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尼泊尔国家公共卫生实验室中产生超广谱β-内酰胺酶的多重耐药临床细菌分离株

Extended spectrum â-lactamase producing multidrug resistant clinical bacterial isolates at National Public Health Laboratory, Nepal.

作者信息

Poudyal S, Bhatta D R, Shakya G, Upadhyaya B, Dumre S P, Buda G, Kandel B P

机构信息

Central Department of Microbiology, Tribhuvan University, Kirtipur, Nepal.

出版信息

Nepal Med Coll J. 2011 Mar;13(1):34-8.

Abstract

Extended Spectrum â-lactamase (ESBL) producing multidrug resistant bacteria complicate therapeutic management and limit treatment options. Therefore, detection of ESBL-producing multidrug resistant (MDR) pathogens has a paramount importance. Between April 2009 and January 2010, a prospective study was carried out in National Public Health Laboratory with an objective to determine the status of ESBL producing MDR bacterial isolates from different clinical samples. Identification of the isolates was done by standard microbiological techniques and antibiotic susceptibility testing was done by Kirby Bauer disc diffusion method following Clinical and Laboratory Standard Institute (CLSI) guidelines. ESBL screening among MDR isolates was done using Ceftriaxone, Aztreonam, Cefotaxime, Ceftazidime and Cefpodoxime followed by confirmation using MASTDISCS ID ES2L Detection Discs (CPD10). Data analysis was done by SPSS 16 software. Of the 314 bacterial isolates from 1601 different clinical specimens, 199 (63.4%) were MDR. Cefotaxime was found the reliable screening agent for ESBL detection with sensitivity and positive predictive value of 98.6% and 76.4% respectively. Sixtey nine (62.7%) isolates of the 110 tested MDR isolates were ESBL positive with at least one of the Combined Disk (CD) Assays. Escherichia coli (80%) was the major ESBL producer followed by Klebsiella pneumoniae (5.8%). A statistically significant relationship was found between increasing spectrum of drug resistance and ESBL production (p<0.05). Thus it is concluded that a higher rate of ESBL production prevail among MDR clinical bacterial isolates underscoring the need for routine ESBL detection in clinical laboratories.

摘要

产超广谱β-内酰胺酶(ESBL)的多重耐药菌使治疗管理复杂化并限制了治疗选择。因此,检测产ESBL的多重耐药(MDR)病原体至关重要。2009年4月至2010年1月期间,在国家公共卫生实验室进行了一项前瞻性研究,目的是确定来自不同临床样本的产ESBL的MDR细菌分离株的情况。通过标准微生物技术对分离株进行鉴定,并按照临床和实验室标准协会(CLSI)指南,采用 Kirby Bauer 纸片扩散法进行抗生素敏感性试验。对MDR分离株进行ESBL筛查时使用头孢曲松、氨曲南、头孢噻肟、头孢他啶和头孢泊肟,随后使用MASTDISCS ID ES2L检测纸片(CPD10)进行确认。使用SPSS 16软件进行数据分析。在来自1601份不同临床标本的314株细菌分离株中,199株(63.4%)为MDR。发现头孢噻肟是ESBL检测的可靠筛查试剂,其敏感性和阳性预测值分别为98.6%和76.4%。在110株检测的MDR分离株中,69株(62.7%)通过至少一种复合纸片(CD)试验检测为ESBL阳性。大肠埃希菌(80%)是主要的ESBL产生菌,其次是肺炎克雷伯菌(5.8%)。发现耐药谱增加与ESBL产生之间存在统计学显著关系(p<0.05)。因此得出结论,MDR临床细菌分离株中产ESBL的比例较高,这突出了临床实验室进行常规ESBL检测的必要性。

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