- Poster presentation
- Open Access
Left ventricular mechanical dyssynchrony by cardiac magnetic resonance is greater in patients with strict vs. conventional ECG criteria for left bundle branch block
© Andersson et al; licensee BioMed Central Ltd. 2013
- Published: 30 January 2013
- Cardiac Magnetic Resonance
- Cardiac Resynchronization Therapy
- Implantable Cardioverter Defibrillator
- Left Bundle Branch Block
- Circumferential Strain
Left bundle branch block (LBBB) is a marker of increased delay between septal and left ventricular (LV) lateral wall electrical activation, and is a predictor of which patients will benefit from cardiac resynchronization therapy (CRT). Recent analysis has suggested that one third of patients meeting conventional ECG criteria for LBBB are misdiagnosed and new strict LBBB criteria have been proposed. We tested the hypothesis that strict LBBB patients have greater LV mechanical dyssynchrony than patients only meeting conventional LBBB criteria, while there is no difference between patients with conventional-only LBBB and LV conduction delay with QRS duration 110-119 ms.
Sixty-four cardiomyopathy patients referred for a primary prevention implantable cardioverter defibrillator (ICD) underwent 12-lead ECG and cardiac magnetic resonance (CMR) myocardial tagging. The patients were classified as strict LBBB, conventional-only LBBB or non-LBBB, indicating nonspecific LV conduction delay with QRS duration 110-119 ms. The time delay between septal and lateral LV wall peak circumferential strain, septal-to-lateral wall delay, was measured by CMR.
Strict LBBB ECG criteria identify patients with greater mechanical dyssynchrony compared to patients only meeting conventional-only LBBB criteria, while there was no significant difference between conventional-only and non-LBBB patients. The greater observed LV dyssynchrony may explain why strict-LBBB patients have better response to CRT.
The study was supported by the National Heart, Lung, and Blood Institute, National Institutes of Health (HL103812 to KCW, HL91062 to GFT, and HL61912 to RGW), the DW
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.