High Sensitivity Cardiac Troponin T Levels after Elective Cardioversion for Atrial Fibrillation/Flutter
Insights
High sensitivity cardiac troponin T (hs-cTnT) levels are elevated in persistent atrial fibrillation/flutter patients but do not increase after cardioversion. Post-cardioversion biomarker levels gradually decrease, indicating changes are not due to the procedure.
Area of Science:
- Cardiology
- Biomarker analysis
Background:
- Persistent atrial fibrillation/flutter is common.
- The impact of cardioversion on cardiac biomarkers is not well understood.
Purpose of the Study:
- To investigate the kinetics of high sensitivity cardiac troponin T (hs-cTnT) after cardioversion.
- To assess changes in other cardiac injury and inflammation markers post-cardioversion.
Main Methods:
- Studied 24 patients undergoing elective cardioversion for persistent atrial fibrillation/flutter.
- Measured hs-cTnT, creatine kinase, aspartate aminotransferase, lactate dehydrogenase, brain natriuretic peptide (BNP), and high sensitivity C-reactive protein (hs-CRP) at multiple time points.
- Analyzed biomarker levels at baseline, 2, 6, 24 hours, 7 days, and 30 days post-cardioversion.
Main Results:
- Baseline hs-cTnT levels were elevated in most patients (14/24 above the 99th percentile).
- Hs-cTnT levels did not significantly increase after cardioversion, showing a non-significant trend towards decrease by 30 days.
- No significant rise in other myocardial injury markers was observed; BNP and hs-CRP were elevated at baseline and decreased over time.
Conclusions:
- Elevated hs-cTnT, BNP, and hs-CRP in atrial fibrillation/flutter patients are not exacerbated by cardioversion.
- Post-cardioversion biomarker changes are not attributable to the procedure itself.
- Cardioversion does not appear to cause acute myocardial injury as indicated by hs-cTnT kinetics.
Background:
The kinetics of high sensitivity cardiac troponin T (hs-cTnT) levels after elective, biphasic, direct-current cardioversion for persistent atrial fibrillation/flutter remains unknown.
Methods:
We examined hs-cTnT kinetics in 24 patients at baseline and at 2, 6 and 24 hours post-cardioversion, and again at 7 and 30 days. We also examined levels of creatine kinase, aspartate aminotransferase, lactate dehydrogenase, brain natriuretic peptide (BNP), and high sensitivity C-reactive protein (hs-CRP).
Results:
Median (25th, 75th interquartiles) baseline hs-cTnT concentration was 19.8 (10.4, 35.2) ng/L with 14 patients presenting with levels above the 99th percentile (13 ng/L). Hs-cTnT levels did not change significantly over time although they tended to decrease by 30 days, 18.8 ng/L (12.5, 23.3). There was no significant rise in other markers of myocardial injury. Similarly, BNP and hs-CRP levels were elevated at baseline and tended to decrease over time.
Conclusions:
Patients with persistent atrial fibrillation/flutter have elevated hs-cTnT levels, as part of a general rise in biomarkers such as BNP and hs-CRP, without a further rise after cardioversion. After cardioversion, there is a gradual non-significant decrease in biomarker levels over time, and thus a rise in hs-cTnT levels should not be attributed to cardioversion.
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