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动脉内与静脉内碘克沙醇给药后持续的肾脏增强。

Persistent renal enhancement after intra-arterial versus intravenous iodixanol administration.

机构信息

Department of Radiology, University of California San Francisco, 505 Parnassus Avenue, San Francisco, CA 94143-0628, United States.

出版信息

Eur J Radiol. 2011 Nov;80(2):378-86. doi: 10.1016/j.ejrad.2011.02.044. Epub 2011 Apr 5.

Abstract

PURPOSE

To examine the clinical significance of persistent renal enhancement after iodixanol administration.

METHODS

We retrospectively studied 166 consecutive patients who underwent non-enhanced abdominopelvic CT within 7 days after receiving intra-arterial (n=99) or intravenous (n=67) iodixanol. Renal attenuation was measured for each non-enhanced CT scan. Persistent renal enhancement was defined as CT attenuation>55 Hounsfield units (HU). Contrast-induced nephropathy (CIN) was defined as a rise in serum creatinine>0.5 mg/dL within 5 days after contrast administration.

RESULTS

While the intensity and frequency of persistent renal enhancement was higher after intra-arterial (mean CT attenuation of 73.7 HU, seen in 54 of 99 patients, or 55%) than intravenous contrast material administration (51.8 HU, seen in 21 of 67, or 31%, p<0.005), a multivariate regression model showed that the independent predictors of persistent renal enhancement were a shorter time interval until the subsequent non-enhanced CT (p<0.001); higher contrast dose (p<0.001); higher baseline serum creatinine (p<0.01); and older age (p<0.05). The route of contrast administration was not a predictor of persistent renal enhancement in this model. Contrast-induced nephropathy was noted in 9 patients who received intra-arterial (9%) versus 3 who received intravenous iodixanol (4%), and was more common in patients with persistent renal enhancement (p<0.01).

CONCLUSION

Persistent renal enhancement at follow-up non-contrast CT suggests a greater risk for contrast-induced nephropathy, but the increased frequency of striking renal enhancement in patients who received intra-arterial rather than intravenous contrast material also reflects the larger doses of contrast and shorter time to subsequent follow-up CT scanning for such patients.

摘要

目的

探讨碘克沙醇给药后持续性肾增强的临床意义。

方法

我们回顾性研究了 166 例连续患者,这些患者在接受动脉内(n=99)或静脉内(n=67)碘克沙醇后 7 天内接受了非增强的腹盆腔 CT。为每次非增强 CT 扫描测量肾衰减值。持续性肾增强定义为 CT 衰减值>55 亨斯菲尔德单位(HU)。对比剂肾病(CIN)定义为对比剂给药后 5 天内血清肌酐升高>0.5mg/dL。

结果

虽然动脉内(99 例患者中有 54 例,或 55%,平均 CT 衰减值为 73.7HU)对比剂给药后的肾增强强度和频率高于静脉内(67 例患者中有 21 例,或 31%,51.8HU,p<0.005),但多元回归模型显示,持续性肾增强的独立预测因素为直至随后非增强 CT 的时间间隔较短(p<0.001);更高的对比剂量(p<0.001);更高的基线血清肌酐(p<0.01);以及年龄较大(p<0.05)。在该模型中,对比剂给药途径不是持续性肾增强的预测因素。动脉内碘克沙醇组有 9 例(9%)发生对比剂肾病,静脉内碘克沙醇组有 3 例(4%),且在持续性肾增强患者中更常见(p<0.01)。

结论

随访非对比 CT 上的持续性肾增强提示对比剂肾病的风险更大,但接受动脉内而非静脉内对比剂的患者中更明显的肾增强发生率增加,也反映了此类患者对比剂剂量更大,以及随后的 CT 扫描时间更短。

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