Sebastian-Valles Fernando, Tapia-Sanchiz Maria Sara, Navas-Moreno Victor, Lopez-Ruano Marta, Martínez-Otero Carmen, Carrillo-López Elena, Sager La Ganga Carolina, Raposo-López Juan José, Amar Selma, González-Castañar Sara, Von Wernitz Teleki Andres, Del Arco Carmen, Arranz-Martín Jose Alfonso, Marazuela Mónica
Department of Endocrinology and Nutrition, Universidad Autónoma de Madrid, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria de La Princesa, Diego de León 62, 28005, Madrid, Spain.
Emergency Department, Hospital Universitario de La Princesa, Madrid, Spain.
Intern Emerg Med. 2025 Mar;20(2):431-440. doi: 10.1007/s11739-024-03813-2. Epub 2024 Nov 18.
SGLT-2 inhibitors (SGLT-2i) are linked to a higher risk of diabetic ketoacidosis (DKA). However, it is still unclear whether the severity of SGLT-2i associated DKA is higher. This is a retrospective cohort study with patients admitted for DKA at a tertiary hospital (2013-2024). Patients were matched by propensity score for age, sex, diabetes duration, type, and ischemic heart disease. ICU admission risk and clinical severity were compared between SGLT-2i users and controls. The matched sample included 105 subjects (35 SGLT-2i users, 70 controls). The average age was 63.1 ± 15.4 years, and 40 (38.1%) patients were women. ICU admission was higher in the treatment group (65.7% versus 24.6%, p < 0.001). A conditional logistic regression showed higher risk of ICU admission in the treatment group (odds ratio 12.7, 95% confidence interval 1.9-84.3, p = 0.009) after adjusting for confounding factors. The treatment group exhibited less favorable blood gas results (pH 7.10 ± 0.17 vs 7.18 ± 0.16, p = 0.024) and shorter symptom duration (2 [1-3] vs 3 [2-7] days, p < 0.002). No significant differences were found in diabetes type, ketonemia, creatinine, or DKA precipitating factors. DKA in patients with diabetes treated with SGLT-2i is associated with more severe acidosis with quicker onset, leading to higher risk of ICU admission compared to patients not receiving this treatment. We recommend temporary discontinuation of SGLT-2i during any acute event until resolution, regardless of diabetes type or the patient's glycemic control.
钠-葡萄糖协同转运蛋白2抑制剂(SGLT-2i)与糖尿病酮症酸中毒(DKA)风险升高有关。然而,SGLT-2i相关DKA的严重程度是否更高仍不清楚。这是一项对一家三级医院(2013年至2024年)因DKA入院患者的回顾性队列研究。通过倾向评分对患者的年龄、性别、糖尿病病程、类型和缺血性心脏病进行匹配。比较SGLT-2i使用者和对照组的重症监护病房(ICU)入院风险和临床严重程度。匹配样本包括105名受试者(35名SGLT-2i使用者,70名对照组)。平均年龄为63.1±15.4岁,40名(38.1%)患者为女性。治疗组的ICU入院率更高(65.7%对24.6%,p<0.001)。条件逻辑回归显示,在调整混杂因素后,治疗组的ICU入院风险更高(比值比12.7,95%置信区间1.9-84.3,p=0.009)。治疗组的血气结果较差(pH值7.10±0.17对7.18±0.16,p=0.024),症状持续时间较短(2[1-3]天对3[2-7]天,p<0.002)。在糖尿病类型、酮血症、肌酐或DKA诱发因素方面未发现显著差异。与未接受该治疗的患者相比,接受SGLT-2i治疗的糖尿病患者发生的DKA与更严重的酸中毒和更快的发作有关,导致ICU入院风险更高。我们建议在任何急性事件期间暂时停用SGLT-2i,直至病情缓解,无论糖尿病类型或患者的血糖控制情况如何。