Professional Documents
Culture Documents
DOI 10.1007/s10840-015-9975-6
174
Special Program and Abstract issue of the 11th Annual Congress of the European
Cardiac Arrhythmia Society (ECAS)
April 19-21, 2015
Paris, France
Hotel Meriden-Etoile
Guest Editor: Prof. Samuel Lvy, MD Aix-Marseille Universit, Marseille, France
PROGRAM AT A GLANCE
11th Annual Congress of the European Cardiac Arrhythmia Society
SCIENTIFIC PROGRAM OF PRE-ARRANGED SESSIONS
ECAS 2015 ABSTRACT SESSIONS 14
Sunday, April 19, 2015, 10:30 AM12:00 PM
Abstract Session 1: Atrial fibrillation ablation
Abstract Session 2: Sudden cardiac death. Prevention and management
Abstract Session 3: Atrial fibrillation and prevention of related thromboembolism
Abstract Session 4: Mechanisms of ventricular arrhythmias
ECAS 2015 ABSTRACT SESSIONS 58
Monday, April 20, 2015, 10:30 AM12:00 PM
Abstract Session 5: Advances in atrial fibrillation ablation II
Abstract Session 6: Cardiac resynchronization therapy: techniques and outcome
Abstract Session 7: Mapping and ablation of ventricular arrhythmias
Abstract Session 8: Clinical and genetic aspects of ARVD/C
ECAS 2015 ABSTRACT SESSIONS 912
Tuesday, April 21, 2015, 08:30 AM10:00 AM
Abstract Session 9: Atrial fibrillation mechanisms and management I
Abstract Session 10: Atrial arrhythmia mechanisms II
Abstract Session 11: Management of atrial arrhythmias
Abstract Session 12: Atrial fibrillation ablation III
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176
Invitation
Dear Colleagues,
This is an invitation to join us at the 11th Annual Scientific Congress of the European Cardiac Arrhythmia Society ECAS 2015
to be held in Paris, France April 19 to 21, 2015, at the Meridien-Etoile Hotel (Porte Maillot). All those who attended previous
editions of ECAS Congress know that it is a highly scientific and educational event in a cheerful atmosphere which facilitates
interaction between the renowned faculty and the audience which is particularly appreciated by fellows. This edition promises to
be successful and we will be delighted to have you among us in Paris next April.
Riccardo Cappato, MD
Nicolas Lellouche, MD
Xavier Jouven, MD
President of ECAS
Congress Chairman
Past President
Treasurer
Secretary General
Continuing Medical Education
Gerhard Steinbeck MD
177
Samuel Levy MD
Nicolas Lellouche, MD
Program Committee
Andrey Ardashev; Alawi Alsheikh-Ali; Serge Barold; Leonardo Calo; David S Cannom; Riccardo Cappato; Sumeet Chugh;
Wyn Davies; Roberto De Ponti; Heidi Estner; Jeronimo Farre; Mark Estes III; John Fisher; Robert Hatala; Richard Hauer; Ellen
Hoffmann; Charles Jazra; Xavier Jouven (Chair); Stefan Kb; Jean-Franois Leclercq; Gilles Lascault; Samuel Lvy; Thorsten
Lewalter; Jean-Yves Le Heuzey; Shaowen Liu; Peter Loh; Pierpaolo Lupo; Chang Sheng Ma; Michal Nbauer; Mohan Nair;
Yuji Nakazato; Andrea Natale; Petr Neuzil; Promund Obel; Eli Ovsyshcher; Douglas L Packer; Luigi Padeletti; Nicholas S.
Peters; Dubravko Petrac; Antonio Raviele; Amiran Revishvilli; Sanjeev Saksena; Richard Schilling; Gerhard Steinbeck;
Massimo Santini; Neil Sulke; Dorwarth Uwe; Reza Wakili; Bruce Wilkoff.
Scientific Advisory Board
Masood Akhtar (Milwaukee, USA)
Philippe Coumel*
178
(continued)
Nabil El-Sherif (New York, USA)
Jeronimo Farre (Madrid, ES)
John Fisher (New-York, USA)
Guy Fontaine (Paris, FR)
Robert Frank (Paris, FR)
Seymour Furman (New York, USA)*
*In memoriam
Abstract Selection
Each abstract has been sent to eight reviewers and been evaluated by a minimum of four of them.
The organizing committee would like to thank the abstract reviewers for their valuable help in the abstract selection for
the ECAS 2015 program:
Etienne Aliot; Elad Anter; Serge Barold; Jean-Jacques Blanc; Poul-Erik Block Thomsen; Gerard Boink; Gunter Breithardt; Hugh
Calkins; Leonardo Calo; John Camm; Riccardo Cappato; Mario Delmar; Roberto De Ponti; Luigi Di Biase; Nils Edvardsson;
Nabil El Sherif; Mark Estes; Heidi Estner; Gerard Guiraudon; Sam Hanon; Richard Hauer; Bengt Herweg; Ellen Hoffman;
Carsten Israel; Michiel Janse; Prapa Kanagaratnam; Helmut Klein; Yusuke Kondo; Jean-Yves Le Heuzey; Nicolas Lellouche;
Thorsten Lewalter; Berndt Lderitz; Marek Malik; Robert Myerburg; Yuji Nakazato; Brian Olshansky; Ali Oto; Eli Ovshyscher;
Dubravko Petrac; Sanjeev Saksena; Walid Saliba; Massimo Santini; Peter Schwartz; Robert Schweikert; Dipen Shah; Claudio
Shuger; Jasbir Sra; Gerhard Steinbeck; Neil Sulke; Richard Sutton; Tamas Szili-Torok; Jacob Tfelt-Hansen; Antonello Vado;
Peter Van Tintelen; Reza Wakili; Albert Waldo; David Wilber; Bruce Wilkoff; Roger Winkle.
General Information
Congress Venue
LE MERIDIEN ETOILE Htel
81 Boulevard Gouvion Saint Cyr,
75848 Paris Cedex 17
Tel: (33) (0)1 40 68 34 34
www.lemeridienetoile.com
Congress Chairman
Nicolas Lellouche, MD Secretary:
Hpital Henri Mondor
51 avenue du Marchal
de Lattre De Tassigny
94000 Crteil, France
Email: nicolas.lellouche@hmn.aphp.fr
Sandrine Bordire
Tel: +33149 814350
Email: sandrinebordiere@hmn.aphm.fr
179
Abstract Awards
Awards for the best oral abstracts will be presented during the opening ceremony to take place on Sunday April 19, 2015, at Room Derain
Presentation of the awards for best poster presentations will take place on Tuesday April 21, 2015, 12:00 PM12:30 PM Room
Diderot (Meridien-Etoile Hotel)
11th Philippe Coumel Lecture 2015
Will be presented on Sunday April 19, 2015, from 5:30 PM to 6:00 PM as part of the opening ceremony
Badges
Badges and Final program will be available for pre-registered participants and faculty at the ECAS welcome desk, Hotel
Meridien Etoile, Paris, starting Sunday April 19, 2015, from 2:00 PM to 6:00 PM
ECAS Congress Secretariat
Josette Razafimbelo
Tel/FAX: + 33 (0)4 89 14 45 33
Cell: +336 26 07 55 74
E-mail: josette.razafimbelo@sfr.fr
Registration
Registration and payment of Congress fees as well as payment of membership dues can be done through the website. Registration
on site will start on Sunday April 19, 2015, at 8:00 AM at Hotel Meridien-Etoile.
Currency
Payment in cash for registration on site must be made in euros only. Payment using Visa credit cards will be accepted on the
Congress site. Personal checks cannot be accepted.
Congress Website
All information, Scientific Program and registration to the congress, abstract submission and membership subscription with
secured payment can be done through our website http://www.ecas-heartrhythm.org
Pre-Arranged Sessions
The program includes 33 pre-arranged sessions and workshops or debates. It can be downloaded from our website as well as the
program of abstracts selected for oral or poster presentations
Publications
180
Sanjeev Saksena MD
JICE Editor-in-Chief
Leonardo Calo MD
Abstract Presentations
The abstracts accepted for oral or poster presentation will be published in a supplement issue of the Journal of Interventional
Cardiac Electrophysiology (JICE), the official journal of ECAS provided the authors attend the congress and present their work.
The oral presentation of abstracts is 10 min plus 5 min for discussion.
All posters accepted for presentation will be chaired. Please check the day and time at which your poster will be presented to the
chairpersons and the time at which the presenter should be near their poster board.
181
Registration
Concurrent Workshops
8:30am
10:00am
Room TBA
Room PASCAL
Room DIDEROT
Session WS-06
Session WS-01
Session WS-02
Atrial Fibrillation
ablation
D L Packer
Cardiac
Resynchronization
therapy
Bruce Wilkoff
Session WS-03
Pacemaker, ICD and
CRT:Case studies
S Barold
E Ovsyshcher
C Israel
B Herweg
Five year
Experience with
NOACs
Room DESCARTES
Chaired poster
session A
8:30-12:00
Coffee break
Concurrent Abstract Sessions
10:30am
12:00pm
2:00pm
3:30pm
Room DERAIN
Room DIDEROT
Room DESCARTES
Room PASCAL
Room GAUGUIN
Oral Abstract 1
Oral Abstract 2
Oral Abstract 3
Oral Abstract 4
Session A cont.
12:150pm-1:45pm
12:15pm-1:45pm
Room DERAIN
Room DIDEROT
Session AB-01
Session HD-01
Pulmonary Vein
Isolation and
related strategies
Inherited
potentially lethal
syndromes
Room DESCARTES
Room PASCAL
Room GAUGUIN
Session SP-07
Session SP-02
ECAS-WSA
New frontiers in cardiac
pacing
Session B
Prevention of sudden
cardiac death
Chaired poster
Room PASCAL
Room GAUGUIN
Room DIDEROT
Room DESCARTES
Session SP-03
Session SP-04
Session AB-02
4.00pm
5:30pm
5:30pm
Ventricular
tachycardia
ablation (I)
Intracardiac imaging
Session SP-05
Stroke prevention in
atrial fibrillation
Session B
Chaired poster
182
6:00pm
Opening ceremony
Chaired By Prof. Samuel LEVY (Marseille, FR) and Prof. Gerhard Steinbeck (Munich, DE) and
OUTSTANDING ACHIEVEMENT AWARDS Presented by
Dr Riccardo Cappato (Milan, IT) President of ECAS
Prof. Nicolas Lellouche (Paris, FR) Congress Chairman
Dr Fernand Hessel (Mulhouse, FR) President Lucien Dreyfus Foundation
183
8:30am
10:00am
Room COROT
Room DIDEROT
Room DESCARTES
Room PASCAL
Room
GAUGUIN
Session SP-06
Session SP-07
Session C
Sudden cardiac
Arrhythmogenic
death : and left
ventricular
Cardiomyopathy I
hypertrophy (LVH)
catheter ablation of
complex arrhythmias
Chaired
posters
Room DIDEROT
Room DESCARTES
Room PASCAL
Oral abstract 5
Oral abstract 6
Oral abstract 7
Oral abstract 8
10:30am
12:00pm
12:15pm-1:45pm
12:15pm-1:45pm
Luncheon Panel 3
Luncheon Panel 4
Room COROT
2:00pm
3:30pm
Room DIDEROT
Room DESCARTES
Room PASCAL
Chaired
Posters
(cont.)
