改良血清肾小球滤过率(GFR)与99mTc-DTPA GFR方法在肝硬化患者中的性能比较

Zaid Haddadin, V. Lee, C. Conlin, Lei Zhang, Kristi Carlston, G. Morrell, Daniel Kim, J. Hoffman, K. Morton
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引用次数: 7

摘要

肾小球滤过率(GFR)的测量在肝硬化患者中是至关重要的,但基于血清肌酐的测量可能是错误的。估计GFR (eGFR)的新公式在肝硬化中显示出不同的性能,可能是因为测量GFR (mGFR)的参考方法不准确。本研究的主要目的是比较4种改进的eGFR方程与1室、2样本血浆斜率截断99mTc-DTPA mGFR方法的性能,以确定是否有任何eGFR计算可以替代肝硬化患者的血浆99mTc-DTPA mGFR。次要目的是验证与仅使用血浆方法相比,使用自愿尿液收集的mGFR是否会引入误差。方法:54例肝硬化患者在静脉注射185mbq 99mTc-DTPA后1和3小时,分别采集2份血浆样本进行mGFR检测。GFR也通过血液和尿液样本的UV/P计算产生。将这些mgfr与4个估算方程产生的egfr进行比较:MDRD(肾脏疾病改良饮食)、CKD-EPI(慢性肾脏疾病流行病学协作)(血清肌酐[SCr])、CKD-EPI(胱抑素[CysC])和CKD-EPI (CysC+SCr)。egfr与mGFR通过Pearson相关性、精度、偏差、百分比偏差和准确性(egfr与相应mGFR的差异<10% [p10]、<20% [p20]或<30% [p30])进行比较。结果:以UV/P 99mTc-DTPA mGFR为对照时,所有egfr的表现都不如以血浆99mTc-DTPA mGFR为对照时。与血浆99mTc-DTPA mGFR方法相比,所有eGFR方程的性能优于大多数已发表的报告。egfr和mgfr之间有中等好的正相关。与血浆99mTc-DTPA mGFR相比,egfr的精度在14-20 mL/min范围内,偏差可以忽略不计。与血浆99mTc-DTPA mGFR相比,CKD-EPI (CysC+SCr)表现出最好的整体性能和准确性,分别为85.19% (p30)、75.93% (p20)和42.59% (p10)。结论:由于使用血浆99mTc-DTPA mGFR方法作为参考,eGFR测量方程的估计效果优于大多数已发表的报告。CKD-EPI (CysC+SCr) eGFR整体表现最佳。然而,当需要精确的GFR测量时,可能需要更多的鉴别方法。与仅使用血浆的方法相比,使用尿液采集mGFR测量可能会引入误差。
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Comparison of Performance of Improved Serum Estimators of Glomerular Filtration Rate (GFR) to 99mTc-DTPA GFR Methods in Patients with Hepatic Cirrhosis
Glomerular filtration rate (GFR) measurements are critical in patients with hepatic cirrhosis but potentially erroneous when based on serum creatinine. New equations for estimated GFR (eGFR) have shown variable performance in cirrhotics, possibly because of inaccuracies in reference methods for measured GFR (mGFR). The primary objective was to compare the performance of 4 improved eGFR equations with a 1-compartment, 2-sample plasma slope intercept 99mTc-DTPA mGFR method to determine whether any of the eGFR calculations could replace plasma 99mTc-DTPA mGFR in patients with cirrhosis. The secondary objective was to test the hypothesis that mGFR using voluntary voided urine collections introduces error compared with plasma-only methods. Methods: Fifty-four patients with hepatic cirrhosis underwent mGFR determinations from 2 plasma samples at 1 and 3 h after intravenous administration of 185 MBq of 99mTc-DTPA. GFR was also generated by a UV/P calculation derived from blood and urine samples. These mGFRs were compared with the eGFRs generated by 4 estimating equations: MDRD (Modified Diet in Renal Disease), CKD-EPI (Chronic Kidney Disease-Epidemiology Collaboration) (serum creatinine [SCr]), CKD-EPI (cystatin [CysC]), and CKD-EPI (CysC+SCr). eGFRs were compared with mGFRs by Pearson correlation, precision, bias, percentage bias, and accuracy (eGFRs varying by <10% [p10], <20% [p20] or <30% [p30] from the corresponding mGFR). Results: All eGFRs showed poorer performance when the UV/P 99mTc-DTPA mGFR was used as the reference than when the plasma 99mTc-DTPA mGFR was used. When compared with the plasma 99mTc-DTPA mGFR method, the performance of all eGFR equations was superior to most published reports. There was a moderately good positive correlation between eGFRs and mGFRs. When compared with plasma 99mTc-DTPA mGFR, precision of eGFRs was in the range of 14–20 mL/min and showed a negligible bias. Compared with the plasma 99mTc-DTPA mGFR, CKD-EPI (CysC+SCr) showed the best overall performance and accuracy, at 85.19% (p30), 75.93% (p20), and 42.59% (p10). Conclusion: Estimating equations for measuring eGFR performed better than in most published reports, attributable to use of the plasma 99mTc-DTPA mGFR method as a reference. CKD-EPI (CysC+SCr) eGFR showed the best overall performance. However, more discriminating methods may be required when accurate GFR measurements are necessary. mGFR measurements using urine collections may introduce error compared with plasma-only methods.
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