Riccardo Fenici, Donatella Brisinda, Maria Pia Ruggieri, Peter Fenici.
Clinical Physiology, Biomagnetism Research Center, Catholic University, Rome, Italy
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BACKGROUND. An advanced development of
the amagnetic catheter (AC) for magnetocardiographically guided intracardiac
electrophysiological recordings and ablation of cardiac arrhythmias is described,
which allows single catheter recording of four monophasic action potentials (MAP)
simultaneously (Multi-MAP function).
METHODS. The 6F AC features five non-polarizable amagnetic electrodes, arranged in
such a way that orthogonal or parallel current dipoles can be generated in the patients
heart. This assembly can be localized by Magnetic Source Imaging (MSI), with a
three-dimensional (3D) accuracy of 2-7 mm, without the use of fluoroscopy. On the
basis of preoperative MCG 3D localization, the AC can be driven, under fluoroscopic
control, as close as possible to the arrhythmogenic zone. Once reached the area of
onset of the arrhythmia the tip electrodes are used to record simultaneously four MAPs
from an area of about 4 mm2. Alternatively two electrodes can be used for local pacing
and two simultaneous MAP recordings. MAP signals are differentially amplified,
bandpass filtered (DC-1kHz) and digitized at the sampling frequency of 2-4 kHz. MAP
duration at 50 and 90% levels of repolarization and local conduction times between
the phase 0 of the four MAPs are automatically calculated with a custom software.
RESULTS. With this AC, the average amplitude of right atrial MAP (10 patients) was
6.2±2.4 mV and that of the right ventricular (RV) MAP (15 patients) was 23±9 mV. Local
variation coefficients of RV MAP duration at 50 and 90% level of repolarization were 7.4
and 3.1%, respectively. Local repolarization inhomogeneity and of areas of slow
conduction or focal block were detected with the multi-MAP recording technique.
CONCLUSION. This new multi-MAP AC in combination with MSI, provides non
fluoroscopy-dependant single-catheter high resolution intracardiac mapping of local
electrophysiological abnormalities from MSI predefined arrhythmogenic areas.
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