“…The SSI rate in patients receiving antimicrobial prophylaxis undergoing spinal procedures with instrumentation has ranged from 2.8% to 9.7%. 165,764,765,769,770 Monosegmental instrumentation has a reported SSI rate of <2%, compared with 6.7% for instrumentation at multiple levels. 771 Several case-control studies of adults undergoing spinal procedures with and without instrumentation have found the following notable patient-related risk factors for SSI: prolonged preoperative hospitalization, 771 [770][771][772][773][774][775]777 Procedure-related risk factors include extended duration of procedure (defined in studies as two to five hours or greater than five hours, 775 greater than three hours, 771 and greater than five hours 776 ), excessive blood loss (>1 L), 771,775 staged procedure, 776 multilevel fusions, 777 foreign-body placement (e.g., screw, rod, plate), 767 combined anterior and posterior fusion, 776 and suboptimal antimicrobial timing (>60 minutes before or after incision).…”