Impact of a multi-strain probiotic administration on peri-rectal colonization with drug-resistant Gram-negative

Marwyn Sowden1, Evette van Niekerk1, Andre Nyandwe Hamama Bulabula2

  • 1Division of Human Nutrition, Department of Global Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.

Frontiers in Pediatrics
|November 21, 2022
PubMed

Insights

A multi-strain probiotic significantly reduced drug-resistant Gram-negative bacteria colonization in preterm neonates. This intervention proved effective in preventing early and late gut colonization by these resistant bacteria.

Area of Science:

  • Neonatal Medicine
  • Microbiology
  • Clinical Trials

Background:

  • Drug-resistant Gram-negative bacteria (DR-GNB) pose a significant threat to hospitalized preterm neonates globally.
  • Investigating interventions to prevent DR-GNB colonization is crucial for improving neonatal outcomes.

Purpose of the Study:

  • To evaluate the efficacy of a multi-strain probiotic in reducing rectal colonization with DR-GNB in preterm neonates.
  • To assess the impact of probiotics on both early and late stages of gut colonization.

Main Methods:

  • A double-blind, placebo-controlled, randomized clinical trial.
  • 200 preterm neonates were randomized to receive either a multi-strain probiotic (n=100) or a placebo (n=100).
  • Peri-rectal colonization with DR-GNB was assessed at enrolment, day 7, and day 14.

Main Results:

  • Initial DR-GNB colonization was observed in 15% of neonates at enrolment.
  • Rapid acquisition of DR-GNB occurred, increasing to 77% by day 7 and 83% by day 14.
  • Probiotic group showed a 57% reduction in DR-GNB colonization by day 7 (OR: 0.43) and a 93% reduction by day 14 (OR: 0.07).

Conclusions:

  • Preterm neonates experience significant DR-GNB colonization early in life.
  • A multi-strain probiotic effectively reduces both early and late neonatal gut colonization with DR-GNB.
  • Probiotic intervention offers a promising strategy to combat DR-GNB in vulnerable preterm infants.
Abstract