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标准透析器配置下的中等稀释度在线血液透析滤过

Mid-dilution on-line haemodiafiltration in a standard dialyser configuration.

作者信息

Krieter Detlef H, Collins Gregory, Summerton James, Spence Edward, Moragues Hélène Leray, Canaud Bernard

机构信息

Nephrology, University Hospital, Montpellier, France.

出版信息

Nephrol Dial Transplant. 2005 Jan;20(1):155-60. doi: 10.1093/ndt/gfh520. Epub 2004 Nov 2.

Abstract

BACKGROUND

Mid-dilution haemodiafiltration (HDF) results in an improved middle molecule removal compared with standard HDF. The OLpur MD 190 haemodiafilter represents a new dialyser design exclusively for mid-dilution on-line HDF. Compared with standard haemodialysers, structural changes in the headers allow the infusion of high replacement fluid volumes after a first post-dilution and before a second pre-dilution stage.

METHODS

We compared in vitro the new device [blood flow (QB) 400 ml/min, substitution flow (QS) 100 and 200 ml/min, dialysate flow (QD) 800 ml/min] with a conventional high-flux dialyser of the same surface area in haemodialysis (HD) (QD 500 ml/min) and post-dilution HDF (at QS 60, QD = 500 ml/min and at QS 100, QD = 800 ml/min) modes. Subsequently, we performed an initial clinical application of the new device in six mid-dilution HDF treatments of five end-stage renal disease patients (QB 400 ml/min, QS 200 ml/min, QD 800 ml/min, treatment duration 205+/-23 min).

RESULTS

In vitro urea and beta2-microglobulin clearances in mid-dilution HDF were, respectively, 309.2+/-5.5 and 144.4+/-15.2 ml/min (QS 100) and 321.6+/-4.1 and 204.9+/-4.1 ml/min (QS 200), compared with 278.6+/- 17.2 and 94.0+/-7.6 ml/min in HD, and 310.8+/-10.2 and 123.0+/-6.5 ml/min (QS 60) and 323.6+/-11.2 and 158.0+/-10.3 ml/min (QS 100) in post-dilution HDF. The in vivo trials showed the clinical utility of the device and confirmed the in vitro data: urea and beta2-microglobulin clearances were, respectively, 324.6+/- 10.9 and 207.9+/-29.3 ml/min, while reduction ratios were 75.0+/-5.5 and 83.6+/-4.7%.

CONCLUSION

Our preliminary results need confirmation in a prospective cross-over study. However, the Nephros MD 190 haemodiafilter promises to be a true technological step ahead in terms of improved beta2-microglobulin removal.

摘要

背景

与标准血液透析滤过(HDF)相比,中稀释血液透析滤过能更好地清除中分子物质。OLpur MD 190血液透析滤过器代表了一种专门用于中稀释在线HDF的新型透析器设计。与标准血液透析器相比,其端盖的结构变化允许在第一次后稀释后和第二次预稀释阶段之前输注高置换液量。

方法

我们在体外将新设备[血流量(QB)400 ml/分钟,置换流量(QS)100和200 ml/分钟,透析液流量(QD)800 ml/分钟]与相同表面积的传统高通量透析器在血液透析(HD)(QD 500 ml/分钟)和后稀释HDF(QS 60时,QD = 500 ml/分钟;QS 100时,QD = 800 ml/分钟)模式下进行比较。随后,我们在5例终末期肾病患者的6次中稀释HDF治疗中对新设备进行了初步临床应用(QB 400 ml/分钟,QS 200 ml/分钟,QD 800 ml/分钟,治疗持续时间205±23分钟)。

结果

在中稀释HDF中,体外尿素和β2-微球蛋白清除率分别为(QS 100时)309.2±5.5和144.4±15.2 ml/分钟,(QS 200时)321.6±4.1和204.9±4.1 ml/分钟;相比之下,HD中的清除率分别为278.6±17.2和94.0±7.6 ml/分钟,后稀释HDF中(QS 60时)为310.8±10.2和123.0±,6.5 ml/分钟,(QS 100时)为323.6±11.2和158.0±10.3 ml/分钟。体内试验显示了该设备的临床实用性并证实了体外数据:尿素和β2-微球蛋白清除率分别为324.6±10.9和207.9±29.3 ml/分钟,而降低率分别为75.0±5.5和83.6±4.7%。

结论

我们的初步结果需要在前瞻性交叉研究中得到证实。然而,Nephros MD 190血液透析滤过器有望在改善β2-微球蛋白清除方面成为真正的技术进步。

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