| Literature DB >> 26002394 |
Archana Rajdev1, William J Groh2.
Abstract
In patients with muscular dystrophies, cardiac involvement leading to cardiomyopathy and arrhythmias occurs with variable prevalence, mirroring the phenotypic variability seen among and within the various hereditary myopathies. Knowledge of the incidence of arrhythmias and predictors of sudden death in the various hereditary myopathies can help guide screening and appropriate management of these patients, thereby improving survival. The noncardiac manifestations can lead to delayed recognition of symptoms, affect the decision to implant a prophylactic device, and once a decision is made to proceed with device implant, increase peri-procedural respiratory and anesthesia-related complications. Published by Elsevier Inc.Entities:
Keywords: Arrhythmia; Genetics; Implantable cardioverter-defibrillator; Muscular dystrophy; Pacemaker; Sudden cardiac death
Mesh:
Year: 2015 PMID: 26002394 PMCID: PMC4441951 DOI: 10.1016/j.ccep.2015.03.011
Source DB: PubMed Journal: Card Electrophysiol Clin ISSN: 1877-9182