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Activation delay-induced mechanical dyssynchrony in single-ventricle heart disease

Published online by Cambridge University Press:  09 June 2017

Daniel Forsha*
Affiliation:
Ward Family Heart Center, Children’s Mercy Hospital, 2401 Gillham Road, Kansas City, Missouri, United States of America
Niels Risum
Affiliation:
Department of Cardiology, Hvidovre University, Hvidovre, Denmark
Piers Barker
Affiliation:
Department of Pediatrics, Duke University Medical Center, 2301 Erwin Road, Durham, North Carolina, United States of America
*
Corresponding author: D. Forsha, MD, Assistant Professor of Pediatrics, Ward Family Heart Center, Children’s Mercy Hospital, 2401 Gillham Road, Kansas City, MI 64108, United States of America. Tel: +303 921 5878; Fax: 816 302 9987; E-mail: Deforsha@cmh.edu
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Abstract

We present the case of an infant with a single functional ventricle who developed ventricular dysfunction and heart failure due to an electrical activation delay and dyssynchrony. Earlier recognition of this potentially reversible aetiology may have changed her poor outcome.

Information

Type
Images in Congenital Cardiac Disease
Copyright
© Cambridge University Press 2017 
Figure 0

Figure 1 Echo and electrocardiographic data before the development of right bundle branch block (left) and after right bundle branch block (right). Lead V1 demonstrates a new right bundle branch block. Two-dimensional images with strain tracking and strain analysis demonstrate increased ventricular dilation, dysfunction, and dyssynchrony following bundle branch block. Longitudinal strain curves show the evolution from normal, synchronous mechanics in the left and right free walls degrading to the pattern of activation-delay-induced mechanical dyssynchrony with severe dysfunction post-right bundle branch block.