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目前对抗多重耐药病原体引起的医院获得性肺炎的抗菌治疗的综述。

Current review of antimicrobial treatment of nosocomial pneumonia caused by multidrug-resistant pathogens.

出版信息

Expert Opin Pharmacother. 2011 Oct;12(14):2145-8. doi: 10.1517/14656566.2011.599320.

Abstract

Nosocomial pneumonia (including ventilator-associated pneumonia; VAP), a consistently difficult-to-treat entity, is frequently caused by multidrug-resistant (MDR) or pandrug-resistant (PDR) bacteria. Given the high mortality rates caused by drug-resistant bacteria and the difficulty of developing new potent antibiotics to target the problematic pathogens, combination regimens are under ardent evaluation as new strategies to overcome increasing drug resistance. Adjustment of the administration method of certain β-lactams (meropenem, or imipenem/cilastatin), or combination of tigecycline with some agents, may show promise with regard to successful management of MDR or PDR Acinetobacter baumannii pneumonia. Additionally, vancomycin plus rifampicin is an effective regimen against nosocomial pneumonia caused by methicillin-resistant Staphylococcus aureus (MRSA) responding poorly to vancomycin monotherapy. The clinical appropriateness of parenteral colistin against pneumonia caused by MDR A. baumannii has been established in a clinical trial. Facing the decline of clinical vancomycin efficacy after initial use, linezolid might be the drug of choice with regard to the treatment of MRSA-VAP. The role of tigecycline monotherapy for the management of nosocomial pneumonia caused by MRSA and extended-spectrum β-lactamase-producing Enterobacteriaceae needs to be cautiously evaluated.

摘要

医院获得性肺炎(包括呼吸机相关性肺炎;VAP)一直是一种难以治疗的疾病,通常由耐多药(MDR)或泛耐药(PDR)细菌引起。鉴于耐药菌引起的高死亡率以及开发新的强效抗生素来靶向这些有问题的病原体的困难,联合治疗方案作为克服日益增加的耐药性的新策略正在受到热烈评估。调整某些β-内酰胺类药物(美罗培南或亚胺培南/西司他丁)的给药方法,或联合替加环素与某些药物,可能在成功治疗 MDR 或 PDR 鲍曼不动杆菌肺炎方面显示出前景。此外,万古霉素加利福平是治疗对万古霉素单药治疗反应不佳的耐甲氧西林金黄色葡萄球菌(MRSA)引起的医院获得性肺炎的有效方案。一项临床试验已经证实了静脉用黏菌素治疗 MDR A. 鲍曼不动杆菌肺炎的临床适宜性。在初始使用后,临床万古霉素疗效下降,利奈唑胺可能是治疗 MRSA-VAP 的首选药物。替加环素单药治疗 MRSA 和产超广谱β-内酰胺酶肠杆菌科引起的医院获得性肺炎的作用需要谨慎评估。

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