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"DTIC ADA630348: Effect Of Recombinant Factor VIIa As An Adjunctive Therapy In Damage Control For Wartime Vascular Injuries: A Case Control Study" and the language of the book is English.


“DTIC ADA630348: Effect Of Recombinant Factor VIIa As An Adjunctive Therapy In Damage Control For Wartime Vascular Injuries: A Case Control Study” Metadata:

  • Title: ➤  DTIC ADA630348: Effect Of Recombinant Factor VIIa As An Adjunctive Therapy In Damage Control For Wartime Vascular Injuries: A Case Control Study
  • Author: ➤  
  • Language: English

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  • Internet Archive ID: DTIC_ADA630348

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"DTIC ADA630348: Effect Of Recombinant Factor VIIa As An Adjunctive Therapy In Damage Control For Wartime Vascular Injuries: A Case Control Study" Description:

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Objectives: Military casualties with vascular injuries often present with severe acidosis and coagulopathy that can negatively influence limb salvage decisions. We previously reported the value of a damage control resuscitation (DCR) strategy that can correct physiologic shock during simultaneous vascular reconstruction. The effect of recombinant factor VIIa (rFVIIa) on the repair of injured vessels and vascular grafts when used as an adjunctive therapy during DCR is unclear in the setting of wartime vascular injuries. The primary aim of this study was to assess the effect of rFVIIa use during DCR for vascular trauma and the impact on vessel repair. Methods: A retrospective two cohort case control study was performed using the Joint Theater Trauma Registry to identify patients with major vascular injury and DCR. Group 1 (n = 12) had DCR and repair of the injured vessels. Group 2 (n = 41) included early rFVIIa as an adjunctive therapy with DCR to control bleeding and perform simultaneous vascular reconstruction. Results: Age, injury severity score, presenting physiology, and operative time were similar between groups. Postoperative data show that early physiologic recovery from acidosis, coagulopathy, and anemia was associated with rFVIIa and DCR. Extremity graft failures in groups 1 and 2 (follow-up range, 10 26 months) were either from early thrombosis (1 vs. 5 p = 1), graft dehiscence (1 vs. 2 p = 0.55), or infection (1 vs. 1 p = 0.41) and were the result of inadequate soft tissue coverage or technical factors that eventually resulted in eight (15%) amputations. All cause mortality (group 1: 0% vs. group 2: 7.3%, p = 1) and amputation rates (group 1: 25% vs. groups 2: 12.2%, p n= 0.36) were similar between the two groups. Conclusions: DCR using rFVIIa is effective for controlling hemorrhage and reversing coagulopathy for severe vascular injuries. Early graft failures seem unrelated to rFVIIa use in the setting of wartime vascular injuries.

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