Room
GAUGUIN
Session HD-06
Session AB-04
Current issues in
atrial fibrillation
Session HD-07
Biomarker-based
HRS-ECAS Session
therapeutic
Arrhythmogenic
decision making in
Cardiomyopathy II
AF
Session SP-15
Approaches in VT
Ablation
Session D
Chaired
poster
4:00pm
5:30pm
Room COROT
Room DIDEROT
Room DESCARTES
Room PASCAL
Room
GAUGUIN
Session AB-05
SP-14
Session SP-13
Session HD-04
Session D
AF ablation not
targetting
pulmonary veins
Automatic nervous
Sudden cardiac death system and
arrhythmias
Chaired
poster
184
8:30am
10:00am
Room DIDEROT
Room DESCARTES
Room PASCAL
Room TBA
Oral abstract 9
Oral abstract 10
Oral abstract 11
Oral abstract 12
Room DESCARTES
Room PASCAL
Room TOCQUEVILLE
12:00pm
12:30pm
Unresolved questions
Session SP-12
Session WS-05
Session WS-04
Nightmares in catheter
ablation
185
186
187
Luncheon Panels
12:15 PM1:45 PM
Seated Luncheon Panel 1
12:15 PM1:45 PM
Seated Luncheon Panel 2
188
189
190
Room DESCARTES
SP-04
Advances in Intracardiac Imaging for Interventional Electrophysiologists: 2015 and beyond
Chairpersons: Andrea Natale (Austin, USA), Roger Winkle (Palo Alto, USA)
1. Cardiac CT for definition of left atrial appendage morphology and risk stratification
Luigi Di Biase (New York, USA)
2. Intracardiac echocardiography performed from and for the pulmonary vasculaturetechnique and application
Sanjeev Saksena (Warren, USA)
3. Magnetic resonance imaging of the atrial substrate and progression of atrial fibrillation: a critical analysis
Mark ONeill (London, GB)
4. Real-time three dimensional imaging of cardiac chambers
Mohammad Shenasa (San Jose, USA)
SUNDAY APRIL 19, 2015
4:00 PM5:30 PM
Room PASCAL
SP-05
Stroke prevention in atrial fibrillation
Chairpersons: John Camm (London, GB), Johannes Brachmann (Coburg, DE)
1. NOACs5 years after RE-LY: What have we learned?
Michael Nbauer (Munich, DE)
2. Interventional therapy by occluder deviceswhich patients should be considered?
Thorsten Lewalter (Munich, DE)
3. Ablation therapy for stroke prevention in patients with AF
John Fisher (New York, USA)
4. Role of continuous rhythm monitoringidentification of cause or bystander?
Albert Waldo (Cleveland, USA)
SUNDAY APRIL 19, 2015
3:30 PM5:00 PM
ROOM GAUGUIN
Chaired poster session B (Cont.)
Room DERAIN
5:30 PM to 6:00 PM
Special lecture: A tribute to Philippe Coumel TBA
Opening ceremony
Prof. Samuel Lvy (Marseille, FR) and Prof. Gerhard Steinbeck (Munich, DE)
Outstanding Achievement Awards
Best Abstracts Awards
Presented by Dr Riccardo Cappato (Milan, IT)
President of ECAS
Prof. Nicolas Lellouche (Paris, FR)
Congress Chairman
Dr Fernand Hessel (Mulhouse, FR)
President Lucien Dreyfus Foundation
Followed by a cocktail reception
MONDAY APRIL 20, 2015
08:30 AM10:00 AM
ROOM COROT
SESSION SP-06
Atrial Fibrillation: Beyond Stroke Prevention
Chairpersons: Nils Edvardsson (Gothenburg, SE), Amiran Revishvili (Moscow, RU)
1. Cardiovascular Morbidity and Mortality of AF
Christine Albert (Boston, USA)
2. Atrial Fibrillation and Sudden Cardiac Death
Eloi Marijon (Paris, FR)
3. Role of Pharmacology
Juan Tamargo (Madrid, ES)
4. Role of Catheter Ablation
Walid Saliba (Cleveland, USA)
MONDAY APRIL 20, 2015
08:30 AM10:00 AM
ROOM DIDEROT
Session SP-07
Sudden cardiac death: Focus on at risk patients with secondary left ventricular hypertrophy (LVH)
Chairpersons: John Fisher (New-York, USA), Dubravko Petrac (Zagreb, HR)
191
192
193
3. Preprocedural imaging and 3-D mapping in patients with ventricular tachycardia associated with structural heart
disease
Richard Schilling (London, GB)
4. 3-D mapping and contact force sensing in ablation of idiopathic ventricular tachycardia
David Wilber (Chicago, USA)
MONDAY APRIL 20, 2015
08:30 AM10:30 AM
ROOM GAUGUIN
Chaired Poster session C Part 1
10:00 AM10:30 AM Coffee break and Posters
MONDAY APRIL 20, 2015
10:30 AM12:00 PM
Concurrent Oral Abstract sessions
ROOM COROT
Abstract session 5
ROOM DIDEROT
Abstract session 6
ROOM DESCARTES
Abstract session 7
ROOM PASCAL
Abstract session 8
12:15 PM1:45 PM
Luncheon Panel 3
Luncheon Panel 4
194
195
196
197
198
199
200
201
202
from an interim analysis of the first multicentre randomised controlled trial studying the impact of this data on the ablation of
paroxysmal atrial fibrillation (PAF). METHODS: At seven UK
centres, patients undergoing first-time PAF ablation were
randomised to ablation with (CF-on) or without CF data (CFoff) available to the operator. Planned recruitment is 120 patients
with 1-year follow-up. Using a 3D mapping system and the
SmartTouch CF-sensing catheter (Biosense Webster), all patients
underwent WACA. Subsequently a 1-h waiting time was observed before assessing acute pulmonary vein (PV) reconnection;
if the PV remained isolated, 18 mg adenosine was administered
intravenously. The primary end point was acute PV reconnection
(spontaneous/adenosine induced). PVs were assessed separately,
but cases of a common trunk were taken as one vein. PVs that
CF-off group
60
CF-on group
56
p value
195 [165216]
193 [171219]
0.97
13 [623]
904 [2921684]
10 [630]
813 [3652187]
0.96
0.88
2446 [18982862]
2446 [20232956]
0.46
Number
68/227 (30 %)
38/202 (18 %)
0.01
35/115 (30 %)
17/103 (17 %)
0.017
33/112 (30 %)
21/99 (21 %)
0.2
high-density mapping. Methods: We analysed the PAF subgroup of the SUBSTRATE HD study (multicentric study with
seven operators involved). Twenty-four patients undergoing
PAF ablation were thus prospectively enrolled for a first ablation procedure (mean age=61.7+10.25). A substrate biatrial
highdensity mapping with a 20-pole-contact electrode
PentaRay NAV catheter (Biosense Webster) was performed.
AF substrate was detected both automatically with a new
CFAE algorithm setting and visually by operators (continuous
CFAE and temporal gradient of activation). Ablation end
points were AF termination (sinus rhythm or atrial tachycardia
conversion), sinus conversion and non-inducibility (atrial
devulnerabilisation). Results: AF was induced in 16 patients
(66.6 %) by rapid atrial pacing. The median mapping times
and number of acquisition points/patient in the right and left
atria were, respectively, as follows: 7 [47] and 14 [9.2515]
min with 569 [285739] and 831 [1052490] points. Substrate ablation without PVI terminated AF in 23/24 (96 %)
patients in 15.3+14.8 mean min RF time. Sinus rhythm was
restored in 23/24 (96 %) patients and non-inducibility was
achieved in 75 %. The total mean procedure and RF time
were, respectively, 153.9+36 and 43 min +18.4. No procedural complications occurred. After a mean follow-up of 6.5+
2.8 months 23/24 (96 %), patients were free from AF and
19/24 (79.16) were free from any atrial arrhythmias. Conclusion: Electrogram-based substrate ablation guided by bi-atrial
high-density mapping for PAF without PVI is feasible, safe,
reproducible and efficient.
203
An easily determined clinical scoring system was derived retrospectively and applied prospectively. CAAP-AF predicted
the final outcome of AF ablation in both a development and a
test cohort of AF ablation patients. CAAP-AF may provide a
realistic AF ablation outcome expectation for individual pts.
14 Abstract 1816
15 Abstract 1832
PREDICTION OF AF ABLATION OUTCOME: THE
CAAP-AF SCORE
Roger Winkle1, Julian Jarman2, R. Hardwin Mead1, Gregory
Engel1, Melissa Kong1, William Fleming1, Rob Patrawala1
1
Silicon Valley Cardiology, E Palo Alto, CA, USA; 2Royal
Brompton Hospital, London, UK
Objectives: To develop a clinical scoring system to predict the
final outcome for all patients undergoing atrial fibrillation (AF)
ablation. Methods: We examined a development cohort (DC) of
1125 consecutive patients undergoing 1.340.53 AF ablations
from 2003 to 2010. Results: Pt. demographics were as follows:
age=62.310.3, male=71.2 %, LA size=4.300.69 cm, paroxysmal AF 30.9 %, drugs failed=1.31.1, hypertension=
46.7 %, diabetes=8.9 %, prior CVA/TIA=6.9 %, prior cardioversion=46.9 % and CHADS2=0.870.97. Multivariate analysis showed six independent variables predicting outcome after
final ablation: CAD (p=0.021), atrial diameter (p=0.0003), age
(p=0.004), persistent or longstanding AF (p<0.0001), antiarrhythmic drugs failed (p<0.0001) and female (p=0.0001). We
created a scoring system (CAAP-AF) using these six variables
with total CAAP-AF scores ranging from 0 to 13 points.
CAAP-AF Score: CAD=1 pt; atrial diameter <4.0=0 pts, 4 to
<4.5=1 pt,.4.5 to <5=2 pts, 5.0 to <5.5=3 pts, 5.5=4 pts; age
<50=0 pts, 50 to <60=1 pt, 60 to <70=2 pts, 70=3 pts;
persistent or longstanding AF=2 pts; antiarrhythmic drugs
failed none=0 pts, 1 or 2=1 pt, 3=2 pts; female=1 pt.
CAAP-AF score predicted final outcome (C statistic=0.691,
p = 0.0006). The 2-year Kaplan-Meier AF free rates by
CAAP-AF scores were as follows: 0=100 %, 1=95.7 %, 2=
96.3 %, 3=83.1 %, 4=85.5 %, 5=79.9 %, 6=76.1 %, 7=
63.4 %, 8 = 51.1 %, 9 = 53.6 % 10 = 29.1 %. CochranArmitage trend test showed worsening 2-year outcome with
higher CAAP-AF scores (p<0.0001). The CAAP-AF score
was then applied prospectively to 937 patients in a test cohort
(TC) undergoing AF ablation from 2010 to 2012. The CAAPAF score also predicted final outcome in the TC (C statistic=
0.651, p=0.009). The 2-year Kaplan-Meier AF free rates by
CAAP-AF scores were as follows: 0=100 %, 1=87.0 %, 2=
89.0 %, 3=91.6 %, 4=90.5 %, 5=84.4 %, 6=70.1 %, 7=
71.0 %, 8 = 60.7 %, 9 = 68.9 % 10 = 51.3 %. CochranArmitage trend test showed worsening 2-year outcome for the
TC with higher CAAP-AF scores (p<0.0001). Conclusions:
204
16 Abstract 1825
USE OF CONTACT FORCE TECHNOLOGY IN AF
ABLATION PROCEDURES DOES NOT IMPROVE
CLINICAL OUTCOME RATESINSIGHTS FROM
A 3 YEAR SINGLE CENTER EXPERIENCE
Stefan Sattler1, Johannes Siebermair1, Eva Klocker1, Lucia
Olesch1, Samira Saraj1, Ina Klier1, Christoph Schuhmann1,
Sebastian Clauss1, Moritz Sinner1, Stephanie Fichtner1,
Stefan Kb1, Heidi Estner1, Reza Wakili1
1
Medical Department I, Klinikum Grosshadern, LudwigMaximilians-University, Munich, Germany
Introduction: Pulmonary vein isolation (PVI) is an established
method to treat atrial fibrillation (AF). Contact force (CF) sensing
catheters have been introduced with the purpose to improve procedural parameters and clinical outcome of AF ablation. In this
205
206
207
22 Abstract 1924
23 Abstract 1925
RANOLAZINE AMELIORATES
POST-RESUSCITATION ELECTRICAL INST
ABILITY AND MYOCARDIAL DYSFUNCTION AND
IMPROVES OUTCOME IN A RAT MODEL OF VENT
RICULAR FIBRILLATION
208
ing structural or electrical heart disease during followup, with VF as first manifestation. These data emphasize the importance of comprehensive follow-up of IVFpatients, regarding its impact on patient diagnosis, treatment and genetic- and family counselling. Keywords:
Follow-up, Idiopathic Ventricular Fibrillation
25 Abstract 1926
24 Abstract 1916
FOLLOW-UP OF PATIENTS WITH IDIOPATHIC
VENTRICULAR FIBRILLATION (THE FU-IVF
STUDY)PRELIMINARY RESULTS
Marloes Visser1, Charlotte Siegers1, Jeroen van der Heijden1,
Peter Loh1, Pieter Doevendans1, Rutger Hassink1
1
UMC Utrecht, Utrecht, Netherlands
Background: Idiopathic ventricular fibrillation (IVF) is the underlying cause of 510 % of out-of-hospital cardiac arrest patients. IVF is defined as VF without structural or electrical heart
disease present upon first presentation. Little is known regarding
long-term outcome and clinical characteristics during follow-up
of IVF patients. The purpose of this study is to further elucidate
underlying causes and to more accurately assess the prognosis.
