Should beta-blockers be given to patients with heart disease and peanut-induced anaphylaxis? A decision analysis

J Allergy Clin Immunol. 2004 May;113(5):977-82. doi: 10.1016/j.jaci.2004.02.043.

Abstract

Background: Beta-blocker therapy postmyocardial infarction is generally recommended because it reduces mortality. However, beta-blockers may increase anaphylaxis mortality in the growing population of patients with peanut-induced anaphylaxis.

Objective: We sought to assess the risks and benefits of beta-blocker therapy among patients with peanut allergy and heart disease.

Methods: We created a Markov model for patients with heart disease at risk for peanut-induced anaphylaxis to compare life expectancy with the following strategies: (1) beta-blocker and (2) no beta-blocker. Meta-analysis and a literature review were used to estimate model parameters. We performed sensitivity analysis to explore parameter uncertainty.

Results: For peanut-allergic patients who are postmyocardial infarction or who have congestive heart failure, the heart disease benefit of beta-blockers outweighs the increased likelihood of dying from anaphylaxis, increasing life expectancy by 9.4 and 17.4 months, respectively. Beta-blocker was preferred unless (1) the annual rate of moderate to severe anaphylaxis exceeded 6.0% for postmyocardial infarction and 15% for congestive heart failure patients; (2) beta-blocker therapy increased the incidence of moderate to severe anaphylaxis >2.5-fold for postmyocardial infarction and >5.8-fold for congestive heart failure patients; (3) anaphylaxis case fatality exceeded 6.5% postmyocardial infarction; or (4) beta-blocker therapy increased anaphylaxis case fatality >25-fold postmyocardial infarction.

Conclusion: Our results suggest that for patients postmyocardial infarction or with congestive heart failure who are at risk for peanut-induced anaphylaxis, beta-blocker use should still improve survival. However, the epidemiology of anaphylaxis and effects of beta-blocker therapy on anaphylaxis incidence and mortality require further study.

MeSH terms

  • Adrenergic beta-Antagonists / adverse effects
  • Adrenergic beta-Antagonists / therapeutic use*
  • Adult
  • Aged
  • Aged, 80 and over
  • Anaphylaxis / etiology
  • Decision Support Techniques
  • Heart Diseases / complications*
  • Heart Diseases / drug therapy*
  • Heart Failure / complications
  • Heart Failure / drug therapy
  • Humans
  • Middle Aged
  • Models, Biological
  • Myocardial Infarction / complications
  • Myocardial Infarction / drug therapy
  • Peanut Hypersensitivity / complications*
  • Risk Factors

Substances

  • Adrenergic beta-Antagonists