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   <subfield code="a">10.1007/s12028-013-9826-1</subfield>
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   <subfield code="a">No Exacerbation of Perihematomal Edema with Intraventricular Tissue Plasminogen Activator in Patients with Spontaneous Intraventricular Hemorrhage</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Wendy Ziai, Tom Moullaali, Saman Nekoovaght-Tak, Natalie Ullman, Jay Brooks, Timothy Morgan, Daniel Hanley]</subfield>
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   <subfield code="a">Introduction: In severe spontaneous intraventricular hemorrhage (IVH), intraventricular (IVR) administration of tissue plasminogen activator (rtPA) clears blood from the ventricles more rapidly than with external ventricular drainage (EVD) alone. However, experimental studies suggest tPA may be neurotoxic in compromised brain tissue and may exacerbate perihematomal edema. Methods: We used computerized volumetrics to assess change in intracerebral hemorrhage (ICH), IVH, ventricular, and perihematomal edema (PHE) volumes at 2-4 (T1) and 5-9 (T2) days following diagnostic CT scans (T0) of 24 patients (12 tPA-treated; 12 controls) with IVH requiring EVD. Controls from a hospital registry were matched by IVH and ICH volume to tPA-treated patients who came from a multicenter trial involving 52 patients with IVH. Results: There were no significant differences between matched pairs in admission ICH and IVH volumes. IVR tPA resulted in more rapid clearance of IVH as determined by T2-T0 decrease in median IVH volume (tPA: −18.7cc, iqr 14.9; control:−6.9cc, iqr 6.4; P=0.002). Median ratios of PHE to ICH volume were not significantly different in control versus tPA-treated patients at T1 and T2 [control:tPA=0.55:0.56 (T1); P=0.84 and 0.81:0.71 (T2); P=1.00]. Total ventricular volume was significantly larger in the control group at T2 (mean: 57.57±10.32 vs. tPA: 24.80±2.67cc; P=0.01). Bacterial ventriculitis was more frequent in the control group (5 vs. 1 episodes; P=0.06) as was shunt dependence (4 vs. 0 cases; P=0.03). Conclusions: For case matched large IVH with small ICH volume, IVR tPA enhances lysis of intraventricular blood clots and has no significant impact on PHE.</subfield>
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   <subfield code="a">Springer Science+Business Media New York, 2013</subfield>
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   <subfield code="a">Intracerebral hemorrhage</subfield>
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   <subfield code="a">Intraventricular fibrinolysis</subfield>
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   <subfield code="a">Intraventricular hemorrhage</subfield>
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   <subfield code="a">Perihemorrhagic edema</subfield>
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   <subfield code="a">Recombinant tissue-type plasminogen activator</subfield>
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   <subfield code="a">Computed tomography</subfield>
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   <subfield code="a">Ziai</subfield>
   <subfield code="D">Wendy</subfield>
   <subfield code="u">Division of Neurosciences Critical Care, Departments of Neurology, Anesthesia and Critical Care Medicine, The Johns Hopkins University School of Medicine, Meyer 8-140, 600 N. Wolfe St., 21287, Baltimore, MD, USA</subfield>
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   <subfield code="u">Division of Brain Injury Outcomes, Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA</subfield>
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   <subfield code="a">Nekoovaght-Tak</subfield>
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   <subfield code="u">Division of Brain Injury Outcomes, Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA</subfield>
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   <subfield code="u">Division of Brain Injury Outcomes, Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA</subfield>
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   <subfield code="u">Division of Brain Injury Outcomes, Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA</subfield>
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   <subfield code="u">Division of Brain Injury Outcomes, Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA</subfield>
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