A comparison of two hybrid closed-loop systems in adolescents and young adults with type 1 diabetes (FLAIR): a multicentre, randomised, crossover trial.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
16 01 2021
Historique:
received: 18 09 2020
revised: 02 11 2020
accepted: 10 11 2020
entrez: 17 1 2021
pubmed: 18 1 2021
medline: 23 2 2021
Statut: ppublish

Résumé

Management of type 1 diabetes is challenging. We compared outcomes using a commercially available hybrid closed-loop system versus a new investigational system with features potentially useful for adolescents and young adults with type 1 diabetes. In this multinational, randomised, crossover trial (Fuzzy Logic Automated Insulin Regulation [FLAIR]), individuals aged 14-29 years old, with a clinical diagnosis of type 1 diabetes with a duration of at least 1 year, using either an insulin pump or multiple daily insulin injections, and glycated haemoglobin (HbA Between June 3 and Aug 22, 2019, 113 individuals were enrolled into the trial. Mean age was 19 years (SD 4) and 70 (62%) of 113 participants were female. Mean proportion of time with daytime glucose levels above 180 mg/dL (>10·0 mmol/L) was 42% (SD 13) at baseline, 37% (9) during use of the 670G system, and 34% (9) during use of the advanced hybrid closed-loop system (mean difference [advanced hybrid closed-loop system minus 670G system] -3·00% [95% CI -3·97 to -2·04]; p<0·0001). Mean 24-h proportion of time with glucose levels below 54 mg/dL (<3·0 mmol/L) was 0·46% (SD 0·42) at baseline, 0·50% (0·35) during use of the 670G system, and 0·46% (0·33) during use of the advanced hybrid closed-loop system (mean difference [advanced hybrid closed-loop system minus 670G system] -0·06% [95% CI -0·11 to -0·02]; p<0·0001 for non-inferiority). One severe hypoglycaemic event occurred in the advanced hybrid closed-loop system group, determined to be unrelated to study treatment, and none occurred in the 670G group. Hyperglycaemia was reduced without increasing hypoglycaemia in adolescents and young adults with type 1 diabetes using the investigational advanced hybrid closed-loop system compared with the commercially available MiniMed 670G system. Testing an advanced hybrid closed-loop system in populations that are underserved due to socioeconomic factors and testing during pregnancy and in individuals with impaired awareness of hypoglycaemia would advance the effective use of this technology FUNDING: National Institute of Diabetes and Digestive and Kidney Diseases.

Sections du résumé

BACKGROUND
Management of type 1 diabetes is challenging. We compared outcomes using a commercially available hybrid closed-loop system versus a new investigational system with features potentially useful for adolescents and young adults with type 1 diabetes.
METHODS
In this multinational, randomised, crossover trial (Fuzzy Logic Automated Insulin Regulation [FLAIR]), individuals aged 14-29 years old, with a clinical diagnosis of type 1 diabetes with a duration of at least 1 year, using either an insulin pump or multiple daily insulin injections, and glycated haemoglobin (HbA
FINDINGS
Between June 3 and Aug 22, 2019, 113 individuals were enrolled into the trial. Mean age was 19 years (SD 4) and 70 (62%) of 113 participants were female. Mean proportion of time with daytime glucose levels above 180 mg/dL (>10·0 mmol/L) was 42% (SD 13) at baseline, 37% (9) during use of the 670G system, and 34% (9) during use of the advanced hybrid closed-loop system (mean difference [advanced hybrid closed-loop system minus 670G system] -3·00% [95% CI -3·97 to -2·04]; p<0·0001). Mean 24-h proportion of time with glucose levels below 54 mg/dL (<3·0 mmol/L) was 0·46% (SD 0·42) at baseline, 0·50% (0·35) during use of the 670G system, and 0·46% (0·33) during use of the advanced hybrid closed-loop system (mean difference [advanced hybrid closed-loop system minus 670G system] -0·06% [95% CI -0·11 to -0·02]; p<0·0001 for non-inferiority). One severe hypoglycaemic event occurred in the advanced hybrid closed-loop system group, determined to be unrelated to study treatment, and none occurred in the 670G group.
INTERPRETATION
Hyperglycaemia was reduced without increasing hypoglycaemia in adolescents and young adults with type 1 diabetes using the investigational advanced hybrid closed-loop system compared with the commercially available MiniMed 670G system. Testing an advanced hybrid closed-loop system in populations that are underserved due to socioeconomic factors and testing during pregnancy and in individuals with impaired awareness of hypoglycaemia would advance the effective use of this technology FUNDING: National Institute of Diabetes and Digestive and Kidney Diseases.

Identifiants

pubmed: 33453783
pii: S0140-6736(20)32514-9
doi: 10.1016/S0140-6736(20)32514-9
pmc: PMC9194961
mid: NIHMS1672134
pii:
doi:

Substances chimiques

Insulin 0

Banques de données

ClinicalTrials.gov
['NCT03040414']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

208-219

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK036836
Pays : United States
Organisme : NIDDK NIH HHS
ID : UC4 DK108611
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

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Auteurs

Richard M Bergenstal (RM)

International Diabetes Center, HealthPartners Institute, Minneapolis, MN, USA. Electronic address: richard.bergenstal@parknicollet.com.

Revital Nimri (R)

Schneider Children's Medical Center, Petah Tikva, Israel.

Roy W Beck (RW)

Jaeb Center for Health Research Foundation, Tampa, FL, USA.

Amy Criego (A)

International Diabetes Center, HealthPartners Institute, Minneapolis, MN, USA.

Lori Laffel (L)

Joslin Diabetes Center, Harvard Medical School, Boston, MA, USA.

Desmond Schatz (D)

Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, USA.

Tadej Battelino (T)

University Medical Center Ljubljana, University Children's Hospital, and Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.

Thomas Danne (T)

Auf der Bult Centre for Children and Adolescents, Diabetology, Endocrinology and General Paediatrics, Hannover, Germany.

Stuart A Weinzimer (SA)

Department of Pediatrics, Yale University, New Haven, CT, USA.

Judy Sibayan (J)

Jaeb Center for Health Research Foundation, Tampa, FL, USA.

Mary L Johnson (ML)

International Diabetes Center, HealthPartners Institute, Minneapolis, MN, USA.

Ryan J Bailey (RJ)

Jaeb Center for Health Research Foundation, Tampa, FL, USA.

Peter Calhoun (P)

Jaeb Center for Health Research Foundation, Tampa, FL, USA.

Anders Carlson (A)

International Diabetes Center, HealthPartners Institute, Minneapolis, MN, USA.

Elvira Isganaitis (E)

Joslin Diabetes Center, Harvard Medical School, Boston, MA, USA.

Rachel Bello (R)

Schneider Children's Medical Center, Petah Tikva, Israel.

Anastasia Albanese-O'Neill (A)

Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, USA.

Klemen Dovc (K)

University Medical Center Ljubljana, University Children's Hospital, and Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.

Torben Biester (T)

Auf der Bult Centre for Children and Adolescents, Diabetology, Endocrinology and General Paediatrics, Hannover, Germany.

Kate Weyman (K)

Department of Pediatrics, Yale University, New Haven, CT, USA.

Korey Hood (K)

Stanford University School of Medicine, Stanford Diabetes Research Center, Palo Alto, CA, USA.

Moshe Phillip (M)

Schneider Children's Medical Center, Petah Tikva, Israel.

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