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A novel approach to mapping the atrial ganglionated plexus network by generating a distribution probability atlas.
Kim, Min-Young; Sikkel, Markus B; Hunter, Ross J; Haywood, Guy A; Tomlinson, David R; Tayebjee, Muzahir H; Ali, Rheeda L; Cantwell, Chris D; Gonna, Hanney; Sandler, Belinda C; Lim, Elaine; Furniss, Guy; Panagopoulos, Dimitrios; Begg, Gordon; Dhillon, Gurpreet; Hill, Nicola J; O'Neill, James; Francis, Darrel P; Lim, Phang Boon; Peters, Nicholas S; Linton, Nick W F; Kanagaratnam, Prapa.
  • Kim MY; Myocardial Function Section, Imperial Centre for Translational and Experimental Medicine, Imperial College London, London, UK.
  • Sikkel MB; Imperial Centre for Cardiac Engineering, Imperial College London, London, UK.
  • Hunter RJ; Myocardial Function Section, Imperial Centre for Translational and Experimental Medicine, Imperial College London, London, UK.
  • Haywood GA; Imperial Centre for Cardiac Engineering, Imperial College London, London, UK.
  • Tomlinson DR; Department of Cardiology, Imperial College Healthcare NHS Trust, London, UK.
  • Tayebjee MH; Department of Cardiology, The Barts Heart Centre, St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.
  • Ali RL; Department of Cardiology, Derriford Hospital, Plymouth Hospitals NHS Trust, Plymouth, UK.
  • Cantwell CD; Department of Cardiology, Derriford Hospital, Plymouth Hospitals NHS Trust, Plymouth, UK.
  • Gonna H; Department of Cardiology, Leeds General Infirmary, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Sandler BC; Myocardial Function Section, Imperial Centre for Translational and Experimental Medicine, Imperial College London, London, UK.
  • Lim E; Imperial Centre for Cardiac Engineering, Imperial College London, London, UK.
  • Furniss G; Myocardial Function Section, Imperial Centre for Translational and Experimental Medicine, Imperial College London, London, UK.
  • Panagopoulos D; Imperial Centre for Cardiac Engineering, Imperial College London, London, UK.
  • Begg G; Myocardial Function Section, Imperial Centre for Translational and Experimental Medicine, Imperial College London, London, UK.
  • Dhillon G; Imperial Centre for Cardiac Engineering, Imperial College London, London, UK.
  • Hill NJ; Myocardial Function Section, Imperial Centre for Translational and Experimental Medicine, Imperial College London, London, UK.
  • O'Neill J; Imperial Centre for Cardiac Engineering, Imperial College London, London, UK.
  • Francis DP; Imperial Centre for Cardiac Engineering, Imperial College London, London, UK.
  • Lim PB; Department of Cardiology, Imperial College Healthcare NHS Trust, London, UK.
  • Peters NS; Department of Cardiology, Derriford Hospital, Plymouth Hospitals NHS Trust, Plymouth, UK.
  • Linton NWF; Department of Cardiology, Derriford Hospital, Plymouth Hospitals NHS Trust, Plymouth, UK.
  • Kanagaratnam P; Department of Cardiology, Derriford Hospital, Plymouth Hospitals NHS Trust, Plymouth, UK.
J Cardiovasc Electrophysiol ; 29(12): 1624-1634, 2018 12.
Article en En | MEDLINE | ID: mdl-30168232
ABSTRACT

INTRODUCTION:

The ganglionated plexuses (GPs) of the intrinsic cardiac autonomic system are implicated in arrhythmogenesis. GP localization by stimulation of the epicardial fat pads to produce atrioventricular dissociating (AVD) effects is well described. We determined the anatomical distribution of the left atrial GPs that influence atrioventricular (AV) dissociation. METHODS AND

RESULTS:

High frequency stimulation was delivered through a Smart-Touch catheter in the left atrium of patients undergoing atrial fibrillation (AF) ablation. Three dimensional locations of points tested throughout the entire chamber were recorded on the CARTO™ system. Impact on the AV conduction was categorized as ventricular asystole, bradycardia, or no effect. CARTO maps were exported, registered, and transformed onto a reference left atrial geometry using a custom software, enabling data from multiple patients to be overlaid. In 28 patients, 2108 locations were tested and 283 sites (13%) demonstrated (AVD-GP) effects. There were 10 AVD-GPs (interquartile range, 11.5) per patient. Eighty percent (226) produced asystole and 20% (57) showed bradycardia. The distribution of the two groups was very similar. Highest probability of AVD-GPs (>20%) was identified in inferoseptal portion (41%) and right inferior pulmonary vein base (30%) of the posterior wall, right superior pulmonary vein antrum (31%).

CONCLUSION:

It is feasible to map the entire left atrium for AVD-GPs before AF ablation. Aggregated data from multiple patients, producing a distribution probability atlas of AVD-GPs, identified three regions with a higher likelihood for finding AVD-GPs and these matched the histological descriptions. This approach could be used to better characterize the autonomic network.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Atlas como Asunto / Fibrilación Atrial / Imagenología Tridimensional / Ganglios Autónomos / Atrios Cardíacos Tipo de estudio: Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Atlas como Asunto / Fibrilación Atrial / Imagenología Tridimensional / Ganglios Autónomos / Atrios Cardíacos Tipo de estudio: Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article