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High Dose Ascorbic Acid During Acute Resuscitation in Critically Burn Patients.
Flores, Eva; Sánchez-Sánchez, Manuel; Gutierrez, Claudio; Estébanez, Belen; Millán, Pablo; Gutierrez, Carola; Gonzalez, Alvaro; Garcia de Lorenzo, Abelardo.
Afiliação
  • Flores E; Department of Intensive Care Medicine, University Hospital La Paz-Carlos III/IdiPAZ, Madrid, Spain.
  • Sánchez-Sánchez M; Department of Intensive Care Medicine, University Hospital La Paz-Carlos III/IdiPAZ, Madrid, Spain.
  • Gutierrez C; Department of Intensive Care Medicine, University Hospital La Paz-Carlos III/IdiPAZ, Madrid, Spain.
  • Estébanez B; Department of Intensive Care Medicine, University Hospital La Paz-Carlos III/IdiPAZ, Madrid, Spain.
  • Millán P; Department of Intensive Care Medicine, University Hospital La Paz-Carlos III/IdiPAZ, Madrid, Spain.
  • Gutierrez C; Department of Intensive Care Medicine, University Hospital La Paz-Carlos III/IdiPAZ, Madrid, Spain.
  • Gonzalez A; Department of Plastic and Reconstructive Surgery, University Hospital La Paz-Carlos III/IdiPAZ, Madrid, Spain.
  • Garcia de Lorenzo A; Department of Intensive Care Medicine, University Hospital La Paz-Carlos III/IdiPAZ, Madrid, Spain.
J Burn Care Res ; 43(1): 149-155, 2022 01 05.
Article em En | MEDLINE | ID: mdl-34142146
ABSTRACT
Ascorbic acid (AA) is a potent oxygen-free radical scavenger. We hypothesized that treating severe burn patients with high doses of AA (HDAA) can reduce fluid resuscitation requirements and prevent organ dysfunction. We performed a unicentric, retrospective case-control study of 75 burn patients 25 patients admitted from 2018 to 2019 with more than 30% Total Surface Body Surface Area (TSBA) burned who received HDAA (66 mg/kg/h as soon as possible after admission until 36 h after injury), and 50 patients admitted from 2014 to 2017 with similar Abbreviated Burn Severity Index (ABSI)/Baux scores who were treated with the same protocol but did not receive HDAA. During the first 24 hours of burn resuscitation the HDAA group required less fluids than the control group (3.06 ± 0.87 ml/kg/%TBSA vs 4.32 ± 1.51 P < .05), but the overall reduction of fluid requirements during the first 72 hours was not significant. There were no significant differences in Sequential Organ Failure Assessment (SOFA), other hemodynamic parameters, complications, or mortality. We also did not find an increase acute kidney injury in patients who received HDAA even though the mean urine oxalate/creatinine ratio was 0.61 (0.02-0.96). We conclude that in severe burn patients treated with a restrictive fluid therapy protocol, administration of HDAA can decrease only the initial fluid requirements but not total fluid intakes. We did not find differences in severity score after resuscitation or in mortality. Nor did we find an increase in renal failure in patients administered with HDAA.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácido Ascórbico / Ressuscitação / Queimaduras / Estado Terminal Tipo de estudo: Guideline / Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Burn Care Res Assunto da revista: TRAUMATOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácido Ascórbico / Ressuscitação / Queimaduras / Estado Terminal Tipo de estudo: Guideline / Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Burn Care Res Assunto da revista: TRAUMATOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Espanha
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