Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 2009;40:1539-1540
Published online before print February 19, 2009, doi: 10.1161/STROKEAHA.108.535757
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
40/4/1539    most recent
STROKEAHA.108.535757v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Torbey, M. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Torbey, M. T.
Related Collections
Right arrow Other Stroke Treatment - Medical

(Stroke. 2009;40:1539.)
© 2009 American Heart Association, Inc.


Emerging Therapies

Intracerebral Hemorrhage

What’s Next?

Michel T. Torbey, MD, MPH, FAHA, FCCM

From Department of Neurology and Neurosurgery, Medical College of Wisconsin, Milwaukee, Wis.

Correspondence to Michel T. Torbey, MD, MPH, FAHA, FCCM, Director, Stroke Critical Care Program, Medical College of Wisconsin, 9200 W. Wisconsin Ave, Milwaukee, WI 53226. E-mail mtorbey@mcw.edu

Marc Fisher MD Kennedy Lees MD Section Editors


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 

A proven and effective treatment for intracerebral hemorrhage (ICH) remains an elusive goal. Results of recent clinical trials have been bitterly disappointing. Neither a surgical approach focusing on evacuation of the hematoma1 nor a medical approach focusing on neuroprotective strategies2,3 have shown any clinically relevant benefit.

The hematoma in ICH is a dynamic expanding mass. An increase in hematoma volume of >33% is seen in 38% of patients scanned within 3 hours of symptoms onset.4 In two-thirds of patients this increase in volume is seen within 1 hour.4 Because volume of the hematoma has been shown to be an important predictor of mortality and functional outcome,5 an approach focusing on preventing further bleeding is worth investigating.

In a recent phase 2 trial, a role for ultra-early hemostatic therapy with recombinant activated factor VII (rFVIIa) was identified.6 In this study, 399 patients with ICH were randomly assigned to receive placebo or 40, 80, or 160 µg of rFVIIa per kg of body weight. Treatment was given within 1 hour of the baseline CT scan and no later than 4 hours of symptoms onset. The primary efficacy endpoint for the study was the percent change in the volume of ICH. Global outcomes at 90 days were assessed using modified Rankin scale and the extended Glasgow Outcome scale. Of note, death and complete dependence on others was defined as modified Rankin Scale scores of 4 to 6. The study was conducted between August 2002 and March 2004 in 73 hospitals and 20 countries. . . . [Full Text of this Article]




This article has been cited by other articles:


Home page
StrokeHome page
M. Hoffman and D. M. Monroe
Tissue Factor in Brain Is Not Saturated With Factor VIIa: Implications for Factor VIIa Dosing in Intracerebral Hemorrhage
Stroke, August 1, 2009; 40(8): 2882 - 2884.
[Full Text] [PDF]