Enteral human IgG for prevention of necrotising enterocolitis: a placebo-controlled, randomised trial

G Lawrence1, D Tudehope, K Baumann

  • 1Queensland Institute of Medical Research, PO Royal Brisbane Hospital, 4029, Brisbane, Australia. gregL@QIMR.edu.au

PubMed

Insights

Enteral immunoglobulin G (IgG) supplementation does not prevent necrotising enterocolitis in premature infants. This study found no significant difference in the incidence of necrotising enterocolitis between infants receiving IgG and those receiving a placebo.

Area of Science:

  • Neonatalogy
  • Immunology
  • Gastroenterology

Background:

  • Neonatal necrotising enterocolitis (NEC) is a life-threatening condition in premature infants.
  • While breast milk and good nursery practices offer some protection, effective preventive measures are still needed.
  • Previous research suggested enteral immunoglobulins (IgA and IgG) might prevent NEC, but IgA is unavailable in Australia.

Purpose of the Study:

  • To determine if enteral immunoglobulin G (IgG) supplementation can prevent necrotising enterocolitis in premature neonates.

Main Methods:

  • A multicentre, double-blind, placebo-controlled trial involving 1529 infants.
  • Infants were randomly assigned to receive either human IgG (1200 mg/kg daily) or a placebo for up to 28 days, starting with enteral feeding.
  • The primary outcome was the incidence of definite necrotising enterocolitis and associated mortality.

Main Results:

  • 43 infants in the IgG group developed definite necrotising enterocolitis, with 10 deaths.
  • 41 infants in the placebo group developed definite necrotising enterocolitis, with 6 deaths (p=0.47).
  • There was no statistically significant difference in the incidence of definite or suspect necrotising enterocolitis between the groups.

Conclusions:

  • Enteral supplementation with human IgG does not reduce the incidence of necrotising enterocolitis in premature infants.
  • The findings do not support the use of enteral IgG as a preventive strategy for NEC.
Abstract