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作 者:夏兆新 杨文苏 朱毅 胡心益 林春晖 蒋童 沈继录[1] Xia Zhaoxin;Yang Wensu;Zhu Yi;Hu Xinyi;Lin Chunhui;Jiang Tong;Shen Jilu(The First Affiliated Hospital of Anhui Medical University,The Anhui Public Health Clinical Center,Laboratory Dept,Hefei 230022)
机构地区:[1]安徽医科大学第一附属医院检验科,安徽省公共卫生临床中心,合肥230022
出 处:《安徽医科大学学报》2023年第5期859-862,共4页Acta Universitatis Medicinalis Anhui
基 金:安徽省高等学校自然科学研究重大项目(编号:KJ2021ZD0032)。
摘 要:目的探究直接靶板微滴法(DOT-MGA)快速检测替加环素和多黏菌素敏感性。方法共收集了67株肺炎克雷伯菌进行DOT-MGA测试,将有或没有替加环素、多黏菌素(药物终浓度为2μg/ml)的6μl微滴一式三份加在靶板上,设置了3、4、6、8 h四个孵育时间点。Bruker Biotyper软件将测试结果判定为敏感(评分<1.7分)或非敏感(评分≥1.7分)。结果孵育4 h后,替加环素和多黏菌素的生长有效率、特异度、阳性预测值均为100.00%,分类一致率分别为98.15%、96.15%,灵敏度分别为96.30%、92.31%,阴性预测值分别为96.45%、92.86%。结论DOT-MGA可以快速准确鉴别对替加环素和多黏菌素的耐药表型,与微量肉汤稀释法比较具有良好的一致性。Objective To explore the direct-on-target micro-droplet growth assay(DOT-MGA)for rapid detection of the susceptibility of tigecycline and polymyxin.Methods A total of 67 strains of Klebsiella pneumoniae were collected for DOT-MGA.6μl droplets with or without tigecycline or polymyxin(The final drug concentration is 2μg/ml)were added in triplicate into the wells of the MALDI plate with four incubation time points(3 h,4 h,6 h,and 8 h).The results were classified as susceptible(score<1.7)and non-susceptible(score≥1.7)according to the Bruker Biotype software.Results After incubation for 4 h,the growth efficiency,specificity and positive predictive value of tigecycline and polymyxin were both 100.00%.The classification consistency rate was 98.15%and 96.15%,the sensitivity was 96.30%and 92.31%,and the negative predictive value was 96.45%and 92.86%,respectively.Conclusion DOT-MGA can provide rapid and reliable drug susceptibility diagnosis of tigecycline and polymyxin,which is of great significance for the clinical anti-infective treatment.
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