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Commentary

Beta 2 antagonism in acute respiratory failure

Rob Mac Sweeney12, PJ Devereaux3 and Daniel F McAuley12*

Author Affiliations

1 Regional Intensive Care Unit, Royal Victoria Hospital, Grosvenor Road, Belfast, BT12 6BA, Northern Ireland

2 Centre for Infection and Immunity, Health Sciences Building, Queen's University Belfast, 97 Lisburn Road, Belfast, BT9 7BL, Northern Ireland

3 McMaster University, Faculty of Health Sciences, 1200 Main Street West, Room 2C8, Hamilton, ON, Canada, L8N 3Z5

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Critical Care 2010, 14:1012  doi:10.1186/cc9359


See related research by Noveanu et al., http://ccforum.com/content/14/6/R198


The electronic version of this article is the complete one and can be found online at: http://ccforum.com/content/14/6/1012


Published:20 December 2010

© 2010 BioMed Central Ltd

Abstract

Post hoc analyses from the B-type natriuretic peptide for Acute Shortness of Breath Evaluation (BASEL)-II-ICU study suggest an association between beta-blocker usage at admission and improved mortality in patients treated in the intensive care unit for acute respiratory failure. Although this evidence is encouraging, there is a need for a phase 2 proof-of-concept randomized controlled trial of beta-blocker therapy in patients admitted with acute respiratory failure.

Commentary

In this issue of Critical Care, Noveanu and colleagues [1] present intriguing observational data from the B-type natriuretic peptide for Acute Shortness of Breath Evaluation (BASEL)-II-ICU study evaluating the association between beta-blocker therapy and mortality in 314 patients. Current dogma suggests a role for beta 2 agonism in the management of respiratory disease, most notably in asthma and chronic obstructive pulmonary disease (COPD). Beta 2 agonism was also recently investigated in the intensive care unit (ICU) for acute respiratory distress syndrome (ARDS) [2]. In addition to bronchodilatation and improvements in ventilatory mechanics, purported beneficial effects include improved endothelial function, cytoprotection, an anti-inflammatory effect, increased surfactant production, and increased alveolar fluid clearance [3]. However, despite these potential beneficial effects, a large randomized controlled trial (RCT) of nebulized salbutamol in ARDS, which has been published only in abstract form, was stopped early for futility. In addition, there is ongoing controversy over the safety of long-acting beta 2 agonists in the management of asthma, and data suggest that beta 2 agonism may increase cardiovascular morbidity in those with risk factors for cardiovascular disease [4].

The BASEL-II-ICU study was a prospective randomized trial evaluating the effect of BNP-guided therapy versus standard care in ICU patients with acute respiratory failure [1]. Beta-blocker therapy instituted before or after ICU care was associated with improved mortality both in-hospital and at 1 year in multivariable analyses. This association was demonstrated in stratified analyses for both cardiac and non-cardiac causes of acute respiratory failure. Among the factors limiting the generalizability of the data were the strict exclusion criteria, and many conditions commonly seen in the ICU, including sepsis, shock, renal failure, trauma, and prior cardiopulmonary resuscitation, were excluded. Furthermore, only 13% of the cohort with acute respiratory failure received invasive mechanical ventilation, although 50% did receive non-invasive mechanical ventilation. It would also be useful to know what causes of death were modified by beta 2 antagonism in acute respiratory failure. Another limitation of this observational data is that the models are at substantial risk of over-fitting given that the authors evaluated 40 variables despite having only 51 in-hospital deaths [5].

Why might beta 2 agonism be ineffective and antagonism be beneficial in acute respiratory failure? First, many patients admitted with acute respiratory failure will suffer cardiac ischemia, a condition that potentially can be prevented with a beta-blocker [6]. Beta-receptors form an integral component of the sympathetic nervous system. The three beta-receptor subtypes help coordinate neural, circulatory, gastrointestinal, digestive, urinary, hematological, metabolic, and immune function during the 'fight-or-flight response' induced by periods of stress. Initially, beta agonism diverts energy to vital organs and upregulates homeostatic mechanisms such as platelet activation and coagulation; however, prolonged beta adrenergic activation may prove detrimental. Data from RCTs have shown a beneficial effect of beta-blocker therapy in the treatment of chronic heart failure [7]. Observational data suggest a possible beneficial role for beta antagonism in trauma [8], including traumatic brain injury [9], and sepsis [10]. Two other studies have highlighted the benefits and risks of beta-blockers. The Clopidogrel and Metoprolol in Myocardial Infarction Trial (COMMIT), an RCT of 45,852 acute myocardial infarction patients randomly assigned to a beta-blocker or placebo, surprised many clinicians when it demonstrated no impact on 30-day mortality [11]. This trial demonstrated less re-infarction and ventricular fibrillation with beta-blocker therapy, but these beneficial effects were counterbalanced by an excess of death due to shock with beta-blocker therapy. Similarly, the Perioperative Ischemic Evaluation Study (POISE-1), an RCT of 8,351 non-cardiac surgery patients randomly assigned to a beta-blocker or placebo, demonstrated that a perioperative beta-blocker prevented perioperative myocardial infarction but increased the risk of death or stroke [12]. In POISE-1, the negative consequences of beta-blockade appeared to have occurred through an excess of clinically important hypotension. This excess is similar to the excess of cardiogenic shock witnessed with beta-blockade in COMMIT. These data highlight the potential benefits of a beta-blocker but also the need to exclude patients in shock or at high risk of shock and to intensely monitor and manage hemodynamic instability. Reassuringly, current data suggest that cardio-selective beta-blockers do not induce respiratory physiological impairment. In particular, beta-blockers are associated with improved outcomes in patients with COPD [13], a group theoretically at high risk from bronchospasm with beta antagonism.

The data emerging from beta adrenergic modulation in respiratory failure mirror those of statins. Statins were initially designed as cholesterol-lowering agents to reduce cardiovascular risk, and their pleiotropic effects were soon realized and matched by observational data showing associations between statin use and improved outcomes in cohorts with pneumonia and lung injury. Because a small prospective phase 2 RCT suggested potential benefit [14], statins are being investigated as a therapy for ARDS in at least two large RCTs in Europe and the US. Now, an appropriate phase 2 proof-of-concept RCT investigating beta 2 antagonism in acute respiratory failure with strict eligibility criteria would be an appropriate approach to define the role of beta-blockers in acute respiratory failure.

Abbreviations

ARDS: acute respiratory distress syndrome; BASEL: B-type natriuretic peptide for Acute Shortness of Breath Evaluation; BNP: B-type natriuretic peptide; COMMIT: Clopidogrel and Metoprolol in Myocardial Infarction Trial; COPD: chronic obstructive pulmonary disease; ICU: intensive care unit; POISE-1: Perioperative Ischemic Evaluation Study; RCT: randomized controlled trial.

Competing interests

AstraZeneca (London, UK) funded the drugs for the POISE-1 trial, for which PJD was the principal investigator. AstraZeneca manufactures metoprolol CR and beta-blockers. RMS and DFM declare that they have no competing interests.

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