Abstract
β-blockers are commonly used in the treatment of cardiovascular diseases and to reduce the risk of re-infarction and the related mortality after myocardial infarction [1]. In fact, they almost universally reduce myocardial oxygen consumption and hence the degree of cardiac ischemia. Two randomized controlled trials (RCT) demonstrated that the perioperative use of β-blockers could reduce the incidence of cardiac complications responsible for significant morbidity and mortality after cardiac surgery [2, 3]. However, these results were not confirmed in three subsequent RCTs and in a large cohort study [4–7]. Similarly, the Perioperative Ischemic Evaluation Study (POISE) found that individuals receiving metoprolol succinate 30 days before surgery had a reduced risk of postoperative myocardial infarction compared to the control group but an increased risk of stroke and death associated with an increased incidence of hypotension, bradycardia and bleeding [8]. Over the years, these surprising results led to different changes in practice guidelines; specifically, the recent 2014 American College of Cardiology/American Heart Association (ACC/AHA) guidelines recommend that perioperative β-blockers should be started only in patients considered to be at intermediate or high risk for myocardial ischemia [9].
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Coppola, S., Froio, S., Chiumello, D. (2015). β-Blockers in Critically Ill Patients: From Physiology to Clinical Evidence. In: Vincent, JL. (eds) Annual Update in Intensive Care and Emergency Medicine 2015. Annual Update in Intensive Care and Emergency Medicine 2015, vol 2015. Springer, Cham. https://doi.org/10.1007/978-3-319-13761-2_11
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DOI: https://doi.org/10.1007/978-3-319-13761-2_11
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