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Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus (MRSA)
Published on: February 9, 2011
Antimicrobial susceptibility of Staphylococcus aureus in children with atopic dermatitis
Ching-Shen Tang1, Chih-Chien Wang, Ching-Feng Huang
1Department of Pediatrics, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Insights
Staphylococcus aureus (S. aureus) nasal carriage and skin infections in children with atopic dermatitis (AD) are common. High rates of methicillin-resistant S. aureus (MRSA) and multi-drug resistance necessitate careful antibiotic selection for effective treatment.
Area of Science:
- Pediatric Dermatology
- Infectious Diseases
- Clinical Microbiology
Background:
- Atopic dermatitis (AD) in children increases risk for Staphylococcus aureus (S. aureus) skin infections and nasal carriage.
- S. aureus colonization and infection can exacerbate AD and lead to recurrent infections.
Purpose of the Study:
- To evaluate antibiotic susceptibilities of S. aureus strains in children with AD.
- To determine optimal antibiotic choices for treating S. aureus in this population.
Main Methods:
- Nasal swabs collected from 168 healthy children with AD and 20 AD children with skin and soft-tissue infections (SSTI).
- S. aureus strains analyzed for antibiotic susceptibilities and prevalence of methicillin-resistant S. aureus (MRSA).
Main Results:
- High prevalence of S. aureus colonization (46.4%) and MRSA (30.8%) in healthy AD children.
- MRSA identified in 60% of SSTI-causing strains.
- High resistance rates to erythromycin; all strains susceptible to vancomycin, rifampin, and mupirocin.
- Multi-drug resistance observed in 70% of colonizing and 50% of SSTI strains; inducible clindamycin resistance common.
Conclusions:
- S. aureus strains from children with AD exhibit significant MRSA and multi-drug resistance.
- Trimethoprim-sulfamethoxazole, rifampin, fusidic acid, and mupirocin are recommended for S. aureus treatment and decolonization in AD patients.
Background:
Skin infection and/or nasal carriage of Staphylococcus aureus in children with atopic dermatitis (AD) is a risk factor for exacerbating disease or subsequent recurrent S. aureus infection. The purpose of the study is to evaluate the antibiotic susceptibilities of S. aureus strains from AD children and determine the most appropriate choice of antibiotics.
Methods:
Nasal swabs from 168 healthy children with AD and 20 AD children with concurrent skin and soft-tissue infections (SSTI) were collected in 2005-2008. S. aureus strains were further analyzed for and compared with antibiotic susceptibilities.
Results:
There were 78 (46.4%) healthy children with AD colonized with S. aureus, and 24 (30.8%) were methicillin-resistant S. aureus (MRSA). Among the 20 SSTI-infecting strains, 12 (60%) were MRSA. Antimicrobial susceptibility testing showed that, after penicillin, colonizing and SSTI-infecting strains had the highest rates of resistance to erythromycin (50% and 70%, respectively). All isolated strains were susceptible to vancomycin, rifampin, and mupirocin. Multi-drug resistance was found in 70% of the colonizing and 50% of the SSTI-infecting strains. D-test assay revealed inducible clindamycin resistance in 75% of the colonizing strains. The most prevalent resistance gene was ermB which was present in 94.9% and 92.9% of colonizing and SSTI-infecting strains, respectively.
Conclusions:
This study found that colonizing and SSTI-infecting strains of S. aureus from AD children had a high prevalence of MRSA and multi-drug resistance. Trimethoprim-sulfamethoxazole, rifampin, fusidic acid and mupirocin appear to be more suitable for treatment and decolonization of S. aureus in AD children.
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