Safety and Effectiveness of Sodium-Glucose Co-transporter 2 Inhibitors on Glycemic Control in Patients with Type 2 Diabetes Mellitus Fasting during Ramadan: A Review.

IF 2.7 Q3 ENDOCRINOLOGY & METABOLISM
Afif Nakhleh, Jomana Mazareeb, Said Darawshi, Amin Masri, Naim Shehadeh
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引用次数: 0

Abstract

This review evaluates the current evidence on the safety and efficacy of sodium-glucose cotransporter 2 (SGLT2) inhibitors for patients with type 2 diabetes mellitus (T2DM) fasting during Ramadan. All studies included in the review were conducted in Asia and the Middle East. Overall, the evidence suggests that SGLT2 inhibitors are a safe and effective treatment option for most T2DM patients fasting during Ramadan. The average incidence of symptomatic hypoglycemia is 12.5%, but ranges from 0.7% to 27%, depending on the study population and concomitant use of other medications. The risk of hypoglycemia is increased when SGLT2 inhibitors are used in combination with insulin and/or sulfonylureas. Therefore, patients taking SGLT2 inhibitors in combination with insulin and/or sulfonylureas can take steps to mitigate this risk, such as having their insulin and/or sulfonylurea doses adjusted and being closely monitored for hypoglycemia. Patients taking SGLT2 inhibitors may be at increased risk of dehydration. To mitigate the risk of dehydration, patients should be advised to consume adequate fluids during the fast-breaking hours. Further research is warranted to validate these findings and extend their applicability to high-risk populations and other regions of the world.

钠-葡萄糖协同转运体 2 抑制剂对斋月期间禁食的 2 型糖尿病患者血糖控制的安全性和有效性:综述。
本综述评估了钠-葡萄糖共转运体 2 (SGLT2) 抑制剂对在斋月期间禁食的 2 型糖尿病 (T2DM) 患者的安全性和有效性的现有证据。纳入综述的所有研究均在亚洲和中东地区进行。总体而言,有证据表明,对于大多数在斋月期间禁食的 T2DM 患者来说,SGLT2 抑制剂是一种安全有效的治疗选择。症状性低血糖的平均发生率为 12.5%,但根据研究人群和同时使用其他药物的不同,发生率从 0.7% 到 27% 不等。当 SGLT2 抑制剂与胰岛素和/或磺脲类药物合用时,发生低血糖的风险会增加。因此,SGLT2 抑制剂与胰岛素和/或磺脲类药物合用的患者可采取措施降低这一风险,例如调整胰岛素和/或磺脲类药物的剂量,并密切监测低血糖情况。服用 SGLT2 抑制剂的患者可能会增加脱水风险。为降低脱水风险,应建议患者在断食期间摄入充足的液体。还需要进一步研究来验证这些发现,并将其推广到高风险人群和世界其他地区。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
15
审稿时长
8 weeks
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