Retrospective, observational study to see the effect of evogliptin on continuous glucose monitoring (CGM) in T2DM Indian patients: A real-world experience

A. Trailokya, S. Erande, Amol Aiwale
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Abstract

This study aimed to assess effectiveness of Evogliptin 5 mg through continues glucose monitoring (CGM) in patients with T2DM in retrospective observational real world settings. Overall 6 patients who received Evogliptin as routine clinical practice in management of T2DM were analyzed retrospectively from single center. Data collected from past medical records. FreeStyle Librepro 1.0.6 was used for CGM. CGM was done 15 days prior to adding Evogliptin and repeated immediately after that for next 15 days. Mean BG level, Percentage time in target range (80-140mg/dl), Percentage time above target and Percentage time below target were assessed prior and after adding Evogliptin in existing treatment regimen. Significant reduction in Mean blood glucose level seen after adding Evogliptin in existing treatment regimen from 215 mg/dl to 138 mg/dl (-77 mg/dl P=0.006). Significant improvement seen in Percentage time in target range (80-140mg/dl) from 17% to 44% (27% P value 0.007) and in Percentage time above target from 81% to 43% (- 38%, P valve 0.003). 13.5 % of the patients seen below target. Evogliptin was found to be effective when added to the patients who were uncontrolled on other oral anti-diabetic medications. It effectively showed improvement in continues glucose monitoring (CGM) parameters like Mean blood glucose, more number of patients were in Time in Target range i.e (80-140mg/dl) after adding Evogliptin to existing anti-diabetic medications & well tolerated. Small sample size and retrospective study
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回顾性观察研究,观察依格列汀对印度T2DM患者持续血糖监测(CGM)的影响:一个真实世界的经验
本研究旨在通过持续血糖监测(CGM)对T2DM患者进行回顾性观察,评估Evogliptin 5mg的有效性。对6例接受依格列汀治疗T2DM的患者进行单中心回顾性分析。从过去的医疗记录中收集数据。使用FreeStyle libpro 1.0.6进行CGM。在加入Evogliptin前15天进行CGM,随后立即重复15天。在现有治疗方案中加入依格列汀之前和之后,评估平均BG水平、达到目标范围(80-140mg/dl)的时间百分比、高于目标的时间百分比和低于目标的时间百分比。在现有治疗方案中加入Evogliptin后,平均血糖水平从215 mg/dl显著降低至138 mg/dl (-77 mg/dl P=0.006)。达到目标范围(80-140mg/dl)的时间百分比从17%提高到44% (27% P值为0.007),高于目标的时间百分比从81%提高到43% (- 38%,P值为0.003)。13.5%的患者低于目标。研究发现,在其他口服抗糖尿病药物不受控制的患者中加入依格列汀是有效的。在现有的抗糖尿病药物中加入依格列汀后,平均血糖等持续血糖监测(CGM)参数得到了有效改善,更多的患者在目标范围内(80-140mg/dl),并且耐受性良好。小样本和回顾性研究
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