Author/Authors :
Giovanni Fazio، نويسنده , , Giovanni Corrado، نويسنده , , Caterina Pizzuto، نويسنده , , Elisabetta Zachara، نويسنده , , Carlo Rapezzi، نويسنده , , Ali K. Sulafa، نويسنده , , Loredana Sutera، نويسنده , , Claudia Stollberger، نويسنده , , Luca Sormani، نويسنده , , Joseph Finsterer، نويسنده , , Abraham Benatar، نويسنده , , Gabriele Di Gesaro، نويسنده , , Giuseppina Novo، نويسنده , , Yuksel Cavusoglu، نويسنده , , Magnus Baumhakel، نويسنده , , Fabrizio Drago، نويسنده , , Scipione Carerj، نويسنده , , Salvatore Pipitone، نويسنده , , Salvatore Novo، نويسنده ,
Abstract :
Background:
Isolated left ventricular noncompaction is the result of incomplete myocardial morphogenesis, leading to persistence of the embryonic myocardium. The condition is recognised by an excessively prominent trabecular meshwork and deep intertrabecular recesses of the left ventricle. Whether these intertrabecular recesses are a favorable substrate for supraventricular arrhythmias is unclear, even if the incidence of chronic heart failure seems to be high.
Results:
We evaluated a continuous series of 238 patients affected by noncompaction. In 4 cases the patients reported palpitations and in 4 an episode of syncope. Periodic holter monitoring was performed every 6 months for 4 years. Only 9 patients had documented atrial fibrillation. In no cases we observed supraventricular tachycardia.
Conclusions:
Noncompaction alone does not seem to be a risk factor for supraventricular arrhythmias.
Keywords :
Isolated left ventricular noncompaction , supraventricular arrhythmias , Atrial fibrillation , Palpitation syncope