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中华实验和临床感染病杂志(电子版) ›› 2018, Vol. 12 ›› Issue (03) : 272 -277. doi: 10.3877/cma.j.issn.1674-1358.2018.03.014

所属专题: 经典病例 文献

临床论著

新生儿感染性疾病127例临床研究
白萌萌1, 孟林2, 李文2,(), 崔玉婕2, 张冬梅2, 桑艳峰2, 刘咏梅2, 唐静2   
  1. 1. 067000 承德市;承德医学院2016级研究生;067000 承德市,承德市中心医院儿科(承德医学院第二临床学院)
    2. 067000 承德市,承德市中心医院儿科(承德医学院第二临床学院)
  • 收稿日期:2017-02-27 出版日期:2018-06-15
  • 通信作者: 李文
  • 基金资助:
    承德市科学技术研究及发展项目(No. 201706A026)

Clinical study on 127 cases with suspected early-onset sepsis

Mengmeng Bai1, Lin Meng2, Wen Li2,(), Yujie Cui2, Dongmei Zhang2, Yanfeng Sang2, Yongmei Liu2, Jing Tang2   

  1. 1. Chengde Medical University, Chengde 067000, China
    2. Chengde Central Hospital (Second Clinical College of Chengde Medical College), Chengde 067000, China
  • Received:2017-02-27 Published:2018-06-15
  • Corresponding author: Wen Li
  • About author:
    Corresponding author: Li Wen, Email:
引用本文:

白萌萌, 孟林, 李文, 崔玉婕, 张冬梅, 桑艳峰, 刘咏梅, 唐静. 新生儿感染性疾病127例临床研究[J]. 中华实验和临床感染病杂志(电子版), 2018, 12(03): 272-277.

Mengmeng Bai, Lin Meng, Wen Li, Yujie Cui, Dongmei Zhang, Yanfeng Sang, Yongmei Liu, Jing Tang. Clinical study on 127 cases with suspected early-onset sepsis[J]. Chinese Journal of Experimental and Clinical Infectious Diseases(Electronic Edition), 2018, 12(03): 272-277.

目的

探讨新生儿感染性疾病实验室非特异性指标相关因素的诊断价值。

方法

选取2016年7月至2017年7月承德市中心医院NICU收治的127例出生0~3 d的感染性疾病患儿为感染组,103例0~3 d非感染性疾病新生儿为对照组,比较两组新生儿的临床症状、围产期因素以及实验室指标等。

结果

与对照组新生儿相比,感染组患儿喂养困难(15.7%)、呼吸困难(30.7%)、呻吟(31.5%)、皮肤黄染(18.1%)和窒息(5%)等初始症状差异均有统计学意义(χ2 = 4.136、24.574、33.282、38.039,P均< 0.001)。围产期因素中两组新生儿母亲孕晚期有感染病史和胎膜早破> 18 h两个因素差异有统计学意义(χ2 = 10.536、10.717,P均= 0.001)。实验室指标结果显示,两组新生儿C-反应蛋白(CRP)、白细胞计数以及中性粒细胞百分比差异均有统计学意义(t = 2.740、P = 0.008,t = 6.378、P < 0.001,t = 4.860、P < 0.001)。感染组患儿ROC曲线分析显示:CRP、白细胞计数、中性粒细胞百分比最佳截断点分别为8.0 mg/dl、12.65 × 109/L和63.15%,敏感性分别为24.3%、62.2%和68.9%,特异性分别为99.0%、81.2%和84.4%,曲线下面积(AUC)分别为0.544、0.707和0.769;CRP、白细胞计数和中性粒细胞百分比三者联合敏感性为83.8%,特异性为75.0%,曲线下面积(AUC)为0.860,显著高于单项指标。

结论

新生儿感染性疾病的发生与多种围产期因素密切相关,以呼吸系统症状为始发临床表现多见。CRP、白细胞计数和中性粒细胞百分比联合诊断可以提高诊断价值。围产期因素、临床表现和实验室指标相结合,有利于早期识别新生儿感染性疾病。

Objective

To investigate the diagnostic value of related nonspecific indexes in the laboratory factors for neonatal infectious diseases.

