دورية أكاديمية

A Randomized Controlled Trial Comparing Glargine U300 and Glargine U100 for the Inpatient Management of Medicine and Surgery Patients With Type 2 Diabetes: Glargine U300 Hospital Trial.

التفاصيل البيبلوغرافية
العنوان: A Randomized Controlled Trial Comparing Glargine U300 and Glargine U100 for the Inpatient Management of Medicine and Surgery Patients With Type 2 Diabetes: Glargine U300 Hospital Trial.
المؤلفون: Pasquel, Francisco J.1, Lansang, M. Cecilia2, Khowaja, Ameer3, Urrutia, M. Agustina1, Cardona, Saumeth1, Albury, Bonnie1, Galindo, Rodolfo J.1, Fayfman, Maya1, Davis, Georgia1, Migdal, Alexandra1, Vellanki, Priyathama1, Peng, Limin4, Umpierrez, Guillermo E.1 geumpie@emory.edu
المصدر: Diabetes Care. Jun2020, Vol. 43 Issue 6, p1242-1248. 7p.
مصطلحات موضوعية: *TYPE 2 diabetes, *RANDOMIZED controlled trials, *BLOOD sugar, *GLYCEMIC control, *HYPOGLYCEMIA, *GASTRIC bypass, *RESEARCH, *HEALTH facilities, *INTERNAL medicine, *RESEARCH methodology, *DEPARTMENTS, *HYPOGLYCEMIC agents, *MEDICAL cooperation, *EVALUATION research, *COMPARATIVE studies, *HOSPITAL care, *DOSE-effect relationship in pharmacology
مصطلحات جغرافية: MINNESOTA
مستخلص: Objective: The role of U300 glargine insulin for the inpatient management of type 2 diabetes (T2D) has not been determined. We compared the safety and efficacy of glargine U300 versus glargine U100 in noncritically ill patients with T2D.Research Design and Methods: This prospective, open-label, randomized clinical trial included 176 patients with poorly controlled T2D (admission blood glucose [BG] 228 ± 82 mg/dL and HbA1c 9.5 ± 2.2%), treated with oral agents or insulin before admission. Patients were treated with a basal-bolus regimen with glargine U300 (n = 92) or glargine U100 (n = 84) and glulisine before meals. We adjusted insulin daily to a target BG of 70-180 mg/dL. The primary end point was noninferiority in the mean difference in daily BG between groups. The major safety outcome was the occurrence of hypoglycemia.Results: There were no differences between glargine U300 and U100 in mean daily BG (186 ± 40 vs. 184 ± 46 mg/dL, P = 0.62), percentage of readings within target BG of 70-180 mg/dL (50 ± 27% vs. 55 ± 29%, P = 0.3), length of stay (median [IQR] 6.0 [4.0, 8.0] vs. 4.0 [3.0, 7.0] days, P = 0.06), hospital complications (6.5% vs. 11%, P = 0.42), or insulin total daily dose (0.43 ± 0.21 vs. 0.42 ± 0.20 units/kg/day, P = 0.74). There were no differences in the proportion of patients with BG <70 mg/dL (8.7% vs. 9.5%, P > 0.99), but glargine U300 resulted in significantly lower rates of clinically significant hypoglycemia (<54 mg/dL) compared with glargine U100 (0% vs. 6.0%, P = 0.023).Conclusions: Hospital treatment with glargine U300 resulted in similar glycemic control compared with glargine U100 and may be associated with a lower incidence of clinically significant hypoglycemia. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:01495992
DOI:10.2337/dc19-1940