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Updated: Feb 6, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Clinical outcomes after initial treatment of methicillin-resistant Staphylococcus aureus infections
Nobuaki Shime1,2, Nobuyuki Saito3, Miya Bokui4
1Department of Emergency and Critical Care Medicine, Graduate School of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan, shime@koto.kpu-m.ac.jp.
Objective:
To evaluate the clinical outcomes associated with anti-methicillin-resistant Staphylococcus aureus (MRSA) antimicrobials.
Methods:
We reviewed a prospective database of 247 consecutive patients with clinically and microbiologically confirmed MRSA infections, hospitalized in 7 Japanese hospitals between April 2014 and March 2015, and treated with anti-MRSA pharmaceuticals. Survival was measured at 30 days. We examined the relationships between initial antimicrobial administered and survival and organ toxicity. HR and 95% CIs were calculated.
Results:
Overall 30-day mortality was 12%. The lungs were infected in 105 (41%), skin and soft tissue in 73 (30%), and bones and joints in 21 (9%) patients. Bacteremia complicated the illness in 69 patients (28%). Among 5 pharmaceuticals, vancomycin was prescribed to 174 (71%), linezolid to 38 (16%), teicoplanin to 22 (9%), and daptomycin to 11 (5%) patients. Vancomycin tended to be associated with the lowest survival (HR=2.47; 95% CI=0.93-6.51; P=0.067), particularly in the lung-infected subgroup (HR=4.85; 95% CI=1.12-20.94; P=0.034) after adjustments for baseline illness severity. The incidence of renal dysfunction tended to be higher in patients with trough serum concentrations of vancomycin >15 mg/dL.
Conclusion:
In this observational study reflecting real-world conditions, vancomycin was associated with higher 30-day mortality and incidence of kidney dysfunction than other anti-MRSA agents. The significance of the differences observed among antimicrobials other than vancomycin is uncertain.
Insights
Vancomycin use in methicillin-resistant Staphylococcus aureus (MRSA) infections was linked to increased 30-day mortality and kidney dysfunction compared to other anti-MRSA drugs. Further research is needed for other agents.
Area of Science:
- Infectious Diseases
- Pharmacology
- Clinical Medicine
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) is a significant cause of hospital-acquired infections.
- Effective antimicrobial therapy is crucial for managing MRSA infections and improving patient outcomes.
Purpose of the Study:
- To evaluate the clinical outcomes, including survival and organ toxicity, associated with different anti-MRSA antimicrobials.
- To compare the efficacy and safety of vancomycin, linezolid, teicoplanin, and daptomycin in treating MRSA infections.
Main Methods:
- Prospective database review of 247 patients with confirmed MRSA infections across 7 Japanese hospitals (April 2014 - March 2015).
- Analysis of 30-day mortality, organ toxicity (specifically renal dysfunction), and initial antimicrobial treatment.
- Calculation of Hazard Ratios (HR) and 95% Confidence Intervals (CIs) to assess treatment associations.
Main Results:
- Overall 30-day mortality was 12%. Common infection sites included lungs (41%), skin/soft tissue (30%), and bones/joints (9%). Bacteremia occurred in 28% of patients.
- Vancomycin, used in 71% of patients, was associated with lower survival (HR=2.47) and higher mortality in lung infections (HR=4.85) compared to other agents.
- Higher incidence of renal dysfunction was observed with vancomycin trough serum concentrations >15 mg/dL.
Conclusions:
- In real-world settings, vancomycin demonstrated a trend towards higher 30-day mortality and increased renal dysfunction compared to other anti-MRSA agents.
- The observed differences among antimicrobials other than vancomycin require further investigation to determine their clinical significance.
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