MRI Contrast

 

MRI Contrast

 

MRI is based on magnetization, not ionizing radiation.  Therefore, the intravenous contrast material must have magnetic properties different from that of the surrounding tissue. The most common agent used is gadolinium diethylenetriamine pentaacetic acid (Gd-DTPA) — a paramagnetic agent that allows positive contrast enhancement, i.e. it shows up as bright on T1-weighted sequences. This provides a new array of diagnostic information, including differentiation of tumor from edema and inflammation and soft tissue from scar tissue (as in recurrent lumbar disc herniation). It also facilitates the dynamic assessment of lesion types such as hepatic hemangiomas vs hepatocellular carcinoma). In the brain, Gd-enhancement reveals areas where the blood-brain barrier has been breached, providing vital information on patients with tumors and other pathologic processes. For multiple sclerosis, Gd-enhancement helps distinguish active demyelination plaques from chronic quiescent ones. Other valuable uses for Gd in brain MRIs include the assessment of early ischemia, parenchymal brain infections and meningeal lesions.

 

MRI contrast is felt to be a safe contrast agent that rarely causes allergic reactions.  It is important, however, that the patient with impaired kidney function not receive MRI contrast.  Patients with the following history are required to have a recent BUN and creatinine/glomeular filtration rate (GFR) assessment prior to receiving intravenous MRI contrast.

  • 60 years of age or older
  • Under 60 years of age with a history of
    • Renal disease
    • Diabetes
    • Multiple myeloma
    • Active Gout

 When to use MRI contrast


BRAIN

SPINE

BODY

MRA

  • Primary brain tumors
  • Metastatic disease
  • Seizures
  • Inflammatory disease
  • Post operative brain
  • Recurrent tumor
  • Acoustic neuroma
  • Pituitary adenoma
  • Differentiation of microvascular infarction
  • Selected cases of complex vascular disease or stroke

 

  • Differentiation of recurrent disc heerniation versus scar granulation tissue (postsurgical scar tissue)
  • Inflammatory cord disease, particularly myelitis or multiple sclerosis
  • Spinal cord neoplasm
  • Any case of myelopathy

 

  • Any case of primary or metastatic organ disease versus benign cystic lesion (Example: Liver, spleen, kidneys, adrenals, pancreas)
  • Evaluation of masses in the extremities

 

  • Any vascular studies of the ascending, thoracic or abdominal aorta
  • Any vascular branches of the aorta including: celiac axis, SMA, renal arteries, IMA, iliac arteries
  • Any venous branches of the superior vena cava or inferior vena cava