Key result
Administration of 2 mg atropine significantly reduced fractionated areas in the right atrium (P<0.001 for supero- and infero-posterior regions, P<0.05 for mid-posterior region).
Why the study?
Does 2 mg atropine alter atrial electrogram fragmentation patterns in ganglionated plexi regions in healthy patients without structural heart disease?
Does 2 mg atropine alter atrial electrogram fragmentation patterns in ganglionated plexi regions in healthy patients without structural heart disease?
Answers are grounded in this paper and cite their sources.
Atropine administration reveals that atrial electrogram fragmentation has a dynamic, vagally-mediated component, suggesting that cardioneuroablation should selectively target the structural central core of ganglionated plexi.
Background and aims Ganglionated plexi (GPs) are the primary target of ablative therapies for neurally mediated syncope (NMS); however, the optimal method for their endocardial localization remains unclear. This study analyzed bipolar atrial electrograms (EGMs) and their response to a vagolytic agent to elucidate their relationship with the parasympathetic network. Methods High–density right atrial mapping was performed before and after 2 mg atropine in healthy patients without structural heart disease undergoing electrophysiological study for standard indications. Offline analysis compared pre– and post–atropine maps, focusing on fragmentation patterns and spectral analysis. Results The study included 13 patients (mean age: 34±12 years, 9 males). Baseline maps exhibited a consistent fragmentation pattern in the posterior–septal wall, reflecting anatomical right GPs distribution. No difference in density of points between the pre–post atropine map was detected (p=0.97). Three primary areas were identified in the supero–(A), mid–(B), and infero–posterior–(C) regions. Fragmentation of EGMs was found to increase from the periphery toward the core of each area. In fact, the fragmentation pattern was consistent across all analyzed GPs areas: a centrally located, rounded high–fragmentation area (≥6 deflections) was surrounded by a low–fragmentation area (≥4 deflections), with a transition zone (≥5 deflections) in between (Figure 1). Atropine significantly reduced fractionated areas (p‹0.001 for A and C, p‹0.05 for B, Figure 1, Figure 2). External areas exhibited “functional“ fragmentation, sensitive to vagal output, whereas central cores displayed " structural" fragmentation, resistant to vagolysis. Conclusion Fragmentation of atrial EGMs is a dynamic property, related to parasympathetic output. Standard fragmentation criteria may overestimate GPs areas. These results could suggest a more selective approach on central core of GPs during Cardioneuroablation procedure, potentially reducing procedural risks and improving long–term outcomes.
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Bernardini et al. (2026) studied Healthy patients without structural heart disease undergoing electrophysiological study (n=13). Atropine vs. Baseline (pre-atropine) was evaluated on Fractionated areas of atrial electrograms (p=<0.001). Administration of 2 mg atropine significantly reduced fractionated areas in the right atrium (P<0.001 for supero- and infero-posterior regions, P<0.05 for mid-posterior region).
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