Hypertrophic Cardiomyopathy (HCM) (2024)

ECG features of HCM
  • Left ventricular hypertrophy with increased precordial voltages and non-specific ST segment and T-wave abnormalities
  • Deep, narrow (“dagger-like”) Q waves in lateral (I, aVL, V5-6) +/- inferior (II, III, aVF) leads

Other associated features may include:

  • Left atrial enlargement (“P mitrale”) — left ventricular diastolic dysfunction may lead to compensatory left atrial hyertrophy
  • Signs of WPW (short PR, delta wave) — ECG features of Wolff-Parkinson-White (WPW) were seen in 33% of patients with HCM in one study, and at least one genetic mutation has been identified that is associated with both conditions
  • Dysrhythmias: atrial fibrillation and supraventricular tachycardias are common; PACs, PVCs, VT
  • Giant precordial T-wave inversions in apical HCM
Q wave morphology
  • Q waves seen in HCM can mimic prior myocardial infarction, although the Q-wave morphology is different:
    • Infarction Q waves are typically > 40 ms duration
    • Septal Q waves in HCM are < 40 ms
  • Lateral Q waves are more common than inferior Q waves in HCM
Overview of HCM

Hypertrophic cardiomyopathy, previously termed hypertrophic obstructive cardiomyopathy (HOCM) or idiopathic hypertrophic subaortic stenosis (IHSS), is one of the most common inherited cardiac disorders:

  • Prevalence ~1 in 500 people
  • Annual mortality ~1-2%
  • Number one cause of sudden cardiac death in young people

It is a heterogenous disorder produced by mutations in multiple genes coding for sarcomeric proteins (e.g. beta-myosin heavy chain, troponin T). Inheritance is primarily autosomal dominant, with variable penetrance. Over 150 mutations have been identified, explaining the variability in the clinical phenotype.

Structural changes
  • The chief abnormality associated with HCM is left ventricular hypertrophy (LVH), occurring in the absence of any inciting stimulus such as hypertension or aortic stenosis
  • The degree and distribution of LVH is variable: mild hypertrophy (13-15 mm) or extreme myocardial thickening (30-60 mm) may be seen.
  • The most commonly observed pattern is asymmetrical thickening of the anterior interventricular septum (= asymmetrical septal hypertrophy). This pattern has been classically associated with systolic anterior motion (SAM) of the mitral valve and dynamic left ventricular outflow tract (LVOT) obstruction
  • However, in the majority of cases (75%), HCM is not associated with LVOT obstruction, hence the name change from HOCM to HCM
  • Other less common patterns of LVH include concentric hypertrophy (20% of cases) and apical hypertrophy (10%)
Pathophysiology of clinical manifestations

Processes responsible for clinical manifestations of HCM:

  • Dynamic obstruction of the LVOT
  • Left ventricular diastolic dysfunction, resulting from impaired relaxation and filling of the stiff and hypertrophied left ventricle (often associated with increased filling pressures)
  • Abnormal intramural coronary arteries with thickened walls and narrowed lumens
  • Chaotic, disorganised left ventricular architecture (“cellular disarray”) predisposing to abnormal transmission of electrical impulses, thus serving as a substrate for arrhythmogenesis
Clinical features
  • Exertional syncope or pre-syncope — this is the most worrying symptom, suggesting dynamic LVOT obstruction ± ventricular dysrhythmia, with the potential for sudden cardiac death
  • Symptoms of pulmonary congestion (e.g. exertional dyspnoea, fatigue, orthopnoea, paroxysmal nocturnal dyspnoea) due to left ventricular dysfunction
  • Chest pain — may be typical anginal pain due to increased demand (thicker myocardial walls) and reduced supply (aberrant coronary arteries)
  • Palpitations due to supraventricular or ventricular arrhythmias
Apical HCM
  • This relatively uncommon form of HCM is seen most frequently in Japanese patients (13-25% of all HCM cases in Japan)
  • There is localised hypertrophy of LV apex, causing a “spade-shaped” configuration of the LV cavity on ventriculography
  • The classic ECG finding in apical HCM is giant T-wave inversion in the precordial leads
Useful Tip
  • There is a small subset of patients with HCM who will have an abnormal ECG with no evidence of LVH on echo
  • If there is clinical concern for HCM — i.e. syncope, chest pain and characteristic ECG changes — patients should be referred for a cardiac MRI if echo is unremarkable
ECG Examples
Example 1

Classic HCM pattern with asymmetrical septal hypertrophy:

  • Voltage criteria for left ventricular hypertrophy.
  • Deep narrow Q waves < 40 ms wide in the lateral leads I, aVL and V5-6.

This ECG was taken from a 30-year old man who presented with exertional lightheadedness and palpitations. The ECG was misread by the cardiology team as showing “left ventricular hypertrophy, lateral infarct age undetermined”.

The patient was discharged home and subsequently died of a VF arrest while running to catch a bus. Autopsy showed septal hypertrophy consistent with HCM.

Teaching Point:In a young patient presenting with exertional symptoms and an ECG that looks this this, think HCM — not “prior lateral infarction“!

This ECG and clinical vignette is reproduced from a fantastic review article by Kelly, Mattu and Brady (2007).

Example 2

HCM showing features of asymmetrical septal hypertrophy:

  • Large precordial voltages.
  • Deep, narrow, septal Q waves most prominent in leads I and aVL; also seen in V5-6.

This great ECG is reproduced from Kelly, Mattu and Brady (2007).

Example 3

This ECG shows the typical pattern of apical HCM:

  • Large precordial voltages.
  • Giant T wave inversions in the precordial leads
  • Inverted T waves are also seen in the inferior and lateral leads.

This great ECG is reproduced from Hansen & Merchant (2007).

Example 4

Another example of apical HCM

  • High precordial voltages.
  • Deep T wave inversions in the precordial and high-lateral leads.
  • There is also evidence of left atrial enlargement (“P mitrale”).
Videos
HCM video education
Related Topics
  • Dilated cardiomyopathy
  • Restrictive cardiomyopathy
  • Left ventricular hypertrophy
  • Yamaguchi Syndrome
Advanced Reading

Online

Textbooks

LITFL Further Reading
  • ECG Library Basics – Waves, Intervals, Segments and Clinical Interpretation
  • ECG A to Z by diagnosis – ECG interpretation in clinical context
  • ECG Exigency and Cardiovascular Curveball – ECG Clinical Cases
  • 100 ECG Quiz – Self-assessment tool for examination practice
  • ECG Reference SITES and BOOKS – the best of the rest

ECG LIBRARY

more EKG…

Robert Buttner

MBBS (UWA) CCPU (RCE, Biliary, DVT, E-FAST, AAA) Adult/Paediatric Emergency Medicine Advanced Trainee in Melbourne, Australia. Special interests in diagnostic and procedural ultrasound, medical education, and ECG interpretation. Editor-in-chief of the LITFL ECG Library. Twitter: @rob_buttner

Ed Burns

Emergency Physician in Prehospital and Retrieval Medicine in Sydney, Australia. He has a passion for ECG interpretation and medical education | ECG Library |

Hypertrophic Cardiomyopathy (HCM) (2024)

FAQs

Is HCM a serious heart condition? ›

HCM causes abnormal growth of the heart muscle. Most people with HCM have few or no symptoms. Most lead long lives. But HCM sometimes causes serious complications, including sudden cardiac death.

What is the average life expectancy for HCM? ›

Research has shown that with proper treatment and follow-ups, most people with HCM live a normal life. A database of 1,297 patients with HCM from the Minneapolis Heart Institute Foundation identified that 2% of the patients can live past 90 years, and 69% of them were women.

What makes HCM worse? ›

Smoking tobacco can worsen some HCM symptoms. It causes a narrowing of the coronary arteries. The combination of HCM and coronary artery disease is dangerous. If you smoke, experts at NYU Langone's Tobacco Cessation Programs can teach you techniques designed to help you quit.

How fast does HCM progress? ›

Although HCM has 4 identified stages [11], patients with HCM can experience a sudden cardiac arrest or the disease can slowly progress over several years.

