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Fecal Recovery of Probiotics Administered as a Multi-Strain Formulation during Antibiotic Treatment.


ABSTRACT: The present study aimed to investigate whether probiotic recovery is affected when consumed together with antibiotics. Fecal samples were collected from an earlier antibiotic associated diarrhea, randomized, placebo-controlled study with a product consisting of a combination of Lactobacillus acidophilus NCFM, Lactobacillus paracasei Lpc-37, and Bifidobacterium lactis Bi-07, B. lactis Bl-04 at equal numbers and at a total dose of 1010 CFU. Fecal samples were collected during the screening visit (T0), i.e., at the time of antibiotic prescription, and then on the last day of the antibiotic treatment (T1) as well as seven days after the subject had stopped taking the antibiotic treatment (T2) and at two weeks after completing antibiotic treatment and one week after probiotic/placebo consumption stopped (T3). Samples were analyzed for the presence of the four administered strains. The study was registered at clinicaltrials.gov as NCT01596829. Detection levels of all four strains were significantly increased from T0 to T1 and returned to baseline level from T2 to T3. There were also significantly more subjects with detectable levels of L. paracasei Lpc-37, B. lactis Bi-07, and B. lactis Bl-04 at T1 and T2 compared to T0 and T3, and compared to placebo. Each of the four strains could be detected in the feces of patients apparently unaffected by the simultaneous consumption of antibiotics.

SUBMITTER: Forssten SD 

PROVIDER: S-EPMC7235824 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

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Fecal Recovery of Probiotics Administered as a Multi-Strain Formulation during Antibiotic Treatment.

Forssten Sofia D SD   Yeung Nicolas N   Ouwehand Arthur C AC  

Biomedicines 20200409 4


The present study aimed to investigate whether probiotic recovery is affected when consumed together with antibiotics. Fecal samples were collected from an earlier antibiotic associated diarrhea, randomized, placebo-controlled study with a product consisting of a combination of <i>Lactobacillus acidophilus</i> NCFM, <i>Lactobacillus paracasei</i> Lpc-37, and <i>Bifidobacterium lactis</i> Bi-07, <i>B. lactis</i> Bl-04 at equal numbers and at a total dose of 10<sup>10</sup> CFU. Fecal samples were  ...[more]

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