Velojic-Golubovic Milena, Ciric Vojislav, Dimitrijevic Marija, Kovic Tijana, Mitic Milica, Olujic Biljana, Pevac Natasa, Radenkovic Sasa, Radojkovic Danijela, Vukadinovic Selena, Popovic Djordje S
Clinical Center Nis, Nis, Serbia.
Medical Faculty, University of Nis, Nis, Serbia.
Diabetes Ther. 2021 Jul;12(7):2049-2058. doi: 10.1007/s13300-021-01074-2. Epub 2021 Jun 23.
Insulin glargine 300 U/mL (Gla-300) is a novel glargine formulation which shows slower and more prolonged absorption following subcutaneous administration in comparison to insulin glargine 100 U/mL. In this prospective, observational, single-arm, multicenter, real-world study conducted in Serbia, we evaluated the effectiveness and safety of Gla-300 in patients with type 2 diabetes mellitus (T2DM) previously inadequately controlled with different basal or premix insulin therapy regimes.
A total of 350 patients with T2DM were enrolled by 27 physicians, from date of the first patient in (12 December 2017) to the date of last patient completed/last patient out (30 October 2018), from both medical centers and general hospitals. Patients' observation and data collection were performed at visit 1 (V1), i.e., the inclusion visit (3-6 months after Gla-300 introduction), including collection of retrospective data from the patients' medical charts at the time of Gla-300 introduction, and at visit 2 (V2) (3-6 months after V1). The primary objective was to assess the change in glycated hemoglobin (HbA1c) level from day of the Gla-300 initiation to the end of the observational period, while the secondary objectives included other effectiveness, as well as safety and other clinically relevant data.
The mean age of the 350 patients was 63.4 ± 8.4 years and 56.3% were female. The mean duration of diabetes was 13.4 ± 7.4 years, while the mean duration of insulin therapy prior to Gla-300 initiation was 5.3 ± 3.9 years. There was a significant reduction in HbA1c level at each visit compared to the previous visit (8.63 ± 1.52% at baseline prior to Gla-300 initiation, 7.87 ± 1.13% at V1, 7.45 ± 1.05% at V2; p < 0.01 vs. previous visit) accompanied by significant reduction of all hypoglycemic events (p < 0.01).
Initiation of Gla-300 therapy significantly improved glycemic control and reduced the risk of hypoglycemia in patients with T2DM inadequately controlled with different basal or premix insulin therapy regimes.
Sanofi Serbia.
甘精胰岛素300 U/mL(Gla-300)是一种新型甘精胰岛素制剂,与甘精胰岛素100 U/mL相比,皮下注射后吸收更缓慢、更持久。在塞尔维亚进行的这项前瞻性、观察性、单臂、多中心、真实世界研究中,我们评估了Gla-300在先前使用不同基础或预混胰岛素治疗方案控制不佳的2型糖尿病(T2DM)患者中的有效性和安全性。
27名医生从2017年12月1日第一名患者入组至2018年10月30日最后一名患者完成/退出,共招募了350例T2DM患者,来自医疗中心和综合医院。在第1次就诊(V1)即纳入就诊时(引入Gla-300后3 - 6个月)进行患者观察和数据收集,包括收集引入Gla-300时患者病历中的回顾性数据,并在第2次就诊(V2)(V1后3 - 6个月)进行。主要目标是评估从开始使用Gla-300至观察期结束时糖化血红蛋白(HbA1c)水平的变化,次要目标包括其他有效性指标以及安全性和其他临床相关数据。
350例患者的平均年龄为63.4±8.4岁,女性占56.3%。糖尿病平均病程为13.4±7.4年,开始使用Gla-300前胰岛素治疗的平均病程为5.3±3.9年。与上一次就诊相比,每次就诊时HbA1c水平均显著降低(开始使用Gla-300前基线时为8.63±1.52%,V1时为7.87±1.13%,V2时为7.45±1.05%;与上一次就诊相比,p<0.01),同时所有低血糖事件显著减少(p<0.01)。
对于先前使用不同基础或预混胰岛素治疗方案控制不佳的T2DM患者,开始使用Gla-300治疗可显著改善血糖控制并降低低血糖风险。
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