Artificial Pancreas: Clinical Study in Latin America Without Premeal Insulin Boluses

Author:

Sánchez-Peña Ricardo12ORCID,Colmegna Patricio234,Garelli Fabricio25,De Battista Hernán25,García-Violini Demián12,Moscoso-Vásquez Marcela12ORCID,Rosales Nicolás5,Fushimi Emilia25,Campos-Náñez Enrique6,Breton Marc3,Beruto Valeria7,Scibona Paula7,Rodriguez Cintia7,Giunta Javier7,Simonovich Ventura7,Belloso Waldo H.7,Cherñavvsky Daniel7,Grosembacher Luis7

Affiliation:

1. Instituto Tecnológico de Buenos Aires, Buenos Aires, Argentina

2. National Scientific and Technical Research Council, Buenos Aires, Argentina

3. University of Virginia, Charlottesville, VA, USA

4. Universidad Nacional de Quilmes, Bernal, Buenos Aires, Argentina

5. Universidad Nacional de La Plata, La Plata, Buenos Aires Argentina

6. TypeZero Technologies, Inc, Charlottesville, VA, USA

7. Hospital Italiano de Buenos Aires, Buenos Aires, Argentina

Abstract

Background: Emerging therapies such as closed-loop (CL) glucose control, also known as artificial pancreas (AP) systems, have shown significant improvement in type 1 diabetes mellitus (T1DM) management. However, demanding patient intervention is still required, particularly at meal times. To reduce treatment burden, the automatic regulation of glucose (ARG) algorithm mitigates postprandial glucose excursions without feedforward insulin boluses. This work assesses feasibility of this new strategy in a clinical trial. Methods: A 36-hour pilot study was performed on five T1DM subjects to validate the ARG algorithm. Subjects wore a subcutaneous continuous glucose monitor (CGM) and an insulin pump. Insulin delivery was solely commanded by the ARG algorithm, without premeal insulin boluses. This was the first clinical trial in Latin America to validate an AP controller. Results: For the total 36-hour period, results were as follows: average time of CGM readings in range 70-250 mg/dl: 88.6%, in range 70-180 mg/dl: 74.7%, <70 mg/dl: 5.8%, and <50 mg/dl: 0.8%. Results improved analyzing the final 15-hour period of this trial. In that case, the time spent in range was 70-250 mg/dl: 94.7%, in range 70-180 mg/dl: 82.6%, <70 mg/dl: 4.1%, and <50 mg/dl: 0.2%. During the last night the time spent in range was 70-250 mg/dl: 95%, in range 70-180 mg/dl: 87.7%, <70 mg/dl: 5.0%, and <50 mg/dl: 0.0%. No severe hypoglycemia occurred. No serious adverse events were reported. Conclusions: The ARG algorithm was successfully validated in a pilot clinical trial, encouraging further tests with a larger number of patients and in outpatient settings.

Funder

Fundación Cellex

Juvenile Diabetes Research Foundation International

Publisher

SAGE Publications

Subject

Biomedical Engineering,Bioengineering,Endocrinology, Diabetes and Metabolism,Internal Medicine

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