Outcomes of Patients with COPD Treated with ICS/LABA Before and After Initiation of Single-Inhaler Triple Therapy with Fluticasone Furoate/Umeclidinium/Vilanterol (FF/UMEC/VI)

被引:2
作者
Mccormack, Meredith [1 ]
Paczkowski, Rosirene [2 ]
Gronroos, Noelle N. [3 ]
Noorduyn, Stephen G. [4 ,5 ]
Lee, Lydia [2 ,6 ]
Veeranki, Phani [3 ]
Johnson, Mary G. [3 ]
Igboekwe, Emmeline [7 ]
Kahle-Wrobleski, Kristin [2 ]
Panettieri, Reynold [8 ]
机构
[1] Johns Hopkins Univ, Pulm & Crit Care Med, Baltimore, MD USA
[2] GSK, R&D Global Med, Value Evidence & Outcomes, Collegeville, PA 19426 USA
[3] Optum, Hlth Econ & Outcomes Res, Eden Prairie, MN USA
[4] GSK, Global Value Evidence & Outcomes, Mississauga, ON, Canada
[5] McMaster Univ, Dept Hlth Res Methods Evidence & Impact, Hamilton, ON, Canada
[6] Rutgers Sch Publ Hlth, Ctr Hlth Outcomes Policy & Econ, Piscataway, NJ USA
[7] GSK, R&D Global Med, US Med Affairs, Durham, NC USA
[8] Rutgers Inst Translat Med & Sci, New Brunswick, NJ USA
关键词
COPD; Dual therapy; Exacerbations; FF/UMEC/VI; HCRU; ICS/LABA; Single-inhaler triple therapy; OBSTRUCTIVE PULMONARY-DISEASE; ECONOMIC BURDEN; EXACERBATIONS; ADHERENCE;
D O I
10.1007/s12325-023-02776-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: Triple therapy (fluticasone furoate/umeclidinium/vilanterol; FF/UMEC/VI) has been shown to improve symptoms and reduce exacerbations in patients with chronic obstructive pulmonary disease (COPD) and a history of exacerbations. This real-world study compared exacerbation rates and healthcare resource utilization (HCRU) before and after initiation of FF/UMEC/VI in patients with COPD previously treated with inhaled corticosteroid (ICS)/long-acting beta(2)-agonist (LABA). Methods: This retrospective cohort study included commercial and Medicare Advantage with Part D administrative claims data from September 01, 2016, to March 31, 2020, of patients diagnosed with COPD. The index date was the date of the first FF/UMEC/VI claim (September 2017-March 2019). The 12 months prior to index (baseline) were used to assess patient characteristics and outcomes; the 12 months following index (follow-up) were used to assess study outcomes. All patients had >= 30 consecutive days' supply of any ICS/LABA dual therapy during the 12 months prior to FF/UMEC/VI initiation. Subgroup analyses included patients with >= 30 consecutive days' supply of budesonide/formoterol (BUD/FORM) during baseline. Analyses of patients with >= 1 COPD exacerbation during baseline were reported as well. Results: The overall population included 1449 patients (mean age 70.75 years; 54.18% female), of whom 540 were patients in the BUD/FORM subgroup. Significantly fewer patients experienced any exacerbation during follow-up versus baseline (overall population 53.49% vs 62.59%; p < 0.001; BUD/FORM subgroup 55.00% vs 62.41%; p = 0.004). Effects on exacerbation reduction were more pronounced among patients with >= 1 exacerbation during baseline. Lower COPD-related HCRU was observed during the follow-up compared with baseline for both the overall population and the BUD/FORM subgroup. Conclusion: Patients with COPD treated with ICS/LABA during baseline, including patients specifically treated with BUD/FORM and those with a history of >= 1 exacerbation, had fewer COPD exacerbations and lower COPD-related HCRU after initiating FF/UMEC/VI.
引用
收藏
页码:1245 / 1261
页数:17
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