Methods: This retrospective cross-sectional study describes the
follow-up of 100 IVF patients diagnosed since 1985. IVF diagnoses were reassessed and reclassified if needed according to
current guidelines. Additional testing (e.g. ajmalin-testing, echocardiography, genetic testing) was performed if needed. Genetic
testing was performed with a custom gene panel containing 33
genes associated with VF and cardiomyopathy. Results: Fiftynine males and 41 females were included, with a mean age at
event of 41.6 years. A previous history of syncope was
reported in 24 % of patients. Ninety patients (90 %)
received an ICD, of which 36 % (32/90) received appropriate ICD therapy. During a mean follow-up of
10 years, diagnosis was revised in 18 % of patients
(e.g. to structural disease such as arrhythmogenic and
dilated cardiomyopathy or electrical disease such as
Brugada and long QT syndrome). A genetic diagnosis
was obtained in 11 patients. The all-cause mortality was
13 %. Conclusion: Our results show a high mortality
and recurrence rate of ventricular arrhythmia requiring
ICD-therapy in IVF patients. A substantial amount of
patients initially diagnosed with IVF reveal an underly-
209
210
31 Abstract 1525
32 Abstract 1557
211
212
213
214
43 Abstract 0116
GAP JUNCTION UNCOUPLING DURING ISCH
AEMIA ACTIVATES NORMALLY QUIESCENT
PURKINJE-MYOCARDIAL JUNCTIONS
RESULTING IN MORE COMPLEX ACTIVATION
PATTERNS
Fu Siong Ng1, Elham Behradfar2, Michael T Debney1, Anders
Nygren2, Adam Hartley1, Alexander Lyon1, Igor Efimov3,
Edward Vigmond4, Nicholas S Peters1
1
Imperial College London, London, UK; 2University of Calgary, Calgary, Canada; 3Washington University in Saint Louis, Saint Louis, MO, USA; 4 Universite Bordeaux 1, Bordeaux,
France
Introduction: The His-Purkinje system activates ventricular
myocardium through Purkinje-myocardial junctions (PMJs).
It has been suggested that most PMJs are normally nonfunctional at baseline due to sourcesink mismatches at these
junctions. We hypothesised that gap junctional uncoupling at
the PMJs during acute ischaemia facilitates propagation across
a greater number of functional PMJs, thereby leading to accelerated but more complex activation patterns. Methods: In
aortic-perfused rabbit hearts (n=8), the right ventricles (RV)
were exposed, preserving the Purkinje system (Figure), and
the endocardium optically mapped. Activation of the RV endocardium during atrial pacing was recorded during 40 min of
global ischemia followed by 30 min reperfusion. A corresponding detailed 3D computer model of rabbit ventricles
with Purkinje system was also constructed to test the hypothesis. Results: Optical mapping studies revealed that the percentage of RV area activated within the first 5 ms decreased
from baseline 53 6 to 43 8 % during early ischemia
(<20 min), and paradoxically then increased to 598 %, with
more complex activation (p<0.001). This coincided with
more surface breakthroughs at more PMJs during late
ischaemia (Figure). Activation normalised after reperfusion. In the computer model, a 6 % reduction in conductivity was sufficient to render quiescent PMJs active.
Increasing the fraction of functioning PMJs from 5 to
100 % accelerated endocardial activation from 27.1 to
15.8 ms, compensating for reduced conduction velocity.
Surface breakthroughs increased, as did the complexity
of activation, matching the experiments. Conclusion: At
baseline, most PMJs are quiescent. Ischaemia-induced
closure of gap junction channels reduces conduction velocity, but as the uncoupling progresses, more PMJs become functional due to reduced sourceload mismatch.
The altered, more complex, activation patterns during
ischaemia may be pro-arrhythmic as they increase the
pathways for meandering wavefronts and the likelihood
of wave collision.
44 Abstract 0214
CELLULAR CHARACTERISATION OF STROMAL
CELL AND CARDIOMYOCYTE COUPLING AT THE
CRITICAL ISTHMUS IN AN IN VIVO SWINE
MODEL OF POST-INFARCTION RE-ENTRANT
VENTRICULAR TACHYCARDIA
Tarvinder Dhanjal1, Nicolas Lellouche2, Chris Von Ruhling1,
David Edwards1, Chris George1, Alan Williams1
1
Wales Heart Research Institute, Cardiff, UK; 2 Henri Mondor
Hopital, Paris, France
Introduction: Electroanatomical- and MRI-based mapping techniques have defined the critical isthmus (CI)
in the post-myocardial infarction (MI) re-entrant VT
215
216
Non-inducible
VT
(n=6)
454112
Inducible
VT
(n=6)
39350
LV mass (g)
1463
14514
0.87
2712
264
0.52
167
101
0.005
115
173
0.055
413
642
0.004
0.34
45 Abstract 01233
46 Abstract 1713
217
218
52 Abstract 2816
FEASIBILITY OF A NON-INVASIVE ELEC
TROCARDIOGRAPHIC MAPPING SYSTEM AT
LOCALISATION OF ECTOPY TO GUIDE ABLATION
IN PATIENTS UNDERGOING REPEAT CATHETER
ABLATION FOR ATRIAL FIBRILLATION
Norman Qureshi1, Cheng Yao2, Shahnaz Jamil-Copley1,
Michael Koa-Wing1, Sajad Hayat1, Fu Siong Ng1, Afzal
Sohaib1, Elaine Lim1, Ian Wright1, Nick Linton1, David
Lefroy 1 , Zachary Whinnett 1 , Nicholas Peters 1 , Prapa
Kanagaratnam1, Phang Boon Lim1, D Wyn Davies1
1
Imperial College, London, UK; 2 CardioInsight Technologies,
Cleveland, OH, USA
Pulmonary vein isolation (PVI) is the cornerstone of
atrial fibrillation (AF) ablation. Long-term outcomes
219
220
53 Abstract 1546
54 Abstract 1537
221
Day case AF
ablation
46
Overnight stay
after ablation
104
Total
A 86 %, B 7 %, C 7 %
A 88 %, B 9 %, C 3 %
A 87 %, B 8 %, C 5 %
NS
1. 86 %, 2. 19 %
66 (44 to 83)
1. 80 %, 2. 18 %
66 (34 to 88)
1. 83 %, 2. 18 %
66 (34 to 88)
NS
NS
Female (%)
50
48
49
NS
100
9h
5 (11 %)
102
27 h
15 (14 %)
102
26 h
20 (13 %)
NS
<0.001
NS
225
705
N
Technology used, A multipolar cathether RF
ablation, B point-to-point ablation, C Cryo ablation
1. Paraxsysmol AF, 2. Persistant AF
Age in years (range)
P value
150
time (RF time needed for PVI) was 12.55.1 min; 98 % of the
targeted veins were isolated with a mean of 23.46.3 RF pulses
per patient. In only four patients, a single point ablation strategy
was required to achieve the PVI. No stroke/TIA, pericardial effusion, or cardiac tamponade were observed. Only one groin
hematoma was reported. Conclusions. In this multicenter registry, irrigated multi-electrode RF ablation resulted widely feasible,
achieving a high rate of isolated PVs. In addition, procedural and
fluoroscopy times were comparable with other techniques and,
importantly, related to low complication rates. Pre-ablation imaging allowed reduced fluoroscopy time.
56 Abstract 1540
222
Department of Cardiology, St Bartholomews Hospital, London, UK; 2 The Bristol Heart Institute, University Hospital
Bristol NHS Foundation Trust, Bristol, UK
223
224
62 Abstract 2414
64 Abstract 3110
225
226
65 Abstract 2419
66 Abstract 2413
NICM and
MSES
3
p value
55
19
Age (mean)
66.7
62.7
0.052
Male (%)
89
74
0.106
LVEF % (mean)
19.8
21.8
0.144
ICD therapy
45 % (25/55)
0 % (0/19)
18.21 (1.16285.47)
0.038
227
228
73 Abstract 2814
229
74 Abstract 1819
230
therapy averaged to a 6-month period. RESULTS: Twelve consecutive patients who underwent robotic VT ablation were compared to 12 consecutive patients undergoing a manual ablation.
Patient demographics and comorbidities were similar in the two
groups. A significantly higher proportion of robotic cases were
urgent (9/12 (75 %)) vs. manual (4/12 (33 %)) (p=0.01). Postablation VT stimulation did not induce clinical VT in 11/12
(92 %) in each group. There were no peri-procedural complications related to ablation delivery. Patients were followed up for
Clinical characteristics
N
Age/year (meanSD)
LVEF 2D echo (meanSD)
Total ATPs 6 months pre abl. (median (IQR))
Total shocks 6 months preabl. (median (IQR))
Previous manual ablation
No. of VTs induced (meanSD)
Scar location
Robotic
12
70.85.5
28.113.7 %
19 (4396)
1.5 (14)
4/12 (33 %)
2.41.9
Manual
12
73.86.7
31.210.7 %
11 (822)
1 (03)
1/12 (8 %)
1.71.0
p value
1a
0.24c
0.53c
0.56c
0.73c
0.32a
0.31c
Anterior
Inferior
Apical
Maximum power/W (meanSD)
Overall procedure duration/min (meanSD)
4
4
4
29.62.7
31291
3
7
2
44.610.0
21893
1a
0.41a
0.65a
<0.001c
0.02c
6/12 (50 %)
5/12 (42 %)
1/12 (8 %)
24.119.1, 27 (540)
3.5 (110)
0.6 (01)
3.5 (111)
Pre 32 (5400)
Post 1 (05)
p=0.023d
3/12 (21 %)
8/12 (67 %)
3/12 (25 %)
1/12 (8 %)
21.114.6, 22 (932)
0.5 (011)
0 (02)
1 (014)
Pre 14 (1025)
0.60b
0.68a
0.67a
1a
0.77b
0.38b
0.52b
0.38b
0.49b
4/12 (29 %)
1a
abl ablation, Atp Anti-tachycardia pacing, ICD implantable cardioverter defibrillator, ind inducible, LVEF left ventricular ejection fraction, proc
procedural
a
Fishers exact test
b
MannWhitney U test
c
Students t test
d
Wilcoxon signed rank test
75 Abstract 1714
CLINICAL EXPERIENCE USING A NEW
FLUOROSCOPY-INTEGRATED CATHETER TRAC
KING SYSTEM (MEDIGUIDE) FOR ABLATION OF
VENTRICULAR TACHYCARDIAA
CASE-MATCHED COMPARISON
Michael Derndorfer1, Elisabeth Sigmund1, Georgios Kollias1,
Siegmund Winter1, Helmut Prerfellner1, Josef Aichinger1,
Martin Martinek1
Elisabethinen University Teaching Hospital of the Universities Innsbruck, Vienna and Graz; Linz, Austria, Linz, Austria
Mediguide (MG) represents a new catheter tracking system
integrated into the C-arm of a standard fluoro unit. After recording of short fluoro loops (RAO, LAO position), the tip of
MG-catheters is precisely visualized onto these, allowing nonfluoroscopic tracking within EnSite NavX. Objective: We
assessed system feasibility, safety and intraprocedural
231
parameters for radiofrequency-ablation of ventricular tachycardias (VT) in patients with structural heart disease (SHD)
or idiopathic VT. Methods: Sixty-three consecutive VTpatients (21 MG, 42 conventional using a standard 3D system) were retrospectively compared in a 2:1, closely casematched comparison. Thirteen patients (61.9 %) in the MGgroup and 23 patients (54.7 %) in the conventional group
showed SHD. Ten (MG, 47.6 %) vs. 25 (conventional,
59.5 %) patients had a history of recurrent ICD shocks. Procedural parameters were compared between both groups. The end
point of non-inducibility was used for all patients. Results:
76 Abstract 1835
232
82 Abstract 0719
233
234
who met ARVD/C 2010 Task Force Criteria during 39 singleton pregnancies >13 weeks (14 per woman). Cardiac and
obstetric outcomes were ascertained in all. Results: Pregnancy
began at a mean age of 31.23.5 years. ARVD/C was diagnosed prior to most pregnancies (n=29; 74 %), whereas in 7
(18 %), ARVD/C was present but not yet clinically recognized
and 3 pregnancies (8 %) were ongoing at diagnosis. Treatment
in pregnancies included beta blockers (n=16), sotalol (n=4),
flecainide (n=1), digoxine (n=1), diuretics (n=3) and ICDs
(n=28). Most pregnancies were uneventful (n=23; 59 %);
new or worsening symptoms were noted in 9 (23 %): 6
palpitations/PVCs and 3 fatigue/dyspnea. A single sustained
VT or appropriate ICD therapy occurred in 5 pregnancies
(13 %): 3 first trimester sustained VTs (ARVD/C not yet
established), 1 second trimester anti-tachycardia pacing
(ARVD/C established) and 1 first trimester ICD discharge in
a woman with a history of sustained VT. In contrast, 9 other
pregnancies in women with VT/ICD discharge history were
without events. AHA Class C heart failure (HF) developed in
2 pregnancies (5 %), in women with either biventricular structural disease or tricuspid valve disease pre-pregnancy. They
were managed outpatient and are stable 2 and 5 years postdelivery. In 9 other pregnancies with significant right ventricular structural disease, no HF developed. All pregnancies resulted in live-born children without major obstetric complications. Of 11 C-sections (28 %), only 1 was exclusively
ARVD/C-related (HF). At last follow-up all children were
healthy (023 years old); mothers had no cardiac mortality
or transplant. Conclusion: Although caution is warranted in
women with established biventricular or valve disease, pregnancy and delivery appear to be reasonably safe in ARVD/C,
especially when it is recognized beforehand. With adequate
guidance and treatment, a favorable outcome for both mother
and child is generally obtained.
