4.6 Article

Cancer Patients Have a Higher Risk of Thrombotic and Ischemic Events After Percutaneous Coronary Intervention

期刊

JACC-CARDIOVASCULAR INTERVENTIONS
卷 14, 期 10, 页码 1094-1105

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.jcin.2021.03.049

关键词

cancer; coronary artery disease; myocardial infarction; stent thrombosis

资金

  1. National Cancer Institute [CA233610]
  2. Miami Heart Foundation
  3. Mayo Clinic Department of Cardiovascular Medicine

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This study found that cancer patients have a higher risk of stent thrombosis and myocardial infarction after PCI compared to noncancer patients, especially in the first year post-PCI. The dual antiplatelet therapy score is predictive of thrombotic and ischemic events in both groups, indicating the importance of this score in decision-making for antiplatelet therapy.
OBJECTIVES This study sought to define the risk of stent thrombosis (ST) and myocardial infarction (MI) in cancer patients compared with noncancer patients after percutaneous coronary intervention (PCI). BACKGROUND Cancer patients are considered to be at high thrombotic risk, but data on whether this is the case after PCI remain inconclusive. METHODS Cancer patients undergoing PCI at Mayo Clinic Rochester from January 1, 2003, to December 31, 2013, were identified by cross-linking institutional cancer and PCI databases and by propensity score matching to noncancer patients. The combined primary endpoint was all-cause mortality, MI, and revascularization rate at 5-year follow-up. Secondary endpoints were the individual primary endpoint components, cause of mortality, ST, and Bleeding Academic Research Consortium 2+ bleeding. RESULTS The primary endpoint occurred in 48.6% of 416 cancer and in 33.0% of 768 noncancer patients (p < 0.001). In competing risk analyses, cancer patients had a higher rate of noncardiac death (24.0% vs. 10.5%; p < 0.001) and a lower rate of cardiac death (5.0% vs. 11.7%; p < 0.001). Cancer patients had a higher rate of MI (16.1% vs. 8.0%; p < 0.001), ST (6.0% vs. 2.3%; p < 0.001), repeat revascularization (21.2% vs. 10.0%; p < 0.001), and bleeding (6.7% vs. 3.9%; p = 0.03). The most critical period for ST in cancer patients was in the first year after PCI. The dual antiplatelet therapy score was predictive of thrombotic and ischemic events in both groups. CONCLUSIONS Cancer patients have a higher risk of thrombotic and ischemic events after PCI, identifiable by a high dual antiplatelet therapy score. These findings have important implications for antiplatelet therapy decisions.

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