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Glycemic Outcomes in Baseline Hemoglobin A1C Subgroups in the International Diabetes Closed-Loop Trial.
Ekhlaspour, Laya; Town, Marissa; Raghinaru, Dan; Lum, John W; Brown, Sue A; Buckingham, Bruce A.
Affiliation
  • Ekhlaspour L; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics, Center for Academic Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Town M; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics, Center for Academic Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Raghinaru D; Jaeb Center for Health Research, Tampa, Florida, USA.
  • Lum JW; Jaeb Center for Health Research, Tampa, Florida, USA.
  • Brown SA; University of Virginia Center for Diabetes Technology, Charlottesville, Virginia, USA.
  • Buckingham BA; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics, Center for Academic Medicine, Stanford University School of Medicine, Stanford, California, USA.
Diabetes Technol Ther ; 24(8): 588-591, 2022 08.
Article in En | MEDLINE | ID: mdl-35020488
ABSTRACT
Using a closed-loop system significantly improves time in range (TIR) 70-180 mg/dL in patients with type 1 diabetes (T1D). In a 6-month RCT, 112 subjects were randomly assigned to closed-loop control (Tandem Control-IQ) after obtaining 2 weeks of baseline Continuous glucose monitoring (CGM) data from sensor-augmented pump therapy. We compared glycemic outcomes from baseline to end of study among subgroups classified by baseline HbA1c levels. All HbA1c subgroups showed an improvement in TIR due to reduction of both hyperglycemia and hypoglycemia. Those with HbA1c <6.5% improved mostly by reducing nocturnal hypoglycemia due to the automated basal insulin adjustments. Those with HbA1c ≥8.5% improved mostly by reducing daytime and nocturnal hyperglycemia due to both automated basal insulin adjustments and correction boluses during the day. There does not appear to be any reason to exclude individuals with T1D from automated insulin delivery based on their HbA1c. Clinical Trial Identifier NCT03563313.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus, Type 1 / Hyperglycemia / Hypoglycemia Type of study: Clinical_trials Limits: Humans Language: En Journal: Diabetes Technol Ther Journal subject: ENDOCRINOLOGIA / TERAPEUTICA Year: 2022 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus, Type 1 / Hyperglycemia / Hypoglycemia Type of study: Clinical_trials Limits: Humans Language: En Journal: Diabetes Technol Ther Journal subject: ENDOCRINOLOGIA / TERAPEUTICA Year: 2022 Document type: Article Affiliation country: United States
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