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Correction: Benefit of prompt initiation of single-inhaler fluticasone furoate, umeclidinium, and vilanterol (FF/UMEC/VI) in patients with COPD in England following an exacerbation: a retrospective cohort study

The Original Article was published on 25 September 2023


Correction: Respiratory Research (2023) 24: 229 https://doi.org/10.1186/s12931-023-02523-1


Following publication of the original article [1], the Authors identified errors in the COPD-related total costs for prompt and delayed initiators and the associated exponentiated coefficient (95% confidence interval) and p-value in Fig. 8b.

The corrected Fig. 8b is given below: 

These errors also impacted some statements under the “Results” and “Discussion” sections and “Conclusions”. This text has now been amended in this Correction.

Results

HCRU and costs following FF/UMEC/VI initiation.

The text in the penultimate sentence under the heading “HCRU and costs following FF/UMEC/VI initiation” in the “Results” section originally read: Prompt initiators had numerically lower all-cause total costs and significantly lower COPD-related costs per-person-per-year compared with delayed initiators (Fig. 8; COPD-related costs: prompt £742, delayed £801, p = 0.0016).

Corrected sentence: Prompt initiators had numerically lower all-cause total costs and similar COPD-related costs per-person-per-year compared with delayed initiators (Fig. 8).

Discussion

The first sentence of the second “Discussion” paragraph originally read: Prompt initiation of FF/UMEC/VI following the index exacerbation was also associated with fewer all-cause and COPD-related hospital readmissions at all time points assessed, as well as lower COPD-related total costs and COPD-related prescription costs compared with delayed initiation.

Corrected sentence: Prompt initiation of FF/UMEC/VI following the index exacerbation was also associated with fewer all-cause and COPD-related hospital readmissions at all time points assessed, as well as lower COPD-related prescription costs compared with delayed initiation.

Conclusions

Finally, an additional discrepancy in the “Conclusions” section is noted.

The first sentence originally read: Compared with delayed initiation, prompt initiation of FF/UMEC/VI following a moderate/severe exacerbation was associated with fewer subsequent exacerbations, fewer hospital readmissions, and lower COPD-related medical costs.

Corrected sentence: Compared with delayed initiation, prompt initiation of FF/UMEC/VI following a moderate/severe exacerbation was associated with fewer subsequent exacerbations, fewer hospital readmissions, and lower COPD-related prescription costs.

The Authors apologise for these discrepancies and for any inconvenience to the journal and to the readers.

The original article has been corrected.

Reference

  1. Ismaila AS, Rothnie KJ, Wood RP, Banks VL, Camidge LJ, Czira A, Compton C, Sharma R, Millard SN, Massey O, Halpin DMG. Benefit of prompt initiation of single-inhaler fluticasone furoate, umeclidinium, and vilanterol (FF/UMEC/VI) in patients with COPD in England following an exacerbation: a retrospective cohort study. Respir Res. 2023;24:229. https://doi.org/10.1186/s12931-023-02523-1.

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Correspondence to Afisi S. Ismaila.

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Ismaila, A.S., Rothnie, K.J., Wood, R.P. et al. Correction: Benefit of prompt initiation of single-inhaler fluticasone furoate, umeclidinium, and vilanterol (FF/UMEC/VI) in patients with COPD in England following an exacerbation: a retrospective cohort study. Respir Res 25, 152 (2024). https://doi.org/10.1186/s12931-024-02745-x

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