Medication management patterns among Medicare beneficiaries with chronic obstructive pulmonary disease who initiate nebulized arformoterol treatment

Int J Chron Obstruct Pulmon Dis. 2019 May 15:14:1019-1031. doi: 10.2147/COPD.S199251. eCollection 2019.

Abstract

Purpose: Global evidence-based treatment strategies for chronic obstructive pulmonary disease (COPD) recommend using long-acting bronchodilators (LABDs) as maintenance therapy. However, COPD patients are often undertreated. We examined COPD treatment patterns among Medicare beneficiaries who initiated arformoterol tartrate, a nebulized long-acting beta2 agonist (LABA), and identified the predictors of initiation. Methods: Using a 100% sample of Medicare administrative data, we identified beneficiaries with a COPD diagnosis (ICD-9 490-492.xx, 494.xx, 496.xx) between 2010 and 2014 who had ≥1 year of continuous enrollment in Parts A, B, and D, and ≥2 COPD-related outpatient visits within 30 days or ≥1 hospitalization(s). After applying inclusion/exclusion criteria, three cohorts were identified: (1) study group beneficiaries who received nebulized arformoterol (n=11,886), (2) a subset of the study group with no LABD use 90 days prior to initiating arformoterol (n=5,542), and (3) control group beneficiaries with no nebulized LABA use (n=220,429). Logistic regression was used to evaluate predictors of arformoterol initiation. Odds ratios (ORs), 95% confidence intervals (CIs), and p values were computed. Results: Among arformoterol users, 47% (n=5,542) had received no LABDs 90 days prior to initiating arformoterol. These beneficiaries were being treated with a nebulized (50%) or inhaled (37%) short-acting bronchodilator or a systemic corticosteroid (46%), and many received antibiotics (37%). Compared to controls, beneficiaries who initiated arformoterol were significantly more likely to have had an exacerbation, a COPD-related hospitalization, and a pulmonologist or respiratory therapist visit prior to initiation (all p<0.05). Beneficiaries with moderate/severe psychiatric comorbidity or dual-eligible status were significantly less likely to initiate arformoterol, as compared to controls (all p<0.05). Conclusion: Medicare beneficiaries who initiated nebulized arformoterol therapy had more exacerbations and hospitalizations than controls 90 days prior to initiation. Findings revealed inadequate use of maintenance medications, suggesting a lack of compliance with evidence-based treatment guidelines.

Keywords: COPD; Medicare; arformoterol; long-acting beta2-agonists; nebulized therapy; treatment patterns.

Publication types

  • Observational Study

MeSH terms

  • Administration, Inhalation
  • Administrative Claims, Healthcare
  • Adrenergic beta-2 Receptor Agonists / administration & dosage*
  • Aerosols
  • Aged
  • Aged, 80 and over
  • Bronchodilator Agents / administration & dosage*
  • Databases, Factual
  • Disease Progression
  • Female
  • Formoterol Fumarate / administration & dosage*
  • Guideline Adherence / trends
  • Hospitalization
  • Humans
  • Lung / drug effects*
  • Lung / physiopathology
  • Male
  • Medicare*
  • Medication Therapy Management / trends*
  • Middle Aged
  • Nebulizers and Vaporizers
  • Practice Guidelines as Topic
  • Practice Patterns, Physicians' / trends*
  • Pulmonary Disease, Chronic Obstructive / diagnosis
  • Pulmonary Disease, Chronic Obstructive / drug therapy*
  • Pulmonary Disease, Chronic Obstructive / physiopathology
  • Retrospective Studies
  • Time Factors
  • Treatment Outcome
  • United States

Substances

  • Adrenergic beta-2 Receptor Agonists
  • Aerosols
  • Bronchodilator Agents
  • Formoterol Fumarate