期刊文献+

临床抗感染治疗不足与耐药菌产生的相关研究 被引量:5

Correlation between insufficient clinical anti-infection treatment and emergence of drug-resistant bacteria
原文传递
导出
摘要 目的探讨临床抗感染治疗不足与耐药菌产生的相关性,指导临床抗感染治疗以及减少耐药菌的产生。方法选取医院2013年9月-2014年1月140例感染性疾病住院患者,将患者均分为试验组和对照组,各70例;其中对照组为抗感染不足患者,采用药物最低抑菌浓度(MIC)的剂量治疗,试验组为治疗充足患者,采用药物防突变浓度(MPC)的剂量治疗;比较两组患者用药后3、6d的白细胞(WBC)计数和治疗后耐药菌产生情况。结果试验组3d后WBC计数为(8.308±0.785)×109/L,6d后WBC计数为(7.986±1.151)×109/L,WBC增值为(-0.391±1.237)×109/L,低于治疗不足组的(9.172±0.799)×109/L、(11.123±1.039)×109/L及(2.381±2.134)×109/L,两组比较差异有统计学意义(P<0.05);试验组患者产生耐药菌125株,对照组产生耐药菌824株,两组比较差异有统计学意义(P<0.05)。结论临床中抗感染治疗不足可导致耐药菌的产生,采用高浓度的MPC治疗剂量在抗感染治疗上的效果优于较低浓度的MIC治疗剂量,能有效减少因抗感染治疗不足而导致的耐药菌产生。 OBJECTIVE To explore the relationship between the insufficient clinical anti-infection treatment and the emergence of drug-resistant bacteria so as to provide guidance for clinical treatment of infections and prevent the emergence of drug-resistant bacteria.METHODS A total of 140 patients with infectious diseases who were hospitalized from Sep 2013 to Jan 2014 were enrolled in the study and divided into the experimental group and the control group,with 70 cases in each.The control group was treated with the dose of minimal inhibitory concentration(MIC)for the insufficient anti-infection treatment,while the experimental group was treated with the dose of mutant prevention concentration(MPC).The white blood cells(WBC)counts and the emergence of drug-resistant bacteria were observed and compared between the two groups after the medication for 3and 6days.RESULTS The mean WBC counts of the experimental group was(8.308±0.785)×10^9/L after the medication for 3days,lower than(9.172±0.799)×10^9/L of the control group;the mean WBC counts of the experimental group was(7.986±1.151)×10^9/L after the medication for 6days,lower than(11.123±1.039)×10^9/L of the control group;the increase of the WBC counts of the experimental group was(-0.391±1.237)×10^9/L,lower than(2.381±2.134)×10^9/L of the control group;there was significant difference between the two groups(P〈0.05).Totally 125 strains of drug-resistant bacteria emerged in the experimental group,and 824 strains of drug-resistant bacteria emerged in the control group,with significance(P〈0.05).CONCLUSIONThe clinical insufficient anti-infection treatment may induce the emergence of drug-resistant bacteria.The high dose of MPC is superior to the low dose of MIC in the clinical treatment of infections,and it can effectively prevent the emergence of the drug-resistant bacteria due to the insufficient treatment.
出处 《中华医院感染学杂志》 CAS CSCD 北大核心 2015年第18期4172-4173,4193,共3页 Chinese Journal of Nosocomiology
基金 教育部高等学校博士学科点专项科研基金资助项目(200803161015)
关键词 抗感染 治疗不足 防突变浓度 耐药菌 Anti-infection Insufficient treatment Mutant prevention concentration Drug-resistant bacteria
  • 相关文献

参考文献3

  • 1刘淼,刘海凤,郑风劲.耐药突变选择窗与抗菌药物防耐药突变浓度的研究进展[J].四川解剖学杂志,2012,20(2):55-58. 被引量:3
  • 2Menendez-Arias L.Molecular basis of human immunodeficiency virus drug resistance:an update[J].Antiviral Res,2010,85(1):210-231.
  • 3Blondeau JM,Hansen G,Metzler K,et al.The role of PK/PD parameters to avoid selection and increase of resistance:mutant prevention concentration[J].J Chemother,2004,16(Suppl 3):1-19.

