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Effect of budesonide/formoterol pressurized metered-dose inhaler on exacerbations versus formoterol in chronic obstructive pulmonary disease: The 6-month, randomized RISE (Revealing the Impact of Symbicort in reducing Exacerbations in COPD) study.
Ferguson, Gary T; Tashkin, Donald P; Skärby, Tor; Jorup, Carin; Sandin, Kristina; Greenwood, Michael; Pemberton, Kristine; Trudo, Frank.
Afiliação
  • Ferguson GT; Pulmonary Research Institute of Southeast Michigan, Farmington Hills, MI, USA. Electronic address: garytferguson@msn.com.
  • Tashkin DP; University of California, Los Angeles, CA, USA. Electronic address: DTashkin@mednet.ucla.edu.
  • Skärby T; AstraZeneca R&D, Gothenburg, Sweden. Electronic address: Tor.Skarby@astrazeneca.com.
  • Jorup C; AstraZeneca R&D, Gothenburg, Sweden. Electronic address: Carin.Jorup@astrazeneca.com.
  • Sandin K; AstraZeneca R&D, Gothenburg, Sweden. Electronic address: Kristina.Sandin@astrazeneca.com.
  • Greenwood M; AstraZeneca R&D, Alderley Park, Cheshire, UK. Electronic address: mike.greenwood@phastar.com.
  • Pemberton K; AstraZeneca R&D, Alderley Park, Cheshire, UK. Electronic address: kristine.pemberton@hotmail.co.uk.
  • Trudo F; AstraZeneca LP, Wilmington, DE, USA. Electronic address: Frank.Trudo@astrazeneca.com.
Respir Med ; 132: 31-41, 2017 Nov.
Article em En | MEDLINE | ID: mdl-29229103
ABSTRACT

BACKGROUND:

Prevention of exacerbations is a primary goal for chronic obstructive pulmonary disease (COPD) therapy. This randomized, double-blind, double-dummy, parallel-group, multicenter study evaluated the effect of budesonide/formoterol pressurized metered-dose inhaler (pMDI) versus formoterol dry powder inhaler (DPI) on reducing COPD exacerbations.

METHODS:

1219 patients aged ≥40 years with moderate-to-very-severe COPD (per lung function) and a history of ≥1 COPD exacerbation received budesonide/formoterol pMDI 320/9 µg twice daily (BID) during a 4-week run-in. Patients were then randomized 11 to receive budesonide/formoterol pMDI 320/9 µg BID (n = 606) or formoterol DPI 9 µg BID (n = 613) for 26 weeks. Exacerbations were identified using predefined criteria for symptom worsening and treatment with systemic corticosteroids and/or antibiotics and/or hospitalization. The primary endpoint was annual rate of exacerbations.

RESULTS:

Budesonide/formoterol pMDI resulted in a 24% reduction in annual rate of exacerbations (0.85 vs 1.12; rate ratio 0.76 [95% CI 0.62, 0.92]; P = 0.006), and a significant risk reduction for time to first exacerbation (hazard ratio 0.78 [95% CI 0.64, 0.96]; P = 0.016) versus formoterol DPI. The most commonly reported adverse events (AEs; ≥3%) in budesonide/formoterol and formoterol groups were COPD (4.5% vs 8.6%) and nasopharyngitis (5.0% vs 5.2%). Pneumonia AEs were reported in 0.5% and 1.0% of budesonide/formoterol-treated and formoterol-treated patients, respectively.

CONCLUSIONS:

Budesonide/formoterol pMDI is an effective treatment option for reducing exacerbation rates in COPD patients with moderate-to-very-severe airflow limitation and history of exacerbations. No increase in pneumonia was observed with budesonide/formoterol; safety data were consistent with its established profile.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Broncodilatadores / Doença Pulmonar Obstrutiva Crônica / Fumarato de Formoterol / Combinação Budesonida e Fumarato de Formoterol / Glucocorticoides Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Broncodilatadores / Doença Pulmonar Obstrutiva Crônica / Fumarato de Formoterol / Combinação Budesonida e Fumarato de Formoterol / Glucocorticoides Idioma: En Ano de publicação: 2017 Tipo de documento: Article