CFDB - Cystic Fibrosis DataBase

primary studies published RCT

Comparison of 6 and 8 hourly tobramycin dosing intervals in treatment of pulmonary exacerbations in cystic fibrosis patients.

Study design (if review, criteria of inclusion for studies)

randomized trial

Participants

CF patients ages 13 to 30 years received 34 treatment courses

Interventions

tobramycin administered either every 6 or 8 hours. Peak serum concentrations were adjusted to 8 to 10 micrograms/ml; thus a larger total daily dosage was administered to patients receiving tobramycin every 6 hours.

Outcome measures

pulmonary function, time to next hospital admission for a pulmonary exacerbation, clinical score, sputum carriage of P. aeruginosa, toxicity or necessary length of hospitalization.

Main results

The shorter dosing interval was associated with better pulmonary function at follow-up and significantly longer time before next hospital admission for a pulmonary exacerbation. During the study hospitalization there were no differences in pulmonary function tests, clinical score, sputum carriage of P. aeruginosa, toxicity or necessary length of hospitalization.

Authors' conclusions

A 6-hour tobramycin dosing interval was more efficacious than an 8-hour dosing interval in the treatment of cystic fibrosis patients.

Keywords: Adolescent; Adult; Anti-Bacterial Agents; Bacterial Infections; Drug Administration Schedule; Infection; pharmacological_intervention; Pneumonia; Pseudomonas aeruginosa; Pseudomonas; Respiratory Tract Diseases; Respiratory Tract Infections; Tobramycin; Exacerbation; Aminoglycosides;