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Published on: April 11, 2014
High Dose Ascorbic Acid During Acute Resuscitation in Critically Burn Patients.
Eva Flores1, Manuel Sánchez-Sánchez1, Claudio Gutierrez1
1Department of Intensive Care Medicine, University Hospital La Paz-Carlos III/IdiPAZ, Madrid, Spain.
High-dose ascorbic acid (AA) in severe burn patients reduced initial fluid needs but not overall intake or organ dysfunction. This antioxidant therapy did not increase acute kidney injury risks.
Area of Science:
- Resuscitation Medicine
- Burn Care
- Antioxidant Therapy
Background:
- Severe burns trigger systemic inflammation and oxidative stress.
- Ascorbic acid (AA) is a potent free radical scavenger with potential therapeutic benefits.
- High-dose ascorbic acid (HDAA) has been explored for its effects on fluid resuscitation and organ function in burn patients.
Purpose of the Study:
- To investigate the efficacy of HDAA in reducing fluid resuscitation requirements in severe burn patients.
- To assess the impact of HDAA on preventing organ dysfunction and complications.
- To evaluate the safety of HDAA, particularly concerning acute kidney injury.
Main Methods:
- Retrospective case-control study of 75 severe burn patients (TSBA > 30%).
- Comparison between 25 patients receiving HDAA (66 mg/kg/h for 36h) and 50 controls.
- Analysis of fluid requirements, Sequential Organ Failure Assessment (SOFA) scores, hemodynamic parameters, complications, and mortality.
Main Results:
- The HDAA group showed significantly lower fluid requirements in the first 24 hours (3.06 vs 4.32 ml/kg/%TBSA, P < .05).
- No significant difference in overall fluid requirements within 72 hours, SOFA scores, hemodynamic parameters, complications, or mortality between groups.
- No increased incidence of acute kidney injury in the HDAA group, despite a mean urine oxalate/creatinine ratio of 0.61.
Conclusions:
- HDAA administration in severe burn patients under restrictive fluid therapy can decrease initial fluid resuscitation needs.
- HDAA did not significantly impact total fluid intake, organ dysfunction, or mortality.
- HDAA appears safe regarding renal function in this patient cohort.
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