期刊文献+

低体重儿、早产儿败血症血培养的病原菌耐药性分析 被引量:4

Pathogen and Antibiotic Resistance in Very-low-birth-weight or Preterm Infants Septicemia
暂未订购
导出
摘要 目的了解低体重儿、早产儿败血症不同阶段感染菌株病原菌分布特点及耐药性。方法回顾性调查医院近3年间低体重儿、早产儿败血症血培养分离的病原菌菌株,结合出生后败血症的发作时间分组。结果970例低体重儿、早产儿可疑标本,细菌培养阳性率为17.5%;大多数败血症为出生3d后的晚期发作,占75.3%,迟发性败血症组主要病原菌为革兰阳性球菌,并以葡萄球菌属为主,占所有感染菌株的80.5%;早发性败血症组革兰阴性菌与革兰阳性菌感染比例大致相同,分别为47.6%和52.4%;并且迟发性败血症的耐药性明显高于早发败血症组。结论治疗新生儿感染的关键,是掌握新生儿不同时期感染病原菌的分布特点及药敏规律,根据药敏结果选用抗菌药物,避免滥用。 OBJECTIVE To understand the distribution of pathogen in very-low-birth-weight or preterm infants septicemia in early-onset and late-onset and drug sensitivity. METHODS Bacterial isolates from inpatients of verylow-birth-weight or preterm infants septicemia over a period of 3 years were retrospectively analyzed,and classified as when septicemia was happened. RESULTS The positive rate of isolates was 43.2% in 970 samples of very-lowbirth-weight or preterm infants septicemia. Most of the sepsis detected by blood culture was late-onset neonatal sepsis (58.6%). Pathogen of late-onset neonatal sepsis mostly was Gram - positive cocci, Staphylococcus were found to be the most common isolates(80.5 %). In early-onset sepsis group, the isolates rates of Gram-negative and Gram-positive bacteria were mostly in proportion, there were 52.4 % and 47.6 %, respeitively. The resistance rate of late-onset sepsis group was higher than that of early-onset one. CONCLUSIONS The key of curing infants septicemia is that we should master the distribution of pathogen of very-low-birth-weight or preterm infants septicemia in early-onset and late-onset and drug sensitivity. Antimicrobial therapy should be initiated under the guidance of anti-microbial sensitivity test, in order to avoid abuse of antimicrobial.
出处 《中华医院感染学杂志》 CAS CSCD 北大核心 2007年第2期236-238,共3页 Chinese Journal of Nosocomiology
关键词 低体重儿 早产儿 败血症 病原菌 抗菌药物 耐药性 Very-low-birth-weight infants Petrerm infants Septicemia Pathogen Antibiotics Drug resistance
  • 相关文献

参考文献6

二级参考文献12

共引文献850

同被引文献46

  • 1黄支密,仵蕾,陈榆,糜祖煌,单浩,郭满盈,秦玲,蔡培泉,王春新.44株阴沟肠杆菌耐药基因分析[J].中华医院感染学杂志,2007,17(2):139-142. 被引量:17
  • 2ANDERSON KF, LONSWAY DR, RASHEED JK, et al. Evalua- tion of methods to identify the Klebsiella pneumoniae carbapene- mase in Enterobacteriaceae[J]. Clin Microbiol, 2007, 45(8): 2723- 2725.
  • 3COUTO RC, CARVALHO EA, PEDROSA TM, et al. A 10-year prospective surveillance of nosocomial infections in neonatal intensive care units[J]. Am J Infect Control, 2007, 35 (3): 183-186.
  • 4Vergnano S, Menson E, Kennea N, et al. Neonatal infections in England: the NeonIN surveillance network[J]. Arch Dis Child Fetal Neonatal Ed, 2011, 96(1 ): F9-F14.
  • 5Stoll B J, Hansen NI, Bell EF, et al. Neonatal outcomes of extreme- ly preterm infants from the NICHD Neonatal Research Network[J]. Pediatrics, 2010, 126(3): 443-456.
  • 6McGuire W, Clerihew L, Fowlie PW, et al. Infection in the preterm infant[J]. BMJ, 2004, 329(7477): 1277-1280.
  • 7Lim WH, Lien R, Huang YC, et al. Prevalence and pathogen dis- tribution of neonatal sepsis among very-low-birth-weight infants[J]. Pediatr Neonatol, 2012, 53 (4): 228-234.
  • 8Lawrence SL, Roth V, Slinger R, et al. Cloxacillin versus van- comycin for presumed late-onset sepsis in the Neonatal Intensive Care Unit and the impact upon outcome of coagulase negative staphylococcal bacteremia:a retrospective cohort study [J]. BMC Pediatr, 2005, 5: 49.
  • 9Puopolo KM, Eichenwald EC. No change in the incidence of ampi- cillin-resistant, neonatal, early-onset sepsis over 18 years [J]. Pediatrics, 2010, 125(5): e1031-e1038.
  • 10Huang Y, Zhuang S, Du M. Risk factors of nosocomial infection with extended-spectrum beta-lactamase-producing bacteria in neonatal intensive care unit in China[J]. Infection, 2007, 35 (5): 339-345.

引证文献4

二级引证文献14

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