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Varicose Veins
Valve Disease
Raynaud’s Phenomenon
Pulmonary Stenosis
Pulmonary embolism
Do you know how serious is Congenital Heart Disease?
A heart defect that develops within the mother’s womb and alters the structure of the baby’s heart is called congenital heart disease (CHD). In CHD, there is abnormal development of the heart and the blood vessels. The flow of blood through the heart is usually affected due to CHD.
As per Indian Pediatrics, the estimated number of children born with congenital heart disease in India is more than 200,000 per year. Of these, about one-fifth are likely to have serious defects, requiring medical attention in the first year of life.
What are the Types of Congenital Heart Disease?
- Atrial septal defect – A hole in the wall between the left and the right atria leads to the accumulation of blood into the right atrium.
- Ventricular septal defect – A hole in the wall between the two ventricles results in extra blood flow into the right ventricle.
- Hypoplastic left heart syndrome – A rare defect in which the left side of the heart doesn’t develop normally and is too small.
- Tricuspid atresia – The tricuspid valve is not formed properly, resulting in the underdevelopment of the right pumping chamber.
- Patent ductus arteriosus – The ductus arteriosus that connects the pulmonary artery and aorta does not close properly, leading to extra blood being pumped into the lungs.
- Pulmonary valve stenosis – Narrowing of the pulmonary valve causes the right heart chamber to work harder to push blood to the lungs.
- Aortic valve stenosis – Flow of blood throughout the body is affected due to narrowing of the aortic valve.
- Tetralogy of Fallot – Rare combination of several heart defects, namely:
- Ventricular septal defect
- Pulmonary valve stenosis
- Right ventricular hypertrophy – Thickening of the right ventricular muscle.
- Overriding aorta – Aorta is not located in its usual position.
- Other types –
- Coarctation of aorta
- Double–outlet right ventricle
- Ebstein’s anomaly
- Total anomalous pulmonary venous connection
- Truncus arteriosus
- Hypoplastic left heart syndrome
Causes:
Risk factors:
- Family history – Though rare, the risk of the child getting CHD is increased if the parents have CHD.
- Genetic conditions – Children with Down’s syndrome, Turner syndrome, and Noonan syndrome are more likely to develop CHD.
- Maternal diabetes – Women with type 1 and type 2 diabetes have a higher risk of giving birth to a baby with CHD.
- Alcohol – Consuming alcohol during pregnancy leads to the development of fetal alcohol syndrome that is associated with CHD.
- Other medical conditions – Rubella infection during the first 8 to 10 weeks of pregnancy and flu during the first trimester increases the risk of having a baby with CHD.
- Medications – Consumption of anti-seizure medications, acne medications, ibuprofen, and other medications during the first trimester is linked to an increased risk.
- Phenylketonuria (PKU) – Pregnant women with PKU are more likely to give birth to a baby with CHD.
- Environmental factors – Smoking, secondhand exposure to smoke, and exposure to organic solvents during pregnancy increases the risk of giving birth to a baby with CHD.
- Gender – CHD is most frequently seen in boys at birth as compared to girls.
What are the Signs and symptoms of Congenital Heart Disease?
- Cyanosis
- Fatigue
- Heart murmurs
- Poor blood circulation
- Rapid breathing
- Underdeveloped limbs and muscles
- Shortness of breath
Complications:
- Arrhythmia
- Blood clots
- Developmental disorders
- Emotional health issues
- Endocarditis
- Endocrine disorders
- Kidney disease
- Pneumonia
- Pregnancy complications
- Pulmonary hypertension
- Stroke
How is Congenital Heart Disease diagnosed?
- The physician examines the newborn for the Signs of heart defect, general appearance, and the baby’s heart sounds.
- Diagnostic tests –
- Echocardiography (echo) – Most CHDs can be diagnosed prenatally by fetal echocardiography during the second trimester of pregnancy.
- Fetal electrocardiogram (ECG)
- Chest x-ray
- Cardiac Magnetic Resonance Imaging (MRI)
- Cardiac catheterization – To determine how the blood is being pumped through the heart.
- Genetic testing – To determine if any genetic syndrome or particular gene is responsible for CHD.
- Pulse oximetry – To measure the amount of oxygen present in the blood.
Treatment: How is Congenital Heart Disease treated?
- Mild heart defects usually don’t require any treatment, but the baby’s condition is monitored throughout adult life.
- Treatment is generally done to relieve the symptoms and stabilize the condition before and after the surgery.
- Surgical procedures –
- Heart transplant – Children with complex CHD that cannot be repaired undergo this procedure.
