Simultaneous Use of Factor XIII and Fibrin Degradation Products in Diagnosing Early Cases of NEC and Neonatal SEPSIS

Mohammad A Sharaf, Heba R. Hashem, W. Ahmed
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引用次数: 1

Abstract

Purpose: The study examined the use of factor XIII and fibrin degradation products in diagnosing early cases of NEC and neonatal sepsis. Methods: Sixty neonates were divided into two groups. 30 preterm neonates suspected with early NEC Diagnosis of NEC was confirmed by modified Bell’s score and 30 preterm neonates with symptoms of neonatal sepsis; where sepsis was confirmed by blood culture and CRP. Laboratory evaluation of FDPs and plasma factor XIII was done for all the patients. The study was carried out in a tertiary NICU of the pediatric department, Ain Shams University Hospital. All enrolled neonates had a matched mean birth weight and gestational age. They were either moderate preterms >32 weeks, but <34 weeks, and late preterms >34 weeks, but <37 weeks). Results: The results indicate a correlation between FDPs and the laboratory data of group B, and it was found out that FDPs were negatively correlated with TLC, Plate-lets, and CRP, reflecting FDPs increase with bone marrow suppression and progression of sepsis. Factor XIII was significantly lower in the group with NEC as compared to the group of sepsis (p<0.001), while FDPs level was significantly higher in the group with sepsis (p<. 0.001). The correlation between the clinical stages of NEC BELL's score and the level of Initial factor XIII level revealed that the factor level is negatively correlated with stage I of BELL's score. The follow-up revealed that there was no correlation between BELL's score and the level of follow-up factor XIII. On follow-up, the current study demonstrated that TLC, CRP, FDPS, PTT were significantly increased in the sepsis group with p values of 0.021,, 0.001, 0.001 and 0.01. The current study found significantly higher partial thromboplastin time (PTT) in the group with sepsis Conclusion: Factor XIII level can predict early cases of NEC and can differentiate it from neo-natal sepsis.
同时使用因子XIII和纤维蛋白降解产物诊断早期NEC和新生儿败血症
目的:探讨因子XIII和纤维蛋白降解产物在早期NEC和新生儿败血症诊断中的应用。方法:60例新生儿分为两组。30例疑似早期NEC的早产儿采用改良Bell评分法确诊NEC, 30例有新生儿败血症症状的早产儿确诊NEC;通过血培养和CRP确诊败血症。对所有患者进行FDPs和血浆因子XIII的实验室评估。该研究是在艾因沙姆斯大学医院儿科的第三重症监护病房进行的。所有入组的新生儿均有匹配的平均出生体重和胎龄。中度早产>32周,但34周,但<37周)。结果:结果显示B组FDPs与实验室数据相关,发现FDPs与TLC、Plate-lets、CRP呈负相关,反映FDPs随骨髓抑制和脓毒症进展而升高。与脓毒症组相比,NEC组的因子XIII显著降低(p<0.001),而脓毒症组的FDPs水平显著升高(p<0.001)。0.001)。NEC BELL评分的临床分期与初始因子XIII水平的相关性显示,因子水平与BELL评分的I期呈负相关。随访发现BELL评分与随访因子XIII水平无相关性。本研究随访发现,败血症组TLC、CRP、FDPS、PTT显著升高,p值分别为0.021、0.001、0.001、0.01。本研究发现败血症组部分凝血活素时间(PTT)明显增高。结论:因子XIII水平可预测NEC早期病例,并可与新生儿败血症鉴别。
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