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严重肾功能受损患者中非离子型X射线造影剂碘克沙醇和碘海醇的消除情况。

Elimination of the non-ionic X-ray contrast media iodixanol and iohexol in patients with severely impaired renal function.

作者信息

Nossen J O, Jakobsen J A, Kjaersgaard P, Andrew E, Jacobsen P B, Berg K J

机构信息

Nycomed Imaging AS, Oslo, Norway.

出版信息

Scand J Clin Lab Invest. 1995 Jul;55(4):341-50. doi: 10.3109/00365519509104972.

Abstract

Iodixanol (Visipaque) and iohexol (Omnipaque) are dimeric and monomeric, respectively, non-ionic X-ray contrast media (CM), with well-characterized pharmacokinetics in healthy volunteers. This study was undertaken to study the pharmacokinetics of the contrast media in patients with severely impaired renal function. A total of 16 patients referred for preoperative abdominal angiography were randomized to form two groups of eight patients, receiving either iodixanol 320 mgI ml-1 or iohexol 350 mgI ml-1. Urine and faeces were sampled before the examination and collected quantitatively for five days afterwards, and blood samples were drawn frequently. The concentrations of iodine and contrast medium in urine and in serum, and the amount of iodine in faeces were determined. Mean baseline creatinine clearance was 13.6 and 9.9 ml min-1 1.73 m-2 in the iodixanol and iohexol groups, respectively. Patients in the iodixanol group received on average 0.34 gI per kg bodyweight (bw) and those in the iohexol group 0.39 gI per kg bw. The semilogarithmic plots of serum concentration of CM vs. time indicated elimination according to a two-compartment model. The mean elimination half-life was 23.0 h for iodixanol and 27.2 h for iohexol, and the mean apparent volume of distribution was similar for the two CM, ranging from 0.20 to 0.30 1 per kg bw. Mean plasma clearance of iodixanol was 10.4 ml min-1 1.73 m-2 and 6.9 ml min-1 1.73 m-2 for iohexol, whereas the mean renal clearances were 8.7 and 6.1 ml min-1 1.73 m-2, respectively. Mean faecal recovery was 8.2% for iodixanol and 6.1% for iohexol, and the respective figures for that in urine were 76.1 and 74.8%. Renal clearance of radiolabelled iothalamate, a marker of glomerular filtration rate (GFR), measured simultaneously, indicated that both CM were eliminated by the kidneys by glomerular filtration only. Thus, both media are suitable as GFR markers.

摘要

碘克沙醇(威视派克)和碘海醇(欧乃派克)分别为二聚体和单体非离子型X射线造影剂(CM),在健康志愿者中的药代动力学特征明确。本研究旨在探讨造影剂在肾功能严重受损患者中的药代动力学。共有16例因术前腹部血管造影而转诊的患者被随机分为两组,每组8例,分别接受320 mgI/ml的碘克沙醇或350 mgI/ml的碘海醇。在检查前采集尿液和粪便样本,并在之后的五天内进行定量收集,同时频繁采集血样。测定尿液和血清中碘及造影剂的浓度,以及粪便中碘的含量。碘克沙醇组和碘海醇组的平均基线肌酐清除率分别为13.6和9.9 ml·min-1·1.73 m-2。碘克沙醇组患者平均每千克体重(bw)接受0.34 gI,碘海醇组患者平均每千克bw接受0.39 gI。CM血清浓度对时间的半对数图表明其消除符合二室模型。碘克沙醇的平均消除半衰期为23.0小时,碘海醇为27.2小时,两种CM的平均表观分布容积相似,范围为每千克bw 0.20至0.30升。碘克沙醇的平均血浆清除率为10.4 ml·min-1·1.73 m-2,碘海醇为6.9 ml·min-1·1.73 m-2,而平均肾清除率分别为8.7和6.1 ml·min-1·1.73 m-2。碘克沙醇的平均粪便回收率为8.2%,碘海醇为6.1%,尿液中的相应回收率分别为76.1%和74.8%。同时测量的放射性标记碘他拉酸盐(肾小球滤过率(GFR)的标志物)的肾清除率表明,两种CM均仅通过肾小球滤过经肾脏消除。因此,两种造影剂均适合作GFR标志物。

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