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作 者:赵建萍[1] 黄金伟[1] 陈丽珠[1] 李爱芳[1] 黄建胜[1] 王晓光[2] 陈秀英[2] 李国雄[1]
机构地区:[1]浙江省丽水市中心医院检验科,浙江丽水323000 [2]浙江省丽水市疾病预防控制中心,浙江丽水323000
出 处:《中国卫生检验杂志》2010年第3期567-569,共3页Chinese Journal of Health Laboratory Technology
摘 要:目的:探讨临床分离的肺炎克雷伯菌的亚胺培南抑菌圈直径大小与KPC型碳青霉烯酶(Carbapenemase KPC)存在的相关性。方法:利用ESBLs确认试验对临床分离的肺炎克雷伯菌产ESBLs检测,并分为ESBLs阳性组与ESBLs阴性组,K-B法检测亚胺培南对所有菌抑菌圈直径,PCR方法检测所有菌KPC。结果:亚胺培南对81株肺炎克雷伯菌ESBLs阳性组抑菌圈直径27.92±0.18 cm,统计学方法推论95%抑菌圈范围27.10~28.48 cm;ESBLs阴性组101株抑菌圈直径28.28±0.11 cm,统计学方法推论95%抑菌圈范围27.40~28.86 cm,2组抑菌环直径比较无明显差异(P0.05)。2株ESBLs阳性肺炎克雷伯菌亚胺培南抑菌圈直径分别为20 cm和19.5 cm,同时检测到KPC。结论:亚胺培南对临床分离的肺炎克雷伯菌抑菌圈直径小于或等于20 cm,该菌检测到KPC型碳青霉烯酶可能是原因之一。Objective:To analyze the relationship between imipenem inhibition zone and KPC type Carbapenemase in Klebsiella pneumoniae.Methods:K.pneumoniae strains were separated in two groups according to ESBLs.Imipenem inhibition zone were measured with disc dilution method,while KPC gene was detected by PCR.Results:Imipenem inhibition zone in 81 ESBLs positive and 101 ESBLs negative strains were 27.92±0.18 cm and 28.28±0.11 cm,respectively,according to statistical method.But there was no significant discrepancy between the two groups(P0.05).KPC gene were detected in 2 ESBLs positive strains with the inhibition zone of 20 cm and 19.5 cm respectively.Conclusion:KPC type Carbapenemase may contribute to imipenem resistant in K.pneumoniae with the inhibition zone = 20 cm.
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