2020
DOI: 10.1111/dom.14238
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Glycaemic profiles of diverse patients with type 2 diabetes using basal insulin: MOBILE study baseline data

Abstract: Basal insulin is often prescribed to patients with suboptimally controlled type 2 diabetes (T2D); however, its therapeutic efficacy is inadequate in many. During the MOBILE study's baseline phase, we evaluated 173 participants' continuous glucose monitoring (CGM) data (mean ± SD age 57 ± 9 years; 50% female; HbA1c 9.1% [range 7.1%‐11.6%]; 40% using sulphonylureas; 19% using NPH; reported self‐monitored blood glucose [SMBG] frequency median 1.0 checks/day) who were using basal, but not prandial insulin. Blinded… Show more

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Cited by 9 publications
(6 citation statements)
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“…Participants could be using any other antidiabetic medication in addition to basal insulin, provided the regimen had been stable for at least 3 months, but not prandial insulin. See eTable 1 in Supplement 2 and a prior publication for a complete listing of the inclusion and exclusion criteria. To characterize the cohort with respect to the generalization of the results, race and ethnicity were recorded through self-report by the study participants from a structured list of choices.…”
Section: Methodsmentioning
confidence: 60%
“…Participants could be using any other antidiabetic medication in addition to basal insulin, provided the regimen had been stable for at least 3 months, but not prandial insulin. See eTable 1 in Supplement 2 and a prior publication for a complete listing of the inclusion and exclusion criteria. To characterize the cohort with respect to the generalization of the results, race and ethnicity were recorded through self-report by the study participants from a structured list of choices.…”
Section: Methodsmentioning
confidence: 60%
“…Mean (±standard deviation [SD]) baseline HbA1c was 9.1% ± 0.9% and mean (±SD) baseline TIR 70–180 mg/dL was 40% ± 25%. 21 , 22 Potential participants were recruited from primary care practices and were not under the care of an endocrinologist to manage their diabetes. Participants could not have been using prandial insulin at the time of enrollment.…”
Section: Methodsmentioning
confidence: 99%
“…Written informed consent was obtained from each participant on entering the initial randomized trial. Methods for the initial 8-month randomized trial have been reported ( 6 , 7 ). Key aspects of the protocol are summarized below.…”
Section: Methodsmentioning
confidence: 99%