Heart Rhythm
Volume 6, Issue 6 , Pages 769-775, June 2009

Prolonged RV endocardial activation duration: A novel marker of arrhythmogenic right ventricular dysplasia/cardiomyopathy

  • Harikrishna Tandri, MD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland
    • Corresponding Author InformationAddress reprint requests and correspondence: Dr. Harikrishna Tandri, Carnegie 568, 600 North Wolfe Street, Baltimore, Maryland 21287
  • ,
  • Angeliki Asimaki, PhD

      Affiliations

    • Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts
  • ,
  • Theodore Abraham, MD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • Darshan Dalal, MD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • Laurens Tops, MD

      Affiliations

    • Department of Cardiology, Leiden University Medical Center, Leiden, the Netherlands
  • ,
  • Rahul Jain, MD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • Jeffrey E. Saffitz, MD, PhD

      Affiliations

    • Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts
  • ,
  • Daniel P. Judge, MD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • Stuart D. Russell, MD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • Marc Halushka, MD, PhD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • David A. Bluemke, MD, PhD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • David A. Kass, MD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • Hugh Calkins, MD

      Affiliations

    • Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland

Received 3 December 2008; accepted 14 February 2009. published online 26 February 2009.

Background

Parietal block, defined as intra right ventricular (RV) conduction slowing, is a major diagnostic criterion for arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C).

Objective

We evaluated the utility of total RV endocardial activation duration (EAD) measured by 3-dimensional electroanatomic mapping during sinus rhythm in the diagnosis of ARVD/C.

Methods

Twenty-five consecutive patients with frequent left bundle branch block morphology premature ventricular complexes who underwent electroanatomic mapping as a part of the evaluation for ARVD/C were included in the study. All patients were evaluated using standard protocol that included electrocardiogram (ECG), signal-averaged ECG, Holter monitoring, echocardiography, and magnetic resonance imaging. Invasive testing was performed as indicated. Total RV EAD was measured as the time interval between the onset of RV activation to the latest activated region in the RV.

Results

The mean age of the study subjects was 38 ± 11 years, and 32% were men. Fourteen subjects were diagnosed with ARVD/C using task force criteria, and the remainder had idiopathic ventricular tachycardia. Although the surface QRS durations were similar, the total RV EAD was significantly prolonged in ARVD/C compared with idiopathic VT (83.9 ± 10 ms vs. 50.8 ± 7 ms, P <.001). None of the idiopathic VT subjects had RV EAD of >65 ms. RV EAD also showed significant negative correlation with RV ejection fraction.

Conclusion

Total RV EAD obtained by 3-dimensional electroanatomic mapping is a sensitive marker of intra-RV conduction delay in ARVD/C, and a total RV EAD of >65 ms accurately differentiates ARVD/C from idiopathic VT.

Keywords: Right ventricular dysplasia, Electroanatomic mapping, Diagnosis

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 Supported by the National Heart, Lung, and Blood Institute (K23HL093350 to Dr. Tandri). The Johns Hopkins ARVD Program is supported by the Bogle Foundation, St. Jude Medical Foundation, the Healing Hearts Foundation, the Campanella family, and the Wilmerding Endowments.

 The authors thank the ARVD patients and families who have made this work possible.

PII: S1547-5271(09)00213-6

doi:10.1016/j.hrthm.2009.02.031

Heart Rhythm
Volume 6, Issue 6 , Pages 769-775, June 2009