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2型糖尿病患者中钠-葡萄糖协同转运蛋白2抑制剂与败血症/感染性休克风险——基于全国医疗理赔数据的回顾性分析

Sodium-glucose cotransporter-2 inhibitor in risk of sepsis/septic shock among patients with type 2 diabetes mellitus-a retrospective analysis of nationwide medical claims data.

作者信息

Hu Wei-Syun, Lin Cheng-Li

机构信息

School of Medicine, College of Medicine, China Medical University, Taichung, Taiwan.

Division of Cardiovascular Medicine, Department of Medicine, China Medical University Hospital, 2, Yuh-Der Road, Taichung, 40447, Taiwan.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2024 Mar;397(3):1623-1631. doi: 10.1007/s00210-023-02685-1. Epub 2023 Sep 12.

Abstract

This research is an attempt to investigate the benefit of sodium-glucose cotransporter-2 inhibitor (SGLT2I) use in patients with diabetes mellitus (DM) for outcomes of sepsis/septic shock. We used Taiwan's national data set to identify patients and patients' characteristics to investigate sepsis/septic shock among diabetes patients who use SGLT2I compared to those who do not. We have compared the two groups for several relevant categories of potential risk factors for sepsis/septic shock and adjusted the Cox regression models accordingly. The adapted diabetes complications severity index (DCSI) was used for stratifying the advancing disease of DM. Compared to patients with DCSI = 0, patients with DCSI ≥ 2 had a significantly higher risk of sepsis/septic shock (adjusted HR = 1.52, 95% CI = 1.37-1.68). A significantly lower risk of sepsis/septic shock events was observed in the SGLT2I cohort than in the non-SGLT2I cohort with the DCSI groups [adjusted HR = 0.6 (DCSI group = 0), adjusted HR = 0.61 (DCSI group = 1), adjusted HR = 0.55 (DCSI group ≥ 2)]. Patients who received SGLT2I for a cumulative duration of ≥ 90 days had a significantly lower risk of sepsis/septic shock than patients with a duration of < 90 days (adjusted HR = 0.36, 95% CI = 0.34-0.39). We described a decreased risk of sepsis/septic shock among diabetic patients who took SGLT2I.

摘要

本研究旨在探讨使用钠-葡萄糖协同转运蛋白2抑制剂(SGLT2I)对糖尿病(DM)患者发生脓毒症/脓毒性休克结局的益处。我们利用台湾的全国数据集来确定患者及其特征,以调查使用SGLT2I的糖尿病患者与未使用该药物的患者相比发生脓毒症/脓毒性休克的情况。我们比较了两组在脓毒症/脓毒性休克潜在风险因素的几个相关类别方面的情况,并相应地调整了Cox回归模型。采用改良的糖尿病并发症严重程度指数(DCSI)对糖尿病进展性疾病进行分层。与DCSI = 0的患者相比,DCSI≥2的患者发生脓毒症/脓毒性休克的风险显著更高(调整后HR = 1.52,95%CI = 1.37 - 1.68)。在DCSI分组中,SGLT2I队列中脓毒症/脓毒性休克事件的风险显著低于非SGLT2I队列[调整后HR = 0.6(DCSI组 = 0),调整后HR = 0.61(DCSI组 = 1),调整后HR = 0.55(DCSI组≥2)]。接受SGLT2I累计持续时间≥90天的患者发生脓毒症/脓毒性休克的风险显著低于持续时间<90天的患者(调整后HR = 0.36,95%CI = 0.34 - 0.39)。我们描述了服用SGLT2I的糖尿病患者发生脓毒症/脓毒性休克的风险降低。

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