Literature DB >> 18294477

Post-myocardial infarction beta-blocker therapy: the bradycardia conundrum. Rationale and design for the Pacemaker & beta-blocker therapy post-MI (PACE-MI) trial.

Jeffrey J Goldberger1, Robert O Bonow, Michael Cuffe, Alan Dyer, Philip Greenland, Yves Rosenberg, Robert O'Rourke, Prediman K Shah, Sidney Smith.   

Abstract

Multiple clinical trials have demonstrated beta-blockers improving survival after myocardial infarction (MI). Patients with "bradycardia-related" contraindications to beta-blockers, such as those with asymptomatic bradycardia or AV conduction abnormalities, have been excluded from clinical trials of beta-blockers and continue to be excluded from post-MI beta-blocker therapy in routine clinical practice. These patients tend to be elderly and have a high 1-year mortality. If beta-blockers provide benefit to the post-MI patient independent of their heart rate-lowering effect, then these patients could benefit substantially from initiation of beta-blocker therapy. However, in this particular group of patients, beta-blockers can be safely initiated only if more severe or significant bradycardia can be prevented by pacemaker implantation. It is unclear whether adverse effects related to pacemaker implantation could also negate some or all of the hypothesized benefit of beta-blocker therapy. Although beta-blockers are particularly effective in the elderly, the benefit of beta-blocker therapy in patients with bradycardia-related contraindications to beta-blockers has not been established. The PACE-MI trial is a randomized controlled trial that will address whether beta-blocker therapy enabled by pacemaker implantation is superior to no beta-blocker and no pacemaker therapy after MI in patients with rhythm contraindications to beta-blockers or in those who have developed symptomatic bradycardia due to beta-blockers. The trial will randomize 1124 patients to standard therapy (not to include beta-blockers as patients must have a contraindication to be enrolled) or standard therapy plus pacemaker implantation and beta-blocker. The primary end point is the composite end point of total mortality plus nonfatal reinfarction.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18294477     DOI: 10.1016/j.ahj.2007.10.041

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  6 in total

1.  Treating cardiac arrhythmias detected with an implantable cardiac monitor in patients after an acute myocardial infarction.

Authors:  Christian Jons; Poul Erik Bloch Thomsen
Journal:  Curr Treat Options Cardiovasc Med       Date:  2012-02

2.  Changes in under-treatment after comprehensive geriatric assessment: an observational study.

Authors:  Linda R Tulner; Jos P C M van Campen; Suzanne V Frankfort; Cornelis H W Koks; Jos H Beijnen; Desiderius P M Brandjes; Paul A F Jansen
Journal:  Drugs Aging       Date:  2010-10-01       Impact factor: 3.923

3.  beta-Blocker use following myocardial infarction: low prevalence of evidence-based dosing.

Authors:  Jeffrey J Goldberger; Robert O Bonow; Michael Cuffe; Alan Dyer; Yves Rosenberg; Robert O'Rourke; Prediman K Shah; Sidney C Smith
Journal:  Am Heart J       Date:  2010-09       Impact factor: 4.749

4.  Antianginal medications and long-term outcomes after elective catheterization in patients with coronary artery disease.

Authors:  Lan Shen; John P Vavalle; Samuel Broderick; Linda K Shaw; Pamela S Douglas
Journal:  Clin Cardiol       Date:  2016-12       Impact factor: 2.882

5.  Effect of Beta-Blocker Dose on Survival After Acute Myocardial Infarction.

Authors:  Jeffrey J Goldberger; Robert O Bonow; Michael Cuffe; Lei Liu; Yves Rosenberg; Prediman K Shah; Sidney C Smith; Haris Subačius
Journal:  J Am Coll Cardiol       Date:  2015-09-29       Impact factor: 24.094

6.  Poor tolerance of beta-blockers by elderly patients with heart failure.

Authors:  Satoshi Yanagisawa; Noriyuki Suzuki; Toshikazu Tanaka
Journal:  Clin Interv Aging       Date:  2010-11-26       Impact factor: 4.458

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.