CFDB - Cystic Fibrosis DataBase

primary studies published RCT

The effect of ipratropium bromide on lung function in patients with cystic fibrosis.

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

Randomised, single-blind, placebo-controlled cross over

Participants

11 participants (8 males), age range 8 - 29 years, mean (SEM) age 18.1 (2.0) years. Normal nutritional status. Schwachman score ranged from 53 to 97. Other medication discontinued before study commenced

Interventions

2 ml placebo (0.9 % hypertonic saline solution) or 2 ml ipratropium bromide solution (Atrovent® = 250 μg in 1 ml hypertonic saline solution) on different days in the space of 2 weeks

Outcome measures

Lung function (FEV1, FEF25-75%, RV, TLC) measured before, then 30, 60 and 120 min after inhalation

Main results

The mean figures for the changes in FEV1.0, FEF25-75%, RV and TLC after inhalation of IB and placebo did not differ significantly. However, FEV1.0 and FEF25-75% after administration of IB increased in 4 out of 11 patients, and decreased in one. The lung volumes changed significantly in only a single case.

Authors' conclusions

This variable effect of inhaled IB in CF patients is in agreement with findings that have been observed for other substances with a "bronchodilatory" effect in patients with CF.

Keywords: Adolescent; Adult; Anticholinergic Agents; Atropine; Biomarker; Bronchodilator Agents; Child; Inhalation OR nebulised; Ipratropium; non pharmacological intervention - diagn; pharmacological_intervention; Respiratory System Agents;