84 Abstract 0715
85 Abstract 0714
ARRHYTHMOGENIC RIGHT VENTRICLAR DYSP
LASIA DURING PREGNANCY: RETROSPECTIVE
STUDY OF 21 PATIENTS
Emilie Varlet1, Jacky Nizard2, Guillaume Duthoit2, Veronique
Fressart2, Nicolas Badenco2, Xavier Waintraub2, Caroline
Himbert2, Carole Maupain2, Thomas Chastre2, Franoise
Hidden-Lucet2, Estelle Gandjbakhch2
1
Hopital Bichat, Paris, France; 2Hopital La Pitie Salpetriere,
Paris, France
IntroductionArrhythmogenic right ventricular dysplasia
(ARVD) is an inherited heart disease responsible for lifethreatening ventricular arrhythmias. There are few data
concerning complications associated with this disease
235
236
86 Abstract 0312
familial arrhythmogenic disorders and underlines that molecular testing and genetic consultation of the entire family
should be performed early in disease management. A genetic
diagnosis allows optimal patient management, identifies relatives at risk for sudden death and allows initiation of preventive measures in those individuals.
Abstract oral session 9: Atrial fibrillation mechanisms I
Tuesday, April 21, 2015, 8:30 AM10:00 AM
91 Abstract 0121
237
near-instantaneous re-initiations of AF and locating these foci critical in sustaining the arrhythmia. This meth-
92 Abstract 1421
of the underlying rhythm as a function of the spatial wavelength, together with a method for estimating the spatial wavelength. Methods: Simulations of rotors and focal sources with
the spatial wavelength within the range for human AF (n=9,
range 3278 mm; downsampling range 0.125 mm) were
used to estimate the minimum number of points (N) per spatial
wavelength. Spatial wavelength was estimated (conduction
velocitycycle length), and the number of points required
for estimation was investigated. Realistic catheter arrangements (spiral, circular, five-spline and basket) were compared.
Results: The minimum value of N necessary to identify a rotor
were as follows: 2.5 (for visual identification), 2.7 (for determining rotor core location with a threshold distance of 4 mm)
and 3.1 (for a distribution of false phase singularity detections
below threshold). Focal sources could be detected with N=3.3
(visual), N=1.6 (maximum divergence location). The spatial
wavelength was determined accurately using 7 points. When
placed over the rotor core, all of the catheters performed well
(core location error for wavelength of 33.5 mm: spiral 0.7 mm,
circular 3.5 mm, five-spline 0.5 mm; for wavelength of
75.2 mm: basket 5.4 mm, Fig). Conclusions: For the range
238
93 Abstract 1420
Introduction: The goal of surgical or catheter-based interventions for atrial fibrillation (AF) is to restore normal cardiac
function, i.e., restoration of normal ventricular function, in
particular left ventricular (LV) function, since good LV function can sustain the entire circulatory need, including atrial
hemodynamics. Restoring cardiac physiology: Normal LV
function requires a normal chronotropic response with early
activation by the Purkinje system of the papillary muscles for
the earliest closing of the mitral valve. The LV is an active
suction pump that, in each beat, aspirates the entire left atrial
(LA) volume. Indeed, we recently, documented that the LV
stroke volume is equal to the LA prediastolic volume. Therefore, the explosive suction of the LV, combined with LA recoil, allows complete flushing of the LA. However, irregular
LV rhythm disables effective flushing of the LA, a major cause
of thrombosis. Restoring normal LV function in chronic or
persistent AF can be achieved by permanently ablating the
AF anatomical substrate using multiple catheter sessions or
surgical access or focusing only on protecting the sinus
node-AV node-His-Purkinje system by isolating, in part or in
full, the right atrium (RA) from the fibrillating LA. The experience with the Corridor operation, which is a variety of RA
isolation, documented excellent cardiac function with normal
flushing of the fibrillating LA. RA isolation: Recent publications have documented that multiple extensive catheter ablations of the LA result in normal LA physiology as
documented for the Corridor or RA isolation: the three approaches listed above produce identical cardiac physiology.
The advantages of RA isolation include the following: (a)
an intervention focusing on discrete, well-defined targets,
i.e. the three discrete interatrial bundles, the Bachmann, the
coronary sinus and the LA-AV nodal bundles; (b) a single
shot intervention that can be delivered, by catheter or surgical access, easily combined with open heart access and
easily performed via minimally invasive access for lone
AF; (c) the single-shot catheter ablation should increase
the effectiveness of electrophysiology procedures and decrease patient wait times, and (d) last but a critical advantage, RA access will eliminate the added risk of stoke which
is currently associated with extensive LA catheter ablation.
Conclusions: We have presented arguments in support of
RA isolation as an addition and alternative to current ablative rationales. RA isolation may become a first choice for
persistent AF, and with more experience, be a valid alternative for paroxysmal AF
95 Abstract 1519
239
240
96 Abstract 0213
canine left atria were used for these studies, with the LA divided
into nine regions (Figure) and frozen for subsequent analysis.
LA structure was assessed by immunohistochemistry of
connexin 40 and 43 proteins and autofluorescence of fibrosis.
For fibrosis, the total amount of fibrosis, the proportion of
stringy (interstitial) and circular (scar) fibrosis were analysed,
and for connexins, the heterogeneity of connexin 40, the
colocalisation of connexin 40 and 43 in intercalated disks, the
size of en-face intercalated disks and the proportional occupation by connexin43 of these en-face disks were calculated. Results: Gap junctional disk size was increased in the midposterior wall of the LA compared with other regions (p=
0.03). We did not detect any other regional differences in fibrosis quantity/proportions nor in connexin heterogeneity or
colocalisation. Conclusion: There were detectable differences
in gap junctional disk size between regions in the LA as
assessed by immunohistochemistry, though we detected no other spatial heterogeneities of fibrosis and connexins. Correlation
of the structural data above with optical mapping data of AF in
these preparations may help to explain if any spatial structural
heterogeneities contribute to the locations of drivers in AF.
241
regulatory function in the progression of LSAF and are involved in atrial arrhythmogenic structural remodeling. Identification of key miRNAs in atrial remodeling will advance our
understanding of the determinants of AF and suggest novel
therapeutic possibilities to prevent clinical AF.
102 Abstract 0114
242
recordings and conduction velocity measurements in isolated rat atrium. Moreover, automated patch-clamping
(Qpatch) was used to access sodium current inhibition.
Results: Runs of atrial fibrillation observed in the isolated right atrium was not inducible after pharmacological
SK channel inhibition. The SK channel inhibitor
N-(pyridin-2 -yl)-4-(pyridin-2-yl)thiazol-2-amine
(ICAGEN) exhibited antiarrhythmic effects. Without directly inhibiting sodium channels, ICAGEN induced atrial post-repolarization-refractoriness and slowed conduction velocity. However, due to a marked prolongation
of ERP, the calculated wavelength was increased. Furthermore, at increased pacing frequencies, SK channel
inhibition showed more prominent effects on sodium
channel-dependent parameters. Contractility was not affected. Conclusion: SK channel inhibition modulates
multiple parameters of the action potential, including
prolongation through direct blockage of the repolarizing
SK current, and shifting the resting membrane potential
towards more depolarized potentials, which leads to an
indirect sodium channel inhibition and ultimately conduction slowing and decreased excitability. Hence, we
propose that the antiarrhythmic mechanism of SK channel inhibition is generated both through direct potassium
channel block and via indirect sodium channel inhibition.
243
244
P=0.0017). Additionally, frequent occurrences of early afterdepolarization on action potentials were noted in MetSVLDL-treated HL-1 cells. Conclusions: The VLDL of MetS
individuals augmented repolarizing calcium currents, increased intracellular calcium release, and significantly shortened action potentials. These changes may contribute in coordination to increased AF vulnerability in MetS.
Abstract oral session 11: Management of atrial
arrhythmias
Tuesday, April 21, 2015, 8:30 AM-10:00 AM
111 Abstract 1532
245
246
INR 1.82.0
INR>2.0
ACT 1
360.52133.249
311.5673.284
348.5890.744
ACT 2
P value
311.67131.192
0.02
297.7691.123
n.s.
319.32112.483
n.s.
PREDICTORS OF CEREBRAL
MICROEMBOLIZATION DURING PHASED
RADIOFREQUENCY ABLATION OF ATRIAL
FIBRILLATION: ANALYSIS OF BIOPHYSICAL
PARAMETERS FROM THE ABLATION GENE
RATOR.
Edina Nagy-Bal1, Alexandra Kiss1, Catherine Condie2,
Mark Stewart2, Zoltn Csndi1
1
University of Debrecen, Institution of Cardiology, Debrecen,
Hungary; 2Medtronic Inc., Minneapolis, MN, USA
BACKGROUND: Pulmonary vein isolation with phased radiofrequency current and use of a pulmonary vein ablation
catheter (PVAC) has recently been associated with a high incidence of clinically silent brain infarcts on diffusionweighted magnetic resonance imaging and a high
microembolic signal (MES) count detected by transcranial
Doppler. OBJECTIVE: The purpose of this study was to investigate the potential correlation between different biophysical parameters of energy delivery (ED) and MES generation
during PVAC ablation. METHODS: MES counts during consecutive PVAC ablations were recorded for each ED and time
stamped for correlation with temperature, power, and impedance data from the GENius 14.4 generator. Additionally,
catheter-tissue contact was characterized by the template
247
248
249
250
right and left atrial flutters are frequently encountered. Aggressive ablative therapy leads to acceptable long-term results.
However, adjunctive anti-arrhythmic therapy is needed in a
third of patients.
comparison to CC group. CF technology is able to significantly reduce procedure time without compromising complication
rate.
