Tantisiriwat Woraphot, Linasmita Patcharasarn
J Med Assoc Thai. 2017 Apr;100(4):469-78.
Sitafloxacin is a newly approved oral fluoroquinolone in Thailand for treatment of respiratory tract and urinary tract infections. Initial in vitro susceptibility testing showed its effect on Escherichia coli with extended-spectrum betalactamases (ESBL), Klebsiella pneumoniae with ESBL, Pseudomonas aeruginosa, and carbapenem resistant Acinetobacter baumannii
To retrospectively review in vitro susceptibility to sitafloxacin on clinical isolates from HRH Princess Maha Chakri Sirindhorn Medical Center, Srinakharinwirot University (SWU) and Samitivej Sukhumvit Hospital (SVH).
Between January 2014 and June 2015, all clinical isolates from SWU and SVH that were added to test in vitro susceptibility to sitafloxacin were included in the present study. The susceptibility for sitafloxacin was identified by disk diffusion method with inhibition zone diameter 19 mm or greater, considered to be sensitive, and smaller than 16 mm considered to be resistance. The comparative activities of sitafloxacin to other antibiotics were determined by organisms. All bacteria with count numbers of more than 30 would be shown in results.
Among 1,288 clinical isolates from 1,163 clinical specimens that were added in vitro susceptibility test to sitafloxacin, there were 728 clinical isolates from SWU and 560 clinical isolates from SVH. The most common specimens were sputum (482), urine (385), pus (96), and blood (81). Organisms with comparative activities included E. coli, K. pneumoniae, P. aeruginosa, A. baumannii, and Stenotrophomonas maltophilia. The susceptible percentage of sitafloxacin was 72.69% for all E. coli (n = 216) (68.26% for E. coli with ESBL and 86.96% for E. coli without ESBL), 39.31% for all K. pneumoniae (n = 173) (50% for K. pneumoniae with ESBL, 61.11% for K. pneumoniae without ESBL and 13.11% for carbapenem resistant enterobacteriaceae (CRE) strain of K. pneumoniae), 60.66% for P. aeruginosa (n = 366), 66.32% for A. baumannii (n = 386) and 93.94% for S. maltophilia (n = 33). Sitafloxacin had more susceptible percentage as compared to ciprofloxacin for all strains of E. coli, K. pneumoniae, P. aeruginosa, and A. baumannii and more susceptible percentage as compared to levofloxacin for S. maltophilia. Although sitafloxacin might not have good activity against CRE strain of K. pneumoniae, at least some (13.11%) were susceptible as compared to 0% for ciprofloxacin.
Sitafloxacin had more susceptible percentage to E. coli, K. pneumoniae, P. aeruginosa, A. baumannii, and S. maltophilia compared to comparative fluoroquinolones. It should be considered an antibiotic for treatment of respiratory tract and urinary tract infections caused by the resistant strains of these bacteria with susceptible proven of in vitro susceptibility.
西他沙星是泰国新批准的一种口服氟喹诺酮类药物,用于治疗呼吸道和泌尿道感染。初步体外药敏试验显示其对产超广谱β-内酰胺酶(ESBL)的大肠埃希菌、产ESBL的肺炎克雷伯菌、铜绿假单胞菌以及耐碳青霉烯类鲍曼不动杆菌有效。
回顾性分析泰国诗琳通公主医疗中心、泰国先皇技术学院(SWU)和三美泰素坤逸医院(SVH)临床分离株对西他沙星的体外药敏情况。
2014年1月至2015年6月期间,SWU和SVH所有用于检测西他沙星体外药敏的临床分离株纳入本研究。采用纸片扩散法鉴定西他沙星药敏情况,抑菌圈直径大于等于19mm为敏感,小于16mm为耐药。根据菌株测定西他沙星与其他抗生素的对比活性。所有菌数超过30的细菌将在结果中显示。
在1163份临床标本的1288株临床分离株中进行了西他沙星体外药敏试验,其中728株来自SWU,560株来自SVH。最常见的标本是痰液(482份)、尿液(385份)、脓液(96份)和血液(81份)。具有对比活性的菌株包括大肠埃希菌、肺炎克雷伯菌、铜绿假单胞菌、鲍曼不动杆菌和嗜麦芽窄食单胞菌。所有大肠埃希菌(n = 216)中西他沙星的敏感率为72.69%(产ESBL的大肠埃希菌为68.26%,非产ESBL的大肠埃希菌为86.96%),所有肺炎克雷伯菌(n = 173)为39.31%(产ESBL的肺炎克雷伯菌为50%,非产ESBL的肺炎克雷伯菌为61.11%,产碳青霉烯类耐药肠杆菌科(CRE)的肺炎克雷伯菌为13.11%),铜绿假单胞菌(n = 366)为60.66%,鲍曼不动杆菌(n = 386)为66.32%,嗜麦芽窄食单胞菌(n = 33)为93.94%。对于所有大肠埃希菌、肺炎克雷伯菌、铜绿假单胞菌和鲍曼不动杆菌菌株,西他沙星的敏感率高于环丙沙星;对于嗜麦芽窄食单胞菌,西他沙星的敏感率高于左氧氟沙星。虽然西他沙星对产CRE的肺炎克雷伯菌活性可能不佳,但至少有部分菌株(13.11%)敏感,而环丙沙星的敏感率为0%。
与对照氟喹诺酮类药物相比,西他沙星对大肠埃希菌、肺炎克雷伯菌、铜绿假单胞菌、鲍曼不动杆菌和嗜麦芽窄食单胞菌的敏感率更高。对于由这些细菌的耐药菌株引起的呼吸道和泌尿道感染,若体外药敏证实敏感,西他沙星应被视为一种治疗用抗生素。