Saikat Mondal, Kanailai Barik, Sudipto Paul, S. Laha, Sayan Bera
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引用次数: 0
摘要
背景:当新生儿在缺氧状态下出生时,由于缺氧组织损伤,尿酸的产生增加,尿酸通过肾脏排出,尿液中尿酸和肌酐(UA/Cr)的比值被用作围产期缺氧的早期预测指标。目的:我们进行了这项研究,比较正常新生儿和窒息新生儿以及HIE不同阶段的尿UA/Cr比值,以评估其作为围产期窒息诊断和预后指标的有效性。患者和方法:本观察性横断面研究以75例HIE不同阶段窒息新生儿和75例健康新生儿为对照,为期一年。尿酸和肌酐值是用自动分析仪从出生后6至24小时内采集的单个尿液样本中测量的。结果:尿UA(38±2.81 mg/dl vs 19.24±0.75 mg/dl)和尿UA/Cr值(2.81±0.32 vs 1.40±0.13)显著高于对照组。尿UA和UA/Cr值随HIE晚期升高(p 2.45, AUC为0.96,准确性为90%,敏感性为98.07%,特异性为85.70%,PPV为78.46%,NPV为98.82%)。结论:尿UA/Cr可作为HIE患儿围生期缺氧风险分层的一种简单、廉价、可靠的指标。
Usefulness of Urine Uric Acid/Creatinine Ratio in Neonate as an Early Detector of Perinatal Hypoxia: A Hospital-Based Observational Study
Background : When a neonate is born under a hypoxic state, there is increased production of uric acid due to hypoxic tissue damage, which is excreted via the kidney, and the ratio of uric acid and creatinine (UA/Cr) in urine is used as an early predictor of perinatal hypoxia. Objectives : We conducted this study to compare urine UA/Cr ratio between normal and asphyxiated newborns and between different stages of HIE to evaluate its usefulness as a diagnostic and prognostic marker of perinatal asphyxia . Patients and method: This observational cross-sectional study is conducted for one year with 75 asphyxiated neonates in different stages of HIE and 75 healthy neonates as control. Uric acid and creatinine values are measured with an auto-analyzer from a single urine sample taken between 6 to 24 hours of birth. Results: We found urine UA(38 ±2.81 mg/dl vs 19.24±0.75 mg/dl ) and urine UA/Cr value (2.81±0.32 vs 1.40±0.13 ) significantly high in cases compared to control. Also, the urine UA and UA/Cr values are increasing with advanced stages of HIE (p <0.001). The optimal cut point value to predict HIE was at urine UA/Cr ratio of >2.45 with an AUC of 0.96, accuracy of 90%, sensitivity of 98.07% , specificity of 85.70% , PPV 78.46%, and NPV 98.82%. Conclusion: Urine UA/Cr appears to be a simple, inexpensive and reliable indicator of perinatal hypoxia for risk stratification based on functional impairment in the HIE babies.