UHFQRS physiology

PJ Pavel Jurak
JH Josef Halamek
JM Jaroslav Meluzin
FP Filip Plesinger
TP Tereza Postranecka
JL Jolana Lipoldova
MN Miroslav Novak
VV Vlastimil Vondra
IV Ivo Viscor
LS Ladislav Soukup
PK Petr Klimes
PV Petr Vesely
JS Josef Sumbera
KZ Karel Zeman
RA Roshini S. Asirvatham
JT Jason Tri
SA Samuel J. Asirvatham
PL Pavel Leinveber
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Fig. Fig.22 demonstrates the physiological origin of UHF oscillations. The depolarization phase of myocardial cell action potentials (AP) serves as a main UHF transmitter (Fig. (Fig.2c).2c). Steep cell membrane potential gradients caused by the sodium ion current change (Phase 0 of AP) represent a unique source of UHF oscillations. The mass of myocardium, especially the left ventricle, defines the main location of UHF transmitters. UHFQRS can be simply interpreted as a histogram of UHF oscillation distribution in time (horizontal time axis) and location (V leads). The UHF transmitters work synchronously in the healthy heart (Fig. (Fig.2b,2b, HEALTHY). In a dyssynchronous left bundle branch block (LBBB) heart, the depolarization in the RV and septum (blue color in Fig. Fig.2b,2b, LBBB) precedes the depolarization in the LV lateral wall (green color).

Physiological origin of UHFQRS electrical activation pattern in ventricular dyssynchrony. Patient 1 with delayed activation of LV lateral wall (LBBB) and subject with HEALTHY conduction system. a Averaged ECG, V1-V6 leads. b Averaged UHF amplitude envelopes 500–1000 Hz (UHFQRS). c Schematic interpretation of myocardial cell action potentials—AP. Blue—V1 lead—mostly interventricular septum and RV, green—V6 lead—mostly LV lateral wall

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