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Patient preferences for thrombolytic therapy in acute myocardial infarction

E J Stanek1, J W Cheng, P J Peeples

  • 1Department of Pharmacy Practice and Pharmacy Administration, Philadelphia College of Pharmacy and Science, PA 19104, USA.

Insights

Patient preferences for acute myocardial infarction thrombolytic therapy reveal a significant shift from tissue plasminogen activator (tPA) to streptokinase (SK) when drug costs are considered, especially for self-payers.

Area of Science:

  • Cardiology
  • Pharmacoeconomics
  • Health Services Research

Background:

  • Optimal thrombolytic therapy for acute myocardial infarction (AMI) remains debated professionally.
  • Patient perspectives on thrombolytic treatment choices for AMI have not been previously explored.

Purpose of the Study:

  • To determine patient preferences for tissue plasminogen activator (tPA) versus streptokinase (SK) in treating AMI.
  • To assess how clinical outcomes (mortality, stroke) and drug costs influence these preferences.

Main Methods:

  • A questionnaire was administered to patients with suspected or known coronary artery disease.
  • Patients evaluated treatment preferences based on GUSTO-1 trial data, drug costs, and payer perspectives (self, third-party, government).

Main Results:

  • Tissue plasminogen activator (tPA) was initially preferred when considering only mortality and stroke rates (78%).
  • Preference for tPA significantly decreased to 43% when drug acquisition costs were introduced, particularly under a self-pay model.
  • A similar, though less pronounced, cost-driven shift towards streptokinase (SK) was observed across different payer designations.

Conclusions:

  • Patient preferences for AMI thrombolytics involve a trade-off between clinical benefits and cost.
  • Incorporating drug costs substantially influences patient choice, favoring SK over tPA, especially in self-pay scenarios.
  • These findings highlight the importance of patient values in guiding thrombolytic therapy decisions and policy discussions.
Abstract

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