Phosphate kinetics during hemodialysis: Evidence for biphasic regulation

被引:139
作者
Spalding, EM [1 ]
Chamney, PW [1 ]
Farrington, K [1 ]
机构
[1] Lister Hosp, Dept Nephrol, Stevenage SG1 4AB, Herts, England
关键词
hyperphosphatemia; kinetic modeling; intracellular fluid; extracellular fluid; two-pool model; three-pool model; four-pool model;
D O I
10.1046/j.1523-1755.2002.00146.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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 Vis-Sim(TM). 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.
引用
收藏
页码:655 / 667
页数:13
相关论文
共 21 条
[1]  
ANSELL D, 1999, UK RENAL REGISTRY RE, pCH8
[2]  
Bazzato G, 1988, Kidney Int Suppl, V24, pS180
[3]   Association of serum phosphorus and calcium x phosphate product with mortality risk in chronic hemodialysis patients: A national study [J].
Block, GA ;
Hulbert-Shearon, TE ;
Levin, NW ;
Port, FK .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 31 (04) :607-617
[4]  
DESOI CA, 1993, J AM SOC NEPHROL, V4, P1214
[5]   Coronary artery calcifications in children and young adults treated with renal replacement therapy [J].
Eifinger, F ;
Wahn, F ;
Querfeld, U ;
Pollok, M ;
Gevargez, A ;
Kriener, P ;
Grönemeyer, D .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2000, 15 (11) :1892-1894
[6]  
GREENWOOD RN, 1985, CLIN NEPHROL, V23, P189
[7]  
HAAS T, 1991, NEPHROL DIAL TRANSPL, V6, P108
[8]   CALCIUM AND PHOSPHORUS FLUXES DURING HEMODIALYSIS WITH LOW CALCIUM DIALYSATE [J].
HOU, SH ;
ZHAO, J ;
ELLMAN, CF ;
HU, J ;
GRIFFIN, Z ;
SPIEGEL, DM ;
BOURDEAU, JE .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1991, 18 (02) :217-224
[9]   DEATH RISK IN HEMODIALYSIS-PATIENTS - THE PREDICTIVE VALUE OF COMMONLY MEASURED VARIABLES AND AN EVALUATION OF DEATH RATE DIFFERENCES BETWEEN FACILITIES [J].
LOWRIE, EG ;
LEW, NL .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1990, 15 (05) :458-482
[10]   UREA, CREATININE AND PHOSPHATE KINETIC MODELING DURING DIALYSIS - APPLICATION TO PEDIATRIC HEMODIALYSIS [J].
MAASRANI, M ;
JAFFRIN, MY ;
FISCHBACH, M ;
BOUDAILLIEZ, B .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 1995, 18 (03) :122-129