Teng Rhea, Kurian Martin, Close Kelly L, Buse John B, Peters Anne L, Alexander Charles M
Close Concerns, San Francisco, CA.
Division of Endocrinology, Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC.
Diabetes Spectr. 2021 Jan;34(1):42-51. doi: 10.2337/ds20-0038.
| Sodium-glucose cotransporter 2 (SGLT2) inhibitors are approved for type 1 diabetes in Europe and Japan, with off-label use in type 1 diabetes in the United States. Although there were no consistent approaches to risk mitigation in clinical trials of these agents, protocols have been developed to try to reduce the risk of diabetic ketoacidosis (DKA). However, a validated risk mitigation strategy does not exist. We reviewed available DKA risk mitigation protocols to better understand the various strategies currently in use. | We conducted a search of the published medical literature and other medical information sources, including conference presentations, for protocols. We then categorized the information provided into guidance on patient selection, initiation of SGLT2 inhibitors, ketone monitoring, necessary patient action in the event of ketosis or DKA, and inpatient treatment of ketosis or DKA. | Patient selection is generally similar among the protocols, although some require a minimum BMI and insulin dose. All protocols advocate routine measurement of ketones, although some insist on blood ketone tests. Although action steps for ketosis varies, all protocols advocate rapid patient intervention. The importance of evaluating ketones and acid-base balance even in the absence of hyperglycemia is emphasized by all protocols, as is the need to continue administering insulin until ketosis has resolved. | DKA risk mitigation must be pursued systematically in individuals with type 1 diabetes, although the best strategy remains to be determined. Given the ongoing need for adjunctive therapies in type 1 diabetes and current use of SGLT2 inhibitors for this purpose, additional education and research are crucial, especially in the hospital environment, where DKA may not be diagnosed promptly and treated appropriately.
钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂在欧洲和日本被批准用于1型糖尿病,在美国则用于1型糖尿病的非标签用药。尽管在这些药物的临床试验中,没有一致的风险缓解方法,但已经制定了方案来试图降低糖尿病酮症酸中毒(DKA)的风险。然而,尚未存在经过验证的风险缓解策略。我们回顾了现有的DKA风险缓解方案,以更好地了解目前正在使用的各种策略。
我们检索了已发表的医学文献和其他医学信息来源,包括会议报告,以查找相关方案。然后,我们将所提供的信息分类为关于患者选择、SGLT2抑制剂的起始使用、酮体监测、酮症或DKA发生时患者的必要行动以及酮症或DKA的住院治疗等方面的指导。
尽管有些方案要求最低体重指数(BMI)和胰岛素剂量,但各方案中的患者选择通常相似。所有方案都提倡常规检测酮体,尽管有些方案坚持进行血酮检测。尽管酮症的行动步骤各不相同,但所有方案都提倡对患者进行快速干预。所有方案都强调即使在没有高血糖的情况下评估酮体和酸碱平衡的重要性,以及在酮症消退之前继续使用胰岛素的必要性。
对于1型糖尿病患者,必须系统地采取DKA风险缓解措施,尽管最佳策略仍有待确定。鉴于1型糖尿病持续需要辅助治疗,以及目前为此目的使用SGLT2抑制剂,额外的教育和研究至关重要,尤其是在医院环境中,因为在那里DKA可能无法及时诊断和得到适当治疗。