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• W1974082012 abstract "Abstract Aims/Introduction Early initiation of basal insulin therapy is recommended for normalizing fasting blood glucose in type 2 diabetes mellitus. However, basal insulin treatment might not adequately control postprandial glucose levels. The present study evaluated whether the combination of the α‐glucosidase inhibitor, acarbose, and basal insulin improved blood glucose control under daily‐life treatment conditions in a large sample of K orean patients. Materials and Methods The present study was a multicenter, prospective, observational study under daily‐life treatment conditions. A total of 539 patients with type 2 diabetes who were treated with basal insulin and additional acarbose were enrolled and followed up for 20 weeks. Changes in hemoglobin A 1c, fasting and postprandial blood glucose were evaluated at baseline and at the end of the observation period. The physician and patient satisfaction of the combination treatment and safety were assessed. Results Hemoglobin A 1c decreased by 0.55 ± 1.05% from baseline ( P < 0.0001). Fasting and postprandial blood glucose levels were reduced by 0.89 ± 3.79 and 2.59 ± 4.77 mmol/L (both P < 0.0001). The most frequently reported adverse drug reactions were flatulence (0.37%) and abnormal gastrointestinal sounds (0.37%), and all were mild in intensity and transient. In the satisfaction evaluation, 79.0% of physicians and 77.3% of patients were ‘very satisfied’ or ‘satisfied’ with the combined basal insulin and acarbose therapy. Conclusions Combination therapy of basal insulin and acarbose in patients with type 2 diabetes improved glucose control, and had no drug‐specific safety concerns, suggesting that the treatment might benefit individuals who cannot control blood glucose with basal insulin alone." @default.
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• W1974082012 date "2014-08-06" @default.
• W1974082012 modified "2023-10-03" @default.
• W1974082012 title "Combined use of basal insulin analog and acarbose reduces postprandial glucose in patients with uncontrolled type 2 diabetes" @default.
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• W1974082012 doi "https://doi.org/10.1111/jdi.12261" @default.
• W1974082012 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4364857" @default.
• W1974082012 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25802730" @default.
• W1974082012 hasPublicationYear "2014" @default.
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