125 Abstract 1411
INTRODUCTION: Three months of empirical antiarrhythmic drug (AAD) therapy after atrial fibrillation ablation (AFA) is common to prevent early AF recurrence
with limited data to support this practice. OBJECTIVE:
The study aims to perform a meta-analysis of published
controlled trials comparing temporary AAD therapy after
AFA with standard care in patients after AFA. The primary outcome was recurrence of arrhythmia. A subgroup analysis stratified patients by durations of
follow-up at 6 months. RESULTS: Seven trials were
included; six were randomized and one was a retrospective controlled study. Among 1245 patients, 763
(61.3 %) had paroxysmal AF, and 318 (25.5 %) had
persistent AF. In total, 747 patients were treated with
AADs and 498 patients served as a control group (no
AA therapy). Various class IC-III antiarrhythmics were
used. Length of AAD administration varied between
6 weeks immediately following AFA to 3 months. The
follow-up duration ranged from 1.5 to 12 months.
Among AAD-treated patients, the recurrence of arrhythmia rate was 33.4 vs. 39.5 % in control patients (odd
ratio 0.75, 95 % CI 0.541.03, P = 0.08)., Subgroup
analysis revealed that among patients followed for
6 months or longer after AFA, AAD-treated patients
had an arrhythmia recurrence rate of 32.9 % compared
with 45.1 % among control (odds ratio 0.55, 95 % CI
0.330.91, P=0.02). However, no significant heterogeneity was noted compared with patients followed for less
than 6 months (I2 =39 %, P=0.18). CONCLUSION: Antiarrhythmic therapy may help to reduce delayed
(6 months or longer) recurrence of AF after AFA. A
definitive large randomized controlled trial appears warranted to confirm these findings.
251
252
month treatment of ivabradine caused a stronger attenuation of mean and maximal Holter ECG HR and of maximal HR at stress test in comparison to bisoprolol.
Ivabradine was also more effective in controlling symptoms and was better tolerated than bisoprolol.
NONINVASIVE ELECTROCARDIOGRAPHIC
IMAGING OF ATRIAL FLUTTER IN HUMANS
USING PHASE MAPPING
Amiran Revishvili1, Dmitry Lebedev2, Michail Chmelevsky2,
Alexander Kalinin3, Vitaly Kalinin1, Evgenii Labartkava1,
Oleg Sopov1, Stepan Zubarev2
1
Bakoulev Scientific Center for Cardiovascular Surgery,
Moscow, Russia; 2Almazov Federal Heart, Blood and Endocrinology Centre, St. Petersburg, Russia; 3Lomonosov Moscow State University, Moscow, Russia
Introduction. Noninvasive electrocardiographic imaging
(ECGi) is a state-of-the-art electrophysiology methodology that has been used to reconstruct local unipolar
electrograms at the epicardium from the body-surface
potentials. We have extended ECGi to map both endo
and epicardium. Here, we introduce phase mapping to
analyze stable reentrant atrial flutter. The stability of
flutter allowed us to validate ECGi with invasive electroanatomic mapping. Methods and results. Nine consecutive patients with type I atrial flutter (AFl) were examined. All patients underwent ECGi using an Amycard
01 C system (Amycard, Moscow, Russia). Data processing included reconstruction of unipolar electrograms,
phase and isochronal mapping. Validation of the methodology was carried out based on electroanatomical
mapping using a CARTO XP EP Navigation system
(Biosense Webster, Diamond Bar, USA). Using isochronal maps of the right atrium, we conducted radiofrequency ablation of cavo-tricuspid isthmus in all patients. We visualized the spread of excitation using noninvasive phase mapping. A typical counterclockwise reentry circuit around the tricuspid valve with a transition
through the cavo-tricuspid isthmus was the mechanism of
AFl. We visualized two types of patterns of atrial activation which are typical for type I (N=8) and lower-loop
(N=1) AFl. The results were confirmed using a CARTO
XP system in all patients. Catheter ablation of the isthmus resulted in successful termination of AFl in all patients. Conclusions. Noninvasive phase mapping enables
accurate detection of the activation pattern in type I AFl,
253
the electrogram voltage-time relationship, gated to a fiduciary time point that enables mapping without point annotation or window-of-interest adjustments. We prospectively tested the RM module on CARTO3 v4 in a consecutive series of atrial tachycardia (AT) ablations. Methods:
3D maps were collected with CARTO3 v4 with color and
fill threshold reduced to 5 mm to ensure dense and even
point collection. RM preferences were set to clip bars at
0.25 mV and exclude points <0.03 mV. During RM playback, the bipolar voltage threshold was modified to display scar as areas devoid of ripple activation. Results:
Nine patients (mean age 66 years, six male) were studied.
The mean number of points collected was 837 (range
1822426) over a mean chamber area of 205 36 cm2
(seven left atrium) and mapping time of 358mins. Five
maps were collected with ConfiDense automated mapping. RM demonstrated a focal origin in four patients
and ablation at the earliest ripple bar terminated all cases.
Macro-re-entry was demonstrated in the remaining five
patients (see figure). Dual-loop re-entry involving the roof
and mitral annulus was evident in three patients. Modifying the voltage threshold identified isthmuses of conduction bounded by islands of scar or previous ablation lines
critical to these circuits. Ablation transecting these isthmuses changed or terminated tachycardia in each case.
Automated isochronal maps were un-interpretable in two
focal cases owing to inappropriate setting of the window
of interest and four re-entrant studies due to the complexity of propagation. Conclusion: In this small series of
prospective AT ablations, RM correctly defined the mechanism of AT and critical sites for ablation delivery.
254
INTERVENTIONAL TREATMENT
SUPRAVENTRICULAR TACHYARRHYTHMIAS IN
CHILDREN WITH CONGENITAL HEART DISEASE
Introduction. A new generation ablation system with an irrigated ablation catheter in conjunction with an advanced electroanatomic mapping and navigation system allows the evaluation
of the electrical coupling index (ECI), an indication of tip-totissue contact. The aim of our study was to evaluate if this index
could also give an indication about ablation lesion efficacy.
Methods. In patients undergoing typical right atrial flutter ablation, we compared the values of the ECI before, during (at the
plateau) and after isthmus ablation. Permanent tissue damage or
ablation lesion efficacy was defined as the reduction in the local
potential >90 % or as potential split in two separate signals. In
the absence of these endpoints, lesions were deemed ineffective.
Results. Fifteen consecutive patients (11 males, age 69.3
11.4 years) with history of typical atrial flutter underwent an
ablation with Contact Therapy Cool Path Cardiac Ablation System in conjunction with EnSite Velocity Contact
technology between Sep 2012 and Aug 2013. The target site for
ablation was the isthmus between the inferior vena cava and the
tricuspid valve. All the procedures were successful, without
complications. The number of radiofrequency (RF) applications
was 10.86.7 (range 628) and RF time was 330.3177.5 s.
ECI values are reported in the table:
Overall
RF effective
shots
RF ineffective
shots
p*
RF duration (s)
31.73.7
31.43.9
36.14.5
0.02
100.110.5
101.610.8
104.819.3
ns
56.39.6
55.89.7
6820.1
ns
81.09.6
79.610.9
95.416.9
0.03
19.15
223.6
9.42.5
<0.001
18.54.2
21.03.6
8.81.2
<0.001
Delta ECI
(pre-post ablation)
Delta% ECI
(pre-post ablation)
Purpose: The study aims to evaluate the results of ablation of supraventricular tachyarrhythmia (SVT) in pediatric patients with congenital heart disease (CHD).
Material and methods: From 2000 to 2014, electrophysiological study and catheter radiofrequency ablation for
atrial tachyarrhythmias was performed in 215 children
with congenital heart disease from 1 to 18 years. The
median age was 104.8 years (132 boys and 83 girls).
Patients performed surgery on the following congenital
heart disease: ASD, VSD, tetralogy of Fallot, Ebstein
anomaly (in some casesoperation Sealy), transposition
of great vessels and Fontan operation. Results: One
hundred and thirteen patients had typical or atypical
atrial flutterallin the postoperative period. Other arrhythmias were as follows: WPW syndrome 65 patients,
AVNRT 18, ectopic atrial tachycardia 17 children, occurrence in preoperative (51 %) and in the postoperative
period (49 %). The overall effectiveness of catheter ablation after repeated treatments was 87.2 %. Repeat procedures were performed totally in 10 % of patients and
5 % of them after Ebstein anomaly correction. Conclusion: the effectiveness of interventional treatment SVT
in child with CHD in all cases depends on the age of
the child, such as congenital heart disease and methods
of surgical correction of congenital heart disease.
137 Abstract 0812
255
Background: It is suggested that adenosine resistance of retrograde fast pathway in slowfast atrioventricular nodal reentrant tachycardia (AVNRT) confirms the participation of a
concealed retrograde atriohisian pathway, rather than a conventional fast pathway in the arrhythmia circuit of slow-fast
AVNRT. Methods: Electrophysiologic parameters and adenosine sensitivity of the retrograde fast pathway were studied in
21 consecutive patients (18 women; age 5710 years) with
slowfast AVNRT and in a control group of 24 patients (11
women; age 4616 years) without documented supraventricular tachycardia in which AVNRT, accessory pathways, and
other supraventricular tachycardias had been excluded. Results: Fifteen patients (71 %) with AVNRT and 18 patients
(75 %) in the control group developed a transient VA block
after intravenous administration of adenosine (P = 0.79).
Among patients with slowfast AVNRT, female gender (P=
256
Life-threatening atrioventricular reentry tachycardia in newborn is a rare disease. We report the case of a 16-day-old
newborn submitted in cardiogenic shock requiring cardio pulmonary resuscitation (CPR) and extracorporeal membrane oxygenation (ECMO). The patient was presented with a history
of occasional vomiting over the past 6 days and an accelerated
heart beat was noticed the evening before admission by the
parents. At the time of admission, the child showed clinical
signs of severe cardiac failure and an atrioventricular reentry
tachycardia with a heart rate of 240 bpm and a left bundle
brunch block. Echocardiography showed highly reduced left
ventricular function and a massive dilatation of the left ventricle. Therapy with adenosine and amiodarone led to conversion to sinus rhythm detecting an antidromic leading accessory pathway conduction but was not sufficient to restore a permanent stable circulation. Regarding a continuous need of
CPR, a venous-arterial ECMO must be established leading
to resumption of proper organ functions. Therapy with intravenous amiodarone and flecainide led up to control of frequency and increasingly normal cardiac rhythm and the extracorporeal circulatory support could be explanted after 4 days.
257
258
259
260
Percentage of success
I-GR
B-GR 8
10
14/33
25/33
<0.002 0.002
42
76
261
Background: Although atrial fibrillation (AF) is commonly associated with sinus node dysfunction (SND), hemodynamic characteristics of those patients have not yet been investigated. Objective: The purpose of this study was to determine whether elevated
LAP plays some role in the pathogenesis of SND among patients
with AF. Methods: We included 182 patients (67.6 % male, 59.0
11.1 years old, 69.2 % paroxysmal AF) who underwent radiofrequency catheter ablation for AF. We measured both
LAPpeak(SR), LAPpeak(AF), and LA pulse pressure [LApp=
LAPpeak(SR)-LAPnadir(SR)] at the beginning of the ablation
procedure, and compared LAPs from 30 patients with SND (19
262
263
00.1
3.72.6
0.50.8
4.73.6
1.62.0
0.30.9
2.33.4
ED [mSv]
0.30.4
0.10.2
0.50.7
Table 1. Radiation exposure of patients undergoing first RMNguided PVAI for PAF. FT fluoroscopy time, DAP dose area
product, ED effective dose. After having finished the learning
curve PVAI in the last 150 patients required a total FT of 3.5
2.2 min corresponding to an ED of 0.280.3 mSv. Total
264
265
266
267
AUC
p value
Framingham score
65.7 [60.85;78.77]
Framingham score+PAC
72.2 [66.35;84.29]
0.0072
Framingham score+NT-proBNP
68.4 [61.98;81.43]
0.23
Framingham score+PAC+NT-proBNP
72.3 [66.43;84.22]
0.013
268
269
270
Conclusion: Supraventricular dysrhythmia occurs in the majority of patients after CABG, whereas PoAF develops in
28 % of the patients. Independent risk factors for development
of AF after CABG were the frequency and burden of SVPBs
and SV-runs. Hence, these parameters could be used to identify patients at risk for developing PoAF and allows preventive measures to be taken.
