Simple ventricular septal defects are the most common form of congenital heart disease. A ventricular septal defect is a hole in the wall between the right and left ventricles (ventricular septum). A VSD can potentially cause a shunting of blood from the left ventricle to the right ventricle or from the right ventricle to the left ventricle. The position and size of the VSD determine the physiology and, in turn, dictate the timing of intervention.
The ventricular septum is made up of two components, the truncal portion and the conoseptal portion. These two sections fit together like two pieces of a puzzle. The position of the VSD among these two portions of the septum determines the type of VSD.
Five Types of VSD
A conoventricular VSD results when there is a space between where the two portions of the ventricular septum meet. This type of VSD is not typically associated with other forms of congenital heart disease. The size of a conoventricular VSD is the predominate indicator of physiology. A small conoventricular VSD may close on its own as the child grows. A larger VSD may cause greater strain on the heart and need to be repaired surgically. Surgical repair entails patch closure of the VSD using a synthetic material.
Muscular VSDs are the most common type of VSD and are not usually associated with other forms of congenital heart disease. A muscular VSD is a hole located in the truncal portion of the ventricular septum. Again, size is the predominate indicator of physiology. This type of VSD has the highest chance of spontaneous closure and therefore requires less surgery.
A conoseptal VSD is a hole located in the conoseptal portion of the ventricular septum. This type of VSD has almost no chance for spontaneous closure and often requires surgical repair.
An Atrioventricular Canal Type VSD is a hole located in the upper portion of the ventricular septum. Often, this type of VSD is associated with a large ASD as well as malformed atrioventricular valves in a complex congenital heart disease known as Complete Common Atrioventricular Canal Defect (see below).
An Atrioventricular Canal Type VSD allows oxygen-rich blood from the left ventricle to pass into the right ventricle resulting in increased blood flow to the lungs. This type of VSD has no chance of spontaneous closure. Surgical repair is required and involves patch closure of the VSD using a synthetic material
Malalignment of the conoseptal portion of the ventricular septum results in a malalignment VSD. This type of VSD causes one of the most common forms of congenital heart disease known as Tetralogy of Fallot. Because the two portions of the ventricular septum have failed to align properly, the anatomy of other structures in the heart are affected. Namely, there is less space for the growth of the pulmonary valve and artery resulting in pulmonary stenosis. In addition, the aorta is not aligned properly resulting in an overriding aorta (i.e. the aorta lies directly over the VSD). Finally, the right ventricle typically works at the lower, pulmonary pressure. Due to the presence of the VSD, the right and left ventricles are pumping at the same pressure. A secondary condition, known as right ventricular hypertrophy (enlargement of the right ventricle), is a result of the right ventricle working at systemic pressure.
The resistance of blood flow through the stenotic pulmonary valve results in deoxygenated blood flowing from the right ventricle through the VSD directly into the left ventricle. This deoxygenated blood is then pumped from the left ventricle out to the body causing the baby to appear cyanotic or blue. Corrective surgery involves patch closure of the VSD and enlargement of the narrow area of the pulmonary artery and right ventricle.
What Is Normal Cardiac Anatomy?
When your child has a congenital heart defect, there's usually something wrong with the structure of his or her heart's structure.
Heart With Normal Cardiac Anatomy
When your child has a congenital heart defect, there's usually something wrong with the structure of his or her heart's structure.
The heart is composed of four chambers. The two upper chambers, known as atria, collect blood as it flows back to the heart. The two lower chambers, known as ventricles, pump blood with each heartbeat to the two main arteries (the pulmonary artery and the aorta). The septum is the wall that divides the heart into right and left sides. The atrial septum separates the right and left atria; likewise, the ventricular septum separates the two ventricles.
There are four valves that control the flow of blood through the heart. These flap-like structures allow blood to flow in only one direction. The tricuspid and mitral valves, also known as the atrioventricular valves, separate the upper and lower chambers of the heart. The aortic and pulmonary valves, also known as the arterial valves, separate the ventricles from the main arteries. Oxygen-depleted blood returns from the body and drains into the right atrium via the superior and inferior vena cavas. The blood in the right atrium then passes through the tricuspid valve and enters the right ventricle.
