Rossetti, P.; Quirós, C.; Moscardo-Garcia, V.; Comas, A.; Giménez, M.; Ampudia-Blasco, F.; León, F.... (2017). Closed-Loop Control of Postprandial Glycemia Using an Insulin-on-Board Limitation Through Continuous Action on Glucose Target. Diabetes Technology & Therapeutics. 19(6):355-362. https://doi.org/10.1089/dia.2016.0443
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/148245
Título:
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Closed-Loop Control of Postprandial Glycemia Using an Insulin-on-Board Limitation Through Continuous Action on Glucose Target
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Autor:
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Rossetti, P.
Quirós, C.
Moscardo-Garcia, Vanessa
Comas, A.
Giménez, M.
Ampudia-Blasco, F.J.
León, F.
Montaser Roushdi Ali, Eslam
Conget, I.
Bondía Company, Jorge
Vehí, J.
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Entidad UPV:
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Universitat Politècnica de València. Departamento de Ingeniería de Sistemas y Automática - Departament d'Enginyeria de Sistemes i Automàtica
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Fecha difusión:
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Resumen:
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[EN] Background: Postprandial (PP) control remains a challenge for closed-loop (CL) systems. Few studies with inconsistent results have systematically investigated the PP period.
Objective: To compare a new CL algorithm ...[+]
[EN] Background: Postprandial (PP) control remains a challenge for closed-loop (CL) systems. Few studies with inconsistent results have systematically investigated the PP period.
Objective: To compare a new CL algorithm with current pump therapy (open loop [OL]) in the PP glucose control in type 1 diabetes (T1D) subjects.
Methods: A crossover randomized study was performed in two centers. Twenty T1D subjects (F/M 13/7, age 40.7 -10.4 years, disease duration 22.6 +/- 9.9 years, and A1c 7.8% +/- 0.7%) underwent an 8-h mixed meal test on four occasions. In two (CL1/CL2), after meal announcement, a bolus was given followed by an algorithmdriven basal infusion based on continuous glucose monitoring (CGM). Alternatively, in OL1/OL2 conventional pump therapy was used. Main outcome measures were as follows: glucose variability, estimated with the coefficient of variation (CV) of the area under the curve (AUC) of plasma glucose (PG) and CGM values, and from the analysis of the glucose time series; mean, maximum (C-max), and time to C-max glucose concentrations and time in range (<70, 70-180, >180 mg/dL).
Results: CVs of the glucose AUCs were low and similar in all studies (around 10%). However, CL achieved greater reproducibility and better PG control in the PP period: CL1 = CL2<OL1<OL2 (PG(mean) 123 +/- 47 and 125 +/- 44 vs. 152 +/- 53 and 159 +/- 54 mg/dL) and C-max OL 217.1 +/- 67.0 mg/dL versus CL 183.3 +/- 63.9 mg/dL, P < 0.0001. Time-in-range was higher with CL versus OL (80% vs. 64%; P < 0.001). Neither the time below 70 mg/dL (CL 6.1% vs. OL 3.2%; P > 0.05) nor the need for oral glucose was significantly different (CL 40.0% vs. OL 22.5% of meals; P = 0.054).
Conclusions: This novel CL algorithm effectively and consistently controls PP glucose excursions without increasing hypoglycemia. Study registered at ClinicalTrials.gov: study number NCT02100488.
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Palabras clave:
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Artificial pancreas
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Glucose control
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Postprandial
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Derechos de uso:
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Reserva de todos los derechos
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Fuente:
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Diabetes Technology & Therapeutics. (issn:
1520-9156
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DOI:
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10.1089/dia.2016.0443
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Editorial:
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Mary Ann Liebert
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Versión del editor:
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https://doi.org/10.1089/dia.2016.0443
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Código del Proyecto:
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info:eu-repo/grantAgreement/MINECO//DPI2013-46982-C2-2-R/ES/NUEVOS METODOS PARA LA EFICIENCIA Y SEGURIDAD DEL PANCREAS ARTIFICIAL DOMICILIARIO EN DIABETES TIPO 1/
info:eu-repo/grantAgreement/MINECO//DPI2013-46982-C2-1-R/ES/NUEVOS METODOS PARA LA EFICIENCIA Y SEGURIDAD DEL PANCREAS ARTIFICIAL DOMICILIARIO EN DIABETES TIPO 1/
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Descripción:
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This is a copy of an article published in the Diabetes Technology & Therapeutics © 2017 [copyright Mary Ann Liebert, Inc.]; Diabetes Technology & Therapeutics is available online at: https://www.liebertpub.com/.
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Agradecimientos:
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This work was supported by the Spanish Ministry of Economy and Competitiveness through Grants DPI2013-46982-C2-1-R and DPI2013-46982-C2-2-R, and the EU through FEDER funds. C.Q. is the recipient of a grant from the Hospital ...[+]
This work was supported by the Spanish Ministry of Economy and Competitiveness through Grants DPI2013-46982-C2-1-R and DPI2013-46982-C2-2-R, and the EU through FEDER funds. C.Q. is the recipient of a grant from the Hospital Clinic i Universitari of Barcelona ("Ajut a la recerca Josep Font 2014-2017").
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Tipo:
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Artículo
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