Tranexamic Acid for Traumatic Brain Injury

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     Tranexamic acid for traumatic braininjury: a systematic review

    and meta-analysis

    Shahriar Zehtabchi, MD a,

    Samah G !bdel "a#i,MDa,$ouise %al&on, "!, Daniel '(ishijima, MD

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     Trauma"rain )njury

    • an estimated *+ million emerency deartment ./D0visits

    • 123444 hositali&ations• 31444 deaths each year

    Secondary

    "rain )njury

    • roressive intracranial bleedin, cerebral edema,increased intracranial ressure, subse5uent cerebral

    ischemia• worsened by osttraumatic coauloathy

    !nti6brinolytic aent

    tranexamicacid .T7!0   • Does administration of T7! .intervention0 comared to

    lacebo .comarison0 imrove atients8 outcomes suchas reduction inmortality, neuroloic function, andhemorrhae roression .outcome09utcome

    )ntroduction

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    Methods

    Study Desin :;andomi&ed controlled trials .;

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    Methods• Data extractionData from the identi6ed studies were abstracted indeendently by 1 of theauthors .SZ and SG!0 usin a standardi&ed form

    • Buality assessmentCGradin 5uality of evidence and strenth of recommendations criteria to assess the

    5uality of the included trial and rate the level of evidence

    • Buantitative data synthesis The eEect of T7! on dichotomous outcomes was assessed usin a random eEects

    model because the trials were exected to be heteroeneous in their desin andatient oulations ;elative ris# and >3F

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    Methods

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    Methods

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    ;esult

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    Discussion

    )mrovin the outcome of brain injury atients larelydeends on minimi&in the secondary brain insults

    • Secondary insults include hematoma

    exansion, cerebral edema, increasedintracerebral ressure, infection, hyoxia, andcoauloathy The brain tissue contains lare amounts of thrombolastin

     This substance is released in hih concentration into theblood stream after hysical trauma to the arenchyma,

    causin disturbance in coaulation rocesses• )n addition, damaed cerebral endothelium

    activates latelets as well as clottin cascadesto roduce intravascular thrombosis and

    deletion of coaulation factors

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    Mechanism* T7!, as an anti6brinolytic aent,may limit 6brinolysis and thus )

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    $imitations

     There was some heteroeneity betweenidenti6ed studies, articularly in theinclusion criteria• The included studies did not account

    for atients receivin anticoaulantsor antilatelet aents

     The mechanism of injury could be a

    confounder that needs to be examinedin future trials• The meta-analysiswas erformedwith

    only 1 trials

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