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DOI 10.1007/s12265-013-9464-1

Медицинская библиотека · Journal of cardiovascular translational research · 2013

Development of a swine model of left bundle branch block for experimental studies of cardiac resynchronization therapy.

Rigol Montserrat, Solanes Núria, Fernandez-Armenta Juan, Silva Etelvino, Doltra Adelina, Duchateau Nicolas, Barcelo Aina, Gabrielli Luigi, Bijnens Bart, Berruezo Antonio, Brugada Josep, Sitges Marta

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Animal models that mimic human electrical and mechanical dyssynchrony often associated with chronic heart failure would provide an essential tool to investigate factors influencing response to cardiac resynchronization therapy. A standardized closed-chest porcine model of left bundle branch block (LBBB) was developed using 16 pigs. Radiofrequency applications were performed to induce LBBB, which was confirmed by QRS widening, a surface electrocardiogram pattern concordant with LBBB, and a prolonged activation time from endocardial. Echocardiography confirmed abnormal motion of the septum, which was not present at the baseline echocardiogram. High susceptibility of pigs to ventricular fibrillation during the endocardial ablation was overcome by applying high-rate pacing during radiofrequency applications. This is the first study to devise a closed-chest porcine model of LBBB that closely reproduces abnormalities found in patients with electrical and mechanical cardiac dyssynchrony, and provides a useful tool to investigate the basic mechanisms underlying cardiac resynchronization therapy benefits in heart failure.

Для цитирования: Rigol Montserrat, Solanes Núria, Fernandez-Armenta Juan, Silva Etelvino, Doltra Adelina, Duchateau Nicolas, Barcelo Aina, Gabrielli Luigi, Bijnens Bart, Berruezo Antonio, Brugada Josep, Sitges Marta. Development of a swine model of left bundle branch block for experimental studies of cardiac resynchronization therapy.. Journal of cardiovascular translational research. 2013. DOI: 10.1007/s12265-013-9464-1.

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