Gadoversetamide

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(Redirected from OptiMARK)

Gadoversetamide is a contrast agent used in magnetic resonance imaging (MRI) to enhance the visibility of internal structures in the body. It is particularly useful in neuroimaging, angiography, and cardiac MRI due to its properties that allow for clearer imaging of blood vessels, the brain, and the heart. Gadoversetamide is a gadolinium-based contrast agent (GBCA), which works by altering the magnetic properties of nearby water molecules in the body, thereby improving the quality of MRI images.

Chemical and Physical Properties[edit | edit source]

Gadoversetamide is a non-ionic, water-soluble, gadolinium-based compound with the chemical formula C_18H_28GdN_5O_9. It is marketed under the brand name OptiMARK and is known for its high relaxivity, which refers to its ability to enhance the contrast of MRI images. Gadoversetamide has a molecular weight of 661.71 g/mol and appears as a clear, colorless to slightly yellowish solution when prepared for use in MRI procedures.

Mechanism of Action[edit | edit source]

The mechanism of action of gadoversetamide involves the interaction of the gadolinium ion with water molecules in the body. Gadolinium ions have unpaired electrons, which significantly alter the magnetic properties of water molecules in their vicinity. This alteration enhances the relaxation rates of hydrogen nuclei in water, thereby increasing the contrast between different tissues in the MRI images. The non-ionic nature of gadoversetamide reduces the risk of osmotic side effects, making it a safer choice for patients.

Clinical Uses[edit | edit source]

Gadoversetamide is used in a variety of MRI procedures to improve the visualization of specific areas of the body, including:

Safety and Side Effects[edit | edit source]

While gadoversetamide is generally safe for use in most patients, it is associated with a low risk of side effects. Common side effects include headache, nausea, dizziness, and a sensation of coldness at the injection site. In rare cases, gadoversetamide can cause nephrogenic systemic fibrosis (NSF) in patients with severe renal impairment. Therefore, it is crucial to assess renal function before administering gadolinium-based contrast agents.

Regulatory Status[edit | edit source]

Gadoversetamide has been approved by various regulatory agencies worldwide, including the Food and Drug Administration (FDA) in the United States. Its use is subject to specific guidelines to minimize the risk of adverse effects, particularly in patients with renal impairment.

Conclusion[edit | edit source]

Gadoversetamide is a valuable tool in the field of magnetic resonance imaging, offering enhanced visualization of internal structures and aiding in the diagnosis and assessment of various medical conditions. Its safety profile and effectiveness make it a widely used contrast agent in clinical practice. However, careful patient selection and adherence to guidelines are essential to minimize the risk of side effects.


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Contributors: Prab R. Tumpati, MD