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Original Research

Closed-Loop Basal Insulin Delivery Over 36 Hours in Adolescents With Type 1 Diabetes

Randomized clinical trial

  1. Daniela Elleri, MD1,2,
  2. Janet M. Allen, RN1,2,
  3. Kavita Kumareswaran, MD2,
  4. Lalantha Leelarathna, MD2,
  5. Marianna Nodale, MSC2,
  6. Karen Caldwell, RN2,
  7. Peiyao Cheng, MPH3,
  8. Craig Kollman, PHD3,
  9. Ahmad Haidar, MSC2,
  10. Helen R. Murphy, MD2,
  11. Malgorzata E. Wilinska, PHD1,2,
  12. Carlo L. Acerini, MD1,
  13. David B. Dunger, MD1,2 and
  14. Roman Hovorka, PHD1,2⇑
  1. 1Department of Paediatrics, University of Cambridge, Cambridge, U.K.
  2. 2Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, U.K.
  3. 3Jaeb Center for Health Research, Tampa, Florida.
  1. Corresponding author: Roman Hovorka, rh347{at}cam.ac.uk.
Diabetes Care 2013 Apr; 36(4): 838-844. https://doi.org/10.2337/dc12-0816
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Abstract

OBJECTIVE We evaluated the safety and efficacy of closed-loop basal insulin delivery during sleep and after regular meals and unannounced periods of exercise.

RESEARCH DESIGN AND METHODS Twelve adolescents with type 1 diabetes (five males; mean age 15.0 [SD 1.4] years; HbA1c 7.9 [0.7]%; BMI 21.4 [2.6] kg/m2) were studied at a clinical research facility on two occasions and received, in random order, either closed-loop basal insulin delivery or conventional pump therapy for 36 h. During closed-loop insulin delivery, pump basal rates were adjusted every 15 min according to a model predictive control algorithm informed by subcutaneous sensor glucose levels. During control visits, subjects’ standard infusion rates were applied. Prandial insulin boluses were given before main meals (50–80 g carbohydrates) but not before snacks (15–30 g carbohydrates). Subjects undertook moderate-intensity exercise, not announced to the algorithm, on a stationary bicycle at a 140 bpm heart rate in the morning (40 min) and afternoon (20 min). Primary outcome was time when plasma glucose was in the target range (71–180 mg/dL).

RESULTS Closed-loop basal insulin delivery increased percentage time when glucose was in the target range (median 84% [interquartile range 78–88%] vs. 49% [26–79%], P = 0.02) and reduced mean plasma glucose levels (128 [19] vs. 165 [55] mg/dL, P = 0.02). Plasma glucose levels were in the target range 100% of the time on 17 of 24 nights during closed-loop insulin delivery. Hypoglycemia occurred on 10 occasions during control visits and 9 occasions during closed-loop delivery (5 episodes were exercise related, and 4 occurred within 2.5 h of prandial bolus).

CONCLUSIONS Day-and-night closed-loop basal insulin delivery can improve glucose control in adolescents. However, unannounced moderate-intensity exercise and excessive prandial boluses pose challenges to hypoglycemia-free closed-loop basal insulin delivery.

Footnotes

  • Clinical trial reg. no. NCT01074801, clinicaltrials.gov.

  • This article contains Supplementary Data online at http://care.diabetesjournals.org/lookup/suppl/doi:10.2337/dc12-0816/-/DC1.

  • Received April 28, 2012.
  • Accepted September 22, 2012.
  • © 2013 by the American Diabetes Association.

Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.

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Diabetes Care: 44 (2)

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Closed-Loop Basal Insulin Delivery Over 36 Hours in Adolescents With Type 1 Diabetes
Daniela Elleri, Janet M. Allen, Kavita Kumareswaran, Lalantha Leelarathna, Marianna Nodale, Karen Caldwell, Peiyao Cheng, Craig Kollman, Ahmad Haidar, Helen R. Murphy, Malgorzata E. Wilinska, Carlo L. Acerini, David B. Dunger, Roman Hovorka
Diabetes Care Apr 2013, 36 (4) 838-844; DOI: 10.2337/dc12-0816

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Closed-Loop Basal Insulin Delivery Over 36 Hours in Adolescents With Type 1 Diabetes
Daniela Elleri, Janet M. Allen, Kavita Kumareswaran, Lalantha Leelarathna, Marianna Nodale, Karen Caldwell, Peiyao Cheng, Craig Kollman, Ahmad Haidar, Helen R. Murphy, Malgorzata E. Wilinska, Carlo L. Acerini, David B. Dunger, Roman Hovorka
Diabetes Care Apr 2013, 36 (4) 838-844; DOI: 10.2337/dc12-0816
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