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Published on: July 2, 2018
Avalanches in cardiology
1Department of Pediatric Cardiology, Frontier Lifeline Hospital, Chennai, Tamil Nadu, India.
Insights
Sudden cardiac death (SCD) can result from right ventricular (RV) overload, not just left ventricular issues. Understanding RV decompensation is key to preventing fatal "cardiac avalanches."
Area of Science:
- Cardiology
- Pathophysiology
- Medical Research
Background:
- Sudden cardiac death (SCD) is a major cause of mortality in heart disease patients.
- Ventricular tachyarrhythmia, often cited, explains only a fraction of SCD cases.
- Implantable cardioverter-defibrillators show variable success in preventing SCD.
Purpose of the Study:
- To explore the pathophysiology of SCD in right ventricular (RV) overload states.
- To review RV adaptive and decompensatory mechanisms.
- To identify therapeutic strategies to prevent SCD in RV overload.
Main Methods:
- Literature review on RV overload and SCD.
- Analysis of compensatory mechanisms in advanced cardiac disease.
- Comparison of RV and left ventricular (LV) dysfunction in SCD.
Main Results:
- A significant proportion of SCD may stem from circulatory failure, not just arrhythmias.
- RV overload conditions, like pulmonary arterial hypertension, are increasingly recognized as SCD causes.
- Limited data exists on RV adaptation and decompensation compared to LV.
Conclusions:
- SCD in RV overload states requires further investigation into its unique mechanisms.
- Understanding RV decompensation is crucial for developing targeted therapies.
- Preventing "cardiac avalanches" in RV overload may involve interrupting specific triggers and decompensatory pathways.
Abstract:
Sudden cardiac death (SCD) accounts for 15%-60% of mortality in patients with heart disease. Generally, this has been attributed to ventricular tachyarrhythmia. However, ventricular tachyarrhythmia has been documented or strongly suspected on clinical grounds in a relatively small proportion of SCD patients (8%-50%). Attempted prophylaxis of SCD by implantation of cardioverter-defibrillator is associated with variable success in different subsets of high-risk cardiac patients (30%-70%). A significant number of SCD, therefore, appear to be due to catastrophic circulatory failure. Multiple interdependent compensatory mechanisms help to maintain circulation in advanced cardiac disease. Rapid, unexpected, and massive breakdown of the compensated state can be precipitated by small and often imperceptible triggers. The initial critical but stable state followed by rapid circulatory failure and death has been considered to be analogous to snow avalanches. It is typically described in patients with left ventricular (LV) dysfunction (ischemic or nonischemic). It is now recognized that SCD can also happen in conditions where the right ventricle (RV) takes the brunt of the hemodynamic load. Advanced pulmonary arterial hypertension and operated patients of tetralogy of Fallot with pulmonary regurgitation are of particular interest to pediatric cardiologists. A large amount of data is available on LV changes and mechanics, while relatively little information is available on the mechanisms of RV adaptation to increased load and RV failure. Whether the triggers and the decompensatory processes are similar for the two ventricles is a moot point. This article highlights the currently available knowledge on the pathophysiology of SCD in RV overload states, with special reference to RV adaptive and decompensatory mechanisms, and therapeutic measures that can potentially interrupt the vicious downward course (cardiac avalanches).
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