Computed Tomography Assessment of Cerebral Perfusion Using a Distributed Parameter Tracer Kinetics Model: Validation with H2(15)O Positron Emission Tomography Measurements and Initial Clinical Experience in Patients with Acute Stroke
Author(s) -
Sotirios Bisdas,
Frank Donnerstag,
Georg Berding,
Thomas J. Vogl,
Choon Hua Thng,
Tong San Koh
Publication year - 2007
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.167
H-Index - 193
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/sj.jcbfm.9600522
Subject(s) - positron emission tomography , nuclear medicine , tomography , positron emission , tracer , emission computed tomography , kinetics , physics , medicine , nuclear physics , radiology , quantum mechanics
We describe a distributed parameter (DP) model for tracer kinetic analysis in brain and validate the derived perfusion values with positron emission tomography (PET) scans. The proposed model is applied on actual clinical cases of hemispheric stroke. Nine patients with experienced transient ischaemic attack or minor stroke and a stenosis of the internal carotid artery were referred for computed tomography (CT) and PET imaging. The applicability of the DP model in clinical practice was tested in seven patients with acute stroke who received a baseline perfusion CT study and a noncontrast follow-up CT study after 2.4 ± 1.8 days. The mean blood flow ( F) value for all patients with carotid stenosis in the pooled data (54 regions of interest (ROIs)) was 37.9 ± 11.2 mL/min per 100 g in perfusion CT and 35.6 ± 9.8 mL/min per 100 g in perfusion PET imaging [ r = 0.77 ( P = 0.00)]. Regression analysis of the pooled ROIs for every patient revealed significant correlation between F values in seven patients [ r = 0.50 to 0.79 ( r 2 -values ranged from 0.45 to 0.79), (0.01 ≤ P ≤ 0.05)]. Parametric maps that corresponded to all physiologic parameters were generated for every perfusion CT in the patients with acute stroke using the DP model. The ischaemic area was better delineated in F, intravascular blood volume and lag time ( t lag ) maps. The correlation coefficient comparing the visually outlined regions of abnormality between the t lag parametric map and the follow-up CT scans was 0.81 ( P = 0.003). In conclusion, DP physiological model using more realistic pharmacokinetics is feasible in dynamic contrast-enhanced CT of the brain in patients with acute and chronic cerebrovascular disease.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom