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The Efficacy and Safety of Saxagliptin in Haemodialysis Patients

机译:沙格列汀在血液透析患者中​​的疗效和安全性

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Introduction: Good glycaemic control without causing excessive hypoglycaemia reduced the risk of macrovascular and microvascular complications in type 2 DM patients on regular haemodialysis (HD). The objectives of this study were to assess the efficacy and safety of add-on saxagliptin to insulin therapy in blood sugar control compared to insulin therapy alone in diabetic patients undergoing HD. Design and Methods: In this prospective open-labelled randomized controlled trial, HD patients with type 2 DM and on stable insulin therapy with HbA1c 7% - 13% were randomized to receive add-on saxagliptin 2.5 mg once daily to insulin therapy or insulin therapy only for 12 weeks. Results: 24 patients were randomized into each arm equally. Baseline and week-12 serum HbA1c, fructosamine, fasting blood glucose (FBS) and mean self monitoring blood glucose (SMBG) were comparable in the groups. Reduction of HbA1c and mean SMBG were significant in both groups. There was a significant drop in fructosamine levels (p = 0.004) and trend of lower FBS (p = 0.097) in add-on saxagliptin group but not in insulin alone group. The incidence of hypoglycaemia was the same in both groups. Conclusion: Add-on saxagliptin to insulin is comparable to insulin therapy alone in blood sugar control in regular HD patients and is safe and generally well tolerated. Add-on saxagliptin group may have more persistent and less fluctuation of glucose control compared to insulin only group.
机译:简介:良好的血糖控制而不会引起过多的低血糖症,可降低定期进行血液透析(HD)的2型DM患者发生大血管和微血管并发症的风险。这项研究的目的是评估与接受HD治疗的糖尿病患者相比,沙格列汀对胰岛素治疗的血糖控制疗效和安全性。设计与方法:在这项前瞻性开放标签随机对照试验中,将患有2型DM且接受HbA1c 7 %-13 %稳定胰岛素治疗的HD患者随机分配至接受每日一次胰岛素治疗的2.5 mg附加沙格列汀或胰岛素治疗仅持续12周。结果:24名患者被平均分为两组。两组的基线和第12周血清HbA1c,果糖胺,空腹血糖(FBS)和平均自我监测血糖(SMBG)相当。两组中HbA1c和平均SMBG的降低均显着。附加沙格列汀组的果糖胺水平显着下降(p = 0.004),FBS降低的趋势(p = 0.097),而胰岛素单独组则没有。两组的低血糖发生率相同。结论:在正常的HD患者中,在胰岛素控制中添加沙格列汀可与单独使用胰岛素疗法相媲美,并且安全且耐受性良好。与仅使用胰岛素的组相比,添加的沙格列汀组可能具有更高的持久性和更少的血糖控制波动。

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