Abstract
Gadolinium (Gd)-based contrast agents (GBCAs) have revolutionized of MR imaging, enabling physicians to obtain life-saving medical information that often cannot be obtained with unenhanced MR imaging or other imaging modalities. Since regulatory approval in 1988, more than 450 million intravenous GBCA doses have been administered worldwide, with an extremely favorable pharmacologic safety profile. Recent evidence has demonstrated, however, that a small fraction of Gd is retained in human tissues. No direct correlation between Gd retention and clinical effects has been confirmed; however, a subset of patients have attributed various symptoms to GBCA exposure. This review details current knowledge regarding GBCA safety.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 497-507 |
| Number of pages | 11 |
| Journal | Magnetic resonance imaging clinics of North America |
| Volume | 28 |
| Issue number | 4 |
| DOIs | |
| State | Published - Nov 2020 |
Keywords
- Gadolinium deposition disease
- Gadolinium retention
- Gadolinium-based contrast agents
- MR imaging contrast agent
- Nephrogenic systemic fibrosis
- Radiology safety
ASJC Scopus subject areas
- Radiology Nuclear Medicine and imaging
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