Pitfalls in assessing renal function in patients with cirrhosis-potential inequity for access to treatment of hepatorenal failure and liver transplantation

被引:50
作者
Davenport, Andrew [1 ]
Cholongitas, Evangelos [2 ]
Xirouchakis, Elias [2 ]
Burroughs, Andrew Kenneth [2 ]
机构
[1] UCL, Sch Med, Royal Free Hosp, UCL Ctr Nephrol, London W1N 8AA, England
[2] UCL, Sch Med, Royal Free Hosp, Royal Free Sheila Sherlock Liver Ctr, London W1N 8AA, England
关键词
chronic liver disease; cirrhosis; cystatin C; GFR; renal function creatinine; GLOMERULAR-FILTRATION-RATE; SERUM CYSTATIN-C; X-RAY ABSORPTIOMETRY; BODY-SURFACE AREA; CREATININE CLEARANCE; BIOELECTRICAL-IMPEDANCE; GENDER-DIFFERENCE; URINE COLLECTIONS; PLASMA-CREATININE; DIAGNOSTIC-VALUE;
D O I
10.1093/ndt/gfr354
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Serum creatinine is universally used to assess renal function in clinical practice. Creatinine and changes in serum creatinine are used to define acute kidney injury and hepatorenal syndrome (HRS) in patients with progressive liver disease. In addition, creatinine is a key variable in the calculation used to determine priority for liver transplantation in many countries. As there is no universal standardized creatinine assay, there is variation in creatinine determinations between laboratory assays, compounded by assay interference due to chromogens, including bilirubin. This leads to patients with the same actual renal function potentially being offered different treatment options, in terms of access to therapy for HRS and priority waiting time for liver transplantation. Alternative methods for assessing renal function either also tend to overestimate renal function or are too time consuming and expensive to provide practical alternatives for standard clinical practice. Standardization of creatinine assays with readily available reference standards would help minimize interlaboratory variation; of the current creatinine assays, enzymatic creatinine appears more accurate, but even this is inaccurate at high bilirubin concentrations. Further work is required to determine whether interpatient variation can be reduced by correcting creatinine and cystatin measurements for muscle mass.
引用
收藏
页码:2735 / 2742
页数:8
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