Double outlet right ventricle with subaortic or doubly committed ventricular septal defect without pulmonary stenosis is a congenital heart defect that affects the structure of the heart. In this condition, both the pulmonary artery and the aorta arise from the right ventricle, instead of the normal arrangement where the pulmonary artery arises from the right ventricle and the aorta arises from the left ventricle. Additionally, there is a hole in the wall that separates the two ventricles, known as a ventricular septal defect (V(版权所有：爱伊AI)SD), which is located just below the aortic valve.
This condition can cause a range of symptoms, including shortness of breath, fatigue, and poor growth in infants. In some cases, the condition may be diagnosed during pregnancy through ultrasound imaging. Treatment for this condition typically involves surgery to repair the VSD and redirect the blood flow to the correct vessels. In some cases, additional surgeries may be necessary to correct any other abnormalities in the heart.
As a doctor, it is important to provide patients with clear and accurate information about their condition, including the potential risks and benefits of treatment options. It is also important to provide emotional support and guidance to patients and their families throughout the treatment process. With proper care and management, many patients with double outlet right ventricle with subaortic or doubly committed VSD can lead healthy and fulfilling lives.

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