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Side Effects of MRI With Contrast

by 
author image Marie Cheour
Marie Cheour had her first article published in 1995, and she has since published more than 40 articles in peer-reviewed publications such as "Nature" and "Nature Neuroscience." She has worked as a college professor in Europe and in the United States. Cheour has a Ph.D. in cognitive psychology from the University of Helsinki.
Side Effects of MRI With Contrast
MRI contrast agents are generally safe, but there are a few potential side effects. Photo Credit: JohnnyGreig/E+/GettyImages

Magnetic resonance imaging (MRI) is a method of scanning the body that provides clear, detailed pictures of organs and tissues. A contrast dye is sometimes injected into a vein during an MRI scan to improve the ability to see certain structures. All dyes used for MRIs contain a metal called gadolinium, which is attached to another molecule that varies from dye to dye.

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These dyes — called gadolinium-based contrast agents (GBCAs) — have been used for nearly 30 years, with over 300 million doses being given throughout the world, according to a review article in the December 2016 issue of “Magnetic Resonance Imaging.” They are generally very safe, but side effects are possible.

Most Common Side Effects

According to a report published by the American College of Radiology (ACR) in 2017, side effects occur in between 0.07 and 2.4 percent of MRIs with contrast. Most of these side effects are mild and temporary. They include nausea, headache, lightheadedness, pins and needles sensations and pain, warmth or coldness at the GBCA injection site.

Some GBCAs temporarily interfere with blood tests for calcium, causing calcium levels to appear falsely low. The actual amount of calcium in the blood is not affected. Some GBCAs may also transiently interfere with blood tests for iron, copper and zinc.

Allergic Reactions

Allergic reactions with GBCAs are rare. The 2017 ACR report noted that allergic reactions occur in 0.004 to 0.7 percent of GBCA injections. Most allergic reactions are mild, producing hives, other rashes, itchiness, a stuffy nose or sneezing. Facial swelling or wheezing may occur with more serious reactions.

Anaphylaxis — a severe, life-threatening allergic reaction — is very rare, occurring in 0.001 to 0.01 percent of GBCA injections, according to the 2017 ACR report. Allergic reactions occur shortly after a GBCA is injected and are usually easily treated with appropriate medications.

The risk of an allergic reaction may be slightly higher in people with asthma or other types of allergic diseases. They are more common in women than men. People with an allergic reaction to a GBCA have a 30 percent chance of a reaction when given a GBCA in the future, according to a study reported in the August 2012 issue of “Radiology.

For individuals with a previous reaction, the radiologist may avoid all GBCAs or may choose a different GBCA and administer a steroid medication beforehand to reduce the likelihood of a reaction.

Nephrogenic Systemic Fibrosis

Nephrogenic systemic fibrosis (NSF) occasionally occurs in people with severe kidney disease who receive a GBCA. In this disorder, fibrous tissue — firm scar-like tissue — develops in many parts of the body. It leads to thick and tight skin, tight muscles, stiff joints, pain primarily in the arms and legs and impaired function of the heart, lungs and esophagus.

NSF occurs when GBCAs accumulate in the body because kidney disease limits their removal through the urine. Gadolinium collects in tissues and organs, where it triggers the formation of fibrous tissue.

The risk of developing NSF is much higher with some types of GBCAs than others. If an MRI with contrast is considered necessary in a person with poor kidney function, the radiologist will likely choose one of the low-risk GBCAs, as explained in the 2017 ACR report.

Brain Deposits

On July 27, 2015, the US Food and Drug Administration (FDA) announced that recent research showed small amounts of gadolinium remaining in the brain of some people for a long time — months to years — after receiving GBCAs. This primarily occurred in people receiving at least 4 MRIs with contrast and was observed even in people with normal kidney function.

In an update on December 19, 2017, the FDA announced that although gadolinium collections can occur, there is no good scientific evidence that they produce any harmful effects in people with normal kidneys. However, it did state that drug labels for all GBCAs must contain a warning that gadolinium can accumulate in the body.

A review article published in the May 2017 issue of “Advances in Chronic Kidney Disease” confirmed that gadolinium may accumulate in the brain, but there is currently no scientific evidence that these deposits are harmful in humans. Additional research is necessary to help clarify this issue.

Other Potential Side Effects

GBCAs can occasionally cause sudden worsening of kidney function in people with pre-existing kidney disease. This may be more common with higher doses of GBCAs, so the FDA-approved drug labels for all GBCAs recommend using the lowest dose that gives adequate MRI results.

Gadolinium may accumulate in other parts of the body besides the brain in people with normal kidney function. The term gadolinium deposition disease (GDD) has been used by some experts to describe a collection of symptoms developing after MRIs with contrast in people without kidney disease. The symptoms include headaches, bone or joint pain and skin thickening, among others.

As explained in the May 2017 review article in “Advances in Chronic Kidney Disease,” GDD is similar in some ways to NSF and may represent a mild form of that disease. But not all experts agree that GDD is an actual disorder, and the December 2017 FDA update indicated that NSF is the only disease definitely caused by GBCA use. More research is needed to resolve this controversy.

Reviewed and revised by Mary D. Daley, M.D.

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