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Original Research

COPD patient satisfaction with ipratropium bromide/albuterol delivered via Respimat: a randomized, controlled study

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Pages 139-150 | Published online: 19 Mar 2013

Figures & data

Table A1 Permitted medications and medication restrictions

Table 1 Summary of study patient demographics

Figure 1 Study population.

Notes: Five randomized patients did not proceed with treatment: three patients decided to not participate, one patient developed a COPD exacerbation, and one patient was unable to stop prohibited medication prior to randomization.
Abbreviations: N, number; CVT-R, ipratropium bromide/albuterol Respimat inhaler; CVT-MDI, ipratropium bromide/albuterol metered-dose inhaler; I+A, ipratropium bromide and albuterol metered dose inhalers delivered as dual monotherapies; AE, adverse event.
Figure 1 Study population.

Figure 2 Kaplan–Meier curves of time to discontinuation.

Abbreviations: CVT-R, ipratropium bromide/albuterol Respimat inhaler; CVT-MDI, ipratropium bromide/albuterol metered-dose inhaler; I + A, ipratropium bromide and albuterol metered dose inhalers delivered as dual monotherapies; d, days.
Figure 2 Kaplan–Meier curves of time to discontinuation.

Figure 3 Adjusted mean of PASAPQ performance domain score time profile.

Abbreviations: PASAPQ, Patient Satisfaction and Preference Questionnaire; CVT-R, ipratropium bromide/albuterol Respimat inhaler; CVT-MDI, ipratropium bromide/albuterol metered-dose inhaler; I + A, ipratropium bromide and albuterol metered dose inhalers delivered as dual monotherapies.
Figure 3 Adjusted mean of PASAPQ performance domain score time profile.

Figure 4 Kaplan-Meier curves for time to first COPD exacerbation.

Abbreviations: COPD, chronic obstructive pulmonary disease; CVT-R, ipratropium bromide/albuterol Respimat inhaler; CVT-MDI, ipratropium bromide/albuterol metered-dose inhaler; I+A, ipratropium bromide and albuterol metered dose inhalers delivered as dual monotherapies; d, day.
Figure 4 Kaplan-Meier curves for time to first COPD exacerbation.

Table 2 Frequency of patients (N, %) with adverse events occurring with incidence in preferred term greater than or equal to 3% by treatment, primary system organ class, and preferred term