Optimising the management of childhood acute diarrhoeal disease using a rapid test-and- treat strategy and/or Lactobacillus reuteri DSM 17938: a multicentre, randomised, controlled, factorial trial in Botswana
- 2022-04
- BMJ Global Health 7(4)
- J. Pernica
- T. Arscott-Mills
- A. Steenhoff
- M. Mokomane
- Banno Moorad
- Mbabi Bapabi
- K. Lechiile
- Oarabile Mangwegape
- Boswa Batisani
- Norah Mawoko
- Charles Muthoga
- T. Vanniyasingam
- Joycelyne E Ewusie
- Amy Lowe
- Janice M Bonsu
- Alemayehu Mekonnen Gezmu
- M. Smieja
- L. Mazhani
- K. Størdal
- L. Thabane
- M. Kelly
- D. Goldfarb
- PubMed: 35418412
- DOI: 10.1136/bmjgh-2021-007826
Abstract
Introduction: The study aim was to determine if rapid enteric diagnostics followed by the provision of targeted antibiotic therapy ('test-and-treat') and/or Lactobacillus reuteri DSM 17938 would improve outcomes in children hospitalised in Botswana with acute gastroenteritis.
Methods: This was a multicentre, randomised, factorial, controlled, trial. Children aged 2-60 months admitted for acute non-bloody diarrhoea to four hospitals in southern Botswana were eligible. Participants were assigned to treatment groups by web-based block randomisation. Test-and-treat results were not blinded, but participants and research staff were blinded to L. reuteri/placebo assignment; this was dosed as 1×108 cfu/mL by mouth daily and continued for 60 days. The primary outcome was 60-day age-standardised height (HAZ) adjusted for baseline HAZ. All analyses were by intention to treat. The trial was registered at Clinicaltrials.gov.
Results: Recruitment began on 12 June 2016 and continued until 24 October 2018. There were 66 participants randomised to the test-and-treat plus L. reuteri group, 68 randomised to the test-and-treat plus placebo group, 69 to the standard care plus L. reuteri group and 69 to the standard care plus placebo group. There was no demonstrable impact of the test-and-treat intervention (mean increase of 0.01 SD, 95% CI -0.14 to 0.16 SD) or the L. reuteri intervention (mean decrease of 0.07 SD, 95% CI -0.22 to 0.08 SD) on adjusted HAZ at 60 days.
Conclusions: In children hospitalised for acute gastroenteritis in Botswana, neither a test-and-treat algorithm targeting enteropathogens, nor a 60-day course of L. reuteri DSM 17938, were found to markedly impact linear growth or other important outcomes. We cannot exclude the possibility that test-and-treat will improve the care of children with significant enteropathogens (such as Shigella) in their stool.
Trial registration number: NCT02803827.
Keywords: Child health; Individual randomized trial; Medical microbiology.
Research Insights
Supplement | Health Outcome | Effect Type | Effect Size |
---|---|---|---|
Lactobacillus reuteri | Adjusted Height-for-Age Z Score | Neutral | Small |
Lactobacillus reuteri DSM 17938 | Improved Age-Standardized Height | Neutral | Small |
Lactobacillus reuteri HA-188 | Improved Growth | Neutral | Small |