Cardiac allograft vasculopathy (CAV) is a serious complication that can occur after heart transplantation. It is the leading cause of long-term mortality in heart transplant recipients.
CAV is a form of chronic rejection that affects the blood vessels of the transplanted heart. Over time, the immune system of the recipient recognizes the transplanted heart as foreign and begins to attack it. This leads to the thickening and narrowing of the blood vessels, which can eventually lead to reduced blood flow to the heart muscle.
CAV can be difficult to diagnose as it often does not cause any symptoms until it has progressed to an advanced stage. Some of the symptoms that may appear in later stages of CAV include chest pain, shortness of breath, fatigue, and heart failure.
The exact causes of CAV are not fully understood. However, there are several factors that are known to increase the risk of developing CAV:
CAV is typically diagnosed through a combination of tests, including:
If CAV is suspected, it is important to undergo regular monitoring and testing to detect any changes in the blood vessels of the transplanted heart.
Cardiac allograft vasculopathy is a serious complication that can occur after heart transplantation. It is important for heart transplant recipients to be aware of the risk factors for CAV and to undergo regular monitoring and testing to detect any changes in the blood vessels of the transplanted heart.
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