Publicación:
Lactobacillus casei strain GG in the treatment of infants with acute watery diarrhea: A randomized, double-blind, placebo controlled clinical trial [ISRCTN67363048]

dc.contributor.authorSalazar-Lindo, Eduardo
dc.contributor.authorMiranda-Langschwager, Percy
dc.contributor.authorCampos-Sanchez, Miguel
dc.contributor.authorChea-Woo, Elsa
dc.contributor.authorSack, R. Bradley
dc.date.accessioned2026-05-14T14:28:50Z
dc.date.issued2004
dc.description.abstractBackground: Adjuvant therapy to ORT with probiotic bacteria for infants with acute watery diarrhea has been under active investigation. Most studies have been done in the developed world showing benefit only for viral mild gastroenteritis. We evaluated the effect of a milk formula containing one billion (109) cfu/ml of Lactobacillus casei strain GG (LGG) upon duration and severity of diarrhea in infants in an environment with more severe acute diarrhea, where etiologic agents other than rotavirus are involved more frequently, and where mixed infections are more prevalent. Methods: Male infants aged 3-36 months brought for treatment of acute watery diarrhea of less than 48 hours were eligible. After rehydration was completed with the WHO's oral rehydration solution, patients were randomly assigned to receive a milk formula either containing LGG or not. Stool volume was periodically measured using a devise suited to collect stools separate from urine. Duration of diarrhea was estimated based on stools physical characteristics. Results: Eighty nine patients received the placebo milk formula and ninety received the LGG containing formula. Both groups were comparable in their baseline characteristics. Total stool output was significantly larger (p = 0.047) in the LGG group (247.8 ml/kg) than in the placebo group (195.0 ml/kg). No significant differences were found in duration of diarrhea (58.5 hours with LGG vs. 50.4 hours with placebo), rate of treatment failure (21.1% with LGG vs. 18.0% with placebo), and proportion of patients with unresolved diarrhea after 120 hours (12.2% with LGG vs. 12.5% with placebo). The rate of stools with reducing substances after 24 hours of treatment increased significantly in both groups (from 41.4% to 72.2% with LGG and from 45.9% to 68.0% with placebo). Conclusion: This study did not show a positive effect of LGG on the clinical course of acute watery diarrhea. Positive beneficial effects of LGG, as had been reported elsewhere, could have been masked in our study by worsening diarrhea due to transient lactose malabsorption. Further studies with low-lactose or non-lactose conveyors of LGG are desirable. © 2004 Salazar-Lindo et al; licensee BioMed Central Ltd.en_US
dc.identifier.doihttps://doi.org/10.1186/1471-2431-4-18
dc.identifier.scopus2-s2.0-12944265073
dc.identifier.urihttps://hdl.handle.net/20.500.12866/19729
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.ispartofurn:issn:1471-2431
dc.relation.ispartofseriesBMC Pediatrics
dc.relation.issn1471-2431
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectDiarrheaen_US
dc.subjectMilk Formulaen_US
dc.subjectOral Rehydration Solutionen_US
dc.subjectAcute Diarrheaen_US
dc.subjectOral Rehydration Salten_US
dc.titleLactobacillus casei strain GG in the treatment of infants with acute watery diarrhea: A randomized, double-blind, placebo controlled clinical trial [ISRCTN67363048]en_US
dc.typehttps://purl.org/coar/resource_type/c_2df8fbb1
dc.type.localArtículo de revista
dc.type.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85
dspace.entity.typePublication

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