No PoAF
PoAF
P value
178/0.02
65
540/0.09
63
0.01/0.00
0.02
22/0.02
6/0.2
45/0.05
34/0.9
0.09/0.05
0.02
271
272
The purpose of the present study was to examine indicators of heart rate turbulence on this 24-h ECG in
older men suffering from essential arterial hypertension
(AH) with high cardiovascular risk. Materials and
methods. The group surveyed was consisted of 75 men
with arterial hypertension of degree III, risk 4, in middle age 67.42.5 years. AG diagnostics was carried out
taking into account the recommendations of the RSC
(Russian Society of Cardiology) (2010). All patients
were evaluated for quality of life (GL) on the scale of
the SF-36. The assessments of the level of depression
by Beck questionnaire and of reactive and personal anxiety on the evaluation scale of Ch. Spilbergera and Y.l.
Hanina had place. A 6-min walk test, the study of biological age by V.P. Voitenko method as well as ECG,
echocardiography, a daily monitoring of ECG in order
to evaluate the heart rate variability and study of heart
rate turbulence with an assessment of turbulence onset
(TO) and turbulence slope (TS) according to the 24-h
ECG monitoring were performed. The comparison group
was consisted of 25 male with AG at the age of 46.3
3.8 years. It was found that elderly patients with high
cardiovascular risk differ from the patients of the comparison group by an increased performance of TO and
decrease of TS (P<0.05). Pathological night values of
TO was associated with a reliable (P<0.05) increase in
body mass index (BMI), the average heart rate (AHR),
the reduction of circadian index, decreased power of the
low- and high-frequency components of heart rate variability spectrum, elongation QT according to standard
ECG, an increase of the minute bloodstream (IOC)
and the index of left ventricular myocardium mass
(iLVMM). An equation of multifactor regression analysis including 12 parameters of clinical-functional status
of elderly patients as independent variables found the
influence of independent myocardial mass index of left
ventricle of the heart on the night TO reducing.
273
using open and closed irrigated RF ablation. Furthermore, prevention of pops and the influences of blood
flow as well as position of tip electrode with a specific
angle to the myocardium could be clearly demonstrated.
Conclusions: In several workshops, the in vitro teaching
system provided excellent requirements for both physicians and medical engineering students, to become
acquainted with the physical science basics of RF
catheter ablation.
1410 Abstract 0411
274
275
patients 63 % vs 121 patients 95 %); this difference was statistically significant (p<0.0001).
AF
not AF
B2B2
27 (37 %)
6 (5 %)
B1B2
B1B1
17 (23 %)
29 (40 %)
80 (63 %)
41 (32 %)
276
277
278
PV-CB ablation/
CTI RF
PV-CB
ablation
p value
Age (years)
6212
6111
0.79
LA diameter (mm)
416
405
0.94
8229
7924
0.76
227
2010
0.51
Nb. of CB applications
8.20.6
8.41.0
0.65
Introduction: Benzodiazepines and opiate boluses are currently widely used for catheter ablation of atrial fibrillation (AF).
However, patient comfort, compliance and prolonged immobility are difficult to manage with conscious sedation. Therefore, we aimed to determine the feasibility and safety of deep
sedation with propofol/fentanyl infusion directed by specialized nurses in patients undergoing an AF ablation procedure.
Methods: Three nurses of our catheterization laboratory completed training for inducing and managing deep sedation under supervision of experienced anesthesiologists in patients
undergoing AF ablation procedures. The training included a
279
280
prospective, observational study is to determine the differences between the 23- and 28-mm CB regarding the LET
during CB ablation. Methods: Thirty consecutive patients
with paroxysmal or persistent atrial fibrillation underwent
CB PVI. The 28-mm, 23-mm, or both balloons were applied
with respect to the LA/PV-anatomy as determined by preprocedural cardiac imaging. Standard freezing time was
180 s with an additional bonus freeze after PVI. LET was
continuously recorded during the whole procedure. Prespecified cutoff value for premature termination of a
cryoapplication was a LET +15 C. Esophagoscopy was
planned in case of symptoms suggestive for esophageal lesions. Results: In total, 395 freeze cycles were applied in
125 veins, 149 (38.0 %) with the 23 mm and 246 (62.0 %)
with the 28 mm CB. PVI was achieved in 100 % of the veins.
Premature termination of the freeze cycle because of low LET
occurred only during ablation of the inferior pulmonary veins.
None of the patients developed symptomatic esophageal
lesions. Minimal LET (median) was 35.3 (14.236.4) C
with the 23-mm CB and 35.4 (12.836.7) C with the
28-mm CB, p=0.30. In subgroup analysis of the pulmonary veins, there was no significant difference either. The
freeze time after which LET started to drop showed a
positive correlation to minimal LET, p=0.001. LET drop
within 25 s predicted a LET +15 C with the
highest sensitivity (83 %) and specificity (92 %) in
ROC curve analysis. Conclusion: Low LET +15 C
occurred rarely with both balloon sizes and was without
statistical significance. Moreover, no symptomatic esophageal lesions were reported. CB ablation following an
individualized anatomic approach seems to be equally
safe with either the 23- or the 28-mm CB concerning
the LET. LET drop within 25 s predicts a minimal
LET +15 C with a high sensitivity and specificity.
Background: The clinical significance of left atrial pressure (LAP) has not yet been clearly elucidated in patients
281
282
navigation, and intracardiac echocardiography. RF delivery was power-controlled with up to 30 W along the
posterior wall and 40 W elsewhere. Esophageal temperature was continuously monitored and RF was
discontinued if temperatures above 39 C or with rapid
rise. Results: Four hundred sixty-six patients underwent
PVI, 108 females (23 %), with a mean age of 62.6
10.0 years, paroxysmal AF in 195 (42 %), persistent AF
in 269 (58 %), and AFL in 2 (0.4 %). The median AF
Duration since diagnosis was 48 months (IQR 24, 96);
mean LVEF was 55.19.8 %. Mean CHA2DS2-VASC
was 2.11.5, CAD 93 (20 %), CHF 101 (22 %), DM
54 (12 %), HTN 252 (54 %); TIA/Stroke 49 (11 %),
age 65, 221 (47 %), age 75, 48 (10 %). Average
procedure time was 24277.3 min and radiation exposure was 0.510.36 Gy. Ninety-nine cases (21 %) were
done under general anesthesia. Thirty-day complications
included four pericardial effusions (0.9 %): acute
tamponade in three (0.6 %),and mild-moderate pericardial effusion requiring no intervention in one (0.2 %),
one ischemic stroke (0.2 %), and seven groin hematoma
(1.5 %). On long-term follow-up, moderate to severe
PV stenosis occurred in nine patients (1.9 %). There
were no atrio-oesophageal fistulae and no deaths. Conclusion: PVI using the 56-hole open-irrigation ablation
catheter was not associated with excess complication on
short and long-term follow-up.
283
esophageal lesions was observed in the MIAC group. Conclusions: In our small cohort, ablation with MIAC, under
phrenic nerve and esophagus temperature monitoring, seems
to still bear a potential for complications along with important
device related limitations to successfully assess and achieve
PV disconnection. Furthermore, ablation with MIAC failed to
show significant benefits regarding relevant procedural parameters or clinical outcome compared to a SAC cohort.
1426 Abstract 2819
284
285
cardioversion at the end of procedure in all patients. Mathematical phase. Ablation formatting (corresponding to linear ablation) transformed 6-wave re-entry to 4-wave re-entry. Following
mathematical simulation of cardioversion effectively terminated
4-wave AF, whereas did not terminate 6-wave re-entry AF.
Conclusion: (1) Mathematical modeling of 6-wave re-entry
and linear ablation formatting may simulate long-lasting persistent AF and subsequent AF organization due to antral and linear
ablation. (2) Transformation of 6-wave re-entry to 4-wave reentry with following AF termination after cardioversion may
be effective ablation end-point recording tj mathematical
approach. Our clinical results are consistent with ablation formatting data.
1429 Abstract 0513
1428 Abstract 0120
286
SR
AF
Initial CF
in a pair
4.5 g SR
and 8 g AF
Median change
in complex
size (%)
110 g
6 [834]
0.06
13 [1660]
<0.005
10 g
3 [822]
0.28
0.3 [2926]
0.43
110 g
0 [1216]
0.28
6 [1141]
<0.005
10 g
2 [1318]
0.09
0 [1624]
0.12
ELECTROCARDIOGRAPHIC AND
ECHOCARDIOGRAPHIC EVALUATION OF A
LARGE COHORT OF YOUNG SOCCER PLAYERS
DURING PRE-PARTICIPATION SCREENING.
Annamaria Martino1, Fabio Sperandii1, Emanuele Guerra1,
Elena Cavarretta 2 , Federico Quaranta 3, Attilio Parisi 3 ,
Antonia Nigro2, Luigi Sciarra1, Ermenegildo de Ruvo1,
Antonio Spataro4, Fabio Pigozzi3, Leonardo Calo1
1
Cardiology Department, Policlinic Casilino, Rome, Italy;
2
FMSI Sport Medicine Institute, Villa Stuart Sport ClinicFIFA Centre of Excellence and Department of MedicalSurgical Sciences and Biotechnologies, Sapienza University,
Rome, Italy; 3Department of Health Sciences, University of
Rome Foro Italico, Rome, Italy; 4Institute of Sports Medicine and Science (CONI), Rome, Italy
Background. The early diagnosis of cardiac abnormalities in
young athletes may be helpful not only to identify subjects
potentially at risk of sudden cardiac death but also to prevent
evolution towards cardiac dysfunction. The aim of our study
was to investigate the prevalence of cardiac abnormalities in a
population of young male soccer players undergoing preparticipation screening (PPS) through ECG and transthoracic
echocardiography (TTE). Methods. All consecutive male
football players undergoing PPS in the FMSI Sport Medicine
Institute in Rome, between January 2008 and March 2009,
were enrolled in the study and underwent standardized medical history, physical examination, 12-lead ECG and TTE. Results. The study population consisted of 2261 consecutive
young athletes aged 12.42.6 years. Positive family history
287
Latest activation
during RV pacing
number of patients
Anterior
10
Antero-lateral
Lateral
8
27
8
18
Postero-lateral
Posterior
8
1
10
0
Delay in RAO
Basal
25
16
Medium
Apical
16
5
15
15
Conclusion. Coronary venous EAM can be used intra procedurally to guide LV lead placement to the latest activated
region. This approach especially contributes to optimization
of LV lead electrical delay in patients with multiple target
veins. Conventional anatomical LV lead placement strategy
does not target the vein with maximal electrical delay in many
of these patients.
152 Abstract 2411
288
Group 2 (8 pts)
Pre-implant
Post-implant
NE 750 pg/ml
E 92 pg/ml
NE 280 pg/ml
E 47 pg/ml
E 89 pg/ml
E 40 pg/ml
Accurate selection of eligible patients as well as optimal specification of their individual left ventricular electrode position
can increase responder-rate in cardiac resynchronization therapy (CRT). This could be fulfilled preoperatively by selecting
patients characterized by a distinct interventricular conduction
delay and intraoperatively by placing the LV electrode within
a desynchronized left ventricular region. Esophageal left heart
electrogram was proposed (applied) in symptomatic heart failure patients in sinus rhythm or atrial fibrillation, preoperatively, to measure interventricular conduction delay (IVCD), to
justify CRT and to intraoperatively guide the left ventricular
electrode placement. Nevertheless, there is a lack concerning
the distribution of esophageal IVCDs in healthy subjects.
