Abstract

BackgroundAcute kidney injury (AKI) is a common and serious complication after cardiac surgery, and current strategies aimed at treating AKI have proven ineffective. Levosimendan, an inodilatating agent, has been shown to increase renal blood flow and glomerular filtration rate in uncomplicated postoperative patients and in patients with the cardiorenal syndrome. We hypothesized that levosimendan through its specific effects on renal vasculature, a preferential vasodilating effect on preglomerular resistance vessels, could improve renal function in AKI-patients with who did not have clinical indication for inotropic support.MethodsIn this single-center, double-blind, randomized controlled study, adult patients with postoperative AKI within 2 days after cardiac surgery, who were hemodynamically stable with a central venous oxygen saturation (ScvO2) ≥ 60% without inotropic support were eligible for inclusion. After randomization, study drug infusions, levosimendan (n = 16) or placebo (n = 13) were given for 5 h. A bolus infusion of levosimendan (12 µg/kg), were given for 30 min followed by 0.1 µg/kg/min for 5 h. Renal blood flow and glomerular filtration rate were measured using infusion clearance of para-aminohippuric acid and a filtration marker, respectively. As a safety issue, norepinephrine was administered to maintain mean arterial pressure between 70–80 mmHg. Intra-group differences were tested by Mann–Whitney U-tests, and a linear mixed model was used to test time and group interaction.ResultsTwenty-nine patients completed the study. At inclusion, the mean serum creatinine was higher in the patients randomized to levosimendan (148 ± 29 vs 127 ± 22 µmol/L, p = 0.030), and the estimated GFR was lower (46 ± 12 vs 57 ± 11 ml/min/1.73 m2, p = 0.025). Levosimendan induced a significantly (p = 0.011) more pronounced increase in renal blood flow (15%) compared placebo (3%) and a more pronounced decrease in renal vascular resistance (− 18% vs. − 4%, respectively, p = 0.043). There was a trend for a minor increase in glomerular filtration rate with levosimendan (4.5%, p = 0.079), which did differ significantly from the placebo group (p = 0.440). The mean norepinephrine dose was increased by 82% in the levosimedan group and decreased by 29% in the placebo group (p = 0.012).ConclusionsIn hemodynamically stable patients with AKI after cardiac surgery, levosimendan increases renal blood flow through renal vasodilatation.Trial registrationNCT02531724, prospectly registered on 08/20/2015. https://clinicaltrials.gov/ct2/show/NCT02531724?cond=AKI&cntry=SE&age=1&draw=2&rank=1

Highlights

  • Acute kidney injury (AKI) is a common complication after cardiac surgery and associated with increased morbidity and mortality [1]

  • The mean serum creatinine was higher in the patients randomized to levosimendan (148 ± 29 vs 127 ± 22 μmol/L, p = 0.030), and the estimated glomerular filtration rate (GFR) was lower (46 ± 12 vs 57 ± 11 ml/min/1.73 ­m2, p = 0.025)

  • In patients with AKI grade 2 (n = 5, all in the levosimendan group), there was a mean increase in serum creatinine on the first day after the study compared to inclusion (+ 10%, n.s.). In this blinded, randomized placebo-controlled trial, we studied the renal effects of the inodilator levosimendan in patients with early cardiac surgery-associated AKI, without the need for inotropic support

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Summary

Introduction

Acute kidney injury (AKI) is a common complication after cardiac surgery and associated with increased morbidity and mortality [1]. Renal oxygenation is severely impaired in patients with early cardiac surgery-associated AKI [8], in turn, caused by a substantial increase (50%) in renal vascular resistance and a 40% lower renal blood flow (RBF), compared with post-cardiac surgery patients with no AKI. In this situation, an ideal agent to treat AKI, would be one that induces a vasodilation of preferentially the preglomerular resistance vessels increasing both RBF and GFR. We hypothesized that levosimendan through its specific effects on renal vasculature, a preferential vasodilating effect on preglomerular resistance vessels, could improve renal function in AKI-patients with who did not have clinical indication for inotropic support

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