4.4 Article

A Lactobacillus casei Shirota probiotic drink reduces antibiotic-associated diarrhoea in patients with spinal cord injuries: a randomised controlled trial

Journal

BRITISH JOURNAL OF NUTRITION
Volume 111, Issue 4, Pages 672-678

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0007114513002973

Keywords

Probiotics; Spinal cord injuries; Diarrhoea; Undernutrition risk

Funding

  1. Healthcare Infection Society (Mike Emmerson Young Investigator Award)
  2. Yakult UK Limited
  3. BRC

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Certain probiotics may prevent the development of antibiotic-associated diarrhoea (AAD) and Clostridium difficile-associated diarrhoea (CDAD), but their effectiveness depends on both strain and dose. There are few data on nutritional interventions to control AAD/CDAD in the spinal cord injury (SCI) population. The present study aimed to assess (1) the efficacy of consuming a commercially produced probiotic containing at least 6.5 x 10(9) live Lactobacilluscasei Shirota (LcS) in reducing the incidence of AAD/CDAD, and (2) whether undernutrition and proton pump inhibitors (PPI) are risk factors for AAD/CDAD. A total of 164 SCI patients (50.1 (sd 17.8) years) with a requirement for antibiotics (median 21 d, range 5-366) were randomly allocated to receive LcS (n 76) or no probiotic (n 82). LcS was given once daily for the duration of the antibiotic course and continued for 7 days thereafter. Nutritional risk was assessed by the Spinal Nutrition Screening Tool. The LcS group had a significantly lower incidence of AAD (17.1 v. 54.9%, P<0.001). At baseline, 65% of patients were at undernutrition risk. Undernutrition (64.1 v. 33.3%, P<0.01) and the use of PPI (38.4 v. 12.1%, P=0.022) were found to be associated with AAD. However, no significant difference was observed in nutrient intake between the groups. The multivariate logistic regression analysis identified poor appetite (<1/2 meals eaten) (OR 5.04, 95% CI 1.28, 19.84) and no probiotic (OR 8.46, 95% CI 3.22, 22.20) as the independent risk factors for AAD. The present study indicated that LcS could reduce the incidence of AAD in hospitalised SCI patients. A randomised, placebo-controlled study is needed to confirm this apparent therapeutic success in order to translate into improved clinical outcomes.

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