IMPACT OF T WAVE AMPLITUDE IN LEAD aVR ON PREDICTING APPROPRIATE THERAPIES IN HYPERTROPHIC CARDIOMYOPATHY PATIENTS WITH AN IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
Abstract
Aims: Although implantable cardioverter defibrillator reduces mortality in hypertrophic cardiomyopathy patients, inappropriate implantable cardioverter defibrillator shocks are related to increased mortality. The aim of this study is to investigate whether a new electrocardiographic marker of T wave amplitude in lead aVR can be used to predict appropriate therapy of implantable cardioverter defibrillator (shock or anti-tachycardia pacing) in hypertrophic cardiomyopathy patients.
Methods: Thirty-six hypertrophic cardiomyopathy patients, who were admitted to the outpatient clinic for pacemaker control, with implantable cardioverter defibrillator were retrospectively examined (mean age: 51 ± 10.2 years, 72.2% male). The primary endpoint was appropriate implantable cardioverter defibrillator therapy. All hematological, biochemical and electrocardiogram parameters were measured before implantable cardioverter defibrillator was implanted.
Results: Over a median follow-up period of 33 months, 9 (25%) patients experienced appropriate implantable cardioverter defibrillator therapy. Heart rate and QRS interval were similar between groups. QT and QTc values were higher in patients that received appropriate shocks. Patients who have T wave inversion were higher in therapy positive group. T wave amplitude in lead aVR values were significantly associated with appropriate therapy.
Conclusion: Using simple ECG parameters, we may predict arrhythmic episodes before ICD implantation and an
improvement of the medical antiarrhythmic therapy might be protective for HCM patients with ICD.
Keywords
References
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Details
Primary Language
English
Subjects
-
Journal Section
Research Article
Authors
Begüm Söyleyici
*
Türkiye
Pelinsu Elif Hünkar
Türkiye
Çağrı Girit
Türkiye
Cansu Kurt
This is me
Türkiye
Fatih Mehmet Uçar
This is me
Türkiye
Publication Date
February 25, 2018
Submission Date
December 6, 2017
Acceptance Date
December 22, 2017
Published in Issue
Year 2018 Volume: 5 Number: 1