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新型造影剂碘海醇的血浆清除率:一种评估肾小球滤过率的方法。

Plasma clearance of a new contrast agent, iohexol: a method for the assessment of glomerular filtration rate.

作者信息

Krutzén E, Bäck S E, Nilsson-Ehle I, Nilsson-Ehle P

出版信息

J Lab Clin Med. 1984 Dec;104(6):955-61.

PMID:6438261
Abstract

We developed a rapid and precise method for the chemical determination of a new contrast agent, iohexol (N,N'-bis(2,3-dihydroxypropyl)-5-N-(2,3-dihydroxypropyl)-acetamido-2,4, 6-triiodoisophtalamide). Its sensitivity allows the monitoring of plasma concentrations for at least 6 hours after the injection of a single small dose. The elimination rate of iohexol was constant after approximately 90 minutes; plasma clearance in healthy volunteers averaged 127 ml/min. The injected dose was quantitatively recovered in urine. Determination of plasma clearance on two different occasions demonstrated a total variation of 11% (coefficient of variation); the methodologic imprecision was minor compared with the biologic variation. In 42 patients with normal to moderately impaired renal function, a comparison of iohexol and 51Cr-ethylenediaminetetraacetic acid clearances demonstrated an excellent correlation (correlation coefficient 0.98). The simplicity and rapidity of the new method makes it an attractive alternative to current methods for the assessment of glomerular filtration rate.

摘要

我们开发了一种快速且精确的化学方法,用于测定一种新型造影剂碘海醇(N,N'-双(2,3-二羟基丙基)-5-N-(2,3-二羟基丙基)-乙酰氨基-2,4,6-三碘间苯二甲酰胺)。其灵敏度能够在单次注射小剂量后至少6小时监测血浆浓度。碘海醇的消除率在约90分钟后保持恒定;健康志愿者的血浆清除率平均为127毫升/分钟。注射剂量在尿液中可定量回收。在两个不同时间测定血浆清除率显示总变异为11%(变异系数);与生物学变异相比,方法学不精密度较小。在42例肾功能正常至中度受损的患者中,碘海醇和51Cr-乙二胺四乙酸清除率的比较显示出极佳的相关性(相关系数0.98)。新方法的简便性和快速性使其成为评估肾小球滤过率的现有方法的一个有吸引力的替代方法。

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