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Mechanisms, time course and predictability of premature ventricular contractions cardiomyopathy-an update on its
C Cojocaru1, D Penela2, Antonio Berruezo3,4
1Clinical Emergency Hospital, Bucharest, Romania.
Insights
Frequent premature ventricular contractions (PVCs) can cause heart muscle dysfunction. This review synthesizes current knowledge on PVC-induced cardiomyopathy, its reversibility, and associated conditions, aiding clinical practice.
Area of Science:
- Cardiology
- Electrophysiology
- Heart Failure Research
Background:
- Frequent premature ventricular contractions (PVCs) are linked to left ventricular systolic dysfunction (LVSD).
- Predictors for cardiomyopathy (CMP) development are known, but precise risk and reversibility after PVC suppression remain unclear.
- Limited data exists on the time course of CMP development/resolution and associated right ventricular (RV) and atrial myopathies.
Purpose of the Study:
- To synthesize recent information on PVC-induced cardiomyopathy (CMP).
- To provide a deeper understanding of this heart failure scenario.
- To describe mechanisms, time course, and predictors of reverse remodeling after arrhythmia suppression.
Main Methods:
- Review of recent scientific literature and clinical experiences.
- Synthesis of information on mechanisms, time course, and predictors of reverse remodeling.
- Exploration of experimental models and clinical data.
Main Results:
- The review details the mechanisms and time course of PVC-induced CMP development and resolution.
- Predictors for reverse remodeling after PVC suppression are described.
- Associated RV and atrial myopathies are discussed.
Conclusions:
- Understanding PVC-induced CMP is crucial for tailored patient monitoring and early treatment.
- The review proposes a new paradigm for multi-level, multi-modality evaluation and potential early intervention.
- Further research into the precise risk and reversibility of PVC-induced CMP is warranted.
Abstract:
Frequent premature ventricular contractions (PVCs) associated left ventricular systolic dysfunction (LVSD) is a well-known clinical scenario and numerous predictors for cardiomyopathy (CMP) development have been already thoroughly described. It may present as a "pure" form of dissynchrony-induced cardiomyopathy or it may be an aggravating component of a multifactorial structural heart disease. However, the precise risk to develop PVC-induced CMP (which would allow for tailored-patient monitoring and/or early treatment) and the degree of CMP reversibility after PVC suppression/elimination (which may permit appropriate candidate selection for therapy) are unclear. Moreover, there is limited data regarding the time course of CMP development and resolution after arrhythmia suppression. Even less known are the other components of PVC-induced CMP, such as right ventricular (RV) and atrial myopathies. This review targets to synthetize the most recent information in this regard and bring a deeper understanding of this heart failure scenario. The mechanisms, time course (both in experimental models and clinical experiences) and predictors of reverse-remodelling after arrhythmia suppression are described. The novel experience hereby presented may aid everyday clinical practice, promoting a new paradigm involving more complex, multi-level and multi-modality evaluation and possible earlier intervention at least in some patient subsets.
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