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dc.contributor.authorEslami, K
dc.contributor.authorMahmoodpoor, A
dc.contributor.authorAhmadi, A
dc.contributor.authorAbdollahi, M
dc.contributor.authorKamali, K
dc.contributor.authorMousavi, S
dc.contributor.authorNajafi, A
dc.contributor.authorBaeeri, M
dc.contributor.authorHamishehkar, H
dc.contributor.authorKouti, L
dc.contributor.authorJavadi, M
dc.contributor.authorMojtahedzadeh, M
dc.date.accessioned2018-08-26T09:32:06Z
dc.date.available2018-08-26T09:32:06Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57251
dc.description.abstractBackground: Septimeb is a new herbal-derived remedy, recently approved for its potential immunomodulatory effects. Regarding the key role of immune system in the pathogenesis of severe sepsis and lack of any standard treatment for improving survival of these patients; we evaluated the effect of Septimeb -as an adjutant to standard treatment-on inflammatory biomarkers and mortality rates in patients with severe sepsis. Methods. In this multicenter, randomized, single-blind trial, we assigned patients with severe sepsis and Acute Physiology and Chronic Health Evaluation (APACHE II) score of more than 20 to receive standard treatment of severe sepsis (control group) or standard treatment plus Septimeb. This group was treated with Septimeb for 14 days then followed up for another14 days. APACHE score, Sequential Organ Failure Assessment (SOFA) and Simplified Acute Physiology Score (SAPS) were calculated daily. Blood samples were analyzed for interleukin 2 tumor necrosis factor-?, total antioxidant power, platelet growth factor and matrix metalloproteinase 2. Results: A total of 29 patients underwent randomization (13 in control group and 16 in Septimeb group). There was significant difference between the Septimeb and control group in the 14 days mortality rate (18.8% vs. 53.85 respectively, P=0.048). Compared to control group, Septimeb was significantly effective in improving SAPS (P= 0.029), SOFA (P=0.003) and APACHE II (P=0.008) scores. Inflammatory biomarkers didnt change significantly between the two groups (P>0.05). Conclusion: Septimeb reduces mortality rates among patients with severe sepsis and it could be added as a safe adjutant to standard treatment of sepsis. © 2012 Eslami et al.; licensee BioMed Central Ltd.
dc.language.isoEnglish
dc.relation.ispartofDARU, Journal of Pharmaceutical Sciences
dc.subjectgelatinase A
dc.subjectimmunomodulating agent
dc.subjectinterleukin 2
dc.subjectplatelet derived growth factor
dc.subjectseptimeb
dc.subjecttumor necrosis factor alpha
dc.subjectunclassified drug
dc.subjectadult
dc.subjectaged
dc.subjectantibiotic therapy
dc.subjectAPACHE
dc.subjectarticle
dc.subjectblood sampling
dc.subjectcentral venous pressure
dc.subjectclinical article
dc.subjectcontrolled study
dc.subjectdisease severity
dc.subjectdrug efficacy
dc.subjectearly intervention
dc.subjectfemale
dc.subjectfollow up
dc.subjectglycemic control
dc.subjectherbal medicine
dc.subjecthuman
dc.subjectmale
dc.subjectmortality
dc.subjectmulticenter study
dc.subjectpatient monitoring
dc.subjectrandomized controlled trial
dc.subjectresuscitation
dc.subjectscoring system
dc.subjectsepsis
dc.subjectsequential organ failure assessment
dc.subjectSimplified Acute Physiology Score
dc.subjectsingle blind procedure
dc.titlePositive effect of septimeb™ on mortality rate in severe sepsis: A novel non antibiotic strategy
dc.typeArticle
dc.citation.volume20
dc.citation.issue1
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1186/2008-2231-20-40


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