Aims: The study aims to compare the esophageal IVCDs between guideline CRT patients and healthy subjects. Methods:
Esophageal IVCD was measured between onsets of QRS in
surface ECG and left ventricular deflection in the esophageal
left heart electrogram by perorally applied 4 F bipolar electrode (Osypka TOslim) in position of maximum left ventricular deflection using the Biotronic ICS3000 esophageal electrogram feature in 32 consecutive symptomatic heart failure
patients (24 male, 8 female, 66.57.8 years) 1 week after
implantation of CRT systems according to the guidelines. Results were compared with IVCDs of 31 healthy medical
289
290
291
CRTD models
Chemistry Capacity
(Ah)
Ratio
Total Usable
Boston Scientific Cognis
LiMnO2
(group 1)
St Jude Medical Promote/Atlas HF LiSVO
(group 2)
Medtronic
Consulta/
LiSVO
(group 3)
Concerto/
Maximo
1.8
0.9
1.87 1.31
0.7
1.4
0.7
1.0
AUC (CI)
p value Correct
Nagelkerke
prediction
R square
(%)
Clinical+wide
QRS
Clinical+wide
QRS+ECHO
Clinical+wide
QRS+ECHO+
Lab
Clinical+wide
QRS+ECHO+
Lab+HM
0.336
0.35
0.423
0.879 (.786;.972)
0.478
<0.001 84.5
Background: Cardiac resynchronization therapy (CRT) improves LV functions and NYHA class in the majority of heart
292
stroke volume (SV) and ejection fraction (EF) were measured on TTE by Simpsons equation. Endocardial
RWSA were correlated with LV dynamic variables (SV
and EF). RESULTS: RWSAs were similar when compared between device types (biventricular versus right
ventricular device; p=0.102), lead locations (apex, right
ventricular outflow tract, septum; p=0.186), EF [%] (<50
and >50, p=0.618). In patients without coronary artery
disease (CAD), there was a significant increase in RWSA
with decrease in SV (p = 0.008) and a non-significant
trend towards increase in RWSA with decrease in EF
(p=0.06) (Figure 1). In the presence of CAD, there was
no significant correlation between RWSA versus SV (p=
0.32) or RWSA versus EF (p=0.30). Conclusion: In the
absence of CAD, RWSA changes are inversely related to
the changes in stroke volume; however, no such association was noted in the presence of CAD.
Arrhythmia mechanisms
1511 Abstract 0215
TISSUE STRUCTURE FUNCTION RELATIONSHIPS SIZE AND DIRECTION DO MATTER.
Junaid Zaman1, Sayed Al-Aidarous1, Samha Alayoubi1,
Pravina Patel1, Cesare Terracciano1, Nicholas Peters1
1
Imperial College London, London, UK
Intro: We tested whether structure (connexin43, Cx43/fibrosis)
function (electrograms Eg, conduction velocity, CV) relations
vary with size of electrode and direction of pacing. Methods:
Macro: Functionpaced (633 Hz) Langendorff perfused rat
hearts (312 m, n=80). Microelectrode array (MiEA) mean and
max CV calculated by isochronal mapping. AF (>30s) dominant
frequency (DF), organizational index (OI), Shannon entropy
(ShEn) andmagnitude squared coherence (MSC) calculated with
small (30 mm), medium (150 mm) and large (1.5 mm) electrodes. Structurewhole atrial Cx43 phosphofractions (P0, P1,
293
294
haemodynamic function recovery after global ischaemia. However, this intervention had no significant effect on the
reperfusional arrhythmias after global normothermic ischaemia.
The purpose of the present study was to assess the effects of Iso/
Ade on cardiac function, including ventricular arrhythmias, and
necrotic damage during regional ischaemia and reperfusion.
Methods: Experiments were performed on isolated
Lengendorff-perfused rat heart. All hearts were subjected to
30-min regional ischaemia and 2-h reperfusion. Regional ischaemia was induced by occlusion of the left anterior descending coronary artery (LAD). The hearts were divided into control
and Iso/Ade groups according to the preischaemic protocol.
Hearts of the Iso/Ade group were perfused with 10 nM isoproterenol for 2 min followed by 5 min perfusion with 30 M
adenosine. Electrocardiogram (ECG) and left ventricular pressure were monitored throughout the experiment. Ventricular arrhythmias (number of ventricular premature beats (VPBs), number and total duration of ventricular tachycardia and ventricular
fibrillation (VT and VF)) were assessed using ECG. At the end
of reperfusion, infarct size-to-area at risk ratio (IS/AAR) was
determined in the hearts. In a separate series of experiments,
mitochondria were isolated from Iso-perfused and control
hearts, and the ability of mitochondria to retain Ca2+ was
assessed fluorimetrically. Results: During LAD occlusion, arrhythmias were dramatically reduced in the treated hearts. Thus,
in the control and Iso/Ade groups, the number of VPBs were
678172 vs. 13539, the number of VT and VF were 9124
vs. 73, and the total duration of VT and VF were 24385 vs. 3
1 s, respectively. During reperfusion, the number of VPBs was
similar in the two groups. However, the number and duration of
VT and VF were still significantly lower in the Iso/Ade group.
Iso/Ade also considerably improved hemodynamic function recovery and reduced IS/AAR during reperfusion. Interestingly,
that perfusion of hearts with Iso significantly enhanced ability of
mitochondria to retain Ca2+. Conclusion: Thus, in contrast to
the global ischaemia, consecutive isoproterenol/adenosine treatment effectively prevented the development of ventricular arrhythmias during regional ischaemia and reperfusion. This treatment also significantly improved functional recovery and reduced infarct size after the LAD ligation. This effect could be
a result of the improved Ca2+ handling by the myocardium in
the treated hearts during regional ischaemia and reperfusion.
1513 Abstract 1919
295
Table 1. *p<0.0001
Full cohort
Assumed nonhealthy
8779
3438
Assumed
healthy
Demographics
n
Age
Male
5341
51.5212.32
45.8 %
ECG parameters
QTcF
ms
416.520.4
420.521.8*
QTcB
ms
420.924.5
427.725.2*
413.919.0
RR
ms
956.0163.9 918.6159.8*
980.2162.0
SemM
Potassium
Se-Sodium mM
3.8830.297 3.8940.342*
3.8760.264
140.702.24 140.522.52*
140.822.03
77.3919.42 80.9425.45*
75.1413.83
416.422.9
Clinical chemistry
Creatinine
QTcF
Univariate 95 % CI
a
Multivariate 95 % CI
a
Age (years)
0.21*
[0.17; 0.25]
0.26*
[0.21; 0.30]
Gender
(M vs. F)
Se-potassium
(mM)
Se-sodium
(mM)
Creatinine
(M)
Intercept
7.4*
[8.4;6.4]
6.7*
[7.7; 5.7]
8.4*
[10.3;6.4]
8.3*
[10.2;6.3]
0.12
[0.12; 0.38]
0.17
[0.21; 0.14]
436*
[429; 443]
296
suggests that GP sites that trigger ectopy are not confined to the PV antrum as suggested by post-mortem
studies.
autopsy rates, and prior known disease have not been systematically investigated in a nationwide setting before. Methods:
All deaths in persons aged 135 years in Denmark in 2000
2009 were included. To chart causes of death and incidence
rates, death certificates, and autopsy reports were collected
and read. By additional use of the extensive health care registries in Denmark, we were also able to investigate prior disease. SCDw were compared to SCDm. Results: During the
10-year study period, there was an average of 2.37 million
persons aged 135 years (49 % women). There were a total
of 8756 deaths from 23.7 million person-years. Of these, 10 %
(n=848) were sudden unexpected deaths. In total, 635 of sudden unexpected deaths were SCD, of which SCDw constituted 205 deaths (32 %). Compared to SCDm, women less often
died in a public place (16 vs 26 %, p=0.02). Women more
often died during sleep, and less often during moderate- to
high-intensity activity (40 and 3 vs 33 and 11 %, respectively,
p=0.036). There were no differences between genders in regard to age at death, witnessed deaths, ratio of autopsies, and
ratio of sudden unexplained deaths. Likewise, there were no
differences in comorbidity between SCDw and SCDm. Most
common structural heart diseases in SCDw were ischemic
heart disease (n=17, 13 % of autopsied SCD), followed by
myocarditis and ARVC (n=9 each, 7 % of autopsied SCD). In
297
298
Secondary
prevention
p value
982773
16071461
0.043
12/39
11/20
0064
Inappropriate therapy
6/39
4/20
0.72
IS IMPLANTABLE CARD
IOVERTER-DEFIBRILLATOR REPLACEMENT
NECESSARY IN THE PRIMARY PREVENTION PATI
ENT WHOSE LEFT VENTRICULAR EJECTION
FRACTION HAS NORMALIZED?
JoEllyn Abraham1, Deepa McGriff1, C. Dennis OHare2,
Raed Abdelhadi1, Jay Sengupta1, Robert Hauser1
1
Minneapolis Heart Institute, Abbott Northwestern Hospital,
part of Allina Health, Minneapolis, MN, USA; 2 Abbott Northwestern Hospital, part of Allina Health, Minneapolis, MN,
USA
Background: There are limited data on the need for implantable cardioverter-defibrillator (ICD) pulse generator
(PG) replacement in primary prevention patients who
have not received appropriate ICD therapy (ICD-Rx)
and whose left ventricular ejection fractions (LVEF) have
normalized. Accordingly, we assessed the outcomes of
such patients at our center who did and did not undergo
ICD replacement for battery depletion. Methods: This
was a single-center retrospective study. Patients were
age 18 years who had ischemic cardiomyopathy
(ICM) or dilated cardiomyopathy (DCM) and who
underwent primary prevention ICD implantation from
2000 to 2014. Patients who had received ICD-Rx for
ventricular tachycardia (VT) or ventricular fibrillation
(VF) were excluded. Results: The cohort included 82
patients (average age 6512 years; 66 % male) whose
average LVEF was 24.27.0 % at initial ICD implant
(range 1037 %) and 49.33.9 % (range 4555 %) when
their PGs reached end-of-battery life. None had received
ICD-Rx for VT or VF. The majority of patients had
DCM (n = 48; 59 %) and the remaining patients had
ICM (41 %). Of the 82 patients, 72 (88 %) underwent
ICD replacement, 6 (7 %) were downgraded to a pacemaker, and 4 (5 %) patients had their ICDs removed or
abandoned. During average follow-up of 19
299
22.56.9
33.122.6
Clinical events
Patientss with appropriate 1 (6.7 %)
shocks (%)
Mortality (%)
6 (40 %)
p value
59.212.9
0.33
22.59.6
34.330.7
0.77
0.76
10 (16.7 %) 0.45
9 (15 %)
0.06
300
301
1
302
1
303
DFT
after
40
42.8
ICM
30
7.7
Fail 40 J
41 J
29
53.1
NICM
35
6.7
Fail 30 J
28 J
52
44.3
NICM
30
6.7
3 shocks of 35 J 20 J
62
29.9
NICM
20
6.4
7 shocks of 41 J 21 J
304
Ulrich Backenkoehler1
1
Praxis fr Kardiologie, Hamburg, Germany
Background: Implantation of subcutaneous ICD (S-ICD) has
become a routine intervention in patients in whom out of
distinct reasons the deployment of a conventional intracardiac
lead system is impossible or contraindicated. However, the
implantation of the S-ICD-can and the subcutaneous lead with
a wide field of detection may typically lead to inappropriate
myopotential detection and S-ICD-therapy as caused by ICDmovement or externally applied mechanical muscle irritation.
Myopotentials are mediated by proprioceptive sensory nerve
receptors (SNR). Therefore, we searched for number, location
and structure of SNR in the adjacent thoracic tissue of the
anterior serratus muscle (ASM) in order to identify optimal
implantation sites allowing for improvement of postoperative
results. Methods: Topography and ultrastructure of SNR in the
anterior serratus muscle were analyzed in 12 models of adult
female NMRI-mice. Three SNR-types were identified using
light and electron microscopy: muscle spindles (MSP),
lamellated Pacini corpucles (PC) and Golgi tendon organs
(GTO). Their location within the skeletal muscle was determined by 3D-image processing of three complete thorax section series. Results: Within the relevant structure of the anterior serratus muscle (ASM), a total amount of n=275 MSP
were found per thorax. The vast majority of SNR of the
MSP-type were identified either within the area of tendinous origin (n=114) or the fibromuscular tissue of
muscle insertion (n=134), respectively; in all samples,
only a very small number of MSP were located within
the central portions of the ASM (n=31). GTO (n=3
1) and rare PC were exclusively found within the fibrous tissue of the tendinous muscle insertions Conclusion: To avoid SNR irritation near the tendinous zones
of origin and insertion of the ASM that are richly supplied with a large number of MSP as well as GTO and
PC, special attention should be paid to the implantation
of the S-ICD-can within the anterolateral central muscle
region close to the landmark of the anterior axillary
line. Thus, the risk of electrical noise and thoracic
myopotential interference resulting in inappropriate SICD therapy may be reduced by a neuroanatomically
guided implantation site
cardiomyopathy. Older age, left ventricular dilatation and absence of diuretic were predictive factors for ICD therapy and
presence of CRTD was close to be significant.
