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Admission EASIX Score Predicts Coronary No-Reflow and In-Hospital Mortality in STEMI Patients Undergoing Primary PCI
Yusuf Bozkurt Şahin1, Veysel Ozan Tanık1, Sinan Boz1
1Department of Cardiology, Ankara Etlik City Hospital, 06170 Ankara, Türkiye.
Insights
The Endothelial Activation and Stress Index (EASIX) effectively predicts no-reflow phenomenon and mortality in ST-elevation myocardial infarction (STEMI) patients. This accessible biomarker aids early risk stratification after primary percutaneous coronary intervention.
Area of Science:
- Cardiology
- Biomarkers
- Clinical Risk Stratification
Background:
- Early risk stratification is crucial for ST-elevation myocardial infarction (STEMI) patients, particularly for predicting adverse outcomes like no-reflow phenomenon (NRP) and early mortality.
- The Endothelial Activation and Stress Index (EASIX), derived from routine labs, indicates systemic endothelial dysfunction and may serve as a prognostic tool.
Purpose of the Study:
- To evaluate the prognostic value of admission EASIX for predicting NRP and in-hospital mortality in STEMI patients undergoing primary percutaneous coronary intervention (pPCI).
Main Methods:
- Retrospective analysis of 1931 STEMI patients treated with pPCI.
- Calculation of admission EASIX and assessment of its association with NRP and in-hospital mortality.
- Utilized multivariable logistic regression, reclassification analyses (NRI/IDI), and ROC analysis for predictive performance evaluation.
Main Results:
- NRP occurred in 14.1% and in-hospital mortality in 2.5% of patients.
- Admission EASIX was independently associated with both NRP (adjusted OR 1.485) and in-hospital mortality (adjusted OR range 1.371-2.096).
- EASIX significantly improved risk reclassification for both outcomes, with ROC-AUCs of 0.706 for NRP and 0.810 for mortality.
Conclusions:
- Admission EASIX is a valuable, independent predictor of NRP and in-hospital mortality in STEMI patients.
- The EASIX score offers an accessible method to enhance early risk stratification in this patient population.
- External validation is recommended prior to widespread clinical implementation of EASIX.
Abstract:
Background: Early risk stratification in ST-elevation myocardial infarction (STEMI) remains critical, particularly for anticipating adverse outcomes such as the coronary no-reflow phenomenon (NRP) and early mortality. The Endothelial Activation and Stress Index (EASIX), calculated from routine laboratory parameters, has emerged as a potential biomarker reflecting systemic endothelial dysfunction. This study evaluated the prognostic value of admission EASIX for the NRP and in-hospital mortality in STEMI patients undergoing primary percutaneous coronary intervention (pPCI). Methods: In this retrospective single-center cohort, 1931 STEMI patients treated with pPCI between January 2023 and January 2025 were included. EASIX was calculated at admission. NRP was defined as post-PCI TIMI flow ≤ 2 or TIMI 3 flow with impaired myocardial blush (TMPG ≤ 1). Multivariable logistic regression, reclassification analyses (NRI/IDI), ROC analysis, and calibration methods were used to assess predictive performance. Sensitivity and interaction analyses were conducted. Results: NRP occurred in 14.1%, and in-hospital mortality was 2.5%. EASIX was independently associated with both outcomes (NRP: adjusted OR 1.485, 95% CI 1.286-1.715; mortality: adjusted OR range 1.371-2.096 across models; all p < 0.001). EASIX significantly improved risk reclassification for both NRP and in-hospital mortality (NRI > 0.20). ROC-AUCs were 0.706 for NRP and 0.810 for mortality. Restricted cubic spline and LOWESS analyses revealed nonlinear risk escalation. Calibration plots and Brier scores confirmed model reliability. Associations persisted across ischemic time and renal function strata. Conclusions: Admission EASIX is independently associated with NRP and in-hospital mortality in STEMI. Easily accessible and integrative, EASIX may enhance early risk stratification. External validation is warranted before clinical implementation.
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