Aortic valve stenosis

Aortic valve stenosis is the most common valvulopathy and describes narrowing of the opening of the aortic valve between the aorta and the left ventricle.

Aortic stenosis is the most common valvulopathy, present in up to one-quarter of all patients with chronic valvular heart disease 1,2. The condition has a male predilection in a 4:1 ratio 1, and the incidence of degenerative aortic valve disease, the most common etiology of aortic stenosis, is increasing 1,2.

The classic triad of symptoms caused by aortic stenosis is angina pectoris, dysnpoea, and syncope, however any left-predominant clinical features of heart failure may be present 1,2. Generally these symptoms do not become prominent until significant stenosis is present (<1 cm2) 1.

Clinical examination classically reveals a narrow pulse pressure, a slow-rising peripheral pulse, pulsus parvus et tardus (weak and delayed pulse) in the carotid pulse, a pressure loaded ('heaving') apex beat, and a crescendo-decrescendo mid-systolic (or ejection systolic) murmur that is heard on praecordial auscultation 1,2. The murmur associated with aortic stenosis also characteristically radiates to the carotid arteries, and may also radiate to the apex which can mimic the murmur of mitral valve regurgitation, known as the Gallavardin phenomenon 3.

Numerous clinical maneuvers can be used to distinguish aortic stenosis from the similar-sounding murmurs of hypertrophic obstructive cardiomyopathy and pulmonary valve stenosis, such as the Valsalva maneuver and auscultation during inspiration respectively 1

Aortic stenosis in adults is most commonly caused by degenerative calcification, especially in the setting of congenital aortic valve disease (most commonly a bicuspid aortic valve), chronic tri-leaflet deterioration, or previous rheumatic heart disease affecting the aortic valve 1,2. This degenerative calcification shares many similarities to the process of atherosclerosis, and indeed many of the risk factors are the same, such as low LDL, diabetes mellitus, smoking, hypertension, chronic kidney disease, and the metabolic syndrome 1,2.

The end-product of this atherosclerotic-like process is thickening of the valve leaflets (initially just 'aortic sclerosis') due to activation of inflammatory cascades, endothelial dysfunction, and valvular lipid accumulation 1,2. Ultimately, the valvular myofibroblasts differentiate into osteoblasts resulting in calcium deposition on the valve ('calcific aortic stenosis') 1,2. This process progressively causes a reduction in aortic valve area, resulting in progressive stenosis 1,2.

This stenosis causes a left ventricular outflow tract (LVOT) obstruction. The turbulent blood flow from this LVOT obstruction explains the timing of the murmur and the various peripheral signs associated with aortic stenosis 1,2. Moreover, this LVOT obstruction causes a systolic gradient to form between the aorta and left ventricle 1,2. This gradient may progressively increase without any significant changes to left ventricular function because of compensatory left ventricular hypertrophy, appreciated clinically by the pressure loaded apex beat 1,2.

However, this adaptive mechanism eventually fails and systolic and diastolic function declines and irreversible myocardial fibrosis develops. It is at this point where patients manifest clinical features of heart failure 1,2

There are numerous other predisposing factors and causes of aortic stenosis. These can be classified by their anatomical position (supravalvular vs valvular vs subvalvular) and whether they are congenital or acquired etiologies 1,2,4. Of note, supravalvular and subvalvular aortic stenosis often do not have the same degenerative pathogenesis as valvular aortic stenosis 1.

Variable appearance on chest radiographs depending on stage and severity of the disease 2,5

In early disease, the chest radiograph can be entirely normal or it may show dilatation of the ascending aorta with a normal heart size. Differentiation with hypertension can usually be made as in hypertension the entire descending aorta is enlarged 2,5.

However, late in the disease, the chest radiograph may reveal valvular calcifications (if valvular aortic stenosis) and/or cardiomegaly with features of heart failure, such as pulmonary venous congestion and pulmonary interstitial/alveolar edema 2,5. At this stage, especially in the absence of valvular calcifications, it is not possible to differentiate aortic stenosis from other causes of heart failure 2,5

Echocardiography is useful for evaluating the anatomical location of the stenosis, either supravalvular, valvular, or subvalvular, for assessing the aortic valve area and jet velocity, and for assessing the left ventricle. Various parameters are used in order to determine severity, such as 2,6:

  • aortic sclerosis
    • aortic jet velocity ≤2.5 m/s
  • mild aortic stenosis
    • aortic jet velocity 2.6-2.9 m/s
    • mean gradient is <20 mmHg
    • aortic valve area (AVA) >1.5 cm2
    • aortic valve area indexed to body surface area (AVA/BSA) >0.85 cm2/m2
  • moderate aortic stenosis
    • aortic jet velocity 3.0-4.0 m/s
    • mean gradient 20-40 mmHg
    • AVA 1.0-1.5 cm2
    • AVA/BSA 0.60-0.85 cm2/m2
  • severe aortic stenosis
    • aortic jet velocity >4 m/s
    • mean gradient >40 mmHg
    • AVA <1 cm2
    • AVA/BSA <0.60 cm2/m2

In cases where there is a low AVA and also a low mean gradient, this may either indicate true severe aortic stenosis or pseudo-severe aortic stenosis due to low cardiac output 6. In these cases, low-dose dobutamine may be given to differentiate between these two entities 6.

Cardiac CT confirms, with greater detail, findings on plain radiograph 7-10. Moreover, it is able to determine an aortic valve calcification score, whereby a high aortic valve calcification score may indicate severe aortic stenosis, particularly in patients with non-rheumatic acquired calcific aortic stenosis 7-10.

Cardiac MRI (CMR) is able to provide a more detailed structural and dynamic assessment of the aortic valve and left ventricle, in particular 5,7:

  • structural assessment on spin echo MR sequence
    • bicuspid or unicuspid aortic valve
    • post stenotic dilatation of ascending aorta
    • symmetrical left ventricular hypertrophy wall thickness (≥12 mm)
    • increased LV mass
  • dynamic assessment on cine GRE or b-SSEP
    • thickened valve leaflets with reduce excursion during systole
    • size and extent of the high-velocity jet into the ascending aorta
    • hyperdynamic LV contraction in compensated state

The decision to treat aortic stenosis is based on the severity 1,2. Management involves a combination of lifestyle and pharmacotherapy measures (a similar armamentarium to that used in heart failure), balloon valvuloplasty and aortic valve replacement1,2

Aortic valve replacement can be in the form of:

  • transcatheter aortic valve implantation (TAVI): percutaneously inserted valve that is deployed within the stenotic native valve, useful in frailer patients but long term resilience unclear at this stage
  • conventional aortic valve replacement: involves midline sternotomy, cardiopulmonary bypass and replacement with a metal or bioprosthetic valve, still the treatment of choice in younger patients

Further details of this management is beyond the scope of this article.

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Article information

rID: 17960
System: Cardiac
Synonyms or Alternate Spellings:
  • Aortic stenosis
  • Aortic valve sclerosis
  • Aortic sclerosis

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