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Development of an outpatient finger-prick glomerular filtration rate procedure suitable for epidemiological studies

机译:制定适合流行病学研究的门诊手指刺肾小球滤过率程序

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Development of an outpatient finger-prick glomerular filtration rate (GFR) procedure suitable for epidemiological studies. In clinical practice, reference GFR procedures are rarely used; in large-scale research studies, a great deal of effort and experience is required to obtain them, which is a considerable disincentive to using GFR as an end point. The major problem for both clinical staff and the subject is the length of time that the procedure takes, requiring continuous attendance in the outpatient clinic or its vicinity. Using iohexol as a marker, we therefore propose an alternative approach, which addresses this fundamental deterrent to a more widespread use of GFR measurement. Eighty-two GFR measurements were performed in a mixture of healthy subjects and patients with differing degrees of renal impairment with a wide range of GFRs. Serum was obtained from blood samples to enable a reference GFR to be calculated. Blood spots were collected on filter paper at the same intervals (120, 180, and 240min), allowed to dry, and then sent through the post. Serum and blood spots were analyzed simultaneously for each individual by automated reverse-phase high-pressure liquid chromatography. Standard linear regression analyses confirmed a good agreement (r2=0.953) between the iohexol serum GFR and iohexol blood spots GFR. Bland–Altman analysis confirmed that there was no concentration bias. Paired comparisons (Wilcoxon's paired signed rank test) showed no significant difference between the two measurements. Capillary sampling is simple, effective, and significantly reduces the time and costs of performing plasma clearance GFR measurements. This approach will make the GFR measurement more accessible for clinical practice and large-scale epidemiological studies may become feasible.
机译:开发适用于流行病学研究的门诊手指刺肾小球滤过率(GFR)程序。在临床实践中,很少使用参考GFR程序。在大规模研究中,获得它们需要大量的努力和经验,这极大地阻碍了将GFR用作终点。对于临床人员和受试者而言,主要问题是该过程花费的时间长,需要持续在门诊诊所或其附近就诊。因此,我们使用碘海醇作为标记物,提出了一种替代方法,该方法解决了对更广泛地使用GFR测量的这种基本威慑作用。在健康受试者和不同程度的肾功能不全的肾功能不全患者中混合进行了八十二次GFR测量。从血液样本中获取血清,以便能够计算参考GFR。以相同的时间间隔(120、180和240分钟)在滤纸上收集血斑,使其干燥,然后将其通过柱子。通过自动反相高压液相色谱仪同时分析每个人的血清和血斑。标准线性回归分析证实了碘海醇血清GFR与碘海醇血斑GFR之间的良好一致性(r2 = 0.953)。 Bland–Altman分析确认没有浓度偏差。配对比较(Wilcoxon的配对符号秩检验)显示两次测量之间没有显着差异。毛细管采样简单,有效,并且显着减少了执行血浆清除率GFR测量的时间和成本。这种方法将使GFR测定更易于临床实践,大规模的流行病学研究可能变得可行。

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