An Exploratory Study on Vectorcardiographic Identification of the Site of Origin of Focally Induced Premature Depolarizations in Horses, Part II: The Ventricles.

Animals (Basel)

Equine Cardioteam, Department of Internal Medicine, Reproduction and Population Medicine, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium.

Published: February 2022

AI Article Synopsis

  • The study aimed to investigate if vectorcardiography (VCG) can differentiate the anatomical origin of pacing-induced ventricular premature depolarizations (VPDs) in horses, given the inconsistent results from previous studies using 12-lead electrocardiograms (ECG).
  • Seven horses were studied under general anesthesia, where researchers recorded a 12-lead ECG during various pacing locations in the heart, using advanced mapping techniques to guide catheter placement.
  • The findings revealed significant differences in electrical axes for VPDs depending on the pacing location and rhythm, indicating that VCG could effectively identify the anatomical origins of ventricular ectopy in horses.

Article Abstract

In human cardiology, the anatomical origin of ventricular premature depolarizations (VPDs) is determined by the characteristics of a 12-lead electrocardiogram (ECG). Former studies in horses had contradictory results regarding the diagnostic value of the 12-lead ECG and vectorcardiography (VCG), which results were attributed to the different cardiac conduction system in this species. The objective of this study was to determine if the anatomical origin of pacing-induced VPDs could be differentiated in horses based upon VCG characteristics. A 12-lead ECG was recorded in seven horses under general anesthesia while right and left ventricular endomyocardial pacing was performed (800−1000 ms cycle length) at the apex, mid and high septum and mid and high free wall, and at the right ventricular outflow tract. Catheter positioning was guided by 3D electro-anatomical mapping and echocardiography. A median complex, obtained from four consecutive complexes, was calculated for each pacing location and sinus rhythm. The VCG was calculated from the 12-lead ECG-derived median complexes using custom-made algorithms and was used to determine the initial and maximum electrical axes of the QRS complex. An ANOVA for spherical data was used to test if VCGs between each paced location and between pacing and sinus rhythm were significantly (p < 0.05) different. The model included the radius, azimuth and elevation of each electrical axis. Pacing induced significantly different initial and maximum electrical axes between different locations and between pacing and sinus rhythm. The current results suggest that VCG is a useful technique to identify the anatomical origin of ventricular ectopy in horses.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8908816PMC
http://dx.doi.org/10.3390/ani12050550DOI Listing

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