Prognostic Implication of Platelet Reactivity According to Procedural Complexity After PCI: Subanalysis of PTRG-DES Consortium
- PMID: 38463677
- PMCID: PMC10920055
- DOI: 10.1016/j.jacasi.2023.10.011
Prognostic Implication of Platelet Reactivity According to Procedural Complexity After PCI: Subanalysis of PTRG-DES Consortium
Abstract
Background: Complex percutaneous coronary intervention (C-PCI) and high platelet reactivity (HPR) have been proposed as representative risk factors for the high ischemic phenotype. Uncertainty remains regarding the relative prognostic importance of these factors.
Objectives: This study aimed to investigate the prognostic implication of HPR according to procedural complexity.
Methods: Patients treated with drug-eluting stent implantation (PTRG-PFT cohort; N = 11,714) were classified according to procedural complexity. HPR criteria were determined using VerifyNow (≥252 P2Y12 reaction units). The major adverse cardiac and cerebrovascular events (MACCE) (the composite of all-cause death, myocardial infarction, definite stent thrombosis, or stroke) and major bleeding were assessed for up to 3 years.
Results: C-PCI was performed in 3,152 patients (26.9%). C-PCI significantly increased the risk of MACCE (HRadjusted: 1.21; 95% CI: 1.01-1.44; P = 0.035), driven by a higher rate of all-cause death (HRadjusted: 1.45; 95% CI: 1.15-1.83; P = 0.002), although it did not increase the risk of major bleeding. Irrespective of procedural complexity, the HPR phenotype was significantly associated with MACCE (Pinteraction = 0.731) and all-cause mortality (Pinteraction = 0.978), in which the prognostic implication appeared prominent within 1 year. The HPR phenotype did not show a significant interaction with any type of C-PCI. In addition, the number of complexity features per procedure did not proportionally increase the risk of MACCE.
Conclusions: C-PCI was significantly associated with 3-year risk of MACCE and all-cause death. The HPR phenotype appears to have a similar prognostic implication irrespective of the type and extent of procedural complexity. (Platelet Function and Genotype-Related Long-Term Prognosis in DES-Treated Patients [PTRG-DES]; NCT04734028).
Keywords: clinical outcomes; complex PCI; platelet reactivity.
© 2024 The Authors.
Conflict of interest statement
The study was designed by the principal investigator and executive committee, and was sponsored by the Korean Society of Interventional Cardiology. Dr Jeong has received honoraria for lectures for AstraZeneca, Daiichi-Sankyo, Sanofi, Hanmi Pharmaceuticals, and Yuhan Corporation; and research grants or support from Yuhan Corporation and U&I Corporation. Dr Joo has received honoraria for lectures for AstraZeneca, Hanmi, Samjin, Dong-A, HK inno, N Pharmaceuticals, and DIO Medical Ltd. Dr Song has received honoraria for lectures for AstraZeneca, Daiichi-Sankyo, Sanofi, Bayer Korea, and Samjin Pharmaceutical. All other authors have reported that they have no relationships relevant to the content of this paper to disclose.
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