Resuscitation Strategies for Burn Injuries Sustained in Austere Environments to Improve Renal Perfusion and Function

Abstract

Our overall hypothesis is that oral or intravenous resuscitation results in distinct improvements in burn-induced SIRS and AKI. Specifically, while oral resuscitation (i.e., drinking) helps in reducing SIRS, MOD and AKI post-burn injury, we predict it will not be as effective as the gold standard IV fluid resuscitation which may relate to fluid volume requirements that cannot be met orally. Moreover, we hypothesize that IV blood products (e.g., fresh frozen plasma) will improve organ perfusion and outcomes when compared to crystalloids, and thus reduce total fluid requirements. Resuscitation strategies will vary in ameliorating burn induced renal perfusion and dysfunction because of a differential effect on circulating cytokines and granulocytes. Subsequently, markers and byproducts of oxidative stress will increase as renal perfusion decreases. Information from the studies described in this proposal will elucidate what effect low volume post-burn resuscitation strategies have on the mechanisms of oxidative stress and systemic and local inflammation. This will not only provide information on the ensuing SIRS, MOD, and AKI, but also allow for future testing of therapies to modulate these mechanisms. The ultimate goal is to improve outcomes after extensive burn in austere environments where large volumes of fluid are not available and the casualty is delayed in transport to a treatment facility.

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Document Details

Document Type
Technical Report
Publication Date
Jan 01, 2021
Accession Number
AD1120120

Entities

People

  • David M Burmeister

Organizations

  • Geneva Foundation

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Biomedical Research
  • Blood
  • Blood Cells
  • Burns
  • Cardiovascular System
  • Casualties
  • Cell Count
  • Cells
  • Chemistry
  • Department Of Defense
  • Electrical Burns
  • Environment
  • Granulocytes
  • Gut Microbiome
  • Inflammation
  • Kidney Diseases
  • Leukocytes
  • Medical Personnel
  • Microbiomes
  • Military Medicine
  • Patient Care
  • Pharmaceutical Solutions
  • Standards
  • Stress (Physiology)
  • Therapy
  • Tissues

Fields of Study

  • Medicine

Readers

  • Immunology and Pathology
  • Trauma Surgery or Emergency Medicine.