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      Efficacy and Safety of Aclidinium Bromide Compared with Placebo and Tiotropium in Patients with Moderate-to-Severe Chronic Obstructive Pulmonary Disease: Results from a 6-week, Randomized, Controlled Phase Iiib Study

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          Abstract

          Background:

          This randomized, double-blind, Phase IIIb study evaluated the 24-hour bronchodilatory efficacy of aclidinium bromide versus placebo and tiotropium in patients with moderate-to-severe chronic obstructive pulmonary disease (COPD). Methods: Patients received aclidinium 400 μg twice daily (morning and evening), tiotropium 18 μg once daily (morning), or placebo for 6 weeks. The primary endpoint was change from baseline in forced expiratory volume in 1 second area under the curve for the 24-hour period post-morning dose (FEV 1 AUC 0–24) at week 6. Secondary and additional endpoints included FEV 1 AUC 12–24, COPD symptoms (EXAcerbations of chronic pulmonary disease Tool-Respiratory Symptoms [E-RS] total score and additional symptoms questionnaire), and safety. Results: Overall, 414 patients were randomized and treated (FEV 1 1.63 L [55.8% predicted]). Compared with placebo, FEV 1 AUC 0–24 and FEV 1 AUC 12–24 were significantly increased from baseline with aclidinium (Δ = 150 mL and 160 mL, respectively; p < 0.0001) and tiotropium (Δ = 140 mL and 123 mL, respectively; p < 0.0001) at week 6. Significant improvements in E-RS total scores over 6 weeks were numerically greater with aclidinium (p < 0.0001) than tiotropium (p < 0.05) versus placebo. Only aclidinium significantly reduced the severity of early-morning cough, wheeze, shortness of breath, and phlegm, and of nighttime symptoms versus placebo (p < 0.05). Adverse-event (AE) incidence (28%) was similar between treatments. Few anticholinergic AEs (<1.5%) or serious AEs (<3%) occurred in any group. Conclusions: Aclidinium provided significant 24-hour bronchodilation versus placebo from day 1 with comparable efficacy to tiotropium after 6 weeks. Improvements in COPD symptoms were consistently numerically greater with aclidinium versus tiotropium. Aclidinium was generally well tolerated.

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          Standardisation of spirometry

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            Standardisation of spirometry

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              Medication adherence issues in patients treated for COPD

              Although medical treatment of COPD has advanced, nonadherence to medication regimens poses a significant barrier to optimal management. Underuse, overuse, and improper use continue to be the most common causes of poor adherence to therapy. An average of 40%–60% of patients with COPD adheres to the prescribed regimen and only 1 out of 10 patients with a metered dose inhaler performs all essential steps correctly. Adherence to therapy is multifactorial and involves both the patient and the primary care provider. The effect of patient instruction on inhaler adherence and rescue medication utilization in patients with COPD does not seem to parallel the good results reported in patients with asthma. While use of a combined inhaler may facilitate adherence to medications and improve efficacy, pharmacoeconomic factors may influence patient’s selection of both the device and the regimen. Patient’s health beliefs, experiences, and behaviors play a significant role in adherence to pharmacological therapy. This manuscript reviews important aspects associated with medication adherence in patients with COPD and identifies some predictors of poor adherence.
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                Author and article information

                Journal
                COPD
                COPD
                COP
                COPD
                Informa Healthcare
                1541-2555
                1541-2563
                1 August 2013
                22 June 2013
                : 10
                : 4
                : 511-522
                Affiliations
                1Insaf Respiratory Research Institute, Wiesbaden, Germany
                2Pulmonary Research Institute at Hospital Grosshansdorf, Grosshansdorf, Germany
                3ISPL Centrum Medyczne and Department of Lung Diseases and Tuberculosis, Medical University of Bialystok, Białystok,Poland
                4Almirall, Barcelona,Spain
                5Forest Research Institute, Jersey City, New Jersey,USA
                Author notes

                Clinical trial registration: This trial was registered on clinicaltrials.gov (NCT01462929).

                Correspondence to: Dr Jutta Beier, insaf Respiratory Research Institute , Biebricher Allee 34, 65187, Wiesbaden, Germany, phone: +49 611 985 4410, email: j.beier@ 123456insaf-wi.de
                Article
                10.3109/15412555.2013.814626
                3787813
                23819698
                363c36c2-7c4f-419c-98b3-bfa414584876
                © 2013 Informa Healthcare USA, Inc.

                This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the source is credited.

                History
                Categories
                Original Research

                Respiratory medicine
                24-hour,bronchodilation,long-acting muscarinic antagonist,nighttime,symptoms
                Respiratory medicine
                24-hour, bronchodilation, long-acting muscarinic antagonist, nighttime, symptoms

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