Presepsin as an early diagnostic marker in Premature infants with neonatal sepsis and septic shock

Ashraf Shahin, Omima Abdel haie, Sahar Fayed, Rime Abdelsalam
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Abstract

Background: Neonatal sepsis is a systemic condition involving hemodynamic changes and clinical manifestations caused by bacterial, viral, or fungal infection that occurs within the first 28 days of life. This study aimed to assess the accuracy of Presepsin for diagnosis and early detection of sepsis and septic shock among preterm neonates. Methods: This Cross-sectional study included 75 preterm neonates with symptoms suspicious of sepsis. They were classified into 3 groups: Group 1; Infection (suspected infection not meeting the criteria for sepsis). Group 2; Sepsis (neonatal systemic inflammatory response syndrome, SIRS, plus suspected or proven infection). Group 3; Septic shock (sepsis plus cardiovascular organ dysfunction). Detailed history, clinical examination, laboratory investigations: Complete blood picture (CBC), C-Reactive Protein (CRP), blood culture and determination of Human Presepsin level in the Blood (PSEP). Results : Presepsin level was significantly lower at D3 and D5 compared to D1 (P<0.001). whereas, in group 3 (Septic shock), Presepsin level was significantly lower at D5 compared to D1 (P=0.007). only PLT count, CRP, Presepsin at D1, Presepsin at D3 and Presepsin at D5-were significant predictors of neonatal sepsis and only APGAR at 5 min, PLT count, CRP, Presepsin at D1, Presepsin at D3 and Presepsin at D5-were significant predictors of septic shock in neonates. Conclusion: Presepsin is an accurate diagnostic biomarker for early diagnosis of sepsis compared to other acute phase reactant and inflammatory markers. Presepsin is a strong predictive marker for sepsis and septic shock from day1 to day 5 with high sensitivity and specificity.
作为新生儿败血症和脓毒性休克早产儿早期诊断标志物的前胃蛋白酶
背景:新生儿败血症是一种全身性疾病,由细菌、病毒或真菌感染引起的血流动力学变化和临床表现,发生在新生儿出生后的 28 天内。本研究旨在评估 Presepsin 诊断和早期检测早产新生儿败血症和脓毒性休克的准确性。方法:横断面研究这项横断面研究包括 75 名有败血症可疑症状的早产新生儿。他们被分为 3 组:第 1 组;感染(疑似感染,不符合败血症标准)。第 2 组;败血症(新生儿全身炎症反应综合征,SIRS,加上疑似或已证实的感染)。第 3 组;脓毒性休克(脓毒症加心血管器官功能障碍)。详细病史、临床检查、实验室检查:全血细胞计数(CBC)、C-反应蛋白(CRP)、血液培养和血液中人血前蛋白水平测定(PSEP)。结果:与第一组相比,第三组(脓毒性休克)的前体蛋白水平在第 3 和第 5 天明显降低(P<0.001);与第一组相比,第三组(脓毒性休克)的前体蛋白水平在第 5 天明显降低(P=0.007)。只有 5 分钟时的 APGAR、PLT 计数、CRP、D1 时的 Presepsin、D3 时的 Presepsin 和 D5 时的 Presepsin 可显著预测新生儿败血症,只有 5 分钟时的 APGAR、PLT 计数、CRP、D1 时的 Presepsin、D3 时的 Presepsin 和 D5 时的 Presepsin 可显著预测新生儿脓毒性休克。结论与其他急性期反应物和炎症标记物相比,前血蛋白是早期诊断脓毒症的准确生物标记物。前血蛋白是第 1 天至第 5 天脓毒症和脓毒性休克的强预测标志物,具有很高的灵敏度和特异性。
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