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Effects of a nine-strain bacterial synbiotic compared to simethicone in colicky babies - an open-label randomised
J Piątek1, M Bernatek1, H Krauss1
1Department of Medicine, The President Stanisław Wojciechowski State University of Applied Sciences in Kalisz, Nowy Šwiat 4, 62-800 Kalisz, Poland.
Insights
A multi-strain synbiotic significantly reduced crying days and duration in colicky infants compared to simethicone. This suggests synbiotics are a promising treatment for infantile colic, warranting further research.
Area of Science:
- Pediatrics
- Gastroenterology
- Microbiology
Background:
- Infantile colic is a common condition in infants, characterized by prolonged crying episodes.
- Current treatments for infantile colic have varying efficacy and potential side effects.
Purpose of the Study:
- To evaluate the efficacy of a multi-strain synbiotic compared to simethicone in managing infantile colic.
- To assess the impact on crying behavior, specifically crying days and duration.
Main Methods:
- An open-label, two-parallel group study involving 87 infants (3-6 weeks old) with infantile colic.
- Infants were randomized to receive either simethicone or a multi-strain synbiotic (containing specific Lactobacillus and Bifidobacterium strains with fructooligosaccharides) for 4 weeks.
- Primary outcomes included responder rates (≥50% reduction) for crying days, evening crying duration, and crying phases per day.
Main Results:
- The multi-strain synbiotic group showed significantly higher responder rates for reduced crying days (72% vs 18%, P<0.0001) and average evening crying duration (85% vs 39%, P=0.0001) compared to simethicone.
- No significant difference was observed in the reduction of average crying phases per day (50% vs 42%, P=0.4852).
- No adverse effects were reported in either treatment group.
Conclusions:
- A multi-strain synbiotic demonstrates significant efficacy in reducing crying days and duration in infants with colic.
- Synbiotics represent a potentially valuable therapeutic option for infantile colic that merits further investigation.
- The safety profile of the multi-strain synbiotic was favorable in this study population.
Abstract:
The aim of the study was to determine effects of administration of simethicone and a multi-strain synbiotic on the crying behaviour of colicky babies. The study design consisted of an open-label, two parallel treatment group study involving 87 infants aged 3-6 weeks with infantile colic (defined as crying episodes lasting 3 or more hours per day and occurring at least 3 days per week within 3 weeks prior to enrolment) randomly, unequally [1:1.5] assigned to receive simethicone (n=33) or a multi-strain synbiotic (n=54) orally for 4 weeks. The multi-strain synbiotic contained Lactobacillus acidophilus LA-14, Lacticaseibacillus casei R0215, Lacticaseibacillus paracasei Lp-115, Lacticaseibacillus rhamnosus GG, Ligilactobacillus salivarius Ls-33, Bifidobacterium lactis Bl-04, Bifidobacterium bifidum R0071, Bifidobacterium longum R0175 and fructooligosaccharides). Primary outcome measures were the responder rates (effect ≥50% reduction from baseline) of the measures 'crying days last 3 weeks', 'average evening crying duration last 3 weeks' and 'reduction of average number of crying phases per day last three weeks' at the end of treatment. The study is registered at ClinicalTrials.gov under NCT04487834. Significantly higher responder rates (effect ≥50% reduction from baseline) of the multi-strain synbiotic compared to simethicone were found for the measures 'crying days last 3 weeks' (72% vs 18%, P<0.0001) and 'average evening crying duration last 3 weeks' (85% vs 39%, P=0.0001). No significant difference was found for the measure 'reduction of average number of crying phases per day last three weeks' (50% vs 42%, P=0.4852). No adverse effects were reported for the two treatment groups. Based on these results, the multi-strain synbiotic can be considered as an interesting therapeutic possibility for the treatment of infantile colic, worthwhile to be investigated further in non-clinical and clinical studies.
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