(Circulation. 1999;100:419-426.)
© 1999 American Heart Association, Inc.
Basic Science Reports |
From the Cardiovascular System Laboratory, The Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, and the Faculty of Medicine, University of Tel-Aviv (D.C.), Israel.
Correspondence to Lior Gepstein, MD, Cardiovascular System Laboratory, The Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Efron St, POB 9649, 31096 Haifa, Israel. E-mail mdlior{at}tx.technion.ac.il
| Abstract |
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Methods and ResultsA nonfluoroscopic mapping and navigation technique was used to generate 3-dimensional (3D) electroanatomic maps of the right atrium in 8 pigs. The catheter was then used to deliver sequential radiofrequency (RF) applications (power output gradually increased until 80% reduction in the amplitude of the unipolar electrogram) to generate a continuous lesion between the superior and inferior venae cavae. The animals were remapped 4 weeks after ablation during septal pacing. Lesion continuity was confirmed in all cases by the following criteria: (1) activation maps indicating conduction block [significant disparities in activation times (52.0±16.0 ms) and opposite orientation of the activation wave front on opposing sides of the lesion], (2) evidence of double potentials (interspike time difference of 52.3±17.1 ms), and (3) low peak-to-peak amplitude of the bipolar electrograms (0.7±0.6 mV) along the lesion. At autopsy, all lesions were continuous and transmural, averaged 50.5±6.7 mm, and were characterized histologically by transmural fibrosis throughout the length of the lesion.
ConclusionsLong linear atrial ablation, created by sequential RF applications (using unipolar amplitude attenuation as the end point for energy delivery), results in long-term continuous and transmural lesions. Lesion continuity is associated with evidence of conduction block in the 3D activation maps and the presence of double potentials and low electrogram amplitude along the lesion.
Key Words: catheter ablation electrophysiology arrhythmia atrium
| Introduction |
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The recent paradigm shift from application of focal ablations to continuous longitudinal lesions, although it significantly increased the spectrum of treatable arrhythmias, has also raised several issues regarding the application and short- and long-term electrophysiological and pathological consequences of these lesions. However, data regarding these issues are lacking in the literature.7 Such information may be crucial for optimal treatment of various arrhythmias and for better understanding of the mechanisms involved in arrhythmia recurrences.
Recently, a nonfluoroscopic, catheter-based, electroanatomic mapping method was introduced.8 9 10 11 12 This method uses magnetic fields to accurately determine the 3-dimensional (3D) location of a mapping and ablation catheter. More recently, it has been shown that this technique can be used to generate precise continuous and longitudinal lesions.10
In this study, we used this technique to study the chronic effects of the generation of longitudinal lesions on the electrophysiological and pathological properties of the atrium. Specifically, we tried to investigate whether chronic healing of an acute lesion may result in the appearance of discontinuities along the line, and also to describe the spatial and electrophysiological parameters associated with the presence of a continuous lesion.
| Methods |
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Animals
Studies were performed on 8 healthy male pigs weighing 25 to 40
kg. Animals were anesthetized with pentobarbital 30 mg/kg,
intubated, and ventilated. Vascular access was obtained by vascular
cutdown of the jugular veins. A 100-U/kg IV bolus of heparin was given
shortly thereafter. The experimental protocol was approved by the
Animal Study Committee of the Technion Faculty of Medicine.
Mapping Procedure
The mapping procedure was based on sequential sampling of
the location of the roving catheter simultaneously with the
local electrogram recorded from its tip, at several endocardial
sites. In our experience, sampling of
50 points was needed to
accurately reconstruct the 3D geometry of the right atrium (RA). The
local activation time (LAT) at each site was determined as the time
interval between a fiducial point on the body-surface ECG and the
steepest negative intrinsic deflection in the unipolar
recordings. We report results that were collected from unipolar
and bipolar recordings filtered at 0.5 to 400 Hz and 30 to 400
Hz, respectively. The activation map was then color-coded and
superimposed on the 3D geometry.
Radiofrequency Energy Application
Radiofrequency (RF) energy was delivered from the distal
tip electrode (4 mm) of the mapping catheter, and the ground
electrode was a large patch placed on the animal's back. RF ablation
was performed with a 500-kHz RF generator (RFG-3C; Radionics) with
power output increased gradually (maximum temperature, 60°C) for up
to 60 seconds, or 10 seconds after 80% reduction in the unipolar
amplitude.
