Bovine Lactoferrin in the Prevention of Antibiotic-Associated Diarrhea in Children: A Randomized Clinical Trial

Michal F Wronowski, Maria Kotowska, Marcin Banasiuk, Artur Kotowski, Weronika Kuzmicka, Piotr Albrecht, Michal F Wronowski, Maria Kotowska, Marcin Banasiuk, Artur Kotowski, Weronika Kuzmicka, Piotr Albrecht

Abstract

Introduction: Antibiotic-associated diarrhea (AAD) is a common adverse reaction to antibiotic treatment affecting up to 21% of children. The aim of the study is to evaluate whether bovine lactoferrin (bLf) might be used for AAD prevention. Materials and Methods: In this prospective, randomized, double-blind, placebo-controlled, single-center study, we enrolled 156 children aged between 1 and 18 years, treated with antibiotic due to acute respiratory or urinary tract infection. We randomly allocated children 1:1 to receive 100 mg of bLf or a placebo twice a day orally for the whole period of antibiotic therapy. The primary outcome was the occurrence of antibiotic-associated diarrhea during and up to 2 weeks after antibiotic therapy. The secondary endpoint was intravenous rehydration or antibiotic withdrawal due to diarrhea. We performed intention-to-treat analysis. Results: We included 150 patients in intention-to-treat analysis. AAD occurred in 16 of 75 (21.3%) patients in bLf group and in 7 of 75 (9.3%) individuals in placebo group [OR = 2.6, (95% CI: 1.01-6.84), p = 0.04]. Relative risk was 2.29 (95% CI: 0.89-5.88). The need for intravenous rehydration occurred in one patient in the placebo group (p = 0.3). We observed no adverse effects in neither of the groups. Discussion: The trial indicated that bLf is not effective in AAD prevention. The risk for AAD was higher in bovine lactoferrin group as compared with placebo. We registered the study protocol on ClinicalTrials.gov (NCT02626104).

Keywords: Clostridioides difficile; antibiotic-associated diarrhea; children; lactoferrin; probiotics.

Conflict of interest statement

The lactoferrin and placebo preparations were donated to the Medical University of Warsaw Public Pediatric Teaching Hospital's Pharmacy by Pharmabest, private limited company, Poland). The manufacturer was not involved in the design of the study, collection, analysis and interpretation of data, the writing of the report and decision to submit this manuscript for publication. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Copyright © 2021 Wronowski, Kotowska, Banasiuk, Kotowski, Kuzmicka and Albrecht.

Figures

Figure 1
Figure 1
Patient study flow diagram.

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Source: PubMed

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