Iotrolan, a nonionic dimeric contrast medium in myelography.

S Bien, M Schumacher, W Berger, B I Wenzel-Hora
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Abstract

As part of a clinical Phase III study of the nonionic, dimeric contrast medium iotrolan, differences in opacification, tolerance, and effects on the electroencephalogram after myelography were examined in a double-blind comparison with iohexol. Two groups of 25 patients each received either 10 ml iotrolan 240 mg I/ml or 10 ml iohexol 240 mg I/ml for lumbar myelography, and two groups of 50 patients each received either 10 ml iotrolan 300 mg I/ml or 10 ml iohexol 300 mg I/ml for lumbar, thoracic or cervical myelography. The overall assessment of the opacification in the subarachnoid space, which was moderate in only one case of each group and otherwise good, showed no differences between the preparations. The tolerance of both concentrations of iotrolan proved to be significantly better than those of iohexol: at a significance level in the chi-square test of p less than 0.001 in a simple size of 25 patients per preparation with 240 mg I/ml and at a significance level of p +/- 0.05 in a sample size of 50 patients per preparation with 300 mg I/ml.

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一种非离子二聚体造影剂,用于骨髓造影术。
作为非离子型二聚体造影剂碘曲兰临床III期研究的一部分,在与碘己醇的双盲比较中,研究了其混浊、耐受性和对脊髓造影后脑电图的影响的差异。两组25例患者各接受10ml iotrolan 240mg I/ml或10ml iohexol 240mg I/ml用于腰椎造影,两组50例患者各接受10ml iotrolan 300mg I/ml或10ml iohexol 300mg I/ml用于腰椎、胸椎或颈髓造影。蛛网膜下腔混浊的总体评估,每组只有一例为中度,其他情况良好,在两种制剂之间没有差异。事实证明,两种浓度的碘曲兰的耐受性都明显优于碘已醇:在每次240 mg I/ml制剂25例患者的简单样本中,卡方检验的显著性水平为p < 0.001;在每次300 mg I/ml制剂50例患者的样本中,显著性水平为p +/- 0.05。
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Recent developments in nonionic contrast media. Renal excretion of iopromide and iopamidol after intravenous administration in digital subtraction angiography. Pharmacokinetics of iohexol, iopamidol, iopromide, and iosimide compared with meglumine diatrizoate. Plasma level and renal excretion of iotrolan after lumbar injection in patients. Left ventricular after load as a result of levocardiography with contrast media of various osmolality.
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