Hypertrophic Cardiomyopathy (HCM)
This infographic provides a structured overview of Hypertrophic Cardiomyopathy (HCM), focusing on its diagnosis, clinical presentation, and management strategies.
- Diagnosis
- Wall thickness ≥15 mm detected via TTE, CT, or MRI.
- HCM is confirmed by ruling out secondary causes of LVH such as hypertension or myocardial infiltration. Genetic testing and MRI findings (e.g., LGE) support diagnosis.
- LVOT Assessment and Obstruction
- Resting gradient >50 mmHg confirms obstruction; for borderline cases (<50 mmHg), obstruction is provoked via:
- Valsalva maneuver
- Amyl nitrate administration
- Stress testing
- Cardiac catheterization
- Clinical Presentation and Physical Exam
- Symptoms: Dyspnea, angina, syncope, and palpitations.
- Physical findings include a holosystolic murmur, which intensifies with Valsalva or standing, and pulsus bisferiens.
- Diagnostic Findings
- Echo Findings:
- Asymmetric septal thickening, SAM (systolic anterior motion of the mitral valve), and posterior jet MR.
- EKG Findings:
- Repolarization abnormalities, LVH, and ST-T wave changes (e.g., apical HCM presenting with deep T-wave inversion).
- Management Strategies
- Prevent Symptoms
- Medical therapy: Beta-blockers (BB), calcium channel blockers (CCB), disopyramide.
- Avoid diuretics, vasodilators, and digoxin.
- Drug-refractory cases: Surgical myectomy, alcohol septal ablation, or heart transplant.
- Lifestyle changes: Avoid alcohol, stimulants, dehydration, and temperature extremes.
- Prevent Stroke
- Atrial fibrillation requires anticoagulation, regardless of CHADSVASc score.
- Prevent Sudden Cardiac Death (SCD)
- Genetic screening for all first-degree relatives.
- Risk factors: Family history of SCD, unexplained syncope, septum ≥3 cm, NSVT (nonsustained VT), or abnormal BP response.
This infographic provides a comprehensive framework for managing HCM by preventing symptoms, stroke, and sudden cardiac death.
Produced by Dr. Carine Hamo
“4 P’s of Prevention” by Dr. Amit Goyal
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