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Twelve-lead and signal-averaged electrocardiographic parameters among beta-thalassemia major patients
Dimitrios Patsourakos1, Konstantinos A Gatzoulis2, Constantina Aggeli2
1State Department of Cardiology General Hospital of Athens Ippokrateio Athens Greece.
Insights
Beta thalassemia major patients show increased cardiac electrical abnormalities, including prolonged PR intervals and late potentials. Signal-averaged electrocardiography is a valuable tool for assessing these risks.
Area of Science:
- Cardiology
- Electrophysiology
- Hematology
Background:
- Beta-thalassemia major (β-TM) is associated with significant cardiac disease and sudden death.
- Cardiac complications in β-TM patients necessitate effective diagnostic tools.
Purpose of the Study:
- To evaluate the utility of 12-lead and signal-averaged electrocardiography (SAECG) in identifying arrhythmiogenic substrates in β-TM patients.
- To assess electrocardiographic parameters and the prevalence of late potentials (LPs) in β-TM patients compared to healthy controls.
Main Methods:
- 47 β-TM patients and 30 healthy controls underwent 12-lead and SAECG.
- Echocardiography and cardiac MRI (T2*) were used to assess cardiac structure and function.
- Prevalence of LPs and basic electrocardiographic parameters were recorded.
Main Results:
- β-TM patients exhibited prolonged PR intervals (P=.043) and a higher prevalence of PR prolongation (P=.013) compared to controls.
- Late potentials (LPs) were significantly more prevalent in β-TM patients (38.3% vs 6.7%, P=.002).
- Higher E/e' ratio (P=.012) and left atrial volume index (LAVI) (P=.002) were observed in β-TM patients. QTc and LAVI predicted LPs in 80.9% of patients.
Conclusions:
- β-TM patients demonstrate a higher incidence of prolonged PR intervals, atrial fibrillation, and LPs.
- 12-lead and SAECG are feasible and effective tools for assessing myocardial electrophysiological alterations in β-TM.
- These ECG findings highlight the importance of SAECG for risk stratification in β-TM patients.
Background:
The majority of beta thalassemia major (β-TM) patients suffer from cardiac disease, while a significant proportion of them die suddenly. Twelve-lead and signal-averaged electrocardiography (SAECG) are simple, inexpensive, readily available tools for identifying an unfavorable arrhythmiological substrate by detecting the presence of arrhythmias, conduction abnormalities, and late potentials (LPs) in these patients.
Methods:
A total of 47 β-TM patients and 30 healthy controls were submitted to 12-lead and signal-averaged electrocardiography. Basic electrocardiographic parameters and prevalence of LPs were recorded. Basic echocardiographic parameters were estimated by transthoracic echocardiography. T2* was calculated by cardiac magnetic resonance imaging wherever available.
Results:
β-TM patients demonstrated a more prolonged PR interval (167.74 msec vs 147.07 msec) (P = .043), a higher prevalence of PR prolongation (21.05% vs 0%) (P = .013), and a higher prevalence of LPs (18/47, 38.3% vs 2/30, 6.7%) (P = .002) compared with controls. The prevalence of atrial fibrillation among b-TM patients was estimated at 10.64%. Patients had also greater E/e' ratio (8.35, SD = 2.2 vs 7, SD = 2.07) (P = .012) and LAVI (30.7 mL/m2, SD = 8.76 vs 24.6 mL/m2, SD = 6.57) (P = .002) than controls. Regression analysis showed that QTc and LAVI could correctly predict the presence of LPs in the 80.9% of the patients.
Conclusions:
β-TM patients have a higher prevalence of a prolonged PR interval, atrial fibrillation, and LPs. Twelve-lead and SAECG performance was feasible in all subjects and constitutes a readily available tool for assessing myocardial electrophysiological alterations in this patient group.
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