# Saccharomyces boulardii in patients with severe acute pancreatitis: a single center, open-label randomized controlled trial

**Authors:** Jia-Lin He, Lei Ran, Xu Xiao, Yu Su, Hui Lin, Cheng Lu, Bo Tang, Shiming Yang

PMC · DOI: 10.1093/burnst/tkag006 · Burns & Trauma · 2026-01-16

## TL;DR

This study found that Saccharomyces boulardii, when combined with nutrition, may reduce infections in patients with severe acute pancreatitis by improving gut and respiratory microbiomes.

## Contribution

The study demonstrates that S. boulardii reduces nosocomial infections in SAP patients by altering gut and respiratory microbiota.

## Key findings

- S. boulardii prevented nosocomial infections in 0/27 patients compared to 5/23 in the control group.
- S. boulardii reduced intestinal bacterial perturbation and inhibited Enterococcus and Candida proliferation.
- Intestinal fungi were closely linked to nosocomial infections in SAP patients.

## Abstract

Nosocomial infections in patients with severe acute pancreatitis (SAP) are frequently driven by impaired intestinal barrier function, which facilitates bacterial translocation and contributes to adverse clinical outcomes. Saccharomyces boulardii (S. boulardii) can reconstitute gut microbiota composition. We investigated whether S. boulardii combined with enteral nutrition (EN) affects the microbiome and nosocomial infections in SAP.

This study is a single centre, open-label randomized controlled trial. We included 50 patients with SAP in a Chinese gastroenterology intensive care unit (ICU), randomized to Probiotic group (S. boulardii and EN) or the Control group (EN). Throat/oropharyngeal and rectal swabs were collected from patients with SAP on days 0, 1, 3, 6, 9, 12, and 15 of ICU admission. The primary endpoints were nosocomial infection and fungemia, whereas the secondary endpoints were ICU mortality, 28-day mortality, ICU stay, and length of hospital stay. All samples were subjected to full-length 16 s rRNA and internal transcribed spacer (ITS) sequencing. Multivariate analysis was performed using normalized microbial and corresponding clinical data.

After data processing, 213 16S rRNA and 120 ITS samples were analysed. S. boulardii prevented nosocomial infections (0/27 in the Probiotic group vs 5/23 in the Control group; P < 0.05). Intestinal fungi were closely associated with nosocomial infections. Bioinformatic analysis showed that S. boulardii prevented nosocomial infections by reducing intestinal bacterial perturbation and inhibiting the proliferation of Enterococcus in the intestine, and Candida in the respiratory tract and intestines.

S. boulardii in patients with SAP may positively alter the respiratory and intestinal microbiome and decrease the incidence of nosocomial infections.

This study was approved by the Ethics Committee of Xinqiao Hospital, Army Medical University, Chongqing China (2021-yd030–01), which was retrospectively registered at the Chinese Clinical Trial Registry (ChiCTR2200056011, Date of Registration: 30/01/2022 https://www.chictr.org.cn/showproj.html?proj=151215).

## Linked entities

- **Species:** Enterococcus (taxon 1350), Candida (taxon 5475)

## Full-text entities

- **Diseases:** organ dysfunction (MESH:D009102), nausea (MESH:D009325), pulmonary infiltrates (MESH:D017254), pneumonia (MESH:D011014), ischemia (MESH:D007511), VAP (MESH:D053717), fever (MESH:D005334), fungemia (MESH:D016469), damage (MESH:D020263), Burns (MESH:D002056), vomiting (MESH:D014839), Respiratory infection (MESH:D012141), Trauma (MESH:D014947), bacteraemia (MESH:C531821), inflammation (MESH:D007249), Critically Ill (MESH:D016638), IPN (MESH:D019283), ICU (MESH:C000657744), abdominal pain (MESH:D015746), Acute Pancreatitis (MESH:D010195), bacterial (MESH:D001424), drug allergy (MESH:D004342), fungal (MESH:D009181), Intestinal infection (MESH:D007410), ulcerative colitis (MESH:D003093), BSI (MESH:D018805), SAP (MESH:D045169), infectious (MESH:D003141), Hospital Infections (MESH:D003428), persistent (MESH:D000088562), diarrheal (MESH:D004403), reperfusion injury (MESH:D015427), death (MESH:D003643), enterococcal infections (MESH:D007239), gastrointestinal dysfunction (MESH:D005767), bacteremia (MESH:D016470), cough (MESH:D003371)
- **Chemicals:** vancomycin (MESH:D014640), carbapenem (MESH:D015780), lactate (MESH:D019344), urea nitrogen (MESH:C530477), creatinine (MESH:D003404), betwcontrol (-)
- **Species:** Pseudomonadota (proteobacteria, phylum) [taxon 1224], Enterococcus (genus) [taxon 1350], Enterobacter (genus) [taxon 547], Enterobacterales (order) [taxon 91347], Fungi (kingdom) [taxon 4751], Candida albicans (species) [taxon 5476], Pseudomonas aeruginosa (species) [taxon 287], Geobacillus sp. g (species) [taxon 422286], Lacticaseibacillus rhamnosus (species) [taxon 47715], S boulardii [taxon 252598], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Enterobacteriaceae (enterobacteria, family) [taxon 543], Enterococcus faecium (species) [taxon 1352], Homo sapiens (human, species) [taxon 9606], Candida [taxon 1535326]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12919443/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12919443/full.md

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Source: https://tomesphere.com/paper/PMC12919443