Related Experiment Video
Updated: Dec 20, 2025

Location, Dissection, and Analysis of the Murine Stellate Ganglion
Published on: December 22, 2020
Role of cardiac sympathetic denervation in ventricular tachycardia: A meta-analysis
Ghulam Murtaza1, Sharan P Sharma2, Krishna Akella1
1Kansas City Heart Rhythm Institute & Research Foundation, Overland Park, Kansas.
Insights
Cardiac sympathetic denervation (CSD) effectively manages refractory ventricular tachycardia (VT), showing a 60% VT nonrecurrence rate. This procedure also significantly reduces implantable cardioverter-defibrillator (ICD) shocks in patients with electrical storm.
Area of Science:
- Cardiology
- Electrophysiology
- Medical Interventions
Background:
- Refractory ventricular tachycardia (VT) and electrical storm pose significant clinical challenges.
- Cardiac sympathetic denervation (CSD) is an emerging therapy for these conditions.
- Limited data exists on the efficacy of CSD in managing ventricular arrhythmias.
Purpose of the Study:
- To evaluate the effectiveness of CSD in patients with refractory VT and electrical storm.
- To determine the pooled rate of VT recurrence after CSD.
- To assess the impact of CSD on implantable cardioverter-defibrillator (ICD) shocks.
Main Methods:
- A meta-analysis of 14 retrospective studies.
- Inclusion of 311 patients with refractory VT or electrical storm.
- Calculation of pooled VT-free rates and mean difference in ICD shocks pre- and post-CSD.
Main Results:
- A pooled VT nonrecurrence rate of 60% was observed at a mean follow-up of 15 months.
- For arrhythmias excluding CPVT and LQTS, the VT nonrecurrence rate was 50%.
- CSD significantly reduced the mean number of ICD shocks per person by 3.01 overall and 0.97 excluding CPVT and LQTS.
Conclusions:
- CSD is associated with a 60% VT nonrecurrence rate in patients with refractory VT or electrical storm.
- CSD significantly decreases the number of ICD shocks.
- Further prospective studies are recommended to confirm these findings.
Background:
Cardiac sympathetic denervation (CSD) is being used in the management of refractory ventricular tachycardia (VT) and electrical storm. However, data on the role of CSD in the management of ventricular arrhythmia is limited.
Methods:
We performed a meta-analysis of retrospective studies to calculate the pooled rate of freedom from VT and the standard mean difference of ICD shocks before and after CSD.
Results:
14 nonrandomized studies with a total of 311 patients with refractory VT or electrical storm were included. At a mean follow up of 15 ± 10.7 months, the pooled rate of freedom from VT (VT nonrecurrence rate) after CSD in all causes of arrhythmia was 60% (range 48.8% to 70%, I2 = 43%). When analysis was restricted to only arrhythmias caused by conditions other than catecholaminergic polymorphic ventricular tachycardia (CPVT) and long QT syndrome (LQTS), the pooled VT non-recurrence rate was 50% (range 41% to 58%, I2 = 5%). After CSD, mean total number of ICD shocks per person diminished by 3.01 (95% CI 1.09-4.94, P = .002, I2 = 96%) in overall analysis and by 0.97(95% CI 0.41-1.5, P = .001, I2 = 45%) when CPVT and LQTS were excluded.
Conclusion:
In patients with refractory VT or electrical storm, CSD is associated with pooled VT nonrecurrence rate of 60% at a mean follow-up of 15 ± 10.7 months. CSD was also associated with significantly lower mean number ICD shocks per person. Further studies are needed to validate this finding in a prospective setting.
More Related Videos
06:57Ablation of Ischemic Ventricular Tachycardia Using a Multipolar Catheter and 3-dimensional Mapping System for High-density Electro-anatomical Reconstruction
Published on: January 31, 2019
08:35Improved Renal Denervation Mitigated Hypertension Induced by Angiotensin II Infusion
Published on: May 26, 2022
Related Concept Videos
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Heart Failure Drugs: β-Blockers
Heart Failure II: Pathophysiology
Dysrhythmias VI: Management of Dysrhythmias
Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers
Cardiomyopathy II: Dilated Cardiomyopathy