Dextro-Transposition of the great arteries: Difference between revisions

Dextro-Transposition of the great arteries
Dextro-Transposition of the great arteries
Specialty	Medical genetics

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dextro-Transposition of the Great Arteries (d-TGA), sometimes also referred to as Complete Transposition of the Great Arteries, is a cyanotic congenital heart defect (CHD) in which the primary arteries (the aorta and the pulmonary artery) are transposed, with the aorta anterior and to the right of the pulmonary artery.

d-TGA is often referred to simply as Transposition of the Great Arteries (TGA), however, TGA is a more general term which may also refer to levo-Transposition of the Great Arteries (l-TGA).

Another term commonly used to refer to both d-TGA and l-TGA is Transposition of the Great Vessels (TGV), although this term might have an even broader meaning than TGA.

Overview

Description

In a normal heart, oxygen-depleted ("blue") blood is pumped from the right side of the heart, through the pulmonary artery, to the lungs where it is oxygenated. The oxygen-rich ("red") blood then returns to the left heart, via the pulmonary veins, and is pumped through the aorta to the rest of the body, including the heart muscle itself.

With d-TGA, blue blood from the right heart is pumped immediately through the aorta and circulated to the body and the heart itself, bypassing the lungs altogether, while the left heart pumps red blood continuously back into the lungs through the pulmonary artery. In effect, two separate "circular" circulatory systems are created, rather than the "figure 8" circulation of a normal cardio-pulmonary system.

Variations and similar defects

Simple and complex d-TGA

d-TGA is often accompanied by other heart defects, the most common type being intracardiac shunts such as atrial septal defect (ASD) including patent foramen ovale (PFO), ventricular septal defect (VSD), and patent ductus arteriosus (PDA). Stenosis of valves or vessels may also be present.

When no other heart defects are present it is called 'simple' d-TGA; when other defects are present it is called 'complex' d-TGA.

Although it may seem illogical, complex d-TGA presents better chance of survival and less developmental risks than simple d-TGA, as well as usually requiring fewer invasive palliative procedures. This is because the left-to-right and bidirectional shunting caused by the defects common to complex d-TGA allow a higher amount of oxygen-rich blood to enter the systemic circulation. However, complex d-TGA may cause a very slight increase to length and risk of the corrective surgery, as most or all other heart defects will normally be repaired at the same time, and the heart becomes "irritated" the more it is manipulated.

Similar defects

The following defects also involve abnormal spatial arrangement and/or structure of the great arteries:

Coarctation of the Aorta
Double Outlet Right Ventricle (DORV)
Left Heart Hypoplasia or Hypoplastic Left Heart Syndrome (HLHS)
levo-Transposition of the Great Arteries (l-TGA)
Overriding Aorta
Patent Ductus Arteriosus (PDA)
Taussig-Bing Syndrome
Tetralogy of Fallot (TOF)
Truncus Arteriosus
Vascular Rings

Symptoms and Diagnoses

Prenatal d-TGA

In utero, a baby with d-TGA experiences no symptoms as the lungs will not be used until after birth, and oxygen is provided by the mother via the placenta and umbilical cord; in order for the red blood to bypass the lungs in utero, the fetal heart has two shunts that begin to close when the newborn starts breathing; these are the foramen ovale and the ductus arteriosus. The foramen ovale is a hole in the atrial septum which allows blood from the right atrium to flow into the left atrium; after birth, the left atrium will be filled with blood returning from the lungs and the foramen ovale will close. The ductus arteriosus is a small, artery-like structure which allows blood to flow from the trunk of the pulmonary artery into the aorta; after birth, the blood in the pulmonary artery will flow into the lungs and the ductus arteriosus will close. Sometimes these shunts will fail to close after birth; these defects are called patent foramen ovale and patent ductus arteriosus, and either may occur independantly, or in combination with one another, or with d-TGA or other heart and/or general defects.

Symptoms

Due to the low oxygen saturation of the blood, cyanosis will appear in peripheral areas: around the mouth and lips, fingertips, and toes; these areas are furthest from the heart, and since the circulated blood is not fully oxygenated to begin with, very little oxygen reaches the peripheral arteries. A d-TGA baby will exhibit indrawing beneath the ribcage and rapid breathing; this is likely a homeostatic reflex of the autonomic nervous system in response to hypoxic hypoxia. The infant will be easily fatigued and may experience weakness, particularly during feeding or playing; this interruption to feeding combined with hypoxia can cause failure to thrive. If d-TGA is not diagnosed and corrected early on, the infant may eventually experience syncopic episodes and develop clubbing of the fingers and toes.

Diagnosis

d-TGA can sometimes be diagnosed in utero with an ultrasound after 18 weeks gestation. However, if it is not diagnosed in utero, cyanosis of the newborn (blue baby) should immediately indicate that there is a problem with the cardiovascular system. Normally, the lungs are examined first, then the heart is examined if there are no apparent problems with the lungs. These examinations are typically performed using ultrasound, known as an echocardiogram when performed on the heart. Chest x-rays and electrocardiograms (EKG) may also be used in reaching or confirming a diagnosis; however, an x-ray may appear normal immediatly following birth. If d-TGA is accompanied by both a VSD and pulmonary stenosis, a systolic murmur will be present.

