Congenital Heart Defects
Fetal blood flow
ACYANOTIC
PDA, VSD, ASD, COA
When a hole allows for communication (blood shunting)... extra volume ends up where it shouldn't be
Higher pressure in left side compared to right side ➔ blood moves from LEFT (high) ➔ RIGHT (low) (Qp > Qs)
Already oxygenated blood moves back to right side ➔ ↑ right sided volume & pressure ➔ ↑ pulmonary blood flow (↑ Qp)
↑ Qp ➔ pulmonary HTN over time ➔ increased pulmonary vasculature on CXR
Qp: pulmonary flow (from heart to lungs) Qs: systemic flow (from heart to body); Normally 1:1
Qp > Qs = pulmonary flow > systemic flow = Left ➔ Right shunt
Qp < Qs = pulmonary flow < systemic flow = Right ➔ Left shunt
Pulmonary over-circulation ➔ dyspnea (bobbing head, nasal flaring, retractions), ↑ respiratory infections
When CO ↓ ➔ sweating, exertional dyspnea (babies exert themselves while feeding)
RAE ➔ arrhythmias
Pulmonary HTN ➔ pulmonary vessel remodeling ➔ RVH to overcome pressure
Once RV pressure > LV pressure ➔ reversal of shunt (Qp < Qs) ➔ cyanosis ➔ polycythemia, finger clubbing...
Eisenmenger syndrome: Acyanotic defect becomes cyanotic defect (when shunt reverses)
CLOSURES ARE CONTRAINDICATED ONCE THIS HAPPENS
Only tx is lung transplant + repair defect or lung & heart transplant
CYANOTIC
Tetralogy of Fallot, Transposition of great vessels
Abnormal cardiac development can cause connections between R and L heart
Right ➔ left shunting ➔ cyanosis ➔ blue babies with failure to thrive and sx of HF