Mitra Piyali, Guha Debasish, Nag Shankha S, Mondal Badal C, Dasgupta Sayantan
Department of Pathology, North Bengal Medical College and Hospital, Sushruta Nagar, District Darjeeling, West Bengal India.
Department of Pathology, Nilratan Sircar Medical College and Hospital, Kolkata, West Bengal India.
Indian J Hematol Blood Transfus. 2017 Jun;33(2):195-199. doi: 10.1007/s12288-016-0683-x. Epub 2016 May 14.
The study was carried out to determine the role of plasma fibrinogen in diagnosis of neonatal sepsis and to evaluate its role in predicting short term outcome. Sixty five neonates with clinical features suggestive of neonatal sepsis were included in this study. Seventy five neonates served as the control group. Plasma fibrinogen, prothrombin time, activated partial thromboplastin time and platelet counts were performed in all the neonates. Cut-off value of plasma fibrinogen for diagnosis of neonatal sepsis was determined with the help of receiver operating characteristic curve. Plasma fibrinogen level was found to be significantly higher among neonates with sepsis when compared to neonates in control group ( < 0.0001). It had sensitivity of 70.8 %, specificity of 82.7 %, positive predictive value (PPV) of 72.3 % and negative predictive value (NPV) of 81.6 % for diagnosis of neonatal sepsis at cut-off value of 301.90 mg/dL. When neonates with septic shock and/or disseminated intravascular coagulation (DIC) were excluded from study population, sensitivity and NPV rose to 91.9 % and 95.4 % at the same cut-off value while specificity and PPV remained the same. Lower level of plasma fibrinogen was detected in neonates with septic shock and/or DIC ( < 0.0001) and in neonates who died ( < 0.0001). Hence plasma fibrinogen can serve as an effective tool in diagnostic work up of neonatal sepsis as well as in assessing development of complications and outcome.
本研究旨在确定血浆纤维蛋白原在新生儿败血症诊断中的作用,并评估其在预测短期预后方面的作用。本研究纳入了65例具有新生儿败血症临床特征的新生儿。75例新生儿作为对照组。对所有新生儿进行了血浆纤维蛋白原、凝血酶原时间、活化部分凝血活酶时间和血小板计数检测。借助受试者工作特征曲线确定了诊断新生儿败血症的血浆纤维蛋白原临界值。与对照组新生儿相比,败血症新生儿的血浆纤维蛋白原水平显著更高(<0.0001)。在临界值为301.90mg/dL时,其诊断新生儿败血症的敏感性为70.8%,特异性为82.7%,阳性预测值(PPV)为72.3%,阴性预测值(NPV)为81.6%。当研究人群中排除患有感染性休克和/或弥散性血管内凝血(DIC)的新生儿时,在相同临界值下,敏感性和NPV分别升至91.9%和95.4%,而特异性和PPV保持不变。在患有感染性休克和/或DIC的新生儿(<0.0001)以及死亡的新生儿(<0.0001)中检测到较低水平的血浆纤维蛋白原。因此,血浆纤维蛋白原可作为新生儿败血症诊断检查以及评估并发症发生和预后的有效工具。