血浆d -二聚体水平与早、晚发型新生儿败血症的关系。

Mohammed Al-Biltagi, Ehab M Hantash, Mohammed Ramadan El-Shanshory, Enayat Aly Badr, Mohamed Zahra, Manar Hany Anwar
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引用次数: 2

摘要

背景:新生儿败血症是一种危及生命的疾病。早期诊断至关重要,但尚未发现单一的感染标志。脓毒症激活凝血级联反应,同时由于纤维蛋白的裂解产生d -二聚体。d -二聚体试验反映凝血系统的激活。目的:探讨d -二聚体在新生儿早、晚发型脓毒症中的临床病理意义。方法:本研究为前瞻性横断面研究,纳入90例新生儿;分为三组:第一组:早发性脓毒症(EOS);第二组:迟发性脓毒症(LOS);第三组:对照组。我们根据方案诊断新生儿败血症。c -反应蛋白(CRP)和d -二聚体测定在EOS和LOS之间进行比较,并与致病微生物因子相关。结果:脓毒症组d -二聚体明显增高,且d -二聚体阳性的病例数明显增多。LOS新生儿的d -二聚体水平明显高于EOS, CRP水平无显著差异。LOS患儿住院时间、革兰氏阴性菌血症和死亡率均显著高于EOS患儿(P < 0.01)。革兰氏阴性菌具有最高的d -二聚体水平(不动杆菌、克雷伯氏菌和假单胞菌)和CRP(沙雷氏菌、克雷伯氏菌和假单胞菌);而革兰氏阳性败血症则与相对较低的水平相关。d -二聚体与血红蛋白水平、血小板计数呈显著负相关;与CRP、住院时间、死亡率呈显著正相关。d -二聚体诊断新生儿脓毒症的最佳临界值为0.75 mg/L,敏感性为72.7%,特异性为86.7%。在目前的研究中,d -二聚体检测具有与CRP相当的特异性和敏感性。结论:本研究揭示了d -二聚体在新生儿败血症诊断中的重要价值。d -二聚体可作为其他脓毒症标志物的辅助,提高诊断新生儿脓毒症的敏感性和特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Plasma D-dimer level in early and late-onset neonatal sepsis.

Plasma D-dimer level in early and late-onset neonatal sepsis.

Plasma D-dimer level in early and late-onset neonatal sepsis.

Background: Neonatal sepsis is a life-threatening disease. Early diagnosis is essential, but no single marker of infection has been identified. Sepsis activates a coagulation cascade with simultaneous production of the D-dimers due to lysis of fibrin. D-dimer test reflects the activation of the coagulation system.

Aim: To assess the D-dimer plasma level, elaborating its clinicopathological value in neonates with early-onset and late-onset neonatal sepsis.

Methods: The study was a prospective cross-sectional study that included ninety neonates; divided into three groups: Group I: Early-onset sepsis (EOS); Group II: Late-onset sepsis (LOS); and Group III: Control group. We diagnosed neonatal sepsis according to our protocol. C-reactive protein (CRP) and D-dimer assays were compared between EOS and LOS and correlated to the causative microbiological agents.

Results: D-dimer was significantly higher in septic groups with a considerably higher number of cases with positive D-dimer. Neonates with LOS had substantially higher levels of D-dimer than EOS, with no significant differences in CRP. Neonates with LOS had a significantly longer hospitalization duration and higher gram-negative bacteriemia and mortality rates than EOS (P < 0.01). Gram-negative bacteria have the highest D-dimer levels (Acinetobacter, Klebsiella, and Pseudomonas) and CRP (Serratia, Klebsiella, and Pseudomonas); while gram-positive sepsis was associated with relatively lower levels. D-dimer had a significant negative correlation with hemoglobin level and platelet count; and a significant positive correlation with CRP, hospitalization duration, and mortality rates. The best-suggested cut-off point for D-dimer in neonatal sepsis was 0.75 mg/L, giving a sensitivity of 72.7% and specificity of 86.7%. The D-dimer assay has specificity and sensitivity comparable to CRP in the current study.

Conclusion: The current study revealed a significant diagnostic value for D-dimer in neonatal sepsis. D-dimer can be used as an adjunct to other sepsis markers to increase the sensitivity and specificity of diagnosing neonatal sepsis.

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