期刊文献+

超敏CRP及IL-6水平变化在新生儿败血症诊治中的价值 被引量:6

Value of determination of Hs-CRP and IL-6 in blood to diagnose neonate hematosepsis
下载PDF
导出
摘要 目的分析超敏CRP及IL-6水平变化,结合中性粒细胞杆状核/分叶核比值、血小板参数等测定,评价其新生儿败血症早期诊断中的价值。方法取35例静脉血测定超敏CRP及IL-6,并作血液分析,超敏CRP测定采用免疫比浊法I、L-6测定采用酶免吸附法,并与对照组比较。结果新生儿败血症时超敏CRP、IL-6、杆状核/分叶核比值、血小板参数与对照组比较有显著差异(P<0.01),治疗前后也有差异(P<0.05)。结论超敏CRPI、L-6、杆状核/分叶核比值、血小板参数水平及动态检测对新生儿败血症的早期诊断及疗效判定具有一定价值。 Objective To analyze the significance of determing Hs-CRP and IL-6 and platelet parameter level in blood, binding the ratio of neutrophic granulocyte band form and neutrophic granulocyte segmentedm form to early diagnose the neonate hematosepsis. Methods The venous blood were obtained in 35 cases with neonatal sepsis and 20 normal neonates for measuring serum Hs-CRP and IL- 6 by immunoassays and then have a blood routine analysis. The changes of serum Hs-CRP and IL-6 were compared before and after the therapy with normal controls. Results There is a significant difference between hematosepsis team and control team in Hs-CRP, IL-6, platelet parameter level and the ratio of neutrophic granulocyte band form and neutrophic granulocyte segmented (P〈0.01),there is also difference between before and after therapy in the same neonate (P〈0. 05). Conclusion Dynamically determing Hs-CRP and IL-6 and platelet parameter level in blood, binding the ratio of neutrophic granulocyte band form and neutrophic granulocyte segmentum form have difinite value in early diagno- sing neonate hematosepsis,and helping to judge the therapeutic effect of this disease.
出处 《国外医学(临床生物化学与检验学分册)》 2005年第10期684-685,688,共3页 Foreign Medical Sciences(section of Clinical Biochemistry and Laboratory Medicine
关键词 败血病 C反应蛋白质 白细胞介素6 Septicemia C-reactive protein Interleukin-6
  • 相关文献

参考文献6

二级参考文献41

  • 1Xiong YQ, Yeaman MR, Bayer AS. In vitro antibacterial activities of platelet microbicidal protein and neutrophil defensin against Staphylococcus aureus are influenced by antibiotics differing in mechanism of action. Antimicrob Agents Chemother, 1999,43(5)
  • 2Mercier RC, Rybak MJ, Bayer AS, et al. Influence of platelets and platelet microbicidal protein susceptibility on the fate of Staphylococcus aureus in an in vitro model of infective endocarditis.Infect Immun, 2000,68(8):4699-4705.
  • 3Dhawan VK, Bayer AS, Yeaman MR. Thrombin-induced platelet microbicidal protein susceptibility phenotype influences the outcome of oxacillin prophylaxis and therapy of experimental Staphylococcus aureus endocarditis. Antimicrob Agents Chemother, 2000,44(11
  • 4Kupferwasser LI, Skurray RA, Brown MH, et al. Plasmid-mediated resistance to thrombin-induced platelet microbicidal protein in staphylococci: role of the qacA locus. Antimicrob Agents Chemother, 1999,43(10):2395-2399.
  • 5Bayer AS, Prasad R, Chandra J, et al. In vitro resistance of Staphylococcus aureus to thrombin-induced platelet microbicidal protein is associated with alterations in cytoplasmic membrane fluidity. Infect Immun,2000,68(6):3548-3553.
  • 6Kupferwasser LI, Yeaman MR, Shapiro SM, et al. In vitro susceptibility to thrombin-induced platelet microbicidal protein is associated with reduced disease progression and complication rates in experimental Staphylococcus aureus endocarditis: microbiologi
  • 7Koo SP, Yeaman MR, Nast CC, et al. The cytoplasmic membrane is a primary target for the staphylocidal action of thrombin-induced platelet microbicidal protein. Infect Immun, 1997,65(11):4795-4800 .
  • 8Koo SP, Yeaman MR, Bayer AS. Staphylocidal action of thrombin-induced platelet microbicidal protein is influenced by microenvironment and target cell growth phase. Infect Immun, 1996,64(9):3758-3764.
  • 9Yeaman MR, Yount NY. Mechanisms of antimicrobial peptide action and resistance. Pharmacol Rev, 2003,55(1):27-55.
  • 10Ganong WF,eds. Review of medical physiology. 20th ed. San Francisco. McGraw-Hill Companies,2001:514-515.

共引文献1044

同被引文献31

引证文献6

二级引证文献49

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部