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Noninvasive diagnosis of electroanatomic abnormalities in arrhythmogenic right ventricular cardiomyopathy

Authors :
Pasquale Santangeli
Andrea Natale
Andrea Macchione
Stefano Bartoletti
Luigi Di Biase
Michela Casella
Costantino Smaldone
Fulvio Bellocci
Maurizio Pieroni
Gemma Pelargonio
Antonio Russo
Antonia Camporeale
Source :
Circulation. Arrhythmia and electrophysiology. 3(6)
Publication Year :
2010

Abstract

Background— The diagnostic reliability and pathophysiologic relevance of different noninvasive diagnostic criteria for arrhythmogenic right ventricular cardiomyopathy (ARVC) are undefined. We tested the association between noninvasive diagnostic criteria for ARVC and the presence of low-voltage areas (LVAs) detected at electroanatomic voltage mapping (EAM). Methods and Results— Noninvasive diagnostic criteria, including ECG, signal-averaged ECG (SAECG), and cardiac magnetic resonance (CMR) criteria, were compared with the presence and location of LVAs detected at right ventricular (RV) EAM in 17 patients (9 men) aged 50±16 years with biopsy specimen-proven ARVC. LVAs were found in 15 (88%) patients. Patients with surface ECG abnormalities showed a higher degree of RV involvement than those without ECG abnormalities (number of LVAs, 1.8±0.5 versus 0.9±0.6, respectively; P P =0.03) but not between SAECG parameters and LVAs in other RV regions. Among CMR findings, RV delayed enhancement was more significantly associated with the distribution of LVAs (free wall, P P P =0.02). Regional RV dysfunction also showed a good correlation with LVAs, with the most significant association being found with the free wall ( P =0.01), whereas RV fat infiltration at CMR was not correlated with LVAs. Conclusion— In patients with ARVC, SAECG abnormalities correlate with the presence of LVAs selectively in the RV outflow tract, whereas surface ECG abnormalities are associated with a more diffuse RV involvement. Myocardial delayed enhancement is the CMR finding more strongly associated with LVAs, thus supporting the appropriateness of its inclusion among diagnostic criteria for ARVC.

Details

ISSN :
19413084
Volume :
3
Issue :
6
Database :
OpenAIRE
Journal :
Circulation. Arrhythmia and electrophysiology
Accession number :
edsair.doi.dedup.....6d4b6a6281855706d333fb6d781de0af