Does in situ replacement of a staphylococcal infected vascular graft with a rifampicin impregnated gelatin sealed Dacron graft reduce the incidence of subsequent infection?

Background The aim of this study was to treat methicillin-resistant Staphyl ococcus aureus (MRSA) or S. epidermidis prosthetic vascular graft infection s by in situ replacement with a rifampicin bonded Gelsoft graft. Methods. Interposition grafts were placed in the carotid artery of 56 sheep and the graft surface directly inoculated with 10(8) colony forming units of MRSA or S. epidermidis. At three weeks, grafts were harvested and sheep allocated to three groups. In the MRSA group, sheep received grafts soaked in 1.2 mg/ml (12), 10 mg/ml (10) and no rifampicin (7). For S. epidermidis, sheep received grafts soaked in 1.2 mg/ml (10), 10 mg/ml (9) and no rifamp icin (8). There were two deaths, in the MRSA study group. Remaining sheep w ere euthanased and grafts harvested three weeks following regrafting. Swabs were taken to assess bacterial growth in the perigraft tissues, and extern al and internal graft surfaces. A 3-5 mm segment of graft tvas incubated in broth medium. Results. For MRSA, no statistical difference between the groups was reached for any of the measured parameters. For S. epidermidis, a significant redu ction was reached for total infected specimens in the 10 mg/ml group compar ed to both control (p<0.001) and 1.2 mg/ml (p<0.005) groups. Graft re-infec tion was also less likely to occur with S. epidermidis than MRSA. Conclusions. Replacement of S. epidermidis infected vascular grafts with 10 mg/ml rifampicin soaked Gelsoft graft is effective in reducing subsequent S. epidermidis infection. This conclusion cannot be extended to MRSA infect ed vascular grafts.