Clinical Chemistry Laboratory, Maasstad Hospital, Rotterdam, The Netherlands.
Clinical Chemistry Laboratory, Treant Health Care Group, Scheper Hospital Location, Emmen, The Netherlands.
Biochem Med (Zagreb). 2021 Feb 15;31(1):010706. doi: 10.11613/BM.2021.010706. Epub 2020 Dec 15.
The intraindividual variability in urinary creatinine excretion is notoriously large. The aims of this study were to investigate the variability of duplicate consecutive 24-hour urinary creatinine excretions in patients and to develop a model for the detection and correction of discrepant creatinine excretions.
A group of 270 patients (82 men and 188 women) were included in the study. We collected the following data: urinary 24-hour volumes (volumetric/gravimetric) and urinary creatinine concentrations (Jaffé/enzymatic) on both collection days. We performed specific calculations to detect discrepant creatinine excretions.
In 60 patients (22%) discrepant collections were found. Among the remaining 78%, 22% of the patients collected very accurately (almost identical urinary creatinine excretions). In this subgroup the volume ratios and the creatinine concentration ratios behave inversely as in a dilution curve. A theoretical model and six collection scenarios were developed to detect, interpret and correct discrepant collections. Practical examples are given to illustrate the use of the model in successful correction of creatinine and other analytes for under- or overcollection.
We conclude that missed or overcollected urine volumes are the largest source of variation in creatinine excretion. Discrepancies in consecutive duplicate 24-hour creatinine excretions can be detected and corrected with specific calculations by means of the presented model. The effectiveness of these corrections is demonstrated with examples from daily practice. These calculations can be easily automated.
尿液肌酐排泄的个体内变异性很大。本研究旨在探讨患者连续两次 24 小时尿液肌酐排泄的变异性,并建立一种检测和纠正肌酐排泄差异的模型。
本研究纳入了 270 例患者(82 名男性和 188 名女性)。我们收集了以下数据:两次收集日的尿液 24 小时量(体积/重量)和尿液肌酐浓度(Jaffé/酶法)。我们进行了特定的计算来检测差异的肌酐排泄。
在 60 例患者(22%)中发现了差异采集。在剩余的 78%中,22%的患者采集非常准确(几乎相同的尿液肌酐排泄)。在这个亚组中,体积比和肌酐浓度比的行为与稀释曲线相反。提出了一个理论模型和六种采集方案来检测、解释和纠正差异采集。给出了实际示例来说明如何使用该模型成功纠正肌酐和其他分析物的欠采或过采。
我们得出结论,漏采或过采的尿液量是肌酐排泄变异性的最大来源。通过所提出的模型,可以通过特定的计算来检测和纠正连续两次 24 小时肌酐排泄的差异。通过日常实践中的示例证明了这些校正的有效性。这些计算可以很容易地自动化。