Cardiac Resynchronization Therapy and Hypertrophic Cardiomyopathy: A Comprehensive Review
Andrei Dan Radu1,2, Cosmin Cojocaru1,2, Sebastian Onciul1,2
1Faculty of Medicine, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Insights
Cardiac resynchronization therapy (CRT) may benefit hypertrophic cardiomyopathy (HCM) patients with heart failure and prolonged QRS duration. Studies suggest CRT can improve symptoms, exercise capacity, and left ventricular function in specific HCM patient groups.
Area of Science:
- Cardiology
- Cardiovascular Medicine
- Genetics
Background:
- Hypertrophic cardiomyopathy (HCM) is an inherited heart muscle disease causing left ventricle (LV) hypertrophy and potential outflow tract obstruction.
- Patients with HCM may develop heart failure (HF) with reduced ejection fraction or left bundle branch block (LBBB), particularly with disease progression or after myectomy.
- Cardiac resynchronization therapy (CRT) is a treatment for heart failure patients with specific electrical conduction abnormalities.
Purpose of the Study:
- To review and reassess the role and importance of CRT in managing patients with hypertrophic cardiomyopathy.
- To contextualize current research on CRT efficacy in diverse HCM patient populations.
- To identify potential patient selection criteria for CRT in HCM.
Main Methods:
- Systematic review and analysis of existing studies on CRT in HCM patients.
- Comparison of outcomes in HCM patients with LBBB or reduced LVEF undergoing CRT.
- Evaluation of electrical and imaging parameters for patient stratification.
Main Results:
- CRT may improve symptoms, exercise capacity, and LV ejection fraction (LVEF) in HCM patients with myectomy-induced LBBB.
- CRT can enhance NYHA class, LV systolic performance, and promote reverse remodeling in end-stage/dilated HCM with prolonged QRS.
- Further research is needed due to limited current data.
Conclusions:
- CRT shows potential benefits for specific subgroups of HCM patients, including those with LBBB or advanced HF.
- Careful patient selection using electrical and imaging markers is crucial for optimizing CRT outcomes in HCM.
- More extensive clinical trials are required to establish definitive guidelines for CRT use in HCM.
Abstract:
Hypertrophic cardiomyopathy (HCM) is an inherited primary myocardial disease characterized by asymmetrical/symmetrical left ventricle (LV) hypertrophy, with or without LV outflow tract (LVOT) dynamic obstruction, and poor prognosis. Cardiac resynchronization therapy (CRT) has emerged as a minimally invasive tool for patients with heart failure (HF) with decreased LV ejection fraction (LVEF) and prolonged QRS duration of over 120 ms with or without left bundle branch block (LBBB). Several HCM patients are at risk of developing LBBB because of disease progression or secondary to septal myomectomy, while others might develop HF with decreased LVEF, alleged end-stage/dilated HCM, especially those with thin myofilament mutations. Several studies have shown that patients with myectomy-induced LBBB might benefit from left bundle branch pacing or CRT to relieve symptoms, improve exercise capacity, and increase LVEF. Otherwise, patients with end-stage/dilated HCM and prolonged QRS interval could gain from CRT in terms of NYHA class improvement, LV systolic performance increase and, to some degree, LV reverse remodeling. Moreover, several electrical and imaging parameters might aid proper selection and stratification of HCM patients to benefit from CRT. Nonetheless, current available data are scarce and further studies are still required to accurately clarify the view. This review reassesses the importance of CRT in patients with HCM based on current research by contrasting and contextualizing data from various published studies.
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