- Palliative surgery – A shunt is installed in babies with only one ventricle to improve oxygen levels till the heart defects are fully repaired.
- Ventricular assist device – This device supports the functioning of the heart until heart transplantation.
- Total artificial heart – An artificial heart is installed permanently to replace the heart if heart transplantation is impossible.
- Cardiac catheterization – To repair simple heart defects like an atrial septal defect and patent ductus arteriosus by opening up the narrowed valves or blood vessels.
- Medications –
- Diuretics – Bumetanide, furosemide, etc., to remove fluid from the body and make breathing easier.
- Anticoagulants – Aspirin, warfarin, etc., to decrease the clotting tendency.
- Digoxin – To lower the heartbeat and enhance the heart’s pumping function.
- Indomethacin or ibuprofen – To constrict or tighten the patent ductus arteriosus and cause it to close.
- Acetaminophen – To close the patent ductus arteriosus.
- Other drugs – Antibiotics, anti-arrhythmic drugs, beta-blockers.
Prevention: how it can be prevented?
- Living with CHD –
- Have regular checkups.
- Take medications to prevent complications.
- Heart-healthy diet.
- Maintaining a healthy weight.
- Increasing physical activity.
- Preventing CHD –
- Vaccinate the mother against Rubella and flu.
- Consume Folic acid supplements during the first trimester of pregnancy.
- Avoiding exposure to organic solvents during pregnancy.
- Avoiding alcohol or medicines that are not safe to take during pregnancy.
When to see a doctor? :
Consult immediately with a pediatric cardiologist if the baby experiences shortness of breath during feeding. If the older children and adults experience this during exercise, consult with an adult congenital heart specialist or cardiologist. The average cost of cardiac catheterization ranges from Rs. 16,000 to Rs. 20,000.
Chronic Obstructive Pulmonary Disease
Carotid Artery Disease
Transesophageal Echocardiography
Transesophageal echocardiography (TEE) is an invasive test that creates high–quality, moving images of the heart. The transducer is passed down the esophagus to get detailed pictures of the heart structures, valves, and blood vessels. TEE guides the positioning of catheters for diagnosis and provides information during surgery to repair the valves. Regurgitation of blood through the valves and valve stenosis can also be diagnosed by it.
TEE is performed to diagnose infective endocarditis, valve disease, pericardial disease, myocardial disease, cardiac masses, and congenital heart disease.
Read: Heart Diseases
How is Transesophageal Echocardiography performed? :
The back of the mouth and the throat are sprayed with an anesthetic to numb the region and suppress the gag reflex. The nurse then puts an intravenous line (IV) in the patient’s arm. A patient is asked to lie down on a table, and a mild sedative is administered to calm him.
Generally, the patient lies down on his left side. Electrodes are then attached to his chest to monitor his heart rate throughout the procedure. Following this, a thin, flexible tube is gently guided down his throat through the mouth. This tube is called a probe and has a transducer in its end. The patient may be asked to swallow the probe to propel it easily into the throat. Once the probe reaches the desired position, it sends sound waves to the heart. These waves are bounced back to the probe and get captured as images. [1]
The doctor views the pictures of the heart through the video screen. After getting the necessary images, the probe, IV, and electrodes are removed from the patient’s body. Occasionally, oxygen is administered through nasal tubes, but this depends on the patient’s condition. The room is often darkened to let the doctor see the images clearly on the echocardiogram monitor.
Know about other diagnostic tests to detect heart diseases.
Are there any risks involved in it? :
There are a few problems associated with Transesophageal Echocardiography. This includes having a sore throat for a day or two, nausea, and bad reactions to the medicine. These usually resolve on their own within a day.
FAQs: Transesophageal Echocardiography
What are preparations required from the patient?
The patient should refrain from consuming alcoholic drinks for a few days before the test. He is also asked to not eat or drink anything for 4 to 6 hours before the TEE. Dentures, oral prostheses, and other objects that interfere with the test must be removed before inserting the probe. He must also arrange for a ride home after the test as he may feel drowsy after the test.
How long does it take?
The test gets over in about 30 to 60 minutes.
Who performs it?
It is done by cardiologists, cardiac anesthesiologists, or physicians as it is an invasive procedure.
How much does Transesophageal Echocardiography cost?
The cost of TEE is around Rs. 800 to Rs. 3 K.
When can I go home after the procedure?
The patient is allowed to go home once his vital signs stabilize and gag reflex returns. He can resume his normal activities and usual diet unless advised by the doctor.