Efficacy and Safety of Recombinant Activated Factor VII for Acute Intracerebral Hemorrhage
Top Cited Papers
- 15 May 2008
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 358 (20) , 2127-2137
- https://doi.org/10.1056/nejmoa0707534
Abstract
Intracerebral hemorrhage is the least treatable form of stroke. We performed this phase 3 trial to confirm a previous study in which recombinant activated factor VII (rFVIIa) reduced growth of the hematoma and improved survival and functional outcomes. We randomly assigned 841 patients with intracerebral hemorrhage to receive placebo (268 patients), 20 μg of rFVIIa per kilogram of body weight (276 patients), or 80 μg of rFVIIa per kilogram (297 patients) within 4 hours after the onset of stroke. The primary end point was poor outcome, defined as severe disability or death according to the modified Rankin scale 90 days after the stroke. Treatment with 80 μg of rFVIIa per kilogram resulted in a significant reduction in growth in volume of the hemorrhage. The mean estimated increase in volume of the intracerebral hemorrhage at 24 hours was 26% in the placebo group, as compared with 18% in the group receiving 20 μg of rFVIIa per kilogram (P=0.09) and 11% in the group receiving 80 μg (P<0.001). The growth in volume of intracerebral hemorrhage was reduced by 2.6 ml (95% confidence interval [CI], −0.3 to 5.5; P=0.08) in the group receiving 20 μg of rFVIIa per kilogram and by 3.8 ml (95% CI, 0.9 to 6.7; P=0.009) in the group receiving 80 μg, as compared with the placebo group. Despite this reduction in bleeding, there was no significant difference among the three groups in the proportion of patients with poor clinical outcome (24% in the placebo group, 26% in the group receiving 20 μg of rFVIIa per kilogram, and 29% in the group receiving 80 μg). The overall frequency of thromboembolic serious adverse events was similar in the three groups; however, arterial events were more frequent in the group receiving 80 μg of rFVIIa than in the placebo group (9% vs. 4%, P=0.04). Hemostatic therapy with rFVIIa reduced growth of the hematoma but did not improve survival or functional outcome after intracerebral hemorrhage. (ClinicalTrials.gov number, NCT00127283.)Keywords
This publication has 23 references indexed in Scilit:
- Guidelines for the Management of Spontaneous Intracerebral Hemorrhage in AdultsStroke, 2007
- Hematoma growth is a determinant of mortality and poor outcome after intracerebral hemorrhageNeurology, 2006
- Recombinant Activated Factor VII for Acute Intracerebral HemorrhageNew England Journal of Medicine, 2005
- Ultra-Early Hemostatic Therapy for Intracerebral HemorrhageStroke, 2003
- The ICH ScoreStroke, 2001
- Guidelines for the Management of Spontaneous Intracerebral HemorrhageStroke, 1999
- Platelet activity of high‐dose factor VIIa is independent of tissue factorBritish Journal of Haematology, 1997
- Early Hemorrhage Growth in Patients With Intracerebral HemorrhageStroke, 1997
- Primary Intracerebral Haemorrhage in the Oxfordshire Community Stroke ProjectCerebrovascular Diseases, 1995
- Volume of intracerebral hemorrhage. A powerful and easy-to-use predictor of 30-day mortality.Stroke, 1993