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阿根廷关于哌拉西林-他唑巴坦对从住院患者中分离出的特定细菌菌株的体外比较活性的多中心合作研究。

Argentinean collaborative multicenter study on the in vitro comparative activity of piperacillin-tazobactam against selected bacterial isolates recovered from hospitalized patients.

作者信息

Casellas José María, Tomé Gabriella, Bantar Carlos, Bertolini Pamela, Blázquez Néstor, Borda Noemí, Couto Elsa, Cudmani Norma, Guerrera Josefina, Juárez María Josefina, López Teresa, Littvik Ana, Méndez Emilce, Notario Rodolfo, Ponce Graciela, Quinteros Mirta, Salamone Francisco, Sparo Mónica, Sutich Emma, Vaylet Susana, Wolff Lidia

机构信息

Centro de Estudios en Antimicrobianos (CEA), Buenos Aires City (Reference Center), Buenos Aires, Argentina.

出版信息

Diagn Microbiol Infect Dis. 2003 Nov;47(3):527-37. doi: 10.1016/s0732-8893(03)00131-7.

Abstract

The in vitro activity of piperacillin-tazobactam and several antibacterial drugs commonly used in Argentinean hospitals for the treatment of severe infections was determined against selected but consecutively isolated strains from clinical specimens recovered from hospitalized patients at 17 different hospitals from 9 Argentinean cities from different geographic areas during the period November 2001-March 2002. Out of 418 Enterobacteriaceae included in the Study 84% were susceptible to piperacillin-tazobactam. ESBLs putative producers were isolated at an extremely high rate since among those isolates obtained from patients with hospital acquired infections 56% of Klebsiella pneumoniae, 32% of Proteus mirabilis and 25% Escherichia coli were phenotypically considered as ESBLs producers Notably P.mirabilis is not considered by for screening for ESBL producers. ESBLs producers were 100% susceptible to imipenem and 70% were susceptible to piperacillin-tazobactam whereas more than 50% were resistant to levofloxacin. The isolates considered as amp C beta lactamase putative producers showed 99% susceptibility to carbapenems while 26.7% were resistant to piperacillin-tazobactam and 38.4% to levofloxacin. Noteworthy only 4% of the Enterobacteriaceae isolates were resistant to amikacin. Piperacillin-tazobactam was the most active agent against Pseudomonas aeruginosa isolates (MIC(90): 128 microg/ml; 78% susceptibility) but showed poor activity against Acinetobacter spp (MIC(90):>256 microg/ml; 21.7% susceptibility). Only 41.7% Acinetobacter spp isolates were susceptible to ampicillin-sulbactam. Piperacillin-tazobactam inhibited 100% of Haemophilus influenzae isolates (MIC(90) < 0.25 microg/ml) but only 16.6% of them were ampicillin resistant. The activity of piperacillin-tazobactam against oxacillin susceptible Staphylococcus aureus or coagulase negative staphylococci was excellent (MIC(90) 2 microg/ml; 100% susceptibility). Out of 150 enterococci 12 isolates (8%) were identified as E.faecium and only three isolates (2%), 2 E.faecium and 1 E.faecalis were vancomycin resistant. All the enterococci isolates were susceptible to linezolid. Piperacillin-tazobactam showed excellent activity (MIC(90) 2 microg/ml; 92% susceptibility). Regarding pneumococci all the isolates showed MICs of 16 microg/ml for piperacillin-tazobactam. Among 34 viridans group streptococci only 67% were penicillin susceptible and 85.2% ceftriaxone susceptible whereas piperacillin-tazobactam was very active (MIC(90) 4 microg/ml).Piperacillin-tazobactam is therefore a very interesting antibacterial drug to be used, preferably in combination (IE: amikacin-vancomycin) for the empiric treatment of severe infections occurring in hospitalized patients in Argentina. Caution must be taken for infections due to ESBL producers considering that the inoculum effect MICs can affect MIC values.

摘要

测定了哌拉西林 - 他唑巴坦及几种阿根廷医院常用于治疗严重感染的抗菌药物对2001年11月至2002年3月期间从阿根廷9个不同城市17家不同医院住院患者临床标本中选取但连续分离的菌株的体外活性。在该研究纳入的418株肠杆菌科细菌中,84% 对哌拉西林 - 他唑巴坦敏感。超广谱β - 内酰胺酶(ESBLs)推定产生菌的分离率极高,因为在医院获得性感染患者分离出的菌株中,56% 的肺炎克雷伯菌、32% 的奇异变形杆菌和25% 的大肠埃希菌在表型上被认为是ESBLs产生菌。值得注意的是,奇异变形杆菌通常不被纳入ESBLs产生菌的筛查范围。ESBLs产生菌对亚胺培南100% 敏感,对哌拉西林 - 他唑巴坦70% 敏感,而对左氧氟沙星超过50% 耐药。被认为是AmpCβ - 内酰胺酶推定产生菌的分离株对碳青霉烯类99% 敏感,而对哌拉西林 - 他唑巴坦26.7% 耐药,对左氧氟沙星38.4% 耐药。值得注意的是,仅4% 的肠杆菌科分离株对阿米卡星耐药。哌拉西林 - 他唑巴坦是对铜绿假单胞菌分离株活性最强的药物(MIC90:128μg/ml;敏感性78%),但对不动杆菌属活性较差(MIC90:>256μg/ml;敏感性21.7%)。仅41.7% 的不动杆菌属分离株对氨苄西林 - 舒巴坦敏感。哌拉西林 - 他唑巴坦抑制100% 的流感嗜血杆菌分离株(MIC90 < 0.25μg/ml),但其中仅16.6% 对氨苄西林耐药。哌拉西林 - 他唑巴坦对苯唑西林敏感的金黄色葡萄球菌或凝固酶阴性葡萄球菌活性极佳(MIC90 2μg/ml;敏感性100%)。在150株肠球菌中,12株(8%)被鉴定为粪肠球菌,仅3株(2%),即2株粪肠球菌和1株屎肠球菌对万古霉素耐药。所有肠球菌分离株对利奈唑胺敏感。哌拉西林 - 他唑巴坦显示出极佳活性(MIC90 2μg/ml;敏感性92%)。对于肺炎球菌,所有分离株对哌拉西林 - 他唑巴坦的MIC均为16μg/ml。在34株草绿色链球菌中,仅67% 对青霉素敏感,85.2% 对头孢曲松敏感,而哌拉西林 - 他唑巴坦活性很强(MIC90 4μg/ml)。因此,哌拉西林 - 他唑巴坦是一种非常值得使用的抗菌药物,最好联合使用(如:阿米卡星 - 万古霉素)用于阿根廷住院患者严重感染的经验性治疗。对于由ESBLs产生菌引起的感染必须谨慎,因为接种物效应MICs可能会影响MIC值。

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