Mechanical Dyssynchrony by Tissue Doppler Cross-Correlation is Associated with Risk for Complex Ventricular Arrhythmias after Cardiac Resynchronization Therapy

Background Tissue Doppler cross-correlation analysis has been shown to be associated with long-term survival after cardiac resynchronization defibrillator therapy (CRT-D). Its association with ventricular arrhythmia (VA) is unknown. Methods From two centers 151 CRT-D patients (New York Heart Associa...

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Published inJournal of the American Society of Echocardiography Vol. 28; no. 12; pp. 1474 - 1481
Main Authors Tayal, Bhupendar, MD, Gorcsan, John, MD, Delgado-Montero, Antonia, MD, Marek, Josef J., MD, Haugaa, Kristina H., MD, PhD, Ryo, Keiko, MD, PhD, Goda, Akiko, MD, PhD, Olsen, Niels Thue, MD, PhD, Saba, Samir, MD, Risum, Niels, MD, PhD, Sogaard, Peter, MD, DMSc
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.12.2015
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Summary:Background Tissue Doppler cross-correlation analysis has been shown to be associated with long-term survival after cardiac resynchronization defibrillator therapy (CRT-D). Its association with ventricular arrhythmia (VA) is unknown. Methods From two centers 151 CRT-D patients (New York Heart Association functional classes II–IV, ejection fraction ≤ 35%, and QRS duration ≥ 120 msec) were prospectively included. Tissue Doppler cross-correlation analysis of myocardial acceleration curves from the basal segments in the apical views both at baseline and 6 months after CRT-D implantation was performed. Patients were divided into four subgroups on the basis of dyssynchrony at baseline and follow-up after CRT-D. Outcome events were predefined as appropriate antitachycardia pacing, shock, or death over 2 years. Results Mechanical dyssynchrony was present in 97 patients (64%) at baseline. At follow-up, 42 of these 97 patients (43%) had persistent dyssynchrony. Furthermore, among 54 patients with no dyssynchrony at baseline, 15 (28%) had onset of new dyssynchrony after CRT-D. In comparison with the group with reduced dyssynchrony, patients with persistent dyssynchrony after CRT-D were associated with a substantially increased risk for VA (hazard ratio [HR], 4.4; 95% CI, 1.2–16.3; P  = .03) and VA or death (HR, 4.0; 95% CI, 1.7–9.6; P  = .002) after adjusting for other covariates. Similarly, patients with new dyssynchrony had increased risk for VA (HR, 10.6; 95% CI, 2.8–40.4; P  = .001) and VA or death (HR, 5.0; 95% CI, 1.8–13.5; P  = .002). Conclusions Persistent and new mechanical dyssynchrony after CRT-D was associated with subsequent complex VA. Dyssynchrony after CRT-D is a marker of poor prognosis.
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ISSN:0894-7317
1097-6795
DOI:10.1016/j.echo.2015.07.021