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基于钆的细胞外造影剂:诊断效能的差异

Extracellular gadolinium-based contrast media: differences in diagnostic efficacy.

作者信息

van der Molen Aart J, Bellin Marie-France

机构信息

Department of Radiology C-2S, Leiden University Medical Centre, Albinusdreef 2, NL-2333 ZA Leiden, The Netherlands.

出版信息

Eur J Radiol. 2008 May;66(2):168-74. doi: 10.1016/j.ejrad.2008.02.010. Epub 2008 Mar 26.

Abstract

Since the introduction of the first gadolinium-based contrast agent (Gd-CA) in 1988 it has become clear that these agents significantly improve the diagnostic efficacy of MRI. Studies on single agents have shown that, in comparison to unenhanced sequences, all agents help to improve the detection and delineation of lesions which can alter diagnosis in up to 40% of patients. Doubling or tripling the standard dose of 0.1 mmol/kg body weight may be beneficial for selected indications (e.g. brain perfusion, equivocal single dose study in MRI for brain metastasis, small vessel MR angiography). A more limited number of studies have compared the various agents. These studies do not show clinically significant differences in diagnostic efficacy between the various extracellular Gd-CA. Agents with higher concentration or protein binding may be relatively better suitable for selected applications (e.g. perfusion MRI). The higher relaxivity agents may be used in somewhat lower doses than the extracellular agents.

摘要

自1988年首款钆基造影剂(Gd-CA)问世以来,很明显这些造影剂显著提高了MRI的诊断效能。对单一造影剂的研究表明,与未增强序列相比,所有造影剂均有助于改善病变的检测与描绘,这在高达40%的患者中可改变诊断结果。将0.1 mmol/kg体重的标准剂量加倍或增至三倍可能对特定适应症有益(例如脑灌注、MRI用于脑转移的单剂量研究结果不明确、小血管磁共振血管造影)。较少数量的研究比较了各种造影剂。这些研究未显示出各种细胞外Gd-CA在诊断效能方面存在临床显著差异。浓度较高或具有蛋白结合能力的造影剂可能相对更适合特定应用(例如灌注MRI)。弛豫率较高的造影剂使用剂量可能比细胞外造影剂略低。

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