On the rare occasion, initial symptoms may go unnoticed, resulting in the infant being discharged without treatment in the event of a hospital or birthing center birth, or a delay in bringing the infant for diagnosis in the event of a home birth. On these occasions, a layperson is likely not to recognize symptoms until the infant is experiencing moderate to serious congestive heart failure (CHF) as a result of the heart working harder in a futile attempt to increase oxygen flow to the body; this overworking of the heart muscle eventually leads to hypertrophy and may result in cardiac arrest if left untreated.

Prognosis

With simple d-TGA, if the foramen ovale and ductus arteriosus are allowed to close naturally, the newborn will likely not survive long enough to receive corrective surgery. With complex d-TGA, the infant will fail to thrive and is unlikely to survive longer than a year if corrective surgery is not performed. In most cases, the patient's condition will deteriorate to the point of inoperability if the defect is not corrected in the first year.

While the foramen ovale and ductus arteriosus are open after birth, some mixing of red and blue blood occurs allowing a small amount of oxygen to be delivered to the body; if ASD, VSD, PFO, and/or PDA are present, this will allow a higher amount of the red and blue blood to be mixed, therefore delivering more oxygen to the body, but can complicate and lengthen the corrective surgery and/or be symptomatic.

Modern repair procedures within the ideal timeframe and without additional complications have an very high success rate.

Treatment

If the diagnosis is made in a standard hospital or other clinical facility, the baby will be transferred to a children's hospital, if such facilities are available, for specialized paediatric treatment and equipment.

The patient will require constant monitering and care in an intensive care unit (ICU).

Palliative

Palliative treatment is normally administered prior to corrective surgery in order to reduce the symptoms of d-TGA (and any other complications), giving the newborn or infant a better chance of surviving the surgery. Treatment may include any combination of:

Medical Imaging

Echocardiogram
Chest x-ray
Magnetic resonance imaging (MRI)
Computed tomography (CT) scan

Each type of medical imaging has it's merits and drawbacks, so they are usually used in combination to provide as complete a model as possible from which to plan and prepare for the corrective surgery. Medical imaging may also be used to moniter how well the heart is functioning, or to determine whether a treatment is having the desired effect.

Surgery

Minor

Cardiac catheterization

Cardiac catheterization is a minimally invasive procedure which provides a means of performing a number of other procedures.

A balloon atrial septostomy is performed with a balloon catheter, which is inserted into a foramen ovale, PFO, or ASD and inflated to enlarge the opening in the atrial septum; this creates a shunt which allows a larger amount of red blood to enter the systemic circulation.

Angioplasty also requires a balloon catheter, which is used to stretch open a stenotic vessel; this relieves restricted blood flow, which could otherwise lead to CHF.

An endovascular stent is sometimes placed in a stenotic vessel immediatly following a balloon angioplasty to maintain the widened passage.

Angiography involves using the catheter to release a contrast medium into the chambers and/or vessels of the heart; this process facilitates examining the flow of blood through the chambers during an echocardiogram, or shows the vessels clearly on a chest x-ray, MRI, or CT scan - this is of particular importance, as the coronary arteries must be carefully examined and "mapped out" prior to the corrective surgery.

It is commonplace for any of these palliations to be performed on a d-TGA patient.

Moderate

Left anterior thoracotomy
- Isolated pulmonary artery banding (PAB)
Left lateral thoracotomy
- PAB (when coarctation or aortic arch repair also required)
Right lateral thoracotomy
- Blalock-Hanlon atrial septectomy

Each of these procedures is performed through an incision between the ribs and visualized by echocardiogram; these are far less common than heart cath procedures.

Pulmonary artery banding is used in a small number of cases of d-TGA, usually when the corrective surgery needs to be delayed, to create an artificial stenosis in order to control pulmonary blood pressure; PAB involves placing a band around the pulmonary trunk, this band can then be quickly and easily adjusted when necessary.

An atrial septectomy is the surgical removal of the atrial septum; this is performed when a foramen ovale, PFO, or ASD are not present and additional shunting is required to raise the oxygen saturation of the blood.

Major

Median sternotomy
- PAB (when intracardiac procedures also required)
- Concomitant atrial septectomy

In recent years, it is quite rare for palliative procedures to be done via median sternotomy. However, if a sternotomy is required for a different procedure, in most cases all procedures that are immediatly required will be performed at the same time.

Monitering and Maintainance

Nasogastric tube (NG tube or simply NG)
Intubation, oxygen mask, or nasal cannula
Intravenous drip (IV)
Arterial line
Central line
Fingerprick
Sphygmomanometer
Pulse oximeter
EKG

An NG tube is used to deliver nourishment, and occasionally medication, to the patient. Since the tube extends right into the stomach, it can also be used to moniter how well the patient is digesting their "food". Paediatric units normally provide facilities and equipment for mothers of infant patients to pump their breastmilk, which can then be fed to the infant through the NG tube, and/or stored for later use.

