D. Giannini et al., The protective effect of salbutamol inhaled using different devices on methacholine bronchoconstriction, CHEST, 117(5), 2000, pp. 1319-1323
Citations number
25
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Study objective: To determine the protective effect of salbutamol, 100 mu g
, inhaled by different devices (pressurized Inetered-dose inhaler [pMDI; Ve
ntolin; GlaxoWellcome; Greenford, UK], pMDI + spacer [Volumatic; GlaxoWellc
ome], or breath-activated PMDI [Autohaler; 3M Pharmaceuticals; St. Paul, MN
]) on bronchoconstriction induced by methacholine.
Design: Randomized, double-blind, cross-over, placebo-controlled study.
Patients: Eighteen subjects with stable, moderate asthma, asymptomatic, rec
eiving regular treatment with salmeterol, 50 mu g bid, and inhaled beclomet
hasone dipropionate, 250 mu g bid, in the last 6 months, with high hyperrea
ctivity to methacholine (baseline provocative dose of methacholine causing
a 20% fall in FEV1 [PD20] geometric mean [GM], 0.071 mg). Subjects were cla
ssified into two groups: subjects with incorrect (n = 5) pMDI inhalation te
chnique, and subjects with correct (n = 13) inhalation technique.
Methods and measurements: After cessation of therapy for 3 days, all subjec
ts underwent four methacholine challenge tests, each test 1 week apart, eac
h time 15 min after inhalation of salbutamol, 100 mu g (via pMDI, pMDI + sp
acer, or Autohaler), or placebo. The protective effect on methacholine chal
lenge test was evaluated as the change in the PD20, and expressed in terms
of doubling doses of methacholine in comparison with placebo treatment,
Results: The PO20 was significantly higher after salbutamol inhalation than
after placebo inhalation, but no significant difference was observed among
the three different inhalation techniques. Only when salbutamol was inhale
d via pMDI + spacer, PD20 was slightly but not significantly higher (pMDI G
M, 0.454 mg; pMDI + spacer GM, 0.559 mg; and Autohaler GM, 0.372 mg; not si
gnificant [NS]) than other inhalation techniques. Similar results (mean +/-
SEM) were obtained with doubling doses of methacholine (pMDI, 2 +/- 0.47;
pMDI + spacer, 3 +/- 0.35; and Autohaler, 2.4 +/- 0.40; NS), No significant
difference was found among techniques when subjects with correct or incorr
ect inhalation technique were separately considered.
Conclusions: Our data show that the protective effect of salbutamol, 100 mu
g, on methacholine-induced bronchoconstriction is not affected by the diff
erent inhalation techniques, although inhalation tia pMDI + spacer tends to
improve the bronchoprotective ability of salbutamol. These data confirm th
e clinical efficacy of salbutamol, whatever the device, and the patient's i
nhalation technique.