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Real-life evaluation of budesonide/formoterol (DuoResp Spiromax) for the management of asthma and COPD in the UK

Nicolas Roche, Hicham Benhaddi, Marianka van der Tol, Jonathan Chambers, Job FM van Boven, Leif Bjermer, Marc miravitlles, David Price, Jaco Voorham
European Respiratory Journal 2017 50: PA937; DOI: 10.1183/1393003.congress-2017.PA937
Nicolas Roche
1Hôpitaux Universitaires Paris Centre, Paris, France
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Hicham Benhaddi
2Teva Pharmaceuticals Europe B.V., Brussels, Belgium
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Marianka van der Tol
3Teva Pharmaceuticals Europe B.V., Amsterdam, Netherlands
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Jonathan Chambers
4Teva Pharmaceuticals Europe B.V., Winchester, United Kingdom
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Job FM van Boven
5Groningen Research Institute for Asthma and COPD (GRIAC), University Medical Center Groningen, University of Groningen, Groningen, Netherlands
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Leif Bjermer
6Skane University Hospital, Lund, Sweden
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Marc miravitlles
7Hospital Universitari Vall d'Hebron, Barcelona, Spain
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David Price
8Observational and Pragmatic Research Institute, Singapore, Singapore
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Jaco Voorham
8Observational and Pragmatic Research Institute, Singapore, Singapore
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Abstract

Background: DuoResp Spiromax is an inhaled corticosteroid (ICS)/long-acting β2-agonist fixed-dose combination inhaler, designed to reduce common inhaler errors and enhance usability (reliable dosing and good lung deposition) for patients (pts) with asthma/COPD.

Aims/Objectives: To evaluate the non-inferiority of DuoResp after changing from Symbicort, vs staying on Symbicort (pts achieving disease control [based on Risk Domain Control, RDC, algorithm]; exacerbation rate; short-acting β2-agonists (SABA) use; and treatment stability [achieved RDC; no treatment boost]).

Methods: Asthma/COPD pts who changed from Symbicort to DuoResp were matched (3:1) with pts staying on Symbicort. Data were from the Optimum Patient Care Research Database and Clinical Practice Research Datalink. To achieve RDC, pts must not have had respiratory related hospitalization, accident/emergency attendance, exacerbations, and oral CS or antibiotic courses.

Results: Compared with 1091 pts (asthma 743; COPD 348) staying on Symbicort, 385 matched pts (asthma 253; COPD 132) who changed to DuoResp had non-inferiority in RDC (adjusted difference +6.6% [95% CI, -0.3–13.5]). In asthma pts, DuoResp (vs Symbicort) resulted in fewer exacerbations (adjusted rate ratio [RR] 0.76; p=0.044); lower odds of being in a high SABA dose category (OR 0.71; p=0.034); used fewer SABA inhalers (RR 0.92; p=0.019) and higher odds of achieving treatment stability (adjusted odds ratio 1.44; p=0.037). No significant differences were found in COPD pts.

Conclusions: In real-life asthma/COPD patients, DuoResp was non-inferior (in RDC) to Symbicort. In asthma pts, DuoResp was associated with better health outcomes.

  • Copyright ©the authors 2017
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Real-life evaluation of budesonide/formoterol (DuoResp Spiromax) for the management of asthma and COPD in the UK
Nicolas Roche, Hicham Benhaddi, Marianka van der Tol, Jonathan Chambers, Job FM van Boven, Leif Bjermer, Marc miravitlles, David Price, Jaco Voorham
European Respiratory Journal Sep 2017, 50 (suppl 61) PA937; DOI: 10.1183/1393003.congress-2017.PA937

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Real-life evaluation of budesonide/formoterol (DuoResp Spiromax) for the management of asthma and COPD in the UK
Nicolas Roche, Hicham Benhaddi, Marianka van der Tol, Jonathan Chambers, Job FM van Boven, Leif Bjermer, Marc miravitlles, David Price, Jaco Voorham
European Respiratory Journal Sep 2017, 50 (suppl 61) PA937; DOI: 10.1183/1393003.congress-2017.PA937
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