Open Fractures, Prophylactic Antibiotic Use in — Update

Published 2011
Citation: J Trauma. 70 (3): 751-4, Mar 2011



Hoff, William S. MD, FACS; Bonadies, John A. MD, FACS; Cachecho, Riad MD, FACS, FCCP; Dorlac, Warren C. MD, FACS

Author Information

From the Division of Trauma (W.S.H.), St. Luke's Hospital, Bethlehem, Pennsylvania; Department of Surgery (J.A.B.), Hospital of St. Raphael, New Haven, Connecticut; Divison of Trauma (R.C.), Crozer Chester Medical Center, Upland, Pennsylvania; Department of Surgery (W.C.D.), University of Cincinnati, Cincinnati, Ohio.

Submitted for publication July 28, 2009

Accepted for publication November 29, 2010.

Presented at the 21st Annual Assembly of the Eastern Association for the Surgery of Trauma, January 19, 2008, Jacksonville, Florida.

Statement of the Problem

An open fracture is defined as one in which the fracture fragments communicate with the environment through a break in the skin. The presence of an open fracture either isolated or as part of a multiple injury complex increases the risk of infection and soft tissue complications. In 1976, Gustilo and Anderson[1] described a system to classify open fractures based on the size of the associated laceration, the degree of soft issue injury, contamination, and presence of vascular compromise. In a subsequent article, Gustilo et al.[2] refined the classification of severe open fractures. In general, risk of infection and incidence of limb loss correlate with the Gustilo type (Table 1).


By using a search methodology similar to Luchette et al.,[3] a MEDLINE search was performed using the key words “open fractures” and “antibiotics.” This search was limited to articles published subsequent to the guidelines published by Luchette et al. This search yielded a total of 49 articles. Sixteen articles were excluded for the following reasons: technical article (6), non-English publication (5), insufficient contribution to the project (2), involved nonextremity fractures (2), and animal study (1). Thirteen secondary citations were obtained from bibliographies in the initial articles yielding 46 articles, which were reviewed by the subcommittee.

Each article was reviewed and classified based on methodology described by the EAST Ad Hoc Committee on Guidelines Development and the Agency for Healthcare Policy and Research of the US Department of Health and Human Services as follows[4][5]:

Class I: prospective, randomized controlled study.

Class II: prospective, randomized, nonblinded trials. That is, studies in which data were prospectively collected and analyzed retrospectively.

Class III: studies based on retrospectively collected data, database and registry reviews, and meta-analysis.

For purposes of this practice management guideline, review articles were classified as class III. Reviewers also determined whether the respective article was relevant to the purpose of the practice management guidelines. Nineteen studies were determined to be nonrelevant and were excluded from further analysis; nonrelevance was based on the following: poor methodology (11), inadequate study size (6), and irrelevant purpose (2).

The remaining 27 articles were used to construct an evidentiary table, which was analyzed to make final recommendations. Recommendations were classified based on the quality of scientific evidence available:

Level I: recommendation is justifiable based on the available scientific evidence alone; recommendation is based on class I or a preponderance of class II evidence.

Level II: recommendation is reasonably justifiable based on the available scientific evidence and supported by expert opinion; recommendation is supported by class II evidence or a preponderance of class III evidence.

Level III: recommendation is supported by available data, but inadequate scientific data are available; recommendation is supported by class III evidence.


Level I

  • Systemic antibiotic coverage directed at gram-positive organisms should be initiated as soon as possible after injury.
  • Additional gram-negative coverage should be added for type III fractures.
  • High-dose penicillin should be added in the presence of fecal or potential clostridial contamination (e.g., farm-related injuries).
  • Fluoroquinolones offer no advantage compared with cephalosporin/aminoglycoside regimens. Moreover, these agents may have a detrimental effect on fracture healing and may result in higher infection rates in type III open fractures.

Level II

  • In type III fractures, antibiotics should be continued for 72 hours after injury or not >24 hours after soft tissue coverage has been achieved.
  • Once-daily aminoglycoside dosing is safe and effective for types II and III fractures.

