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Discrimination between His-bundle and the right bundle branch during electrophysiologic studies
Yoshiaki Kaneko1, Tadashi Nakajima, Akihiro Saito
1Department of Medicine and Biological Science, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan. kanekoy@showa.gunma-u.ac.jp
Insights
Identifying the His-bundle (HB) and right bundle branch (RBB) using the V3 phenomenon is feasible. However, measuring the His-ventricular (H-V) interval can lead to misidentifying the RBB as the HB.
Area of Science:
- Electrophysiology
- Cardiac conduction system
Background:
- Accurate identification of the His-bundle (HB) and right bundle branch (RBB) is crucial in electrophysiologic studies.
- Distinguishing between HB and RBB can be challenging, impacting diagnostic accuracy.
Purpose of the Study:
- To identify the His-bundle (HB) versus right bundle branch (RBB) during electrophysiologic studies.
- To utilize the V3 phenomenon for HB and RBB identification.
- To compare the His-ventricular (H-V) interval timing for HB and RBB potentials.
Main Methods:
- Electrophysiologic studies were performed on 16 patients without structural heart disease.
- The V3 phenomenon was induced to record HB and RBB potentials using a multi-electrode catheter.
- Specific recording sites were defined: HB branching portion (HBBP), proximal HB, and distal RBB.
Main Results:
- The HBBP was successfully identified in all patients.
- The H-V interval at the HB adjacent to the HBBP was ≥35 ms in most patients.
- The H-V interval at the RBB adjacent to the HBBP was also ≥35 ms in 12 patients.
Conclusions:
- Simultaneous recording of HB and RBB potentials during V3 phenomenon induction allows for feasible electrophysiologic identification.
- Relying solely on H-V interval measurements for discrimination frequently leads to misidentification of the proximal RBB as the HB.
Background:
The purpose of this study was to identify the His-bundle (HB) versus right bundle branch (RBB) during electrophysiologic studies, using the V3 phenomenon, and to compare the timing of HB versus RBB potentials of sinus cycles (His-ventricular [H-V] interval).
Methods:
The study enrolled 16 patients without structural heart disease, who underwent electrophysiologic studies during which the H-V interval was within normal limits and the V3 phenomenon was induced during recordings of the HB and the RBB potentials by a multi-electrode catheter. The recording site of the earliest HB potential just before the V3 phenomenon was defined as the branching portion of His bundle (HBBP), the site immediately proximal to the HBBP as the HB, and the site immediately distal to the HBBP as the RBB.
Results:
The HBBP was identified in all patients. In all cases but one patient, the H-V interval measured at the HB adjacent to the HBBP was > or =35 ms. However, in 12 patients, the H-V interval measured at the RBB adjacent to the HBBP was also > or =35 ms.
Conclusions:
The electrophysiologic identification of HB versus RBB by simultaneous recordings of HB and RBB potentials during induction of the V3 phenomenon was feasible. When the discrimination between HB and RBB was based on the measurement of the H-V interval, the proximal portion of the RBB was frequently misidentified as the HB.
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