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Assessment of Meal Anticipation for Improving Fully Automated Insulin Delivery in Adults With Type 1 Diabetes.
Garcia-Tirado, Jose; Colmegna, Patricio; Villard, Orianne; Diaz, Jenny L; Esquivel-Zuniga, Rebeca; Koravi, Chaitanya L K; Barnett, Charlotte L; Oliveri, Mary C; Fuller, Morgan; Brown, Sue A; DeBoer, Mark D; Breton, Marc D.
Afiliação
  • Garcia-Tirado J; Center for Diabetes Technology, University of Virginia, Charlottesville, VA.
  • Colmegna P; University Clinic for Diabetes, Endocrinology, Nutritional Medicine, and Metabolism, Inselspital-University Hospital Bern, University of Bern, Bern, Switzerland.
  • Villard O; Center for Diabetes Technology, University of Virginia, Charlottesville, VA.
  • Diaz JL; Center for Diabetes Technology, University of Virginia, Charlottesville, VA.
  • Esquivel-Zuniga R; Department of Diabetes Endocrinology and Metabolism, CHU Montpellier, Montpellier, France.
  • Koravi CLK; Center for Diabetes Technology, University of Virginia, Charlottesville, VA.
  • Barnett CL; Department of Pediatrics, University of Virginia, Charlottesville, VA.
  • Oliveri MC; Center for Diabetes Technology, University of Virginia, Charlottesville, VA.
  • Fuller M; Center for Diabetes Technology, University of Virginia, Charlottesville, VA.
  • Brown SA; Center for Diabetes Technology, University of Virginia, Charlottesville, VA.
  • DeBoer MD; Center for Diabetes Technology, University of Virginia, Charlottesville, VA.
  • Breton MD; Center for Diabetes Technology, University of Virginia, Charlottesville, VA.
Diabetes Care ; 46(9): 1652-1658, 2023 09 01.
Article em En | MEDLINE | ID: mdl-37478323
OBJECTIVE: Meals are a consistent challenge to glycemic control in type 1 diabetes (T1D). Our objective was to assess the glycemic impact of meal anticipation within a fully automated insulin delivery (AID) system among adults with T1D. RESEARCH DESIGN AND METHODS: We report the results of a randomized crossover clinical trial comparing three modalities of AID systems: hybrid closed loop (HCL), full closed loop (FCL), and full closed loop with meal anticipation (FCL+). Modalities were tested during three supervised 24-h admissions, where breakfast, lunch, and dinner were consumed per participant's home schedule, at a fixed time, and with a 1.5-h delay, respectively. Primary outcome was the percent time in range 70-180 mg/dL (TIR) during the breakfast postprandial period for FCL+ versus FCL. RESULTS: Thirty-five adults with T1D (age 44.5 ± 15.4 years; HbA1c 6.7 ± 0.9%; n = 23 women and n = 12 men) were randomly assigned. TIR for the 5-h period after breakfast was 75 ± 23%, 58 ± 21%, and 63 ± 19% for HCL, FCL, and FCL+, respectively, with no significant difference between FCL+ and FCL. For the 2 h before dinner, time below range (TBR) was similar for FCL and FCL+. For the 5-h period after dinner, TIR was similar for FCL+ and FCL (71 ± 34% vs. 72 ± 29%; P = 1.0), whereas TBR was reduced in FCL+ (median 0% [0-0%] vs. 0% [0-0.8%]; P = 0.03). Overall, 24-h control for HCL, FCL, and FCL+ was 86 ± 10%, 77 ± 11%, and 77 ± 12%, respectively. CONCLUSIONS: Although postprandial control remained optimal with hybrid AID, both fully AID solutions offered overall TIR >70% with similar or lower exposure to hypoglycemia. Anticipation did not significantly improve postprandial control in AID systems but also did not increase hypoglycemic risk when meals were delayed.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 1 / Insulina Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Care Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 1 / Insulina Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Care Ano de publicação: 2023 Tipo de documento: Article