Thompson W M, Foster W L, Halvorsen R A, Dunnick N R, Rommel A J, Bates M
AJR Am J Roentgenol. 1984 Feb;142(2):329-32. doi: 10.2214/ajr.142.2.329.
Iopamidol, a new, nonionic contrast agent, was evaluated in 18 patients undergoing excretory urography. None of the 18 patients experienced any side effects or adverse reactions. No abnormalities were noted in serum chemistries, complete blood cell counts, urinalyses, or electrocardiograms. The half-life of iopamidol in 17 patients with normal renal function was 2.5 hr. The urograms were judged to be of good or excellent quality in 15 of 16 patients using doses of 200 and 250 mg l/kg of iopamidol. Two patients who were studied using a dose of only 120 mg l/kg had urograms rated poor. Fifteen iopamidol urograms (mean iodine dose, 17.4 g) were compared in a blind fashion with 15 meglumine diatrizoate studies (iodine dose, 29 g). No qualitative difference could be detected between the two groups of urograms. Iopamidol may provide equal-quality diagnostic studies with a lower iodine dose and perhaps greater safety than the currently used ionic agents.
碘帕醇是一种新型非离子型造影剂,对18例接受排泄性尿路造影的患者进行了评估。18例患者均未出现任何副作用或不良反应。血清化学、全血细胞计数、尿液分析或心电图均未发现异常。17例肾功能正常患者体内碘帕醇的半衰期为2.5小时。在16例使用200和250毫克碘/千克碘帕醇剂量的患者中,15例的尿路造影被判定质量良好或优秀。仅使用120毫克碘/千克剂量进行研究的2例患者的尿路造影评级为差。将15例碘帕醇尿路造影(平均碘剂量17.4克)与15例泛影葡胺研究(碘剂量29克)进行了盲法比较。两组尿路造影之间未发现定性差异。与目前使用的离子型造影剂相比,碘帕醇可能以更低的碘剂量提供同等质量的诊断研究,并且安全性可能更高。