Literature DB >> 28802751

Acute Management of Hemostasis in Patients With Neurological Injury.

M Irem Baharoglu1, Anneke Brand2, Maria M Koopman3, Marinus Vermeulen4, Yvo B W E M Roos5.   

Abstract

Neurological injuries can be divided into those with traumatic and nontraumatic causes. The largest groups are traumatic brain injury (TBI) and nontraumatic stroke. TBI patients may present with intracranial hemorrhages (contusions, or subdural or epidural hematomas). Strokes are ischemic or hemorrhagic. In all these disorders, thrombosis and hemostasis play a major role. Treatment aims to either cease bleeding and/or restore perfusion. We reviewed hemostatic and thrombolytic therapies in patients with neurological injuries by MEDLINE and EMBASE search using various key words for neurological disorders and hemostatic therapies restricted to English language and human adults. Review of articles fulfilling inclusion criteria and relevant references revealed that, in patients with ischemic stroke, intravenous thrombolytic therapy with recombinant tissue plasminogen activator within 4.5-5 hours after onset of symptoms improves clinical outcome. In contrast, there are no hemostatic therapies that are proven to improve clinical outcome of patients with hemorrhagic stroke or TBI. In patients with hemorrhagic stroke who use vitamin K antagonist or direct oral anticoagulants, there is evidence that specific reversal therapies improve hemostatic laboratory parameters but without an effect on clinical recovery. In patients with hemorrhagic stroke or TBI who use concomitant antiplatelet therapy, there is evidence for harm of platelet transfusion. In patients with aneurysmal subarachnoid hemorrhage, tranexamic acid was shown to reduce rebleeding rate without improving clinical outcome. The effects of tranexamic acid in patients with TBI are still under investigation. We conclude that, in patients with ischemic stroke, thrombolytic therapy improves outcome when given within 4.5-5 hours. In hemorrhagic stroke and TBI, most hemostatic therapies improved or corrected laboratory parameters but not clinical outcome. Currently, in several trials, the effects of tranexamic acid are being studied of which the results are eagerly awaited. Because improving clinical outcome should be the goal of new therapies, we encourage to use clinical outcome scales as the primary outcome measure in trials that investigate effects of hemostatic therapies in patients with neurological injury.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Hemostasis; Hemostatic therapy; Intracerebral hemorrhage; Stroke; Subarachnoid hemorrhage; Transfusion; Traumatic brain injury

Mesh:

Substances:

Year:  2017        PMID: 28802751     DOI: 10.1016/j.tmrv.2017.07.002

Source DB:  PubMed          Journal:  Transfus Med Rev        ISSN: 0887-7963


  3 in total

1.  Microvesicles generated following traumatic brain injury induce platelet dysfunction via adenosine diphosphate receptor.

Authors:  Grace E Martin; Amanda M Pugh; Ryan Moran; Rose Veile; Lou Ann Friend; Timothy A Pritts; Amy T Makley; Charles C Caldwell; Michael D Goodman
Journal:  J Trauma Acute Care Surg       Date:  2019-04       Impact factor: 3.313

2.  Protective effect of hypoxia inducible factor-1α gene therapy using recombinant adenovirus in cerebral ischaemia-reperfusion injuries in rats.

Authors:  Ya-Qi Li; Zhi-Rong Hui; Tao Tao; Kang-Yu Shao; Zhi Liu; Min Li; Li-Ling Gu
Journal:  Pharm Biol       Date:  2020-12       Impact factor: 3.503

3.  Benign Paroxysmal Positional Vertigo and Occult Subarachnoid Hemorrhage Complicated after Head Trauma.

Authors:  Qinghua Li; Shuangxing Hou; Hualan Yang
Journal:  Case Rep Med       Date:  2020-03-30
  3 in total

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