Cardioprotective medication use in hemodialysis patients

Lisa M Miller1, Wilma M Hopman, Jocelyn S Garland

  • 1Section of Nephrology, University of Manitoba, Winnipeg, Canada. lmiller@exchange.hsc.mb.ca

Insights

Cardioprotective medication use is low in hemodialysis patients, despite high cardiovascular disease risk. Increased attention to prescribing these vital medications is needed to reduce mortality in this population.

Area of Science:

  • Nephrology
  • Cardiology
  • Clinical Pharmacy

Background:

  • Cardiovascular disease (CVD) is the primary cause of death in end-stage renal disease (ESRD) patients, exceeding 50% of mortality.
  • Cardioprotective medications like ACEIs, beta-blockers, ASA, and statins reduce mortality in the general population.
  • Optimizing cardioprotective medication use in ESRD patients is crucial for improving outcomes.

Purpose of the Study:

  • To assess the prescription rates of key cardioprotective medications in a hemodialysis population.
  • To identify factors associated with the use of these medications in hemodialysis patients.

Main Methods:

  • A cross-sectional study involving 185 prevalent hemodialysis patients.
  • Data collected via chart review, focusing on medication use and patient demographics.
  • No exclusion criteria were applied, and contraindications were not assessed.

Main Results:

  • Only 24.9% of patients received ACEIs/ARBs, 31.9% beta-blockers, 37.8% ASA, and 45.4% statins.
  • Patients with established coronary artery disease (CAD) were significantly more likely to receive these medications.
  • No significant difference in medication use was observed between diabetic and non-diabetic patients.

Conclusions:

  • A substantial proportion of hemodialysis patients do not receive recommended cardioprotective medications.
  • The high cardiovascular mortality in this population underscores the need for improved risk factor management.
  • Increased focus on prescribing cardioprotective therapies is warranted for hemodialysis patients.
Abstract

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