Next, the blood passes through the pulmonary valve, enters the pulmonary artery, and travels to the lungs where it is replenished with oxygen. The oxygen-rich blood returns to the heart via the pulmonary veins, draining into the left atrium. The blood in the left atrium passes through the bicuspid, or mitral, valve and enters the left ventricle.
Finally, the oxygen-rich blood flows through the aortic valve into the aorta and out to the rest of the body.
From Nemours' KidsHealth
- Cardiac Catheterization
- ECG (Electrocardiogram)
- If Your Child Has a Heart Defect
- Atrial Septal Defect
- Coarctation of the Aorta
- When Your Child Needs a Heart Transplant
- Congenital Heart Defects
- Patent Ductus Arteriosus (PDA)
- Heart Murmurs
- A to Z: Atrial Flutter
- A to Z: Hypoplastic Left Heart Syndrome
- A to Z: Patent Ductus Arteriosus (PDA)
- A to Z: Tetralogy of Fallot
- Heart and Circulatory System
- Congenital Heart Defects Special Needs Factsheet
- Tetralogy of Fallot
- Ventricular Septal Defect
Trusted External Resources
It's normal to be nervous about a procedure that involves your child's heart. But cardiac catheterizations are usually no cause for alarm. These procedures are often successful in kids and teens and carry a very low risk of complications.
Kids are usually released from the hospital the very same day and can resume most regular activities within a week.
About Cardiac Catheterizations
Cardiac catheterizations help doctors perform diagnostic tests on the heart and its blood vessels, and even treat some heart conditions. During the procedure, doctors put a long, thin tube (catheter) into a blood vessel and thread it through blood vessels to the heart. Once the catheter is in place, doctors can use instruments to see into the heart and its chambers (via X-ray) and perform certain procedures.
Often, a cardiac catheterization can make open-heart surgery unnecessary, although for more serious heart problems, it's common for cardiac catheterization to be done in addition to open-heart surgical procedures.
Cardiac catheterization is what is called an invasive procedure, meaning it involves going into the body through the skin. However, it is a minimally invasive procedure and is not considered "open" surgery since it's performed without making any large incisions. Usually the only sign that a person has had the procedure is a small puncture hole where the catheter was inserted, usually in the groin area, but sometimes in the arm or neck.
Diagnostic Tests & Treatments
By performing a cardiac catheterization for diagnostic purposes, a doctor can:
- obtain a sample of heart tissue (biopsy)
- evaluate congenital heart defects (those that are present from birth)
- measure the blood pressure inside the heart
- measure the amount of oxygen in the heart
- check for problems with heart valves
- locate narrowed or blocked blood vessels
- determine the need for further treatment or surgery
A number of treatments for heart conditions can be performed during a cardiac catheterization. These include:
- closing holes in the heart that are the result of a congenital defect
- repairing leaky or narrow heart valves
- treating an irregular heartbeat (arrhythmia) by destroying the abnormal heart tissue that's causing the heart to beat irregularly
- removing blood clots
- inflating tiny balloons in obstructed blood vessels or heart valves to increase blood flow (angioplasties or valvuloplasties)
- placing wire devices (stents) in narrowed blood vessels to help keep them open
Cardiac catheterizations are generally safe procedures, particularly in comparison with open-heart surgery. Although complications are rare, any procedure that involves the heart and blood vessels does carry risks, such as:
- bruising or bleeding at the site where the catheter is inserted
- an allergic reaction to the medications or contrast material used during the procedure. Contrast material is a special dye put into the blood vessels that helps doctors see the vessels, valves, and chambers of the heart more clearly.
- skin reactions (similar to a sunburn) from exposure to X-rays
- chest pain
- blood clots
- heart attack, stroke, or kidney damage
Your doctor will discuss these risks with you and your child before the procedure is performed.
