Renal Insufficiency After Contrast Media Administration Trial II (REMEDIAL II) RenalGuard System in High-Risk Patients for Contrast-Induced Acute Kidney Injury

被引:180
作者
Briguori, Carlo [1 ,2 ]
Visconti, Gabriella [1 ,2 ]
Focaccio, Amelia [1 ,2 ]
Airoldi, Flavio [3 ]
Valgimigli, Marco [4 ]
Sangiorgi, Giuseppe Massimo [5 ]
Golia, Bruno [1 ,2 ]
Ricciardelli, Bruno [1 ,2 ]
Condorelli, Gerolama [6 ]
机构
[1] Clin Mediterranea, Lab Intervent Cardiol, I-80121 Naples, Italy
[2] Clin Mediterranea, Dept Cardiol, I-80121 Naples, Italy
[3] IRCCS Multimed, Lab Intervent Cardiol, Milan, Italy
[4] Univ Ferrara, Cardiovasc Res Ctr, I-44100 Ferrara, Italy
[5] Univ Modena & Reggio Emilia, Div Cardiol, Modena, Italy
[6] Univ Naples Federico II, Dept Cellular & Mol Biol & Pathol, Naples, Italy
关键词
complications; contrast media; kidney; prevention; SERUM CYSTATIN-C; INDUCED NEPHROPATHY; SODIUM-BICARBONATE; N-ACETYLCYSTEINE; PREVENTION; FUROSEMIDE; PATHOPHYSIOLOGY; HYDRATION; MANNITOL; DIURESIS;
D O I
10.1161/CIRCULATIONAHA.111.030759
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-The RenalGuard System, which creates high urine output and fluid balancing, may be beneficial in preventing contrast-induced acute kidney injury. Methods and Results-The Renal Insufficiency After Contrast Media Administration Trial II (REMEDIAL II) trial is a randomized, multicenter, investigator-driven trial addressing the prevention of contrast-induced acute kidney injury in high-risk patients. Patients with an estimated glomerular filtration rate <= 30 mL.min(-1).1.73 m(-2) and/or a risk score >= 11 were randomly assigned to sodium bicarbonate solution and N-acetylcysteine (control group) or hydration with saline and N-acetylcysteine controlled by the RenalGuard System and furosemide (RenalGuard group). The primary end point was an increase of >= 0.3 mg/dL in the serum creatinine concentration at 48 hours after the procedure. The secondary end points included serum cystatin C kinetics and rate of in-hospital dialysis. Contrast-induced acute kidney injury occurred in 16 of 146 patients in the RenalGuard group (11%) and in 30 of 146 patients in the control group (20.5%; odds ratio, 0.47; 95% confidence interval, 0.24 to 0.92). There were 142 patients (48.5%) with an estimated glomerular filtration rate <= 30 mL.min(-1).1.73 and 149 patients (51.5%) with only a risk score >= 11. Subgroup analysis according to inclusion criteria showed a similarly lower risk of adverse events (estimated glomerular filtration rate <= 30 mL.min(-1).1.73 m(-2): odds ratio, 0.44; risk score >= 11: odds ratio, 0.45; P for interaction = 0.97). Changes in cystatin C at 24 hours (0.02 +/- 0.32 versus -0.08 +/- 0.26; P = 0.002) and 48 hours (0.12 +/- 0.42 versus 0.03 +/- 0.31; P = 0.001) and the rate of in-hospital dialysis (4.1% versus 0.7%; P = 0.056) were higher in the control group. Conclusion-RenalGuard therapy is superior to sodium bicarbonate and N-acetylcysteine in preventing contrast-induced acute kidney injury in high-risk patients.
引用
收藏
页码:1260 / 1269
页数:10
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