二级参考文献18

  • 1陈愉,张智洁,孙继梅,白晓红,李胜歧.4种氟喹诺酮类药物对嗜麦芽寡养单胞菌防耐药变异浓度的测定[J].中国抗生素杂志,2006,31(4):216-219. 被引量:8
  • 2李朝霞,刘又宁.细菌耐药突变选择窗理论与抗菌药物合理应用[J].中国药学杂志,2006,41(16):1201-1205. 被引量:31
  • 3Zhao X. Restricting the selection ofantibiotic-resistant mu- tant: a general strategy drived from fluoroquinolones studies [J]. Clin infect Dis, 2001,33 : S147-156.
  • 4Drlica K. A strategy for fighting antibiotic resistance [ J ]. ASM News,2001,67 :27-33.
  • 5Zhao X, Drlica K. Restricting the selection of antibiotic re- sistants: a general strategy derived from fIuoroquinolones studies[J]. Clin Infect Dis, 2001,33(suppl) :147-156.
  • 6Zhao X, Drlica K. Restricting the selection of antibiotic re- sistant mutant bacteria: measurement and potential use of the mutant selection window[J]. J Infect Dis, 2002, 185, 561- 565.
  • 7Dong Y, Zhao X, Donmagal AJ, et al. Effect of fluoroquin- olone concentration on selection of resistant mutants of myco- bacterium-bovis BCG and staphylococcus aureus[J]. Antimi- crGb Agents Chem-other, 1999, 43(7): 1756-1758.
  • 8Metzler K,Hansen GM,Hedlin P, et ah Comparison of mini- mal inhibitory and mutant prevention drug concentrations of 4 fluoroquinolones against clinical isolates of methicillin suscep- tible and resistant. Staphylococcus aureus[J]. Int J Anticicrob Agents, 2004,24 :161-167.
  • 9Zhao X. Clarification of MPC and the mutant selection win- dow concept [J]. Antimicrob Chemother, 2003,52 : 731.
  • 10Zhao X,Drlica K. Restricting the selection of antibiotic-resist- ant mutant baeteriaz Ageneral strategy derived from fluoro- quinoione studies [J]. Clin Infect Dis, 2001,33 (Suppl3) : S147.

共引文献2

同被引文献52

  • 1刘又宁,陈民钧,赵铁梅,王辉,王睿,刘庆锋,蔡柏蔷,曹彬,孙铁英,胡云建,修清玉,周新,丁星,杨岚,卓建生,唐英春,张扣兴,梁德荣,吕晓菊,李胜歧,刘勇,俞云松,魏泽庆,应可净,赵峰,陈萍,侯晓娜.中国城市成人社区获得性肺炎665例病原学多中心调查[J].中华结核和呼吸杂志,2006,29(1):3-8. 被引量:788
  • 2崔俊昌,刘又宁,王睿,童卫杭,梁蓓蓓.左氧氟沙星药代动力学/药效动力学参数与金黄色葡萄球菌耐药的相关性研究[J].中国临床药理学与治疗学,2007,12(9):989-992. 被引量:25
  • 3CREDITO K, K0S0WSKA - SHICK K, APPELBAUM P C. Mu-tant prevention concentrations of four carbapenems against gram -negative rods [ J]. Antimicrob Agents Chemother, 2010,54 (6):2692 -2695.
  • 4DONG Y,ZHAO X’ DOMAGALA J, et al. Effect of fluoroquinolo-ne concentration on selection of resistant mutants of Mycobacteriumbovis BCG and Staphylococcus aureus [ J]. Antimicrob Agents Che-mother, 1999t43(7):1756 -1758.
  • 5ZHAO X, DRLICA K. Restricting the selection of antibiotic - re-sistant mutant bacteria : measurement and potential use of the mutantselection window [J]. J Infect Dis,2002,185(4) :561 -565.
  • 6FIRSOV A A,VOSTROV S N, LUBENKO I Y, et al. In vitropharmacodynamic evaluation of the mutant selection window hypo-thesis using four fluoroquinolones against Staphylococcus aureus[J]. Antimicrob Agents Chemother, 2003 ,47(5) :1604 -1613.
  • 7CROISIER D,ETIENNE M, CHARLES P, et al. In vivo phannaco-dynamic efficacy of gatiiloxacin a^inst Streptococcus pneumoniae inan experimental model of pneumonia: impact of the low levels offluoroquinolone resistance on the enrichment of resistant mutants[J ]. J Antimicrob Chemother,2004 ’54(3) :640 - 647.
  • 8LIU Y,CUI J,WANG R,et al. Selection of rifampicin resistantStaphylococcus aureus during tuberculosis therapy : concurrent bacte-rial eradication and acquisition of resistance [ J]. J Antimicrob Che-mother, 2005,56(6):1172-1175.
  • 9ZHAO X,DRLICA K. Restricting the selection of antibiotic - re-sistant mutants : a general strategy derived from fluoroquinolonestudies [ J ]. 2001 - 09 - 15 [ 2015 - 11 -25]. http://www. nc-bi. nlm. nih. gov/pubmed/? term.
  • 10CAI Y, YANG J, KAN Q, et al. Mutant prevention concentrationof colistin alone and in combination with levofloxacin or tobramycinagainst multidrug - resistant Acinetobacter baumannii [ J] . Int J An-timicrob Agents, 2012, 40(5) :477 -478.

引证文献5

二级引证文献16

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