Four-week nebulized beclomethasone dipropionate in stable COPD patients with exertional dyspnoea

Monaldi Arch Chest Dis. 1999 Jun;54(3):224-7.

Abstract

Twenty male outpatients with severe-but-stable chronic obstructive pulmonary disease handicapped by exertional dyspnoea (aged 69.7 +/- 5.68 yrs; forced expiratory volume in one second (FEV1) 1.02 +/- 0.18 L or 34.6 +/- 6.5% of the predicted value; forced vital capacity (FVC) 2.51 +/- 0.34 L; arterial oxygen tension (Pa,O2) 9.11 +/- 0.32 kPa (68.5 +/- 2.4 mmHg); arterial carbon dioxide tension (Pa,CO2) 5.20 +/- 0.23 kPa (39.1 +/- 1.7 mmHg)) completed a randomized double-blind crossover study to evaluate the effects of a 4-week regular treatment with inhaled beclomethasone dipropionate via nebulizers at a dosage of 2 mg twice daily. After active and placebo treatment, no peak expiratory flow rate variation in FEV1, FVC, rescue use of beta 2-agonists, exercise tolerance and dyspnoea was observed. In conclusion, a regular short-term treatment with nebulized beclomethasone dipropionate does not give any improvement in lung function or exercise capacity in severe-but-stable chronic obstructive pulmonary disease patients handicapped by exertional dyspnoea.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Administration, Inhalation
  • Aerosols
  • Aged
  • Beclomethasone / administration & dosage
  • Beclomethasone / therapeutic use*
  • Cross-Over Studies
  • Double-Blind Method
  • Dyspnea / drug therapy*
  • Dyspnea / etiology
  • Dyspnea / physiopathology
  • Glucocorticoids / administration & dosage
  • Glucocorticoids / therapeutic use*
  • Humans
  • Lung Diseases, Obstructive / complications*
  • Lung Diseases, Obstructive / physiopathology
  • Male
  • Physical Exertion
  • Respiratory Function Tests
  • Statistics, Nonparametric
  • Treatment Outcome

Substances

  • Aerosols
  • Glucocorticoids
  • Beclomethasone