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- W4382808575 abstract "Hypertrophic cardiomyopathy (HCM) is a common heridetary cardiac disorder characterized by a wide range of symptoms. The pharmacological treatment of HCM is currently limited to beta blockers, non-dihydropyridine calcium channel blockers and disopyramide. Mavacamten is a novel cardiac myosin inhibitor, which was recently added to the limited pharmacological list of treatment options for HCM. This editorial elaborates on current evidence evaluating the use of mavacamten in patients with symptomatic obstructive HCM, comments on its current use and its expanded potential applications in the future." @default.
- W4382808575 created "2023-07-02" @default.
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- W4382808575 date "2023-01-01" @default.
- W4382808575 modified "2023-10-18" @default.
- W4382808575 title "Mavacamten, an Alternative to Septal Reduction Therapy for Patients with Hypertrophic Cardiomyopathy" @default.
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- W4382808575 doi "https://doi.org/10.17925/hi.2023.17.1.2" @default.
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