Dynamics of intraventricular hemorrhage in patients with spontaneous intracerebral hemorrhage: Risk factors, clinical impact, and effect of hemostatic therapy with recombinant activated factor VII

被引:206
作者
Steiner, Thorsten
Diringer, Michael N.
Schneider, Dietmar
Mayer, Stephan A.
Begtrup, Kamilla
Broderick, Joseph
Skolnick, Brett E.
Davis, Stephen M.
机构
[1] Univ Heidelberg, Dept Neurol, D-69120 Heidelberg, Germany
[2] Washington Univ, Sch Med, Intens Care Unit, St Louis, MO 63130 USA
[3] Univ Leipzig, Neurol Intens Care & Stroke Unit, D-7010 Leipzig, Germany
[4] Columbia Univ, Coll Phys & Surg, Dept Neurol, New York, NY 10027 USA
[5] Columbia Univ, Coll Phys & Surg, Dept Neurosurg, New York, NY 10027 USA
[6] Novo Nordisk AS, DK-2880 Bagsvaerd, Denmark
[7] Univ Cincinnati, Med Ctr, Dept Neurol, Cincinnati, OH 45267 USA
[8] Novo Nordisk AS, Princeton, NJ USA
[9] Univ Melbourne, Royal Melbourne Hosp, Dept Neurol, Parkville, Vic 3052, Australia
关键词
hemorrhage growth; hemostatic treatment; intracerebral hemorrhage; intraventricular hemorrhage; recombinant activated factor VII;
D O I
10.1227/01.NEU.0000232837.34992.32
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: To evaluate predictors of intraventricular hemorrhage (IVH) and IVH growth, impact of IVH growth on outcome, and impact of recombinant activated factor VII (rFVIIa) in patients with intracerebral hemorrhage (ICH). METHODS: We analyzed 374 patients out of 399 who were randomized to rFVIIa (40, 80, or 160 mu g/kg) or placebo for ICH (diagnosed within 3 h of symptoms). Risk factors for IVH growth (> 2 ml increase in IVH volume at 24 h), and death or severe disability (modified Rankin scale score 4-6) at 3 months were identified (logistic regression). RESULTS: IVH was present in 38% (n = 141) of patients at baseline and 45% (n = 169) by 24 hours. IVH growth, by 24 hours, occurred in 17 and 10% of placebo- and rFVIIa-treated patients, respectively (P = 0.037). Risk factors for IVH growth included baseline mean arterial pressure greater than 120 mmHg, larger baseline ICH volume, IVH present at baseline, shorter time from symptom onset to baseline computed tomographic scan, and treatment (rFVIIa versus placebo) (all, P:5 0.037). Predictors of death or severe disability included older age, lower baseline Glasgow Coma Score, larger baseline ICH volume, IVH growth greater than 2 ml, IVH present at baseline or 24 hours, and treatment (rFVIIa versus placebo) (all, P <= 0.0405). CONCLUSION: Presence of IVH at any time and early IVH growth worsen clinical outcome and increase mortality. Elevated mean arterial pressure at baseline may be a modifiable risk factor for IVH growth. Beneficial effects of rFVIIa on ICH outcome may be mediated, at least in part, by reducing IVH growth.
引用
收藏
页码:767 / 773
页数:7
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