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Review: Reducing the Use of Gadolinium-based Contrast Agents for Abdominal MRI in Children

Key findings

  • Radiologists should make every effort to minimize the exposure of young patients to gadolinium-based contrast agents (GBCAs), since they face the prospect of undergoing serial MRI examinations over their lifetime
  • Reasons to reduce GBCA use in pediatric patients include the risk of gadolinium tissue deposition, need for IV access, allergic-like and physiologic adverse reactions and safety concerns in patients with impaired renal function
  • Major strategies for reducing GBCA use are to implement unenhanced abdominal MRI protocols when indicated and use unenhanced techniques for serial MRI to assess for change in known pathology such as cancer
  • Ferumoxytol is used off-label at some centers as an MRI contrast agent, and other alternative contrast agents are under development

Both medical literature and the lay press have raised various concerns about the risks of gadolinium-based contrast agents (GBCAs). Radiologists should make every effort to minimize the exposure of young patients to GBCAs, since they face the prospect of undergoing serial MRI examinations over their lifetime.

In the American Journal of Roentgenology, Mark A. Anderson, MD, resident physician in the Department of Radiology at Massachusetts General Hospital, Michael Gee, MD, PhD, chief of Pediatric Radiology and associate program director of the Radiology Residency Program, and colleagues review strategies for reducing the use of GBCAs for pediatric abdominal MRI.

Reasons to Reduce GBCA Use

Gadolinium has been detected in tissues, most commonly the brain, of patients with normal renal function who have undergone numerous MRI studies. The clinical significance of this deposition is unknown, as are any long-term consequences of gadolinium deposition in the pediatric population.

Other reasons to reduce GBCA usage in pediatric patients include avoiding the need for venous cannulation, allergic-like and physiologic adverse reactions and safety concerns in patients with impaired renal function.

Alternative Contrast Agents

Ferumoxytol is FDA-approved for parenteral iron supplementation and is used off-label at some centers as an MRI contrast agent. Like GBCAs it provides positive contrast through T1 shortening of local tissues, and it provides significant negative contrast through T2 shortening. The dose for MRI contrast is typically about half that for iron supplementation.

Ferumoxytol is likely to be as good as GBCAs for most MR angiography and MR venography studies, and it is being investigated for evaluation of lymphadenopathy. It cannot reliably be used for characterization of focal lesions. Ferumoxytol carries a boxed warning about the potential for serious allergic reactions, which have not been well evaluated in children, and this is currently a major limitation on pediatric use.

Manganese-based contrast agents are still preclinical, and no safety data are available in pediatric patients. Like gadolinium, manganese is a paramagnetic contrast agent that leads to T1 shortening. Unlike gadolinium, it is an essential nutritional component and the body has efficient mechanisms to regulate its levels, a theoretical safety advantage.

Nonrelaxation-inducing contrast agents—GBCAs, ferumoxytol and manganese-based contrast agents all generate MRI contrast by inducing tissue relaxation. Agents under development generate contrast through other mechanisms, including chemical exchange saturation transfer and direct probe detection via nonwater protons such as carbon or fluorine. Clinical investigation of these agents is still in early stages.

Unenhanced Sequences

Two of the best-studied pediatric abdominal MRI protocols that do not require GBCAs are pediatric appendicitis MRI and MR enterography for patients with inflammatory bowel disease, such as Crohn's disease. 

Diffusion-weighted imaging (DWI) is being used increasingly often in pediatric abdominal MRI protocols, including oncologic applications: whole-body MRI for tumor staging and screening, detection and characterization of malignant lesions and assessment of treatment response.

Finally, a major way to reduce GBCAs is to eliminate them from serial follow-up examinations of pediatric patients who have established cancer or an infectious or inflammatory condition, where the purpose of the repeat MRI is to assess for change. If lesions are visible on both unenhanced and contrast-enhanced images from initial MRI, assessment for interval change generally does not require a GBCA.

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