Literature DB >> 1356781

The role of beta receptor blockade in preventing sudden death.

J Wikstrand1, M Kendall.   

Abstract

The high mortality rate from coronary heart disease in hypertensives can only be substantially reduced if sudden coronary death rates can be decreased. The aim of this review is to discuss how treatment may be tailored to reduce the risk of sudden death in high-risk patients. Clinical trials have not yet produced long-term primary prevention data on the effects of angiotensin converting enzyme (ACE) inhibitors, calcium antagonists or alpha-blockers on cardiovascular complications and sudden death in hypertensive patients. Further, the conclusion from large-scale secondary preventive studies presently available on ACE inhibitors and calcium antagonists is that their impact on sudden death has been disappointing. By contrast, some beta-blockers have reduced sudden death and other coronary events both in primary and secondary preventive studies. The benefits have been attributed to beta 1-blockade, and seem to be independent of blood pressure control. It cannot be assumed that all beta-blockers are equally effective in preventing ventricular fibrillation, sudden death and other coronary events. To date, the best documented data cover the lipophilic beta-blockers and it is speculated that by increasing levels of cardiac vagal tone and electrical stability in the heart, beta 1-blockade in the brain might contribute to the reduction in sudden death risk seen with these beta-blockers.

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Year:  1992        PMID: 1356781

Source DB:  PubMed          Journal:  Eur Heart J        ISSN: 0195-668X            Impact factor:   29.983


  10 in total

Review 1.  Beta-blockers in the management of hypertension in patients with type 2 diabetes mellitus: is there a role?

Authors:  F Dunne; M J Kendall; U Martin
Journal:  Drugs       Date:  2001       Impact factor: 9.546

2.  Prolonged QT interval as a predictor of mortality in diabetic nephropathy.

Authors:  P T Sawicki; R Dähne; R Bender; M Berger
Journal:  Diabetologia       Date:  1996-01       Impact factor: 10.122

Review 3.  Approaches to meeting the criteria for fixed dose antihypertensive combinations. Focus on metoprolol.

Authors:  M J Kendall
Journal:  Drugs       Date:  1995-09       Impact factor: 9.546

4.  Lipophilic versus hydrophilic beta(1) blockers and the cardiac sympatho-vagal balance during stress and daily activity in patients after acute myocardial infarction.

Authors:  A Kardos; V Long; J Bryant; J Singh; P Sleight; B Casadei
Journal:  Heart       Date:  1998-02       Impact factor: 5.994

5.  Clinical covariates of abnormal heart rate turbulence in coronary patients.

Authors:  Iwona Cygankiewicz; Jerzy Krzysztof Wranicz; Janusz Zaslonka; Halina Bolinska; Wojciech Zareba
Journal:  Ann Noninvasive Electrocardiol       Date:  2003-10       Impact factor: 1.468

6.  Comparative effectiveness of 2 β-blockers in hypertensive patients.

Authors:  Emily D Parker; Karen L Margolis; Nicole K Trower; David J Magid; Heather M Tavel; Susan M Shetterly; P Michael Ho; Bix E Swain; Patrick J O'Connor
Journal:  Arch Intern Med       Date:  2012-10-08

Review 7.  A risk-benefit assessment of celiprolol in the treatment of cardiovascular disease.

Authors:  M J Kendall; I Rajman
Journal:  Drug Saf       Date:  1994-03       Impact factor: 5.606

8.  Exercise metabolism in healthy volunteers taking atenolol, high and low doses of metoprolol CR/Z0K, and placebo.

Authors:  A Head; S Maxwell; M J Kendall; C Eagles
Journal:  Br J Clin Pharmacol       Date:  1994-12       Impact factor: 4.335

Review 9.  Sudden cardiac death and the potential role of beta-adrenoceptor-blocking drugs.

Authors:  I Rajman; M J Kendall
Journal:  Postgrad Med J       Date:  1993-12       Impact factor: 2.401

10.  Metoprolol reduces proinflammatory cytokines and atherosclerosis in ApoE-/- mice.

Authors:  Marcus A Ulleryd; Evelina Bernberg; Li Jin Yang; Göran M L Bergström; Maria E Johansson
Journal:  Biomed Res Int       Date:  2014-07-08       Impact factor: 3.411

  10 in total

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