# A Comprehensive Review of a Mechanism-Based Ventricular Electrical Storm Management

**Authors:** Alina Gabriela Negru, Diana Carina Iovanovici, Ana Lascu, Alexandru Silviu Pescariu, Gabriel Cismaru, Simina Crișan, Ștefan Ailoaei, Diana Luiza Bebec, Caius Glad Streian, Mariela Romina Bîrza, Andrei Raul Manzur, Silvia Ana Luca, Dana David, Svetlana Moșteoru, Dan Gaiță, Constantin Tudor Luca

PMC · DOI: 10.3390/jcm14155351 · Journal of Clinical Medicine · 2025-07-29

## TL;DR

This paper reviews the best strategies for managing ventricular electrical storms, focusing on tailored treatments and long-term stability.

## Contribution

The paper offers a comprehensive, mechanism-based review of therapeutic approaches for ventricular electrical storms.

## Key findings

- VES management requires a stepwise, team-based, and tailored approach.
- Therapeutic options include ICD reprogramming, sedation, and catheter ablation.
- Genetic arrhythmia syndromes require detailed and specific management strategies.

## Abstract

The electrical ventricular storm (VES) is defined as multiple sustained ventricular arrhythmias arising in a short time, often refractory to standard antiarrhythmic treatment. The three pillars of the physiopathogenesis of the VES are autonomic dysfunction, triggers, and an altered ventricular substrate. Incessant or highly recurrent ventricular arrhythmia impacts the hemodynamic status by worsening heart failure and increasing mortality. A stepwise, team-based, and tailored therapeutic approach is required to stop ventricular arrhythmia and regain the hemodynamic and electric stability of the patient. The authors focused on describing all currently available therapeutic approaches for VES, intending to establish the best VES therapeutic approaches. This process involves considering the patient’s specific condition, responses to previous treatments, and the potential risks and benefits of each approach. The options range from adjusting antiarrhythmic therapy to reprogramming of the ICD, sedation, epidural anaesthesia, stellate ganglia anaesthetic block, and the use of ECMO or left ventricular assist devices and radiofrequency catheter ablation. Particular attention is paid to the detailed management of genetic primary arrhythmia syndromes like long-QT syndrome, catecholaminergic polymorphic ventricular tachycardia, Brugada syndrome and Wolff–Parkinson–White syndrome, early repolarisation syndrome, right ventricular arrhythmogenic dysplasia, and idiopathic ventricular fibrillation. After overcoming the acute events of VES and obtaining hemodynamic stability, the treatment should shift toward an optimal balance of heart failure therapy, controlling the substrate by revascularisation procedures and resolving other pathology-generating ventricular arrhythmias. This article provides a comprehensive overview of ESV’s current management options using the most efficient strategies known to date.

## Linked entities

- **Diseases:** long-QT syndrome (MONDO:0002442), catecholaminergic polymorphic ventricular tachycardia (MONDO:0017990), Brugada syndrome (MONDO:0015263), Wolff–Parkinson–White syndrome (MONDO:0008685), idiopathic ventricular fibrillation (MONDO:0100234)

## Full-text entities

- **Diseases:** long-QT syndrome (MESH:D008133), idiopathic ventricular fibrillation (MESH:C537182), Brugada syndrome (MESH:D053840), VES (MESH:C566109), arrhythmia (MESH:D001145), catecholaminergic polymorphic ventricular tachycardia (MESH:C536334), heart failure (MESH:D006333), ventricular arrhythmogenic dysplasia (MESH:D019571), early repolarisation syndrome (MESH:C580055), Wolff-Parkinson-White syndrome (MESH:D014927)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

225 references — full list in the complete paper: https://tomesphere.com/paper/PMC12347519/full.md

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Source: https://tomesphere.com/paper/PMC12347519