Delgado Acosta Fernando, Jiménez Gómez Elvira, Bravo Rey Isabel, Valverde Moyano Roberto, de Asís Bravo-Rodriguez Francisco, Oteros Fernández Rafael
Neuroradiology Unit, Hospital Reina Sofía, Córdoba, Spain.
Interv Neuroradiol. 2020 Feb;26(1):33-37. doi: 10.1177/1591019919883755. Epub 2019 Oct 23.
The aim is to report the incidence and risk factors of contrast-induced nephropathy after the use of iodine-based contrast for the endovascular treatment of acute ischemic stroke.
Data from patients who underwent neuroendovascular procedures in a center over a period of 22 months were analysed retrospectively. Contrast-induced nephropathy was determined by an increase in serum creatinine level of >25% of baseline or an absolute increase in serum creatinine level of at least 44 µmol/L (0.50 mg/dL) occurring after intravascular administration of contrast media without alternative explanation. The primary outcome measure of this study was the presence of contrast-induced nephropathy in these treated patients. Continuous data were presented as mean ± standard deviation, and categorical data as frequencies or percentages. The comparison was made using Student's t-test or Fisher's test. Logistic regression was performed to find independent contrast-induced nephropathy predictors. All statistical analyses were performed using Microsoft Excel. A p value of less than 0.05 was considered statistically significant.
One hundred and eighty-nine patients undergoing endovascular treatment for acute ischemic stroke. Twenty cases of the total cohort (n = 189) presented contrast-induced nephropathy (10.58%). Only diabetes and creatinine levels between 1.3 and 2.5 mg/dL were associated with contrast-induced nephropathy. No patient was treated with dialysis.
Contrast-induced nephropathy is a relatively common complication after endovascular treatment of acute ischemic stroke and is associated with worse outcome in patients with this condition. However, there is no increase in the frequency of hemodialysis after the use of iodinated contrast medium.
报告在使用碘基造影剂进行急性缺血性卒中血管内治疗后对比剂肾病的发生率及危险因素。
回顾性分析某中心22个月期间接受神经血管介入手术患者的数据。对比剂肾病通过血管内注射造影剂后血清肌酐水平较基线升高>25%或血清肌酐水平绝对升高至少44µmol/L(0.50mg/dL)且无其他解释来确定。本研究的主要结局指标是这些接受治疗患者中对比剂肾病的发生情况。连续数据以均数±标准差表示,分类数据以频数或百分比表示。采用Student t检验或Fisher检验进行比较。进行逻辑回归以寻找对比剂肾病的独立预测因素。所有统计分析均使用Microsoft Excel进行。p值<0.05被认为具有统计学意义。
189例接受急性缺血性卒中血管内治疗的患者。整个队列(n = 189)中有20例出现对比剂肾病(10.58%)。仅糖尿病以及肌酐水平在1.3至2.5mg/dL之间与对比剂肾病相关。无患者接受透析治疗。
对比剂肾病是急性缺血性卒中血管内治疗后相对常见的并发症,且与该疾病患者的不良结局相关。然而,使用碘化造影剂后血液透析频率并未增加。