Article ID Journal Published Year Pages File Type
3373256 Journal of Hospital Infection 2008 8 Pages PDF
Abstract

SummaryPrevalence of hospital-acquired meticillin-resistant Staphylococcus aureus (MRSA) infection or colonisation has been associated with antimicrobial consumption. The impact of antibiotic treatment on nasal colonisation is unknown. We conducted a three-month prospective study of 116 patients with extranasal MRSA infection or colonisation, whose nasal MRSA bacterial loads were determined during and after various antibiotic courses over a period of three weeks. Environmental swabs were also taken from the near patient environment. Concomitant nasal MRSA carriage was observed in 76.7% of extranasal MRSA-colonised or -infected patients. The median nasal MRSA bacterial load increased significantly from 2.78 (range 0–6.15) to 5.30 (range 2.90–8.41) log10 cfu per swab (cfu/swab) (P < 0.001) over 21 days during β-lactam therapy. It also increased from 0 (range 0–4.00) to 4.30 (range 0–7.46) log10 cfu/swab (P = 0.039) over 14 days during fluoroquinolone therapy. Median bacterial loads were significantly higher for β-lactam- and fluoroquinolone-treated patients on day 7 [4.78, range 0–7.30], day 14 [4.30, range 0–7.60] and day 21 [5.30, range 2.90–8.41] than controls not receiving antibiotics (P < 0.05). These loads then decreased by 2–5 log10 cfu/swab 2 weeks after discontinuation of antibiotics. The environment of patients receiving β-lactam agents (relative risk: 3.55; 95% confidence interval: 1.30–9.62; P = 0.018) or fluoroquinolones (4.32; 1.52–12.31; P = 0.008) demonstrated more MRSA contamination than the environment around control patients (0.79; 0.67–0.93; P = 0.002). Patients on β-lactam or fluoroquinolone therapy have increased incidence of MRSA colonisation and higher nasal bacterial loads, and appear to spread their MRSA into the near patient environment.

Related Topics
Life Sciences Immunology and Microbiology Applied Microbiology and Biotechnology
Authors
, , , , , , , , , ,