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Long-acting antimuscarinic therapy in patients with chronic obstructive pulmonary disease receiving beta-blockers.

AbstractBACKGROUND:
Beta-blocker therapies for cardiovascular comorbidities are often withheld in patients with chronic obstructive pulmonary disease (COPD) due to potential adverse effects on airway obstruction. We carried out a post hoc analysis to determine the efficacy and safety of aclidinium in patients with moderate-to-very severe COPD and increased cardiovascular risk receiving beta-blockers at baseline versus non-users.
METHODS:
ASCENT-COPD was a Phase 4, multicenter, double-blind, randomized, placebo-controlled, parallel-group study. Patients were randomized 1:1 to aclidinium or placebo twice-daily for up to 3 years. Outcomes included risk of (time to first) major adverse cardiovascular events (MACE), all-cause mortality, and lung function over 3 years, and exacerbations over 1 year.
RESULTS:
Of 3589 patients, 1269 (35.4%) used beta-blockers and 2320 (64.6%) were non-users at baseline. Aclidinium did not statistically increase the risk of MACE (beta-blocker user: hazard ratio 1.01 [95% CI 0.62-1.64]; non-user: 0.80 [0.51-1.24]; interaction P = 0.48) or all-cause mortality (beta-blocker user: 1.13 [0.78-1.64]; non-user: 0.89 [0.62-1.26]; interaction P = 0.35), in patients using beta-blockers. Aclidinium reduced annualized rate of moderate-to-severe COPD exacerbation (beta-blocker user: rate ratio 0.75 [95% CI 0.60-0.94, P = 0.013]; non-user: 0.79 [0.67-0.93, P = 0.005]), delayed time to first exacerbation, and improved lung function versus placebo. There was greater trough FEV1 benefit in beta-blocker users versus non-users (least squares mean difference at 52 weeks: 111 mL [95% CI 74 mL-147 mL] versus 69 mL [42 mL-97 mL]; interaction P = 0.041).
CONCLUSIONS:
This post hoc analysis supports long-acting anti-muscarinic use with concomitant beta-blockers in patients with moderate-to-very severe COPD and cardiovascular comorbidity.
TRIAL REGISTRATION:
ClinicalTrials.gov, NCT01966107, Registered 16 October 2013, https://clinicaltrials.gov/ct2/show/NCT01966107 .
AuthorsKenneth R Chapman, Robert A Wise, Benjamin M Scirica, Deepak L Bhatt, Sami Z Daoud, Dan Lythgoe, Esther Garcia Gil
JournalRespiratory research (Respir Res) Vol. 22 Issue 1 Pg. 272 (Oct 22 2021) ISSN: 1465-993X [Electronic] England
PMID34686204 (Publication Type: Clinical Trial, Phase IV, Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial)
Copyright© 2021. The Author(s).
Chemical References
  • Adrenergic beta-Antagonists
  • Muscarinic Antagonists
  • Tropanes
  • aclidinium bromide
Topics
  • Adrenergic beta-Antagonists (adverse effects, therapeutic use)
  • Aged
  • Canada
  • Disease Progression
  • Double-Blind Method
  • Drug Therapy, Combination
  • Female
  • Forced Expiratory Volume
  • Humans
  • Lung (drug effects, physiopathology)
  • Male
  • Middle Aged
  • Muscarinic Antagonists (adverse effects, therapeutic use)
  • Pulmonary Disease, Chronic Obstructive (diagnosis, drug therapy, mortality, physiopathology)
  • Recovery of Function
  • Severity of Illness Index
  • Time Factors
  • Treatment Outcome
  • Tropanes (adverse effects, therapeutic use)
  • United States
  • Vital Capacity

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