Oxygen therapy is commonplace for hospitalized d-TGA patients. This may range from an oxygen mask resting on the bed nearby their head to intubation. In some cases, patients are intubated as a precaution; the machine can monitor breathing and supplement the patient as much or as little as they need.

IV's are used to deliver medication, blood products, or other fluids to the patient. Arterial lines provide a constant monitor of blood pressure, as well as a method of obtaining samples for blood gas tests; central lines can also monitor blood pressure and provide blood samples, as well as provide a means to deliver medication and nourishment; fingerpricks (or heelpricks on small babies) are used to obtain blood samples for certain tests.

A sphygmomanometer may be used for intermittant blood pressure monitoring even if a patient is being otherwise monitored using a central or arterial line.

A pulse oximeter is attached to a finger or toe and provides constant or intermittant monitoring of the blood's oxygen saturation level.

An EKG creates a visual readout of how well the heart is functioning.

Medication

When PGE is administered to a newborn, it prevents the ductus arteriosus from closing, therefore providing an additional shunt through which to provide the systemic circulation with a higher level of oxygen.

Antibiotics may be administered preventatively. However, due to the physical strain caused by uncorrected d-TGA, as well as the potential for introduction of bacteria via arterial and central lines, infection is not uncommon in pre-operative patients.

Diuretics aid in flushing excess fluid from the body, thereby easing strain on the heart.

Analgesics normally are not used pre-operatively, but they may be used in certain cases. They are occasionally used partially for their sedative effects.

Cardiac glycosides are used to maintain proper heart rhythm while increasing the strength of each contraction.

Sedatives may be used palliatively to prevent a young child from thrashing about or pulling out any of their lines.

Corrective

Arterial Switch

The Arterial Switch surgery is the preferred, and most frequently used, method of correcting d-TGA; ideally, it is performed on an infant between 8-14 days old.

The heart and vessels are accessed via median sternotomy, and a cardiopulmonary bypass machine is used; as this machine needs it's "circulation" to be filled with blood, a child will require a blood transfusion for this surgery. The procedure involves detaching the base of both the aorta and pulmonary artery, including the associated valve from the surface of the heart; the coronary arteries are then detached from the pulmonary trunk and reattached to the aorta, before reattaching both the aorta and pulmonary arteries to their normal positions. Including the anaesthesia and immediate post operative recovery, this surgery takes an average of approximately six hours to complete

Some arterial switch recipients may present with post-operative pulmonary stenosis, which would then be repaired with angioplasty, pulmonary stenting via heart cath or median sternotomy, and/or xenograph.

Atrial Switch

In some cases, it is not possible to perform an arterial switch, either because of late diagnosis, sepsis, or a contraindicative coronary artery pattern. In the case of sepsis or late diagnosis, a delayed Arterial Switch can sometimes be made possible by PAB, which may also require a concomitant construction of an aortic-to-pulmonary artery shunt.

When an arterial switch is impossible, an atrial switch will be attempted using either the Senning or Mustard procedure. Both methods involve creating a baffle to redirect red and blue blood flow to the appropriate artery.

Post-Operative

Following corrective surgery but prior to cessation of anaesthesia, two small incisions are made immediately below the sternotomy incision which provide exit points for chest tubes used to drain fluid from the thoracic cavity, with one tube placed at the front and another at the rear of the heart.

The patient returns to the ICU post-operatively for recovery, maintenance, and close observation; recovery time may vary, but tends to average approximately two weeks, after which the patient may be transferred to a Transitional Care Unit (TCU), and eventually to a cardiac ward.

Post-operative care is very similar to the palliative care received, with the exception that the patient no longer requires PGE or the surgical palliation procedures. Additionally, the patient is kept on a cooling blanket for a period of time to prevent fever, which could cause brain damage. The sternum is not closed immediatly which allows extra space in the thoracic cavity, preventing excess pressure on the heart, which swells considerably following the surgery; the sternum and incision are closed after a few days, when swelling is sufficiently reduced.

Follow-Up

The infant will continue to see a cardiologist on a regular basis. Although these appointments are required less frequently as time goes on, they will continue throughout the lifetime of the individual, and may increase in the event of complications or as the individual approaches middle age.

The cardiology exam may include an echocardiogram, EKG, and/or cardiac stress test in addition to to consultation.

Additionally, some individuals may require ongoing medication therapy at home, which may include diuretics (such as lasix or spironolactone), analgesics (such as tylenol), cardiac glycosides (such as digoxin), anticoagulants (such as heparin or aspirin), or other medications. If the individual has undergone stenting, an anticoagulant will be a necessity to prevent build-up around the stent(s), as the body will perceive the foreign body as a wound and attempt to heal it.

Statistics

Heart defects are the most common birth defect, occurring in approximately 1% of live births
Approximately one million people worldwide are currently living with a CHD
Having a child with a CHD increases an individual’s chances of having another child with a CHD from 1% to 3%. Subsequent children born with a CHD increase that individual’s chances further.

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