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Postconditioning with Lactate-enriched Blood for Cardioprotection in ST-segment Elevation Myocardial Infarction
Published on: May 28, 2019
Contrast-induced nephropathy in patients undergoing primary percutaneous coronary intervention without acute left
Stylianos A Pyxaras1, Gianfranco Sinagra, Fabio Mangiacapra
1Cardiovascular Center Aalst, Onze-Lieve-Vrouwziekenhuis Clinic, Aalst, Belgium.
Insights
Contrast-induced nephropathy (CIN) negatively impacts outcomes in ST-elevation myocardial infarction patients after primary percutaneous coronary intervention, especially those without left ventricular ejection fraction impairment. CIN is an independent predictor of major adverse cardiovascular events at one year.
Area of Science:
- Cardiology
- Nephrology
- Interventional Cardiology
Background:
- The prognostic significance of contrast toxicity in primary percutaneous coronary intervention (PCI) is debated due to confounding hemodynamic effects on kidney function.
- Left ventricular ejection fraction (LVEF) impairment can influence estimated glomerular filtration rate (eGFR) calculations, complicating the assessment of contrast-induced nephropathy (CIN).
Purpose of the Study:
- To clarify the prognostic relevance of CIN in ST-segment elevation myocardial infarction (STEMI) patients undergoing primary PCI.
- To investigate the interaction between LVEF and eGFR in predicting CIN and its association with adverse cardiovascular events.
Main Methods:
- Prospective enrollment of 644 STEMI patients undergoing primary PCI.
- CIN defined as serum creatinine increase >25% or eGFR decrease <25% within 72 hours post-procedure.
- Primary endpoint: major adverse cardiovascular events (MACE) at 1 year, including death, myocardial infarction, target lesion revascularization, and bleeding.
Main Results:
- A significant interaction between LVEF and eGFR in predicting CIN was observed in the overall cohort (p <0.001).
- In patients without LVEF impairment (LVEF ≥40%), 7% developed CIN, associated with a significantly higher 1-year MACE rate (38% vs 9%; p <0.001).
- CIN independently predicted worse outcomes, with hazard ratios of 3.81 for creatinine-based and 3.77 for eGFR-based definitions.
Conclusions:
- LVEF significantly interacts with eGFR in STEMI patients undergoing primary PCI.
- In patients without acute LVEF impairment, CIN is a confirmed independent negative prognostic factor for 1-year clinical outcomes.
- These findings highlight the importance of considering LVEF when assessing CIN risk and prognosis post-primary PCI.
Abstract:
The prognostic relevance of direct contrast toxicity in patients treated with primary percutaneous coronary intervention remains unclear, owing to the confounding hemodynamic effect of acute left ventricular ejection fraction (LVEF) impairment on kidney function estimation. In the present study, 644 consecutive patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention were prospectively enrolled. Contrast-induced nephropathy (CIN) was defined as an increase in serum creatinine >25% or a decrease in the estimated glomerular filtration rate (eGFR) <25% from baseline in the first 72 hours. The primary end point of the study was major adverse cardiovascular events at 1 year (composite of death, myocardial infarction, target lesion revascularization, and bleeding). Among the global population, the interaction between the LVEF and eGFR at admission to define CIN was statistically significant (p <0.001). When only the 385 patients without acute LVEF impairment (i.e., those with LVEF ≥40%) were considered, 27 (7%) developed postprocedural CIN that was associated with increased major adverse cardiovascular events rate at 1 year of clinical follow-up (38% vs 9%; p <0.001). On adjusted Cox multivariate analysis, CIN was an independent predictor of worse outcomes, both when defined according to creatinine (hazard ratio 3.81, 95% confidence interval 1.71 to 8.48, p = 0.001) or eGFR (hazard ratio 3.77, 95% confidence interval 1.53 to 9.28, p = 0.004) variations. In conclusion, in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention, LVEF has a significant interaction with eGFR. When only patients without acute LVEF impairment were considered, CIN confirmed its negative prognostic effect on the 1-year clinical outcomes.
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