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用于测定肾小球滤过率的菊粉清除率:使用新分析方法对各种方法的重新评估。

Sinistrin clearance for determination of glomerular filtration rate: a reappraisal of various approaches using a new analytical method.

作者信息

Buclin T, Pechère-Bertschi A, Séchaud R, Décosterd L A, Munafo A, Burnier M, Biollaz J

机构信息

Division of Clinical Pharmacology, University Hospital, Lausanne, Switzerland.

出版信息

J Clin Pharmacol. 1997 Aug;37(8):679-92. doi: 10.1002/j.1552-4604.1997.tb04355.x.

Abstract

Several approaches are available to estimate the glomerular filtration rate (GFR) from the sinistrin clearance. To compare such approaches, GFR was estimated in six healthy volunteers, both after a bolus injection and a bolus dose followed by a 6-hour infusion. A recently developed high-performance liquid chromatography method was used for the determination of sinistrin levels, enabling precise measurements in plasma and urine samples with high sensitivity. Blood and urine were sampled up to 6 hours. Four calculation methods for estimating GFR were applied: 1) classical ratio of urinary excretion rate over plasma concentration (UV/P); 2) two-point (log-linear regression slope times monocompartmental volume of distribution) after bolus; 3) ratio of dose over area under the curve (D/AUC) after bolus; and 4) ratio of infusion rate over steady-state concentration during infusion (Rinf/P). The results obtained by fitting a pharmacokinetic model to all the plasma and urine data served as the standard against which the performance of the respective calculation methods were examined. The UV/P method performed poorly on bolus data, mainly by underestimating GFR at late times; on both bolus and infusion data, it suffered from important imprecisions on the urinary volume. The two-point method appeared applicable only between 2 and 4 hours after the bolus dose. The D/AUC method with extrapolation to infinity was highly reliable when integrating the concentrations up to 3 hours or more after the bolus dose. The Rinf/P method was satisfactory if applied later than 2 to 3 hours after the loading dose. The advantages and drawbacks of each method have to be evaluated in relation to the particular clinical setting in which GFR is to be estimated.

摘要

有几种方法可通过氨基葡聚糖清除率来估算肾小球滤过率(GFR)。为比较这些方法,对6名健康志愿者在静脉推注和静脉推注后持续6小时输注两种情况下进行了GFR估算。采用一种最近开发的高效液相色谱法测定氨基葡聚糖水平,该方法能够对血浆和尿液样本进行高灵敏度的精确测量。在6小时内采集血液和尿液样本。应用了四种估算GFR的计算方法:1)尿排泄率与血浆浓度的经典比值(UV/P);2)推注后两点法(对数线性回归斜率乘以单室分布容积);3)推注后剂量与曲线下面积的比值(D/AUC);4)输注期间输注速率与稳态浓度的比值(Rinf/P)。通过对所有血浆和尿液数据拟合药代动力学模型得到的结果作为标准,据此检验各计算方法的性能。UV/P方法在推注数据上表现不佳,主要是在后期低估了GFR;在推注和输注数据上,它在尿量方面存在重大不精确性。两点法似乎仅在推注剂量后2至4小时适用。推注剂量后3小时或更长时间积分浓度时,外推至无穷大的D/AUC方法高度可靠。如果在负荷剂量后2至3小时以后应用,Rinf/P方法令人满意。每种方法的优缺点必须根据估算GFR的特定临床情况进行评估。

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