| Literature DB >> 33851372 |
Fabio Mangiacapra1, Alessandro Sticchi2, Edoardo Bressi2, Roberto Mangiacapra3,4, Michele Mattia Viscusi2, Iginio Colaiori2, Elisabetta Ricottini2, Ilaria Cavallari2, Silvia Spoto5, Gian Paolo Ussia2, Pietro Manuel Ferraro3,4, Francesco Grigioni2.
Abstract
We investigated the interaction between chronic kidney disease (CKD) and high platelet reactivity (HPR) in determining long-term clinical outcomes following elective PCI for stable coronary artery disease (CAD). A total of 500 patients treated with aspirin and clopidogrel were divided based on the presence of CKD (defined as glomerular filtration rate of < 60 ml/min/1.73 m2) and HPR (defined as a P2Y12 reaction unit value ≥ 240 at VerifyNow assay). Primary endpoint was the occurrence of major adverse clinical events (MACE) at 5 years. Patients with both CKD and HPR showed the highest estimates of MACE (25.6%, p = 0.005), all-cause death (17.9%, p = 0.004), and cardiac death (7.7%, p = 0.004). The combination of CKD and HPR was an independent predictor of MACE (HR 3.12, 95% CI 1.46-6.68, p = 0.003). In conclusion, the combination of CKD and HPR identifies a cohort of patients with the highest risk of MACE at 5 years.Entities:
Keywords: Chronic kidney disease; Coronary artery disease; Percutaneous coronary intervention; Platelet reactivity
Mesh:
Year: 2021 PMID: 33851372 DOI: 10.1007/s12265-021-10126-8
Source DB: PubMed Journal: J Cardiovasc Transl Res ISSN: 1937-5387 Impact factor: 4.132