Successful electrical cardioversion in a massive concentric hypertrophic cardiomyopathy with atrial fibrillation

Servet Altay1, Huseyin Altug Cakmak, Serhan Ozcan

  • 1Department of Cardiology, Siyami Ersek Thoracic and Cardiovascular Surgery Center, Training and Research Hospital, Istanbul, Turkey. svtaltay@gmail.com

Insights

This study highlights successful electrical cardioversion for a patient with hypertrophic cardiomyopathy and atrial fibrillation. The procedure restored sinus rhythm, improving cardiac function and reducing outflow tract obstruction.

Area of Science:

  • Cardiology
  • Cardiac Electrophysiology

Background:

  • A 59-year-old male with hypertrophic cardiomyopathy (HCM) and chronic atrial fibrillation (AF) presented with symptoms of heart failure.
  • Initial evaluation revealed AF with rapid ventricular response, intraventricular conduction delay, and left ventricular (LV) hypertrophy.

Observation:

  • Transthoracic echocardiography demonstrated significant LV concentric hypertrophy with midventricular turbulent flow, despite no baseline LV outflow tract (LVOT) gradient.
  • Transesophageal echocardiography excluded left atrial thrombus.
  • Electrical cardioversion successfully converted AF to sinus rhythm.

Findings:

  • Post-cardioversion echocardiography revealed a significant LVOT gradient (54 mm Hg resting, increasing to 84 mm Hg with Valsalva).
  • Cardiac MRI confirmed marked concentric LV hypertrophy (35 mm diastolic thickness), mild anterior wall scarring, and right ventricular hypertrophy (10 mm diastolic thickness).
  • 24-hour Holter and exercise ECG testing showed no significant arrhythmias.

Implications:

  • Electrical cardioversion can be effective in managing AF in patients with HCM, potentially unmasking or increasing LVOT gradients.
  • Careful hemodynamic monitoring and advanced imaging are crucial for assessing gradient changes post-cardioversion in HCM patients.
  • This case underscores the complex interplay between AF, HCM, and dynamic LVOT obstruction.

Related Concept Videos

ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias01:25

ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias

Arrhythmia is a condition characterized by an irregular heart rhythm, with ECG changes that differ based on its origin and nature. The types of arrhythmias discussed below include atrial, junctional, and ventricular arrhythmias.Atrial ArrhythmiasPremature Atrial Complexes (PACs): PACs are early atrial beats caused by stress, caffeine, alcohol, electrolyte imbalances, hypoxia, hyperthyroidism, or certain medications (e.g., bronchodilators and decongestants). The ECG shows early P waves with an...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

Dysrhythmia management involves a multifaceted approach, incorporating pharmacological treatments, medical procedures, surgical interventions, lifestyle modifications, and patient education.Pharmacological ManagementAntiarrhythmic Drugs:Class I (Sodium Channel Blockers): This class includes quinidine and procainamide, which reduce the speed of impulse conduction in the heart, stabilize the cardiac membrane, and control arrhythmias. Quinidine and procainamide are Class IA agents that prolong the...
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...