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Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis
BACKGROUND: Cystic fibrosis is an inherited condition resulting in thickened, sticky respiratory secretions. Respiratory failure, due to recurrent pulmonary infection and inflammation, is the most common cause of mortality. Muco‐active therapies (e.g. dornase alfa and nebulized hypertonic saline) ma...
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| Vydáno v: | Cochrane Database Syst Rev |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley & Sons, Ltd
2013
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8078644/ https://ncbi.nlm.nih.gov/pubmed/23852992 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD007168.pub3 |
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