Acute kidney injury clinical trial design: old problems, new strategies

被引:10
作者
Endre, Zoltan H. [1 ,2 ,3 ]
Pickering, John W. [1 ]
机构
[1] Univ Otago, Christchurch Kidney Res Grp, Dept Med, Christchurch, New Zealand
[2] Univ New S Wales, Dept Nephrol, Prince Wales Clin Sch, Sydney, NSW, Australia
[3] Prince Wales Hosp, Dept Nephrol, Sydney, NSW 2031, Australia
关键词
Biomarkers; Acute kidney injury; Phase-specific renal injury; Early intervention; Late intervention; ACUTE-RENAL-FAILURE; GELATINASE-ASSOCIATED LIPOCALIN; ATRIAL-NATRIURETIC-PEPTIDE; LOW-DOSE DOPAMINE; DECOMPENSATED HEART-FAILURE; ACUTE TUBULAR-NECROSIS; GROWTH-FACTOR I; CARDIAC-SURGERY; DOUBLE-BLIND; URINARY BIOMARKERS;
D O I
10.1007/s00467-012-2171-3
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Apart from supportive dialysis there are no universally accepted interventions in acute kidney injury (AKI). We have summarized the outcomes of all published randomized, placebo-controlled studies of non-dialysis treatment of AKI. Forty-nine trials were identified, only one of which was in a paediatric population. Sixteen trials had positive outcomes; these trials are not comparable in terms of methodology used or outcomes assessed, and they share many of the problems of the negative trials. We discuss the flaws in clinical trial design that have contributed to poor or uncertain outcomes and propose minimum requirements for future trials. In particular, future trials should incorporate biomarkers specific to the etiology of the AKI, and treatment should match the phase of injury.
引用
收藏
页码:207 / 217
页数:11
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