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Levetiracetam-induced transaminitis in a young male with traumatic brain injury
Abstract Levetiracetam is a commonly prescribed antiepileptic drug for seizure prophylaxis in patients with traumatic brain injury (TBI). Levetiracetam metabolism has been reported to be non-dependent on hepatic cytochrome P450 (CYP450) isoenzyme system. Furthermore, levetiracetam and its metabolite...
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Published in: | Oxford Medical Case Reports 2017-11, Vol.2017 (11), p.omx067 |
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creator | Rachamallu, Vivekananda Song, Michael M Reed, Jace M Aligeti, Manish |
description | Abstract
Levetiracetam is a commonly prescribed antiepileptic drug for seizure prophylaxis in patients with traumatic brain injury (TBI). Levetiracetam metabolism has been reported to be non-dependent on hepatic cytochrome P450 (CYP450) isoenzyme system. Furthermore, levetiracetam and its metabolites are reported to be eliminated from systemic circulation via renal excretion. Therefore, due to its well-known renal clearance mechanism with no dosage adjustments recommended for hepatic impairment, levetiracetam is often chosen as the drug of choice in patients with suspected or ongoing hepatic dysfunction. Furthermore, monitoring of liver enzymes is often not considered to be critical in levetiracetam therapy. However, hepatotoxicity is still possible with levetiracetam. Here, we report on an 18-year-old male with TBI who developed transaminitis with levetiracetam therapy which resolved following the discontinuation of levetiracetam. A close monitoring of liver enzymes and early recognition of hepatotoxicity is still necessary and critical to preventing major sequelae stemming from levetiracetam-induced hepatotoxicity. |
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Levetiracetam is a commonly prescribed antiepileptic drug for seizure prophylaxis in patients with traumatic brain injury (TBI). Levetiracetam metabolism has been reported to be non-dependent on hepatic cytochrome P450 (CYP450) isoenzyme system. Furthermore, levetiracetam and its metabolites are reported to be eliminated from systemic circulation via renal excretion. Therefore, due to its well-known renal clearance mechanism with no dosage adjustments recommended for hepatic impairment, levetiracetam is often chosen as the drug of choice in patients with suspected or ongoing hepatic dysfunction. Furthermore, monitoring of liver enzymes is often not considered to be critical in levetiracetam therapy. However, hepatotoxicity is still possible with levetiracetam. Here, we report on an 18-year-old male with TBI who developed transaminitis with levetiracetam therapy which resolved following the discontinuation of levetiracetam. A close monitoring of liver enzymes and early recognition of hepatotoxicity is still necessary and critical to preventing major sequelae stemming from levetiracetam-induced hepatotoxicity.</description><identifier>ISSN: 2053-8855</identifier><identifier>EISSN: 2053-8855</identifier><identifier>DOI: 10.1093/omcr/omx067</identifier><identifier>PMID: 29744119</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Case Report</subject><ispartof>Oxford Medical Case Reports, 2017-11, Vol.2017 (11), p.omx067</ispartof><rights>The Author 2017. Published by Oxford University Press. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-c42d41388d5b1b2cd3186f1bacba23d4f30f64e40dc30d7246e8391bdb1785d3</citedby><cites>FETCH-LOGICAL-c405t-c42d41388d5b1b2cd3186f1bacba23d4f30f64e40dc30d7246e8391bdb1785d3</cites><orcidid>0000-0002-4198-0119</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934633/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934633/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,733,786,790,891,1591,27957,27958,53827,53829</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29744119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rachamallu, Vivekananda</creatorcontrib><creatorcontrib>Song, Michael M</creatorcontrib><creatorcontrib>Reed, Jace M</creatorcontrib><creatorcontrib>Aligeti, Manish</creatorcontrib><title>Levetiracetam-induced transaminitis in a young male with traumatic brain injury</title><title>Oxford Medical Case Reports</title><addtitle>Oxf Med Case Reports</addtitle><description>Abstract
