Congenital malformation of cardiac septum, unspecified - what does this mean
Congenital malformation of the cardiac septum is a birth defect in which the wall that separates the left and right sides of the heart (the septum) is incomplete or improperly formed. this can lead to an abnormal flow of blood between the two sides of the heart, resulting in a wide variety of symptoms, including shortness of breath, fatigue, and an irregular heartbeat.
What happens during the disease - congenital malformation of cardiac septum, unspecified
Congenital malformation of the cardiac septum is a condition in which the walls of the heart do not form correctly during fetal development. this can lead to a hole between the two sides of the heart and/or abnormal connections between the heart chambers, resulting in irregular blood flow and inefficient pumping of the heart. depending on the severity of the malformation, additional symptoms such as fatigue, shortness of breath, and chest pain may be present.
Treatment and Medical Assistance
Main goal of the treatment: To repair the congenital malformation of the cardiac septum.
- Diagnose the malformation with an echocardiogram or other imaging tests.
- Prescribe medications to reduce symptoms such as shortness of breath and fatigue.
- Refer the patient to a cardiologist for further evaluation.
- Perform a cardiac catheterization to assess the extent of the malformation.
- Perform a corrective surgery to repair the malformation.
- Monitor the patient's progress after the surgery.
- Provide follow-up care and lifestyle advice to help prevent future complications.
12 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Congenital malformation of cardiac septum, unspecified - Prevention
Congenital malformation of cardiac septum, unspecified can be prevented by monitoring pregnant women for any risk factors and making sure they are getting regular prenatal care, as well as taking steps to reduce the risk of infections during pregnancy. it is also important to be aware of any family history of congenital heart defects.