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High-resolution Optical Mapping of the Mouse Sino-atrial Node
Published on: December 2, 2016
First Clinical Experience With Reversible Electroporation Mapping in Atrial Flutter
María Cespón-Fernández1,2, Kazutaka Nakasone1, Luigi Pannone1
1Heart Rhythm Management Centre, Postgraduate Program in Cardiac Electrophysiology and Pacing, Universitair Ziekenhuis Brussel-Vrije Universiteit Brussel, European Reference Networks Guard-Heart, Brussels, Belgium (M.C.-F., K.N., L.P., J.S., D.G.D.R., A.A., I.O., G.B., E.S., I.E., A.P., G.V., P.B., G.-B.C., C.d.A., A.S.).
Background:
Reversible pulsed field ablation (PFREV) can temporarily block cardiomyocyte conduction, potentially identifying critical target sites before creating definitive lesions. However, PFREV local capture might interfere with the tachycardia mechanism. The aim of the study was to characterize the responses of nontriggered PFREV pulses to serve as a novel clinical mapping tool in reentrant atrial flutter.
Methods:
PFREV pulses were delivered in and outside of the circuit using a 9-mm lattice-tip catheter in 30 reentrant atrial tachycardias in 26 patients. The presence of local capture and responses to PFREV pulses was characterized.
Results:
Out of 163 PFREV pulses analyzed, 56 (34.4%) showed atrial capture and propagation. Propagated versus Nonpropagated PFREV cohorts were compared. The coupling interval of propagated PFREV pulses was significantly longer (195.3±69.2 msec versus 98.9±77.2 msec; P<0.001). Globally, 4 responses were observed: tachycardia termination (11.0%), stable tachycardia cycle length (TCL) prolongation (9.8%), transient irregular TCL variations (3.1%), and no change in activation sequence and TCL (76.1%). Propagation was only associated with irregular TCL variations (8.9% versus 0%, P=0.002). Tachycardia termination or TCL prolongation occurred only when PFREV was delivered in the reentry circuit (100% specificity). Termination occurred exclusively in the critical isthmus (100% specificity regardless of propagation), and stable TCL prolongation occurred in 93.8% and 6.2% of the cases in the isthmus and outer loop, respectively (100% specificity for nonpropagated and 83.3% specificity for propagated PFREV to localize the isthmus). Sensitivity of termination or stable TCL prolongation for identifying the critical isthmus was moderate (38.8%) and influenced by isthmus width (11.7±1.7 mm versus 22.9±2.1 mm; P<0.001). Reproducibility of PFREV pulses, determined by consecutive pulses delivered at the same site producing identical responses, was high (82.9%).
Conclusions:
PFREV mapping is a novel, feasible, and reproducible tool for identifying critical sites in reentrant atrial tachycardia with narrow isthmuses that may be improved through optimized triggering and dose titration.
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