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Non-selective vs. selective beta-blocker treatment and the risk of thrombo-embolic events in patients with heart failure

  • Olav R. De Peuter
  • , Patrick C. Souverein
  • , Olaf H. Klungel
  • , Harry R. Bller
  • , Anthonius De Boer
  • , Pieter W. Kamphuisen

Research output: Contribution to journalArticleAcademicpeer-review

13 Citations (Scopus)

Abstract

Aims Heart failure (HF) is associated with a prothrombotic state, resulting in an increased risk for thrombo-embolic events. Studies suggest a reduced prothrombotic state when non-selective beta-blockers relative to selective beta-blockers are given. We studied the influence of non-selective beta-blockers compared with selective beta-blockers on the occurrence of arterial and venous thrombo-embolic events in patients with HF. Methods and results Data were obtained from the PHARMO Record Linkage System, a population-based registry of pharmacy records linked with hospital discharge records in The Netherlands. In the period of 1998-2007, 20 870 patients were hospitalized for HF.We used Cox regression analysis with time-varying beta-blocker covariate to assess the difference in the incidence of thrombo-embolic events [acute coronary syndrome (ACS), stroke, or pulmonary embolism] among patients. Median follow-up was 2.0 years (inter-quartile range: 0.7-4.1). Directly after discharge, 6558 patients were prescribed a selective beta-blocker and 2202 patients a non-selective beta-blocker. The hazard ratio (HR) for any thrombo-embolic event for non-selective beta-blockers compared with selective beta-blockers was 0.76 [95% confidence interval (CI): 0.64-0.89]. After adjustment, the difference remained (HR 0.84, 95% CI: 0.72-0.99). The effect was most prominent for ACS (HR 0.78, 95% CI: 0.65-0.93), and not clear for stroke (HR 1.00, 95% CI: 0.67-1.50) or pulmonary embolism (HR 1.33, 95% CI: 0.66-2.71). Conclusion In patients with HF, the use of non-selective beta-blockers was associated with a lower risk of thrombo-embolic events than selective beta-blockers. Whether this beneficial effect is caused by the additional beta2-receptor blockade remains to be elucidated. These findings need to be validated in a well-designed randomized study. © 2010 The Author.
Original languageEnglish
Pages (from-to)220-226
Number of pages7
JournalEuropean Journal of Heart Failure
Volume13
Issue number2
DOIs
Publication statusPublished - 1-Feb-2011
Externally publishedYes

Keywords

  • Beta-blockers
  • Epidemiology
  • Heart failure
  • Pharmacology
  • Thromboembolism
  • acebutolol
  • atenolol
  • beta adrenergic receptor blocking agent
  • bisoprolol
  • bumetanide
  • carvedilol
  • celiprolol
  • furosemide
  • labetalol
  • metoprolol
  • nebivolol
  • oxprenolol
  • pindolol
  • propranolol
  • sotalol
  • acute coronary syndrome
  • adult
  • aged
  • article
  • brain ischemia
  • cardiovascular risk
  • clinical assessment
  • confidence interval
  • female
  • follow up
  • hazard ratio
  • heart arrhythmia
  • heart failure
  • heart infarction
  • hospital discharge
  • hospitalization
  • human
  • lung embolism
  • major clinical study
  • male
  • medical record
  • Netherlands
  • population research
  • priority journal
  • proportional hazards model
  • register
  • cerebrovascular accident
  • thromboembolism

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