Learning Radiology xray montage
 
 
 
 
 

Aortic Stenosis


General Considerations 

  • Most often as result of degeneration of bicuspid aortic valve
  • Less commonly rheumatic heart disease or secondary to degeneration
    of a tricuspid aortic valve in person > 65
     

Location

  • Supravalvular
    • Uncommon
    • Associated with William’s Syndrome
      • Hypercalcemia
      • Elfin facies
      • Pulmonary stenoses
      • Hypoplasia of aorta
      • Stenoses in
        • Renal, celiac, superior mesenteric arteries
  • Valvular
    • Most common
    • Either congenital (from a bicuspid aortic valve) or acquired
      • Bicuspid aortic valve is the most common congenital cardiac anomaly
        • 0.5 –2%
  • Subvalvular
    • Associated with
      • Hypoplastic left heart syndrome
      • Idiopathic Hypertrophic Subaortic Stenosis
      • Hypertrophic cardiomyopathy
      • Subaortic fibrous membrane 

Types

  • Congenital aortic stenosis (more common)
    • Most frequent congenital heart disease associated with
      intra-uterine growth retardation (IUGR)
      • Subvalvular (30%)
      • Valvular (70%)
        • Degeneration of bicuspid valve
      • Supravalvular
  • Acquired aortic stenosis
    • Rheumatic valvulitis
      • Almost invariably associated with mitral valve disease
    • Fibrocalcific senile aortic stenosis
      • Degenerative 

Clinical Findings

  • Asymptomatic for many years
  • Classical triad
    • Angina
    • Syncope
    • Shortness of breath (heart failure)
  • Systolic ejection murmur
  • Carotid pulsus parvus et tardus
  • Diminished aortic component of 2nd heart sound
  • Sudden death in severe stenosis after exercise
    • Diminished flow in coronary arteries causes ventricular dysrhythmias
      and fibrillation
    • Decompensation leads to left ventricular dilatation and pulmonary
      venous congestion

Imaging Findings 

  • In older children or young adults
    • Prominent ascending aorta
      • Poststenotic dilatation of ascending aorta
        • Due to turbulent flow
    • Left ventricular heart configuration
      • Normal-sized or enlarged left ventricle
      • Concentric hypertrophy of left ventricle produces a relatively small
        left ventricular chamber with thick walls
    • Heart size is frequently normal
  • In adults >30 years
    • Prominent ascending aorta
      • Poststenotic dilatation of ascending aorta
        • Due to turbulent flow
    • Calcification of aortic valve (best seen on RAO)
      • In females, usually indicates hemodynamically significant aortic stenosis
      • Calcification of the valve usually indicates a gradient across
        valve of > 50mm Hg
      • Calcification begins in bicuspid and rheumatic valve in 4th decade
        but not until > 65 in tricuspid
      • DDx
        • Calcification of aortic annulus in elderly
        • Calcified coronary artery ostium (thickened cusp echoes only in diastole)
    • Normal to enlarged left ventricle

Echocardiographic findings

  • Thickened and calcified aortic valve with multiple dense cusp echoes
    throughout cardiac cycle
  • Right > non-coronary > left coronary cusp
  • Decreased separation of leaflets in systole with reduced opening orifice
  • (13-14 mm = mild AS; 8-12 mm = moderate AS; <8 mm = severe AS)
  • ± Doming in systole
  • Dilated aortic root
  • Increased thickness of LV wall (= concentric LV hypertrophy)
  • Hyperdynamic contraction of LV (in compensated state)
  • Decreased mitral EF slope (reduced LV compliance)
  • LA enlargement
  • Increased aortic valve gradient (Doppler)
  • Decreased aortic valve area (unreliable)

Angiographic findings

 

  • Simultaneous LV and aortic pressures recordings yield valve gradients from left heart
    catheterization
  • Angiographic technique uses standard RAO left ventriculogram and an aortogram
    using a 40° LAO projection
  • A non-calcified, bicuspid valve reveals thickening and doming of the valve leaflets
    in systole
  • A jet of non-opacified blood is visible through stenotic valve
    • Congenitally bicuspid valves still usually have three aortic sinuses with one large
      non-coronary sinus equal in size to the other two
    • Calcification begins in the bicuspid and rheumatic valve in the 4th decade
      but not until >65 in tricuspid
    • In rheumatic disease, the aortic valve commissures usually fuse whereas they
      do not in the degenerated tricuspid valve

 Differentiating Causes of Aortic Stenosis

Etiology/Findings Calcification Other clues
Congenital Bicuspid Valve 30’s Jet effect on aortogram
Degeneration of Tricuspid Valve > 65 Coronary artery ca++
Commissures don’t fuse
Rheumatic dz in Tricuspid Valve 30’s here; teens in 3rd
world countries
MS or MR almost always present;
commissures fuse

 

Valve areas

 

Normal

Mild

Severe

Critical

2.6-3.5cm2

1.3-1.7

1.0

0.5

Aortic Stenosis. Top: Axial CT scan through heart demonstrates a heavily
calcified aortic valve (white arrow). Bottom: Frontal chest radiograph in
another patient with aortic stenosis shows a dilated ascending
aorta (white arrow) that abnormally projects farther
to the right than the right heart border. This is caused by
post-stenotic dilatation of the aorta.

For these same photos without the arrows, click here and here

 

aortic stenosis

Aortic Stenosis. Frontal radiograph on left demonstrates isolated enlargement of the ascending aorta
(white arrow). The left ventricle is enlarged (red arrow) and the heart is mildly enlarged overall. The lateral view on the right demonstrates calcifications in the region of the aortic valve leaflets (circle). generally, the aortic valve lies above a line drawn from the carina to the junction of the diaphragm with the anterior chest wall. The mitral valve lies below the line.


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