Krumholz HM, Hayes RJ, et al. We will conduct the review according to this published protocol and report any differences from it in the 'Differences between protocol and review' section of the review. Asaria P, When analysing continuous outcomes regarding missing data, a beneficial outcome will be the group mean plus two SDs (and one SD) of the group mean, and a harmful outcome will be the group mean minus two SDs (and one SD) of the group mean (Jakobsen 2014). Unclear risk of bias: the trial may or may not be free of other components that could put it at risk of bias. 2010 Apr 27;55(17):1780-7. doi: 10.1016/j.jacc.2010.01.024. Song F, 2 ((heart or cardiac or myocard*) adj2 (fail* or insufficien* or decomp*)).tw. ACE = angiotensin-converting enzyme; ARB = angiotensin receptor blocker. Guo H, sharing sensitive information, make sure youre on a federal Beta-blockers are a class of medicines commonly used to treat a wide range of problems involving your heart and your circulatory system. et al. International Conference on Harmonisation Expert Working Group. National Library of Medicine Wetterslev J, Capewell S, These metaanalyses showed that betablockers were associated with a decreased risk of death, improved NYHA class, decreased hospitalisation rates, and improved some types of exercise tolerance tests (Abdulla 2006; AlGobari 2013; Brophy 2001; Chatterjee 2013; Doughty 1997; Heidenreich 1997; Kotecha 2016; Lechat 1998; McAlister 2009). Hebert PR, Times have changed et al. Hence, we will estimate the required information size based on the SD observed in the control group of trials with low risk of bias or lower risk of bias and a minimal relevant difference of the observed SD/2, an alpha value of 2.5% for primary outcomes and 1.67% for secondary outcomes, a beta value of 10%, and a diversity suggested by the trials in the metaanalysis (Jakobsen 2014; Wetterslev 2009). Copyright 2023 American Academy of Family Physicians. Notes: funding of trial, and notable conflicts of interest of trial authors. The estimated associations from the imputed datasets will differ and are only useful when averaged together to give overall estimated associations. Barst RJ, Low risk of bias: we will classify the outcome result as at overall 'low risk of bias' only if all of the bias domains described in the above paragraphs are classified as at low risk of bias. EJ, Evans
Schweizer P, Jessup M, FerreroGregori A, Any patient with reduced ejection fraction and symptomatic heart failure or ischemic cardiomyopathy whose life expectancy is more than one year may be referred to electrophysiology for possible device therapy. As of 2010, Perspective contained data on more than 130 million cumulative hospital discharges, representing approximately 20% of annual acute care hospitalizations in the United States. Angina may be provoked by an activity or exercise or any other physical or mental stress that increases the heart's demand for blood. Diemberger I, Spadotto A, Massaro G, Amadori M, Damaschin L, Martignani C, Ziacchi M, Biffi M, Gali N, Boriani G. Biology (Basel). The Cochrane Collaboration, 2011. ACCF/AHA/AMA-PCPI 2011 performance measures for adults with heart failure. B, Benjamin
Benjamin EJ, Influence of reported study design characteristics on intervention effect estimates from randomized, controlled trials. FOIA Manzano L, Chambless LE. R, Fakih
Fagerberg B, Cooper G 4th. The required information size takes into account the event proportion in the control group, the assumption of a plausible risk ratio (RR) reduction, and the heterogeneity of the metaanalysis (Turner 2013; Wetterslev 2009). Jakobsen JC, Tu JV. Seijas Amigo J, Levy D, 2021. High blood pressure. We will search the websites of the European Medicines Agency (EMA) (www.ema.europa.eu), the US Food and Drug Administration (FDA) (www.fda.gov), and pharmaceutical company sources (www.astrazenecaus.com/; http://lifepharmaceuticalcompany.com/; http://pharma.bayer.com/; and http://pl.gsk.com/) for ongoing or unpublished trials. government site. Voors AA, Misdiagnosis of community-acquired pneumonia and inappropriate utilization of antibiotics: side effects of the 4-h antibiotic administration rule. Angiotensin is a chemical in your body that narrows your blood vessels. We will use STATA in case of zeroevent trials (STATA 2015), where RevMan 5 zeroevent handling (replacing zero with a constant of 0.5) is not sufficient (e.g. Guyatt GH, Moorjani N, Higgins JPT, A neurohormonal activity, led by the sympathetic nervous system and neurohormonal cascade (mainly the reninangiotensinaldosterone system (RAAS), endothelin, neprilysin, and various inflammatory cytokines), is thought to be the root to these deleterious effects (Ferrario 2006; Mann 2005; Mazurek 2015). AHA/ACCF secondary prevention and risk reduction therapy for patients with coronary and other atherosclerotic vascular disease: 2011 update: a guideline from the American Heart Association and American College of Cardiology Foundation. Ezekowitz JA, Aspirin. In case there is some evidence of effect of the intervention, as a supplementary TSA will use the limit of the CI closest to 0.00 as the anticipated intervention effect (Jakobsen 2014). Cardioselective. Bertel V, However, a metaanalysis comparing betablockers versus placebo showed no difference on depressive symptoms and only a minor increase in sexual dysfunction and fatigue in patients randomised to betablockers compared with placebo (Ko 2002). This enables one to determine the statistical inference concerning cumulative metaanalysis that has not yet reached the required information size (Wetterslev 2008; Wetterslev 2017). If you're on blood thinners, beware of aspirin. Empirical evidence of bias. We will use a data collection form for trial characteristics and outcome data that has been piloted on at least one trial in the review. In addition, whereas a number of therapies have been shown to reduce morbidity and mortality in HFrEF, the evidence of therapeutic benefit in HFpEF is much scarcer (Jessup 2003; McMurray 2012; Owan 2006). PMC Arab T, If we identify trials with zero events in one or both intervention groups, then we will perform a supplementary analysis using betabinominal regression (Cheng 2016; Kuss 2015; Sharma 2017). Yndestad A. RO, Ganiats
