Abstract
MPH is a condition associated with very high mortality. In 1981 in our Unit 7/8 neonates with MPH died. MPH was defined as hypoxemia(PaO2 40 in FiO2 .9)with fresh blood from the endotracheal tube & compatible chest X-ray features. Pathophysiologically MPH was considered as hemorrhagic pulmonary edema secondary to left ventricular dysfunction.1 We therefore attempted to improve left ventricular function by optimising ventilation (muscle relaxants, sedation, positive end expiratory pressure 8-10 cm H20, high mean airway pressure 18-25) & improving myocardial contraction(Dopamine 5-10mcg/kg/min ± Isuprel 0.1 - 0.3mcg/kg/min). 5 patients have been successfully managed with this protocol. Also, ventricular function was assessed in 2/5 patients with M-mode echocardiogram & showed improvement in left ventricular ejection fraction & resolution of paradoxical septal motion.
We suggest that aggressive cardiopulmonary support including inotropes can alter the previous poor prognosis of MPH.
1Cole: Pediatrics 512: 175-187, 1973.
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Coe, A., Butt, W., Coe, Y. et al. CARDIOPULMONARY SUPPORT FOR NEONATAL MASSIVE PULMONARY HEMORRHAGE (MPH). Pediatr Res 18 (Suppl 4), 313 (1984). https://doi.org/10.1203/00006450-198404001-01322
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DOI: https://doi.org/10.1203/00006450-198404001-01322