Key result
Early delta troponin I fails to predict in-hospital major cardiovascular events in STEMI.
Why the study?
The relationship between the rate of increase in troponin I levels and in-hospital cardiovascular endpoints in patients with STEMI was unclear.
Do delta troponin I levels predict in-hospital major cardiovascular endpoints in patients with acute STEMI?
Cohort (n=84)
No
Do delta troponin I levels predict in-hospital major cardiovascular endpoints in patients with acute STEMI?
p-value: p=>0.05
Delta troponin I levels measured at 2, 4, and 6 hours after admission do not predict in-hospital major cardiovascular endpoints in patients with STEMI.
Delta troponin I changes should not yet inform in-hospital risk stratification in STEMI; leaves open the prognostic role of serial measurements.
Objectives. In this study, we investigated the relationship between the rate of increase in troponinI levels and in-hospital cardiovascular endpoints (outcomes) in patients with ST-elevation myocardial infarction (STEMI). Methods. Eighty-four patients with acute STEMI who received thrombolytic treatment or who underwent primary percutaneous coronary intervention (PCI) were enrolled. After admission to hospital, delta troponinI levels, which were determinedby serial measurements after 2, 4, and 6h of admission, and in-hospital major cardiovascular events were evaluated. Results. There were 35(41.7%) patients in the thrombolytic group and 49(58.3%) patients in the primary PCI group. As major cardiovascular endpoints, death from cardiovascular events was seen in 7(8.3%) patients, stroke/transient ischemic attack in 2(2.4%), recurrent ischemia in 5(6%), arrhythmia in 8(9.5%), and urgent revascularization was performed in 5(6%) cases. In patients with arrhythmia, ventricular fibrillation was seen in 3(3.6%) patients, atrial fibrillation in 3(3.6%), and ventricular tachycardia in 2(2.4%) patients. The ventricular septal defect was observed only in 1(1.2%) patient as a mechanical complication, and the patient underwent urgent surgery. The analysis of all patients and sub-groups of thrombolytic and primary PCI patients revealed no statistically significant difference between delta troponinI levels at time intervals of (02), (04), and (06)h and in-hospital major cardiovascular endpoints (p0.05). Conclusion. The analysis of delta troponinI levels is not a predicting factor of in-hospital endpoints (outcomes) in patients with STEMI treated by thrombolytic therapy or primary PCI. Randomized controlled studies with a larger study population are needed on this subject.
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Aydın et al. (2019) conducted a cohort in Acute ST-elevation myocardial infarction (STEMI) (n=84). Delta troponin I levels vs. Below vs above median delta troponin I levels was evaluated on In-hospital major cardiovascular endpoints (including cardiovascular death, re-infarction, recurrent ischemia, emergency revascularization, cardiac insufficiency, cardiogenic shock, arrhythmia, stroke/TIA, mechanical complication) (p=>0.05). Delta troponin I levels at 0-2, 0-4, and 0-6 hours were not significantly associated with in-hospital major cardiovascular endpoints in patients with STEMI treated by thrombolytic therapy or primary PCI (p >0.05).
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