Scientific Foundation

In 1998, Luchette et al.[3] presented the results of the EAST Practice Management Guidelines Workgroup at the 11th Annual Scientific Assembly. These guidelines were published in 2000 on the EAST Web site. Based on a review of 54 articles published from 1975 to 1997, the workgroup offered three level I and two level II recommendations specific to choice of antibiotic coverage and duration of therapy. The original guidelines recommend preoperative dosing with antibiotics as soon as possible after the injury has been sustained. Antibiotics should be directed at gram-positive organisms with additional gram-negative coverage for type III fractures. In the presence of potential clostridial contamination, penicillin should also be initiated irrespective of fracture type.

With regard to duration of antibiotic coverage, the original guidelines recommend that antibiotics be discontinued 24 hours after successful wound closure for type I and type II fractures. For type III fractures, antibiotics should be continued for 72 hours subsequent to the injury or not >24 hours subsequent to successful soft tissue coverage of the wound.

In 1999, DeLong et al.[6] published a case series designed to compare rates of infection as well as delayed union and nonunion in patients with open fractures based on the type of wound closure performed. Ninety patients with 119 open fractures were reviewed. All patients received cefazolin plus gentamicin if severe contamination was identified. Antibiotics were discontinued 2 days to 3 days after the last surgical procedure. By using this antibiotic regimen, the rate of deep wound infection or osteomyelitis was 7% irrespective of the wound management technique. In a prospective study of 227 patients with open fractures, Vasenius et al. compared clindamycin with cloxacillin. Clindamycin was demonstrated to be effective in type I and type II fractures with infection rates of 3.3% and 1.8%, respectively. Unacceptably high rates of infection were reported in grade III fractures for both clindamycin (29.0%) and cloxacillin (51.8%). This study demonstrates the efficacy of gram-positive coverage for types I and II fractures and confirms the need for additional gram-negative coverage in higher Gustilo type fractures.[7]

In a study of pediatric patients with open forearm fractures, Greenbaum et al.[8] reported a 3% incidence of wound infections using an antibiotic regimen similar to that recommended by the original EAST guidelines. In a retrospective study by Yang and Eisler,[9] 91 patients with grade I open fractures received cefazolin. Initial surgical debridement was not performed on an emergent basis, and no infectious complications were documented in the study cohort.

Citing several advantages of fluoroquinolones (e.g., oral administration, less nephrotoxicity), Patzakis et al. performed a prospective study of intravenous ciprofloxacin in 163 patients with 171 open fractures: type I (65), type II (54), and type III (52). Patients were randomized to an antibiotic regimen of ciprofloxacin or ceftazadime/gentamicin. In types I and II fractures, the infection rate for the ciprofloxacin group and the ceftazadime/gentamicin group was 5.8% and 6.0%, respectively. For type III fractures, an unacceptably high rate of infection was demonstrated in the ciprofloxacin group (31%) compared with the ceftazadime/gentamicin group (7.7%).[10] In response to a clinical observation that delayed union and nonunion were associated with ciprofloxacin, Huddleston et al. published a laboratory investigation of the effect of this fluoroquinolone on fracture healing. Wistar rats with experimentally induced femur fractures were randomized to receive cefazolin and ciprofloxacin. A third group that received no antibiotics was used as a control group. Radiographic, histologic, and mechanical parameters all demonstrated inhibition of fracture healing in the ciprofloxacin group.[11] Similarly, using a murine model, Holtom et al.[12] demonstrated a dose-dependent cytotoxic effect of fluoroquinolones.

In 1999, Sorger et al. published a study comparing the efficacy of once-daily dosing of aminoglycosides with the traditional divided-dose regimen. Two hundred nineteen patients with type II or type III open fractures all received standard surgical treatment of their fractures. All patients received cefazolin but were randomized to receive gentamicin in divided-dose regimen (5 mg/kg divided twice daily) or once-daily (6 mg/kg). Although a statistical difference could not be demonstrated, infection rate in the once-daily patients was lower than in the patients receiving divided dose (6.7% vs. 13.6%).[13] In a preliminary study, Russel et al.[14] demonstrated safety and efficacy of once-daily aminoglycoside dosing in conjunction with cefazolin in the treatment of 16 patients with open tibia fractures.


Based on a review of the literature published subsequent to their original presentation, the recommendations published in the original EAST guidelines remain valid. Antibiotics are an important adjunct to the management of open fractures and should be initiated as soon as possible. Gram-positive coverage is recommended for type I and type II fractures. Broader antimicrobial coverage is recommended for type III fractures.

