New and Emerging Therapies for Pulmonary Complications of Cystic Fibrosis

被引:0
作者
Mark R. Tonelli
Moira L. Aitken
机构
[1] University of Washington,Division of Pulmonary and Critical Care Medicine Department of Medicine
[2] UWMC,undefined
来源
Drugs | 2001年 / 61卷
关键词
Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Colistin; Early Clinical Trial; Pulmonary Exacerbation;
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摘要
In the decade since the gene for cystic fibrosis (CF) was discovered, research into potential therapeutic interventions has progressed on a number of different fronts. The vast majority of morbidity and mortality in CF results from inflammation and infection of the airways. Direct delivery of antibacterials to the airway secretions via a nebuliser is an attractive therapeutic option, and a novel formulation of tobramycin designed for such a purpose has been demonstrated to improve spirometry and decrease the need for intravenous antibacterials. In addition, early clinical trials are studying the effects of small peptides with antibiotic properties (defensins) delivered directly to the airways.
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页码:1379 / 1385
页数:6
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