Association of Race and Ethnicity With High-Potency P2Y12 Inhibitors Prescription Among Patients With Acute MI

Hend Mansoor1, Rebecca Young2,3, Lisa A Kaltenbach2,3

  • 1Department of Pharmacy Practice and Science (H.M.), University of Kentucky, Lexington.

Insights

Black and Hispanic patients with myocardial infarction (AMI) undergoing percutaneous coronary intervention (PCI) were less likely to receive high-potency P2Y12 inhibitors upon discharge. This disparity persists regardless of socioeconomic status, indicating a need for equitable care in AMI pharmacotherapy.

Area of Science:

  • Cardiovascular Medicine
  • Health Disparities Research
  • Pharmacotherapy Outcomes

Background:

  • Racial and ethnic disparities are documented in post-acute myocardial infarction (AMI) care.
  • High-potency P2Y12 inhibitors are guideline-recommended (Class I) for patients with AMI undergoing percutaneous coronary intervention (PCI).

Purpose of the Study:

  • To investigate racial and ethnic disparities in the prescription of high-potency P2Y12 inhibitors at discharge for AMI patients who underwent PCI.

Main Methods:

  • Analysis of consecutive patients with AMI undergoing PCI from the NCDR Cath PCI registry (April 2018 - June 2023).
  • Logistic regression models were used to assess the likelihood of high-potency P2Y12 inhibitor discharge prescription, adjusted for social deprivation and patient/procedure variables.

Main Results:

  • Among 1,662,387 patients, 9.9% were Black, 3.5% Asian, and 78.3% White; 8.1% were Hispanic.
  • 52.7% of patients received a high-potency P2Y12 inhibitor at discharge.
  • Black patients (aOR 0.93) and Hispanic patients (aOR 0.95) were less likely to receive these inhibitors compared to White and non-Hispanic patients, respectively. Asian patients were more likely (aOR 1.08).

Conclusions:

  • Significant racial and ethnic disparities exist in the discharge prescription of high-potency P2Y12 inhibitors for AMI patients post-PCI, even after accounting for socioeconomic status.
  • These findings underscore the need to address inequities in guideline-directed pharmacotherapy for AMI to improve patient outcomes.
Abstract

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