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.
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We are grateful to Health Data Science Center, China Medical University Hospital for providing administrative, technical, and funding support.
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This study is supported in part by the Taiwan Ministry of Health and Welfare Clinical Trial Center (MOHW112-TDU-B-212–144004), China Medical University (CMU110-AWARD-01), and China Medical University Hospital (DMR-HHC-110–4; DMR-111–105; DMR-112–009). No additional external funding was received for this study.
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Hu, WS., Lin, CL. 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. Naunyn-Schmiedeberg's Arch Pharmacol 397, 1623–1631 (2024). https://doi.org/10.1007/s00210-023-02685-1
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DOI: https://doi.org/10.1007/s00210-023-02685-1