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Randomized Controlled Trial
. 2019 Sep;20(6):794-799.
doi: 10.1111/pedi.12872. Epub 2019 Jun 13.

Reduced burden of diabetes and improved quality of life: Experiences from unrestricted day-and-night hybrid closed-loop use in very young children with type 1 diabetes

Affiliations
Randomized Controlled Trial

Reduced burden of diabetes and improved quality of life: Experiences from unrestricted day-and-night hybrid closed-loop use in very young children with type 1 diabetes

Gianluca Musolino et al. Pediatr Diabetes. 2019 Sep.

Abstract

Objective: To evaluate the experiences of families with very young children aged 1 to 7 years (inclusive) with type 1 diabetes using day-and-night hybrid closed-loop insulin delivery.

Methods: Parents/caregivers of 20 children aged 1 to 7 years with type 1 diabetes completed a closed-loop experience survey following two 3-week periods of unrestricted day-and-night hybrid closed-loop insulin therapy using Cambridge FlorenceM system at home. Benefits, limitations, and improvements of closed-loop technology were explored.

Results: Responders reported reduced burden of diabetes management, less time spent managing diabetes, and improved quality of sleep with closed-loop. Ninety percent of the responders felt less worried about their child's glucose control using closed-loop. Size of study devices, battery performance and connectivity issues were identified as areas for improvement. Parents/caregivers wished for more options to input information to the system such as temporary glucose targets.

Conclusions: Parents/caregivers of very young children reported important quality of life benefits associated with using closed-loop, supporting adoption of this technology in this population.

Keywords: artificial pancreas; closed-loop insulin delivery; type 1 diabetes; very young children.

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Conflict of interest statement

M.T. reports having received speaker honoraria from Minimed Medtronic and Novo Nordisk. M.Fr. has received speaker honoraria from Minimed Medtronic and has served on advisory boards for Eli Lilly. J.K.M. is a member in the advisory board of Becton‐Dickinson, Boehringer Ingelheim, Eli Lilly, Medtronic and Sanofi, and has received speaker honoraria from Abbott Diabetes Care, Astra Zeneca, Eli Lilly, Nintamed, Novo Nordisk, Roche Diabetes Care, Sanofi, Servier, and Takeda. M.E.W. has received license fees from Becton‐Dickinson and has served as a consultant to Beckton‐Dickinson. S.E.H. declares speaker honoraria from Eli Lilly and Sanofi. E.F.R. reports having received speaker honoraria from Minimed Medtronic and Eli Lilly, serving on advisory boards for Eli Lilly. T.M.K. has received speaker honoraria from Minimed Medtronic, Roche, and Eli Lilly and is member of an advisory board for Abbott Diabetes Care. C.dB. has received speaker honoraria from Minimed Medtronic, and is member of their European Psychology Advisory Board. F.C. does attend Advisory Boards and obtain speaking fees for Abbott, Medtronic, Lilly, and NovoNordisk. B.R.M. reports having received speaker honoraria from Minimed Medtronic, Eli Lilly, Roche, Menarini, and Novo Nordisk, serving on advisory boards for Eli Lilly. R.H. reports having received speaker honoraria from Minimed Medtronic, Eli Lilly, BBraun, and Novo Nordisk, serving on advisory panel for Eli Lilly, receiving license fees from BBraun and Medtronic; and having served as a consultant to BBraun, Sanofi‐Aventis, and Profil. R.H. and M.E.W. report patents and patent applications. G.M., K.D., C.B., J.M.A., K.N., J.Y., E.M., D.S., M.Fi., U.S., A.G.T., D.A., H.K., S.S., N.A., J.S., N.C., C.K., and C.L.A. declare no competing financial interests exist.

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