Despite the potential clinical and resource advantages of fluoroquinolones, current research does not support their use as single-agent therapy, and studies suggest these agents may impair fracture healing. When required, aminoglycosides may be prescribed in a once-daily regimen.

Future Investigation

The available class I literature on fluoroquinolones has several limitations. Not all studies used an open fracture model. In addition, as these were animal studies, dosages and duration of therapy may not be equivalent to that which may be used clinically. Therefore, given the significant advantages of this class of antibiotics over aminoglycosides, research should continue in an effort to demonstrate efficacy in a clinical model. The systemic side effects of antibiotics may also be reduced through the use of local antibiotic therapy. Future research should also consider the use of this modality in the acute phase of open fracture management.


  1. Gustilo RB, Anderson JT. Prevention of infection in the treatment of 1025 open fractures of long bones: retrospective and prospective analyses. J Bone Joint Surg Am. 1976;58:453–458.
  2. Gustilo RB, Mendoza RM, Williams DN. Problems in the management of type III (severe) open fractures: a new classification of type III open fractures. J Trauma. 1984;24:742–746.
  3. Luchette FA, Bone LB, Born CT, et al. EAST Practice Management Guidelines Workgroup: practice management guidelines for prophylactic antibiotic use in open fractures. Eastern Association for the Surgery of Trauma. 2000. Available at: Accessed November 15, 2009.
  4. Pasquale M, Fabian TC. Practice management guidelines for trauma from the Eastern Association for the Surgery of Trauma. J Trauma. 1998;44:941–956.
  5. Agency for Health Care Policy and Research. Interim Manual for Clinical Practice Guideline Development. Rockville, MD: Agency for Health Care Policy and Research; 1991.
  6. DeLong WG Jr, Born CT, Wei SY, Petrik ME, Ponzio R, Schwab CW. Aggressive treatment of 119 open fracture wounds. J Trauma. 1999;46:1049–1054.
  7. Vasenius J, Tulikoura I, Vainionpää S, Rokkanen P. Clindamycin versus cloxacillin in the treatment of 240 open fractures. A randomized prospective study. Ann Chir Gynaecol. 1998;87:224–228.
  8. Greenbaum B, Zionts LE, Ebramzadeh E. Open fractures of the forearm in children. J Orthop Trauma. 2001;15:111–118.
  9. Yang EC, Eisler J. Treatment of isolated type I open fractures: is emergent operative debridement necessary? Clin Orthop Relat Res. 2003;410:269–294.
  10. Patzakis MJ, Bains RS, Lee J, et al. Prospective, randomized, double-blind study comparing single-agent antibiotic therapy, ciprofloxacin, to combination antibiotic therapy in open fracture wounds. J Orthop Trauma. 2000;14:529–533.
  11. Huddleston PM, Steckelberg JM, Hanssen AD, Rouse MS, Bolander ME, Patel R. Ciprofloxacin inhibition of experimental fracture healing. J Bone Joint Surg Am. 2000;82:161–173.
  12. Holtom PD, Pavkovic SA, Bravos PD, Patzakis MJ, Shepherd LE, Frenkel B. Inhibitory effects of the quinolone antibiotics trovafloxacin, ciprofloxacin, and levofloxacin on osteoblastic cells in vitro. J Orthop Res. 2000;18:721–727.
  13. Sorger JI, Kirk PG, Ruhnke CJ, et al. Once daily, high dose versus divided low dose gentamicin for open fractures. Clin Orthop Relat Res. 1999;366:197–204.
  14. Russel GV Jr, King C, May CG, Pearsall AW IV. Once daily high-dose gentamicin to prevent infection in open fractures of the tibial shaft: a preliminary investigation. South Med J. 2001;94:1185–1191.

Previous version of this guideline

Open Fractures Prophylactic Antibiotics (1998)


Open Fractures—Gustilo Classification[1-2]

Type I

Open fracture with a skin wound <1 cm in length and clean.

Type II

Open fracture with a laceration >1 cm in length without extensive soft tissue damage, flaps, or avulsions.

Type III




Open segmental fracture with >10 cm wound with extensive soft tissue injury or a traumatic amputation (special categories in Type III include gunshot fractures and open fractures caused by farm injuries).

Adequate soft tissue coverage.

Significant soft tissue loss with exposed bone that requires soft tissue transfer to achieve coverage.

Associated vascular injury that requires repair for limb preservation.

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