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Management of refractory Pseudomonas aeruginosa infection in cystic fibrosis

机译:囊性纤维化难治性铜绿假单胞菌感染的处理

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Abstract: Cystic fibrosis (CF) is the most common life-limiting inherited disease in Caucasian populations. The main cause of death in CF patients is respiratory failure resulting from chronic pulmonary infection. Pseudomonas aeruginosa is the most prevalent organism in the airway colonization of CF patients, and its persistence in the airways has been related to greater morbidity with a more rapid deterioration in lung function. P. aeruginosa has enormous genetic and metabolic flexibility that allows it to adapt and persist within the airways of CF patients, and it has the ability to easily acquire antimicrobial resistance. For these reasons, the management of infections and chronic colonization by P. aeruginosa remains a challenge for physicians. This article reviews the current and future antibacterial chemotherapy options for respiratory pseudomonal infection in CF patients.
机译:摘要:囊性纤维化(CF)是高加索人群中最常见的限制生命的遗传疾病。 CF患者的主要死亡原因是慢性肺部感染导致的呼吸衰竭。铜绿假单胞菌是CF患者气道定植中最常见的生物,其在气道中的持久性与发病率更高,肺功能恶化更快有关。铜绿假单胞菌具有巨大的遗传和代谢灵活性,使其能够适应CF患者的气道并在其中持久存在,并且具有轻松获得抗菌素耐药性的能力。由于这些原因,铜绿假单胞菌的感染和慢性定植的管理仍然是医师的挑战。本文回顾了当前和将来用于CF患者呼吸道假性肺炎的抗菌化学治疗方案。

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