Clinical Management and Pump Parameter Adjustment of the Control-IQ Closed-Loop Control System: Results from a 6-Month, Multicenter, Randomized Clinical Trial

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O'Malley, Grenye | Messer, Laurel | Levy, Carol | Pinsker, Jordan | Forlenza, Gregory | Isganaitis, Elvira | Kudva, Yogish | Ekhlaspour, Laya | Raghinaru, Dan | Lum, John | Brown, Sue | Kovatchev, Boris | Anderson, Stacey | Emory, Emma | Voelmle, Mary | Conshafter, Katie | Morris, Kim | Oliveri, Mary | Gondor-Fredrick, Linda | Mitchell, Harry | Calvo, Kayla | Wakeman, Christian | Breton, Marc | Laffel, Lori | Ambler-Osborn, Louise | Flint, Emily | Kim, Kenny | Roethke, Lindsay | Church, Mei Mei | Andre, Camille | Piper, Molly | Lam, David | Levister, Camilla | Ogyaadu, Selassie | Lovett, Jessica | Simha, Vinaya | Dadlani, Vikash | Mccrady-Spitzer, Shelly | Reid, Corey | Kumari, Kanchan | Wadwa, R. Paul | Alonso, G. Todd | Slover, Robert | Jost, Emily | Berget, Cari | Towers, Lindsey | Rossick-Solis, Alex | Buckingham, Bruce | Jacobson, Tali | Town, Marissa | Tabatabai, Ideen | Keller, Jordan | Salas, Evalina | Paulson, John | Beck, J.L. Roy | Passman, Samantha | Campos, Tiffany | Kollman, D.R. Craig | Murphy, Carlos | Patibandla, Nandan | Borgman, Sarah | Arreza-Rubin, Guillermo | Eggerman, Thomas | Green, Neal | Renard, Eric | Cobelli, Claudio | Reznik, Yves | Beck., J.L. Roy

Edité par CCSD ; Mary Ann Liebert -

International audience. Background: Data are limited on the need for and benefits of pump setting optimization with automated insulin delivery. We examined clinical management of a closed-loop control (CLC) system and its relationship to glycemic outcomes. Materials and Methods: We analyzed personal parameter adjustments in 168 participants in a 6-month multicenter trial of CLC with Control-IQ versus sensor-augmented pump (SAP) therapy. Preset parameters (BR = basal rates, CF = correction factors, CR = carbohydrate ratios) were optimized at randomization, 2 and 13 weeks, for safety issues, participant concerns, or initiation by participants' usual diabetes care team. Time in range (TIR 70-180 mg/dL) was compared in the week before and after parameter changes. Results: In 607 encounters for parameter changes, there were fewer adjustments for CLC than SAP (3.4 vs. 4.1/participant). Adjustments involved BR (CLC 69%, SAP 80%), CR (CLC 68%, SAP 50%), CF (CLC 44%, SAP 41%), and overnight parameters (CLC 62%, SAP 75%). TIR before and after adjustments was 71.2% and 71.3% for CLC and 61.0% and 62.9% for SAP. The highest baseline HbA1c CLC subgroup had the largest TIR improvement (51.2% vs. 57.7%). When a CR was made more aggressive in the CLC group, postprandial time >180 mg/dL was 43.1% before the change and 36.0% after the change. The median postprandial time <70 mg/dL before making CR less aggressive was 1.8%, and after the change was 0.7%. Conclusions: No difference in TIR was detected with parameter changes overall, but they may have an effect in higher HbA1c subgroups or following user-directed boluses, suggesting that changes may matter more in suboptimal control or during discrete periods of the day. Clinical Trials Registration number: NCT03563313.

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