Cyanotic heart defect

• Tetralogy of Fallot (ToF)
• Total anomalous pulmonary venous connection
• Hypoplastic left heart syndrome (HLHS)
• Transposition of the great arteries (d-TGA)
• Truncus arteriosus (Persistent)
• Tricuspid atresia
• Interrupted aortic arch
• Pulmonary atresia (PA)
• Pulmonary stenosis (critical)
• Eisenmenger syndrome (reversal of shunt due to pulmonary hypertension).^[2]

Presentation includes the following:^{[citation needed]}

• Clubbing
• The patient assuming a crouching position
• Cyanosis - bluish face, particularly the lips; and bluish fingers and toes
• Crying
• Crabbiness/irritability
• Tachycardia
• Tachypnea
• A history of inadequate feeding
• Unusually large toe and fingernails
• Delayed development (both biological and physiological)

• Morphine during Tet spells to decrease associated infundibular spasm.
• Prophylactic: Propranolol/Inderall
• Prostaglandin E (to keep the ductus arteriosus patent)
• Prophylactic antibiotic to prevent endocarditis
• Surgery: Variable. Superior Cavopulmonary Bypass (Bidirectional Glenn or Hemi-Fontan Procedure), Total Cavopulmonary Bypass (Fontan Completion Procedure). The purpose of these operations is to redirect the blood flow of the deoxygenated blood to the lungs by attaching the Vena Cava directly to the Pulmonary Artery causing the blood that flows into the lungs to be oxygenated before entering the chambers on the right side of the heart. Mathematical models are used to address the issue of pressure level alterations of circulation after the procedures. The pulmonary pressure resistance in the cavopulmonary connection is increased, and these models permit clear analyses of the pressure increase allowing doctors to avoid possible venous circulation congestion.

• what is cyanotic heart disease?
• Acyanotic heart defect