Measuring GFR: A Systematic Review

被引:397
作者
Soveri, Inga [1 ]
Berg, Ulla B. [2 ]
Bjork, Jonas [3 ]
Elinder, Carl-Gustaf [4 ]
Grubb, Anders [5 ]
Mejare, Ingegerd [6 ]
Sterner, Gunnar [7 ]
Back, Sten-Erik [5 ]
机构
[1] Univ Uppsala Hosp, Dept Med Sci, S-75185 Uppsala, Sweden
[2] Karolinska Univ Hosp Huddinge, Dept Clin Sci Intervent & Technol, Div Pediat, Karolinska Inst, Stockholm, Sweden
[3] Lund Univ, Dept Occupat & Environm Med, Lund, Sweden
[4] Karolinska Inst, Stockholm Cty Council, Dept Clin Sci Intervent & Technol, Div Renal Med, Stockholm, Sweden
[5] Univ Lund Hosp, Dept Clin Chem, S-22185 Lund, Sweden
[6] Swedish Council Hlth Technol Assessment, Stockholm, Sweden
[7] Skane Univ Hosp Malmo, Dept Nephrol, Malmo, Sweden
关键词
Glomerular filtration rate (GFR); glomerular filtration rate (GFR) measurement; renal function; clearance marker; accuracy; GLOMERULAR-FILTRATION-RATE; RENAL PLASMA-FLOW; PREDICTED CREATININE CLEARANCE; SERUM CREATININE; ENDOGENOUS CREATININE; SUBCUTANEOUS INJECTION; INULIN-CLEARANCE; CONTRAST-MEDIA; EDETIC ACID; CYSTATIN-C;
D O I
10.1053/j.ajkd.2014.04.010
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: No comprehensive systematic review of the accuracy of glomerular filtration rate (GFR) measurement methods using renal inulin clearance as reference has been published. Study Design: Systematic review with meta-analysis of cross-sectional diagnostic studies. Setting & Population: Published original studies and systematic reviews in any population. Selection Criteria for Studies: Index and reference measurements conducted within 48 hours; at least 15 participants studied; GFR markers measured in plasma or urine; plasma clearance calculation algorithm verified in another study; tubular secretion of creatinine had not been blocked by medicines. Index Tests: Endogenous creatinine clearance; renal or plasma clearance of chromium 51 labeled ethylenediaminetetraacetic acid (Cr-51-EDTA), diethylenetriaminepentaacetic acid (DTPA), iohexol, and iothalamate; and plasma clearance of inulin. Reference Test: Renal inulin clearance measured under continuous inulin infusion and urine collection. Results: Mean bias, 10%, median bias, 5%, the proportion of errors in the index measurements that did not exceed 30% (P-30) >= 80%, and P-10 >= 50% were set as requirements for sufficient accuracy. Based on the GRADE (Grading of Recommendations Assessment, Development and Evaluation) approach, the quality of evidence across studies was rated for each index method. Renal clearance of iothalamate measured GFR with sufficient accuracy (strong evidence). Renal and plasma clearance of Cr-51-EDTA and plasma clearance of iohexol were sufficiently accurate to measure GFR (moderately strong evidence). Renal clearance of DTPA, renal clearance of iohexol, and plasma clearance of inulin had sufficient accuracy (limited evidence). Endogenous creatinine clearance was an inaccurate method (strong evidence), as was plasma clearance of DTPA (limited evidence). The evidence to determine the accuracy of plasma iothalamate clearance was insufficient. With the exception of plasma clearance of inulin, only renal clearance methods had P-30 > 90%. Limitations: The included studies were few and most were old and small, which may limit generalizability. Requirements for sufficient accuracy may depend on clinical setting. Conclusions: At least moderately strong evidence suggests that renal clearance of Cr-51-EDTA or iothalamate and plasma clearance of Cr-51-EDTA or iohexol are sufficiently accurate methods to measure GFR. (C) 2014 by the National Kidney Foundation, Inc.
引用
收藏
页码:411 / 424
页数:14
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