beta-Blockers, heart disease and COPD: current controversies and uncertainties.

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Citation

Baker JG, Wilcox RG

beta-Blockers, heart disease and COPD: current controversies and uncertainties.

Thorax. 2017 Mar;72(3):271-276. doi: 10.1136/thoraxjnl-2016-208412. Epub 2016 Dec 7.

PubMed ID
27927840 [ View in PubMed
]
Abstract

Treating people with cardiovascular disease and COPD causes significant clinician anxiety. beta-Blockers save lives in people with heart disease, specifically postinfarction and heart failure. COPD and heart disease frequently coexist and people with both disorders have particularly high cardiovascular mortality. There are concerns about giving beta-blockers to people with concomitant COPD that include reduced basal lung function, diminished effectiveness of emergency beta-agonist treatments, reduced benefit of long-acting beta-agonist treatment and difficulty in discriminating between asthma and COPD. beta-Blockers appear to reduce lung function in both the general population and those with COPD because they are poorly selective for cardiac beta1-adrenoceptors over respiratory beta2-adrenoceptors, and studies have shown that higher beta-agonist doses are required to overcome the beta-blockade. COPD and cardiovascular disease share similar environmental risks and both disease states have high adrenergic and inflammatory activation. beta-Blockers may therefore be particularly helpful in reducing cardiovascular events in this high-risk group. They may reduce the background inflammatory state, and inhibit the tachycardia and hypertension associated with both the endogenous adrenaline and high-dose beta-agonist treatment associated with acute exacerbations of COPD. Some studies have suggested no increased and, at times, reduced mortality in patients with COPD taking beta-blockers for heart disease. However, these are all observational studies and there are no randomised controlled trials. Potential ways to improve this dilemma include the development of highly beta1-selective beta-blockers or the use of non-beta-blocking heart rate reducing agents, such as ivabridine, if these are proven to be beneficial in randomised controlled trials.

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