Persistent pulmonary hypertension of the new-born (PPHN)
- There is, in essence, a persistent foetal circulation owing to high pulmonary pressures
- This leads to right-to-left shunting:
- The foramen ovale opens
- Ductus arteriosus opens (R arm sats are better than leg sats)
- There is consequent deterioration in cardiac function and cardiac failure
- Often there is not a cardiac abnormality, but some other cause for the raised pulmonary pressures:
- Intense pulmonary vasoconstriction e.g. from meconium, sepsis, hypoxia, acidosis
- Arteriole hypertrophy e.g. from intra-uterine hypoxia
- Abnormalities of the pulmonary vasculature e.g. congenital diaphragmatic hernia, pulmonary hypoplasia
- The best management is avoidance of factors which may contribute (see above)
- If present, treatment should be aggressive, with:
- Oxygen
- Fluids
- Ventilatory support including surfactant
- Cardiac support e.g. inotropy - dopamine often the inotrope of choice
- Reducing PA pressure e.g. sildenafil, iNO, magnesium, adenosine
- Some patients may require ECMO
Respiratory distress syndrome
- An ARDS caused typically by prematurity due to surfactant deficiency
- Best managed by ante-natal steroid prevention
- Treatment involves:
- Surfactant
- CPAP
- High-flow oscillatory ventilation