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Published on: February 9, 2011
Staphylococcus aureus nasal carriage in children receiving long-term peritoneal dialysis
1Children's Mercy Hospital, Kansas City, Missouri, USA.
Insights
Staphylococcus aureus nasal carriage is common in children on peritoneal dialysis and linked to exit-site infections. Mupirocin treatment may minimize peritonitis risk, but carriage risk increases with dialysis duration.
Area of Science:
- Pediatric Nephrology
- Infectious Diseases
- Clinical Microbiology
Background:
- Staphylococcus aureus (SA) nasal carriage prevalence and effects of antibiotic therapy are unclear in pediatric peritoneal dialysis (PD) patients.
- Understanding these factors is crucial for managing infections in this vulnerable population.
Purpose of the Study:
- To determine the frequency of SA nasal carriage in children undergoing long-term PD.
- To assess the impact of SA nasal carriage and intranasal mupirocin treatment on exit-site infections (ESI) and peritonitis.
Main Methods:
- Prospective study of 21 children on PD, with nasal cultures for SA every 4-12 weeks.
- SA nasal carriage (NSA+) was treated with 7-day intranasal mupirocin.
- Infection rates (ESI, peritonitis) were compared between SA-positive (NSA+) and SA-negative (NSA-) patients.
Main Results:
- SA nasal carriage (NSA+) was detected in 61.9% of patients.
- NSA+ patients had a higher incidence of SA exit-site infections (ESI) (0.42 infections/patient-year) compared to NSA- patients (0 infections/patient-year).
- The incidence of non-SA infections did not differ between groups; SA peritonitis risk appeared minimal with mupirocin treatment.
Conclusions:
- SA nasal carriage is associated with SA exit-site infections in children on PD.
- Intranasal mupirocin may reduce the risk of SA peritonitis.
- The likelihood of SA nasal carriage may increase with longer duration of PD treatment.
Abstract:
The frequency of Staphylococcus aureus (SA) nasal carriage and the impact of antibiotic therapy remain undefined in children receiving long-term peritoneal dialysis (PD). We obtained a nasal culture for SA every 4-12 weeks in 21 children (mean age 7.03 +/- 5.8 years) receiving PD from January 1992 to August 1996 (total of 35.3 patient-years). In each case, SA nasal carriage (NSA+) was treated with intranasal mupirocin for 7 days. NSA+ was detected in 13 patients (61.9%) who received dialysis for 28.9 patient-years. Eight (61.5%) of 13 patients became NSA+ during the initial 3 months of dialysis. Seven (53.8%) of the NSA+ patients had 11 exit-site infections (ESI) and one episode of peritonitis (0.42 total infections/patient-year) due to SA. The 8 patients without SA nasal carriage (NSA-) received dialysis for 6.4 patient-years. None of the NSA-patients had an ESI or peritonitis with SA. Finally, the incidence of non-SA infections in the NSA+ and NSA- groups was not different (0.62 vs 0.31 total infections/patient-year, p > 0.05). In conclusion, there appears to be an association between SA nasal carriage and SA ESI in children on PD. The risk of SA peritonitis in NSA+ patients treated with mupirocin may be minimal. The risk of SA nasal carriage may increase with time on dialysis.
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