Lactobacillus rhamnosus GG in the middle ear after randomized, double-blind, placebo-controlled oral administration

Int J Pediatr Otorhinolaryngol. 2014 Oct;78(10):1637-41. doi: 10.1016/j.ijporl.2014.07.011. Epub 2014 Jul 18.

Abstract

Objective: Probiotics may have potency in reducing upper respiratory infections, in particular in children. We studied findings from middle ear effusion (MEE) samples after randomized, placebo-controlled 3-week oral administration of probiotic Lactobacillus rhamnosus GG (L.

Gg) methods: 40 children referred to tympanostomy were randomized to receive either L. GG or placebo (1:1) for 3 weeks before surgery. MEE samples were collected from 13 children (in total, 25 samples, 19 from the L. GG group and 6 from the placebo group) and analyzed for L. GG and pathogenic bacterial and viral findings.

Results: L. GG was present in 5 of the 25 MEE samples (4 from the L. GG group). Haemophilus infuenzae was the most prominent pathogen in 12 samples (10 from the L. GG group). Rhinovirus was present in 12 samples (10 from the L. GG group) and enterovirus in 1 sample (L. GG group).

Conclusions: L. GG was present in the middle ear of children suffering from otitis media with effusion, but did not reduce the presence of pathogenic bacteria or viruses.

Trial registration: ClinicalTrials.gov NCT02110732.

Keywords: Children; Lactobacillus rhamnosus GG; Middle ear effusion; Otitis media; Probiotics; Tympanostomy.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Child
  • Child, Preschool
  • Double-Blind Method
  • Ear, Middle / microbiology
  • Exudates and Transudates
  • Humans
  • Lacticaseibacillus rhamnosus / chemistry*
  • Male
  • Otitis Media with Effusion / drug therapy*
  • Otitis Media with Effusion / microbiology
  • Probiotics / administration & dosage*
  • Probiotics / therapeutic use

Associated data

  • ClinicalTrials.gov/NCT02110732