CORRESPONDING AUTHOR
Philipp Sommer, MD
Clinic for Electrophysiology
Herz- und Diabeteszentrum NRW
Georgstr. 11
32545 Bad Oeynhausen, Germany
Phone: +49(0)5731971327
Fax: +49(0)5731972123
E-mail: psommer@hdz-nrw.de
Ablation of ventricular tachycardia (VT) has emerged an effective
therapy in patients with ischemic heart disease. Electroanatomical
mapping is currently considered the gold standard in terms of VT
ablation (1). Bipolar voltage mapping is the standard tool to
characterize substrate with commonly used cut-off values of 0.5 to 1.5
mV to discriminate between dense scar and intermediate border zones
(1,2,3). Nevertheless, several limitations arise when bipolar voltage
mapping is utilized. Cut-off values for electroanatomical mapping were
derived from studies with small patient populations and based on
experiences with single-tip catheters with limited resolution (2,3).
Mapping is mainly performed at endocardial ventricular sites without
implementation of information from epicardial or intramural myocardium.
Additionally, automatic annotation algorithms are limited in
discrimination between ventricular far-field and near-field signals
especially in case of local signals with low amplitudes. Preprocedural
radiologic imaging may add valuable information to electroanatomical
mapping. Current society guidelines recommend the use of preprocedural
cardiac magnetic resonance imaging (MRI) for planning and
intraprocedural guidance of VT ablation (1). Recently, cardiac computed
tomography (CT) has been investigated as a novel imaging modality using
a commercially available software (InHEART, Pessac, France). The
software may enable preprocedural assessment of myocardial fibrosis as
well as derivation of information on myocardial wall thickness. These
data can be used to guide catheter ablation and to detect specific VT
mechanisms. Wall thinning has been demonstrated to be a powerful
predictor of localizations of abnormal electrical substrate in patients
with ischemic cardiomyopathy (4). Additionally, ablation sites derived
from conventional electrophysiological criteria such as pace mapping or
entrainment mapping were commonly found adjacent to areas of wall
thinning (5).
In this issue, Ene et al. report 40 patients with previous myocardial
infarction who underwent preprocedural CT imaging and consecutive image
integration into 3D-electroanatomical mapping using a commercially
available software (6). The study sought to analyze currently used
voltage cut-off values in its relation to myocardial thinning estimated
by CT imaging. The authors found that current cut-off values of 0.5 mV
may overestimate the myocardial substrate if merely electroanatomical
mapping is used. In detail, thin myocardial layers were detected more
precisely when a lower cut-off value of 0.2 mV was used. Ene et al.
analyzed patients undergoing 3D-electroanatomic mapping with
multielectrode catheters enabling high-density mapping. Differences
between bipolar mapping using single-tip catheters and multipolar
catheters can be assumed. Multipolar catheters are widely available
today and should be seen as gold standard for complex atrial and
ventricular procedures. Again, this study confirms to individualize
patient treatment- also in VT ablation. Each patient is different, each
scar is different and imaging certainly can help to identify areas of
interest and plan lesion deployment preprocedurally.
The main findings of the study are in line with previous studies which
found arrhythmogenic substrate even in thin myocardial layers with low
voltage, which would have been denoted as dense scar when usual cut-off
values would have been applied (7). Interestingly, VT channels were
exclusively found in regions of myocardial thinning of 1-4 mm (7).
The authors elegantly demonstrate the value of a comprehensive setup
consisting of preprocedural CT imaging and high-density mapping to
enable optimal characterization of the substrate. Based on the present
results, ablation targets may be found in regions of 0.2 to 1.0 mV of
bipolar voltage. The findings may be especially relevant in patients in
whom VT is not inducible or hemodynamically unstable and detailed
activation mapping to guide substrate-based ablation is not possible.
Using the above-mentioned criteria derived from 3D-electroanatomical
mapping and CT imaging, regions of interest may be identified even at
sites with marked low voltage in which validity of electroanatomic
mapping is generally limited. Furthermore, CT imaging has several
distinct advantages over MRI in patients undergoing VT ablation. CT
offers a higher spatial resolution compared to MRI and is widely
available. Additionally, presence of implantable cardiac devices can be
a contraindication for MRI imaging in distinct patients and may impair
MRI quality. The current study by Ene et al. focused on the potentially
most suitable patient cohort: post myocardial infarct patients. The
impact of CT information in non-ischemic cardiomypathies is still
limited- although some groups try to perform late-enhancement imaging
using CT as an imaging modality as well. In this cohort, MRI will
probably remain the method of choice to identify the arrhythmogenic
substrate. Further studies need to evaluate the currently used cut-off
values in other heart diseases such as non-ischemic cardiomyopathy or
arrhythmogenic cardiomyopathy. However, contrast-enhanced computed
tomography in ventricular tachycardia ablation is a promising tool for
preprocedural substrate analysis.
References:
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Aguinaga L, Leite LR, Al-Khatib SM, Anter E, Berruezo A, Callans DJ,
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Dickfeld TM, Hadid C, Haqqani HM, Kay GN, Latchamsetty R, Marchlinski F,
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