Massoth Christina, Küllmar Mira, Enders Dominic, Kellum John A, Forni Lui G, Meersch Melanie, Zarbock Alexander
Department of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Muenster, Muenster, Germany.
Institute of Biostatistics and Clinical Research, University of Münster, Münster, Germany.
J Thorac Cardiovasc Surg. 2023 Jan;165(1):199-207.e2. doi: 10.1016/j.jtcvs.2021.03.016. Epub 2021 Mar 10.
Outcomes after acute kidney injury are affected by both the severity and the duration of the insult. Patients with persistent acute kidney injury have higher major adverse kidney events, including 90-day mortality, renal replacement therapy, and persistent kidney dysfunction. Methods to identify these patients are urgently needed to improve outcomes. The purpose of this study was to evaluate whether biomarkers, including C-C motif chemokine ligand 14, were able to predict persistent acute kidney injury and major adverse kidney events after cardiac surgery.
This study was a single-center, prospective, observational study. Patients who developed moderate or severe acute kidney injury (Kidney Disease Improving Global Outcomes 2 or 3) within 72 hours after cardiac surgery were enrolled with a primary end point of persistent severe acute kidney injury (Kidney Disease Improving Global Outcomes 3) lasting 72 hours or more.
A total of 100 patients were available for the primary analysis, and 37 met the primary end point. C-C motif chemokine ligand 14 was the most predictive biomarker for the primary end point with an area under the curve of 0.930 (95% confidence interval, 0.881-0.979). The area under the curve of C-C motif chemokine ligand 14 was significantly higher than the area under the curve for the other biomarkers analyzed. C-C motif chemokine ligand 14 was significantly higher in end point positive patients at enrollment (4.47 ng/mL [2.35-11.5] vs 0.67 ng/mL [0.38-1.07]; P = .001). Sensitivity and specificity were 78% and 95% at a cutoff value of 2.21 ng/mL, respectively. C-C motif chemokine ligand 14 was also highly accurate for predicting renal replacement therapy within 7 days (area under the curve, 0.915; 95% confidence interval, 0.858-0.972; P < .001).
Elevated C-C motif chemokine ligand 14 levels predict persistent acute kidney injury in cardiac surgery patients with moderate or severe acute kidney injury. This new biomarker may help stratify patients destined to receive renal replacement therapy and identify patients who may benefit from novel therapeutic approaches to acute kidney injury.
急性肾损伤后的预后受损伤的严重程度和持续时间影响。持续性急性肾损伤患者发生主要不良肾脏事件的风险更高,包括90天死亡率、肾脏替代治疗及持续性肾功能障碍。迫切需要找到识别这些患者的方法以改善预后。本研究旨在评估包括C-C基序趋化因子配体14在内的生物标志物能否预测心脏手术后的持续性急性肾损伤和主要不良肾脏事件。
本研究为单中心、前瞻性观察性研究。纳入心脏手术后72小时内发生中度或重度急性肾损伤(改善全球肾脏病预后组织2期或3期)的患者,主要终点为持续性重度急性肾损伤(改善全球肾脏病预后组织3期)持续72小时或更长时间。
共有100例患者可用于初步分析,其中37例达到主要终点。C-C基序趋化因子配体14是主要终点最具预测性的生物标志物,曲线下面积为0.930(95%置信区间,0.881-0.979)。C-C基序趋化因子配体14的曲线下面积显著高于所分析的其他生物标志物的曲线下面积。入组时,终点阳性患者的C-C基序趋化因子配体14显著更高(4.47 ng/mL [2.35-11.5] 对比0.67 ng/mL [0.38-1.07];P = 0.001)。在截断值为2.21 ng/mL时,敏感性和特异性分别为78%和95%。C-C基序趋化因子配体14对预测7天内的肾脏替代治疗也具有高度准确性(曲线下面积,0.915;95%置信区间,0.858-0.972;P < 0.001)。
C-C基序趋化因子配体14水平升高可预测中度或重度急性肾损伤的心脏手术患者发生持续性急性肾损伤。这种新的生物标志物可能有助于对注定要接受肾脏替代治疗的患者进行分层,并识别可能从急性肾损伤新治疗方法中获益的患者。