新生儿缺氧缺血性脑病心功能的评价。

IF 0.7 4区 医学 Q4 PATHOLOGY
Fetal and Pediatric Pathology Pub Date : 2025-05-01 Epub Date: 2025-04-21 DOI:10.1080/15513815.2025.2490029
Leyla Sero, Duygu Tuncel, Mehmet Nur Talay, Mehmet Salih Karaca, Ozlem Gul, Nilufer Okur
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引用次数: 0

摘要

简介:本研究的目的是评估心脏标志物在围产期窒息(PA)新生儿预后中的作用。方法:以pH mmol/L为PA。分析NT-proBNP、心肌肌钙蛋白I (cTnI)、肌酸激酶MB水平。随访期间出现兴奋的患者比较MRI病理表现和心脏指标。结果:本研究共纳入115例围产期窒息患儿。死亡患者的cTnI水平中位数为0.63(最小0.1-最大4.2)ng/ml,显著高于死亡患者(p = 0.006)。评估cTnI的预测能力,确定cTnI预测死亡率的阈值为0.428 ng/ml,敏感性为87.5%,特异性为87.2%。结论:我们发现,在新生儿PA出生后最初几个小时内分析cTnI水平对预测死亡率和颅脑病变都有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Cardiac Functions in Neonates with Hypoxic Ischemic Encephalopathy.

Introduction: The aim of our study was to evaluate the role of cardiac markers in determining prognosis in newborns with Perinatal Asphyxia (PA). Method: Patients with a pH <7-7.15 base deficit -12> mmol/L were defined as PA. NT-proBNP, cardiac Troponin I (cTnI), creatine kinase MB levels were analyzed. Patients with excitus during follow-up were compared with patients with pathological MRI findings and cardiac markers. Results: A total of 115 infants with perinatal asphyxia were included in the study.cTnI levels was median 0.63 (min 0.1-max 4.2) ng/ml significantly higher in patients who died (p = .006). The predictive power of cTnI was evaluated and the threshold value of cTnI for predicting mortality was determined as 0.428 ng/ml with 87.5% sensitivity and 87.2% specificity. Conclusion: We found that cTnI level analyzed in the first hours of life in newborn infants with PA has value in predicting both mortality and cranial affections.

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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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