CFDB - Cystic Fibrosis DataBase

primary studies published RCT

The effect of high doses of inhaled salbutamol and ipratropium bromide in patients with stable cystic fibrosis.

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

Dual intervention cross-over trial over 2 days

Participants

Only those with previous positive response to salbutamol SK score 35 - 90 9 participants (4 males), age range 6 - 22 years

Interventions

Sequence A: salbutamol 200 mcg, salbutamol 400 mcg and ipratropium 80 mcg by MDI and aerochamber separated by 45 minutes; or Sequence B: ipratropium 80 mcg, salbutamol 200 mcg, salbutamol 400 mcg Randomised to:

Outcome measures

Only 4 hour data used Changes in spirometry (FVC, FEV1, FEF25-75, FEF50, PEFR, FRC, RV, Raw ) measured at baseline, before each drug in the sequence and at 4 hours and 8 hours from baseline

Main results

The FEV1 and Raw improved from baseline after each inhalation, and at 4 and 8 h during both days (p < 0.05). Forty-five minutes after S 200 micrograms, plus S 400 micrograms, FEV1, FRC, and Raw were not significantly different compared with the values 45 min after IB 80 micrograms, plus S 200 micrograms (1.67 +/- 0.1 vs 1.63 +/- 0.1 L; 2.81 +/- 0.6 vs 2.65 +/- 0.5 L; and 2.98 +/- 0.2 vs 2.66 +/- 0.1 cm H2O/L/s, respectively). The PFTs were not significantly different after maximal doses of IB (80 micrograms) compared with S (600 micrograms). The HR and SaO2 were not significantly different from baseline throughout the study period.

Authors' conclusions

These results indicate that both single and sequential therapy have a similar acute bronchodilator effect provided that large doses are used. We speculate that adrenergic and muscarinic pathways are equally important in airflow obstruction in patients with CF.

Related topics

Keywords: Adolescent; Adult; Albuterol; Biomarker; Bronchodilator Agents; Child; Combined Modality Therapy; Inhalation OR nebulised; Ipratropium; non pharmacological intervention - diagn; pharmacological_intervention; Salbutamol; High-Dose; Adrenergic beta-Agonists; Respiratory System Agents; Anticholinergic Agents;