Literature DB >> 16864616

Biventricular stimulation to prevent cardiac desynchronization: rationale, design, and endpoints of the 'Biventricular Pacing for Atrioventricular Block to Prevent Cardiac Desynchronization (BioPace)' study.

Reinhard C Funck1, Jean-Jacques Blanc, Hans-Helge Mueller, Carmen Schade-Brittinger, Christophe Bailleul, Bernhard Maisch.   

Abstract

Despite the deleterious effects of cardiac dyssynchrony and the positive effects of cardiac resynchronization therapy, patients with high-degree atrioventricular block continue to receive desynchronizing right ventricular (RV) pacing systems. Although it is unclear whether the negative effects of RV pacing and left bundle branch block (LBBB) are comparable, and whether they depend on the presence and the degree of structural heart disease, one may hypothesize that RV pacing may have similar effects to LBBB. In the BioPace trial, the long-term effects of RV pacing vs. biventricular pacing will be prospectively compared in 1200 pacemaker patients with high likelihood of mostly paced ventricular events, regardless of whether in sinus rhythm or in atrial fibrillation (AF). After echocardiographic examination of left ventricular (LV) function, patients will be randomly assigned to the implantation of an RV vs. a biventricular pacing system and followed for up to 5 years. Primary study endpoints are survival, quality of life (QoL), and the distance covered in a 6-min hall walk (6-MHW) at 24 months after implantation. Secondary endpoints are QoL and the 6-MHW result at 12 months after implantation, hospitalization rate, LV dimensions, LV ejection fraction, and the development of chronic AF and other adverse events.

Entities:  

Mesh:

Year:  2006        PMID: 16864616     DOI: 10.1093/europace/eul075

Source DB:  PubMed          Journal:  Europace        ISSN: 1099-5129            Impact factor:   5.214


  25 in total

Review 1.  Strategic choices to reduce implantable cardioverter-defibrillator-related morbidity.

Authors:  Oussama Wazni; Bruce L Wilkoff
Journal:  Nat Rev Cardiol       Date:  2010-04-20       Impact factor: 32.419

Review 2.  Cardiac resynchronization therapy in mild heart failure: a review of the REVERSE and MADIT-CRT trials.

Authors:  Carl R Reynolds; Michael R Gold
Journal:  Curr Cardiol Rep       Date:  2010-09       Impact factor: 2.931

Review 3.  [His-bundle stimulation and alternative RV stimulation sites].

Authors:  G Fröhlig; M Kindermann
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2008-03

Review 4.  [Is resynchronization therapy necessary when optimizing right ventricular stimulation?].

Authors:  G Fröhlig
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2008-12

Review 5.  The importance of avoiding unnecessary right ventricular pacing in clinical practice.

Authors:  Finn Akerström; Miguel A Arias; Marta Pachón; Jesús Jiménez-López; Alberto Puchol; Justo Juliá-Calvo
Journal:  World J Cardiol       Date:  2013-11-26

Review 6.  The changing landscape of cardiac pacing.

Authors:  S Serge Barold; Carsten W Israel
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2015-03

Review 7.  The role of biventricular pacing in the prevention and therapy of pacemaker-induced cardiomyopathy.

Authors:  Maya Guglin; S Serge Barold
Journal:  Ann Noninvasive Electrocardiol       Date:  2015-01-06       Impact factor: 1.468

Review 8.  Should His Bundle Pacing Be Preferred over Cardiac Resynchronization Therapy Following Atrioventricular Junction Ablation?

Authors:  Zak Loring; Albert Y Sun
Journal:  Cardiol Clin       Date:  2019-02-10       Impact factor: 2.213

9.  Expanding indications for resynchronization therapy.

Authors:  Christophe Leclercq; Nathalie Behar; Philippe Mabo; Jean-Claude Daubert
Journal:  Curr Cardiol Rep       Date:  2012-10       Impact factor: 2.931

Review 10.  Cardiac resynchronization therapy guided by cardiovascular magnetic resonance.

Authors:  Francisco Leyva
Journal:  J Cardiovasc Magn Reson       Date:  2010-11-09       Impact factor: 5.364

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.