高渗透压造影剂和低渗透压造影剂的肾毒性:潜在风险患者数字减影血管造影后的病例对照研究。

J E Scherberich, A Fischer, E Rautschka, J Kollath, H Riemann
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引用次数: 0

摘要

静脉注射高渗或低渗造影剂(CM)前后120小时尿液中肾脏特异性标记蛋白的排泄情况;在数字血管成像后,对患者进行斜移,iopamidol 370)监测。随机临床研究纳入标准共40例患者(15例女性,25例男性;平均年龄64.5岁),年龄≥50岁或有糖尿病,血清肌酐浓度正常。与对照组相比,注射CM后所有患者肾小管指示酶丙氨酸氨基肽酶、γ -谷氨酰转肽酶、碱性磷酸酶以及肾小球局部血管紧张酶A的消除均显著升高。在48小时后观察到最显著的差异。相比之下,尿标本中的溶酶体n -乙酰- β - d -氨基葡萄糖酶活性反应不太清楚,似乎是评估CM肾毒性的一个不太敏感的参数。静脉注射低渗CM - iopamidol 370 (832 mOsm/kg)后,毛囊边界的消除以及肾小球标记蛋白的减少明显低于静脉注射异位胺76 (2100 mOsm/kg)后。在所有40例患者中,观察到肌酐清除率显著降低;然而,接受分流酯治疗的患者肌酐清除率显著降低(CM后0至24 - 48小时),而接受iopamidol治疗的患者则没有。两组CM注射后48小时肌酐清除率无差异。由于肾损伤的非离子型无创参数,低渗透性CM对潜在风险患者的肾毒性较小,应优先于常规CM。
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Nephrotoxicity of high and low osmolar contrast media: case control studies following digital subtraction angiography in potential risk patients.

The urinary excretion of kidney-specific marker proteins before and 120 hours after intravenous injection of either high- or low-osmolar contrast media (CM; diatrizoate, iopamidol 370) was monitored in patients after digital vascular imaging. Inclusion criteria for the randomized clinical study in a total of 40 patients (15 women, 25 men; mean age, 64.5 years) were at least 50 years of age or diabetes mellitus with normal creatinine concentration in serum. Compared with the control period, the elimination of tubular indicator enzymes alanine aminopeptidase, gamma-glutamyltranspeptidase, alkaline phosphatase, as well as of glomerular localized angiotensinase A was significantly higher in all patients after injection of the CM. The most significant differences were observed after 48 hours. In contrast, lysosomal N-acetyl-beta-D-glucosaminidase activity in urine specimens reacted less clearly and appears to be a less sensitive parameter in assessing CM nephrotoxicity. Elimination of brush border as well as of glomerular marker proteins was significantly lower after intravenous injection of low-osmolar CM iopamidol 370 (832 mOsm/kg) than after meglumine diatrizoate 76 (2100 mOsm/kg). In all 40 patients a significant decrease in creatinine clearance was observed; however, patients receiving diatrizoate had a significant decrease in creatinine clearance (period 0 versus 24 to 48 hours after CM), whereas patients after administration of iopamidol had not. No difference was found between creatinine clearance after 48 hours of CM injection within both groups of CM. Due to noninvasive parameters of kidney damage nonionic, low-osmolar CM are less nephrotoxic in potential risk patients, and should be preferred to conventional CM.

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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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