(Stroke. 2000;31:726.)
© 2000 American Heart Association, Inc.
Original Contributions |
From the Divisions of Neurosciences Critical Care (J.R.C., D.F.H.) and Neuroradiology (P.Y.W., N.J.B., P.B.B.) and the Department of Emergency Medicine (P.M.K.), The Johns Hopkins Medical Institutions, Baltimore, Md.
Correspondence to Juan R. Carhuapoma, MD, Division of Neurosciences Critical Care, Meyer 8140, Johns Hopkins Hospital, 600 N Wolfe St, Baltimore, MD 21287-7840. E-mail jrcarhuapoma{at}sprintmail.com
Background and PurposeCerebral ischemia has been proposed as contributing mechanism to secondary neuronal injury after intracerebral hemorrhage (ICH). Possible tools for investigating this hypothesis are diffusion-weighted (DWI) and proton magnetic resonance spectroscopic imaging (1H-MRSI). However, magnetic field inhomogeneity induced by paramagnetic blood products may prohibit the application of such techniques on perihematoma tissue. We report on the feasibility of DWI and 1H-MRSI in the study of human ICH and present preliminary data on their contribution to understanding perihematoma tissue functional and metabolic profiles.
MethodsPatients with acute supratentorial ICH were prospectively evaluated using DWI and 1H-MRSI. Obscuration of perihematoma tissue with both sequences was assessed. Obtainable apparent diffusion coefficient (Dav) and lactate spectra in perihematoma brain tissue were recorded and analyzed.
ResultsNine patients with mean age of 63.4 (36 to 87) years were enrolled. Mean time from symptom onset to initial MRI was 3.4 (1 to 9) days; mean hematoma volume was 35.4 (5 to 80) cm3. Perihematoma diffusion values were attainable in 9 of 9 patients, and 1H-MRSI measures were obtainable in 5 of 9 cases. Dav in perihematoma regions was 172.5 (120.0 to 302.5)x10-5 mm2/s and 87.6 (76.5 to 102.1)x10-5 mm2/s in contralateral corresponding regions of interest (P=0.002). One patient showed an additional area of reduced Dav with normal T2 intensity, which suggests ischemia. 1H-MRSI revealed lactate surrounding the hematoma in 2 patients.
ConclusionsDWI and 1H-MRSI can be used in the study of ICH patients. Our preliminary data are inconsistent with ischemia as the primary mechanism for perihematoma tissue injury. Further investigation with advanced MRI techniques will give a clearer understanding of the role that ischemia plays in tissue injury after ICH.
Key Words: intracerebral hemorrhage magnetic resonance imaging, diffusion-weighted neuronal damage spectroscopy, nuclear magnetic resonance
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