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(99m)Tc-HEPIDA肝脏清除率测定的不确定性分析

Uncertainty analysis of (99m)Tc-HEPIDA liver clearance determination.

作者信息

Surma Marian J

机构信息

Nuclear Medicine Department of the Medical University of Łódź, Poland.

出版信息

Nucl Med Rev Cent East Eur. 2005;8(2):116-24.

Abstract

BACKGROUND

The aim of the study was to obtain information on the accuracy and precision of (99m)Tc-HEPIDA hepatic (Cl(Hp)) and plasma (Cl(Pl)) clearances and selection of an appropriate estimator of the measurement uncertainty of a single determination of these quantities.

MATERIAL AND METHODS

In a simulation (Monte Carlo) experiment, it was assumed that the recorded results of plasma and hepatic clearances, as obtained from 185 patients, provided authentic information about (99m)Tc-HEPIDA behaviour in the body over a wide range of the clearances studied. The time course (99m)Tc-HEPIDA concentration in blood plasma has been described by means of biexponential function with parameter values derived for each patient. For each patient, using these data and urinary excretion data, there had been 5000 simulations performed; in each of the latter, the directly measured numbers have been substituted by simulated ones, obtained by means of varying the real ones, using random generated values. These reflected errors of plasma and radioactive standard pipetting (from 1 to 5%) and stochasticity of counting radioactive decay (1%). The time of blood sampling and urine voiding was also varied, assuming realistic uncertainty. The varied values were then used for computation of the simulated clearances. From the 5,000 calculated clearances for each patient, mean-values were calculated, as well as mean standard errors, standard deviations and mean uncertainty of measurements using a widely accepted rule of partial error propagation, and, in addition, a modified rule of the latter. Accuracy of clearance (Cl(Pl), Cl(Hp), Cl(Ur)) determination was assessed on the basis of comparison of mean values from simulations with those from directly recorded values. Precision was identified with standard deviation of each of the 5000 simulations. The uncertainty thus obtained was compared with results of calculated traditional and modified uncertainty. There was good agreement between standard deviation of the simulations with results of the modified calculation of total differential. Therefore, a coefficient of variation from simulation computations and a modified means of calculation of the propagated errors was accepted as a measure of uncertainty of a single determination.

RESULTS/CONCLUSIONS: There was a very high correlation between the mean values from simulations and those from direct determinations (r > 0.98 in each case). The regression lines practically corresponded to the lines of identity. These correlations were not affected by the assumed range of pipetting uncertainty. In conclusion, the methods of (99m)Tc-HEPIDA clearance determination are satisfactory. Precision of clearance measurements depends substantially upon uncertainty of pipetting. For plasma clearance, the coefficients of variations at Cl(Pl) > 350 ml/min and at ab.80 ml/min amounted to 2 and 11% respectively, at pipetting uncertainty of 2%. Similarly, for hepatic clearances of (99m)Tc-HEPIDA of 300 ml/min and 30 ml/min, CV was 2.5 and 25%, respectively (at the same uncertainty of pipetting).

摘要

背景

本研究的目的是获取有关(99m)锝 - 海派达(Tc-HEPIDA)肝脏清除率(Cl(Hp))和血浆清除率(Cl(Pl))的准确性和精密度的信息,并选择一个合适的估计量来评估这些量单次测定的测量不确定度。

材料与方法

在一个模拟(蒙特卡洛)实验中,假设从185名患者获得的血浆和肝脏清除率的记录结果,能提供关于(99m)Tc-HEPIDA在体内在所研究的广泛清除率范围内行为的真实信息。血浆中(99m)Tc-HEPIDA浓度随时间的变化过程用双指数函数描述,其参数值针对每个患者得出。对于每个患者,利用这些数据和尿液排泄数据进行了5000次模拟;在每次模拟中,直接测量的数值被通过改变真实值并使用随机生成值得到的模拟值所替代。这些反映了血浆和放射性标准移液的误差(从1%到5%)以及放射性衰变计数的随机性(1%)。采血和排尿时间也有所变化,假设了实际的不确定度。然后将这些变化值用于计算模拟清除率。对于每个患者的5000个计算出的清除率,计算平均值、平均标准误差、标准差以及使用广泛接受的部分误差传播规则计算的测量平均不确定度,此外还使用了该规则的修正版。基于模拟平均值与直接记录值的比较来评估清除率(Cl(Pl)、Cl(Hp)、Cl(Ur))测定的准确性。精密度用5000次模拟中每次的标准差来确定。将由此获得的不确定度与传统和修正不确定度的计算结果进行比较。模拟的标准差与总微分修正计算结果之间有很好的一致性。因此,模拟计算的变异系数和传播误差的修正计算方法被接受为单次测定不确定度的度量。

结果/结论:模拟平均值与直接测定值之间存在非常高的相关性(每种情况下r > 0.98)。回归线实际上与恒等线相对应。这些相关性不受假定的移液不确定度范围的影响。总之,(99m)Tc-HEPIDA清除率测定方法是令人满意的。清除率测量的精密度很大程度上取决于移液的不确定度。对于血浆清除率,当Cl(Pl) > 350 ml/min且约为80 ml/min时,在移液不确定度为2%的情况下,变异系数分别为2%和11%。同样,对于(99m)Tc-HEPIDA肝脏清除率为300 ml/min和30 ml/min时,变异系数分别为2.5%和25%(在相同的移液不确定度下)。

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