CFDB - Cystic Fibrosis DataBase

primary studies published RCT

Intravenous administration of antibiotics at home in patients with cystic fibrosis improves quality of life.

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

Randomised 4-way cross-over design

Participants

n = 12 Males = 5 Females = 7. Mean age 29.9 years, range 16 years to 46 years (SD 9.4 years)

Interventions

Mannitol 300 mg (encapsulated dry powder) Pre-treated with terbutaline 1000 mcg (turbulhaler) HS 6% 7 ml IS (0.9%)+ matched voluntary cough Empty capsules with matched voluntary coughs All given as a single dose

Outcome measures

Sputum isotope % clearance at 30 minutes Sputum isotope clearance at 90 minutes* Mucociliary clearance*

Main results

Eight patients did not complete the study for diverse reasons. Fifteen of 17 patients taking placebo had decreased respiratory function status by the end of the study while 9 of 16 patients under piroxicam treatment retained their baseline values or improved their respiratory status. Piroxicam- treated patients required less hospitalization (192 d) than those receiving placebo (301 d).

Authors' conclusions

A long-term, large scale study would now be required to confirm the results of this preliminary investigation and to establish the significance of anti-inflammatory treatment with cyclooxgenase inhibitors to prevent lung tissue damage in patients with chronic obstructive pulmonary disease and Gram-negative pulmonary infection.

Keywords: Adolescent; Adult; Anti-Inflammatory Agents; Bacterial Infections; Child; Infection; pharmacological_intervention; Piroxicam; Pneumonia; Pseudomonas aeruginosa; Pseudomonas; Respiratory Tract Infections; Capsules; Powders; Mannitol; Airway clearance drugs -expectorants- mucolytic- mucociliary-; Respiratory System Agents; Anti-Inflammatory Agents - excl Steroids; Respiratory Tract Diseases;