The Bronchodilator Test with Increasing Doses of Terbutaline in Chronic Obstructive Pulmonary Disease Patients

Visualitza/ Obre
Data de publicació
2001Autor/a
Rodríguez-Carballeira, M.
Heredia, J. L.
Quintana, Salvador
Gómez, S.
Citació recomanada
Rodríguez-Carballeira, M.;
Heredia, J. L.;
Rué i Monné, Montserrat;
Quintana, Salvador;
Gómez, S.;
.
(2001)
.
The Bronchodilator Test with Increasing Doses of Terbutaline in Chronic Obstructive Pulmonary Disease Patients.
Pulmonary Pharmacology and Therapeutics, 2001, vol. 14, núm. 1, p. 61-65.
https://doi.org/10.1006/pupt.2000.0272.
Metadades
Mostra el registre d'unitat completResum
There is no uniform consensus on the dose of bronchodilator to be used in the bronchodilator test
(BDT). The objective of the study was to determine the dose of inhaled terbutaline that can safely achieve a
greater number of positive BDT in patients with chronic obstructive pulmonary disease (COPD). The study was
prospective and single blinded. One-hundred and fifty patients with stable COPD were included. Their mean
(±SD) age was 67.4 (8.8) years. Their mean forced expiratory volume in the first second (FEV1) was 1.14 (0.48) l
(41% of the predicted value). A baseline spirometry was performed and a second 20 min after the inhalation of
placebo. Three consecutive doses of 500 g of inhaled terbutaline were administered and a new spirometry was
performed after each one. A multivariate analysis based on the comparison of the repeated means was performed
in order to analyse the spirometric changes achieved after the different doses of bronchodilator. The increase of
FEV1 and forced vital capacity (FVC) with the two first doses of terbutaline was statistically significant; the
increase of the peak expiratory flow (PEF) was significant after the three doses administered. The number of
positive BDT were 40, 47 and 60 after each dose of terbutaline (P=0.004). The higher dose of terbutaline was
more useful in identifying patients with significant bronchoreversibility and, moreover, was well tolerated. We
suggest that this dose (1500 g) should be routinely used in performing the BDT