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.
Administration, Inhalation
Adult
Benzyl Alcohols
/ adverse effects
Bronchodilator Agents
/ adverse effects
Budesonide
Chlorobenzenes
/ adverse effects
Cohort Studies
Comorbidity
Drug Combinations
Fluticasone-Salmeterol Drug Combination
/ adverse effects
Formoterol Fumarate
/ therapeutic use
Humans
Pulmonary Disease, Chronic Obstructive
/ diagnosis
Quinuclidines
/ adverse effects
Retrospective Studies
Tiotropium Bromide
/ adverse effects
COPD
LAMA/LABA
comorbidities
medical costs
severe exacerbations
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
1149-1161Informations 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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