Experimental Protocol
After creation of the RA electroanatomic map during sinus
rhythm, the catheter was navigated to the most distal site of the
planned ablation path. RF energy was delivered to create a point
ablation at that site. The catheter was withdrawn slightly and then
navigated to a nearby site, where another ablation point was created
(Figure 1
, left). Each ablation site was
tagged on the map, resulting in a continuous lesion (Figure 1
, right). After completion of the line, the catheter was navigated back
along the entire lesion to assess the presence of low-amplitude
electrograms (bipolar amplitude, <0.5 mV) and the presence of double
potentials. If "viable" electrograms that did not comply with these
criteria were noted, additional energy was delivered at these sites.
Consequentially, a lesion extending from the superior vena cava (SVC)
to the inferior vena cava (IVC) was created in all
animals.
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Four weeks after the first procedure, the RA was remapped during septal pacing. Between 30 and 50 points were sampled along the lesion, providing a high-density map (distance of 2 to 5 mm between adjacent points) of this region.
Electrophysiological Verification of the
Lesion
We investigated 3 different
electrophysiological methods for the
determination of lesion continuity.
Activation Mapping to Determine Conduction Block
A high-density RA activation map was generated by use of
LATs determined from the unipolar recordings. When split
electrograms were recorded, the LAT was derived from the steeper of
the two. Conduction block was defined as a LAT difference >30 ms
between adjacent points on opposite sides of the lesion (<10 mm
apart) and opposite orientation of the wave front on opposing sides of
the lesion.
Presence of Double Potentials Along the Line
The presence of double potentials in the local unipolar
electrogram and their spatial distribution relative to the lesion was
assessed at all sampled sites.
Amplitude of the Bipolar Electrogram
The peak-to-peak amplitude of the local bipolar electrogram was
determined at each sampled site.
Pathological Verification
At the end of each study, the animals were killed and the hearts
excised. Histochemical staining was obtained with
2,3,5-triphenyltetrazolium chloride (TTC),
followed by preservation in 4% neutralized formalin for further
analysis. The length, shape, location, and continuity of each
ablation line was measured on the fresh tissue and compared with the
line demonstrated on the electroanatomic map.
After fixation, each lesion was blocked and sectioned into a number of longitudinal cuts parallel to the long axis of the lesion, and the sections were then stained with hematoxylin-eosin and Masson's trichrome for microscopic examination.
Statistical Analysis
Results are reported as mean±SD. Unpaired t test or
ANOVA was used to determine statistical significance
| Results |
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The reduction in the amplitude of the local electrogram during energy
delivery was evident in all lesions (Figure 2
). The characteristic morphological
changes in the unipolar electrogram consisted of an initial ST-segment
elevation, followed by a gradual decrease in the amplitude of the
intrinsic atrial deflection. Thus, in most sites (>95%), RF
application lasted <60 seconds before the threshold criterion was
achieved (80% reduction in the unipolar amplitude).
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In the majority of animals studied, no additional RF applications were needed before the completeness criteria were met. In 3 animals, a number of RF applications (1 to 4) were applied to ensure completeness of the lesion in sites at which viable electrograms were recorded. Interestingly, these sites were usually located at the middle of the SVC-IVC line, which suggested a possible problem of inadequate catheter-wall contact in this area. After these additional applications, lesion continuity was ensured in all animals.
Electroanatomic Maps in the Chronic Stage
Four weeks after ablation, the RA was remapped during pacing
from the fossa ovalis. The following
electrophysiological parameters
were assessed to define the lesion continuity.
Presence of Conduction Block
Figure 3
shows a posteroanterior
view of a typical activation map of the pig's RA during pacing. The
earliest activation (red) was located at the inferoseptal aspect of the
atrium. Note the appearance of a well-defined line of block with very
late LATs (blue and purple) located at the lateral aspect of the lesion
just adjacent to sites with early LATs. The presence of conduction
block can also be viewed in the propagation map (Figure 4
). Note that activation originates at
the pacing site and then propagates medially, upward, and downward
along the posterior wall but is blocked laterally. The activation is
then directed around the lesion, using the roof and floor of the
atrium, terminating with collision of the 2 wave fronts on the lateral
aspect of the lesion.
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A line of conduction block characterized by significant LAT differences (52.0±16.0 ms) and by opposite orientation of the activation wave front on opposing sides of the lesion was noted in all animals.
Spatial Distribution of Double Potentials
As can be seen from Figure 5
, most
double potentials were located at the posterior intercaval area
straddling the ablation line. The presence of double potentials along
the lesion was confirmed in all animals.
