abdominal distentionIncreased riskRR = 0.39, 95% CI: 0.26-0.59
abdominal distention (RR = 0.39, 95% CI: 0.26-0.59)
from: Effect of Saccharomyces boulardii supplementation to bismuth quadruple therapy on HelicobaconstipationIncreased riskRR = 0.32, 95% CI: 0.18-0.55
constipation (RR = 0.32, 95% CI: 0.18-0.55)
from: Effect of Saccharomyces boulardii supplementation to bismuth quadruple therapy on HelicobadiarrheaIncreased riskRR = 0.28, 95% CI: 0.22-0.36
Specifically, it reduced the incidence of some gastrointestinal adverse effects and nonspecific adverse effects, including diarrhea (RR = 0.28, 95% CI: 0.22-0.36)
from: Effect of Saccharomyces boulardii supplementation to bismuth quadruple therapy on HelicobanauseaIncreased riskRR = 0.59, 95% CI: 0.36-0.97
nausea (RR = 0.59, 95% CI: 0.36-0.97)
from: Effect of Saccharomyces boulardii supplementation to bismuth quadruple therapy on HelicobarashIncreased riskRR = 0.49, 95% CI: 0.28-0.86
rash (RR = 0.49, 95% CI: 0.28-0.86)
from: Effect of Saccharomyces boulardii supplementation to bismuth quadruple therapy on HelicobaOverall tolerabilityNo significant differenceThe H. pylori eradication rates of VAS and ECAB groups by intention-to-treat analysis were 87.3% and 88.9% (P = 1.000) and by per-protocol analysis were 87.3% and 91.8% (P = 0.560), respectively. The ECAB group had a significantly higher incidence of adverse events than the VAS group.
The ECAB group had a significantly higher incidence of adverse events than the VAS group.
from: Effectiveness and safety of vonoprazan and amoxicillin dual regimen with Saccharomyces bouOverall tolerabilityReported
The VAS group had a significantly lower incidence of adverse events than the ECAB group.
from: Effectiveness and safety of vonoprazan and amoxicillin dual regimen with Saccharomyces bouOverall tolerabilityReported
S. boulardii supplementation to bismuth quadruple therapy significantly improved H. pylori eradication rates (RR = 1.08, 95% CI: 1.04-1.12) and reduced the incidence of total adverse effects (RR = 0.53, 95% CI: 0.45-0.62).
from: Effect of Saccharomyces boulardii supplementation to bismuth quadruple therapy on HelicobaOverall tolerabilityReported
this approach demonstrated advantages in alleviating symptoms, exhibited favorable tolerance, and maintained a high level of clinical safety.
from: Saccharomyces boulardii combined with triple therapy alter the microbiota in the eradicatiadverse reactionsReported
Microbial composition, eradication rates, symptom alleviation, and adverse reactions were monitored on the 14th and 44th days post-treatment.
from: Saccharomyces boulardii combined with triple therapy alter the microbiota in the eradicatidiarrhoeaReportedRR = 0.46; 95% CI: 0.22-0.93; Z = 2.15; p = 0.03
pronounced reductions in diarrhoea (n = 2,091; RR = 0.46; 95% CI: 0.22-0.93; Z = 2.15; p = 0.03)
from: Efficacy and Safety of Saccharomyces Boulardii with Standard Quadruple Therapy for Eradicagastrointestinal side effectsReported
the combination of Saccharomyces boulardii powder with triple therapy displayed notable efficacy and smaller gastrointestinal side effects in eradicating initial H. pylori infections among non-ulcer dyspepsia patients.
from: Saccharomyces boulardii combined with triple therapy alter the microbiota in the eradicatirashReportedRR = 0.33; 95% CI: 0.14-0.77; Z = 2.55; p = 0.01
and rash occurrence (n = 1,271; RR = 0.33; 95% CI: 0.14-0.77; Z = 2.55; p = 0.01)
from: Efficacy and Safety of Saccharomyces Boulardii with Standard Quadruple Therapy for Eradicatreatment-related adverse eventsReportedRR = 0.46; 95% CI: 0.28-0.74; Z = 3.16; p = 0.002
the probiotic combination also substantially reduced treatment-related adverse events (n = 2,183; RR = 0.46; 95% CI: 0.28-0.74; Z = 3.16; p = 0.002)
from: Efficacy and Safety of Saccharomyces Boulardii with Standard Quadruple Therapy for Eradica