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dc.contributor.authorShiehmorteza, M
dc.contributor.authorAhmadi, A
dc.contributor.authorAbdollahi, M
dc.contributor.authorNayebpour, M
dc.contributor.authorMohammadi, M
dc.contributor.authorHamishehkar, H
dc.contributor.authorNajaf, A
dc.contributor.authorPazoki, M
dc.contributor.authorMojtahedzadeh, M
dc.date.accessioned2018-08-26T09:33:25Z
dc.date.available2018-08-26T09:33:25Z
dc.date.issued2011
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57549
dc.description.abstractBackground and the purpose of the study: Besides its hematopoietic effects, erythropoietin (EPO) by mobilization of iron and modulation of some inflammatory cytokines has antioxidant and anti-inflammatory properties. The purpose of this study was to evaluate these effects of erythropoietin and its impact on organ function in traumatized patients. Methods: Twenty-six ICU-admitted traumatized patients within 24 hrs after trauma were randomly assigned to the EPO (received EPO, 300 units/Kg/day) and Control (not received EPO) groups. The inflammatory biomarkers including Tumor Necrosis Factor alpha (TNF-?), Interleukin 1 (IL-1), Plasminogen Activator Inhibitor 1 (PAI-1) and Nitrotyrosine were recorded at the admission, 3, 6 and 9 days thereafter. Acute Physiology and Chronic Health Evaluation (APACHE II) and Sequential Organ Failure Assessment (SOFA) scores were also recorded. Results: Among 12 patients (EPO group) TNF-? level at the day of 9 (P=0.046), and within EPO group at the days of 3 (P=0.026 ameliorate), 6 (P=0.016), and 9 (P=0.052) were significantly lowered. Level of IL-1 and PAI-1 decreased significantly at days of 3, 6 and 9 post intervention. Also there were significant differences between two groups in the SOFA score during three measured time intervals (the first, third and seventh days).Conclusion: From the results of this study it seems that injection of erythrocyte stimulating agent is well tolerated and inhibits the inflammatory response and oxidative stress following trauma.
dc.language.isoEnglish
dc.relation.ispartofDARU, Journal of Pharmaceutical Sciences
dc.subject3 nitrotyrosine
dc.subjectbiological marker
dc.subjectinterleukin 1
dc.subjectplasminogen activator inhibitor
dc.subjectrecombinant erythropoietin
dc.subjecttumor necrosis factor alpha
dc.subjectantiinflammatory activity
dc.subjectantioxidant activity
dc.subjectAPACHE
dc.subjectarticle
dc.subjectclinical article
dc.subjectcontrolled study
dc.subjectdrug effect
dc.subjectdrug tolerability
dc.subjecthuman
dc.subjectinflammation
dc.subjectinjury
dc.subjectintensive care unit
dc.subjectopen study
dc.subjectoxidative stress
dc.subjectrandomization
dc.subjectrandomized controlled trial
dc.subjectscoring system
dc.titleRecombinant human erythropoietin reduces plasminogen activator inhibitor and ameliorates pro-infammatory responses following trauma
dc.typeArticle
dc.citation.volume19
dc.citation.issue2
dc.citation.spage159
dc.citation.epage165
dc.citation.indexScopus
dc.citation.URLhttp://daru.tums.ac.ir/index.php/daru/article/view/431


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