SonoVue in transcranial Doppler investigations of the cerebral arteries
| Autor: | C Pezzoll, D.A. Legemate, H Markus, A. Spinazzi, F Ries, R G Ackerstaff, J.B. Llull, Manfred Kaps |
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| Přispěvatelé: | Other departments |
| Jazyk: | angličtina |
| Rok vydání: | 2001 |
| Předmět: |
Male
medicine.medical_specialty Dose Ultrasonography Doppler Transcranial Sulfur Hexafluoride Contrast Media Neurological examination Statistics Nonparametric medicine Humans Radiology Nuclear Medicine and imaging Adverse effect Phospholipids Analysis of Variance Cross-Over Studies medicine.diagnostic_test business.industry Ultrasound Videotape Recording Blood flow Middle Aged Crossover study Transcranial Doppler Cerebrovascular Disorders Tolerability Cerebrovascular Circulation Female Neurology (clinical) Radiology business Blood Flow Velocity |
| Zdroj: | Journal of neuroimaging, 11(3), 261-267. Wiley-Blackwell |
| ISSN: | 1051-2284 |
| DOI: | 10.1111/j.1552-6569.2001.tb00044.x |
| Popis: | Background and Purpose. The authors investigated the safety and diagnostic potential of a new ultrasound contrast agent (SonoVue™) using transcranial color-coded duplex sonography (TCCS). Methods. Forty patients were enrolled in a multicenter, open-label (on-site), blind (off-site), randomized, dose-ranging crossover study. SonoVue™ was administered as an intravenous bolus injection of 4 different dosages (0.3, 0.6, 1.2, and 2.4 mL). Efficacy was evaluated as (1) off-site assessment of global quality of the Doppler investigation (based on color or power Doppler images and spectral analysis) at baseline and following each dose of SonoVue™ according to a 4-point scale (from very poor to excellent imaging of blood flow) and (2) duration of clinically useful signal enhancement and color or power Doppler visualization of blood flow. Additional on-site efficacy assessments performed following each dose of SonoVue™ included confidence in diagnosis and global consequences of contrast enhancement on diagnosis. Safety evaluations included clinical laboratory tests, neurological examination, injection site tolerability, and incidence of adverse events and their relationship to the study agent. Results. All doses of SonoVue™ significantly improved the global quality of Doppler examinations (P < .05). The median duration of clinically useful enhancement was dose related (P < .001) and ranged from 2 to 6 minutes at the highest dose. The administration of the contrast agent changed a nondiagnostic study to a diagnostic one in 66% of patients and increased the confidence in diagnosis in 74% of cases. No serious adverse events were recorded following SonoVue™ administration. The observed adverse reactions were all transient and mild in intensity. Conclusions. The results obtained from this multicenter study demonstrate that the administration of SonoVue™ to patients with ischemic cerebrovascular disease who undergo TCCS examination of cerebral vessels improves the visualization of intracranial arteries, providing a dose-dependent contrast enhancement and a clinically useful duration of signal enhancement related to the dose. During this multicenter study, SonoVue™ proved to be a safe and well-tolerated compound. |
| Databáze: | OpenAIRE |
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