HOCM Flashcards

1
Q

Hypertrophic (obstructive) cardiomyopathy presentation

A

This young man has complained of palpitations whilst playing football. Examine his cardiovascular system.

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2
Q

Clinical signs of Hypertrophic (obstructive) cardiomyopathy

A
  1. Jerky pulse character
  2. Double apical impulse (palpable atrial and ventricular contraction)
  3. Thrill at the lower left sternal edge
  4. Auscultation:
    - Ejection systolic murmur (ESM) at the lower left sternal edge that radiates throughout the precordium.
    - A fourth heartsound (S4) is present due to blood hitting a hypertrophied stiff LV during atrial systole.
    - Dynamic ESM accentuated by reducing LV volume, e.g. standing from squatting or during a strain phase of Valsalva.
  5. There may be associated mitral valve prolapse (MVP)
  6. There may be features of Friedreich’s ataxia or myotonic dystrophy
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3
Q

Auscultation in HOCM

A
  1. Ejection systolic murmur (ESM) at the lower left sternal edge that radiates throughout the precordium.
  2. A fourth heartsound (S4) is present due to blood hitting a hypertrophied stiff LV during atrial systole.
  3. Dynamic ESM accentuated by reducing LV volume, e.g. standing from squatting or during a strain phase of Valsalva.
  4. There may be associated mitral valve prolapse (MVP)
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4
Q

Investigation for HOCM

A
  1. ECG: LVH with strain (deep T‐wave inversion across precordial leads)
  2. CXR: often normal
  3. TTE:
    - Asymmetrical septal hypertrophy
    - Systolic ant. motion of the ant. mitral leaflet across the LVOT due to misalignment of septal papillary muscle,
    - LVOT gradient (rest/exercise or dobutamine stress)
  4. Cardiac MR: identifies apical HCM more reliably than TTE
  5. Cardiac catheterization:
    - gradient accentuated by a ventricular ectopic or pharmacological stress,
    - identification of septals
  6. Genetic tests: sarcomeric proteins mutation

LVOT = left ventricular outflow tract, ant. = anterior

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5
Q

Management of HOCM

A

1. Asymptomatic: Avoidance of strenuous exercise, dehydration and vasodilators
2. Symptomatic and LVOT gradient >30 mm Hg
- β‐Blockers
- Pacemaker
- Alcohol septal ablation
- Surgical myomectomy
3. Rhythm disturbance/high‐risk SCD:
- ICD
4. Refractory:
- Cardiac transplant
* Genetic counselling of first‐degree relatives (autosomal dominant inheritance)

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6
Q

Prognosis of HOCM

A

i. Annual mortality rate in adults is 2.5%
ii. Poor prognosis factors:
1. Young age at diagnosis
2. Syncope
3. Family history of sudden death
4. Septal thickness > 3 cm

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