Umeclidinium/Vilanterol Compared with Fluticasone Propionate/Salmeterol, Budesonide/Formoterol, and Tiotropium as Initial Maintenance Therapy in Patients with COPD Who Have High Costs and Comorbidities.


Journal

International journal of chronic obstructive pulmonary disease
ISSN: 1178-2005
Titre abrégé: Int J Chron Obstruct Pulmon Dis
Pays: New Zealand
ID NLM: 101273481

Informations de publication

Date de publication:
Historique:
received: 18 12 2020
accepted: 29 03 2021
entrez: 29 4 2021
pubmed: 30 4 2021
medline: 28 7 2021
Statut: epublish

Résumé

Comorbidities in patients with chronic obstructive pulmonary disease (COPD) are associated with increased medical costs and risk of exacerbations. This study compared COPD-related medical costs and exacerbations in high-cost, high-comorbidity patients with COPD receiving initial maintenance treatment (IMT) with umeclidinium/vilanterol (UMEC/VI) versus fluticasone propionate/salmeterol (FP/SAL), budesonide/formoterol (B/F), or tiotropium (TIO). This retrospective, matched cohort study identified patients from Optum's de-identified Clinformatics Data Mart database who initiated UMEC/VI, FP/SAL, B/F, or TIO between January 1, 2014 and December 31, 2018 (index date defined as date of the first fill). Eligibility criteria included age ≥40 years at index, ≥1 pre-index COPD diagnosis, no pre-index asthma diagnosis, 12 months of continuous insurance coverage pre-index, and high pre-index costs (≥80th percentile of IMT population) and comorbidities (Quan-Charlson comorbidity index ≥3). Propensity score matching was used to control for potential confounders. On-treatment COPD-related medical costs (primary endpoint) and exacerbations were evaluated. Matched cohorts were well balanced on baseline characteristics (UMEC/VI vs FP/SAL: n=1194 each; UMEC/VI vs B/F: n=1441 each; UMEC/VI vs TIO: n=1277 each). Patients receiving UMEC/VI had significantly lower COPD-related medical costs versus FP/SAL (difference: $6587 per patient per year; These findings suggest that high-cost, high-comorbidity patients with COPD receiving UMEC/VI compared with FP/SAL, B/F, and TIO as IMT may have lower medical costs and exacerbation risk.

Sections du résumé

BACKGROUND BACKGROUND
Comorbidities in patients with chronic obstructive pulmonary disease (COPD) are associated with increased medical costs and risk of exacerbations. This study compared COPD-related medical costs and exacerbations in high-cost, high-comorbidity patients with COPD receiving initial maintenance treatment (IMT) with umeclidinium/vilanterol (UMEC/VI) versus fluticasone propionate/salmeterol (FP/SAL), budesonide/formoterol (B/F), or tiotropium (TIO).
METHODS METHODS
This retrospective, matched cohort study identified patients from Optum's de-identified Clinformatics Data Mart database who initiated UMEC/VI, FP/SAL, B/F, or TIO between January 1, 2014 and December 31, 2018 (index date defined as date of the first fill). Eligibility criteria included age ≥40 years at index, ≥1 pre-index COPD diagnosis, no pre-index asthma diagnosis, 12 months of continuous insurance coverage pre-index, and high pre-index costs (≥80th percentile of IMT population) and comorbidities (Quan-Charlson comorbidity index ≥3). Propensity score matching was used to control for potential confounders. On-treatment COPD-related medical costs (primary endpoint) and exacerbations were evaluated.
RESULTS RESULTS
Matched cohorts were well balanced on baseline characteristics (UMEC/VI vs FP/SAL: n=1194 each; UMEC/VI vs B/F: n=1441 each; UMEC/VI vs TIO: n=1277 each). Patients receiving UMEC/VI had significantly lower COPD-related medical costs versus FP/SAL (difference: $6587 per patient per year;
CONCLUSION CONCLUSIONS
These findings suggest that high-cost, high-comorbidity patients with COPD receiving UMEC/VI compared with FP/SAL, B/F, and TIO as IMT may have lower medical costs and exacerbation risk.

Identifiants

pubmed: 33911860
doi: 10.2147/COPD.S298032
pii: 298032
pmc: PMC8075186
doi:

Substances chimiques

Benzyl Alcohols 0
Bronchodilator Agents 0
Chlorobenzenes 0
Drug Combinations 0
Fluticasone-Salmeterol Drug Combination 0
GSK573719 0
Quinuclidines 0
vilanterol 028LZY775B
Budesonide 51333-22-3
Formoterol Fumarate W34SHF8J2K
Tiotropium Bromide XX112XZP0J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1149-1161

Informations de copyright

© 2021 Kalhan et al.

Déclaration de conflit d'intérêts

RK reports grants and personal fees from AstraZeneca, Boehringer Ingelheim, and GSK; grants from PneumRx (BTG) and Spiration; and personal fees from Aptus Health, Boston Scientific, Boston Consulting Group, and CVS Caremark (all outside of the submitted work). DS, RR, QS, and BH are employees of GSK and own stocks/shares in GSK. CM was an employee of GSK at the time of the study. GG, FL, MSD, and SDM are employees of Analysis Group, Inc., a consulting company that has received research funds from GSK to conduct the study. The authors report no other conflicts of interest in this work.

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Auteurs

Ravi Kalhan (R)

Asthma and COPD Program, Division of Pulmonary and Critical Care Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

David Slade (D)

US Medical Affairs, GlaxoSmithKline, Research Triangle Park, NC, USA.

Riju Ray (R)

US Medical Affairs, GlaxoSmithKline, Research Triangle Park, NC, USA.

Chad Moretz (C)

US Value Evidence and Outcomes, GlaxoSmithKline, Research Triangle Park, NC, USA.

Guillaume Germain (G)

Groupe d'Analyse, Ltée, Montréal, QC, Canada.

François Laliberté (F)

Groupe d'Analyse, Ltée, Montréal, QC, Canada.

Qin Shen (Q)

US Value Evidence and Outcomes, GlaxoSmithKline, Collegeville, PA, USA.

Mei Sheng Duh (MS)

Analysis Group, Inc., Boston, MA, USA.

Sean Dale MacKnight (SD)

Groupe d'Analyse, Ltée, Montréal, QC, Canada.

Beth Hahn (B)

US Value Evidence and Outcomes, GlaxoSmithKline, Research Triangle Park, NC, USA.

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Classifications MeSH