国际检验医学杂志
國際檢驗醫學雜誌
국제검험의학잡지
INTERNATIONAL JOURNAL OF LABORATORY MEDICINE
2014年
16期
2144-2146
,共3页
区云枝%刘春林%韩福郎%黄德兵%关幼华
區雲枝%劉春林%韓福郎%黃德兵%關幼華
구운지%류춘림%한복랑%황덕병%관유화
多重耐药%泛耐药%铜绿假单胞菌%鲍曼不动杆菌%碳青霉烯酶
多重耐藥%汎耐藥%銅綠假單胞菌%鮑曼不動桿菌%碳青黴烯酶
다중내약%범내약%동록가단포균%포만불동간균%탄청매희매
multidrug-resistant%extensively drug-resistant%Pseudomonas aeruginosa%acinetobacter%carbapenemase
目的:了解铜绿假单胞菌和鲍曼不动杆菌院内感染分布、耐药特点以及产碳青霉烯酶表型情况。方法回顾性收集2012年7月到2013年7月该院分离非重复铜绿假单胞菌和鲍曼不动杆菌医院感染菌株及病例。采用纸片扩散法(K-B 法)进行药敏试验,改良 Hodge 试验进行碳青霉烯酶初筛,初筛阳性菌株应用2-巯基丙酸协同法进一步检测金属酶。结果在研究期间,共纳入非重复铜绿假单胞菌250株,鲍曼不动杆菌132株。菌株标本类型以痰液(55.5%)为主,科室分布以重症监护病房(20.9%)为主。药敏试验显示:铜绿假单胞菌对测试药物敏感性较好,均大于70%以上,对 IPM 和 MEM 耐药率较低分别为8.5%、9.5%,然而鲍曼不动杆菌对测试药物耐药率较高达35.2%~77.4%,对 IPM 和 MEM 耐药率分别为35.2%、39.1%。多重耐药及泛耐药鲍曼不动杆菌医院感染发生率要高于铜绿假单胞菌分别为44.7%和24.0%;9.1%和2.8%。40株耐碳青霉烯类铜绿假单胞菌,碳青霉烯酶初筛阳性11株占27.5%,金属酶表型阳性2株占18.2%;49株耐碳青霉烯类鲍曼不动杆菌,碳青霉烯酶初筛阳性37株占75.5%,金属酶表型阳性1株占2.7%。结论该院铜绿假单胞菌和鲍曼不动杆菌对常用抗菌药物呈现不同耐药性,应加强监测。产碳青霉烯酶是鲍曼不动杆菌耐碳青霉烯类药物主要机制之一。产金属酶铜绿假单胞菌和鲍曼不动杆菌检出率较低。
目的:瞭解銅綠假單胞菌和鮑曼不動桿菌院內感染分佈、耐藥特點以及產碳青黴烯酶錶型情況。方法迴顧性收集2012年7月到2013年7月該院分離非重複銅綠假單胞菌和鮑曼不動桿菌醫院感染菌株及病例。採用紙片擴散法(K-B 法)進行藥敏試驗,改良 Hodge 試驗進行碳青黴烯酶初篩,初篩暘性菌株應用2-巰基丙痠協同法進一步檢測金屬酶。結果在研究期間,共納入非重複銅綠假單胞菌250株,鮑曼不動桿菌132株。菌株標本類型以痰液(55.5%)為主,科室分佈以重癥鑑護病房(20.9%)為主。藥敏試驗顯示:銅綠假單胞菌對測試藥物敏感性較好,均大于70%以上,對 IPM 和 MEM 耐藥率較低分彆為8.5%、9.5%,然而鮑曼不動桿菌對測試藥物耐藥率較高達35.2%~77.4%,對 IPM 和 MEM 耐藥率分彆為35.2%、39.1%。多重耐藥及汎耐藥鮑曼不動桿菌醫院感染髮生率要高于銅綠假單胞菌分彆為44.7%和24.0%;9.1%和2.8%。40株耐碳青黴烯類銅綠假單胞菌,碳青黴烯酶初篩暘性11株佔27.5%,金屬酶錶型暘性2株佔18.2%;49株耐碳青黴烯類鮑曼不動桿菌,碳青黴烯酶初篩暘性37株佔75.5%,金屬酶錶型暘性1株佔2.7%。結論該院銅綠假單胞菌和鮑曼不動桿菌對常用抗菌藥物呈現不同耐藥性,應加彊鑑測。產碳青黴烯酶是鮑曼不動桿菌耐碳青黴烯類藥物主要機製之一。產金屬酶銅綠假單胞菌和鮑曼不動桿菌檢齣率較低。
목적:료해동록가단포균화포만불동간균원내감염분포、내약특점이급산탄청매희매표형정황。방법회고성수집2012년7월도2013년7월해원분리비중복동록가단포균화포만불동간균의원감염균주급병례。채용지편확산법(K-B 법)진행약민시험,개량 Hodge 시험진행탄청매희매초사,초사양성균주응용2-구기병산협동법진일보검측금속매。결과재연구기간,공납입비중복동록가단포균250주,포만불동간균132주。균주표본류형이담액(55.5%)위주,과실분포이중증감호병방(20.9%)위주。약민시험현시:동록가단포균대측시약물민감성교호,균대우70%이상,대 IPM 화 MEM 내약솔교저분별위8.5%、9.5%,연이포만불동간균대측시약물내약솔교고체35.2%~77.4%,대 IPM 화 MEM 내약솔분별위35.2%、39.1%。다중내약급범내약포만불동간균의원감염발생솔요고우동록가단포균분별위44.7%화24.0%;9.1%화2.8%。40주내탄청매희류동록가단포균,탄청매희매초사양성11주점27.5%,금속매표형양성2주점18.2%;49주내탄청매희류포만불동간균,탄청매희매초사양성37주점75.5%,금속매표형양성1주점2.7%。결론해원동록가단포균화포만불동간균대상용항균약물정현불동내약성,응가강감측。산탄청매희매시포만불동간균내탄청매희류약물주요궤제지일。산금속매동록가단포균화포만불동간균검출솔교저。