Methods

From July 2016 to July 2017, a total of 127 cases with infectious diseases in NICU of Chengde Central Hospital were selected as infection group, while 103 cases of non-infection newborns (0-3 day) were taken as the control group. Perinatal factors, laboratory indicators and other clinical factors were compared between the two groups.

Results

Compared with the control group, initial symptoms such as feeding difficulties (15.7%), breathing difficulties (30.7%), groans (31.5%), yellow skin stains (18.1%) and suffocation (5%) were significantly different in the infection group (χ2 = 4.136, 24.574, 33.282, 38.039; all P < 0.001). There were significant differences of perinatal factors between the two groups of newborns with a history of infection in the late stages of pregnancy and premature rupture of the fetal membrane > 18 h (χ2 = 10.536, 10.717; both P = 0.001). The results of laboratory indicators showed that the C-reactive protein (CRP), count of white blood cell (WBC) and percentage of neutrophils between newborns in the two groups were all significantly different (t = 2.740, P = 0.008; t = 6.378, P < 0.001; t = 4.860, P < 0.001). The ROC curve analysis of infection group showed that the best cut-off points for CRP, count of WBC and neutrophils were 8.0 mg/dl, 12.65 × 109/L and 63.15%, respectively; the sensitivity were 24.3%, 62.2% and 68.9%, respectively; the specificity were 99.0%, 81.2% and 84.4%, respectively; and the area under the curve (AUC) were 0.544, 0.707 and 0.769, respectively. The combined sensitivity of CRP, count of WBC and neutrophils was 83.8%, the specificity was 75.0%, and the AUC was 0.860, which was significantly higher than the individual index.

Conclusions

The incidence of neonatal infectious diseases is closely related to many perinatal factors, and mainly showed the clinical manifestations of respiratory symptoms. The combined diagnosis of leukocyte count and neutrophil percentage could improve the diagnostic value. The combination of perinatal factors, clinical manifestations and laboratory indexes are beneficial to the early identification of neonatal infectious diseases.

