Effect of Antibiotic Prophylaxis on Surgical Site Infections Following Removal of Orthopedic Implants Used for Treatment of Foot, Ankle, and Lower Leg Fractures: A Randomized Clinical Trial.

Trauma Unit, Department of Surgery, Academic Medical Center Amsterdam, the Netherlands. Clinical Research Unit, Academic Medical Center, Amsterdam, the Netherlands. Department of Surgery, Onze Lieve Vrouwe Gasthuis East Amsterdam, the Netherlands. Department of Surgery, Flevo Hospital, Almere, the Netherlands. Department of Surgery, Haaglanden Medical Center Den Haag, the Netherlands. Department of Surgery, Medical Center Alkmaar Alkmaar, the Netherlands. Department of Surgery, Alrijne Hospital Leiderdorp, the Netherlands. Department of Surgery, Deventer Hospital Deventer, the Netherlands. Department of Surgery, Catharina Hospital Eindhoven, the Netherlands. Department of Surgery, Spaarne Gasthuis Hoofddorp, the Netherlands. Department of Microbiology, Academic Medical Center Amsterdam, the Netherlands. Department of Surgery, BovenIJ Hospital Amsterdam, the Netherlands. Department of Surgery, Onze Lieve Vrouwe Gasthuis West Amsterdam, the Netherlands. Department of Surgery, Spaarne Gasthuis Haarlem, the Netherlands. Department of Surgery, Amphia Hospital Breda, the Netherlands. Department of Surgery, Westfries Gasthuis Hoorn, the Netherlands.

JAMA. 2017;(24):2438-2445

Abstract

IMPORTANCE Following clean (class I, not contaminated) surgical procedures, the rate of surgical site infection (SSI) should be less than approximately 2%. However, an infection rate of 12.2% has been reported following removal of orthopedic implants used for treatment of fractures below the knee. OBJECTIVE To evaluate the effect of a single dose of preoperative antibiotic prophylaxis on the incidence of SSIs following removal of orthopedic implants used for treatment of fractures below the knee. DESIGN, SETTING, AND PARTICIPANTS Multicenter, double-blind, randomized clinical trial including 500 patients aged 18 to 75 years with previous surgical treatment for fractures below the knee who were undergoing removal of orthopedic implants from 19 hospitals (17 teaching and 2 academic) in the Netherlands (November 2014-September 2016), with a follow-up of 6 months (final follow-up, March 28, 2017). Exclusion criteria were an active infection or fistula, antibiotic treatment, reimplantation of osteosynthesis material in the same session, allergy for cephalosporins, known kidney disease, immunosuppressant use, or pregnancy. INTERVENTIONS A single preoperative intravenous dose of 1000 mg of cefazolin (cefazolin group, n = 228) or sodium chloride (0.9%; saline group, n = 242). MAIN OUTCOMES AND MEASURES Primary outcome was SSI within 30 days as measured by the criteria from the US Centers for Disease Control and Prevention. Secondary outcome measures were functional outcome, health-related quality of life, and patient satisfaction. RESULTS Among 477 randomized patients (mean age, 44 years [SD, 15]; women, 274 [57%]; median time from orthopedic implant placement, 11 months [interquartile range, 7-16]), 470 patients completed the study. Sixty-six patients developed an SSI (14.0%): 30 patients (13.2%) in the cefazolin group vs 36 in the saline group (14.9%) (absolute risk difference, -1.7 [95% CI, -8.0 to 4.6], P = .60). CONCLUSIONS AND RELEVANCE Among patients undergoing surgery for removal of orthopedic implants used for treatment of fractures below the knee, a single preoperative dose of intravenous cefazolin compared with saline did not reduce the risk of surgical site infection within 30 days following implant removal. TRIAL REGISTRATION clinicaltrials.gov Identifier: NCT02225821.

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