Glycemic Effects and Predictors of Increased Time-in-Range After Initiating MiniMed 670G: A 12-Month Observational Study

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Glycemic Effects and Predictors of Increased Time-in-Range After Initiating MiniMed 670G : A 12-Month Observational Study. / Jacobsen, Sabine Schade; Hommel, Eva; Ranjan, Ajenthen G.; Nørgaard, Kirsten.

In: Diabetes Technology & Therapeutics, Vol. 24, No. 8, 2022, p. 592-597.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jacobsen, SS, Hommel, E, Ranjan, AG & Nørgaard, K 2022, 'Glycemic Effects and Predictors of Increased Time-in-Range After Initiating MiniMed 670G: A 12-Month Observational Study', Diabetes Technology & Therapeutics, vol. 24, no. 8, pp. 592-597. https://doi.org/10.1089/dia.2021.0532

APA

Jacobsen, S. S., Hommel, E., Ranjan, A. G., & Nørgaard, K. (2022). Glycemic Effects and Predictors of Increased Time-in-Range After Initiating MiniMed 670G: A 12-Month Observational Study. Diabetes Technology & Therapeutics, 24(8), 592-597. https://doi.org/10.1089/dia.2021.0532

Vancouver

Jacobsen SS, Hommel E, Ranjan AG, Nørgaard K. Glycemic Effects and Predictors of Increased Time-in-Range After Initiating MiniMed 670G: A 12-Month Observational Study. Diabetes Technology & Therapeutics. 2022;24(8):592-597. https://doi.org/10.1089/dia.2021.0532

Author

Jacobsen, Sabine Schade ; Hommel, Eva ; Ranjan, Ajenthen G. ; Nørgaard, Kirsten. / Glycemic Effects and Predictors of Increased Time-in-Range After Initiating MiniMed 670G : A 12-Month Observational Study. In: Diabetes Technology & Therapeutics. 2022 ; Vol. 24, No. 8. pp. 592-597.

Bibtex

@article{0cb3deeee2eb4d5caca6b16d944cf996,
title = "Glycemic Effects and Predictors of Increased Time-in-Range After Initiating MiniMed 670G: A 12-Month Observational Study",
abstract = "We aimed to evaluate the glycemic effect and detect any predictors of improved time-in-range (TIR) in persons with type 1 diabetes after initiating hybrid closed-loop (HCL) treatment with MiniMed 670G in a 12-month retrospective observational study. Before starting HCL treatment, the 62 participants followed a Steno-developed training program; 7 participants (6.5%) discontinued the HCL therapy; the remaining 55 (58% female) had an age (mean +/- standard deviation) of 45.6 +/- 12.6 years and diabetes duration of 28.2 +/- 10.9 years. After 12 months' HCL therapy, glycated hemoglobin A1c decreased from 7.4% +0.7% to 7.1% +0.5%, TIR increased from 59.3% +/- 13.5% to 72% +/- 9.3%, time in 54-70 mg/dL (3.0-3.9 mM) decreased from 2.4% +/- 2.0% to 1.4% +/- 1.0%, and time in 180-250 mg/dL (10.0-13.9 mM) decreased from 26.4% +/- 8.3% to 20.8% +/- 5.5%, all P < 0.001. Improvement in TIR was significantly associated with lower total daily insulin dose, higher amount of total carbohydrate, and more time spent in Auto Mode. Our findings support the promising results on glycemic outcomes seen with HCL treatment.",
keywords = "Hybrid closed-loop, Type 1 diabetes, MiniMed 670G, Training, HYBRID CLOSED-LOOP, INSULIN DELIVERY-SYSTEM, ADULTS, ADOLESCENTS, THERAPY, PUMP",
author = "Jacobsen, {Sabine Schade} and Eva Hommel and Ranjan, {Ajenthen G.} and Kirsten N{\o}rgaard",
year = "2022",
doi = "10.1089/dia.2021.0532",
language = "English",
volume = "24",
pages = "592--597",
journal = "Diabetes Technology & Therapeutics",
issn = "1520-9156",
publisher = "Mary AnnLiebert, Inc. Publishers",
number = "8",

}

RIS

TY - JOUR

T1 - Glycemic Effects and Predictors of Increased Time-in-Range After Initiating MiniMed 670G

T2 - A 12-Month Observational Study

AU - Jacobsen, Sabine Schade

AU - Hommel, Eva

AU - Ranjan, Ajenthen G.

AU - Nørgaard, Kirsten

PY - 2022

Y1 - 2022

N2 - We aimed to evaluate the glycemic effect and detect any predictors of improved time-in-range (TIR) in persons with type 1 diabetes after initiating hybrid closed-loop (HCL) treatment with MiniMed 670G in a 12-month retrospective observational study. Before starting HCL treatment, the 62 participants followed a Steno-developed training program; 7 participants (6.5%) discontinued the HCL therapy; the remaining 55 (58% female) had an age (mean +/- standard deviation) of 45.6 +/- 12.6 years and diabetes duration of 28.2 +/- 10.9 years. After 12 months' HCL therapy, glycated hemoglobin A1c decreased from 7.4% +0.7% to 7.1% +0.5%, TIR increased from 59.3% +/- 13.5% to 72% +/- 9.3%, time in 54-70 mg/dL (3.0-3.9 mM) decreased from 2.4% +/- 2.0% to 1.4% +/- 1.0%, and time in 180-250 mg/dL (10.0-13.9 mM) decreased from 26.4% +/- 8.3% to 20.8% +/- 5.5%, all P < 0.001. Improvement in TIR was significantly associated with lower total daily insulin dose, higher amount of total carbohydrate, and more time spent in Auto Mode. Our findings support the promising results on glycemic outcomes seen with HCL treatment.

AB - We aimed to evaluate the glycemic effect and detect any predictors of improved time-in-range (TIR) in persons with type 1 diabetes after initiating hybrid closed-loop (HCL) treatment with MiniMed 670G in a 12-month retrospective observational study. Before starting HCL treatment, the 62 participants followed a Steno-developed training program; 7 participants (6.5%) discontinued the HCL therapy; the remaining 55 (58% female) had an age (mean +/- standard deviation) of 45.6 +/- 12.6 years and diabetes duration of 28.2 +/- 10.9 years. After 12 months' HCL therapy, glycated hemoglobin A1c decreased from 7.4% +0.7% to 7.1% +0.5%, TIR increased from 59.3% +/- 13.5% to 72% +/- 9.3%, time in 54-70 mg/dL (3.0-3.9 mM) decreased from 2.4% +/- 2.0% to 1.4% +/- 1.0%, and time in 180-250 mg/dL (10.0-13.9 mM) decreased from 26.4% +/- 8.3% to 20.8% +/- 5.5%, all P < 0.001. Improvement in TIR was significantly associated with lower total daily insulin dose, higher amount of total carbohydrate, and more time spent in Auto Mode. Our findings support the promising results on glycemic outcomes seen with HCL treatment.

KW - Hybrid closed-loop

KW - Type 1 diabetes

KW - MiniMed 670G

KW - Training

KW - HYBRID CLOSED-LOOP

KW - INSULIN DELIVERY-SYSTEM

KW - ADULTS

KW - ADOLESCENTS

KW - THERAPY

KW - PUMP

U2 - 10.1089/dia.2021.0532

DO - 10.1089/dia.2021.0532

M3 - Journal article

C2 - 35099298

VL - 24

SP - 592

EP - 597

JO - Diabetes Technology & Therapeutics

JF - Diabetes Technology & Therapeutics

SN - 1520-9156

IS - 8

ER -

ID: 325888857