Evidence map›Paper›PMID 38519563›Full record

Trial reportSpinal cord2024

Lactobacillus casei Shirota probiotic drinks reduce antibiotic associated diarrhoea in patients with spinal cord injuries who regularly consume proton pump inhibitors: a subgroup analysis of the ECLISP multicentre RCT.

Samford Wong, Shashivadan P Hirani, Alastair Forbes, Naveen Kumar, Ramaswamy Hariharan, Jean O'Driscoll, Ravi Sekhar, Ali Jamous

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Spinal cord, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

Samford WongNational Spinal Injuries Centre, Stoke Mandeville Hospital, Aylesbury, UK. samford.wong.1@city.ac.uk.ORCID 0000-0002-3975-5684
Shashivadan P HiraniSchool of Health & Psychological Sciences, City, University of London, London, UK.
Alastair ForbesUniversity of Tartu, Estonia, and Norwich Medical School, University of East Anglia, Norwich, UK.
Naveen KumarMidland Centre for Spinal Injury, Robert Jones and Agnes Hunt Orthopaedic Hospital, Gobowen, UK.
Ramaswamy HariharanThe Princess Royal Spinal Injuries Centre, Northern General Hospital, Sheffield, UK.
Jean O'DriscollDepartment of Microbiology, Stoke Mandeville Hospital, Aylesbury, UK.
Ravi SekharDepartment of Gastroenterology, Stoke Mandeville Hospital, Aylesbury, UK.
Ali JamousINRES Neuro, Wendover, UK.
City, University of London · GBStoke Mandeville Hospital · GBNorthern General Hospital · GBRobert Jones and Agnes Hunt Orthopaedic Hospital · GBUniversity of East Anglia · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

STUDY

designThis was a sub-group analysis of a multicentre, randomised, placebo-controlled, double-blind trial (ECLISP trial)

objectivesTo assess the efficacy of a probiotic containing at least 6.5 × 10

settingThree SCI centres (National Spinal Injuries Centre, Midland Centre for Spinal Injuries and Princess Royal Spinal Cord Injuries Centre) in the United Kingdom

methodsBetween November 2014, and November 2019, 95 eligible consenting SCI patients (median age: 57; IQ range: 43-69) were randomly allocated to receive LcS (n = 50) or placebo (n = 45). The primary outcome is the occurrence of AAD up to 30 days after finishing LcS/placebo.

resultsThe LcS group had a significantly lower incidence of AAD at 30 days after finishing the antibiotic course (28.0 v 53.3%, RR: 95% CI: 0.53, 0.31-0.89; z = 2.5, p = 0.01). Multivariate logistic regression analysis identified that LcS can reduce the risk of AAD at 30 days (OR: 0.36, 95% CI 0.13, 0.99, p < 0.05). No intervention-related adverse events were reported during the study.

conclusionsLcS has the potential to prevent AAD in what could be considered a defined vulnerable group of SCI patients on regular PPI. A confirmatory, randomised, placebo-controlled study is needed to confirm this apparent therapeutic success to translate it into appropriate clinical outcomes. SPONSORSHIP: Yakult Honsha Co., Ltd.

Indexed as

Anti-Bacterial AgentsDiarrheaLacticaseibacillus caseiProbioticsProton Pump InhibitorsSpinal Cord InjuriesAdultAgedDouble-Blind MethodFemaleHumansMaleMiddle AgedAnti-Bacterial AgentsProton Pump Inhibitors

Identifiers

PMID38519563
PMCPMC11176055
OpenAlexW4393097543

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.