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Budesonide/formoterol pressurized metered-dose inhaler for patients with persistent asthma
被引:3
|作者:
Korenblat, Phillip E.
[1
]
Rosenwasser, Lanny J.
[2
]
机构:
[1] Clin Res Ctr, St Louis, MO 63141 USA
[2] Childrens Mercy Hosp, Kansas City, MO 64108 USA
关键词:
Budesonide;
combination therapy;
efficacy;
formoterol;
inhaled corticosteroid;
long-acting beta(2)-adrenergic agonist;
persistent asthma;
pharmacology;
pressurized metered-dose inhaler;
safety;
ACTING BETA-AGONISTS;
LONG-TERM TREATMENT;
SINGLE INHALER;
FLUTICASONE PROPIONATE;
DOUBLE-BLIND;
BETA(2)-ADRENERGIC RECEPTOR;
REPORTED OUTCOMES;
RELIEVER THERAPY;
BUDESONIDE;
FORMOTEROL;
D O I:
10.2500/aap.2010.31.3356
中图分类号:
R392 [医学免疫学];
学科分类号:
100102 ;
摘要:
The combination of budesonide and formoterol administered in one hydrofluoroalkane pressurized metered-dose inhaler (pMDI) is approved in the United States in two dosage strengths (budesonide/formoterol pMDI 80/4.5 mu g x 2 inhalations [160/9 mu g] or 160/4.5 mu g x 2 inhalations [320/9 mu g]) in a fixed-dose, twice-daily regimen for the treatment of patients >= 12 years old with persistent asthma not adequately controlled with an inhaled corticosteroid (ICS) alone. This article reviews the clinical profile of budesonide/formoterol pMDI in patients with persistent asthma, including information on pharmacogenetics, efficacy, and tolerability. Studies of budesonide/formoterol pMDI in patients with asthma were identified through PubMed and respiratory meeting abstract databases. Budesonide/formoterol pMDI 160/9 jig has shown a rapid onset (within 15 minutes) of clinically significant bronchodilation that is faster than fluticasone propionate/salmeterol dry powder inhaler (DPI) 250/50 mu g (within 30 minutes). The efficacy and tolerability profile of budesonide/formoterol pMDI 320/9 mu g was similar to fluticasone propionate/salmeterol DPI 250/50 mu g, and budesonide/formoterol DPI 320/9 jig in adults and adolescents with persistent asthma. Short-term (12-week) and long-term (6- to 12-month) studies have established greater efficacy and similar tolerability of budesonide/formoterol pMDI compared with its monocomponents and placebo in patients with mild/moderate or moderate/severe persistent asthma. Studies evaluating patient-reported outcomes, including health-related quality of life and patient satisfaction with treatment, further support the benefits of budesonide/formoterol pMDI in patients with persistent asthma. In summary, budesonide/formoterol pMDI is an effective, well-tolerated treatment option for patients with persistent asthma for whom ICS/long-acting beta(2)-adrenergic agonist combination therapy is appropriate. (Allergy Asthma Proc 31:190-202, 2010; doi: 10.2500/aap.2010.31.3356)
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页码:190 / 202
页数:13
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