AIMS: To understand the needs of people with asthma and COPD, and to identify opportunities for improved care. METHODS: Quantitative questionnaire-based survey performed in five European countries on patients with asthma and COPD. Questionnaires were administered to patients using Computer Assisted Web Interview methodology. RESULTS: 1022 patients with asthma (UK [n=190]; Germany [n=214]; France [n=200]; Italy [n=222]; Spain [n=196]) and 719 patients with COPD (UK [n=153]; Germany [n=147]; France [n=145]; Italy [n=140]; Spain [n=134]) were enrolled in the study. 32% of those with asthma and 67% of those with COPD considered that their condition had a significant effect on their quality of life, and stigma and emotional distress was common. Many expressed concern regarding potential medication side effects or that medicines might lose their effect with time. Major discrepancies between expectations and patient satisfaction with the doctor-patient relationship were observed, including a need to be consulted in the choice of inhalers. Consultations were infrequent, and 75% of respondents sought additional information beyond that received during consultations - commonly from the internet. CONCLUSIONS: Patient satisfaction was high but information needs were not addressed and the emotional burden of disease is underappreciated.
AIMS: To understand the needs of people with asthma and COPD, and to identify opportunities for improved care. METHODS: Quantitative questionnaire-based survey performed in five European countries on patients with asthma and COPD. Questionnaires were administered to patients using Computer Assisted Web Interview methodology. RESULTS: 1022 patients with asthma (UK [n=190]; Germany [n=214]; France [n=200]; Italy [n=222]; Spain [n=196]) and 719 patients with COPD (UK [n=153]; Germany [n=147]; France [n=145]; Italy [n=140]; Spain [n=134]) were enrolled in the study. 32% of those with asthma and 67% of those with COPD considered that their condition had a significant effect on their quality of life, and stigma and emotional distress was common. Many expressed concern regarding potential medication side effects or that medicines might lose their effect with time. Major discrepancies between expectations and patient satisfaction with the doctor-patient relationship were observed, including a need to be consulted in the choice of inhalers. Consultations were infrequent, and 75% of respondents sought additional information beyond that received during consultations - commonly from the internet. CONCLUSIONS:Patient satisfaction was high but information needs were not addressed and the emotional burden of disease is underappreciated.
Authors: Aaron M Mulhall; Laura A Lach; Sara M Krzywkowski-Mohn; Jeffrey A Welge; Ralph J Panos Journal: Respir Med Date: 2013-07-01 Impact factor: 3.415
Authors: Julia Walters; Helen Cameron-Tucker; Karen Wills; Natalie Schüz; Jenn Scott; Andrew Robinson; Mark Nelson; Paul Turner; Richard Wood-Baker; E Haydn Walters Journal: BMJ Open Date: 2013-09-06 Impact factor: 2.692
Authors: Deborah Morrison; Frances S Mair; Rekha Chaudhuri; Marilyn McGee-Lennon; Mike Thomas; Neil C Thomson; Lucy Yardley; Sally Wyke Journal: BMC Med Inform Decis Mak Date: 2015-07-28 Impact factor: 2.796
Authors: Deborah Morrison; Sally Wyke; Karolina Agur; Euan J Cameron; Robert I Docking; Alison M Mackenzie; Alex McConnachie; Vandana Raghuvir; Neil C Thomson; Frances S Mair Journal: J Med Internet Res Date: 2014-02-18 Impact factor: 5.428