Management of Spontaneous Intracerebral Hemorrhage
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Published version
Author(s)
Veltkamp, Roland
Purrucker, Jan
Type
Journal Article
Abstract
Purpose of Review
We review the current evidence for medical and surgical treatments of spontaneous intracerebral hemorrhage (ICH).
Recent Findings
Therapy with hemostatic agents (e.g. factor VIIa and tranexamic acid) if started early after bleeding onset may reduce hematoma expansion, but their clinical effectiveness has not been shown. Rapid anticoagulation reversal with prothrombin concentrates (PCC) plus vitamin K is the first choice in vitamin K antagonist-related ICH. In ICH related to dabigatran, anticoagulation can be rapidly reversed with idarucizumab. PCC are recommended for ICH related to FXa inhibitors, whereas specific reversal agents are not yet approved. While awaiting ongoing trials studying minimally invasive approaches or hemicraniectomy, the role of surgery in ICH remains to be defined. Therapies targeting downstream molecular cascades in order to prevent secondary neuronal damage are promising, but the complexity and multi-phased nature of ICH pathophysiology is challenging. Finally, in addition to blood pressure control, antithrombotic prevention after ICH has to consider the risk of recurrent bleeding as well as the risk of ischemic events.
Summary
Treatment of acute ICH remains challenging, and many promising interventions for acute ICH await further evidence from trials.
We review the current evidence for medical and surgical treatments of spontaneous intracerebral hemorrhage (ICH).
Recent Findings
Therapy with hemostatic agents (e.g. factor VIIa and tranexamic acid) if started early after bleeding onset may reduce hematoma expansion, but their clinical effectiveness has not been shown. Rapid anticoagulation reversal with prothrombin concentrates (PCC) plus vitamin K is the first choice in vitamin K antagonist-related ICH. In ICH related to dabigatran, anticoagulation can be rapidly reversed with idarucizumab. PCC are recommended for ICH related to FXa inhibitors, whereas specific reversal agents are not yet approved. While awaiting ongoing trials studying minimally invasive approaches or hemicraniectomy, the role of surgery in ICH remains to be defined. Therapies targeting downstream molecular cascades in order to prevent secondary neuronal damage are promising, but the complexity and multi-phased nature of ICH pathophysiology is challenging. Finally, in addition to blood pressure control, antithrombotic prevention after ICH has to consider the risk of recurrent bleeding as well as the risk of ischemic events.
Summary
Treatment of acute ICH remains challenging, and many promising interventions for acute ICH await further evidence from trials.
Date Issued
2017-10-01
Date Acceptance
2017-09-01
Citation
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2017, 17 (10)
ISSN
1528-4042
Publisher
SPRINGER
Journal / Book Title
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS
Volume
17
Issue
10
Copyright Statement
© 2017 The Author(s). Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000411159800008&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Science & Technology
Life Sciences & Biomedicine
Clinical Neurology
Neurosciences
Neurosciences & Neurology
Hematoma growth
Hemostatic therapy
Antihypertensive
Anticoagulation
PROTHROMBIN COMPLEX CONCENTRATE
ACUTE-CEREBRAL-HEMORRHAGE
VITAMIN-K ANTAGONISTS
INITIAL CONSERVATIVE TREATMENT
PREDICTS HEMATOMA EXPANSION
DIRECT ORAL ANTICOAGULANTS
BLOOD-PRESSURE REDUCTION
ACTIVATED FACTOR-VII
RANDOMIZED-TRIAL
INTRACRANIAL HEMORRHAGE
Publication Status
Published
Article Number
ARTN 80
Date Publish Online
2017-09-08