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    Ultrarapid Insulin Use Can Reduce Postprandial Hyperglycemia and Late Hypoglycemia, Even in Delayed Insulin Injections: A Connected Insulin Cap-Based Real-World Study

    Autor: 
    Gómez-Peralta, Fernando
    ;
    Valledor, Xoan
    ;
    López-Picado, Amanda
    ;
    Abreu, Cristina
    ;
    Fernández-Rubio, Elsa
    ;
    Cotovad, Laura
    ;
    Pujante, Pedro
    ;
    García-Fernández, Elena
    ;
    Azriel, Sharona
    ;
    Corcoy, Rosa
    ;
    Pérez-González, Jesús
    ;
    Ruiz-Valdepeñas, Luis
    Fecha: 
    2024
    Palabra clave: 
    insulin; Postprandial Hyperglycemia; Hypoglycemia; study; Scopus
    Revista / editorial: 
    Diabetes Technology & Therapeutics
    Citación: 
    Gómez-Peralta, F., Valledor, X., López-Picado, A., Abreu, C., Fernández-Rubio, E., Cotovad, L., ... & Ruiz-Valdepeñas, L. (2024). Ultrarapid Insulin Use Can Reduce Postprandial Hyperglycemia and Late Hypoglycemia, Even in Delayed Insulin Injections: A Connected Insulin Cap-Based Real-World Study. Diabetes Technology & Therapeutics, 26(1), 1-10.
    Tipo de Ítem: 
    Articulo Revista Indexada
    URI: 
    https://reunir.unir.net/handle/123456789/17323
    DOI: 
    https://doi.org/10.1089/dia.2023.0321
    Dirección web: 
    https://www.liebertpub.com/doi/pdf/10.1089/dia.2023.0321?download=true
    Resumen:
    Objectives: Reaching optimal postprandial glucose dynamics is a daily challenge for people with type 1 diabetes (T1D). This study aimed to analyze the postprandial hyperglycemic excursion (PHEs) and late postprandial hypoglycemia (LPH) risk according to prandial insulin time and type. Research Design and Methods: Real-world, retrospective study in T1D using multiple daily injections (MDI) analyzing 5 h of paired continuous glucose monitoring and insulin injections data collected from the connected cap Insulclock®. Meal events were identified using the rate of change detection methodology. Postprandial glucometrics and LPH (glucose <70 mg/dL 2–5 h after a meal) were evaluated according to insulin injection time and rapid (RI) or ultrarapid analog, Fiasp® (URI), use. Results: Meal glycemic excursions (n = 2488), RI: 1211, 48.7%; UR: 1277, 51.3%, in 82 people were analyzed according to injection time around the PHE: −45 to −15 min; −15 to 0 min; and 0 to +45 min. In 63% of the meals, insulin was injected after the PHE started. Lower PHE was observed with URI versus RI (glucose peak-baseline; mg/dL; mean ± standard deviation): 106.7 ± 35.2 versus 111.2 ± 40.3 (P = 0.003), particularly in 0/+45 injections: 111.6 ± 40.2 versus 118.1 ± 43.3; (P = 0.002). One third (29.1%) of participants added a second (correction) injection. The use of URI and avoiding a second injection were independently associated with less LPH risk, even in delayed injections (0/+45), (−36%, odds ratio [OR] 0.641; confidence interval [CI]: 0.462–0.909; P = 0.012) and −56% (OR 0.641; CI: 0.462–0.909 P = 0.038), respectively. Conclusions: URI analog use as prandial insulin reduces postprandial hyper- and hypoglycemia, even in delayed injections.
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