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dc.contributor.authorMahmoodpoor, A
dc.contributor.authorShokouhi, G
dc.contributor.authorHamishehkar, H
dc.contributor.authorSoleimanpour, H
dc.contributor.authorSanaie, S
dc.contributor.authorPorhomayon, J
dc.contributor.authorRasouli, F
dc.contributor.authorNader, ND
dc.date.accessioned2018-08-26T07:11:26Z
dc.date.available2018-08-26T07:11:26Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44306
dc.description.abstractObjective: To investigate the effects of L-Carnitine on neuron specific enolase (NSE) as a marker of inflammation in patients with traumatic brain injury (TBI). Methods: Forty patients with severe TBI were randomized into 2 groups. The (LCA-) group received standard treatment with placebo while the (LCA+) group received l-Carnitine 2 g/day for one week. NSE was measured on days 1, 3 and 7 after the initiation of the study. Neurocognitive and neurobehavioral disorders were recorded on the first and third months. Results: Neurocognitive function and NSE significantly improved within one week in both groups. Patient mortality was similar in LCA+ and LCA- groups (P value: 0.76). Brain edema was present in 7 patients in LCA+ group and 13 patients in LCA-group (P value: 0.044). While there was no difference in NSE levels between the two groups. Neurological function was preserved in the LCA+ group with an exception of attention deficit, which was frequent in the LCA+ group. Conclusion: We concluded that despite improvements in neurobehavioral function and the degree of cerebral edema, 7-days of treatment with L-Carnitine failed to reduce serum NSE levels or improve mortality rate at 90 days in patients with TBI. Published by Elsevier Inc.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF CRITICAL CARE
dc.subjectL-Carnitine
dc.subjectTraumatic brain injury
dc.subjectNeuron specific enolase
dc.subjectOutcome
dc.titleA pilot trial of L-carnitine in patients with traumatic brain injury: Effects on biomarkers of injury
dc.typeArticle
dc.citation.volume45
dc.citation.spage128
dc.citation.epage132
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/j.jcrc.2018.01.029


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