主要革兰氏阴性菌株对选定抗菌药物的体外药敏模式

Shalini Gupta, P. Mandale
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Antibiotic sensitivity testing was done in accordance with the recommendations of Clinical Laboratory Standard Institute (CLSI) guidelines. \nResults: Of the total 1201 Gram negative isolates included in this study, 51.6% were from wounds and pus specimens, 40.1% were from respiratory and 8.2% from blood. P. aeruginosa (49.7%) was the most frequently isolated pathogen distantly followed by A. baumannii (21.6%), K. pneumoniae (16.6%) and E. coli (12.1%). The highest susceptibility was reported to polymyxins (100%) including Colistin and Polymyxin B, among all the tested bacteria’s and system wise. 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引用次数: 0

摘要

背景:医院选择正确的抗微生物治疗取决于对当地抗微生物药敏概况的了解。本回顾性研究旨在评估斋浦尔市多家医院不同病原菌对头孢吡肟-阿米卡辛-耐药破药剂(ARBs)*等多种抗生素的体外药敏模式。方法:对来自斋浦尔市各医院的不同分离株的抗生素谱资料进行回顾性观察分析,以表征其药敏模式。2017年1月至2017年12月收集的1201株革兰氏阴性分离株纳入研究。抗生素敏感性试验按照临床实验室标准协会(CLSI)指南的建议进行。结果:1201株革兰氏阴性分离株中,51.6%来自伤口和脓液,40.1%来自呼吸道,8.2%来自血液。铜绿假单胞菌(49.7%)是最常见的病原菌,其次是鲍曼不动杆菌(21.6%)、肺炎克雷伯菌(16.6%)和大肠杆菌(12.1%)。据报道,在所有被测细菌和系统中,对粘菌素和多粘菌素B等多粘菌素的敏感性最高(100%)。在所有检测的抗生素中,头孢吡肟-阿米卡辛- arbs *对皮肤、软组织、呼吸道、血液样本中病原菌(大肠杆菌、肺炎克雷伯菌、铜绿假单胞菌)的敏感性为87.9% ~ 52%,其次是美罗培南对病原菌(大肠杆菌、肺炎克雷伯菌、铜绿假单胞菌)的敏感性为78.4% ~ 55%,其次是头孢他啶-他唑巴坦对病原菌(大肠杆菌、肺炎克雷伯菌、铜绿假单胞菌)的敏感性为82.7% ~ 58%,鲍曼假单胞菌对头孢哌酮舒巴坦的敏感性为22.7%。根据病原菌类型,大肠杆菌总体敏感性最高,鲍曼不动杆菌总体敏感性最低。鲍曼不动杆菌对除多粘菌素为100%外的所有抗生素的敏感性为1 ~ 26%。结论:体外敏感性数据表明,头孢吡肟-阿米卡辛- arbs *可作为治疗各种耐药革兰氏阴性菌感染的重要治疗选择,以减轻对最后手段抗生素的过度压力。根据药敏数据,头孢吡肟-阿米卡辛- arbs *可视为碳青霉烯类药物治疗革兰氏阴性细菌感染的有效治疗选择,可视为碳青霉烯类、粘菌素、多粘菌素B等广谱抗生素的选择。
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In vitro Susceptibility Pattern of Major Gram Negative Isolates to Selected Antimicrobial Agents
Background: The choice of choosing right anti-microbial therapy in hospitals depends on the knowledge of local anti-microbial susceptibility profile. This retrospective study was conducted to assess the in vitro susceptibility pattern of different pathogen isolates to various antibiotics including Cefepime-Amikacin-Antibiotic resistant breakers (ARBs)* in various hospitals across the Jaipur City. Methods: To characterize the antimicrobial susceptibility pattern of different isolates from various hospitals across the Jaipur City, a retrospective, observational analysis was done for antibiogram data. A total of 1201 Gram negative isolates collected during the period from January 2017 to December 2017 were included in the study. Antibiotic sensitivity testing was done in accordance with the recommendations of Clinical Laboratory Standard Institute (CLSI) guidelines. Results: Of the total 1201 Gram negative isolates included in this study, 51.6% were from wounds and pus specimens, 40.1% were from respiratory and 8.2% from blood. P. aeruginosa (49.7%) was the most frequently isolated pathogen distantly followed by A. baumannii (21.6%), K. pneumoniae (16.6%) and E. coli (12.1%). The highest susceptibility was reported to polymyxins (100%) including Colistin and Polymyxin B, among all the tested bacteria’s and system wise. Among all the antibiotic tested, (Cefepime-Amikacin-ARBs*) sensitivity ranged for 87.9% to 52% on pathogens (E. coli, K. pneumonia, P. aeruginosa) tested from samples of skin and soft tissue, respiratory tract, blood stream, followed by Meropenem ranged for 78.4% to 55% on pathogens (E. coli, K. pneumonia, P. aeruginosa), followed by ceftazidime-tazobactam ranged for 82.7% to 58% on pathogens (E. coli, K. pneumonia, P. aeruginosa) and 22.7% sensitive for A. baumannii to Cefoperazone sulbactam. Based on pathogen type, E. coli exhibited highest overall susceptibility and the lowest was reported by A. baumannii. The susceptibility of A. baumannii ranged from 1-26% to all the tested antibiotics except polymyxins with 100% susceptibility. Conclusions: This in vitro susceptibility data suggests that Cefepime-Amikacin-ARBs* can serve as important therapeutic option for the treatment of various resistant Gram-negative bacterial infections to relieve the excess pressure on last resort antibiotics, carbapenems and other drugs including Colistin and polymyxin B. Cefepime-Amikacin-ARBs*on the basis of antimicrobial susceptibility data can be considered as an effective therapeutic option for carbapenems in treating gram negative bacterial infections, and could be considered as a broad spectrum antibiotic sparer’s like carbapenem, colistin and Polymyxin B.
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