Levetiracetam is a commonly prescribed antiepileptic drug for seizure prophylaxis in patients with traumatic brain injury (TBI). Levetiracetam metabolism has been reported to be non-dependent on hepatic cytochrome P450 (CYP450) isoenzyme system. Furthermore, levetiracetam and its metabolites are reported to be eliminated from systemic circulation via renal excretion. Therefore, due to its well-known renal clearance mechanism with no dosage adjustments recommended for hepatic impairment, levetiracetam is often chosen as the drug of choice in patients with suspected or ongoing hepatic dysfunction. Furthermore, monitoring of liver enzymes is often not considered to be critical in levetiracetam therapy. However, hepatotoxicity is still possible with levetiracetam. Here, we report on an 18-year-old male with TBI who developed transaminitis with levetiracetam therapy which resolved following the discontinuation of levetiracetam. A close monitoring of liver enzymes and early recognition of hepatotoxicity is still necessary and critical to preventing major sequelae stemming from levetiracetam-induced hepatotoxicity.</description><subject>Case Report</subject><issn>2053-8855</issn><issn>2053-8855</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kL1rwzAQxUVpaUKaqXvx1KW4lSzJlpdCCekHBLJkF_pyohDJQbLT5r-vjduQLl3uDu537x4PgFsEHxEs8VPtVOjKF8yLCzDOIMUpY5Rens0jMI1xCyFEOEeYsWswysqCEITKMVguzME0NghlGuFS63WrjE6aIHwUznrb2JhYn4jkWLd-nTixM8mnbTY90jrRWJXIIDrC-m0bjjfgqhK7aKY_fQJWr_PV7D1dLN8-Zi-LVBFIm65mmvRmNJVIZkpjxPIKSaGkyLAmFYZVTgyBWmGoi4zkhuESSS1RwajGE_A8yO5b6YxWxnd2dnwfrBPhyGth-d-Ntxu-rg-clpjkGHcCD4OACnWMwVSnWwR5nyzvk-VDsh19d_7uxP7m2AH3A1C3-3-VvgE38IWX</recordid><startdate>20171101</startdate><enddate>20171101</enddate><creator>Rachamallu, Vivekananda</creator><creator>Song, Michael M</creator><creator>Reed, Jace M</creator><creator>Aligeti, Manish</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4198-0119</orcidid></search><sort><creationdate>20171101</creationdate><title>Levetiracetam-induced transaminitis in a young male with traumatic brain injury</title><author>Rachamallu, Vivekananda ; Song, Michael M ; Reed, Jace M ; Aligeti, Manish</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-c42d41388d5b1b2cd3186f1bacba23d4f30f64e40dc30d7246e8391bdb1785d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Case Report</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rachamallu, Vivekananda</creatorcontrib><creatorcontrib>Song, Michael M</creatorcontrib><creatorcontrib>Reed, Jace M</creatorcontrib><creatorcontrib>Aligeti, Manish</creatorcontrib><collection>Open Access: Oxford University Press Open Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oxford Medical Case Reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rachamallu, Vivekananda</au><au>Song, Michael M</au><au>Reed, Jace M</au><au>Aligeti, Manish</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Levetiracetam-induced transaminitis in a young male with traumatic brain injury</atitle><jtitle>Oxford Medical Case Reports</jtitle><addtitle>Oxf Med Case Reports</addtitle><date>2017-11-01</date><risdate>2017</risdate><volume>2017</volume><issue>11</issue><spage>omx067</spage><pages>omx067-</pages><issn>2053-8855</issn><eissn>2053-8855</eissn><abstract>Abstract
Levetiracetam is a commonly prescribed antiepileptic drug for seizure prophylaxis in patients with traumatic brain injury (TBI). Levetiracetam metabolism has been reported to be non-dependent on hepatic cytochrome P450 (CYP450) isoenzyme system. Furthermore, levetiracetam and its metabolites are reported to be eliminated from systemic circulation via renal excretion. Therefore, due to its well-known renal clearance mechanism with no dosage adjustments recommended for hepatic impairment, levetiracetam is often chosen as the drug of choice in patients with suspected or ongoing hepatic dysfunction. Furthermore, monitoring of liver enzymes is often not considered to be critical in levetiracetam therapy. However, hepatotoxicity is still possible with levetiracetam. Here, we report on an 18-year-old male with TBI who developed transaminitis with levetiracetam therapy which resolved following the discontinuation of levetiracetam. A close monitoring of liver enzymes and early recognition of hepatotoxicity is still necessary and critical to preventing major sequelae stemming from levetiracetam-induced hepatotoxicity.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>29744119</pmid><doi>10.1093/omcr/omx067</doi><orcidid>https://orcid.org/0000-0002-4198-0119</orcidid><oa>free_for_read</oa></addata></record> |
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title | Levetiracetam-induced transaminitis in a young male with traumatic brain injury |
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