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A randomized double-blind placebo-controlled trial of Lactobacillus GG for abdominal pain disorders in children.

AbstractBACKGROUND:
Functional abdominal pain disorders (FAPD) are common in school-aged children; however, there is no reliable treatment.
AIM:
To determine the efficacy of Lactobacillus rhamnosus GG (LGG) for treating FAPD in children.
METHODS:
A total of 104 children who fulfilled the Rome II criteria for functional dyspepsia (FD), or irritable bowel syndrome (IBS), or functional abdominal pain (FAP) were enrolled in a double-blind, randomized controlled trial in which they received LGG (n = 52), or placebo (n = 52) for 4 weeks.
RESULTS:
For the overall study population, those in the LGG group were more likely to have treatment success (no pain) than those in the placebo group (25% vs. 9.6%, relative benefit (RB) 2.6, 95% confidence interval (CI): 1.05-6.6, number needed to treat (NNT) 7, 95% CI: 4-123). For children with IBS (n = 37), those in the LGG group were more likely to have treatment success than those in the placebo group (33% vs. 5%, RB 6.3, 95% CI: 1.2-38, NNT 4, 95% CI: 2-36) and reduced frequency of pain (P = 0.02), but not pain severity (P = 0.10). For the FD group (n = 20) and FAP group (n = 47), no differences were found.
CONCLUSION:
The LGG appears to moderately increase treatment success, particularly among children with IBS.
AuthorsA Gawrońska, P Dziechciarz, A Horvath, H Szajewska
JournalAlimentary pharmacology & therapeutics (Aliment Pharmacol Ther) Vol. 25 Issue 2 Pg. 177-84 (Jan 15 2007) ISSN: 0269-2813 [Print] England
PMID17229242 (Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Topics
  • Abdominal Pain (diet therapy)
  • Adolescent
  • Child
  • Double-Blind Method
  • Dyspepsia (diet therapy)
  • Female
  • Humans
  • Irritable Bowel Syndrome (diet therapy)
  • Lacticaseibacillus rhamnosus
  • Male
  • Probiotics (therapeutic use)
  • Treatment Outcome

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