Literature DB >> 28877128

Antioxidant and Trace Element Supplementation Reduce the Inflammatory Response in Critically Ill Burn Patients.

Sarah Rehou1, Shahriar Shahrokhi1,2, Rimona Natanson3, Mile Stanojcic4, Marc G Jeschke2,4,5.   

Abstract

Oxidative stress after burn injury induces inflammatory and hypermetabolic responses associated with adverse outcomes. We propose that antioxidant and trace element supplementation may reduce oxidative stress and subsequently alleviate inflammation and hypermetabolism, thus improving clinical outcomes. We conducted a cohort study of adult patients with an acute burn injury admitted to our provincial burn center. Patients in the antioxidant group received an intravenous infusion of multivitamins and trace elements for the first 14 days after admission. The inflammatory profile was assessed at early time points, < 14 days postburn, and later time points, ≥ 15 days postburn, and included interleukin (IL)-1β, interferon-γ, IL-1 receptor antagonist, IL-6, granulocyte-macrophage colony-stimulating factor, and FMS-like tyrosine kinase 3 ligand. Hypermetabolism was assessed by resting energy expenditure. Clinical outcomes included mortality, morbidities, hospital length of stay, and infections including days to the last positive culture after injury. We studied 172 patients, mean age 49 ± 17 years and 33 ± 13% TBSA burned, with 91 controls and 81 patients in the antioxidant group. Patients in the antioxidant group had significantly lower levels of inflammatory markers at both early and late time points, P < .05. Antioxidant treatment was associated with decreased measure of hypermetabolism, P < .05. Morbidity and mortality were not significantly different between groups. Length of hospital stay was significantly shorter in the antioxidant group when adjusted for patient demographics and injury characteristics (risk ratio (RR), 0.78; 95% confidence interval (CI), 0.66-0.92). In the antioxidant group, while infections were not different, the last positive culture post-injury was documented at median 19 days (Interquartile range (IQR), 11-43 days) compared with controls at 35 days (IQR, 15-59 days), P = .012. Patients receiving antioxidant and trace element supplementation had reduced markers of burn stress-induced inflammation; they were also associated with a decreased hypermetabolic response, shorter length of stay, and improved bacterial clearance.

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Year:  2018        PMID: 28877128      PMCID: PMC6053770          DOI: 10.1097/BCR.0000000000000607

Source DB:  PubMed          Journal:  J Burn Care Res        ISSN: 1559-047X            Impact factor:   1.845


  25 in total

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Authors:  David N Herndon; Ronald G Tompkins
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3.  Trace element supplementation after major burns modulates antioxidant status and clinical course by way of increased tissue trace element concentrations.

Authors:  Mette M Berger; Malcolm Baines; Wassim Raffoul; Messod Benathan; René L Chiolero; Chris Reeves; Jean-Pierre Revelly; Marie-Christine Cayeux; Isabelle Sénéchaud; Alan Shenkin
Journal:  Am J Clin Nutr       Date:  2007-05       Impact factor: 7.045

4.  Temporal cytokine profiles in severely burned patients: a comparison of adults and children.

Authors:  Celeste C Finnerty; Marc G Jeschke; David N Herndon; Richard Gamelli; Nicole Gibran; Matthew Klein; Geoff Silver; Brett Arnoldo; Daniel Remick; Ronald G Tompkins
Journal:  Mol Med       Date:  2008 Sep-Oct       Impact factor: 6.354

Review 5.  Trace Element Supplementation Following Severe Burn Injury: A Systematic Review and Meta-Analysis.

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Journal:  J Burn Care Res       Date:  2016 May-Jun       Impact factor: 1.845

Review 6.  Free radicals and lipid peroxidation mediated injury in burn trauma: the role of antioxidant therapy.

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10.  Are serum cytokines early predictors for the outcome of burn patients with inhalation injuries who do not survive?

Authors:  Gerd G Gauglitz; Celeste C Finnerty; David N Herndon; Ronald P Mlcak; Marc G Jeschke
Journal:  Crit Care       Date:  2008-06-18       Impact factor: 9.097

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Review 7.  Innate Immune System Response to Burn Damage-Focus on Cytokine Alteration.

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