Preparing for the Procedure
Before the procedure, the doctor will perform a number of diagnostic tests, including an echocardiogram (ECHO), which uses sound waves to create a picture of the heart. The doctor also might do an electrocardiogram (EKG or ECG) to record the electrical activity of the heart. In rare cases, the doctor might call for a cardiac magnetic resonance imaging (MRI) scan or a CAT scan.
Before the procedure, make sure you discuss any allergies your child has with the doctor, particularly if they involve contrast material, iodine, seafood, latex, or rubber products. Also discuss any medications your child takes. The doctor might have your child stop taking medications or adjust the doses for a few days before the procedure. Bring a list of your child's medications and dosages with you to the hospital.
Your child will be instructed not to eat or drink anything for about 8–12 hours before the procedure. Having something in the stomach can increase the risk of complications from anesthesia. After the procedure, your child will be able to eat and drink.
When it's time to go to the hospital, have your child wear comfortable clothes and remove any jewelry, especially necklaces that may interfere with the pictures to be taken of the heart. At check-in, your child's blood pressure and pulse will be recorded. It's important to keep your child relaxed and distracted at this point so that the heart beats at a normal rate.
If there's a possibility that your child may have to stay in the hospital after the procedure, bring toiletries and any other items that can make the stay more comfortable.
The cardiac catheterization will be performed by a pediatric cardiologist in a catheterization lab. The lab has special X-ray and imaging machines not found in normal operating rooms.
A team of doctors and nurses will be on hand to make sure your child is comfortable and the procedure goes smoothly. In the lab, your child will lie on a small table surrounded by heart monitors and other equipment. The room is kept cool to protect this sensitive equipment, so your child may be offered blankets to keep warm.
First, an intravenous (IV) line will be inserted into your child's arm to deliver medications and fluids during the procedure. A sedative will be given to help your child relax and sleep. Small, sticky patches called electrodes will be placed on the chest; these are attached to an electrocardiograph (ECG) monitor, which will monitor the heartbeat during the procedure.
A nurse will clean and possibly shave the area where the catheter will be inserted, and your child will be given an injection of a local anesthetic (a drug that numbs only a small, specific part of the body, like a hand or patch of skin). Once the area is numb, a plastic sheath (a short, hollow tube used to guide the catheter into the blood vessel) will be inserted into the groin or arm, and then the catheter will follow.
The cardiologist will use X-rays to help guide the catheter as it moves up the blood vessels toward your child's heart. When the catheter is in place, a small amount of contrast material will be injected into the blood vessels and heart.
X-rays will be taken of the heart and if your child needs a treatment (like a valve repair or angioplasty), it will be performed at this time.
After the cardiac catheterization is finished, the catheter will be removed and the site where it was inserted will be bandaged. Your child will recover for several hours while the nursing staff monitors his or her progress. If the catheter was inserted into the groin, your child will need to keep the affected leg straight for a few hours after the procedure to minimize the chances of bleeding at the catheterization site.
If you have a long drive home, stop every hour and have your child walk for 5-10 minutes. If you'll be on a plane, have your child stretch his or her legs and walk in the aisle at least once an hour.
The day after the catheterization, your child may remove the bandage. This is easily done by getting it wet in the shower and taking it off. Once the area is dry, replace the bandage with a small adhesive bandage. It's normal for the site to be bruised, red, or slightly swollen for a couple of days after the procedure.
Have your child gently wash the site with soap and water at least once a day, but he or she should avoid baths, hot tubs, and swimming for 1 week after the catheterization. Don't use any creams, lotions, or ointments on the area.
The doctor will tell you when it's safe for your child to resume activities. In general, your child can expect to feel tired and weak the day after the procedure and will need to take it easy for the first couple of days. This means no heavy lifting (more than 10 pounds) and no sports. After about a week, your child probably will get the go-ahead to return to all normal activities./p>
Reviewed by: Elana Pearl Ben-Joseph, MD
Date reviewed: September 05, 2017