Tobramycin Injection to Prevent Infection in Open Fractures

Purpose

The goal of open extremity fracture (OEF) treatment is to promote fracture healing and restore function while preventing the development of infection. This is achieved through systematic and timely wound debridement and irrigation, fracture stabilization, tetanus prophylaxis, systemic and local antimicrobial therapy, and judicious timing of wound closure based on cleanliness. Early prophylactic systemic antibiotics lower infection rates in open fractures but have limitations of achieving adequate concentration at the hypoperfused wound area. OEF wounds are frequently poor in vasculature secondary to the soft tissue injury, hence adequate concentration of antibiotic cannot permeate to the tissue at risk. If systemic antibiotic concentrations are increased to achieve minimum inhibitory concentration (MIC) for pathogens at the wound, there is heightened concern for systemic drug toxicity. In sharp contrast, locally administered antibiotics achieve high drug concentration directly within the wound cavity with minimal systemic side effects. Local antibiotic therapy has shown to reduce rates of open fracture wound infection. With the serious implications of postoperative infections in OEF, it is imperative that all measures including further use of prophylactic local antibiotics be considered to prevent fracture-related infection (FRI). The overarching hypothesis for this project is that a novel synergistic combination of local aqueous tobramycin plus perioperative weight-based IV cephalosporin antibiotic prophylaxis will reduce the rate of FRI one year after OEF surgery. This in turn will improve OEF patient outcomes, decreasing morbidity and return to the operating room (OR) without any adverse effect on fracture healing. Regardless of the treatment group, bacterial speciation will be determined for patients that do develop FRI to help guide future treatment. The goal is to improve the clinical outcome and recovery of the population that sustains an OEF by decreasing the rate of FRI and fracture nonunions while concurrently educating on bacterial speciation and resistance.

Conditions

  • Wound Infection
  • Fractures, Open
  • Surgical Site Infection

Eligibility

Eligible Ages
Between 18 Years and 80 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Open fracture to arm, leg, or both - Over the age of 18

Exclusion Criteria

  • Under the age of 18 - Allergy to tobramycin or any other antibiotic in the aminoglycoside family - Previously treated with a resorbable antibiotic carrier - Pregnancy

Study Design

Phase
Phase 3
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Tobramycin Treatment Group
Participants in this group receive a local aqueous tobramycin injection (2mg/mL) plus standard of care treatment.
  • Drug: Tobramycin Injection
    80 milligrams of tobramycin diluted in 40 milliliters of normal saline
No Intervention
Standard of Care Treatment Group
Participants in this group receive standard of care treatment.

Recruiting Locations

Vanderbilt University Medical Center
Nashville, Tennessee 37232
Contact:
William Obremskey, MD
william.obremskey@vumc.org

More Details

Status
Recruiting
Sponsor
Massachusetts General Hospital

Study Contact

Arun Aneja, MD, PhD
617-726-6546
aaneja@mgh.harvard.edu