Jin Bo-Yeong, Lee Sukyo, Kim Woosik, Park Jong-Hak, Cho Hanjin, Moon Sungwoo, Ahn Sejoong
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Republic of Korea.
Department of Emergency Medicine, Korea University Ansan Hospital, 123, Jeokgeum-ro, Danwon-gu, Ansan-si, Gyeonggi-do, 15355, Republic of Korea.
Ann Intensive Care. 2025 May 21;15(1):68. doi: 10.1186/s13613-025-01490-8.
In addition to glycemic control, the anti-inflammatory effects and protective effect of metformin on sepsis have been reported in animal studies, which may be beneficial for patients with septic shock. Few observational studies have evaluated metformin administration after sepsis or bacteremia; however, these studies did not specifically analyze septic shock or long-term outcomes. Therefore, this study aimed to evaluate the associations between metformin administration after septic shock and the short- and long-term survival in septic shock patients with type 2 diabetes mellitus.
This retrospective observational study used data from a prospectively collected sepsis registry. From October 2016 to June 2022, adult septic shock patients with type 2 diabetes mellitus were included in this study. The variable of interest was metformin administration within 48 h after diagnosis of septic shock. The 90-day mortality and 365-day mortality were evaluated as outcomes. A multivariable Cox proportional hazards model was conducted.
A total of 320 patients were included in the study. Metformin administration within 48 h after diagnosis of septic shock was associated with lower 90-day mortality (13.0% vs. 39.8%, P < 0.001), 365-day mortality (23.3% vs. 48.3%, P = 0.001), and in-hospital mortality (9.3% vs. 28.6%, P = 0.002) than those who did not administer metformin within 48 h. Metformin administration within 48 h was independently associated with decreased 90-day mortality (adjusted hazard ratio [aHR]: 0.371, 95% confidence interval [CI]: 0.153-0.900, P = 0.028) and 365-day mortality (aHR 0.453, 95% CI 0.219-0.937, P = 0.033) after adjusting for potential confounders. Similar results were found for metformin administration within 72 h after septic shock (aHR 0.433, 95% CI 0.235-0.797, P = 0.007 for 90-day mortality and aHR 0.450, 95% CI 0.264-0.767, P = 0.003 for 365-day mortality).
In septic shock patients with type 2 diabetes mellitus, metformin administration within 48 h was associated with lower 90-day and 365-day mortality. While these findings suggest potential benefits of metformin administration after septic shock, further large, multicenter studies are warranted.
除血糖控制外,动物研究已报道二甲双胍对脓毒症具有抗炎作用和保护作用,这可能对感染性休克患者有益。很少有观察性研究评估脓毒症或菌血症后使用二甲双胍的情况;然而,这些研究并未具体分析感染性休克或长期预后。因此,本研究旨在评估2型糖尿病感染性休克患者在感染性休克后使用二甲双胍与短期和长期生存之间的关联。
这项回顾性观察性研究使用了前瞻性收集的脓毒症登记数据。2016年10月至2022年6月,纳入了成年2型糖尿病感染性休克患者。感兴趣的变量是感染性休克诊断后48小时内使用二甲双胍的情况。将90天死亡率和365天死亡率作为结局进行评估。进行了多变量Cox比例风险模型分析。
本研究共纳入320例患者。感染性休克诊断后48小时内使用二甲双胍与90天死亡率较低(13.0%对39.8%,P<0.001)、365天死亡率较低(23.3%对48.3%,P=0.001)以及住院死亡率较低(9.3%对28.6%,P=0.002)相关,相比于在48小时内未使用二甲双胍的患者。在调整潜在混杂因素后,感染性休克诊断后48小时内使用二甲双胍与90天死亡率降低(调整后风险比[aHR]:0.371,95%置信区间[CI]:0.153 - 0.900,P=0.028)和365天死亡率降低(aHR 0.453,95%CI 0.219 - 0.937,P=0.033)独立相关。对于感染性休克后72小时内使用二甲双胍也发现了类似结果(90天死亡率aHR 0.433,95%CI 0.235 - 0.797,P=0.007;365天死亡率aHR 0.450,95%CI 0.264 - 0.767,P=0.003)。
在2型糖尿病感染性休克患者中,48小时内使用二甲双胍与较低的90天和365天死亡率相关。虽然这些发现提示感染性休克后使用二甲双胍可能有益,但仍需要进一步的大型多中心研究。