Efficacy of oral fluoroquinolones versus conventional intravenous antipseudomonal chemotherapy in treatment of cystic fibrosis

Author:

Jensen T.,Pedersen S. S.,HøSiby N.,Koch C.

Publisher

Springer Science and Business Media LLC

Subject

Microbiology (medical),Microbiology,Infectious Diseases,Microbiology (medical),General Medicine

Reference20 articles.

1. Pedersen, S. S., Jensen, T., Pressler, T., Rosendal, K.: Does centralized treatment of cystic fibrosis increase the risk ofPseudomonas aeruginosa infection? Acta Paediatrica Scandinavia 1986, 75: 840–845.

2. Høiby, N., Flensborg, E. W., Beck, B., Friis, B., Vidar-Jacobsen, S., Jacobsen, L.:Pseudomonas aeruginosa infection in cystic fibrosis. Diagnostic and prognostic significance ofPseudomonas aeruginosa precipitins determined by means of crossed immunoelectrophoresis. Scandinavian Journal of Respiratory Diseases 1977, 58: 65–79.

3. Høiby, N., Friis, B., Jensen, K., Koch, C., Møller, N. E., Støvring, S., Szaff, M.: Antimicrobial chemotherapy in cystic fibrosis patients. Acta Paediatrica Scandinavica 1982, 301, Supplement: 75–100.

4. Cherny, F. J., Cropp, G. J. A., Bye, M. R.: Hospital therapy improves exercise tolerance and lung function in cystic fibrosis. American Journal of Diseases of Children 1984, 133: 261–265.

5. Szaff, M., Høiby, N., Flensborg, E. W.: Frequent antibiotic therapy improves survival of cystic fibrosis patients with chronicPseudomonas aeruginosa infection. Acta Paediatrica Scandinavica 1983, 72: 651–657.

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