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Marfan's syndrome

Since there is an increased risk of aortic dissection or rupture when the aortic caliber reaches a dimension of (1) mm, elective aortic root replacement is indicated.

User Corno
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Final answer:

The question is about the threshold for elective aortic root replacement in Marfan syndrome to prevent aortic dissection or rupture. This is a serious complication where the aorta may become dangerously enlarged, often requiring surgery when it reaches a certain size, typically around 50 mm.

Step-by-step explanation:

The student appears to be asking about the indications for elective aortic root replacement in the context of Marfan's syndrome, which is a genetic condition causing abnormalities in fibrillin, a protein that helps to maintain the structural integrity of connective tissue. An important complication of Marfan syndrome is the increased risk of aortic dissection or rupture, which can be life-threatening. The condition creates a vulnerable aortic root that may expand and once it exceeds a certain diameter (which is not specified in the question but typically around 50 mm based on clinical guidelines), it indicates the need for surgery. Loeys-Dietz syndrome is a related condition also defining an emphasis on vascular problems. Both conditions make managing cardiovascular risk extremely important as they are associated with a higher incidence of cardiovascular events, such as myocardial infarction and stroke. Moreover, aortic stenosis is a pathological narrowing of the aortic valve leading to a compromised blood flow and an increased workload on the heart, which is common in the elderly and may require surgical intervention if severe.

User Anandu Viswan
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