University of Cambridge
Wellcome-MRC Institute of Metabolic Science-Metabolic Research Laboratories and Medical Research Council Metabolic Diseases Unit
Julia Ware (née Fuchs) is a clinical research fellow with the Artificial Pancreas Group under Prof Hovorka at the University of Cambridge, and paediatric registrar at Addenbrooke’s Hospital, Cambridge University Hospitals NHS Foundation Trust. Dr Ware‘s current PhD research focuses on the impact of closed-loop technology on glycaemic control and quality of life in children and young people with type 1 diabetes. Her special interest is in very young children with type 1 diabetes, and investigating how optimising new technologies might ease diabetes burden and improve outcomes in this challenging population.

Presenter of 2 Presentations

KidsAP02 study – closed loop in very young children

Session Type
Industry Symposium
Date
Fri, 29.04.2022
Session Time
16:40 - 18:00
Room
Hall 118
Lecture Time
16:55 - 17:10

Closed-loop in very young children

Session Type
Parallel Session
Date
Thu, 28.04.2022
Session Time
13:00 - 14:30
Room
Hall 114
Lecture Time
13:00 - 13:20

Abstract

Abstract Body

It is well recognised that hybrid closed-loop insulin delivery improves glycaemic control and quality of life in older children and adolescents with type 1 diabetes, but data in very young children is limited. As a result, the majority of commercially available closed-loop systems are not licensed for use in this age-group. While challenging to manage at any age, maintaining recommended glycaemic control is particularly difficult in very young children, due to their high variability of insulin requirements and unpredictable eating and activity patterns. In this talk we discuss the specific challenges of diabetes management in very young children and how hybrid closed-loop therapy might address these. We review most recent published evidence in this age-group, including results of the longest randomised closed-loop study in very young children to date, which showed significant improvements in glycaemic control with closed-loop therapy. Finally, we identify areas for future research with regards to closed-loop technology tailored for very young children and how these might alleviate disease burden.

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