Nephrogenic system fibrosis: A radiologist's practical perspective

被引:20
作者
Martin, Diego R. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Radiol, Atlanta, GA 30322 USA
关键词
gadolinium; gadolinium-chelates; gadolinium based contrast agents; iodinated contrast; magnetic resonance imaging; MRI; CT; nephrogenic systemic fibrosis; NSF; contrast induced nephropathy; CIN; kidney; renal; dialysis; informed consent;
D O I
10.1016/j.ejrad.2008.01.029
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 [临床医学]; 100207 [影像医学与核医学]; 1009 [特种医学];
摘要
This manuscript will provide the background current understanding of Nephrogenic Systemic Fibrosis (NSF) necessary to be appreciated by radiologists who are practicing cross-sectional imaging including gadolinium based contrast agent (Gd-CA) enhanced MRI. Examination of the known risk factors for NSF provides a practical list of considerations including an appreciation of the degree of patient renal function, or dysfunction, and the type and dose of Gd-CA used. Data is presented to argue that we must consider not only the one-time dose, but particularly the cumulative Gd-CA life-time dose administered to a patient. Using the foundation of known risk factors for NSF, we can then assemble a working list of strategies that can be utilized in an imaging practice to minimize the risk of NSF for all patients, including those at highest risk for this disorder. This list includes a discussion of high stability Gd-CAs, cumulative dose monitoring and limits, dialysis, and more specific documentation in the medical records. Finally, the issues required to understand the information that should be provided to the patient prior to obtaining informed consent are discussed. The objectives of an informed consent is to ensure that the patient is properly informed and involved in the decision to proceed with a contrast enhanced MRI, and to provide documentation to establish that the medical facilities and the radiologist are themselves well-versed in the risks and benefits when making the decision to use contrast enhanced MRI for particular patients. The process of informed consent requires that there be a consideration of the risks of not performing the contrast enhanced MRI, or the relative risk of performing another test, particularly a contrast enhanced CT. This requires an appreciation of the risks of CT-related ionizing radiation and cancer, and the risk of iodine based contrast agents (I-CA) and contrast induced nephropathy (CIN). Data is presented to show that many, and perhaps the vast majority, of renal dysfunction patients are at greater risk of harm from I-CA related to CT as compared to high stability Gd-CAs used for MRI. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:220 / 224
页数:5
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