静脉数字减影血管造影中非离子和离子造影剂对肾脏和肝脏的耐受性。

M Langer, W Junge, R Keysser, J Hasford, U A Jänicke
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引用次数: 0

摘要

在两项对照双盲研究中,以血清和尿液酶测定为基础,通过静脉数字减影血管造影术检测了碘丙胺370与异位异位钠370或iopamidol 370在2 ml/kg体重剂量下对肝脏和肾脏的耐受性。在肾功能正常的患者中,注射碘丙胺或三聚氰胺钠后72小时内血清中肝酶GPT、GOT和γ谷氨酰转肽酶(GGT)水平未见变化。肾特异性酶中,注射碘丙胺和iopamidol后尿中GGT的排泄量增加。然而,与iopamidol组相比,使用ioproide组GGT排泄的最大增加量有统计学意义上的显著降低。在72小时内,两组的活动都恢复到初始值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Renal and hepatic tolerance of nonionic and ionic contrast media in intravenous digital subtraction angiography.

The liver and kidney tolerance of iopromide 370 in comparison to that of sodium meglumine diatrizoate 370 or iopamidol 370 in doses of 2 ml/kg body weight was examined in two controlled double-blind studies with intravenous digital subtraction angiography on the basis of enzyme assays in serum and urine. In patients with normal kidney function no changes were observed in the levels of the liver enzymes GPT, GOT, and gamma glutamyl transpeptidase (GGT) serum up to 72 hours after injection of iopromide or sodium meglumine diatrizoate. Among the kidney-specific enzymes, the excretion of GGT in urine increased after injection of iopromide and iopamidol. The maximum increase of GGT excretion was, however, statistically significantly lower in the group treated with iopromide than in the iopamidol group. Within 72 hours, the activities had been returned to the initial values in both groups.

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