Department of Pediatrics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada.
Department of Surgery, University of Sherbrooke, Quebec, Canada; Vitality Health Network, North West Zone, Edmundston, New Brunswick, Canada.
Am J Obstet Gynecol. 2024 Sep;231(3):348.e1-348.e8. doi: 10.1016/j.ajog.2024.03.042. Epub 2024 Apr 3.
Umbilical artery gas results help obstetricians assess fetal well-being during labor and guide screening decisions on eligibility for therapeutic hypothermia (ie, whole-body or head cooling). The accuracy of results, especially for the base deficit on arterial cord gas analysis, in predicting brain injury is questioned. A novel biomarker specifically calculated for fetal acid-base physiology and response to asphyxia-neonatal eucapnic pH as a marker of neonatal metabolic acidosis-has the potential to be an accurate predictor of hypoxic-ischemic encephalopathy.
We aimed to compare false-negative rates of hypoxic-ischemic encephalopathy for umbilical artery pH, base deficit, and neonatal eucapnic pH in assessing fetal acid-base balance as a marker of fetal well-being and predicting acute brain injury.
This is a retrospective single-center cohort study of newborns ≥ 35 weeks of gestation diagnosed with hypoxic-ischemic encephalopathy. We compared false-negative rates for any grade of hypoxic-ischemic encephalopathy using unilateral paired chi-square statistical analysis based on cutoff values for umbilical artery pH ≤7.00, base deficit ≥16 mmol/L, base deficit ≥12 mmol/L and neonatal eucapnic pH ≤7.14. We performed an analysis of variance between umbilical artery pH, base deficit, and neonatal eucapnic pH for each hypoxic-ischemic encephalopathy grade.
We included 113 newborns. False-negative rate for hypoxic-ischemic encephalopathy was significantly higher for base deficit <16 mmol/L (n=78/113; 69.0%) than <12 mmol/L (n=46/113; 40.7%), pH >7.00 (n=41/113; 36.3%), or neonatal eucpanic pH >7.14 (n=35/113; 31.0%) (P<.0001). All true-positive cases were identified using only umbilical artery pH and neonatal eucapnic pH. Base deficit ≥16 or ≥12 mmol/L did not add any value in identifying newborns with hypoxic-ischemic encephalopathy when using umbilical artery pH and neonatal eucapnic pH. No association emerged between any marker and hypoxic-ischemic encephalopathy severity grading.
Our findings support the accuracy of neonatal eucapnic pH to assess fetal well-being during labor and to improve predictive performance for acute brain injury. Neonatal eucpanic pH, in addition to umbilical artery pH, may be a viable alternative in identifying newborns at risk for hypoxic-ischemic encephalopathy.
脐带血气结果有助于产科医生在分娩期间评估胎儿的健康状况,并指导治疗性低体温(即全身或头部降温)的筛选决策。其结果,尤其是动脉脐带血气分析的基础缺陷,在预测脑损伤方面的准确性受到质疑。一种专门为胎儿酸碱生理学和对窒息的反应而计算的新型生物标志物——新生儿碱剩余作为新生儿代谢性酸中毒的标志物——有可能成为缺氧缺血性脑病的准确预测指标。
我们旨在比较脐带血 pH 值、基础缺陷和新生儿碱剩余作为胎儿健康状况的标志物评估胎儿酸碱平衡和预测急性脑损伤时,对缺氧缺血性脑病的假阴性率。
这是一项回顾性单中心队列研究,纳入了≥35 孕周诊断为缺氧缺血性脑病的新生儿。我们比较了单侧配对卡方统计分析基于脐带血 pH 值≤7.00、基础缺陷≥16mmol/L、基础缺陷≥12mmol/L 和新生儿碱剩余 pH 值≤7.14 的截断值时,任何程度缺氧缺血性脑病的假阴性率。我们对每个缺氧缺血性脑病分级的脐带血 pH 值、基础缺陷和新生儿碱剩余进行方差分析。
我们纳入了 113 名新生儿。基础缺陷<16mmol/L(n=78/113;69.0%)的缺氧缺血性脑病假阴性率明显高于<12mmol/L(n=46/113;40.7%)、pH 值>7.00(n=41/113;36.3%)或新生儿碱剩余 pH 值>7.14(n=35/113;31.0%)(P<.0001)。所有真正的阳性病例仅使用脐带血 pH 值和新生儿碱剩余 pH 值即可识别。当使用脐带血 pH 值和新生儿碱剩余 pH 值时,基础缺陷≥16mmol/L 或≥12mmol/L 并不能增加识别缺氧缺血性脑病新生儿的价值。任何标志物与缺氧缺血性脑病严重程度分级之间均无关联。
我们的研究结果支持新生儿碱剩余 pH 值用于评估分娩期间胎儿健康状况,并提高急性脑损伤的预测性能。除了脐带血 pH 值外,新生儿碱剩余 pH 值可能是识别缺氧缺血性脑病风险新生儿的一种可行替代方法。