Evolving Characteristics of Gadolinium‐Based Contrast Agents for MR Imaging: A Systematic Review of the Importance of Relaxivity

Author:

Kanal Emanuel12ORCID,Maki Jeffrey H.3ORCID,Schramm Peter4,Marti‐Bonmati Luis5

Affiliation:

1. Department of Radiology University of Pittsburgh Medical Center Pittsburgh Pennsylvania USA

2. Division of Emergency Radiology University of Pittsburgh Medical Center Pittsburgh Pennsylvania USA

3. Department of Radiology University of Colorado Anschutz Medical Center Aurora Colorado USA

4. Department of Neuroradiology University Luebeck and Universitaetsklinikum Schleswig‐Holstein Campus Luebeck Luebeck Germany

5. Department of Radiology and GIBI230 Research Group on Biomedical Imaging Hospital Universitario y Politécnico de La Fe and Instituto de Investigación Sanitaria La Fe Valencia Spain

Abstract

Gadolinium‐based contrast agents (GBCAs) are widely and routinely used to enhance the diagnostic performance of magnetic resonance imaging and magnetic resonance angiography examinations. T1 relaxivity (r1) is the measure of their ability to increase signal intensity in tissues and blood on T1‐weighted images at a given dose. Pharmaceutical companies have invested in the design and development of GBCAs with higher and higher T1 relaxivity values, and “high relaxivity” is a claim frequently used to promote GBCAs, with no clear definition of what “high relaxivity” means, or general concurrence about its clinical benefit. To understand whether higher relaxivity values translate into a material clinical benefit, well‐designed, and properly powered clinical studies are necessary, while mere in vitro measurements may be misleading. This systematic review of relevant peer‐reviewed literature provides high‐quality clinical evidence showing that a difference in relaxivity of at least 40% between two GBCAs results in superior diagnostic efficacy for the higher‐relaxivity agent when this is used at the same equimolar gadolinium dose as the lower‐relaxivity agent, or similar imaging performance when used at a lower dose. Either outcome clearly implies a relevant clinical benefit.Level of Evidence2Technical EfficacyStage 3

Publisher

Wiley

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