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Probiotics for infantile colic: a randomized, double-blind, placebo-controlled trial investigating Lactobacillus
Kim Chau1, Eddy Lau2, Saul Greenberg3
1Department of Pharmacology and Toxicology, University of Toronto, Ontario, Canada; Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children, Ontario, Canada.
Insights
Lactobacillus reuteri DSM 17938 significantly reduced crying and fussing in breastfed infants with colic. This probiotic intervention offers an effective treatment for infantile colic, improving infant well-being.
Area of Science:
- Pediatrics
- Microbiology
- Gastroenterology
Background:
- Infantile colic is a common condition affecting breastfed infants.
- Current treatments for infantile colic have limited efficacy.
- Probiotics are being explored as a potential therapeutic option.
Purpose of the Study:
- To evaluate the effectiveness of Lactobacillus reuteri DSM 17938 in treating infantile colic.
- To compare L. reuteri DSM 17938 with a placebo in breastfed Canadian infants.
Main Methods:
- A randomized, double-blind, placebo-controlled trial was conducted.
- 52 infants diagnosed with colic received either L. reuteri DSM 17938 (10^8 CFU) or placebo daily for 21 days.
- Infant crying, fussing times, and adverse events were monitored via diaries and questionnaires.
Main Results:
- Infants receiving L. reuteri DSM 17938 experienced significantly shorter total crying and fussing times compared to the placebo group (P = .028).
- A significant reduction in daily crying and fussing was observed by day 21 in the probiotic group (P = .045).
- A higher proportion of infants in the L. reuteri DSM 17938 group showed a ≥50% reduction in crying time (P = .035).
Conclusions:
- Lactobacillus reuteri DSM 17938 administration effectively improved colic symptoms in breastfed infants.
- The probiotic significantly reduced crying and fussing times, indicating its therapeutic potential for infantile colic.
Objective:
To investigate the effectiveness of Lactobacillus reuteri DSM 17938 for the treatment of infantile colic in breastfed Canadian infants, compared with placebo.
Study Design:
A randomized, double-blind, placebo-controlled trial was conducted involving 52 infants with colic, according to modified Wessel criteria, who were assigned at random to receive L reuteri DSM 17938 (10(8) colony-forming units) (n = 24) or placebo (n = 28) for 21 days. Daily crying and fussing times were recorded in a structured diary, and maternal questionnaires were completed to monitor changes in infant colic symptoms and adverse events.
Results:
Total average crying and fussing times throughout the study (from baseline to day 21) were significantly shorter among infants with colic in the probiotic group compared with infants in the placebo group (1719 ± 750 minutes [29 ± 13 hours] vs 2195 ± 764 minutes [37 ± 13 hours]; P = .028) (relative risk, 0.78; 95% CI, 0.58-0.98). Infants given L reuteri DSM 17938 showed a significant reduction in daily crying and fussing times at the end of treatment period compared with those receiving placebo (median, 60 minutes/day [IQR, 64 minutes/day] vs 102 minutes/day [IQR, 87 minutes/day]; P = .045). On day 21, a significantly higher proportion of infants in the L reuteri DSM 17938 group responded to treatment with a ≥50% crying time reduction compared with infants given placebo (17 vs 6, P = .035; relative risk, 3.3; 95% CI, 1.55-7.03).
Conclusion:
Administration of L reuteri DSM 17938 significantly improved colic symptoms by reducing crying and fussing times in breastfed Canadian infants with colic.
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