Annals of the American Thoracic Society: Published on October, 2022
Chronic obstructive pulmonary disease (COPD) is a leading
cause of death worldwide [1, 2]. COPD exacerbations that are related to poor
prognosis and severe COPD exacerbations requiring hospital admission.
Beta-adrenoceptor (β-ADR) antagonists, or “beta blockers,”
are indicated for the treatment of heart failure, hypertension, and ischaemic
heart disease, all of which are more common in patients with COPD.
There was a historic concern over prescribing beta-blocker
therapy in patients with COPD due to the fear of increased exacerbation
frequency, as exacerbations of COPD are associated with increased mortality and
lung function decline.
Cardioselective beta blockers are well-tolerated in patients
with moderate to severe COPD, demonstrating no negative impact on
pulmonary function, objective measures of dyspnea, and 6-minute walk distance.
This study evaluated the change in lung function (FEV1 and
FVC) and chronic obstructive pulmonary disease (COPD) exacerbations in patients
using less cardioselective beta blockers metoprolol versus placebo.
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While metoprolol did not yield promising results in
reducing exacerbations, Authors reinforced the evidence that metoprolol was
well-tolerated in terms of pulmonary function.
This study found decreases in FEV1 and
FVC values in the metoprolol group early during treatment; it did not find
other clear associations between more severe exacerbations and metoprolol use.
Furthermore, this study demonstrated that FVC
bronchodilator responsiveness, independent of metoprolol use, was
associated with a higher rate of severe COPD exacerbations.
This study supports the idea that COPD is a heterogeneous
disease, and some phenotypes are more prone to severe exacerbations (regardless
of metoprolol or other medication use).
Conclusions: Metoprolol was associated with reduced lung function
during the early part of the treatment period, but these effects were modest
and did not persist.
Early lung function reduction and baseline bronchodilator
responsiveness did not interact with the treatment arm to predict exacerbations;
however, baseline FVC bronchodilator responsiveness was associated with a 60%
higher rate of severe or very severe exacerbations.
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