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. 2022 Jul 20;39(11):4961–5010. doi: 10.1007/s12325-022-02234-x

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© The Author(s) 2022, corrected publication 2022

Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

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Fig. 6 — Fixed effects model of incidence ratio of annualised moderate/severe exacerbations rates of UMEC/VI versus a dual therapy and b monotherapy at 24 weeks. Assessment of heterogeneity/inconsistency: I² = 38.86%; Q = 6.54; p = 0.1622. ACL aclidinium, CFB change from baseline, CI confidence interval, FOR formoterol fumarate, FP fluticasone propionate, GLY glycopyrronium, IND indacaterol, PBO placebo, SAL salmeterol, TIO tiotropium, UMEC umeclidinium, VI vilanterol