A multicenter, prospective observational study for severe sepsis induced by Streptococcus pneumoniae, beta-hemolytic streptococci, and Staphylococcus aureus
Not Applicable
- Conditions
- S. pneumonia, beta-hemolytic streptococci, and S. aureus-induced severe sepsis
- Registration Number
- JPRN-UMIN000019702
- Lead Sponsor
- Japanese Association for Acute Medicine
- Brief Summary
62 were included in the current study (29 cases with S. pneumoniae sepsis and 33 with BHS). The CCI and completion of a 3-h bundle did not differ between normal and high virulence groups. Risk of 28-day mortality was significantly higher for high-virulence compared to normal-virulence when adjusted for CCI and completion of a 3-h bundle (Cox proportional hazards regression analysis, hazard ratio 3.848; 95% confidence interval, 1.108-13.370; P = 0.034).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 62
Inclusion Criteria
Not provided
Exclusion Criteria
None
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method