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      Symptoms and quality of life in patients with chronic obstructive pulmonary disease treated with aclidinium in a real-life setting

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          Abstract

          Introduction

          Chronic obstructive pulmonary disease (COPD) is a progressive disease with symptoms that can have a major impact on patients’ physical health. The aim of this study was to evaluate quality of life (QoL), symptom severity and dyspnoea in COPD patients treated with aclidinium up to 24 weeks.

          Methods

          In this prospective non-interventional multicentre study (198 centres in Sweden, Denmark, and Norway), COPD patients (age ≥40 years) who started treatment with aclidinium (initial therapy, change of treatment, or add-on therapy) could be included. Health-related QoL was obtained by COPD assessment test (CAT). Symptoms were evaluated on a 6-point Likert scale. The modified Medical Research Council (mMRC) Dyspnoea Scale was used as a simple grading system to assess the level of dyspnoea/shortness of breath from0 to 4. Patients on treatment with aclidinium who completed baseline and at least one follow-up visit (week 12 or 24) were included in the study population.

          Results

          Overall, 1,093 patients were enrolled (mean 69 years, 54% females), one-third had ≥1 exacerbation the year prior to baseline. At enrolment, 48% were LAMA naïve. Mean (standard deviation, SD) CAT score decreased from 16.9 (7.7) at baseline to 14.3 (7.3) at week 24 ( p<0.01) with a decrease in all individual CAT items ( p<0.05). Mean difference in morning and night-time symptoms from baseline to week 24 was −0.60 (SD 2.51) and −0.44 (SD 2.48), respectively (both p<0.001). Mean (SD) mMRC Dyspnoea Scale changed from 1.6 (1.0) at baseline to 1.5 (1.0) at week 24 ( p<0.001).

          Conclusion

          In this observational study of a Nordic real-life COPD population, treatment with aclidinium was associated with a clinically important improvement in QoL and morning and night-time symptoms, most pronounced in the LAMA naïve group. However, there is still room for improvement in the management of symptomatic COPD patients.

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          Most cited references17

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          A technique for the measturement of attittudes

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            Global strategy for the diagnosis, management and prevention of COPD

            (2016)
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              Night-time symptoms: a forgotten dimension of COPD.

              Sleep quality is often poor in patients with chronic obstructive pulmonary disease (COPD), but these night-time symptoms are frequently unnoticed by physicians and/or not reported by patients themselves. Therefore, the prevalence and clinical impact of sleep disturbances and night-time symptoms in COPD is not well understood and has not been a clinical focus to date. To address this gap, an expert panel meeting was convened in Barcelona, Spain, in March 2011 to discuss the aetiology, evolution, burden, long-term clinical consequences and optimal management of night-time symptoms in COPD. The term "night-time symptoms" in COPD has not been distinctly defined in an objective sense but epidemiological data suggests that the prevalence of nocturnal symptoms and symptomatic sleep disturbance may exceed 75% in patients with COPD. The panel concluded that night-time symptoms in COPD are prevalent and bothersome; that their cause(s) are multiple and include demographic factors, such as age and obesity, pharmacotherapy, disease-specific symptoms and the presence of comorbid sleep disorders, and other medical conditions; and that potential long-term consequences can include lung function changes, increased exacerbation frequency, emergence or worsening of cardiovascular disease, cognitive effects, depression, impaired quality of life and increased mortality. To date, few interventional studies have investigated them, but emerging data suggest that bronchodilator therapy can improve them if deployed appropriately. In summary, night-time symptoms in COPD warrant further clinical investigation with validated tools.
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                Author and article information

                Journal
                Eur Clin Respir J
                Eur Clin Respir J
                ECRJ
                European Clinical Respiratory Journal
                Co-Action Publishing
                2001-8525
                05 July 2016
                2016
                : 3
                : 10.3402/ecrj.v3.31232
                Affiliations
                [1 ]Section of Social Medicine, Department of Public Health, Copenhagen University, Copenhagen, Denmark
                [2 ]Respiratory Section, Hvidovre Hospital, Copenhagen University, Copenhagen, Denmark
                [3 ]Airway Inflammation Unit, Department of Experimental Medical Science, Lund University, Lund, Sweden
                [4 ]Department of Internal Medicine, Trelleborg Hospital, Trelleborg, Sweden
                [5 ]Vårdcentralen Näsby, Kristianstad, Sweden
                [6 ]Clinical Trial Center, Gothia Forum, Sahlgrenska University Hospital, Gothenburg, Sweden
                [7 ]Clinic of Allergology and Respiratory Medicine, Oslo, Norway
                [8 ]AstraZeneca Nordic-Baltic, Södertälje, Sweden
                [9 ]Department of Applied Mathematics and Computer Science, Technical University of Denmark, Lyngby, Denmark
                [10 ]Department of Respiratory Medicine and Allergology, Lund University, Lund, Sweden
                Author notes
                [* ]Correspondence to: Peter Lange, Respiratory Section, Hvidovre Hospital, Copenhagen University, Copenhagen, Denmark, Email: peter.lange@ 123456sund.ku.dk

                Responsible Editor: Vibeke Backer, University of Copenhagen, Denmark.

                Article
                31232
                10.3402/ecrj.v3.31232
                4937723
                27387608
                0c6120ad-12cb-447a-a644-b77777988061
                © 2016 Peter Lange et al.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.

                History
                : 15 February 2016
                : 30 May 2016
                Categories
                Original Article

                patient-reported outcomes,patient satisfaction,dyspnoea,copd,lama,observational study

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