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Hypertrophic Cardiomyopathy 2024

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30 Treatment 8.2. Management of Patients With Nonobstructive HCM With Preserved EF COR LOE Recommendations 1 C-LD 1. In patients with nonobstructive HCM with preserved EF and symptoms of exertional angina or dyspnea, beta blockers or nondihydropyridine calcium channel blockers are recommended. 2a C-EO 2. In patients with nonobstructive HCM with preserved EF, it is reasonable to add oral diuretics when exertional dyspnea persists despite the use of beta blockers or nondihydropyridine calcium channel blockers. 2b C-LD 3. In patients with nonobstructive HCM with preserved EF, the usefulness of angiotensin-converting enzyme inhibitors and angiotensin receptor blockers in the treatment of symptoms (angina and dyspnea) is not well established. 2b C-LD 4. In highly selected patients with apical HCM with severe dyspnea or angina (NYHA class III or class IV) despite maximal medical therapy, and with preserved EF and small LV cavity size (LV end-diastolic volume <50 mL/m 2 and LV stroke volume <30 mL/m 2 ), apical myectomy by experienced surgeons at comprehensive centers may be considered to reduce symptoms. 2b C-EO 5. In asymptomatic patients with nonobstructive HCM, the benefit of beta blockers or calcium channel blockers is not well established. 2b B-R 6. For younger (eg, ≤45 years of age) patients with nonobstructive HCM due to a pathogenic or likely pathogenic cardiac sarcomere genetic variant, and a mild phenotype,* valsartan may be beneficial to slow adverse cardiac remodeling. * Mild phenotype indicates NYHA class I or II, maximal le ventricular wall thickness 13 to 25 mm, no secondary prevention ICDs, no history of appropriate ICD shocks, and no atrial fibrillation.

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