Quest Diagnostics, Chantilly, Virginia, USA.
Ann N Y Acad Sci. 2013 Jan;1277:1-7. doi: 10.1111/nyas.12022.
Cell envelope-active agents, particularly β-lactams, play a pivotal role in the treatment of bacterial infections and the extent to which their activity is affected by the emergence of multidrug-resistant organisms is of concern. We analyzed the Surveillance Network (TSN) database to evaluate resistant trends for key cell envelope-active drugs among ESKAPE pathogens. Analysis demonstrated that the activity of these drugs has been notably influenced by the emergence of multidrug resistance; this was especially evident for the β-lactam drugs. For example, Acinetobacter baumannii resistance to imipenem increased from 23.9% to 34.3%, and resistance to piperacillin-tazobactam increased from 37.0% to 49.7% between 2007 and 2011. During the same time period Klebsiella pneumoniae resistance to imipenem increased from 0.8% to 3.8%. As β-lactams are a cornerstone of anti-infective therapy, it is important to closely monitor the activity of the agents being used today and to aggressively pursue new strategies that can augment current drugs and thwart ever-emerging β-lactam resistance mechanisms that are continuously encountered.
细胞包膜活性药物,特别是β-内酰胺类药物,在治疗细菌感染中起着关键作用,其活性受多药耐药菌出现的影响程度令人关注。我们分析了监测网络(TSN)数据库,以评估 ESKAPE 病原体中关键细胞包膜活性药物的耐药趋势。分析表明,这些药物的活性明显受到多药耐药性的影响;β-内酰胺类药物尤其明显。例如,鲍曼不动杆菌对亚胺培南的耐药性从 2007 年至 2011 年从 23.9%增加到 34.3%,对哌拉西林-他唑巴坦的耐药性从 37.0%增加到 49.7%。在此期间,肺炎克雷伯菌对亚胺培南的耐药性从 0.8%增加到 3.8%。由于β-内酰胺类药物是抗感染治疗的基石,因此密切监测目前使用的药物的活性并积极寻求新的策略来增强现有药物并阻止不断出现的β-内酰胺类耐药机制非常重要。