Can you live a full life with HCM? ›

Hypertrophic cardiomyopathy (HCM) is a disease that causes your heart muscle to enlarge (hypertrophy). Most people who have it can have a normal life, but it can be serious for some people. If this is the case for you, there are several treatment options.

What are the four stages of hypertrophic cardiomyopathy? ›

The stages of HCM, which are based on the clinical evidence of disease progression, were previously defined by Olivotto et al. [16]. These clinical stages include subclinical HCM, the classic HCM phenothype, adverse remodelling and overt dysfunction, or end-stage HCM.

Is HCM considered a disability? ›

HCM, or hypertrophic cardiomyopathy (or hypertrophic obstructed cardiomyopathy), affects between 1 in 200 and 1 in 300 worldwide. If you have HCM and you are unable to work due to severe symptoms, you might be eligible for Social Security disability benefits in the United States.

What is end stage HCM? ›

Introduction: End-Stage (ES) Hypertrophic Cardiomyopathy (HCM) is defined when left ventricular ejection fraction (LVEF) falls below 50% and is associated with poor prognosis. Early identification is paramount, but reliable predictors have not been characterized.

At what age does HCM develop? ›

In many cases, muscle thickening begins early in adolescence or adulthood. Nearly half of all people with HCM have evidence of heart muscle enlargement by age 30. However, muscle thickening can start at any age, and roughly 1 in 4 people do not develop structural evidence of HCM until age 60 .

Is coffee bad for HCM? ›

Of course, if your doctor recommends avoiding coffee or dark, bitter chocolate, you should. If you don't like them (or don't like the way you react to them), by all means, avoid them! But there is no evidence that heart patients generally should avoid them, and they may even be good for you.

Does HCM cause weight gain? ›

In addition, there is a higher prevalence of obesity among patients with HCM, building a strong case for an interaction between the two conditions. The established cardiovascular changes in obesity are also present in patients with HCM.

What are the red flags for hypertrophic cardiomyopathy? ›

Signs and symptoms of HCM include: Chest pain, especially with physical exertion. Shortness of breath, especially with physical exertion. Fatigue.

What should you not do with hypertrophic cardiomyopathy? ›

Avoid intense burst of exercise, weightlifting, and competitive sports. Don't lift heavy objects while performing household chores. Avoid environmental extremes (heat/cold) Follow a heart-healthy diet.

What drugs should be avoided in hypertrophic cardiomyopathy? ›

Drugs to avoid in obstructive HCM.
  • Nitrates.
  • ACE, ARB: . . . . ...
  • Dihydropyridine CaCB: Nifedipine, Amlodipine; . . . ...
  • Alpha blockers: Terazosin (Hytrin), Tamsulosin (Flomax), Doxazosin (Cardura), . . . ...
  • PDE5 inhibitors: Sildenafil (Viagra), Vardenafil (Levitra), . . . . ...
  • Dobutamine, Dopamine, Digoxin.

Can exercise reverse HCM? ›

Exercise can prevent and reverse the severity of hypertrophic cardiomyopathy. Circ Res 2006;98:540-8.

Is HCM a critical illness? ›

But in a small number of people with HCM , the thickened heart muscle can cause serious symptoms. These include shortness of breath and chest pain. Some people with HCM have changes in the heart's electrical system. These changes can result in life-threatening irregular heartbeats or sudden death.

Is hypertrophic cardiomyopathy a terminal illness? ›

Some people do not have any symptoms and do not need treatment. But that does not mean the condition cannot be serious. Hypertrophic cardiomyopathy is the most common cause of sudden unexpected death in childhood and in young athletes.

What are the chances of dying from hypertrophic cardiomyopathy? ›

It can occur at any age, but it is most shocking when it happens to young adults or athletes. While the media often highlight these tragic deaths, sudden death is rare. It occurs in about 1 out of 100 adults with hypertrophic cardiomyopathy each year.

Is HCM a terminal? ›

There is a rare risk of developing a life-threatening abnormal heart rhythm, which can cause a cardiac arrest and sudden death. This is why it's so important to diagnose people who have HCM, so they can have treatment to stop this from happening.

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