How does a predictive low glucose suspend (PLGS) system tackle pediatric lifespan challenges in diabetes treatment? Real world data analysis.


Journal

Pediatric diabetes
ISSN: 1399-5448
Titre abrégé: Pediatr Diabetes
Pays: Denmark
ID NLM: 100939345

Informations de publication

Date de publication:
03 2020
Historique:
received: 05 05 2019
revised: 17 09 2019
accepted: 28 10 2019
pubmed: 13 11 2019
medline: 17 2 2021
entrez: 13 11 2019
Statut: ppublish

Résumé

The aim of the study was to assess the benefits of a predictive low glucose suspend (PLGS) system in real-life in children and adolescents with type 1 diabetes of different age and age-related clinical challenges. Real life retrospective and descriptive analysis included 44 children (26 girls) with type 1 diabetes who were introduced to PLGS system. We divided them in three age groups: I (3-6 years old, n = 12), II (7-10 y/o, n = 16), III (11-19 y/o, n = 16). All children and their caregivers received unified training in self-management during PLGS therapy. Patients' data included: age, HbA1C levels, sex. While from the CGM metric, we obtained: time of sensor use (SENSuse), time in range (TiR): in, below and over target range and average blood glycemia (AVG), insulin suspension time (INSsusp). SENSuse was 93% in total, with 92%, 94%, and 87% in age groups I, II, III, respectively. In total the reduction of mean HbA1C from 7.61% to 6.88% (P < .05), while for the I, II, and III it was 7.46% to 6.72%, 6.91% to 6.41%, and 8.46 to 7.44%, respectively (P < .05). Although we observed a significant reduction of HbA1C, the time below target range was minimal. Specific findings included: group I-longest INSsusp (17%), group II-lowest glycemic variability (CV) (36%), and group III-highest AVG (169 mg/dL). There was a reverse correlation between suspend before low and age (-0.32, P < .05). In group I CV reduced TiR in target range (TiRin) (-0.82, P < .05), in group II use of complex boluses increased TiRin (0.52, P < .05). In group III higher CV increased HbA1C (0.64, P < .05) while reducing TiRin (-0.72, P < .05). PLGS is a suitable and safe therapeutic option for children with diabetes of all age and it is effective in addressing age-specific challenges. PLGS improves glycemic control in children of all age, positively affecting its different parameters.

Identifiants

pubmed: 31715059
doi: 10.1111/pedi.12944
doi:

Substances chimiques

Blood Glucose 0
Hypoglycemic Agents 0
Insulin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

280-287

Informations de copyright

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Auteurs

Władysław B Gaweł (WB)

Students' Scientific Association at the Department of Children's Diabetology, Medical University of Silesia, Katowice, Poland.

Grażyna Deja (G)

Department of Children's Diabetology, Medical University of Silesia, Katowice, Poland.

Halla Kamińska (H)

Department of Children's Diabetology, Medical University of Silesia, Katowice, Poland.

Aleksandra Tabor (A)

Students' Scientific Association at the Department of Children's Diabetology, Medical University of Silesia, Katowice, Poland.

Eliza Skała-Zamorowska (E)

Department of Children's Diabetology, Medical University of Silesia, Katowice, Poland.

Przemysława Jarosz-Chobot (P)

Department of Children's Diabetology, Medical University of Silesia, Katowice, Poland.

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