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A Linear Ablating System in the Left and Right Atrium: Feasibility, Catheter Performance and Clinical Results
INTRODUCTION: We describe the use of a ablating system to compartmentalise and regionally isolate the atria in paroxysmal and persistent atrial fibrillation (AF). METHODS: 40 patients were studied, 25 paroxysmal AF and 14 persistent AF. One patient enrolled was later found to be in left atrial flutt...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Indian Heart Rhythm Society
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356588/ https://www.ncbi.nlm.nih.gov/pubmed/22665957 |
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author | Arujuna, Aruna Murphy, Cliona Hayat, Azmat Seffens, Hollie Gill, Jaswinder S |
author_facet | Arujuna, Aruna Murphy, Cliona Hayat, Azmat Seffens, Hollie Gill, Jaswinder S |
author_sort | Arujuna, Aruna |
collection | PubMed |
description | INTRODUCTION: We describe the use of a ablating system to compartmentalise and regionally isolate the atria in paroxysmal and persistent atrial fibrillation (AF). METHODS: 40 patients were studied, 25 paroxysmal AF and 14 persistent AF. One patient enrolled was later found to be in left atrial flutter and was excluded. The Cardima Revelation® TX catheter system with Intellitemp® Radiofrequency (RF) energy control device and a Medtronic Atakar® RF generator were used to place wide area circumferential ablations to achieve conduction block into the left and right sided pulmonary veins. Roof lines and mitral isthmus lines were also performed. In patients with persistent AF and in repeat procedures, right atrial compartmentalisation was performed with an anterior superior vena cava (SVC) to inferior vena cava (IVC) line and a septal SVC to IVC line. RESULTS: At 6 months, 18 of the 39 patients were asymptomatic, 10 had improved symptoms and 22 were in sinus rhythm. In the paroxysmal group, 11 were asymptomatic, 7 had improved symptoms and 16 (64%) were in sinus rhythm. In the persistent group, 7 were asymptomatic, 3 had improved symptoms and 6 (43%) were in sinus rhythm. The total group AF burden was 37.8 ± 5.4 hrs pre-procedure and 23.1 ± 5.1 hrs at 6 months post procedure. Mean temperature, impedance and power recorded at each pole demonstrated effective power delivery at all poles. No catheter charring was observed, complication rates were comparable to standard AF ablation technique. CONCLUSION: Linear ablation in the left and right atria to mimic Cox's Maze is feasible and safe using this ablating system. |
format | Online Article Text |
id | pubmed-3356588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Indian Heart Rhythm Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-33565882012-06-04 A Linear Ablating System in the Left and Right Atrium: Feasibility, Catheter Performance and Clinical Results Arujuna, Aruna Murphy, Cliona Hayat, Azmat Seffens, Hollie Gill, Jaswinder S Indian Pacing Electrophysiol J Original Article INTRODUCTION: We describe the use of a ablating system to compartmentalise and regionally isolate the atria in paroxysmal and persistent atrial fibrillation (AF). METHODS: 40 patients were studied, 25 paroxysmal AF and 14 persistent AF. One patient enrolled was later found to be in left atrial flutter and was excluded. The Cardima Revelation® TX catheter system with Intellitemp® Radiofrequency (RF) energy control device and a Medtronic Atakar® RF generator were used to place wide area circumferential ablations to achieve conduction block into the left and right sided pulmonary veins. Roof lines and mitral isthmus lines were also performed. In patients with persistent AF and in repeat procedures, right atrial compartmentalisation was performed with an anterior superior vena cava (SVC) to inferior vena cava (IVC) line and a septal SVC to IVC line. RESULTS: At 6 months, 18 of the 39 patients were asymptomatic, 10 had improved symptoms and 22 were in sinus rhythm. In the paroxysmal group, 11 were asymptomatic, 7 had improved symptoms and 16 (64%) were in sinus rhythm. In the persistent group, 7 were asymptomatic, 3 had improved symptoms and 6 (43%) were in sinus rhythm. The total group AF burden was 37.8 ± 5.4 hrs pre-procedure and 23.1 ± 5.1 hrs at 6 months post procedure. Mean temperature, impedance and power recorded at each pole demonstrated effective power delivery at all poles. No catheter charring was observed, complication rates were comparable to standard AF ablation technique. CONCLUSION: Linear ablation in the left and right atria to mimic Cox's Maze is feasible and safe using this ablating system. Indian Heart Rhythm Society 2012-05-20 /pmc/articles/PMC3356588/ /pubmed/22665957 Text en Copyright: © 2012 Arujuna et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Arujuna, Aruna Murphy, Cliona Hayat, Azmat Seffens, Hollie Gill, Jaswinder S A Linear Ablating System in the Left and Right Atrium: Feasibility, Catheter Performance and Clinical Results |
title | A Linear Ablating System in the Left and Right Atrium: Feasibility, Catheter Performance and Clinical Results |
title_full | A Linear Ablating System in the Left and Right Atrium: Feasibility, Catheter Performance and Clinical Results |
title_fullStr | A Linear Ablating System in the Left and Right Atrium: Feasibility, Catheter Performance and Clinical Results |
title_full_unstemmed | A Linear Ablating System in the Left and Right Atrium: Feasibility, Catheter Performance and Clinical Results |
title_short | A Linear Ablating System in the Left and Right Atrium: Feasibility, Catheter Performance and Clinical Results |
title_sort | linear ablating system in the left and right atrium: feasibility, catheter performance and clinical results |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356588/ https://www.ncbi.nlm.nih.gov/pubmed/22665957 |
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