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Tetralogy of Fallot

Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart condition with many cases presenting after the newborn period. It has been classically characterized by the combination of ventricular septal defect (VSD), right ventricular outflow tract obstruction (RVOTO), overriding aorta, and late right ventricular hypertrophy.

Tetralogy of Fallot accounts for 5 to 10% of all congenital heart disease and has an estimated prevalence of 1 in 2000 births 10.

The presentation relies on the degree of right ventricular outflow tract obstruction (RVOTO). Typically this is significant, resulting in cyanosis evident in the neonatal period, as a consequence of the right to left shunt across the ventricular septal defect. In cases where outflow obstruction is minimal, cyanosis may be inapparent (pink tetralogy) resulting in delayed presentation, even into adulthood, although this is rare.

Tetralogy of Fallot is classically characterized by four features which are:

  1. ventricular septal defect (VSD)
    • maybe multiple in ~5% of cases 6
  2. right ventricular outflow tract obstruction (RVOTO) due to
  3. overriding aorta
  4. right ventricular hypertrophy: only develops after birth

The right ventricular hypertrophy is a result of the ventricular septal defect and right ventricular outlet obstruction, both contributing to elevated resistance to right heart emptying 6.

In ~15% of cases, it is associated with a deletion on chromosome 22q11 13.

Chest radiographs may classically show a "boot-shaped" heart with an upturned cardiac apex due to right ventricular hypertrophy and concave pulmonary arterial segment. Most infants with tetralogy of Fallot, however, may not show this finding 2.

Pulmonary oligaemia occurs due to decreased pulmonary arterial flow. A right-sided aortic arch is seen in 25%.

Echocardiography allows direct visualization of the abnormal anatomy and remains the primary modality for the diagnosis of tetralogy of Fallot. It has limitations on assessing associated extracardiac anomalies (e.g. peripheral pulmonary stenosis and atresia). Salient features which may be assessed during a standard sequence of transthoracic echocardiographic views include 16;

  • parasternal long-axis view
    • left and right ventricular size/function
    • degree of aortic override
      • override of the aortic root over the ventricular septal defect should be less than half of the aortic diameter 17
    • analysis of the ventricular septal defect
    • confirmation of aorto-mitral continuity
  • parasternal short-axis view
    • location of the ventricular septal defect
    • anatomy of the right ventricular outflow tract
      • dilation of the RVOT may be observed
      • dynamic obstruction of the RVOT may be noted, resulting from incursion of the infundibulum into the outflow tract
      • continuous-wave Doppler through the RVOT may demonstrate a late-peaking, high-velocity envelope is consistent with dynamic obstruction
      • right ventricular systolic pressure (RVSP) may also be quantified using the velocity of the tricuspid regurgitant jet if visible
    • pulmonic valve
      • leaflet number and degree of mobility
      • dimensions of the annulus
      • spectral Doppler interrogation for the presence and grading of associated pulmonic regurgitation or stenosis
    • presence or absence of associated coronary artery anomalies
  • apical 4 chamber view
    • assess right and left ventricular size and function

CT is useful in demonstrating the complex cardiovascular morphology of tetralogy of Fallot, especially the anatomy of the pulmonary and coronary arteries as well as identification of major aortopulmonary collateral arteries (MAPCAs). CT can be used to evaluate post-surgical changes (e.g. patency of palliative shunts) and complications.

MRI has the great advantage of providing both exquisite anatomical detail and functional information without ionizing radiation. A detailed assessment of the pulmonary artery is of particular importance because the repair of the cardiac defects without addressing pulmonary artery hypoplasia or stenosis has a poor outcome 8.

The main pulmonary artery or right pulmonary artery diameter should be compared to that of the ascending aorta. A ratio of <0.3 usually signifies that primary repair would be unsuccessful, and a bridging shunt operation may be of benefit 8.

Assessment of coronary artery origin is also essential to surgical planning.

Approximately 90% of untreated tetralogy of Fallot patients succumb by the age of 10 years 6. Over the years many surgical approaches were performed until the current primary repair was developed. Shunts are nowadays only performed as a palliative procedure in inoperable cases or to bridge patients until the repair can be carried out, typically in the setting of pulmonary arterial hypoplasia 8.

Shunt operations included 6:

Primary repair (total correction (a.k.a. repair) of tetralogy of Fallot) is now the preferred treatment and is usually performed at the time of diagnosis.

Common postsurgical complications include 6:

  • conduction abnormalities
    • right bundle branch block (RBBB): 80-90% of cases
    • bifascicular block: 15% of cases
    • premature ventricular contractions (PVC): ~50% of cases
    • sustained ventricular tachycardias (VT): ~5% of cases
    • atrial arrhythmias: common
  • valvular dysfunction
    • tricuspid regurgitation
    • pulmonary regurgitation

Prognosis is largely dependent on how soon the defect is diagnosed and corrected, with the best outcome seen in patients repaired before the age of 5 6. Overall there is a 90-95% survival rate at 10 years of age, however, residual right ventricular dysfunction is common. Up to 10% of patients require reoperation within 20 years 6.

It is named after Étienne-Louis Arthur Fallot (1850-1911) 19, a French physician, who described the tetralogy of defects in 1888 14.

Findings on a chest radiograph are commonly non-specific, and other cyanotic congenital heart diseases should be considered.
Other conditions involving an outflow tract overriding a VSD are 15:

  • pulmonary atresia with ventricular septal defect: considered an extreme form of tetralogy of Fallot, the pulmonary atresia is obstructed with anterograde flow. The ductus arteriosus is tortuous with retrograde flow in the pulmonary arteries. Surgery and prognosis is related to the anatomy of the pulmonary arteries
    • type 1 features a simple diaphragm at the pulmonary annulus
    • type 2 has no pulmonary trunk but the pulmonary arteries are preserved
    • type 3 is like type 2 but also with atretic pulmonary arteries
    • type 4 does not feature any pulmonary arteries but a systemic-pulmonary vascularization by major aortopulmonary collateral arteries (MAPCAs)
  • absent pulmonary valve syndrome: aortic root is overriding but not enlarged. PA trunk is, conversely, very large with to-and-fro flow due to both stenosis and insufficiency. Ductus arteriosus is classically absent or atretic.
  • common arterial trunk: pulmonary is arising from the overriding vessel, the common valve often regurgitates.
  • double outlet right ventricle: mimics transposition of the great vessels, combined with a ventricular septal defect
Congenital heart disease

There is more than one way to present the variety of congenital heart diseases. Whichever way they are categorized, it is helpful to have a working understanding of normal and fetal circulation, as well as an understanding of the segmental approach to imaging in congenital heart disease.

Article information

rID: 7356
Synonyms or Alternate Spellings:
  • TOF
  • Fallot tetralogy
  • Fallot's tetralogy
  • Tetralogy of Fallot (TOF)

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Cases and figures

  • Figure 1: illustration
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  • Case 1
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  • Case 2
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  • Case 3
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  • Case 4: with boot shaped heart configuration
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  • Case 5
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  • Case 6: tetralogy of Fallot with pulmonary stenosis
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    Case 7: corrected with RVOT stent
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  • Case 8
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  • Case 9: with a boot shaped heart
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  • Case 10: RV hypertrophy, VSD and overriding aorta
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  • Case 10: RVOTO and RV hypertrophy
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