Key result
A novel nomogram predicts 1-year pathologic ventricular remodeling post-STEMI with an AUC of ~0.91.
Why the study?
Heart failure develops due to post-infarction ventricular remodeling, prompting the need to identify routine clinical and biochemical parameters that predict pathologic remodeling.
Does a nomogram containing simple routine clinical and biochemical parameters predict pathologic ventricular remodeling in STEMI patients?
Observational (n=101)
No
Does a nomogram containing simple routine clinical and biochemical parameters predict pathologic ventricular remodeling in STEMI patients?
Effect estimate: AUC 0.907 (95% CI 0.842-0.973)
A simple nomogram incorporating NTproBNP, AST, systolic blood pressure, and culprit coronary artery can accurately predict pathologic left ventricular remodeling 1 year after STEMI.
May aid post-STEMI risk stratification; leaves open external validation before clinical use.
Heart failure is the leading cause of morbidity and mortality worldwide, with ischemic heart disease being one of the most important etiologic factors. Heart failure develops due to ventricular remodeling, which leads to increases in left ventricular end-systolic and end-diastolic volumes. In this prospective observational study, we included 101 patients with first episode of ST-segment elevation myocardial infarction in whom percutaneous coronary intervention was conducted within 12 h and Thrombolysis in Myocardial Infarction III flow was achieved. The aim was to determine which clinical and biochemical parameters can help predict pathologic ventricular remodeling 1 year after myocardial infarction. We created a nomogram based on routinely used blood tests and vital parameters which showed highest correlation with pathologic ventricular remodeling. The nomogram included NTproBNP value 12 h after reperfusion, aspartate transaminase value 12 h after reperfusion, systolic blood pressure value on admission, and culprit coronary artery. We performed ROC analysis which yielded great predictive value of the nomogram. The area under curve was 0.907 (95% CI 0.842-0.973). The nomogram value of -3.54 had 91.4% sensitivity and 74.0% specificity. We believe that this nomogram, once validated, could offer a widely available, low-cost option that would help identify patients at risk of developing pathologic left ventricular remodeling and achieve this at a very early stage of myocardial infarction (12 h after reperfusion has been achieved).
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Ozren Vinter (2021) conducted an observational in ST-segment elevation myocardial infarction (STEMI) (n=101). Nomogram (NTproBNP, AST, systolic blood pressure, culprit coronary artery) was evaluated on Pathologic ventricular remodeling 1 year after myocardial infarction (AUC 0.907, 95% CI 0.842-0.973). A nomogram incorporating NTproBNP, AST, systolic blood pressure, and culprit coronary artery accurately predicted pathologic ventricular remodeling 1 year after STEMI with an AUC of 0.907.
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