Abstract

BackgroundComplex traumatic injuries sustained by military personnel, particularly when involving extremities, often result in infectious complications and substantial morbidity. One factor that may further impair patient recovery is the persistence of infections. Surface-attached microbial communities, known as biofilms, may play a role in hindering the management of infections; however, clinical data associating biofilm formation with persistent or chronic infections are lacking. Therefore, we evaluated the production of bacterial biofilms as a potential risk factor for persistent infections among wounded military personnel.MethodsBacterial isolates and clinical data from military personnel with deployment-related injuries were collected through the Trauma Infectious Disease Outcomes Study. The study population consisted of patients with diagnosed skin and soft-tissue infections. Cases (wounds with bacterial isolates of the same organism collected 14 days apart) were compared to controls (wounds with non-recurrent bacterial isolates), which were matched by organism and infectious disease syndrome. Potential risk factors for persistent infections, including biofilm formation, were examined in a univariate analysis. Data are expressed as odds ratios (OR; 95% confidence interval [CI]).ResultsOn a per infected wound basis, 35 cases (representing 25 patients) and 69 controls (representing 60 patients) were identified. Eight patients with multiple wounds were utilized as both cases and controls. Overall, 235 bacterial isolates were tested for biofilm formation in the case–control analysis. Biofilm formation was significantly associated with infection persistence (OR: 29.49; CI: 6.24-infinity) in a univariate analysis. Multidrug resistance (OR: 5.62; CI: 1.02-56.92), packed red blood cell transfusion requirements within the first 24 hours (OR: 1.02; CI: 1.01-1.04), operating room visits prior to and on the date of infection diagnosis (OR: 2.05; CI: 1.09-4.28), anatomical location of infected wound (OR: 5.47; CI: 1.65-23.39), and occurrence of polymicrobial infections (OR: 69.71; CI: 15.39-infinity) were also significant risk factors for persistent infections.ConclusionsWe found that biofilm production by clinical strains is significantly associated with the persistence of wound infections. However, the statistical power of the analysis was limited due to the small sample size, precluding a multivariate analysis. Further data are needed to confirm biofilm formation as a risk factor for persistent wound infections.

Highlights

  • Complex traumatic injuries sustained by military personnel, when involving extremities, often result in infectious complications and substantial morbidity

  • It should be noted that the 25 case and 60 control subjects included eight patients with multiple wounds were used in both groups

  • Patients included in the study were predominantly young men injured via a blast mechanism (>83%) in support of Operation Enduring Freedom in Afghanistan (>88%; Table 1)

Read more

Summary

Introduction

Complex traumatic injuries sustained by military personnel, when involving extremities, often result in infectious complications and substantial morbidity. Due to the usage of improvised explosive devices combined with the utilization of body armor protecting the abdomen and thorax during the recent conflicts in Iraq and Afghanistan (Operations Iraqi Freedom and Enduring Freedom), complex extremity wounds are prevalent among military personnel with deployment-related injuries. This injury pattern often results in infectious complications with considerable morbidity (e.g., limb amputation), extended periods of rehabilitation, and high utilization of hospital resources [1,2,3,4,5,6,7,8]. An analysis of 454 civilian patients with osteomyelitis, primarily resulting from soft-tissue wounds and surgical procedures, reported that 31% experienced an infection recurrence, of which 16% were determined to be relapses (original pathogen), 16% reinfections (different pathogen), and 68% could not be specified as either a relapse or reinfection [11]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call