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血液透析期间的磷酸盐动力学:双相调节的证据。

Phosphate kinetics during hemodialysis: Evidence for biphasic regulation.

作者信息

Spalding Elaine M, Chamney Paul W, Farrington Ken

机构信息

Department of Nephrology, Lister Hospital, Herts, England, United Kingdom.

出版信息

Kidney Int. 2002 Feb;61(2):655-67. doi: 10.1046/j.1523-1755.2002.00146.x.

Abstract

BACKGROUND

Hyperphosphatemia in the hemodialysis population is ubiquitous, but phosphate kinetics during hemodialysis is poorly understood.

METHODS

Twenty-nine hemodialysis patients each received one long and one short dialysis, equivalent in terms of urea clearance. Phosphate concentrations were measured during each treatment and for one hour thereafter. A new model of phosphate kinetics was developed and implemented in VisSim. This model characterized additional processes involved in phosphate kinetics explaining the departure of the measured data from a standard two-pool model.

RESULTS

Pre-dialysis phosphate concentrations were similar in long and short dialysis groups. Post-dialysis phosphate concentrations in long dialysis were higher than in short dialysis (P < 0.02) despite removal of a greater mass of phosphate (P < 0.001). In both long and short dialysis serum phosphate concentrations initially fell in accordance with two-pool kinetics, but thereafter plateaued or increased despite continuing phosphate removal. Implementation of an additional regulatory mechanism such that a third pool liberates phosphate to maintain an intrinsic target concentration (1.18 +/- 0.06 mmol/L; 95% confidence intervals, CI) explained the data in 24% of treatments. The further addition of a fourth pool hysteresis element triggered by critically low phosphate levels (0.80 +/- 0.07 mmol/L, CI) yielded an excellent correlation with the observed data in the remaining 76% of treatments (cumulative standard deviation 0.027 +/- 0.004 mmol/L, CI). The critically low concentration correlated with pre-dialysis phosphate levels (r=0.67, P < 0.0001).

CONCLUSION

Modeling of phosphate kinetics during hemodialysis implies regulation involving up to four phosphate pools. The accuracy of this model suggests that the proposed mechanisms have physiological validity.

摘要

背景

血液透析人群中高磷血症很普遍,但血液透析过程中的磷动力学却鲜为人知。

方法

29名血液透析患者每人接受一次长时间透析和一次短时间透析,两次透析的尿素清除率相当。在每次治疗期间及之后一小时测量磷浓度。开发了一种新的磷动力学模型并在VisSim中实现。该模型描述了磷动力学中涉及的其他过程,解释了测量数据与标准双池模型的偏差。

结果

长时间透析组和短时间透析组的透析前磷浓度相似。尽管长时间透析清除的磷质量更多(P < 0.001),但其透析后磷浓度高于短时间透析(P < 0.02)。在长时间和短时间透析中,血清磷浓度最初均按照双池动力学下降,但此后尽管持续清除磷,浓度却趋于平稳或上升。实施一种额外的调节机制,即第三个池释放磷以维持固有目标浓度(1.18±0.06 mmol/L;95%置信区间,CI),在24%的治疗中解释了数据。由极低磷水平(0.80±0.07 mmol/L,CI)触发的第四个池滞后元素的进一步添加,在其余76%的治疗中与观察数据具有极好的相关性(累积标准差0.027±0.004 mmol/L,CI)。极低浓度与透析前磷水平相关(r = 0.67,P < 0.0001)。

结论

血液透析期间磷动力学建模意味着涉及多达四个磷池的调节。该模型的准确性表明所提出的机制具有生理有效性。

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