Effectiveness of cardioneuroablation in different subtypes of vasovagal syncope

Bin Tu1,2, Zi-Hao Lai1, Ai-Yue Chen1

  • 1Arrhythmia Center, Fuwai Hospital, National Center for Cardiovascular Diseases, National Key Laboratory, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Insights

Cardioneuroablation (CNA) shows varied success in vasovagal syncope (VVS) subtypes. Patients with vasodepressive VVS and low deceleration capacity (DC) have higher recurrence risk post-CNA.

Area of Science:

  • Cardiology
  • Neuroscience
  • Medical Devices

Background:

  • Vasovagal syncope (VVS) is a common condition.
  • Cardioneuroablation (CNA) is a treatment option for VVS.
  • Limited data exists on CNA outcomes across different VVS subtypes.

Purpose of the Study:

  • To analyze the effectiveness of CNA in various VVS subtypes.
  • To identify factors influencing recurrence after CNA.
  • To evaluate the role of deceleration capacity (DC) in predicting outcomes.

Main Methods:

  • Retrospective observational study of 141 VVS patients.
  • Analysis of patient characteristics and outcomes post-CNA.
  • Kaplan-Meier survival analysis and subgroup comparisons.

Main Results:

  • Overall recurrence rate of 29.1% after 4.3 years.
  • Cardioinhibitory VVS had the lowest recurrence (16.7%), vasodepressive the highest (45.0%).
  • Low baseline DC (< 8.4 ms) significantly increased recurrence risk (HR=8.1) in vasodepressive VVS.

Conclusions:

  • VVS subtypes demonstrate distinct event-free rates after CNA.
  • Vasodepressive VVS shows the lowest event-free rate.
  • Patients with vasodepressive VVS and DC ≥ 8.4 ms may benefit from CNA.
Abstract

Related Concept Videos

Antiarrhythmic Drugs: Class II Agents as &#946;-Adrenergic Blockers01:24

Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers

Adrenergic stimulation generally impacts cardiac rate and rhythm. Specifically, stimulation of the β-adrenoceptors triggers an increase in intracellular calcium ion influx and pacemaker currents, which may cause arrhythmias. Catecholamines like adrenaline also demonstrate β2-adrenoceptor-mediated hypokalemia, impacting cardiac action potential and disrupting the normal cardiac rhythm. Class II antiarrhythmic drugs are β-adrenoceptor antagonists or β-blockers, which...
733
Heart Failure Drugs: &#946;-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
336
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
419
Antianginal Drugs: Calcium Channel Blockers and Ranolazine01:25

Antianginal Drugs: Calcium Channel Blockers and Ranolazine

Angina pectoris, a primary symptom of ischemic heart disease, requires careful pharmacological interventions. In this context, calcium channel blockers (CCBs) and ranolazine have emerged as crucial pharmacotherapeutic agents, providing deep insights into the complexities of angina management.
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
486
Mechanism of Cardiac Arrhythmias01:28

Mechanism of Cardiac Arrhythmias

Arrhythmias are irregular heart rhythms occurring when the heart's electrical impulses become abnormal. These disturbances can lead to various symptoms, depending on their severity and the underlying cause. Some common factors contributing to arrhythmias include hypoxia, ischemia, electrolyte imbalances, excessive catecholamine exposure, drug toxicity, and muscle overstretching. Arrhythmias can be classified into two main types based on the rate and site of origin of abnormal heart rhythms.
909
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers01:22

Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers

Class I antiarrhythmic drugs are used to treat various types of arrhythmias or irregular heart rhythms. These drugs block the sodium (Na+) channels in the cardiac cells, thereby affecting the movement of electrical impulses across the heart. Class I antiarrhythmic drugs are divided into three subgroups: Class IA, Class IB, and Class IC, each with distinct mechanisms of action and effects on the heart.
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
1.3K