Abolfazl Jokar,Koorosh Ahmadi,Tayyebeh Salehi,Mahdi Sharif-Alhoseini,Vafa Rahimi-Movaghar.[J].Chin J Traumatol,2017,20(1):49-51. [doi]
The effect of tranexamic acid in traumatic brain injury: A randomized controlled trial
  
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KeyWord: Traumatic brain injuriesIntracranial hemorrhageTraumaticTranexamic acid
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Author NameAffiliation
Abolfazl Jokar Department of Emergency Medicine, Arak University of Medical Science, Arak, Iran 
Koorosh Ahmadi Department of Emergency Medicine, Alborz University of Medical Sciences, Karaj, Iran 
Tayyebeh Salehi Department of Emergency Medicine, Arak University of Medical Science, Arak, Iran 
Mahdi Sharif-Alhoseini Sina Trauma and Surgery Research Center, Tehran University of Medical Sciences, Tehran, Iran 
Vafa Rahimi-Movaghar Sina Trauma and Surgery Research Center, Tehran University of Medical Sciences, Tehran, Iran
Department of Neurosurgery, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran 
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Abstract:
      Purpose: Traumatic brain injury (TBI) is a leading cause of death and disability. Intracranial hemorrhage (ICH) secondary to TBI is associated with a high risk of coagulopathy which leads to increasing risk of hemorrhage growth and higher mortality rate. Therefore, antifibrinolytic agents such as tranexamic acid (TA) might reduce traumatic ICH. The aim of the present study was to investigate the extent of ICH growth after TA administration in TBI patients. Methods: This single-blind randomized controlled trial was conducted on patients with traumatic ICH (with less than 30 ml) referring to the emergency department of Vali-Asr Hospital, Arak, Iran in 2014. Patients, based on the inclusion and exclusion criteria, were divided into intervention and control groups (40 patients each). All patients received a conservative treatment for ICH, as well as either intravenous TA or placebo. The extent of ICH growth as the primary outcome was measured by brain CT scan after 48 h. Results: Although brain CT scan showed a significant increase in hemorrhage volume in both groups after 48 h, it was significantly less in the TA group than in the control group (p ¼ 0.04). The mean total hemorrhage expansion was (1.7 ± 9.7) ml and (4.3 ± 12.9) ml in TA and placebo groups, respectively (p < 0.001). Conclusion: It has been established that TA, as an effective hospital-based treatment for acute TBI, could reduce ICH growth. Larger studies are needed to compare the effectiveness of different doses.
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