Dessì Angelica, Corsello Giovanni, Stronati Mauro, Gazzolo Diego, Caboni Pierluigi, Carboni Roberta, Fanos Vassilios
Neonatal Intensive Care Unit, Puericulture Institute and Neonatal Section, Azienda Ospedaliera Universitaria, University of Cagliari, Cagliari, Italy.
Operative Unit of Pediatrics and Neonatal Intensive Therapy, Mother and Child Department, University of Palermo, Palermo, Italy.
Early Hum Dev. 2014 Mar;90 Suppl 1:S19-21. doi: 10.1016/S0378-3782(14)70007-6.
Systemic neonatal infection is a serious complication in preterm and term infants and is defined as a complex clinical syndrome caused by bacteria, fungi and virus. Sepsis remains among the leading causes of death in both developed and underdeveloped countries above all in the neonatal period. Earlier diagnosis may offer the ability to initiate treatment to prevent adverse outcomes. There have been many studies on various diagnostic haematological markers like acute phase reactants, C-reactive protein, procalcitonin, interleukins and presepsin. However, there is still no single test that satisfies the criteria as being the ideal marker for the early diagnosis of neonatal sepsis. In this regard, metabolomic analysis seems to be a promising method for determining metabolic variations correlated with systemic neonatal infections.
新生儿全身性感染是早产和足月婴儿的一种严重并发症,被定义为由细菌、真菌和病毒引起的复杂临床综合征。败血症仍然是发达国家和不发达国家主要的死亡原因之一,尤其是在新生儿期。早期诊断有助于启动治疗以预防不良后果。关于各种诊断血液学标志物,如急性期反应物、C反应蛋白、降钙素原、白细胞介素和 presepsin,已经有很多研究。然而,仍然没有一种单一的检测方法能满足作为新生儿败血症早期诊断理想标志物的标准。在这方面,代谢组学分析似乎是一种有前景的方法,用于确定与新生儿全身性感染相关的代谢变化。