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| Clinical data | |
|---|---|
| Trade names | Amipaque |
| Other names | 3-aAcetamido-2,4,6-triiodo-5-(N-methylacetamido)-N-[(3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]benzamide |
| AHFS/Drugs.com | Micromedex Detailed Consumer Information |
| ATC code | |
| Identifiers | |
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| CAS Number | |
| PubChem CID | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.045.872 |
| Chemical and physical data | |
| Formula | C18H22I3N3O8 |
| Molar mass | 789.100 g·mol−1 |
  (what is this?) (verify) | |
Metrizamide is a non-ionic iodine-based radiocontrast agent.[1] It is also a density gradient medium for the centrifugation of biological particles.[2]
Historically metrizamide replaced both iodized oil (trade names: Ethiodol, Lipiodol) and iofendylate (trade names: Pantopaque, Myodil) as the contrast agent of choice for myelography (an X-ray study of the spine now largely replaced by MRI). The radio opacity characteristics are such that finer detail is displayed with metrizamide, as well as the advantage of reabsorption from spinal fluid and excretion from the body – since unlike iofendylate, metrizamide is a water-soluble substance.
All three agents are administered by lumbar puncture (also referred to as a spinal tap or cisternal puncture), at the cervicocranial junction. The human patient is rolled from the lateral decubitus (lying on the side) to prone. Ankles are strapped to the end of a hard X-ray, CT, or MRI table. To obtain images of the cervical region the patient is then carefully tilted in the Trendelenberg position (head down) so the contrast agent (particularly iofendylate) can enter the neck region. Care is given to prevent spilling dye into the posterior cranial fossa (back of the head) or to enter the cranial cavity in general. This speaks to the inability to remove the heavier or more viscous iofendylate without aspirating it with spinal fluid through a lumbar puncture needle in the low back (sticking up vertically) or back of the neck. Removal of iofendylate is necessary since it is not water-soluble. With metrizamide the issue is that if entering the cranial cavity and high dose exposure to the blood brain barrier, side effects are more likely encountered. Issues related to absorption into the general circulation are also encountered.
Side effects
edit- Headache
- Nausea
- Vomiting
- Mass effect, herniation, and major central nervous system complications including spinal cord compression
- Seizures
- Muscle rigidity and dystonic reaction
- Aphasia[3]
- Adverse neurobehavioral reactions[4]
History
editMetrizamide was approved in the US in 1978. Its marketing is discontinued as of 2021.[5]
References
edit- ^ Hanus, P. M. (1980). "Metrizamide: a review with emphasis on drug interactions". American Journal of Hospital Pharmacy. 37 (4): 510–513. ISSN 0002-9289. PMID 6103672.
- ^ Inaba, Kayo (2011). Current Protocols in Immunology. Isolation of Dendritic Cells: Wiley. p. 3.7.14.
- ^ Kassicieh et al. (1988), Conduction aphasia following metrizamide myelography, J Am Osteopath Assoc 1988 Vol. 88 Issue 3 Pages 384-6
- ^ Killebrew K, Whaley RA, Hayward JN, Scatliff JH (February 1983). "Complications of metrizamide myelography". Archives of Neurology. 40 (2): 78–80. doi:10.1001/archneur.1983.04050020040007. PMID 6824454.
- ^ "Drugs@FDA: FDA-Approved Drugs: Amipaque". Food and Drug Administration. Archived from the original on January 25, 2017. Retrieved 2021-03-31.
Further reading
edit- Ozdoba C, Gralla J, Rieke A, Binggeli R, Schroth G (2011). "Myelography in the Age of MRI: Why We Do It, and How We Do It". Radiology Research and Practice. 2011 329017. doi:10.1155/2011/329017. PMC 3197073. PMID 22091378.
- Boyd WR, Gardiner GA (September 1977). "Metrizamide myelography". AJR. American Journal of Roentgenology. 129 (3): 481–4. doi:10.2214/ajr.129.3.481. PMID 409203.
External links
edit- "Metrizamide". The Free Dictionary.
- "Metrizamide". Drugs.com.
