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Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Methicillin-Resistant Staphylococcus aureus Carriage in Hemodialysis Vicinity: Prevalence and Decolonization Approach
Khaled M A Elzorkany1, Asmaa M Elbrolosy2, Eman H Salem2
1Nephrology Unit, Department of Internal Medicine, Faculty of Medicine, Menoufia University, Menoufia, Egypt.
Abstract:
Hemodialysis (HD) patients are at risk for developing serious infections. Methicillin- resistant Staphylococcus aureus (MRSA) is one of the most prevalent pathogens in healthcare facilities with a major threat to the medical community. We aimed to determine the prevalence of MRSA colonization among patients and medical staff members in a HD Unit and determine efficacy of mupirocin as a decolonizing agent. This cross-sectional study enrolled 250 patients and 35 health care providers of a HD unit. Nasal and hand swabs were collected to assess the prevalence of MRSA carriage. Those exhibiting MRSA phenotype were subjected to conventional Polymerase chain reaction (PCR) assay for detection of mecA gene. Colonized patients and medical personnel with MRSA were prescribed mupirocin ointment (2%) for decolonization. The screening approach identified 54/285 (18.9%) nasal MRSA carriers (41/250 of HD patients and 13/35 of the medical staff members). Concomitant extranasal MRSA colonization of the hands was observed in 10 (18.5%) of these 54 MRSA carriers. In relation to PCR results the sensitivity, specificity, and diagnostic accuracy of cefoxitin disk test were 98.2%, 75%, and 93.9% respectively and for MRSA Select II agar screening method, the sensitivity, specificity, and diagnostic accuracy were 92.6%, 66.7%, and 87.9% respectively. Decolonization approach using mupirocin ointment revealed an overall success rate up to 77.8% (42/54) and failure rate of 16.7% (9/54), while 5.6% (3/54) of decolonized carriers showed recolonization. There is still high prevalence of MRSA colonization in HD vicinity. Implementation of strict infection control measures is essential in dialysis units to avoid MRSA cross-transmission and invasive infections.
Insights
Methicillin-resistant Staphylococcus aureus (MRSA) nasal colonization is prevalent in 18.9% of hemodialysis patients and staff. Mupirocin decolonization achieved a 77.8% success rate, highlighting the need for infection control in dialysis units.
Area of Science:
- Infectious Diseases
- Microbiology
- Public Health
Background:
- Hemodialysis (HD) patients face significant infection risks, with Methicillin-resistant Staphylococcus aureus (MRSA) being a major healthcare-associated pathogen.
- MRSA poses a substantial threat to healthcare facilities, particularly impacting vulnerable patient populations like those undergoing dialysis.
Purpose of the Study:
- To determine the prevalence of MRSA colonization among patients and healthcare providers in a hemodialysis unit.
- To evaluate the efficacy of mupirocin as a decolonizing agent for MRSA carriers within the HD setting.
Main Methods:
- A cross-sectional study involving 250 HD patients and 35 healthcare providers.
- Collection of nasal and hand swabs for MRSA carriage assessment, with Polymerase Chain Reaction (PCR) for mecA gene detection.
- Evaluation of cefoxitin disk test and MRSA Select II agar screening methods, followed by mupirocin treatment for colonized individuals.
Main Results:
- MRSA nasal colonization was identified in 18.9% (54/285) of individuals (41 patients, 13 staff).
- Extranasal colonization (hands) was found in 18.5% of nasal carriers. Cefoxitin disk test showed 98.2% sensitivity and 93.9% accuracy.
- Mupirocin decolonization had a 77.8% success rate, with a 16.7% failure rate and 5.6% recolonization.
Conclusions:
- A high prevalence of MRSA colonization persists in hemodialysis units, posing a continuous risk.
- Mupirocin demonstrates significant efficacy in decolonizing MRSA carriers, though recolonization can occur.
- Strict infection control measures are crucial in dialysis units to prevent MRSA transmission and subsequent invasive infections.
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