Objective To understand the nosocomial infection distribution,drug resistance characteristics and carbapenemases-producing phenotype of Pseudomonas aeruginosa (PAE)and Acinetobacter baumannii (ABA).Methods The nosocomial infection strains of non-repeated PAE and ABA isolated in this hospital and the infected cases from July 2012 to July 2013 were retrospec-tively collected.The antimicrobial susceptibility test was conducted by the disk diffusion method(K-B method).The modified Hodge test was adopted to preliminarily screen carbapenemase and the positive strains of preliminary screening were further detected met-allo-beta-lactamase(MBL)by 2-mercaptopropionic acid synergy test.Results During the study period,250 strains of non-repeated PAE and 132 strains of ABA were included.All of them were primarily isolated from sputum specimens,accounting for 55.5%.The department distribution was dominated by the intensive care units(ICU),accounting for 20.9%.The antimicrobial susceptibility test showed that the sensitivity of PAE to the testing anti-microbial drugs was more than 70%,its resistance rates to IPM and MEM were 8.5% and 9.5% respectively.However,the resistance rates of ABA to the testing anti-microbial drugs were up to 35.2%-77.4%,its resistance rates to IPM and MEM were 35.2%,39.1% respectively.The occurrence rates of multidrug-resist-ant and pandrug-resistant ABA nosocomial infection was higher than that of PAE,which were 44.7% and 24.0% and 9.1% and 2.8%,respectively.Among 40 strains of carbapenem-resistant PAE,11 strains(27.5%)were positive in the preliminary screening and 2 strains(18.2%)were positive of MBL phenotype.Among 49 strains of carbapeneme-resistant ABA,37 strains(75.5%)were positive in the preliminary screening and only 1 strain(2.7%)was positive of MBL phenotype.Conclusion PAE and ABA in our hospital exhibit different resistance to common antibacterial drugs.The monitoring should be strengthened.The production of car-bapenemsa is one the main mechanisms for PAE resistance to carbapenems.The detection rate of MBL-producing PAE and ABA is lower in our hospital.