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Objective. To review literature about risk factors of neonatal hypoxic-ischemic encephalopathy (HIE).
Materials. Search in PubMed, MEDLINE, Embase, Clinicaltrials.gov and reference lists from 1999 to 2018. Study population
was composed of neonates with diagnosed HIE within 28 days from delivery, data reported as proportional rate. Studies were
excluded if they included preterm pregnancies, postnatal conditions leading to HIE and/or fetal malformations, focused on
a single risk factor. PRISMA guidelines were followed. Interstudies heterogeneity was assessed and a random/fixed models
were generated as appropriate. Comparison between neonates with HIE vs. controls was performed by calculating odds
ratio-95% confidence interval (OR-95% CI). Differences were significant if 95% CI did not encompass 1.
Results.Twelve articles were included. Fetuses with growth restriction (OR: 2.87; 95% CI: 1.77-4.67), nonreassuring
cardiotocography (OR: 6.38; 95% CI: 2.56-15.93), emergency cesarean section (OR: 3.69; 95% CI: 2.75-4.96), meconium
(OR: 3.76; 95% CI: 2.58-5.46) and chorioamnionitis (OR: 3.46: 95% CI: 2.07-5.79) were at higher risk of developing HIE.
Nulliparity, gestational diabetes, hypertension, oligohydramnios, polyhydramnios, male sex, induction of labor, labor
augmentation, premature rupture of membrane, and vacuum delivery were not significantly different.
Conclusion. Neonatal HIE has multifactorial origin and its cause is often undetermined and not preventable. (PROSPERO
Registration number: CRD42018106563).
Biography
I received both my degree in Medicine and Surgery, and my Residency in Obstetrics and Gynecology at University of Bari, Bari, Italy. I work as Obstetrician at Clinic of Obstetrics and Gynecology, “San Paolo” Hospital, Bari, Italy. I have special interests in Prenatal diagnosis, Maternal and fetal medicine, and Obstetrics.
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