Efficacy of aerosolized tobramycin in patients with cystic fibrosis
Article Abstract:
Aerosolized tobramycin may be an effective treatment for Pseudomonas aeruginosa infections in patients with cystic fibrosis. Pseudomonas aeruginosa infections are a major complication of cystic fibrosis. Sixty-six cystic fibrosis patients with documented Pseudomonas aeruginosa infections participated in a crossover study of aerosolized tobramycin. Approximately half inhaled the antibiotic through a nebulizer three times a day for 28 days, then switched to a placebo, or inactive substance. The others started on the placebo, then switched to tobramycin. Both groups experienced an improvement in lung function on tobramycin compared to placebo. In addition, the concentration of the bacterium in sputum samples dropped substantially during tobramycin treatment. Few patients experienced kidney damage or hearing loss. These are both side effects of aminoglycosides, the group of antibiotics to which tobramycin belongs.
Publication Name: The New England Journal of Medicine
Subject: Health
ISSN: 0028-4793
Year: 1993
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Management of pulmonary disease in patients with cystic fibrosis
Article Abstract:
Improvements in the treatment for cystic fibrosis have significantly prolonged lifespans. Cystic fibrosis is caused by a defect in the gene for a protein that transports chloride. The defect in chloride transport causes an overproduction of secretions that block the pancreas and cause lung infections. The primary treatment is replacing pancreatic enzymes and clearing abnormal lung secretions. In addition, many CF patients have to take antibiotics to prevent lung infections. These can often be administered using an inhaler. The defective gene has been sequenced, leading to the possibility of gene therapy for this disease.
Publication Name: The New England Journal of Medicine
Subject: Health
ISSN: 0028-4793
Year: 1996
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Intermittent administration of inhaled tobramycin in patients with cystic fibrosis
Article Abstract:
Inhaled tobramycin may improve lung function in cystic fibrosis patients. Researchers randomly assigned 520 cystic fibrosis patients to inhale tobramycin or a placebo twice a day for four weeks. The patients alternated between inhalations of placebo or tobramycin for 24 weeks total. Tobramycin improved lung function, reduced the rate of infection with Pseudomonas aeruginosa, and led to lower hospitalization rates. The drug caused few side effects. Intermittent treatment may prevent Pseudomonas aeruginosa from becoming resistant to the drug.
Publication Name: The New England Journal of Medicine
Subject: Health
ISSN: 0028-4793
Year: 1999
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