Association between endothelial activation and stress index and 30-day mortality risk in acute myocardial infarction patients: a study based on the medical information mart for intensive care-IV database

被引:0
作者
Sang, Mingmin [1 ]
Ma, Xiaofeng [1 ]
Zhu, Fangyi [1 ]
Zhu, Cunkui [1 ]
Ying, Zuohua [1 ]
机构
[1] Qinghai Prov Cardiocerebrovasc Dis Specialist Hosp, Dept Arrhythmia 2, 7 Zhuanchang Rd, Chengzhong Dist 810012, Qinghai, Peoples R China
来源
BMC CARDIOVASCULAR DISORDERS | 2024年 / 24卷 / 01期
关键词
Association; Endothelial activation and stress index; Mortality; Acute myocardial infarction; AGE;
D O I
10.1186/s12872-024-04353-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective This study aimed to evaluate the association between the Endothelial Activation and Stress Index (EASIX) and 30-day mortality risk in acute myocardial infarction (AMI) patients. Methods Using a retrospective cohort design, data were extracted from the Medical Information Mart for Intensive Care-IV (MIMIC-IV) database between 2008 and 2019. Patients diagnosed with AMI at intensive care unit (ICU) admission were included. EASIX score was calculated as follows: lactate dehydrogenase (LDH) level (U/L) x creatinine level (mg/dL)/platelet count (10(9)/L). Cox regression models assessed the association between EASIX and 30-day mortality, with subgroup analyses based on age, gender, AMI subtype, and sepsis status. Results A total of 1,036 patients were analyzed, among whom 323 did not survive beyond 30 days post-ICU admission. Higher EASIX scores were associated with increased 30-day mortality in AMI patients [Hazard ratio (HR): 1.70, 95% confidence interval (CI): 1.17-2.46, P = 0.005). Subgroup analyses supported these findings and revealed significant interactions between EASIX and variables such as gender and AMI subtype (P < 0.05). Conclusion Elevated EASIX scores are significantly correlated with increased 30-day mortality risk in AMI patients, suggesting EASIX as a valuable prognostic tool that may inform clinical management strategies to improve outcomes in AMI. Clinical trial numberNot applicable.
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