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尿中性粒细胞明胶酶相关脂质运载蛋白:迟发性脓毒症的潜在生物标志物。

Urinary neutrophil gelatinase-associated lipocalin: potential biomarker for late-onset sepsis.

作者信息

Pynn Jennifer M, Parravicini Elvira, Saiman Lisa, Bateman David A, Barasch Jonathan M, Lorenz John M

机构信息

Department of Pediatrics, Stony Brook University School of Medicine, Stony Brook, New York.

Department of Pediatrics, College of Physicians and Surgeons, Columbia University, New York, New York.

出版信息

Pediatr Res. 2015 Jul;78(1):76-81. doi: 10.1038/pr.2015.62. Epub 2015 Mar 25.

Abstract

BACKGROUND

To assess the ability of urinary neutrophil gelatinase-associated lipocalin (UNGAL) to discriminate between culture-positive vs. culture-negative late-onset sepsis evaluations.

METHODS

This is a prospective observational study of 136 neonates who underwent ≥1 sepsis evaluation at >72 h of age. Urine was obtained at the time of sepsis evaluation to measure UNGAL concentration. Using generalized estimating equations controlling for gender, gestational and postnatal age, acute kidney injury, and within-patient correlations, pair-wise contrasts between mean log UNGAL concentrations of infants with negative sepsis evaluations vs. culture-positive sepsis and presumed sepsis were assessed. Discrimination characteristics at several UNGAL cutoff concentrations were assessed using receiver-operating characteristic curves.

RESULTS

The predicted mean log UNGAL values of culture-positive sepsis and presumed sepsis vs. negative sepsis evaluations differed significantly (P < 0.001 and P = 0.02, respectively). At a cutoff ≥ 50 ng/ml, UNGAL discriminated between culture-positive sepsis and culture-negative sepsis evaluations with sensitivity = 86%, specificity = 56%, positive predictive value = 41%, negative predictive value = 92%, and number needed to treat = 3.

CONCLUSION

UNGAL is a noninvasive biomarker with high negative predictive value at the time of late-onset sepsis evaluation in neonates and could be a useful adjunct to traditional components of sepsis evaluations.

摘要

背景

评估尿中性粒细胞明胶酶相关脂质运载蛋白(UNGAL)在鉴别晚发性败血症血培养阳性与血培养阴性评估中的能力。

方法

这是一项对136例年龄大于72小时接受≥1次败血症评估的新生儿进行的前瞻性观察研究。在败血症评估时采集尿液以测量UNGAL浓度。使用广义估计方程控制性别、胎龄和出生后年龄、急性肾损伤以及患者内相关性,评估败血症评估阴性的婴儿与血培养阳性败血症和疑似败血症婴儿的平均对数UNGAL浓度之间的成对对比。使用受试者工作特征曲线评估几个UNGAL临界浓度下的鉴别特征。

结果

血培养阳性败血症和疑似败血症与败血症评估阴性的预测平均对数UNGAL值有显著差异(分别为P < 0.001和P = 0.02)。在临界值≥50 ng/ml时,UNGAL在血培养阳性败血症和血培养阴性败血症评估之间进行鉴别,敏感性 = 86%,特异性 = 56%,阳性预测值 = 41%,阴性预测值 = 92%,治疗所需人数 = 3。

结论

UNGAL是一种无创生物标志物,在新生儿晚发性败血症评估时具有较高的阴性预测值,可能是败血症评估传统组成部分的有用辅助手段。

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