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To further characterize the nature of the double potentials, they were divided into 3 groups according to their spatial distribution. Interestingly, significant differences (P<0.01) in the interspike interval of the double potentials were noted between the groups. Double potentials located along the lesion were characterized by the longest time difference between the 2 components (52.3±17.1 ms), those located at the edges of the lesion had an interspike interval of 37.1±10.5 ms, and double potentials located at areas not related to the lesion displayed the shortest interval between the 2 deflections (23.4±8.3 ms). The double potentials in the third group accounted for 11.3% of the points in the map not related to the lesion and were associated with the presumed anatomic location of the cristae terminalis, the eustachian ridge, and areas of activation wave collision.
Voltage Maps
Figure 6
presents a typical
voltage map of the RA, depicting the peak-to-peak bipolar amplitude at
each site. Note that the low voltage (red, bipolar amplitude <0.5 mV)
located in the posterior wall depicts the lesion. This phenomenon was
noted in all maps, with the average amplitude along the lesion
(0.7±0.6 mV) being significantly lower (P<0.01) than that
found at other sites (2.3±1.5 mV).
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Pathological Examination
Pathological examination revealed the presence of complete,
continuous, and transmural lesions in all animals. Average lesion
length was 50.5±6.7 mm. A typical lesion stained with TTC
is shown in Figure 7
. Note that the
lesion is continuous, with no apparent gaps, and that it extends in the
smooth posterior RA from the SVC to the IVC.
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Histological examination of the lesions (Figure 8
) revealed transmural myocardial
fibrosis with areas of chronic inflammatory cell infiltration.
Occasionally, foci of preserved myocardium could be
observed within the necrotic zones, which, however, were
continuous.
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| Discussion |
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Chronic Pathological Changes
Using the ability of the new technique to accurately combine
sequential point ablations into continuous lesions, we were able to
generate an anatomic and
electrophysiological model to study the
chronic changes of such lesions. We found that the initial linear
ablations resulted in long-term continuous and transmural lesions as
assessed by TTC staining and serial pathological examination.
Histologically, all lesions were characterized by
well-defined transmural fibrosis, similar to the
histological changes described for focal
ablations.13 14
Use of Atrial Local Electrogram Attenuation for Energy
Titration
Throughout the years, a number of techniques were developed for
energy titration during RF application. These include power
titration,14 temperature control,15 and
impedance measurements.16 Common to all strategies is the
aim of creating transmural atrial lesions with minimal risk (of
endocardial charring, thromboembolism, barotrauma, and damage to
adjacent structures). Nevertheless, the information acquired by these
techniques is restricted to the electrode-tissue interface and lacks
online data regarding intramyocardial changes during energy
delivery.
This study demonstrated that in the RA smooth muscle, energy titration based on electrogram attenuation was safe and resulted in chronic contiguous and transmural lesions. The rational behind this method is that a single application results in a transmural lesion whose area is just larger than the catheter tip, consequently leading to a marked reduction of local electrogram amplitude. As in our study, Nakagawa et al,17 using the canine isolated heart model, found that an 80% decrease in the unipolar atrial electrogram was associated with the creation of an acute continuous and transmural atrial lesion.
Electrophysiological Evidence of Lesion
Continuity
Using the SVC-IVC linear ablation as a model, we were able to
study the endocardial electrophysiological
parameters associated with a continuous lesion.
Presence of Conduction Block in the Activation Maps
Conduction block was confirmed in all cases and correlated
well with the findings of continuous lesions in pathology. The location
of the pacing electrode and the orientation of the activation wave
front relative to the lesion may be of importance because conduction in
the normal atrium is relatively fast using several possible pathways.
The ability to assess block was facilitated here by the use of an
activation wave front, which originated in close proximity and was
perpendicular to the line. The rationale behind this setting was to
shorten conduction time to the proximal side of the lesion and to
lengthen conduction time to its distal part. This resulted in opposite
orientation of the activation wave front and maximal time delay
(52.0±16.0 ms) between opposite sides of the lesion.
Spatial Distribution of Double Potentials
The appearance of double-spike electrograms has been shown to
occur under a variety of conditions, including slow
conduction,18 tissue anisotropy,19 conduction
block,20 atrial anatomic barriers,21 and
collision of activation waves.22
Our results demonstrate a tight spatial correlation between the distribution of double potentials and the presence of the linear lesion. Thus, double potentials spanning the gap in activation times between opposite sides of the lesion were recorded along its entire length.
Examining the spatial distribution of all double potentials, we noted that they could be divided into 3 groups: (1) double potentials located along the lesion displayed the longest interspike interval (52.3±17.1 ms) and were related to the activation time difference between the 2 sides of the lesion; (2) double potentials located at the edges of the ablation line were characterized by intermediate interspike intervals (37.1±10.5 ms); and (3) double potentials recorded at sites not related to the lesion were associated with the shortest interval between the 2 deflections (23.4±8.3 ms) and may have been related to anatomic barriers in the RA and to activation wave collision.
