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Multicenter closed-loop/hybrid meal bolus insulin delivery with type 1 diabetes.

Authors :
Chase HP
Doyle FJ 3rd
Zisser H
Renard E
Nimri R
Cobelli C
Buckingham BA
Maahs DM
Anderson S
Magni L
Lum J
Calhoun P
Kollman C
Beck RW
Source :
Diabetes technology & therapeutics [Diabetes Technol Ther] 2014 Oct; Vol. 16 (10), pp. 623-32. Date of Electronic Publication: 2014 Sep 04.
Publication Year :
2014

Abstract

Background: This study evaluated meal bolus insulin delivery strategies and associated postprandial glucose control while using an artificial pancreas (AP) system.<br />Subjects and Methods: This study was a multicenter trial in 53 patients, 12-65 years of age, with type 1 diabetes for at least 1 year and use of continuous subcutaneous insulin infusion for at least 6 months. Four different insulin bolus strategies were assessed: standard bolus delivered with meal (n=51), standard bolus delivered 15 min prior to meal (n=40), over-bolus of 30% delivered with meal (n=40), and bolus purposely omitted (n=46). Meal carbohydrate (CHO) intake was 1 g of CHO/kg of body weight up to a maximum of 100 g for the first three strategies or up to a maximum of 50 g for strategy 4.<br />Results: Only three of 177 meals (two with over-bolus and one with standard bolus 15 min prior to meal) had postprandial blood glucose values of <60 mg/dL. Postprandial hyperglycemia (blood glucose level >180 mg/dL) was prolonged for all four bolus strategies but was shorter for the over-bolus (41% of the 4-h period) than the two standard bolus strategies (73% for each). Mean postprandial blood glucose level was 15.9 mg/dL higher for the standard bolus with meal compared with the prebolus (baseline-adjusted, P=0.07 for treatment effect over the 4-h period).<br />Conclusions: The AP handled the four bolus situations safely, but at the expense of having elevated postprandial glucose levels in most subjects. This was most likely secondary to suboptimal performance of the algorithm.

Details

Language :
English
ISSN :
1557-8593
Volume :
16
Issue :
10
Database :
MEDLINE
Journal :
Diabetes technology & therapeutics
Publication Type :
Academic Journal
Accession number :
25188375
Full Text :
https://doi.org/10.1089/dia.2014.0050