Hypertrophic Cardiomyopathy 2020.
James KogutEric D PopjesPublished in: Current cardiology reports (2020)
HCM-related mortality remains low; however, symptoms due in large part to LVOT obstruction remain a clinical dilemma. Several medical therapies have been shown to reduce symptoms and improve functional capacity, including several recent phase 2 clinical trials involving the novel myosin modulator mavacamten. In patients with refractory symptoms, septal reduction therapy or advanced therapies remain viable options in many cases. HCM is a complex and heterogeneous disease with diverse presentations and variable anatomy and clinical outcomes. The majority of patients will remain asymptomatic or with minimal symptoms and long-term survival remains high. For symptomatic patients, a variety of medical therapies, along with septal reduction therapies, have been shown to reduce symptoms and improve functional capacity.
Keyphrases
- hypertrophic cardiomyopathy
- end stage renal disease
- clinical trial
- newly diagnosed
- ejection fraction
- healthcare
- left ventricular
- chronic kidney disease
- sleep quality
- peritoneal dialysis
- type diabetes
- randomized controlled trial
- coronary artery disease
- cardiovascular disease
- mesenchymal stem cells
- risk factors
- bone marrow
- depressive symptoms