AI Article Synopsis

  • Premature infants with intraventricular hemorrhage (IVH) experience high rates of morbidity and mortality, especially those with severe hemorrhage, with the risk increasing as gestation age decreases.
  • The study analyzed 130 premature infants under 32 weeks gestation, dividing them into four groups based on treatments involving Indocid, Phenobarbital, and surfactant to assess their impact on IVH outcomes.
  • Results indicated that the group receiving all three treatments (Indocid, Phenobarbital, and surfactant) had the lowest incidence of IVH, highlighting the importance of comprehensive neonatal care in reducing complications.

Article Abstract

Prematurely born infants with intraventricular haemorrhage (IVH) suffer significant morbidity and mortality, particularly those infants with high grade haemorrhage. The more premature infants have a higher incidence, experiencing more severe IVH. The etiology of IVH is clearly multifactorial. Prevention, both prenatal and postnatal. These include efforts to prevent preterm delivery. Postnatally, the importance of optimal resuscitation and neonatal care practices is stressed, particularly those which minimize cerebral blood flow fluctuation. 130 premature infants of less than 32 weeks gestation with a very low birth weight (VLBW) and extremely low birth weight (ELBW) were studied. They were divided in four groups: group I (n=35) received Indocid; group II (n=42) received Indocid and Phenobarbital; group III (n=53) received Indocid and Phenobarbital; surfactant. These three groups were compare to a reference group (n=45). Newborns from the main group were given Indocid 0.1 mg/kg from 6-12 h of life and during next three days, Phenobarbital 5 mg/kg first five days after delivery and surfactant in the first 4 hours of life according to the protocol provided with the specific surfactant replacement product. Cerebral netrasaund in 24 hours, day 3, 5 and 10 of life and follow up till one year age were performed. We found that IVH/PVH percentage is lowest in newborns from group III, followed by newborns from group II and group I.

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