Low Electrogram Amplitude Along the Lesion
The association of low-amplitude electrograms with
successful ablation sites was confirmed during 3 different stages: (1)
initially, during RF application when the reduction in the
amplitude of the local electrogram was used as an end point for
delivery of energy; (2) after deployment of the lesion, when the
catheter was navigated along the lesion to ensure that no viable
electrograms remained; and (3) in the chronic stage, when the lesions
could be delineated by the voltage map.
Although all 3 criteria were met in the chronic maps, we did not use activation mapping in the acute state to determine lesion continuity. Hence, the presence of "nonviable" (low-amplitude) electrograms and double potentials along the entire path of the lesion was enough to ensure lesion continuity. Activation mapping, however, besides providing additional evidence for the presence of conduction block, may also provide additional information regarding the different routes of ingress of atrial activation after lesion deployment.
Clinical Significance
The results of the present study may possess important
clinical consequences. For a linear ablation to be effective, several
steps have to be taken. First, one must select the desired site for
ablation and then navigate the catheter to this area. Next, energy
application must result in the generation of a continuous lesion. This
can be achieved only if sites at which RF energy was delivered were
continuous and RF application resulted in transmural necrosis. Finally,
one must establish whether the lesion achieved the desired
electrophysiological effect. The unique
abilities of the technique presented here may possess several
advantages for each of these stages, as follows.
Developing Ablation Strategy
The ability to determine the location of the mapping catheter
superimposed on the 3D map and to relocate the catheter back to
predefined sites allows dissociation between the mapping and ablation
procedures. Hence, one may first generate a detailed 3D electroanatomic
map; next, develop the ablation strategy; and finally, using the
reconstruction as a "road map," navigate the catheter back to the
desired path for delivery of RF energy.
Generation of the Lesions
The combination of the ability to navigate the catheter precisely
to predefined sites, to estimate the effects of RF energy (by
monitoring electrogram changes during energy delivery), and to tag
ablated sites ensured the generation of chronic continuous and
transmural lesions. Aside from ensuring lesion continuity, these
qualities may also minimize ablation burden and allow the usage of a
number of different catheters or sheaths for the generation of a single
lesion.
Assessment of Lesion Continuity
Our results demonstrate that a continuous lesion is associated
with the presence of conduction block and spatial association of double
potentials and low-amplitude electrograms along its path. Recent
complementary work has shown that these criteria can be used to
accurately determine the position of gaps within such lesions and that
the catheter could then be renavigated to these sites for completion of
the lesion.23 24 25
Despite the growing number of atrial arrhythmias treated by application of linear lesions, the early and late recurrence rate is still significant. These recurrences may result from (1) generation of an incomplete lesion; (2) healing and remodeling of the initial lesion, resulting in the appearance of discontinuities. Previous studies have shown that the acute lesion is characterized by a central zone of coagulation necrosis and a peripheral zone of hemorrhage and edema and that the chronic lesion contracts significantly in volume.13 It can thus be speculated that healing of this transitional zone may account for the late electrophysiological recovery after an apparently successful ablation26 ; and (3) lesion application in an area not critical for the perpetuation of the arrhythmia.
This study demonstrated that initial generation of continuous lesions resulted in chronic conduction block. Thus, with the limitation of the model studied, we can speculate that precise deployment and assessment of the initial lesion might prevent recurrences related to the first 2 mechanisms.
Limitations
The implications of the present study may be restricted
to the smooth-RA animal model in which they were acquired. Thus,
further studies will be necessary to define the parameters
associated with the generation and assessment of such lesions in
trabeculated parts of the atrium, in the left atrium, and
in humans.
In addition, the precise location of the lesion in the chronic maps is not known directly. However, its position could be approximated rather accurately by anatomic correlation of the 2 maps and by the tight spatial correlation between the 3 electrophysiological parameters assessed.
A further limitation of the present study is the interpolation of the reconstructed geometry and the electrophysiological information between acquired sites. This may generate difficulties in the correct interpretation of the activation sequence and increase the chance of missing gaps. By sampling a large number of sites specifically in the area of the lesion, we were able to partially compensate for this limitation.
Conclusions
This study demonstrated that the generation of long atrial
lesions by combining sequential point ablations guided by 3D magnetic
navigation and by electrogram attenuation during RF ablation results in
short- and long-term conduction block as well as pathological evidence
of continuous and transmural lesions. We have also shown that a
continuous lesion is associated with conduction block in the activation
maps and the presence of double potentials and low-amplitude
electrograms along the line.
Received June 1, 1998; revision received April 1, 1999; accepted April 9, 1999.
| References |
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