Aortic valve disease
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Aortic valve disease
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Angina
aortic stenosis p. 296
aortic stenosis
presentation p. 722
Aortic stenosis
ejection click and p. 731
heart murmurs p. 296
macroangiopathic anemia p. 415
paradoxical splitting in p. 294
presentation p. 722
pulse pressure in p. 290
S4 heart sound and p. 731
systolic murmur in p. 295
Williams syndrome p. 304
Dyspnea
aortic stenosis p. 296
Heart murmurs p. 296
aortic stenosis p. 722
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The aortic valve is typically made up of three leaflets: the left, the right, and the posterior leaflet and it opens during systole to allow blood to be ejected to the body. During diastole, it closes to allow the heart to fill with blood and get ready for another systole. If the aortic valve doesn’t open all the way, it gets harder to pump out to the body and this is called aortic stenosis. If it doesn’t close all the way, then blood leaks back into the left ventricle called aortic valve regurgitation or aortic insufficiency.
Usually, the aortic valve opens to about 3-4 cm2, but with stenosis it can become less than 1 cm2. This is usually caused by mechanical stress over time, which damages endothelial cells around the valves, causing fibrosis and calcification, which hardens the valve and makes it more difficult to open completely. This type usually shows up in late adulthood, with patients over 60 years old.
Similarly, patients that have a bicuspid valve — with two leaflets — as opposed to a tricuspid — with three — are more at risk of fibrosis and calcification because the mechanical stress that’s usually distributed between three leaflets is now being split by two leaflets and therefore, they see more stress per leaflet. Another important cause of aortic stenosis is chronic rheumatic fever, which can cause repeated inflammation and repair, leading to fibrosis. In this case, the leaflets can actually fuse together — called commissural fusion — which is an important distinction from the type caused by mechanical stress over time.
When the valve fuses together or hardens, it doesn’t open as easily, right? And so as the left ventricle contracts, it creates this high pressure that eventually pushes on the valve until it finally snaps open, causing a characteristic “ejection click.” Since the blood has to flow through a narrow opening, there’s turbulence which creates noise, or a murmur, which gets initially louder as more blood flows past the opening, and then quieter as the amount of blood flowing subsides because less remains in the ventricle. This is called a crescendo-decrescendo murmur.
Since now it’s harder to open and push blood past this hardened valve, the left ventricle has to generate higher pressures each time it contracts to get the same amount of blood through. To accomplish this, the left ventricle can thicken its muscles, called concentric left ventricular hypertrophy. This happens because new sarcomeres are added in parallel to the existing ones.
Sources
- "Robbins Basic Pathology" Elsevier (2017)
- "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
- "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
- "Aortic Stenosis: Pathophysiology, Diagnosis, and Therapy" The American Journal of Medicine (2017)
- "Medical Treatment of Aortic Stenosis" Circulation (2016)
- "Aortic Valve Sparing in Different Aortic Valve and Aortic Root Conditions" Journal of the American College of Cardiology (2016)
- "Functional Mitral Regurgitation After Aortic Valve Replacement for Aortic Insufficiency" Journal of Cardiothoracic and Vascular Anesthesia (2018)