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Systematic review: Limosilactobacillus reuteri DSM 17938 for preventing antibiotic-associated diarrhoea in children
Hania Szajewska1, Maciej Kołodziej1, Bartłomiej M Zalewski1
1Department of Paediatrics, The Medical University of Warsaw, Warsaw, Poland.
Objectives:
Probiotic effects are strain-specific; each strain needs to be assessed individually. In this review, we evaluated the effectiveness of Limosilactobacillus reuteri DSM 17938 in preventing antibiotic-associated diarrhoea (AAD) in children receiving systemic antibiotics.
Methods:
We searched the Cochrane Library, MEDLINE, EMBASE and trial registries (January 2016-July 2025) for randomized controlled trials (RCTs) comparing L. reuteri DSM 17938 with placebo, no treatment, or other probiotics in children. Risk of bias was assessed with Risk of Bias 2 (ROB-2), and certainty of evidence with Grading of Recommendations, Assessment, Development and Evaluation (GRADE).
Results:
Three RCTs (1070 randomized, 998 analysed) were included. No significant effect was observed with ≤14-day administration (two RCTs, n = 901; risk ratio [RR] 0.85, 95% confidence interval [CI]: 0.26-2.77; low certainty evidence), with interpretation limited by heterogeneity (I2 = 91%) and analytical differences. A regimen of up to 21 days reduced AAD risk (two RCTs, n = 751; RR: 0.50, 95% CI: 0.33-0.75; moderate certainty evidence). A post hoc analysis of trials with follow-up up to 56 days showed no significant effect (three RCTs, n = 998; RR: 0.85, 95% CI: 0.29-2.46; I2 = 83%). A subgroup analysis limited to children receiving amoxicillin-clavulanate showed benefit (two RCTs, n = 690; RR: 0.49, 95% CI: 0.32-0.76; I2 = 0%).
Conclusions:
L. reuteri DSM 17938 may reduce the risk of AAD in children when administered for up to 21 days or in those receiving amoxicillin-clavulanate. No benefit was found with shorter administration or extended follow-up. Further high-quality trials are needed before routine use can be recommended.
Insights
Limosilactobacillus reuteri DSM 17938 may prevent antibiotic-associated diarrhea (AAD) in children when given for up to 21 days, especially with amoxicillin-clavulanate. Shorter durations or longer follow-up showed no significant benefit.
Area of Science:
- Microbiology and Immunology
- Pediatric Gastroenterology
Background:
- Probiotic efficacy is strain-specific, requiring individual assessment.
- Antibiotic-associated diarrhea (AAD) is a common concern in pediatric patients receiving systemic antibiotics.
Purpose of the Study:
- To evaluate the effectiveness of Limosilactobacillus reuteri DSM 17938 in preventing AAD in children.
- To analyze strain-specific probiotic effects in a pediatric population.
Main Methods:
- Systematic review of randomized controlled trials (RCTs) from major databases and trial registries (January 2016-July 2025).
- Included studies compared L. reuteri DSM 17938 with placebo, no treatment, or other probiotics in children.
- Risk of bias and certainty of evidence were assessed using ROB-2 and GRADE criteria, respectively.
Main Results:
- Three RCTs involving 1070 children were analyzed.
- A 21-day regimen of L. reuteri DSM 17938 showed moderate certainty evidence for reducing AAD risk (RR: 0.50, 95% CI: 0.33-0.75).
- A subgroup analysis indicated benefit for children receiving amoxicillin-clavulanate (RR: 0.49, 95% CI: 0.32-0.76).
Conclusions:
- L. reuteri DSM 17938 may reduce AAD risk in children when administered for up to 21 days or with amoxicillin-clavulanate.
- No significant benefit was observed with shorter administration periods or extended follow-up.
- Further high-quality trials are recommended to support routine use.
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