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碘海醇血浆清除率测定肾小球滤过率的准确性:单次采样与双重采样的比较。

Accuracy of iohexol plasma clearance for GFR-determination: a comparison between single and dual sampling.

作者信息

Zhang Yong, Sui Zhun, Yu Ze, Li Tai Feng, Feng Wan Yu, Zuo Li

机构信息

Department of Nephrology, Peking University People's Hospital, No. 11 Xizhimen South Street, Xi Cheng District, Beijing, 100044, China.

Department of Pharmacy, Peking University People's Hospital, No. 11 Xizhimen South Street, Xi Cheng District, Beijing, China.

出版信息

BMC Nephrol. 2018 Jul 11;19(1):174. doi: 10.1186/s12882-018-0965-7.

Abstract

BACKGROUND

Current guidelines regarding plasma-sampling techniques for glomerular filtration rate (GFR) determination are inconsistent. Single-sample methods are commonly believed not to be precise enough to meet clinical demands. The present study compared the agreement between single- and dual- plasma sampling methods with a three-point plasma clearance of iohexol.

METHODS

A total of 46 healthy volunteers and 124 chronic kidney disease (CKD) patients with varying degrees of renal dysfunction received 5 ml iohexol (300 mgI/ml) i.v. and plasma samples were drawn at 2-, 3- and 4-h post-injection. Plasma-iodine concentrations were detected by high-performance liquid chromatography (HPLC).

RESULTS

Bias was similar among single-plasma sampling methods (SPSM) and dual-plasma sampling methods (DPSM). The best correlation was obtained from the 2- and 4-h DPSM (concordance correlation coefficient [CCC]: 0.9988) with none of the estimates differed by more than 30% from the reference GFR and only one (0.06%) estimate differed by more than 10% (P, 100%; P, 99.4%). SPSM using samples around 3- or 4-h demonstrated acceptable accuracy at a GFR level of ≥60 ml/min/1.73m (P = 100% and P > 75% for both measurements).

CONCLUSION

4-h SPSM is advantageous in clinical practice in subjects with GFR ≥ 60 ml/min/1.73m. For patients with an expected GFR < 60 ml/min/1.73m, a prolonged sampling time is more reliable.

摘要

背景

目前关于用于测定肾小球滤过率(GFR)的血浆采样技术的指南并不一致。单样本方法通常被认为不够精确,无法满足临床需求。本研究比较了单血浆采样方法和双血浆采样方法与碘海醇三点血浆清除率之间的一致性。

方法

共有46名健康志愿者和124名不同程度肾功能不全的慢性肾脏病(CKD)患者静脉注射5毫升碘海醇(300毫克碘/毫升),并在注射后2小时、3小时和4小时采集血浆样本。通过高效液相色谱法(HPLC)检测血浆碘浓度。

结果

单血浆采样方法(SPSM)和双血浆采样方法(DPSM)之间的偏差相似。2小时和4小时的DPSM相关性最佳(一致性相关系数[CCC]:0.9988),所有估计值与参考GFR的差异均不超过30%,只有一个估计值(0.06%)差异超过10%(P,100%;P,99.4%)。在GFR水平≥60毫升/分钟/1.73平方米时,使用3小时或4小时左右样本的SPSM显示出可接受的准确性(两次测量的P均为100%且P>75%)。

结论

对于GFR≥60毫升/分钟/1.73平方米的受试者,4小时SPSM在临床实践中具有优势。对于预期GFR<60毫升/分钟/1.73平方米的患者,延长采样时间更可靠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f257/6042400/dedbcc377664/12882_2018_965_Fig1_HTML.jpg

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