Evaluating the Rates of Mortality and Cardiac Catheterization Using High-Sensitivity Troponin and Conventional
Agostino Grittani1, Saul Ramos2, Chabelly Gomez3
1Internal Medicine, St. George's University, Toronto, CAN.
Insights
This study found no significant difference in cardiac catheterization or mortality rates between conventional troponin I (cTnI) and high-sensitivity troponin I (hs-cTn) assays for non-ST elevation myocardial infarction (NSTEMI) patients.
Area of Science:
- Cardiology
- Clinical Diagnostics
- Biomarker Research
Background:
- Non-ST segment elevation myocardial infarction (NSTEMI) diagnosis relies on cardiac troponin levels.
- Troponin I (cTnI) is a cardiac biomarker, with high-sensitivity troponin I (hs-cTn) being a newer assay.
- Understanding assay performance in patient outcomes is crucial for clinical practice.
Purpose of the Study:
- To investigate if different troponin assays (cTnI vs. hs-cTn) impact patient outcomes in NSTEMI.
- To determine if assay type influences rates of cardiac catheterization or mortality in NSTEMI patients.
Main Methods:
- Retrospective observational study of 75 NSTEMI patients (2018-2023).
- Compared outcomes between patients tested with conventional troponin I (cTnI) and high-sensitivity troponin I (hs-cTn) assays.
- Excluded patients with non-ischemic ECG or echocardiogram findings.
Main Results:
- No significant association was found between troponin assay type and rates of cardiac catheterization.
- No significant association was found between troponin assay type and patient mortality.
- hs-cTn showed a 4.99% increase in sample variation, while cTnI showed a 2.53% decrease.
Conclusions:
- The type of troponin assay used (cTnI vs. hs-cTn) did not significantly affect cardiac catheterization or mortality outcomes in NSTEMI patients.
- Further research may explore the clinical significance of assay variation in hs-cTn.
- Current NSTEMI diagnostic and prognostic strategies appear consistent regardless of the troponin assay used.
Abstract:
Non-ST segment elevation myocardial infarction (NSTEMI) is an acute coronary syndrome event where myocardial ischemia is present, with an increase of cardiac troponins without an elevation of the ST segment. One of the fundamental measures used to diagnose or rule out acute coronary syndrome (ACS) is troponin levels in the blood. Troponin is a broad term used for the category of muscle contraction regulatory proteins and is commonly measured during ACS evaluation. Troponin I is only released by cardiac tissue, while some assay measurements will also pick up troponin released by skeletal muscle injury. This retrospective observational study was performed investigating troponin assays and how they relate to patient's outcomes. The troponin assays used in this Miami hospital where the database of patients was collected between 2018 and 2023 were troponin I (cTnI), the conventional troponin assay, and the newer high-sensitivity troponin I assay (hs-cTn). In this observational study patients who received an admitting diagnosis of NSTEMI corroborated by an independent cardiologist had their respective troponin assay levels included. Patients found to have ECG changes significant for non-ischemic pathologies, or echocardiogram findings suggestive of myocardial dysfunction not clinically correlated to an ACS were excluded from the study. A total of 75 patients were included in this study and the mean age was 75.97 ±14.72 years, with a presentation of chest pain, dyspnea and general weakness recorded in 59% (n = 45) of patients. The median time between troponin samples was 6.63 hours across both assays and hs-cTn showed a 4.99% increase in variation between samples while cTnI had a decrease of 2.53%. The study objective is to support whether there is a difference in rates of cardiac catheterization or mortality based on the type of troponin testing. There was no significant association found between, the type of troponin assay used during hospital admission, and the outcomes of catheterization and death (p > 0.009).
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