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. 2020 Jul 26;36(5):920-928.
doi: 10.1002/joa3.12412. eCollection 2020 Oct.

Twelve-lead and signal-averaged electrocardiographic parameters among beta-thalassemia major patients

Affiliations

Twelve-lead and signal-averaged electrocardiographic parameters among beta-thalassemia major patients

Dimitrios Patsourakos et al. J Arrhythm. .

Abstract

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.

Keywords: beta thalassemia; late potentials; risk stratification; signal‐averaged ECG; sudden cardiac death.

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Conflict of interest statement

Authors declare no conflict of interests for this article.

Figures

FIGURE 1
FIGURE 1
Signal‐averaged electrocardiogram of a 42‐y‐old, female, β‐TM patient. Note the low‐voltage signals at the terminal portion of the filtered QRS complex. All criteria are fulfilled (3/3) for the presence of late potentials (see main text)
FIGURE 2
FIGURE 2
Continuous Holter electrocardiography recording revealing an episode of high‐degree atrioventricular block with an asystole period of 4.2 s during daytime
FIGURE 3
FIGURE 3
Recordings from electrophysiological study. Tracing A shows intranodal suprahisian Wenckebach at 644 msec cycle length. Tracing B shows intranodal suprahisian 2:1 atrioventricular block at 630 msec cycle length. Note that the HV interval remains within normal limits (48 msec). HIS, His bundle catheter
FIGURE 4
FIGURE 4
Recording from electrophysiological study showing the induction of atrial flutter with high‐degree atrioventricular block during programmed atrial stimulation. HRA, High right atrial catheter

References

    1. Higgs DR, Engel JD, Stamatoyannopoulos G. Thalassaemia. Lancet. 2012;379:373‐83. 10.1016/S0140-6736(11)60283-3 - DOI - PubMed
    1. Williams TN, Weatherall DJ. World distribution, population genetics, and health burden of the hemoglobinopathies. Cold Spring Harb Perspect Med. 2012;9:a011692 10.1101/cshperspect.a011692 - DOI - PMC - PubMed
    1. Pennell DJ, Udelson JE, Arai AE et al. Cardiovascular function and treatment in β‐thalassemia major: a consensus statement from the American Heart Association. Circulation. 2013;128(3):281‐308. 10.1161/CIR.0b013e31829b2be6 - DOI - PubMed
    1. Ladis V, Karagiorga‐Lagana M, Tsatra I, Chouliaras G. Thirty‐year experience in preventing haemoglobinopathies in Greece: achievements and potentials for optimisation. Eur J Haematol. 2013;90(4):313‐22. 10.1111/ejh.12076 - DOI - PubMed
    1. Voskaridou E, Kattamis A, Fragodimitri C et al. National registry of hemoglobinopathies in Greece: updated demographics, current trends in affected births, and causes of mortality. Ann Hematol. 2019;98(1):55‐66. 10.1007/s00277-018-3493-4 - DOI - PubMed