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利奈唑胺对在美国分离出的关键革兰氏阳性菌的体外活性:2004年LEADER监测项目的结果

In vitro activity of linezolid against key gram-positive organisms isolated in the united states: results of the LEADER 2004 surveillance program.

作者信息

Draghi Deborah C, Sheehan Daniel J, Hogan Patricia, Sahm Daniel F

机构信息

Focus Bio-Inova, Inc., 13665 Dulles Technology Drive, Suite 200, Herndon, Virginia 20171-4603, USA.

出版信息

Antimicrob Agents Chemother. 2005 Dec;49(12):5024-32. doi: 10.1128/AAC.49.12.5024-5032.2005.

Abstract

Since the approval of linezolid in 2000, sporadic reports of resistance have been given and a greater understanding of the underlying mechanisms of resistance has been gained. However, since these developments, an updated status of the in vitro activity of linezolid against gram-positive organisms from the United States has not been reported. The LEADER 2004 surveillance initiative was undertaken to obtain current and representative data on the activity of linezolid against key species, including isolates with significant resistance phenotypes. Organisms were isolated during 2004 and included 2,872 Staphylococcus aureus, 496 coagulase-negative staphylococcus (CNS), 428 Enterococcus faecalis, 196 Enterococcus faecium, and 422 Streptococcus pneumoniae isolates. All S. aureus isolates (54.2% oxacillin resistant) were susceptible to linezolid (MIC90 = 2 microg/ml); MIC distributions were consistent, regardless of oxacillin or multidrug resistance status. For CNS, one nonsusceptible isolate was encountered (Staphylococcus epidermidis; MIC = 32 microg/ml), but overall, the MIC(90) (1 microg/ml) was lower than that obtained with S. aureus. For E. faecalis and E. faecium, 99.5% and 96.4% of isolates, respectively, were linezolid susceptible. Both species had an MIC90 of 2 microg/ml, and MIC distributions did not vary with the vancomycin susceptibility status of the populations analyzed. Linezolid nonsusceptibility was not encountered among the S. pneumoniae isolates. These findings indicate that linezolid nonsusceptibility has remained rare among staphylococci and uncommon and sporadic among enterococci. Nonetheless, careful and ongoing monitoring of the in vitro effectiveness of linezolid will be needed so that any changes to the current status may be detected as soon as possible.

摘要

自2000年利奈唑胺获批以来,已有关于耐药性的零星报道,并且对耐药性的潜在机制有了更深入的了解。然而,自这些进展以来,尚未有关于利奈唑胺在美国针对革兰氏阳性菌的体外活性的最新情况报道。开展了2004年LEADER监测计划,以获取关于利奈唑胺针对关键菌种活性的当前代表性数据,包括具有显著耐药表型的分离株。在2004年分离出的菌株包括2872株金黄色葡萄球菌、496株凝固酶阴性葡萄球菌(CNS)、428株粪肠球菌、196株屎肠球菌和422株肺炎链球菌分离株。所有金黄色葡萄球菌分离株(54.2%对苯唑西林耐药)对利奈唑胺敏感(MIC90 = 2微克/毫升);无论苯唑西林或多药耐药状态如何,MIC分布都是一致的。对于CNS,遇到1株不敏感分离株(表皮葡萄球菌;MIC = 32微克/毫升),但总体而言,MIC(90)(1微克/毫升)低于金黄色葡萄球菌。对于粪肠球菌和屎肠球菌,分别有99.5%和96.4%的分离株对利奈唑胺敏感。两种菌种的MIC90均为2微克/毫升,且MIC分布不因所分析群体的万古霉素敏感性状态而有所不同。在肺炎链球菌分离株中未发现对利奈唑胺不敏感的情况。这些发现表明,葡萄球菌中对利奈唑胺不敏感的情况仍然很少见,而肠球菌中则不常见且呈散发性。尽管如此,仍需要对利奈唑胺的体外有效性进行仔细且持续的监测,以便能尽快检测到当前状况的任何变化。

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