Acute Kidney Injury Biomarkers Predict an Increase in Serum Milrinone Concentration Earlier Than Serum Creatinine-Defined Acute Kidney Injury in Infants After Cardiac Surgery

被引:22
作者
Gist, Katja M. [1 ]
Cooper, David S. [2 ]
Wrona, Julia [1 ]
Faubel, Sarah [3 ]
Altmann, Christopher [3 ]
Gao, Zhiqian [4 ]
Marino, Bradley S. [5 ,6 ]
Alten, Jeffrey [7 ]
Hock, Kristal M. [7 ]
Mizuno, Tomoyuki [8 ]
Vinks, Alexander A. [8 ]
Joy, Melanie S. [9 ]
Wempe, Michael F. [9 ]
Bennett, Michael R. [10 ]
Goldstein, Stuart L. [2 ,4 ,10 ]
机构
[1] Univ Colorado, Div Pediat Cardiol, Dept Pediat, Heart Inst,Childrens Hosp Colorado, Aurora, CO USA
[2] Cincinnati Childrens Hosp Med Ctr, Dept Pediat, Heart Inst, Cincinnati, OH 45229 USA
[3] Univ Colorado, Dept Internal Med, Div Renal Dis & Hypertens, Anschutz Med Campus, Aurora, CO USA
[4] Cincinnati Childrens Hosp Med Ctr, Heart Inst Res Core, Cincinnati, OH 45229 USA
[5] Ann & Robert H Lurie Childrens Hosp Chicago, Heart Ctr, Div Cardiol, Chicago, IL 60611 USA
[6] Ann & Robert H Lurie Childrens Hosp Chicago, Heart Ctr, Div Crit Care Med, Chicago, IL 60611 USA
[7] Univ Alabama Birmingham, Dept Pediat, Pediat Cardiac Crit Care Med, Childrens Alabama, Birmingham, AL USA
[8] Cincinnati Childrens Hosp Med Ctr, Div Clin Pharmacol, Cincinnati, OH 45229 USA
[9] Univ Colorado, Skaggs Sch Pharm & Pharmaceut Sci, Dept Pharmaceut Sci, Anschutz Med Campus, Aurora, CO USA
[10] Cincinnati Childrens Hosp Med Ctr, Dept Pediat, Ctr Acute Care Nephrol, Cincinnati, OH 45229 USA
关键词
acute kidney injury; milrinone; biomarkers; cardiac surgery; HEART-FAILURE; PHARMACOKINETICS; CHILDREN; EFFICACY; SAFETY; ADULTS;
D O I
10.1097/FTD.0000000000000496
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Milrinone, an inotropic agent used ubiquitously in children after cardiac surgery, accumulates in acute kidney injury (AKI). We assessed if urinary AKI biomarkers are predictive of an increase in milrinone concentrations in infants after cardiac surgery. Methods: Multicenter prospective pilot study of infants undergoing cardiac surgery. Urinary AKI biomarkers were measured in the urine at specific time intervals after cardiopulmonary bypass initiation. AKI was defined using the Kidney Disease: Improving Global Outcomes serum creatinine criteria. Serum milrinone concentrations were measured at specific intervals after drug initiation, dose changes, and termination. Excessive milrinone activity was defined as a 20% increase in serum concentration between 6 and 36 hours after initiation. The temporal relationship between urinary AKI biomarker concentrations and a 20% increase in milrinone concentration was assessed. Results: AKI occurred in 31 (33%) of infants. Milrinone clearance was lower in patients with AKI (4.2 versus 5.6 L/h/70 kg; P = 0.02). Excessive milrinone activity was associated with development of serum creatinine-defined AKI [odds ratio (OR) 3.0; 95% confidence interval (CI), 1.21-7.39; P = 0.02] Both tissue inhibitor metalloproteinase type 2 and insulin-like growth factor-binding protein type 7 (TIMP-2*IGFEP-7) >= 0.78 at 12 hours (OR 2.72; 95% CI, 1.01-7.38; P = 0.04) and kidney injury molecule 1 (KIM-1) >= 529.57 at 24 hours (OR 2.76; 95% CI, 1.06-7.17; P = 0.04) predicted excessive milrinone activity before a diagnosis of AKI. Conclusions: In this pilot study, urine TIMP-2*IGFBP-7 and KIM-1 were predictive of AKI and excessive milrinone activity. Future studies that include a pharmacodynamics assessment of patient hemodynamics, excessive milrinone activity, and AKI biomaker concentrations may be warranted to integrate this concept into clinical practice.
引用
收藏
页码:186 / 194
页数:9
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