ICU患者脑卒中后血糖-钾比值的死亡率:MIMIC-IV数据库分析。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY
Frontiers in Neurology Pub Date : 2025-04-16 eCollection Date: 2025-01-01 DOI:10.3389/fneur.2025.1578268
Zhen Yuan, Aoli Chen, Yunqing Zeng, Jiwei Cheng
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引用次数: 0

摘要

急性缺血性脑卒中(AIS)患者入住重症监护病房(ICU)死亡率高,需要早期识别预后不良的风险。本研究探讨了血糖钾比(GPR)与AIS患者预后的关系。方法:我们使用重症监护医学信息市场IV (MIMIC-IV)数据库的数据进行了回顾性队列研究。主要结局是ICU入院后28天、90天和1年的死亡率。采用多变量Cox比例风险回归模型估计校正风险比(hr),置信区间为95%。采用亚组分析、Kaplan-Meier生存曲线和限制性三次样条模型进一步评价AIS患者GPR与死亡率之间的关系。结果:研究共纳入2636例AIS患者,平均年龄69.4±15.6岁。1年死亡率为36.8% (n = 969)。调整混杂因素后,与第1四分位数(Q1, GPR≤1.39)相比,第2四分位数(Q2, 1.39 < GPR≤1.74)、第3四分位数(Q3, 1.74 < GPR≤2.25)和第4四分位数(Q4, GPR≥2.25)的1年死亡风险分别为HR = 1.17 (95% CI: 0.95-1.43, p = 0.132)、HR = 1.42 (95% CI: 1.17-1.73, p < 0.001)和HR = 1.61 (95% CI: 1.33-1.96, p < 0.001)。28天和90天的死亡率也观察到类似的趋势。Kaplan-Meier (KM)分析显示,gpr较高的组在28天、90天和1年时的死亡率较高。非线性分析进一步证实了GPR与365天死亡率之间存在一个拐点,即GPR = 2.75。在低于该阈值的比率下,死亡风险随着GPR的增加而显著增加(HR: 1.466;95% ci: 1.239-1.735;P < 0.001)。然而,高于该比值,相关性趋于稳定,不再具有统计学意义(HR: 0.899;95% ci: 0.726-1.113;P = 0.095)。结论:GPR是AIS患者入住ICU时预后不良的独立预测因子。较高的gpr与28天和90天死亡率增加相关,突出了该比率在风险分层和临床决策中的潜在效用。GPR与365天死亡率呈非线性关系,在GPR = 2.75处出现拐点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-stroke mortality in ICU patients with serum glucose-potassium ratio: an analysis of MIMIC-IV database.

Introduction: Acute ischemic stroke (AIS) patients admitted to the intensive care unit (ICU) have a high mortality rate, necessitating the early identification of those at risk of a poor prognosis. This study investigated the association between the blood glucose-to-potassium ratio (GPR) and the prognosis of AIS patients.

Methods: We conducted a retrospective cohort study using data from the Medical Information Mart for Intensive Care IV (MIMIC-IV) database. The primary outcomes were 28-day, 90-day, and 1-year mortality rates following ICU admission. Multivariate Cox proportional hazards regression models were used to estimate adjusted hazard ratios (HRs) with 95% confidence intervals (CIs). Subgroup analyses, Kaplan-Meier survival curves, and restricted cubic spline models were employed to further evaluate the relationship between the GPR and mortality in AIS patients.

Results: A total of 2,636 AIS patients were included in the study, with a mean age of 69.4 ± 15.6 years. The 1-year mortality rate was 36.8% (n = 969). After adjusting for confounders, compared with the first quartile (Q1, GPR ≤ 1.39), the 1-year mortality risks for the second quartile (Q2, 1.39 < GPR ≤ 1.74), third quartile (Q3, 1.74 < GPR ≤ 2.25), and fourth quartile (Q4, GPR ≥ 2.25) were HR = 1.17 (95% CI: 0.95-1.43, p = 0.132), HR = 1.42 (95% CI: 1.17-1.73, p < 0.001), and HR = 1.61 (95% CI: 1.33-1.96, p < 0.001), respectively. Similar trends were observed for 28-day and 90-day mortality. Kaplan-Meier (KM) analysis revealed that groups with higher GPRs had higher mortality rates at 28 days, 90 days, and 1 year. Non-linear analysis further confirmed the presence of an inflection point in the association between the GPR and 365-day mortality, which was identified at GPR = 2.75. At ratios less than this threshold, the risk of mortality increased significantly with increasing GPR (HR: 1.466; 95% CI: 1.239-1.735; p < 0.001). However, above this ratio, the association plateaued and was no longer statistically significant (HR: 0.899; 95% CI: 0.726-1.113; p = 0.095).

Conclusion: The GPR is an independent predictor of poor prognosis in AIS patients admitted to the ICU. Higher GPRs are associated with increased 28-day and 90-day mortality rates, highlighting the potential utility of this ratio in risk stratification and clinical decision-making. A non-linear relationship was observed between the GPR and 365-day mortality, with an inflection point identified at GPR = 2.75.

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来源期刊
Frontiers in Neurology
Frontiers in Neurology CLINICAL NEUROLOGYNEUROSCIENCES -NEUROSCIENCES
CiteScore
4.90
自引率
8.80%
发文量
2792
审稿时长
14 weeks
期刊介绍: The section Stroke aims to quickly and accurately publish important experimental, translational and clinical studies, and reviews that contribute to the knowledge of stroke, its causes, manifestations, diagnosis, and management.
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