Potentially multidrug-resistant non-fermentative Gram-negative pathogens causing nosocomial pneumonia

嗜麦芽窄食单胞菌 鲍曼不动杆菌 粘菌素 铜绿假单胞菌 医学 头孢吡肟 舒巴坦钠 肺炎 呼吸机相关性肺炎 抗菌剂 多重耐药 哌拉西林 微生物学 抗生素耐药性 头孢他啶 重症监护医学 抗生素 重症监护室 亚胺培南 生物 内科学 细菌 遗传学
作者
Antonella Ferrara
出处
期刊:International Journal of Antimicrobial Agents [Elsevier BV]
卷期号:27 (3): 183-195 被引量:57
标识
DOI:10.1016/j.ijantimicag.2005.11.005
摘要

Owing to its high morbidity and mortality, nosocomial pneumonia represents a particularly serious illness and one of the most frequent complications in ventilated patients admitted to the Intensive Care Unit. Gram-negative microorganisms, such as Pseudomonas aeruginosa, Acinetobacter baumannii and Stenotrophomonas maltophilia, are the most relevant pathogens responsible for particularly difficult-to-treat nosocomial pneumonia. The intrinsic resistance of these bacteria to many antimicrobial agents and, in addition, the variety of their increasingly recognised acquired resistance mechanisms make their management in the hospital setting problematic. Antimicrobials that retain the best activity against P. aeruginosa include carbapenems, piperacillin, cefepime, ceftazidime, ciprofloxacin and certain aminoglycosides, whilst carbapenems and sulphamethoxazole/trimethoprim remain the most active agents against A. baumannii and S. maltophilia, respectively. However, the growing emergence among these microorganisms of multidrug-resistant (MDR) isolates and the severity of associated infections call for potential alternative drugs. Sulbactam alone or in combination with ampicillin may represent an acceptable option for MDR A. baumannii as well as colistin, which also covers MDR P. aeruginosa. Newer fluoroquinolones and some tetracyclines may be alternative drugs both for MDR S. maltophilia and A. baumannii. However, large-scale controlled clinical trials are needed to confirm these promising therapeutic options.

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