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Updated: May 30, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus (MRSA)
Published on: February 9, 2011
Increased mortality associated with methicillin-resistant Staphylococcus aureus (MRSA) infection in the intensive
Håkan Hanberger1, Sten Walther, Marc Leone
1Division of Infectious Diseases, Institution of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, Linköping, Sweden.
Abstract:
Controversy continues regarding whether the presence of meticillin resistance increases mortality risk in Staphylococcus aureus infections. In this study, we assessed the role of meticillin resistance in survival of patients with S. aureus infection included in the EPIC II point-prevalence study of infection in critically ill patients performed on 8 May 2007. Demographic, physiological, bacteriological and therapeutic data were collected for 13796 adult patients in 1265 participating Intensive Care Units (ICUs) from 75 countries on the study day. ICU and hospital outcomes were recorded. Characteristics of patients with meticillin-sensitive S. aureus (MSSA) and meticillin-resistant S. aureus (MRSA) infections were compared. Co-morbidities, age, Simplified Acute Physiology Score (SAPS) II, site of infection, geographical region and MRSA/MSSA were entered into a multivariate model, and adjusted odds ratios (ORs) [95% confidence interval (CI)] for ICU and hospital mortality rates were calculated. On the study day, 7087 (51%) of the 13796 patients were classified as infected. There were 494 patients with MRSA infections and 505 patients with MSSA infections. There were no significant differences between the two groups in use of mechanical ventilation or haemofiltration/haemodialysis. Cancer and chronic renal failure were more prevalent in MRSA than in MSSA patients. ICU mortality rates were 29.1% and 20.5%, respectively (P<0.01) and corresponding hospital mortality rates were 36.4% and 27.0% (P<0.01). Multivariate analysis of hospital mortality for MRSA infection showed an adjusted OR of 1.46 (95% CI 1.03-2.06) (P=0.03). In ICU patients, MRSA infection is therefore independently associated with an almost 50% higher likelihood of hospital death compared with MSSA infection.
Insights
Meticillin-resistant Staphylococcus aureus (MRSA) infections in intensive care units (ICUs) are linked to a higher risk of death. This study found MRSA significantly increases hospital mortality compared to meticillin-sensitive Staphylococcus aureus (MSSA).
Area of Science:
- Infectious Diseases
- Critical Care Medicine
- Microbiology
Background:
- Meticillin resistance in Staphylococcus aureus (S. aureus) infections raises concerns about patient mortality.
- The EPIC II study provided a large dataset on infections in critically ill patients worldwide.
Purpose of the Study:
- To determine if meticillin resistance in S. aureus infections increases mortality risk in intensive care unit (ICU) patients.
- To compare outcomes between patients with meticillin-sensitive S. aureus (MSSA) and meticillin-resistant S. aureus (MRSA) infections.
Main Methods:
- Analysis of data from the EPIC II point-prevalence study, including 13,796 adult patients across 1265 ICUs in 75 countries.
- Comparison of demographic, physiological, bacteriological, and therapeutic data between MRSA and MSSA infected patients.
- Multivariate analysis to calculate adjusted odds ratios for ICU and hospital mortality, controlling for co-morbidities, age, and disease severity (SAPS II).
Main Results:
- Of 7087 infected patients, 494 had MRSA and 505 had MSSA infections.
- MRSA patients had higher prevalence of cancer and chronic renal failure.
- MRSA infection was independently associated with a 46% increased likelihood of hospital death (OR 1.46, 95% CI 1.03-2.06, P=0.03) compared to MSSA.
Conclusions:
- Meticillin-resistant S. aureus (MRSA) infection is an independent risk factor for increased hospital mortality in critically ill patients.
- These findings highlight the significant impact of antibiotic resistance on patient outcomes in intensive care settings.
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