1. Inflammatory biomarkers in combat wound healing.
- Author
-
Hawksworth JS, Stojadinovic A, Gage FA, Tadaki DK, Perdue PW, Forsberg J, Davis TA, Dunne JR, Denobile JW, Brown TS, and Elster EA
- Subjects
- Afghan Campaign 2001-, Chemokines blood, Chemokines genetics, Cytokines genetics, Follow-Up Studies, Gene Expression Regulation, Hand Injuries diagnosis, Hand Injuries genetics, Humans, Inflammation genetics, Inflammation pathology, Iraq War, 2003-2011, Leg Injuries diagnosis, Leg Injuries genetics, Male, Military Personnel, Prognosis, Prospective Studies, RNA genetics, ROC Curve, Trauma Severity Indices, Wound Healing genetics, Wounds, Penetrating diagnosis, Wounds, Penetrating genetics, Young Adult, Biomarkers blood, Cytokines blood, Hand Injuries blood, Inflammation blood, Leg Injuries blood, Wound Healing physiology, Wounds, Penetrating blood
- Abstract
Background: Modern war ballistics and blast injuries inflict devastating extremity injuries, violating soft tissue, bone, and neurovascular structures. Despite advances in complex wound management, appropriate timing of war wound closure remains subjective. In addition, the pathophysiology of acute wound failure is poorly defined., Methods: Patients with penetrating extremity wounds sustained during combat were prospectively studied and followed for 30 days after definitive wound closure. The primary outcome was wound healing. Wound dehiscence was defined as spontaneous partial or complete wound disruption after closure. Serum, wound effluent, and wound bed tissue biopsy were collected at each surgical wound debridement. Serum and wound effluent were analyzed with a multiplex array of 22 cytokines and chemokines, and wound tissue for corresponding gene transcript expression., Results: Fifty-two penetrating extremity war wounds in 33 male patients were investigated. Nine (17%) wounds dehisced. Concomitant vascular injury, increased wound size, and higher injury severity score correlated with wound dehiscence. Both serum and wound effluent cytokine and chemokine protein profiles were statistically associated with healing outcome at various time points. Wound biopsy gene transcript expression demonstrated increased tissue inflammation associated with wound failure. Multiple protein and gene transcript biomarkers predictive of wound healing were identified., Conclusions: The cytokine and chemokine protein and gene transcript expression patterns demonstrate a condition of inflammatory dysregulation associated with war wound failure. A molecular biomarker panel may predict combat wound healing outcome and warrants prospective validation.
- Published
- 2009
- Full Text
- View/download PDF