Study of adverse events in patients treated with linezolid and vancomycin (Retrospective study)
Not Applicable
- Conditions
- Bacterial infections
- Registration Number
- JPRN-UMIN000010759
- Lead Sponsor
- Sapporo Medical University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
Not provided
Exclusion Criteria
Patients had a treatment duration of less than 3 days, were discharged during treatment, or had missing clinical data. For the renal dysfunction aspect of the study, patients demonstrated end-stage renal failure or were undergoing hemodialysis. For the thrombocytopenia aspect of the study, patients developed disseminated intravascular coagulation or received a transfusion.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Occurrence rate of thrombocytopenia and renal dysfunction
- Secondary Outcome Measures
Name Time Method