Association of Cord Blood Total Protein and Albumin Levels with Respiratory Distress Syndrome

Background: Respiratory distress syndrome (RDS) is one of the major causes of morbidity and mortality in preterm newborns. The severity and treatment of RDS affect the outcomes of premature neonates in neonatal intensive care units. Some studies have claimed that hypoalbuminemia and hypoproteinemia...

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Veröffentlicht in:Iranian journal of neonatology 2020-12, Vol.11 (4), p.32-38
Hauptverfasser: Behzad Barekatain, Amir-Mohammad Armanian, Armin dokht Shahsanaei, Marjaneh Shokrani Chaharsoughi
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Sprache:eng
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Zusammenfassung:Background: Respiratory distress syndrome (RDS) is one of the major causes of morbidity and mortality in preterm newborns. The severity and treatment of RDS affect the outcomes of premature neonates in neonatal intensive care units. Some studies have claimed that hypoalbuminemia and hypoproteinemia are associated with poorer outcomes in preterm neonates. The current study aimed to assess the association of serum total protein and albumin with the presentation of RDS among this group of newborns.Methods: This cross-sectional study was carried out on a total of 100 preterm newborns. The study population included a control group of healthy neonates (n=50) and case group of newborns diagnosed with RDS (n=50). For each neonate, a 2 ml sample of the arterial blood was taken from the umbilical artery, and laboratory indices, including total serum protein and albumin, were measured. Statistical analysis was conducted to compare potential variations between the samples of the healthy and RDS groups.Results: According to the obtained findings, no statistical difference was observed between the healthy and RDS preterm neonates regarding total protein (P=0.16) and serum albumin (P=0.27) levels. Total serum protein and albumin were not affected by the newborn’s birth weight and gender (P>0.05) among both the healthy preterm neonates and those with RDS. However, a significant association was observed regarding gestational age (P
ISSN:2251-7510
2322-2158
DOI:10.22038/ijn.2020.43236.1718