Oj. Dempsey et al., Evaluation of the effect of a large volume spacer on the systemic bioactivity of fluticasone propionate metered-dose inhaler, CHEST, 116(4), 1999, pp. 935-940
Citations number
31
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Background: Inhaled corticosteroids such as fluticasone propionate (FP) hav
e dose-related systemic effects, including adrenal suppression.: We have th
erefore investigated the effect of adding a large volume spacer on the syst
emic bioactivity of FP given via a pressurized metered-dose inhaler (pMDI).
Methods: Fourteen healthy volunteers (mean age, 29.9 years old) were studie
d using an open, randomized, placebo-controlled, three-way crossover design
, Single doses of the following were given at 5:00 par in a randomized sequ
ence: (1) eight-puffs of FP by pMDI, 1.76 mg (250 mu g ex-valve, 220 mu g e
x-actuator); (2) eight puffs of FP by pPMDI, 250 mu g, with 750-mL spacer (
Volumatic; Allen & Hanburys; Uxbridge, UK); and (3) eight puffs of placebo
by pMDI. Measurements were made after each dose, including:overnight and ea
rly morning urinary cortisol/creatinine ratios and 8:00 AM serum cortisol,
Results: Significant (p < 0.05) suppression of all three end-points occurre
d with each active treatment compared to treatment with placebo, Furthermor
e, significant (p < 0.05) additional suppression occurred when comparing FP
by pMDI alone to FP by pMDI with spacer. Geometric mean fold differences (
95% confidence interval for fold difference) between FP by pMDI alone and F
P by pMDI with spacer were 1.94-fold (1.00-3.78) for overnight urinary cort
isol/creatinine ratio and 1.98-fold (1.26-3.10) for 8:00 AM serum cortisol.
This was mirrored by a twofold rise in the number of values for uncorrecte
d overnight urinary cortisol < 10 nmol/10 h: placebo treatment (none of 1 1
subjects); FP by pMDI (6 of 14 subjects;:43%); and FP by pMDI with spacer
(12 of 14 subjects; 86%),
Conclusions: The use of a large volume spacer with FP by: pMDI results in a
twofold increase in the systemic bioavailability as assessed by sensitive
measures of adrenal suppression. This, in turn, reflects a twofold improvem
ent in respirable dose delivery with the spacer device.