Ceschia Giovanni, Gist Katja M, Clover-Brown Imogen, Krallman Kelli A, Navarro Ana C, Goldstein Stuart L
Center for Acute Care Nephrology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Department for Women's and Children's Health, University-Hospital of Padua, Padua, Italy.
Pediatr Res. 2025 Sep 19. doi: 10.1038/s41390-025-04430-1.
Early identification of kidney recovery in critically ill children and young adults undergoing continuous kidney support therapy (CKST) is essential to optimize care and minimize complications. Urinary neutrophil gelatinase-associated lipocalin (uNGAL) is a biomarker of acute kidney injury, but its utility in predicting CKST duration and guiding timely liberation remains unclear.
We retrospectively analyzed urinary uNGAL levels in pediatric intensive care unit (PICU) patients (aged 2 months to 25 years) who received CKST between July 2018 and April 2024. We evaluated two outcomes: (1) the ability of peak uNGAL levels during the first four days of CKST to predict prolonged therapy (>7 days), and (2) the performance of uNGAL measured during KST liberation attempts in predicting successful liberation.
Among 57 patients, early peak uNGAL predicted CKST duration >7 days with good accuracy (AUC-ROC 0.85 [95% CI, 0.73-0.97], optimal cutoff 2600 ng/mL). uNGAL also showed excellent performance in predicting successful KST liberation (AUC-ROC 0.95 [95% CI, 0.89-1.00], optimal cutoff 900 ng/mL).
uNGAL may be useful for predicting prolonged CKST duration and guiding KST liberation in critically ill children. Larger prospective studies are needed to confirm its role in personalized CKST management.
Peak uNGAL levels within the first four days of CKST are strongly associated with treatment duration >7 days, showing good predictive accuracy. uNGAL demonstrates excellent performance in identifying patients likely to achieve successful KST liberation. uNGAL measured during KST may support clinical decision-making by providing timing insights, potentially optimizing treatment duration in critically ill pediatric patients.
对于接受持续肾脏支持治疗(CKST)的危重症儿童和青年,早期识别肾脏恢复情况对于优化治疗和减少并发症至关重要。尿中性粒细胞明胶酶相关脂质运载蛋白(uNGAL)是急性肾损伤的生物标志物,但其在预测CKST持续时间和指导及时撤机方面的效用仍不明确。
我们回顾性分析了2018年7月至2024年4月期间在儿科重症监护病房(PICU)接受CKST的患者(年龄2个月至25岁)的尿uNGAL水平。我们评估了两个结果:(1)CKST前四天的uNGAL峰值水平预测延长治疗(>7天)的能力,以及(2)在尝试进行CKST撤机时测量的uNGAL在预测成功撤机方面的表现。
在57例患者中,早期uNGAL峰值预测CKST持续时间>7天具有良好的准确性(AUC-ROC为0.85 [95% CI,0.73 - 0.97],最佳截断值为2600 ng/mL)。uNGAL在预测成功的CKST撤机方面也表现出色(AUC-ROC为0.95 [95% CI,0.89 - 1.00],最佳截断值为900 ng/mL)。
uNGAL可能有助于预测危重症儿童CKST持续时间延长并指导CKST撤机。需要更大规模的前瞻性研究来证实其在个性化CKST管理中的作用。
CKST前四天的uNGAL峰值水平与治疗持续时间>7天密切相关,显示出良好的预测准确性。uNGAL在识别可能成功实现CKST撤机的患者方面表现出色。在CKST期间测量的uNGAL可以通过提供时间方面的见解来支持临床决策,有可能优化危重症儿科患者的治疗持续时间。