Abstract
As detailed earlier, Levovist produces fragile microbubbles lacking shells. Therefore, the pharmacokinetics of Levovist is quite different from those of water-soluble contrast agents. The enhancement patterns observed on computed tomography (CT), angiography, and dynamic magnetic resonance imaging (MRI) do not apply to contrast-enhanced ultrasonography (US) with Levovist. In a certain way, the behavior of Levovist is similar to that of water-soluble contrast agents during the arterial phase, but its subsequent behavior is very different. Table 6–1 broadly summarizes the differences between contrast agents. Water-soluble contrast agents are regarded as free-pass or through-pass type contrast agents. They can freely pass through the thinnest capillaries in the body. It is known that water-soluble contrast agents leak into the extravascular inter-stitium during the delayed phase, which may result in the false-positive diagnosis of fibrotic changes. However, the dynamic behavior during the 2–3 min from early to late phase is generally described as free pass.
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© 2003 Springer Japan
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Kudo, M. (2003). Comparative Pharmacokinetic Behavior of Levovist with Water-Soluble Contrast Agents. In: Contrast Harmonic Imaging in the Diagnosis and Treatment of Hepatic Tumors. Springer, Tokyo. https://doi.org/10.1007/978-4-431-65904-4_6
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DOI: https://doi.org/10.1007/978-4-431-65904-4_6
Publisher Name: Springer, Tokyo
Print ISBN: 978-4-431-65906-8
Online ISBN: 978-4-431-65904-4
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