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J Am Soc Nephrol ; 15(7): 1927-35, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15213283

RESUMO

Clinical hemodialysis systems achieve high single pass extraction of small solutes that are not bound to plasma proteins. But they clear protein-bound solutes much less effectively. This study examines the extent to which clearance of a protein-bound test solute is improved by increasing the dialyzer mass transfer area coefficient (KoA) and the dialysate flow rate (Qd). A reservoir containing test solutes and artificial plasma with albumin concentration approximately 4 g/dl was dialyzed with a standard clinical dialysate delivery system. The clearance of phenol red (ClPR) was compared with the clearances of urea and creatinine at a plasma flow rate (Qp) of 200 ml/min with varying values of KoA and Qd. ClPR increased from 11 +/- 2 ml/min to 23 +/- 2 ml/min when KoA for phenol red, KoAPR, was increased from 238 to 640 ml/min and Qd was increased from 286 +/- 6 ml/min to 734 +/- 9 ml/min. Increasing either KoAPR or Qd alone had lesser effects. Clearance values for phenol red were much lower than clearance values for the unbound solutes urea and creatinine, which ranged from 150 to 200 ml/min and were less affected by varying KoA and Qd. A mathematical model was developed to predict ClPR from values of Qp, Qd, the fraction of phenol red bound to albumin (94% +/- 1%) and KoAPR. The model accurately predicts the pattern of measured results and shows further that ClPR can be made to approach Qp only by very large increases in both KoAPR and Qd.


Assuntos
Albuminas/metabolismo , Falência Renal Crônica/terapia , Diálise Renal/métodos , Soluções para Diálise , Hemofiltração , Humanos , Membranas Artificiais , Modelos Estatísticos , Modelos Teóricos , Fenolsulfonaftaleína/química , Fenolsulfonaftaleína/farmacologia , Ligação Proteica , Proteínas/química , Fatores de Tempo , Ureia/metabolismo
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