About Double outlet right ventricle with subaortic or doubly committed ventricular septal defect
What is Double outlet right ventricle with subaortic or doubly committed ventricular septal defect?
Double outlet right ventricle with subaortic or doubly committed ventricular septal defect (DORV-SCVSD) is a congenital heart defect in which the aorta and pulmonary artery both arise from the right ventricle. This defect is usually accompanied by a ventricular septal defect (VSD), which is an abnormal opening between the two ventricles. The VSD is usually located in the lower part of the septum, near the outlet of the right ventricle. This defect can cause a variety of symptoms, including difficulty breathing, poor feeding, and failure to thrive. Treatment typically involves surgery to close the VSD and reconstruct the heart.
What are the symptoms of Double outlet right ventricle with subaortic or doubly committed ventricular septal defect?
The symptoms of Double outlet right ventricle with subaortic or doubly committed ventricular septal defect can vary depending on the severity of the defect. Common symptoms include:
- Rapid breathing
- Poor feeding
- Poor weight gain
- Sweating
- Bluish skin color (cyanosis)
- Heart murmur
- Heart failure
- Abnormal heart rhythms (arrhythmias)
- Chest pain
- Shortness of breath
- Fatigue
- Swelling in the legs, abdomen, or around the eyes
What are the causes of Double outlet right ventricle with subaortic or doubly committed ventricular septal defect?
Double outlet right ventricle with subaortic or doubly committed ventricular septal defect is a congenital heart defect that is caused by abnormal development of the heart during fetal development. It is believed to be caused by a combination of genetic and environmental factors, such as maternal diabetes, maternal alcohol or drug use, and certain viral infections.
What are the treatments for Double outlet right ventricle with subaortic or doubly committed ventricular septal defect?
The treatment for double outlet right ventricle with subaortic or doubly committed ventricular septal defect depends on the severity of the defect. In mild cases, the defect may be monitored with regular check-ups and echocardiograms. In more severe cases, surgery may be necessary to repair the defect. Surgery may involve closing the ventricular septal defect, reconstructing the aortic and pulmonary valves, and/or enlarging the right ventricle. In some cases, a heart transplant may be necessary.
What are the risk factors for Double outlet right ventricle with subaortic or doubly committed ventricular septal defect?
1. Genetic syndromes such as Down syndrome, DiGeorge syndrome, and Turner syndrome.
2. Maternal diabetes.
3. Maternal use of certain medications during pregnancy.
4. Maternal alcohol or drug use during pregnancy.
5. Maternal exposure to certain environmental toxins during pregnancy.
6. Family history of congenital heart defects.
7. Low birth weight.
8. Premature birth.
Is there a cure/medications for Double outlet right ventricle with subaortic or doubly committed ventricular septal defect?
Yes, there is a cure for Double Outlet Right Ventricle with Subaortic or Doubly Committed Ventricular Septal Defect. The treatment for this condition is typically surgical repair. This involves closing the ventricular septal defect and reconstructing the right ventricular outflow tract. Medications may also be prescribed to help manage symptoms and reduce the risk of complications.