The impact of hemoadsorption in patients with chronic kidney disease undergoing coronary artery bypass grafting

医学 急性肾损伤 肾脏疾病 围手术期 肾脏替代疗法 肾功能 肌酐 内科学 降钙素原 冠状动脉疾病 临床终点 外科 心脏病学 泌尿科 败血症 随机对照试验
作者
Erdal Şimşek,Serdar Günaydın
出处
期刊:Ndt Plus [Oxford University Press]
卷期号:18 (9): sfaf241-sfaf241
标识
DOI:10.1093/ckj/sfaf241
摘要

ABSTRACT Background With an annual incidence of up to 30%, cardiac surgery-associated acute kidney injury (CSA-AKI) may be one of the most underestimated yet common complications, hence reno-protective interventions are critical. We evaluated the impact of hemoadsorption (HA) on clinical outcomes in KDIGO (Kidney Disease: Improving Global Outcomes) G2/A2 patients (GFR 60–89 ml/min/1.73 m2 and 30–300 mg/g albuminuria) undergoing coronary artery bypass grafting (CABG). Method Forty patients with chronic kidney disease (KDIGO G2/A2) were treated with intraoperative HA therapy during CABG surgery (HA group) and were compared with 40 propensity-score matched control CABG patients without intraoperative HA (control group). Primary endpoints were the need for renal replacement therapy (RRT) and/or worsening of the KDIGO stage during the perioperative period. Secondary endpoints included changes in inflammatory biomarkers, vasopressor use, and ICU/hospital stay. Results No significant differences were observed in demographics between groups. Worsened KDIGO stages were more frequent in the control group (P = .04), and the HA group had less RRT use and shorter ICU stays (P = .02 and P = .03). On the first postoperative day, levels of serum creatinine (1.85 ± 0.6 vs 2.75 ± 0.6 mg/dl; P = .035), myoglobin (210±75 vs 310 ± 80 μg/l; P = .04), NT-proBNP (130 ± 30 vs 180 ± 40 pg/ml; P = .04), IL-6 (8.2±4 vs 22.2 ± 4 pg/ml; P = .012), procalcitonin (1.4 ± 0.1 vs 1.76 ± 0.2 μg/l, P = .02), C-reactive protein (7.6 ± 2 vs 14.2 ± 4 mg/l, P = .01), and D-dimer (0.76 ± 0.04 vs 2.2 ± 0.07 mg/l, P = .002) were significantly lower in the HA group. Conclusion This pioneering study highlights the potential benefits of HA in mitigating kidney function and inflammation in CABG patients with borderline chronic kidney disease. These findings require validation in large, multicenter trials.
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