Cefuroxime is a
second-generation cephalosporin with in vitro activity against the organisms that are commonly associated with neurosurgical
wound infections. Other properties of
cefuroxime are an elimination half-life of 1.3 hours, which yields prolonged serum concentrations, and its ability to penetrate the blood-brain barrier in proportion to the degree of
inflammation. A prospective, multicenter, open-label study was conducted to evaluate the efficacy and safety of
cefuroxime for
antibiotic prophylaxis in patients undergoing clean neurosurgery.
Cefuroxime 1.5 g was given intravenously 25 to 60 minutes before surgery; for procedures lasting more than 3 hours,
cefuroxime 750 mg was given intravenously 8 hours after the initial dose. Patients were examined before surgery, daily during hospitalization, and at 8 weeks after surgery. A total of 956 adults were enrolled in the study. The most common procedures in study patients were
laminectomy (41.8% of patients) or
craniotomy (24.3%), and the mean duration of surgery was 3.2 hours.
Infection occurred in 2 (0.3%) of 592 assessable patients by the time of discharge and in 1 additional patient by the 8-week follow-up evaluation for a total of 3 (0.5%) of 560 assessable patients.
Drug-related adverse events occurred in 5 (0.5%) of 956 patients. These results indicate that
antibiotic prophylaxis with
cefuroxime is associated with a low incidence of
postoperative wound infection and is well tolerated in patients undergoing clean neurosurgery.