首页> 外文期刊>Diabetes, obesity & metabolism >Sodium‐glucose co‐transporter inhibitors, their role in type 1 diabetes treatment and a risk mitigation strategy for preventing diabetic ketoacidosis: The STOP DKA Protocol
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Sodium‐glucose co‐transporter inhibitors, their role in type 1 diabetes treatment and a risk mitigation strategy for preventing diabetic ketoacidosis: The STOP DKA Protocol

机译:钠葡萄糖共转运蛋白抑制剂,它们在1型糖尿病治疗中的作用和预防糖尿病ketoacidosis的风险缓解策略:止损DKA方案

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Abstract Recent phase 3 clinical trials have evaluated the impact of adding sodium‐glucose co‐transporter (SGLT) inhibitors to the type 1 diabetes armamentarium. These trials studied SGLT2 inhibitors (dapagliflozin and empagliflozin) and a dual SGLT1 and SGLT2 inhibitor (sotagliflozin), and demonstrated that these oral non‐insulin antihyperglycaemic medications are able not only to improve glycaemic control, but also to reduce body weight and extend time in range without increasing rates of hypoglycaemia in type 1 diabetes. Diabetic ketoacidosis (DKA) is a feature of type 1 diabetes and the risk is increased when SGLT inhibitors are used in type 1 diabetes. To minimize the risk of DKA and still gain the multiple benefits, we developed the “STOP DKA Protocol “, an easily accessible and practical tool, that provides a risk mitigation strategy for reducing DKA in patients with type 1 diabetes being treated with SGLT inhibitors.
机译:摘要近期第3期临床试验评估了将钠 - 葡萄糖共转运蛋白(SGlT)抑制剂添加到1型糖尿病患者的影响。 这些试验研究了SGLT2抑制剂(Dapagliflozin和Empagliflozin)和双Sglt1和Sotaglit2抑制剂(Sotagliflozin),并证明这些口腔非胰岛素抗血糖药物不仅能够改善血糖控制,还可以降低体重并延长时间 范围而不增加1型糖尿病患者的低血糖率。 糖尿病酮症症(DKA)是1型糖尿病的特征,当SGLT抑制剂用于1型糖尿病时,风险增加。 为了最大限度地减少DKA的风险并仍然获得多种效益,我们开发了“停止DKA协议”,易于访问和实用的工具,为减少用SGLT抑制剂治疗1型糖尿病患者减少DKA的风险缓解策略。

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