心脏手术后婴儿尿液生物标志物与急性肾损伤和体液超载的关联:婴儿心脏手术后类固醇减少全身炎症的单中心辅助队列试验

Elizabeth J Thompson, Reid C Chamberlain, Kevin D Hill, Rebecca D Sullenger, Eric M Graham, Rasheed A Gbadegesin, Christoph P Hornik
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引用次数: 0

摘要

探讨三种围手术期尿液生物标志物浓度(尿胱抑素C [uCysC]、尿中性粒细胞明胶酶相关脂钙蛋白[uNGAL]和尿肾损伤分子1 [uKIM-1])与体外循环手术先天性心脏病婴儿心脏手术相关急性肾损伤(CS-AKI)和液体过载(FO)之间的关系。探讨尿液生物标志物与不同CS-AKI表型之间的关系。设计:辅助前瞻性队列研究。环境:美国单一儿科心脏ICU。患者:1岁以下的婴儿在2019年6月至2020年5月期间接受了心脏手术,并选择在单一中心收集生物标志物,参加了婴儿心脏手术后类固醇减少全身性炎症的试验(NCT03229538)。排除术前CS-AKI的婴儿。干预措施:没有。测量和主要结果:40例婴儿符合纳入标准。手术时的中位(四分位数)年龄为103天(5.5-161天)。改良肾脏疾病改善了总体结果定义的CS-AKI, 22名(55%)婴儿和21名(53%)婴儿被诊断为FO。UCysC和uNGAL在术后早期达到高峰,uKIM-1在术后后期达到高峰。在未经调整的分析中,CS-AKI婴儿的旁路时间更长,24小时血管活性-肌力评分更高。在多变量分析中,较高的uCysC(优势比[OR], 1.023;95% CI, 1.004-1.042)和uNGAL (OR, 1.019;95% CI, 1.004-1.035)与心脏搭桥后0-8小时的FO相关。UCysC、uNGAL、uKIM-1与CS-AKI无显著相关性。在CS-AKI表型的探索性分析中,uCysC和uNGAL在CS-AKI+/FO+婴儿中最高。结论:在本研究中,uCysC和uNGAL在术后早期48小时与FO相关。UCysC、uNGAL和uKIM-1与CS-AKI无关。进一步的研究应侧重于确定这些生物标志物的预期浓度,探索CS-AKI的表型和结果,并为心脏手术后的婴儿建立具有临床意义的终点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of Urine Biomarkers With Acute Kidney Injury and Fluid Overload in Infants After Cardiac Surgery: A Single Center Ancillary Cohort of the Steroids to Reduce Systemic Inflammation After Infant Heart Surgery Trial.

Association of Urine Biomarkers With Acute Kidney Injury and Fluid Overload in Infants After Cardiac Surgery: A Single Center Ancillary Cohort of the Steroids to Reduce Systemic Inflammation After Infant Heart Surgery Trial.

Association of Urine Biomarkers With Acute Kidney Injury and Fluid Overload in Infants After Cardiac Surgery: A Single Center Ancillary Cohort of the Steroids to Reduce Systemic Inflammation After Infant Heart Surgery Trial.

To examine the association between three perioperative urine biomarker concentrations (urine cystatin C [uCysC], urine neutrophil gelatinase-associated lipocalin [uNGAL], and urine kidney injury molecule 1 [uKIM-1]), and cardiac surgery-associated acute kidney injury (CS-AKI) and fluid overload (FO) in infants with congenital heart disease undergoing surgery on cardiopulmonary bypass. To explore how urine biomarkers are associated with distinct CS-AKI phenotypes based on FO status.

Design: Ancillary prospective cohort study.

Setting: Single U.S. pediatric cardiac ICU.

Patients: Infants less than 1 year old enrolled in the Steroids to Reduce Systemic Inflammation after Infant Heart Surgery trial (NCT03229538) who underwent heart surgery from June 2019 to May 2020 and opted into biomarker collection at a single center. Infants with preoperative CS-AKI were excluded.

Interventions: None.

Measurements and main results: Forty infants met inclusion criteria. Median (interquartile) age at surgery was 103 days (5.5-161 d). Modified Kidney Disease Improving Global Outcomes-defined CS-AKI was diagnosed in 22 (55%) infants and 21 (53%) developed FO. UCysC and uNGAL peaked in the early postoperative period and uKIM-1 peaked later. In unadjusted analysis, bypass time was longer, and Vasoactive-Inotropic Score at 24 hours was higher in infants with CS-AKI. On multivariable analysis, higher uCysC (odds ratio [OR], 1.023; 95% CI, 1.004-1.042) and uNGAL (OR, 1.019; 95% CI, 1.004-1.035) at 0-8 hours post-bypass were associated with FO. UCysC, uNGAL, and uKIM-1 did not significantly correlate with CS-AKI. In exploratory analyses of CS-AKI phenotypes, uCysC and uNGAL were highest in CS-AKI+/FO+ infants.

Conclusions: In this study, uCysC and uNGAL in the early postoperative period were associated with FO at 48 hours. UCysC, uNGAL, and uKIM-1 were not associated with CS-AKI. Further studies should focus on defining expected concentrations of these biomarkers, exploring CS-AKI phenotypes and outcomes, and establishing clinically meaningful endpoints for infants post-cardiac surgery.

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