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Abstract
Objectives:
High protein high fat (HPHF) meals are considered “difficult” foods because they can cause prolonged hyperglycemia after ingestion. The potential of hybrid closed loop therapy in managing postprandial glucose excursions with these difficult foods remains unknown. This pilot study aimed to explore the impact of manual mode in standard insulin pump therapy and auto mode with hybrid closed loop pump therapy in managing glucose excursions caused by HPHF foods and to obtain feedback from families about each mode.
Material and Methods:
Children and adolescents (8–18 years) with type 1 diabetes and using the MiniMed™ 670G were recruited to a free-living randomized cross-over study. Participants consumed a standardized lasagne or pizza meal two nights a week for 4 weeks while in auto mode and manual mode. Postprandial continuous glucose monitoring data were collected for 7 h post-meal. The primary outcomes were mean postprandial net incremental area under the glucose × time curve. User experiences were collected during end-of-study interviews administered to parents.
Results:
Postprandial excursions from 38 meals in seven participants were analyzed. There were no significant differences between auto mode and manual mode for the mean net incremental area under the glucose × time curve, irrespective of meal type. Semi-structured end-of-study interviews revealed that five of seven families felt more confident eating HPHF meals in auto mode.
Conclusion:
Although most families felt confident with auto mode for postprandial HPHF excursions, this was not reflected in the postprandial glucose levels.
High protein high fat (HPHF) meals are considered “difficult” foods because they can cause prolonged hyperglycemia after ingestion. The potential of hybrid closed loop therapy in managing postprandial glucose excursions with these difficult foods remains unknown. This pilot study aimed to explore the impact of manual mode in standard insulin pump therapy and auto mode with hybrid closed loop pump therapy in managing glucose excursions caused by HPHF foods and to obtain feedback from families about each mode.
Material and Methods:
Children and adolescents (8–18 years) with type 1 diabetes and using the MiniMed™ 670G were recruited to a free-living randomized cross-over study. Participants consumed a standardized lasagne or pizza meal two nights a week for 4 weeks while in auto mode and manual mode. Postprandial continuous glucose monitoring data were collected for 7 h post-meal. The primary outcomes were mean postprandial net incremental area under the glucose × time curve. User experiences were collected during end-of-study interviews administered to parents.
Results:
Postprandial excursions from 38 meals in seven participants were analyzed. There were no significant differences between auto mode and manual mode for the mean net incremental area under the glucose × time curve, irrespective of meal type. Semi-structured end-of-study interviews revealed that five of seven families felt more confident eating HPHF meals in auto mode.
Conclusion:
Although most families felt confident with auto mode for postprandial HPHF excursions, this was not reflected in the postprandial glucose levels.
Original language | English |
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Number of pages | 8 |
Journal | Journal of Pediatric Endocrinology & Diabetes |
Volume | 3 |
Issue number | 2 |
DOIs | |
Publication status | Published - 18 Nov 2023 |
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Dive into the research topics of 'Efficacy of the MiniMed™ 670G hybrid closed loop system in managing postprandial glucose excursion with high protein high fat foods in children and adolescents under free-living conditions.'. Together they form a unique fingerprint.Projects
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Jones Improving the Lives of Young People with Type 1 Diabetes using State of the Art Therapies
Jones, T. (Investigator 01), Davis, E. (Investigator 02), Fournier, P. (Investigator 03), Keenan, D. (Investigator 04), Grey, M. (Investigator 05), Weinzimer, S. (Investigator 06), Geelhoed, E. (Investigator 07), Cross, D. (Investigator 08) & Tamborlane, W. (Investigator 09)
NHMRC National Health and Medical Research Council
1/01/15 → 30/04/21
Project: Research