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Published on: May 28, 2019
Association between pan-immune-inflammation value and no-reflow in patients with ST elevation myocardial infarction
Adil Bayramoğlu1, Şıho Hidayet1
1Department of Cardiology, Inonu University, Malatya, Turkey.
Insights
The novel pan-immune-inflammation value (PIV) effectively predicts the no-reflow phenomenon in ST-elevation myocardial infarction patients. Higher PIV levels indicate a greater risk of no-reflow, outperforming the systemic immune-inflammation index (SII).
Area of Science:
- Cardiovascular Medicine
- Inflammation and Immunology
- Biomarker Discovery
Background:
- No-reflow is a critical complication in ST-segment elevation myocardial infarction (STEMI) associated with poor patient prognosis.
- Several inflammatory markers, including C-reactive protein and neutrophil-to-lymphocyte ratio, are linked to the no-reflow phenomenon.
- The systemic immune-inflammation index (SII) has shown predictive value, but novel indices require investigation.
Purpose of the Study:
- To retrospectively evaluate the relationship between the pan-immune-inflammation value (PIV) and the occurrence of no-reflow in STEMI patients.
- To determine if PIV can serve as an independent predictor of no-reflow.
- To compare the predictive performance of PIV against the SII for no-reflow.
Main Methods:
- A retrospective analysis included 1212 STEMI patients, with 145 experiencing no-reflow.
- Multivariate logistic regression analysis identified independent predictors of no-reflow.
- Receiver Operating Characteristic (ROC) curve analysis assessed the diagnostic accuracy of PIV, comparing it with SII.
Main Results:
- PIV emerged as an independent predictor of no-reflow (OR: 1.025, p < 0.001), alongside baseline ejection fraction, stent length, age, and pain-to-PCI time.
- The optimal PIV cutoff for predicting no-reflow was ≥889, demonstrating 77.2% sensitivity and 77.5% specificity (AUC: 0.828).
- PIV exhibited significantly higher predictive power for no-reflow compared to SII (p < 0.001).
Conclusions:
- Elevated PIV is an independent predictor of no-reflow in STEMI patients.
- PIV offers superior predictive capability for no-reflow compared to SII.
- PIV represents a promising novel biomarker for assessing no-reflow risk in STEMI.
Abstract:
Noreflow is a condition associated with a poor prognosis in ST segment elevation myocardial infarction patients. It has been shown that many inflammatory markers and index such as procalcitonin, C-reactive protein, neutrophil to lymphocyte ratio, systemic immune inflammatory index (SII), are associated with noreflow. We used a brand-new index pan-immune-inflammation value (PIV) to retrospectively evaluate the relationship between PIV and noreflow. A total of 1212 patients were included for analysis. Noreflow was observed in 145 patients. In multivariate analysis, PIV (odds ratio (OR): 1.025; [1.002-1.115], p < 0.001), baseline ejection fraction (OR: 0.963; [0.934-0.993], p = 0.015), stent length (OR: 1.032; [1.010-1.054], p = 0.004), age (OR: 1.034; [1.014-1.053], p = 0.001) and pain to PCI time (OR: 1.003 [1.002-1.005], p < 0.001) were observed to be the independent predictors of noreflow. ROC curve analysis showed that the best cut off value of PIV for predicting noreflow was ≥889 with 77.2% sensitivity and 77.5% specificity (AUC, 0.828; 95% CI [0.806-0.849]). A ROC curve comparison analysis was performed to compare PIV and SII. The predictive power of PIV was higher than SII (differences between areas: 0.154; p < 0.001). According to our findings, an increase in PIV is an independent predictor of noreflow in patients with STEMI.
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