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Cited 16 time in webofscience Cited 18 time in scopus
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The Impact of platelet-fibrin clot strength on occurrence and clinical outcomes of peripheral artery disease in patients with significant coronary artery disease

Authors
Bae, Jae SeokAhn, Jong-HwaJang, Jeong YoonCho, Sang YoungKang, Min GyuKim, Kye-HwanPark, Hyun WoongKoh, Jin-SinPark, YongwhiHwang, Seok-JaeKwak, Choong HwanHwang, Jin-YongTantry, Udaya S.Gurbel, Paul A.Jeong, Young-Hoon
Issue Date
Nov-2020
Publisher
Kluwer Academic Publishers
Keywords
Clot; Inflammation; Peripheral artery disease; Coronary artery disease
Citation
Journal of Thrombosis and Thrombolysis, v.50, no.4, pp 969 - 981
Pages
13
Indexed
SCIE
SCOPUS
Journal Title
Journal of Thrombosis and Thrombolysis
Volume
50
Number
4
Start Page
969
End Page
981
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/5967
DOI
10.1007/s11239-020-02103-w
ISSN
0929-5305
1573-742X
Abstract
Patients with peripheral artery disease (PAD) have shown the increased risk of cardiovascular (CV) morbidity and mortality. This study sought to evaluate the impact of clot strength on prevalence and major adverse CV events (MACE) of PAD in high-risk patients. We enrolled patients undergoing percutaneous coronary intervention (PCI) (n = 1667) with available platelet-fibrin clot strength [thrombin-induced maximal amplitude (MA(thrombin)) measured by thromboelastography] and inflammation [high sensitivity C-reactive protein (hs-CRP)]. PAD was defined with abnormal ankle-brachial index (<= 0.9 or > 1.4). MACE was defined as a composite of CV death, myocardial infarction or stroke. PAD was observed in 201 patients (12.1%). In the multivariate analysis, high clot strength [MA(thrombin) >= 68 mm: odds ratio (OR) 1.70, 95% confidence interval (CI) 1.20 to 2.41, p = 0.003] and enhanced inflammation (hs-CRP >= 3.0 mg/L: OR 2.30, 95% CI 1.56 to 3.41, p < 0.001) were associated with PAD occurrence. During the follow-up post-PCI (median, 25 months), MACE was more frequently occurred in patients with vs. without PAD (18.7% vs. 6.4% at 3 years; hazard ratio 1.72, 95% CI 1.03 to 2.87, p = 0.039). Furthermore, combined presence of PAD and high clot strength significantly increased the risk of MACE. In conclusion, this study is the first to show the impact of clot strength on prevalence and clinical outcomes of PAD in coronary artery disease patients undergoing PCI. Whether antithrombotic strategy according to level of this biomarker can improve clinical outcomes in PAD patients deserves the further study.
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