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An Inflammation-renal composite approach to predict contrast-induced nephropathy in acute myocardial infarction
Ahmet Ferhat Kaya1, Görkem Ayhan1, Veysi Can1
1Department of Cardiology, Van Regional Education and Research Hospital, Van, Turkey.
Insights
Contrast-induced nephropathy (CIN) is common in acute myocardial infarction (MI) patients undergoing percutaneous coronary intervention (PCI). An inflammation-renal composite (IRIS) score predicts CIN and may aid risk stratification.
Area of Science:
- Cardiology
- Nephrology
- Medical Diagnostics
Background:
- Contrast-induced nephropathy (CIN) is a significant complication following percutaneous coronary intervention (PCI) in acute myocardial infarction (MI) patients.
- Systemic inflammation and pre-existing renal dysfunction are key factors contributing to CIN susceptibility.
- CIN is linked to poorer clinical outcomes and increased in-hospital mortality.
Purpose of the Study:
- To develop and validate an inflammation-renal composite (IRIS) score for predicting CIN in acute MI patients undergoing PCI.
- To assess the association between CIN and in-hospital mortality.
- To evaluate the IRIS score's predictive performance compared to existing clinical models.
Main Methods:
- A retrospective cohort study included 1286 patients with ST-elevation MI (STEMI) or non-ST-elevation MI (NSTEMI) undergoing PCI.
- CIN was defined by serum creatinine increase (≥0.5 mg/dL or ≥25%) within 48-72 hours post-contrast.
- An IRIS score was derived using penalized regression, integrating inflammatory and renal parameters.
Main Results:
- CIN occurred in 33.2% of patients.
- Independent predictors of CIN included age, chronic kidney disease, and the IRIS score.
- The IRIS score modestly improved model discrimination for CIN prediction (AUC 0.686 vs. 0.698).
- CIN was independently associated with increased in-hospital mortality (OR 3.35).
Conclusions:
- CIN is prevalent in acute MI patients undergoing PCI and independently predicts in-hospital mortality.
- The IRIS score, using routine parameters, is associated with CIN and offers a practical bedside tool for risk stratification.
- External validation in prospective multicenter studies is recommended to confirm the IRIS score's clinical utility.
Background:
Contrast-induced nephropathy (CIN) remains an important complication in patients with acute myocardial infarction (MI) undergoing percutaneous coronary intervention (PCI) and is associated with adverse clinical outcomes. Both systemic inflammation and baseline renal dysfunction may contribute to susceptibility to contrast-related renal injury. We aimed to develop and internally validate an inflammation-renal composite score for predicting CIN and to examine the association between CIN and in-hospital mortality.
Methods:
In this retrospective cohort study, 1286 consecutive patients with STEMI or NSTEMI undergoing PCI were included. CIN was defined as an increase in serum creatinine ≥0.5 mg/dL or ≥25% within 48-72 h after contrast exposure. An inflammation-renal composite (IRIS) score integrating inflammatory and renal parameters was derived using penalized regression. Model discrimination and calibration were evaluated, and the incremental predictive value beyond a clinical model was assessed.
Results:
CIN occurred in 427 patients (33.2%). In multivariable analysis, age (OR 1.03 per year, 95% CI 1.02-1.04), chronic kidney disease (OR 5.05, 95% CI 2.64-9.63), and the IRIS score (OR 2.72 per standard deviation increase, 95% CI 2.16-3.42) were independently associated with CIN. Incorporation of the IRIS score resulted in a modest improvement in model discrimination (AUC 0.686 vs. 0.698). CIN was independently associated with increased in-hospital mortality (OR 3.35, 95% CI 1.58-7.11).
Conclusion:
In patients with acute MI undergoing PCI, CIN was common and independently associated with in-hospital mortality. The IRIS score, derived from routinely available inflammatory and renal parameters, was independently associated with CIN and may represent a practical bedside tool for risk stratification before PCI. Prospective multicenter studies are warranted to externally validate its clinical utility.
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