Ticagrelor and Infection Risk in Patients with Coronary Artery Disease

Lourdes Vicent1,2, Vanesa Bruña3,4, Carolina Devesa4,5,6

  • 1Servicio de Cardiología, Hospital General Universitario 12 de Octubre, Madrid, Spain, mlourdesvicent@gmail.com.

Cardiology
|September 22, 2021
PubMed

Insights

Ticagrelor, a P2Y12 inhibitor, was associated with a lower infection risk in coronary artery disease patients compared to prasugrel and clopidogrel. This finding suggests a potential benefit of ticagrelor in managing infections in this population.

Area of Science:

  • Cardiology
  • Infectious Diseases
  • Pharmacology

Background:

  • Ticagrelor exhibits in vitro bactericidal properties.
  • Clinical observations suggest ticagrelor may be beneficial in treating infections.

Purpose of the Study:

  • To investigate and compare the incidence of infections in patients treated with three different P2Y12 receptor inhibitors: ticagrelor, prasugrel, and clopidogrel.

Main Methods:

  • A retrospective registry study was conducted in a cardiology department.
  • Patients with coronary artery disease (CAD) discharged on ticagrelor, prasugrel, or clopidogrel between March 2017 and June 2019 were analyzed.
  • Infection risk was assessed during the P2Y12 inhibitor treatment period (mean 12.4 months).

Main Results:

  • Of 250 patients, 87 (34.8%) experienced infections. Ticagrelor (25.3%) was associated with fewer infections than prasugrel (33.7%) and clopidogrel (48.6%) (p=0.009).
  • Ticagrelor use was independently linked to a reduced likelihood of infection (HR 0.52; 95% CI 0.28-0.95; p=0.035) compared to clopidogrel.
  • ST-segment elevation myocardial infarction (STEMI) was the primary indication for drug use, with prasugrel predominantly used in STEMI cases.

Conclusions:

  • Ticagrelor-treated patients with coronary artery disease showed a lower incidence of infections compared to those on other P2Y12 inhibitors.
  • Further research is warranted to elucidate the specific bactericidal mechanisms of ticagrelor in this clinical context.
Abstract

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