Key result
Sympathetic neuromodulatory therapies suppress refractory ventricular arrhythmias by reducing cardiac sympathetic tone.
Why the study?
Current peripheral sympathetic neuromodulatory therapies for ventricular arrhythmia in structural heart disease have limitations and side effects, highlighting the need for more targeted strategies and evaluation of emerging therapies.
Do peripheral sympathetic neuromodulatory therapies reduce the burden of refractory ventricular arrhythmias in patients with structural heart disease?
Do peripheral sympathetic neuromodulatory therapies reduce the burden of refractory ventricular arrhythmias in patients with structural heart disease?
Sympathetic neuromodulation provides critical therapeutic pathways for treating refractory ventricular arrhythmias in structural heart disease, though future research is required to optimize targeted approaches and minimize side effects.
May support neuromodulation for refractory VA in SHD; leaves open optimal targets and efficacy in prospective trials.
Over the past several decades, substantial evidence has pointed to the role of the autonomic nervous system in the genesis and maintenance of ventricular arrhythmia. In particular, sympathetic activation has been shown to increase the risk of ventricular arrhythmia, particularly in the context of structural heart diseases, and is a key target of neuromodulatory therapies. Current peripheral sympathetic neuromodulatory approaches include temporary interventions, such as stellate ganglion block, proximal intercostal block, and thoracic epidural anaesthesia, as well as more definitive therapies, such as cardiac sympathetic denervation and renal denervation. Each of these approaches presents distinct strengths and limitations, as well as side effects that warrant careful consideration in clinical practice and highlight the need for more targeted strategies. Emerging interventions focusing on neuropeptide Y, sympathetic afferents ablation, high-frequency block of efferent nerves, and the restoration of sympathetic innervation after MI have shown promising potential. However, further research is needed to evaluate the feasibility and safety of these novel therapies prior to their implementation in patients with cardiovascular diseases.
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Benabou et al. (2025) conducted a review in Structural heart disease and ventricular arrhythmias. Peripheral sympathetic neuromodulatory therapies (e.g., stellate ganglion block, CSD, RDN) was evaluated. Peripheral sympathetic neuromodulatory therapies and emerging targeted strategies can suppress refractory ventricular arrhythmias by disrupting sympathetic input to the heart in structural heart disease.
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