +/- 9vs 146 +/- 9 mg/dL (P = .03) in adults and 162 +/- 6vs 175 +/- 9 mg/dL (P = .01) in adolescents. Adaptive meal-priming boluses improved mean PG without increasing time spent with PG less than 60 mg/dL: 1.4% vs 2.3% (P = .6) in adults and 0.1% vs 0.1% (P = 1.0) in adolescents. Large increases in adaptive meal-priming boluses and shifts in the timing and size of automatic insulin doses occurred in adolescents. Much less adaptation occurred in adults. There was nearly a 4-fold variation in the total daily insulin dose across all cohorts (0.36-1.41 U/kg.d). Conclusions: A single control algorithm, initialized only with subject weight, can quickly adapt to regulate glycemia in patients with TID and highly variable insulin requirements.
引用
收藏
页码:1701 / 1711
页数:11
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