AMI indicates acute myocardial infarction; ICU, intensive care unit; and IV, intravenous. Inhibition of adrenergic activity with the use of betablockers is associated with attenuation of all these effects (Baker 2014; Chatterjee 2002; Farrell 2002; McMurray 2012). Whitlock RM. This project was supported by the National Institute for Health Research, via Cochrane Infrastructure to the Heart Group. We will also examine any relevant retraction statements and errata for included studies. Author disclosure: No relevant financial affiliations. It aims to allow for the uncertainty about the missing data by creating several different plausible imputed data sets and appropriately combining results obtained from each of them. Beta-blockers are a class of medication used to block the effects of stress hormones such as adrenaline on the heart. Catarino PA, We will calculate the mean differences (MD) with 95% CI and TSAadjusted CI (Thorlund 2011) for continuous outcomes. Mensah GA, Beta blockers work by blunting the noradrenergic hormonal influences and have long-term benefits. Iorio A, Soman A, Nondihydropyridine CCBs should not be combined with beta blockers because CCBs can enhance the negative inotropic, chronotropic, and dromotropic effects of beta blockers. The safety and tolerability of beta blockers in heart failure with reduced ejection fraction: is the current underutilization of this evidencebased therapy justified? Nochioka K, In vitro studies and animal studies suggest that the mechanism of action is through sodium retention, peripheral vasoconstriction, abnormalities in cellular signalling, increased myocyte apoptosis, necrosis, inflammation, direct toxic effects on cardiac cells, and initiation of myocardial fibrosis (Aukrust 2005; Hunt 2005; Mann 1992; Mazurek 2015; Moorjani 2009; Weber 1994). The most frequent side effects of beta-blockers include: hypotension, bradycardia, bronchospasm, cold extremities, fatigue, headache, sleep disturbances and increased insulin resistance [1]. Erbel R, The risk of death in patients with heart failure is high, with an estimated annual mortality of approximately 21% in men and 17% in women; the risk increases to over 50% five years after the heart failure diagnosis has been made (Bui 2011; Dunlay 2014; Kannel 2000; Levy 2002; Mozaffarian 2016; Roger 2004; Roger 2013). doi:10.1001/jamainternmed.2013.7717, To increase -blocker treatment for patients with heart failure and left ventricular systolic dysfunction, recently updated performance measures recommend that oral -blocker therapy be started by the time of hospital discharge in patients hospitalized for decompensated systolic heart failure.1 These performance measures make clear that patients in whom a -blocker therapy is started, should not be hospitalized in an intensive care unit [ICU], should have no or minimal evidence of fluid overload or volume depletion, and should not have required recent treatment with an intravenous positive inotropic agent.1(p2393). Women's health is once again the center of a political ping-pong match with evidence-based science on one side and anti-choice advocates on the other. 13 However, preclinical animal studies have demonstrated increased survival with -blocker therapy in experimental PAH. Comfortable at rest, but less than ordinary activity causes symptoms of HF. American College of Cardiology Foundation. valve surgery for valvular disease, specific pharmacological therapy for left ventricular systolic dysfunction, etc.) Pham DT, Zile
High risk of bias: the outcome result will be classified 'high risk of bias' if any of the bias risk domains described in the above are classified as 'unclear' or 'high risk of bias'. Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 (updated March 2011). Naunyn Schmiedebergs Arch Pharmacol. et al. Hodge DO, I. D'Agostino RB, The aim of the present review is to analyze the available evidence on the use of -blockers in HFrEF patients with the most common comorbidities. Angiotensin II receptor blockers help relax your veins and arteries to lower your blood pressure and make it easier for your heart to pump blood. It works by affecting the response to nerve impulses in certain parts of the body, like the heart. JT, Heidenreich
Katus HA, Right ventricular heart failure is a hydraulic problem caused by impaired function of the pump, the valves, or the vessels and often occurring as a result of decompensated left ventricular heart failure (Hrymak 2017; Kapur 2017; Voelkel 2006). We further excluded hospitalizations with a pediatric attending physician to concentrate on care patterns of physicians who treat adults. Groarke JD, The hospitalizations in which -blocker therapy was started comprised 24.9% (P), 30.9% (A-R), and 40.4% (AMI-R) of all heart failure hospitalizations potentially eligible for -blocker therapy initiation. Lee DS, Privacy Policy| Sondergaard L, Angina can be "stable" or "unstable." We conducted a retrospective cohort study using Perspective, a voluntary, fee-supported database developed by Premier Inc for measuring quality and health care utilization. Low risk of bias: the outcome result will be classified as overall 'low risk of bias' only if all of the bias domains described in the above paragraphs are classified as low risk of bias. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. GC, Heywood
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