305
306
single Reference Center. Results. The results were demonstrated in the figure (Fig 1). Multivariable Cox analysis effect
of test parameters on the probability of the formation of vegetations in LDIE patients Conclusions: ICD leads presence
was a key positive factors in formation of RHV (HR 2746;
95 %CI (19143938)). Other prognostic factors were amount
of leads (increased risk by 22 %) and previous pocket inter-
Patients/procedures
Number
280 (67.6 %)
134 (32.4 %)
65.514.4
67.514.8
0.2
186 (66.4 %)
98 (73.1 %)
0.17
2.120.93
2.070.90
0.61
ICD lead
65 (23.21 %)
22 (16.4 %)
0.11
CS lead
58 (20.71 %)
22 (16.42 %)
0.30
84.6561.33
77.2458.74
0.24
25 (8.93 %)
10 (7.46 %)
0.61
Conclusions: Both groups of patients with LDIE were comparable in terms of procedural risk factors. TLE in patients
with LDIE was safety and efficacy, but presence of vegetations increased the risk of procedure. Nevertheless, clinical
success and frequency of major and minor complications were
also comparable.
307
308
66.1
34.4
58.7
85.6
0.0001
28.3
17.8
0.02
66.1
75.3
0.06
Laboratory parameters
99184852
90505818
44.330.2
52.566.2
39.628.5
35.052.8
0.41
0.01
1.94.8
0.20.2
0.09
Echocardio-graphy findings
49.414.4
52.513.5
53.710.5
54.49.4
0.55
34.717.1
29.717.0
0.06
0.0001
0.12
0.05
309
310
BMI
Number of leads in heart before
lead extraction (SD)
Number of extracted leads in
one patient (SD)
Number of leads in the system
Number of abandoned leads
29.45.0
1.930.76
26.98.0
1.990.80
<0.0001
0.22
1.640.82
1.650.79
0.84
1.780.67
0.160.50
1.800.63
0.230.57
0.61
0.04
CS lead extraction
ICD lead extraction
4513.93 %
9629.72 %
19,514.01 %
846.03 %
0.97
<0.0001
5115.79 %
34,124.50 %
<0.01
1.751.03
1.921.19
0.02
71.857.9
84.360.6
0.0008
5517.03 %
27,019.40 %
0.31
106.939.7
109.246.7
0.41
20.62 %
221.58 %
0.18
Minor complications
61.86 %
201.44 %
0.58
4012.38 %
22,616.24 %
0.09
Clinical success
31,296.59
131,994.76 % 0.17
20.62 %
60.43 %
0.63
Conclusion. Safety and efficacy of TLE procedures were comparable in two groups of patients butparadoxicallypatients with diabetes had less potential procedural risk factors.
Especially, the lead dwelling time was significantly longer in
non-diabetic population. Additionally, abandoned leads and
loops of the leads, often ingrown, were also more often in
patients without diabetes mellitus. Probably, these differences
balanced the risk of TLE in patients with vegetationsmore
often in diabetic subjects.
Atrial fibrillation and anticoagulant therapy
Patient/system/procedure
information
Diabetes
No diabetes
Number of patients
323
69.0010.28 63.7016.85
<0.0001
Sex (female)
11,134.37 % 56640.66 %
0.04
6319.50 %
21,715.59 %
0.09
Vegetations
Infective indications (pocket
infection)
Infective indications (total)
7924.46 %
8526.32 %
26,819.25 %
32,323.20 %
0.04
0.23
14,845.82 % 54,038.79 %
0.03
Non-infective indications
17,554.18 % 85,261.21 %
0.03
Prior sternotomy
4915.17 %
20,214.51 %
0.75
154.64 %
332.37 %
0.03
311
312
313
314
Arrhythmias in childhood
1616 Abstract 0122
underwent to RA vagal denervation. An extensive ablation approach at anatomical site of GP (previously described in anatomical study) was performed until atrial
electrical activity was completely eliminated (<0.1 mV)
and/or vagal reflexes disappeared. Heart rate variability
(HRV) and HUT evaluation was assessed at baseline, at
1 day after ablation and at 1,3, 6 and 12 months followup. Results. Six patients were free from new syncopal
episodes (and cardioinhibitory response at HUT) at a
mean FU of 13.24.4 months. The patient with early
315
vagal tone restoration suffering from 3 episodes of nausea and dizziness, not followed by the loss of consciousness for effective counter-pressure maneuvers.
Conclusions. Cardioneuroablation in RA could be considered an alternative and safe strategy to reduce CNS
episodes especially in young patients avoiding or
delaying as much as possible PMK implant. A study
including a greater number of patients and long term
FU is necessary to understand the real efficacy of this
procedure.
316
Parameter
Age (SD)
in years
Weight
4316.5
44.616.6
42.116.6
0.01
72.414.0
81.511.7
63.710.5
<0.0001
Height
168.49.5
177.36.8
162.75.9
<0.0001
BMI
24.64.0
25.73.8
23.94.1
NS
30.717.4
23.210.7
0.01
7.86.6
13.311.0
0.02
13.826.9
26.622.9
0.01
Age at first
27.114.2
syncope
(years)
Number of
11.110.4
syncopal
episodes
before
admission
Number of
18.325.6
presyncopal
episodes
Parameter
Whole
studied
group
n=80n
(%)
62 (77.5)
Men
n=40n
(%)
Women
n=40n
(%)
p (women
vs. men)
30 (75)
32 (80)
NS
Syncope in a standing
position n (%)
Syncope in a sitting
position n (%)
Syncope in a standing
position n (%)
Syncope during walking
n (%)
Syncope after urination
n (%)
Syncope after Defecation
n (%)
Prodromal signs n (%)
73 (91.3) 36 (90)
37 (92.5) NS
49 (61.3) 22 (55)
46 (57.5) 20 (50)
27 (67.5) 0.02
26 (66)
0.01
1 (2.5)
2 (5)
NS
34 (42.5) 12 (30)
24 (55)
0.01
3 (3.8)
3 (7.5)
0.001
7 (8.8)
4 (10)
3 (7.5)
NS
0.01
0.001
42 (52.5) 18 (45)
0.002
24 (60)
Dizziness n (%)
Tinnitus n (%)
Headache n (%)
0.01
0.02
Stomachache n (%)
13 (16.3) 5 (12.5)
NS
Nausea n (%)
28 (35)
8 (20)
13 (32.5) 15 (37.5) NS
317
Spontaneus syncope
(%)
HUTT n
(%)
73 (91.3)
78 (98.8)
0.001
Dyspnea n (%)
46 (57.5)
52 (65)
NS
45 (56.3)
66 (82.5)
0.001
37 (46.3)
42 (52.5)
43 (53.8)
48 (60)
NS
NS
56 (70)
43 (53.8)
59 (73.8)
61 (76.25)
NS
0.001
Tinnitus n (%)
Headache n (%)
35 (43.8)
27 (33.8)
52 (65)
31 (38.8)
0.001
NS
Stomachache n (%)
Nausea n (%)
13 (16.3)
28 (35)
17 (21.3)
32 (40)
NS
NS
318
ment may be considered a valid technique useful to identify the site of origin of focal arrhythmias.
319
320
321
aspect (as occurs with sequential unipolar ablation) is replaced with another heat source (namely, simultaneous
heating via the second catheter), which may produce higher
intramural tissue temperatures during an application. Possible risks and limitations of the approach are discussed,
and SURF ablation is placed in the context of alternative
options in the management of the inaccessible substrate
(including the bipolar configuration, intramyocardial techniques such as the needle electrode, and ethanol delivery).
We conclude that SURF ablation may be an effective option
in the management of VT refractory to conventional
unipolar ablation.
322
Outcome
Survival to mean
follow up, N (%)
Survival to hospital
discharge, N (%)
Symptom control,
N (%)
Length of
hospitalization,
median (IQR)
Major bleeding
event, N (%)
Systemic embolism,
N (%)
Worsening heart
failure, N (%)
Procedure related
complication,
N (%)
Beta
blocker
Calcium
channel
blocker
Digoxin
[PB1]
Atrioventricular
node ablation
and permanent
pacemaker
placement
No
P value Yes
No
P value Yes
No
P value
25 (56.8) 0.275 18 (81.8) 19 (63.3) 0.146 2 (100)
35 (70) 0.358
Yes
No
33 (78.6) 4 (40)
P value Yes
0.016 9 (90)
34 (80.9) 5 (50)
0.042
2 (100)
37 (74) 0.405
34 (80.9) 5 (50)
0.501
2 (100)
37 (74) 0.643
5 (6)
6.5 (8)
4 (6)
0.288
6 (11)
5 (5)
0.448
0.5 ()
5 (6)
0.541
1 (2.4)
1 (10)
0.260
0 (0)
2 (4.5)
0.432
0 (0)
2 (6.7)
0.217
0 (0)
2 (4)
0.773
3 (7.1)
0 (0)
0.384
1 (10)
1 (2.3)
0.346
0 (0)
3/(10)
0.127
0 (0)
3 (6)
0.721
17 (40.5) 4 (40)
0.826
5 (50)
14 (31.8) 0.673
11 (50)
10 (33.3) 0.174
2 (100)
19 (38) 0.085
0 (0)
0.000
0 (0)
2 (4.5)
0 (0)
2 (6.7)
0 (0)
2 (4)
2 (20)
0.401
0.193
0.724
323
Outcome
Survival to mean follow up,
N (%)
Survival to hospital discharge,
N (%)
Symptom control, N (%)
Length of hospitalization,
median days (IQR)
Major bleeding event, N (%)
Systemic embolism, N (%)
30 (75)
1.000
8 (66.7)
31 (77.5)
0.834
4.0 (10)
5.0 (7)
0.980
0 (0)
1 (8.3)
2 (0.05)
2 (0.05)
0.430
0.664
16 (40)
0.969
2 (0.05)
0.515
324
Control group
(n=35)
Age (years)
7011
6612
0.20
LVEF (%)
CRT-devices (%)
298
61
287
71
0.39
0.50
No. of alerts/patient
NYHA
161.4
0.0 (2.01.5)
1.21.0
0.0 (1.01.0)
0.19
0.61
6MWT (m)
3597
1457
0.78
BNP (pg/mL)
3193
2144
0.80
MLWHF
516
512
0.005
Outcome
Amiodarone
Yes
19 (63.3)
Electrical
cardioversion
No
P value Yes
No
P value
18 (81.8) 0.146
15 (78.9)
22 (66.7) 0.347
Catheter ablation
(AFL)
Yes
No
P value
10 (100)
27 (64.3) 0.025
20 (66.7)
19 (86.4) 0.105
17 (89.5)
22 (66.7) 0.067
10 (100)
22 (73.3)
17 (77.3) 0.473
15 (78.9)
24 (72.7) 0.653
8 (80)
31 (73.8) 0.834
5 (7)
0.713
4 (7)
6 (6)
0.463
2.5 (5)
5.5 (10)
0.431
0 (0)
0.217
1 (5.3)
1 (3.0)
0.687
0 (0)
2 (4.8)
0.482
1 (3.3)
2 (9.1)
0.379
2 (10.5)
1 (3.0)
0.264
0 (0)
3 (7.1)
0.384
12 (40)
9 (40.9)
0.973
10 (52.6)
11 (33.3) 0.200
4 (40)
17 (40.5) 0.933
0 (0)
0.274
1 (5.3)
1 (3.0)
0 (0)
2 (4.8)
0.806
29 (69.0) 0.042
0.401
325
326