表1 两组新生儿的一般资料
表2 两组患儿的临床表现[例(%)]
表3 两组患儿的围产期因素[例(%)]
表4 两组患儿的实验室非特异性指标( ± s
图1 感染组患儿单指标和多指标联合检测诊断新生儿早发型败血症的ROC曲线
表5 单指标和多指标联合检测诊断新生儿早发型败血症的参数
[1]
任晓旭. 脓毒性休克早期识别[J]. 中国实用儿科杂志,2017,32(6):417-422.
[2]
Liu L, Johnson HL, Cousens S, et al. Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000[J]. Lancet,2012,379(9832):2151-2161.
[3]
Ericson JE, Laughon MM. Chorioamnionitis: Implications for the Neonate[J]. Clinics in perinatology,2015,42(1):155-165.
[4]
Polin RA. Management of neonates with suspected or proven early-onset bacterial sepsis[J]. Pediatrics,2012,129(5):1006-1015.
[5]
Hornik CP, Benjamin DK, Becker KC, et al. Use of the complete blood cell count in early-onset neonatal sepsis[J]. Pediatr Infect Dis J,2012,31(8):799-802.
[6]
邵肖梅, 叶鸿瑁, 丘小汕. 实用新生儿学[M]. 4版. 北京: 人民卫生出版社,2015:337-353.
[7]
Stronati M, Bollani L, Mavagliano R, et al. Neonatal sepsis: new preventive strategies[J]. Minerva Pediatr,2013,65(1):103-110.
[8]
王雪莲, 陈超. 中国新生儿死亡原因变迁[J]. 中华围产医学杂志,2014,17(6):425-427.
[9]
Blackburn RM, Muller-Pebody B, Planche T, et al. Neonatal sepsis-many blood samples, few positive cultures: implications for improving antibiotic prescribing[J]. Arch Dis Child Fetal Neonatal Ed,2012,97(6):487-488.
[10]
楚燕芳, 余加林, 杜立中. 区分早发型和晚发型新生儿败血症的临床意义[J]. 中华实用儿科临床杂志,2015,30(10):743-746.
[11]
van Herk W, Stocker M, van Rossum AM. Recognising early onset neonatal sepsis: An essential step in appropriate antimicrobial use[J]. J Infect,2016,72(1):S77-S82.
[12]
Chan GJ, Lee AC, Baqui AH, et al. Prevalence of early-onset neonatal infection among newborns of mothers with bacterial infection or colonization: a systematic review and Meta-analysis[J]. BMC Infect Dis,2015,15(1):1-16.
[13]
Shane AL, Stoll BJ. Recent developments and current issues in the epidemiology, diagnosis, and management of bacterial and fungal neonatal sepsis[J]. Am J Perinatol,2013,30(2):131-141.
[14]
Ognean ML, Boicean A, Sular FL, et al. Complete blood count and differential in diagnosis of early onset neonatal sepsis[J]. Revista Romana de Medicina de Lab,2017, 25(1):101-108.
[15]
殷静. 血清超敏C-反应蛋白,降钙素原,血小板参数在新生儿感染中的变化及临床意义[J]. 中国妇幼保健,2017,32(15):3539-3541.
[16]
Mikhael M, Brown LS, Rosenfeld CR. Serial neutrophil values facilitate predicting the absence of neonatal early-onset sepsis[J]. J Pediatr,2014,164(3):522-528.
[17]
Benitz WE. Adjunct laboratory tests in the diagnosis of early-onset neonatal sepsis[J]. Clin Perinatol,2010,37(2):421-438.
[18]
Perrone S, Lotti F, Longini M, et al. Creactive protein in healthy term newborns during the first 48 hours of life[J]. Arch Dis Child Fetal Neonatal Ed,2018,103(2):F163-F166.
[19]
Ince Z. Diagnosis of neonatal sepsis: what the clinician expects, what the laboratory tells[J]. Clin Biochem,2014,47(9):754-755.
[20]
Edgar JD, Gabriel V, Gallimore JR, et al. A prospective study of the sensitivity, specificity and diagnostic performance of soluble intercellular adhesion molecule 1, highly sensitive C-reactive protein, soluble E-selectin and serum amyloid A in the diagnosis of neonatal infection[J]. BMC Pediatr,2010,10(1):22.
[21]
Liu S, Hou Y, Cui H. Clinical values of the early detection of serum procalcitonin, C-reactive protein and white blood cells for neonates with infectious diseases[J]. Pak J Med Sci,2016,32(6):1326-1329.
[22]
Kordek A, Torbé A, Tousty J, et al. The determination of procalcitonin concentration in Early-Onset Neonatal Infection[J]. Clin Pediatr (Phila),2017,56(4):333-340.
[23]
Meem M, Modak JK, Mortuza R, et al. Biomarkers for diagnosis of neonatal infections: A systematic analysis of their potential as a point-of-care diagnostics[J]. J Glob Health,2011,1(2):201-209.
[24]
Chiesa C, Pacifico L, Osborn JF, et al. Early-onset neonatal sepsis: still room for improvement in procalcitonin diagnostic accuracy studies[J]. Medicine (Baltimore),2015,94(30):e1230-e1246.
[25]
Altunhan H, Annagür A, Örs R, et al. Procalcitonin measurement at 24 hours of age may be helpful in the prompt diagnosis of early-onset neonatal sepsis[J]. Int J Infect Dis,2011,15(12):854-858.
[26]
Su H, Chang SS, Han CM, et al. Inflammatory markers in cord blood or maternal serum for early detection of neonatal sepsis--a systemic review and meta-analysis[J]. J Perinatol,2014,34(4):268-274.
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