Safety of User-Initiated Intensification of Insulin Delivery Using Cambridge Hybrid Closed-Loop Algorithm

被引:1
作者
Ware, Julia [1 ,2 ]
Wilinska, Malgorzata E. [1 ,2 ]
Ruan, Yue [1 ]
Allen, Janet M. [1 ]
Boughton, Charlotte K. [1 ,3 ]
Hartnell, Sara [3 ]
Bally, Lia [4 ]
de Beaufort, Carine [5 ,6 ]
Besser, Rachel E. J. [7 ,8 ]
Campbell, Fiona M. [9 ]
Draxlbauer, Katharine [10 ]
Elleri, Daniela [11 ]
Evans, Mark L. [1 ,3 ]
Frohlich-Reiterer, Elke [12 ]
Ghatak, Atrayee [13 ]
Hofer, Sabine E. [14 ]
Kapellen, Thomas M. [15 ]
Leelarathna, Lalantha [16 ,17 ]
Mader, Julia K. [18 ]
Mubita, Womba M. [19 ]
Narendran, Parth [10 ,19 ]
Poettler, Tina [18 ]
Rami-Merhar, Birgit [20 ]
Tauschmann, Martin [20 ]
Randell, Tabitha [21 ]
Thabit, Hood [16 ,17 ]
Thankamony, Ajay [2 ]
Trevelyan, Nicola [22 ]
Hovorka, Roman [1 ,2 ]
机构
[1] Univ Cambridge, Wellcome Trust MRC Inst Metab Sci, Metab Res Labs, Cambridge, England
[2] Univ Cambridge, Dept Paediat, Cambridge, England
[3] Cambridge Univ Hosp NHS Fdn Trust, Dept Diabet & Endocrinol, Cambridge, England
[4] Bern Univ Hosp, Inselspital, Dept Diabet Endocrinol Nutr Med & Metab, Bern, Switzerland
[5] Ctr Hosp Luxembourg, Diabet & Endocrine Care Clin Pediat, Luxembourg, Luxembourg
[6] UZ VUB, Dept Paediat Endocrinol, Brussels, Belgium
[7] Oxford Univ Hosp NHS Fdn Trust, NIHR Oxford Biomed Res Ctr, Oxford, England
[8] Univ Oxford, Dept Paediat, Oxford, England
[9] Leeds Childrens Hosp, Dept Paediat Diabet, Leeds, W Yorkshire, England
[10] Univ Hosp Birmingham NHS Fdn Trust, Birmingham, W Midlands, England
[11] Royal Hosp Sick Children, Dept Diabet, Edinburgh, Midlothian, Scotland
[12] Med Univ Graz, Dept Pediat & Adolescent Med, Graz, Austria
[13] Alder Hey Childrens NHS Fdn Trust, Dept Diabet, Liverpool, Merseyside, England
[14] Med Univ Innsbruck, Dept Pediat 1, Innsbruck, Austria
[15] Univ Leipzig, Hosp Children & Adolescents, Leipzig, Germany
[16] Manchester Univ NHS Fdn Trust, Manchester Acad Hlth Sci Ctr, Diabet Endocrinol & Metab Ctr, Manchester, Lancs, England
[17] Univ Manchester, Fac Biol Med & Hlth, Div Diabet Endocrinol & Gastroenterol, Manchester, Lancs, England
[18] Med Univ Graz, Dept Internal Med, Div Endocrinol & Diabetol, Graz, Austria
[19] Univ Birmingham, Inst Immunol & Immunotherapy, Birmingham, W Midlands, England
[20] Med Univ Vienna, Dept Paediat & Adolescent Med, Vienna, Austria
[21] Nottingham Univ Hosp NHS Trust, Nottingham Childrens Hosp, Dept Paediat Diabet & Endocrinol, Nottingham, England
[22] Southampton Childrens Hosp, Southampton Gen Hosp, Dept Paediat Endocrinol & Diabet, Southampton, Hants, England
来源
JOURNAL OF DIABETES SCIENCE AND TECHNOLOGY | 2024年 / 18卷 / 04期
基金
欧盟地平线“2020”; 英国惠康基金;
关键词
artificial pancreas; automated insulin delivery; closed-loop; hypoglycemia; personalized medicine; type; 1; diabetes; TYPE-1; ADULTS; THERAPY; REQUIREMENTS; EXPERIENCES;
D O I
10.1177/19322968221141924
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Many hybrid closed-loop (HCL) systems struggle to manage unusually high glucose levels as experienced with intercurrent illness or pre-menstrually. Manual correction boluses may be needed, increasing hypoglycemia risk with overcorrection. The Cambridge HCL system includes a user-initiated algorithm intensification mode ("Boost"), activation of which increases automated insulin delivery by approximately 35%, while remaining glucose-responsive. In this analysis, we assessed the safety of "Boost" mode. Methods: We retrospectively analyzed data from closed-loop studies involving young children (1-7 years, n = 24), children and adolescents (10-17 years, n = 19), adults (>= 24 years, n = 13), and older adults (>= 60 years, n = 20) with type 1 diabetes. Outcomes were calculated per participant for days with >= 30 minutes of "Boost" use versus days with no "Boost" use. Participants with Results: Eight weeks of data for 76 participants were analyzed. There was no difference in time spent <70 and <54 mg/dL between "Boost" days and "non-Boost" days; mean difference: -0.10% (95% confidence interval [CI] -0.28 to 0.07; P = .249) time <70 mg/dL, and 0.03 (-0.04 to 0.09; P = .416) time < 54 mg/dL. Time in significant hyperglycemia >300 mg/dL was 1.39 percentage points (1.01 to 1.77; P < .001) higher on "Boost" days, with higher mean glucose and lower time in target range (P < .001). Conclusions: Use of an algorithm intensification mode in HCL therapy is safe across all age groups with type 1 diabetes. The higher time in hyperglycemia observed on "Boost" days suggests that users are more likely to use algorithm intensification on days with extreme hyperglycemic excursions.
引用
收藏
页码:882 / 888
页数:7
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