c反应蛋白作为新生儿败血症早期诊断的指标

P. Eniowo, A. Kareem, Akinbowale R. Eniowo, E. Adejuyigbe, Korede O. Oluwatuyi, Opeyemi O. Akinmadelo
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引用次数: 0

摘要

新生儿败血症是发病/死亡的主要原因,最终诊断是从血培养中分离病原体,这可能需要2-7天。因此,需要进行早期确诊感染的检测。因此,c反应蛋白(CRP)被建议作为诊断新生儿败血症的早期筛查工具。目的:探讨CRP在新生儿脓毒症早期诊断中的价值。研究设计:这是一项前瞻性纵向研究。研究地点:奥巴费米·阿沃洛沃大学附属教学医院Ile-Ife儿科。方法:连续招募新生儿。接触时和24小时进行血培养和CRP检测。对资料进行分析,P = 0.05被认为是显著的。结果:共纳入新生儿180例,其中男106例(58.9%),男女比例为1.4:1。新生儿培养证实脓毒症32例(17.8%),本组患病率为10.1%,外组患病率为23.8%,差异有统计学意义(χ2 = 5.638, P = 0.018)。脓毒症患者的初始和重复CRP均值分别为41.4 (23.6)mg/l和10.6 (4.3)mg/l,无脓毒症患者的初始和重复CRP均值分别为9.2 (11.3)mg/l和6.1 (2.6)mg/l (P < 0.001)。CRP敏感性为93.8%,特异性为91.9%,阴性预测值为98.6%,阳性预测值为71.4%。CRP≥10mg/L且培养阳性受试者的受试者操作者特征曲线曲线下面积为0.909 (P < 0.001)。结论:CRP具有较高的敏感性、特异性和阴性预测值,可用于新生儿败血症的筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C-Reactive Protein as an Index of Early Diagnosis of Neonatal Sepsis
Introduction: Neonatal sepsis is a major cause of morbidity/mortality and the definitive diagnosis is an isolation of the pathogen from blood culture which might take 2-7 days. A test for early confirmation of infection is therefore required. C-reactive protein (CRP) is therefore suggested as an early screening tool in the diagnosis of neonatal sepsis. Aim: To determine the usefulness of CRP in the early diagnosis of neonatal sepsis among neonates. Study design: This was a prospective longitudinal study. Place of the study: Department of Paediatrics, Obafemi Awolowo University Teaching Hospital Complex Ile-Ife. Methods: Consecutive neonates were recruited. Blood culture was done and CRP was done at contact and 24 hours. Data were analysed and P = .05 was considered significant. Results: A total of 180 neonates comprising 106 (58.9%) males with a male to female ratio of 1.4:1 were studied. Thirty-two (17.8%) of the neonates had culture-proven sepsis with a prevalence of 10.1% among the inborn and 23.8% among the out-born with statistically significant difference (χ2 = 5.638, P = .018). The means of initial and repeat CRP for subjects with culture-proven sepsis were 41.4 (23.6) mg/l and 10.6 (4.3) mg/l respectively while subjects without sepsis were 9.2 (11.3) mg/l and 6.1 (2.6) mg/l respectively (P < .001). The CRP has a sensitivity of 93.8%, specificity 91.9%, negative predictive value 98.6%, and positive predictive value of 71.4%. The area under the curve for the receiver operator characteristic curve for subjects with CRP ≥ 10mg/L and positive culture was 0.909 (P < .001). Conclusion: The CRP has a high sensitivity, specificity, and negative predictive value and can therefore be used to screen neonates with sepsis.
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