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Paediatr Respir Rev. 2010 Sep;11(3):177-84. doi: 10.1016/j.prrv.2010.05.003. Epub 2010 Jun 16.
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本文引用的文献

1
Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: the ELITE trial.囊性纤维化患者早期铜绿假单胞菌感染的治疗:ELITE 试验。
Thorax. 2010 Apr;65(4):286-91. doi: 10.1136/thx.2009.121657. Epub 2009 Dec 8.
2
Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis.根除囊性纤维化患者体内铜绿假单胞菌的抗生素策略。
Cochrane Database Syst Rev. 2009 Oct 7(4):CD004197. doi: 10.1002/14651858.CD004197.pub3.
3
Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: A European consensus.囊性纤维化患者肺部疾病的吸入药物和吸入装置:欧洲共识
J Cyst Fibros. 2009 Sep;8(5):295-315. doi: 10.1016/j.jcf.2009.04.005. Epub 2009 Jun 25.
4
Early anti-pseudomonal acquisition in young patients with cystic fibrosis: rationale and design of the EPIC clinical trial and observational study'.早期抗假单胞菌在年轻囊性纤维化患者中的获得:EPIC 临床试验和观察研究的原理和设计'。
Contemp Clin Trials. 2009 May;30(3):256-68. doi: 10.1016/j.cct.2009.01.003. Epub 2009 Jan 15.
5
New aerosol delivery devices for cystic fibrosis.用于囊性纤维化的新型气溶胶输送装置。
Respir Care. 2009 Jun;54(6):754-67; discussion 767-8. doi: 10.4187/002013209790983250.
6
Eradication of early Pseudomonas infection in cystic fibrosis.根除囊性纤维化患者的早期铜绿假单胞菌感染
Chron Respir Dis. 2009;6(2):99-107. doi: 10.1177/1479972309104661.
7
Bugs, biofilms, and resistance in cystic fibrosis.囊性纤维化中的细菌、生物膜与耐药性
Respir Care. 2009 May;54(5):628-40. doi: 10.4187/aarc0492.
8
Relationship between antimicrobial proteins and airway inflammation and infection in cystic fibrosis.囊性纤维化中抗菌蛋白与气道炎症及感染之间的关系。
Pediatr Pulmonol. 2009 Apr;44(4):402-9. doi: 10.1002/ppul.21028.
9
Neutrophils in cystic fibrosis.囊性纤维化中的中性粒细胞。
Thorax. 2009 Jan;64(1):81-8. doi: 10.1136/thx.2007.082388.
10
Vaccines for preventing infection with Pseudomonas aeruginosa in cystic fibrosis.用于预防囊性纤维化患者感染铜绿假单胞菌的疫苗。
Cochrane Database Syst Rev. 2008 Oct 8(4):CD001399. doi: 10.1002/14651858.CD001399.pub2.

早期清除囊性纤维化患者中的铜绿假单胞菌。

Early eradication of Pseudomonas aeruginosa in patients with cystic fibrosis.

机构信息

Eudowood Division of Pediatric Respiratory Sciences, Johns Hopkins Medical Institutions, Baltimore, Maryland 21287-2533, USA.

出版信息

Paediatr Respir Rev. 2010 Sep;11(3):177-84. doi: 10.1016/j.prrv.2010.05.003. Epub 2010 Jun 16.

DOI:10.1016/j.prrv.2010.05.003
PMID:20692633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4001925/
Abstract

Pseudomonas aeruginosa (Pa) is the predominant organism infecting the airways of patients with cystic fibrosis (CF). This organism has an armamentarium of survival mechanisms that allows it to survive in the CF airway. Since colonization and chronic infection with Pa is associated with poorer lung function and increased morbidity and mortality, therapies that can prevent infection could significantly improve the lives of patients with CF. Numerous studies have examined the effects of treatment on the eradication of Pa as a means to ameliorate disease. This article outlines the pathophysiology and clinical implication of Pa acquisition, and reviews the existing treatment regimens aimed at early eradication of Pa in patients with CF.

摘要

铜绿假单胞菌(Pa)是引起囊性纤维化(CF)患者气道感染的主要病原体。该病原体具有一系列生存机制,使其能够在 CF 气道中存活。由于 Pa 的定植和慢性感染与肺功能下降、发病率和死亡率增加有关,因此能够预防感染的治疗方法可以显著改善 CF 患者的生活。许多研究已经研究了治疗对消除 Pa 的影响,以期改善疾病。本文概述了 Pa 获得的病理生理学和临床意义,并回顾了旨在早期消除 CF 患者 Pa 的现有治疗方案。