Persistent pulmonary arterial hypertension of the new born

Persistent pulmonary hypertension of the newborn (PPHN) characterised by right to left shunting with intense cyanosis is difficult to manage, and in the best of centres carries a 40–60 percent mortality. We report our one year's experience of managing six neonates with PPHN. There were 5 males and 1 female with mean birth weight of 2.59±0.487 kg and gestation period 39±2.0 wks and 1 minute Apgar score 2.8±2.1. Four to six babies were born by cesarean section and 3–6 babies had aspiration pneumonia. All babies presented within 12 hours of age (mean 5.08±5 hrs) with intense cyanosis and respiratory distress. Diagnosis were confirmed in all by (a) hyperoxia test, (b) simultaneous determination of preductal and postductal paO₂ (c) contrast echocardiography and (d) hyperoxia-hyperventilation test. Babies were managed with hyperventilation using mean ventilatory rates of 100±45 per minute, an inspired oxygen concentration of 100%, peak inspiratory pressures 27±9 cm of H₂O, and expiratory pressures 5±1.6 cms of H₂O, and mean air way pressures of 10.4±2.7 cms H₂O. Alkali therapy was used in 3 of the six babies whereas low dose dopamine was infused in all six babies. Inspite of aggressive ventilatory therapy, only 3 out of 6 babies could be salvaged.