Outcome in neonates with necrotizing enterocolitis and patent ductus arteriosus

World J Pediatr. 2016 Feb;12(1):55-9. doi: 10.1007/s12519-015-0059-6. Epub 2015 Dec 18.

Abstract

Background: There is no agreement of the influence of patent ductus arteriosus (PDA) on outcomes in patients with necrotizing enterocolitis (NEC). In this study, we assessed the influence of PDA on NEC outcomes.

Methods: A retrospective study of 131 infants with established NEC was performed. Outcomes (death, disease severity, need for surgery, hospitalization duration), as well as multiple clinical parameters were compared between NEC patients with no congenital heart disease (n=102) and those with isolated PDA (n=29). Univariate, multivariate and stepwise logistic regression analyses were performed.

Results: Birth weight and gestational age were significantly lower in patients with PDA [median (95% CI): 1120 g (1009-1562 g), 28.4 wk (27.8-30.5 wk)] than in those without PDA [median (95% CI): 1580 g (1593-1905 g), 32.4 wk (31.8-33.5 wk); P<0.05]. The risk of NEC-attributable fatality was higher in NEC patients with PDA (35%) than in NEC patients without PDA (14%)[univariate odds ratio (OR)=3.3, 95% CI: 1.8-8.6, P<0.05; multivariate OR=2.4, 95% CI: 0.82-2.39, P=0.111]. Significant independent predictors for non-survival within the entire cohort were advanced disease severity stage III (OR=27.9, 95% CI: 7.4-105, P<0.001) and birth weight below 1100 g (OR=5.7, 95% CI: 1.7-19.4, P<0.01).

Conclusions: In patients with NEC, the presence of PDA is associated with an increased risk of death. However, when important differences between the two study groups are controlled, only birth weight and disease severity may independently predict mortality.

Keywords: congenital heart disease; necrotizing enterocolitis; neonatal mortality; patent ductus arteriosus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ductus Arteriosus, Patent / complications*
  • Enterocolitis, Necrotizing / complications*
  • Female
  • Humans
  • Infant, Newborn
  • Male
  • Prognosis
  • Retrospective Studies
  • Risk Assessment