2017
DOI: 10.1016/j.ihj.2017.10.012
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Sub-acute stent thrombosis secondary to ticagrelor resistance—Myth or reality!!

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Cited by 9 publications
(9 citation statements)
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“…Also, the asymptomatic status of the patient after his COVID-19 illness makes this possibility highly unlikely. The occurrence of stent thrombosis due to ticagrelor resistance has been reported rarely in the literature [ 13 - 16 ], and could have been contributory toward the development of stent thrombosis in our case, but the occurrence of true resistance to ticagrelor therapy is still debated [ 17 ]. Nevertheless, we kept this possibility in mind and ticagrelor was switched to prasugrel.…”
Section: Discussionmentioning
confidence: 95%
“…Also, the asymptomatic status of the patient after his COVID-19 illness makes this possibility highly unlikely. The occurrence of stent thrombosis due to ticagrelor resistance has been reported rarely in the literature [ 13 - 16 ], and could have been contributory toward the development of stent thrombosis in our case, but the occurrence of true resistance to ticagrelor therapy is still debated [ 17 ]. Nevertheless, we kept this possibility in mind and ticagrelor was switched to prasugrel.…”
Section: Discussionmentioning
confidence: 95%
“…Two weeks after initiating DAPT with ticagrelor, the patient was found to have subacute stent thrombosis, per angiography, after symptoms of acute chest discomfort. A bolus of eptifibatide was given for treatment, and the patient was discharged on ticagrelor, 90 mg twice daily, and aspirin, 75 mg daily 19 . Platelet function testing was absent.…”
Section: Discussionmentioning
confidence: 99%
“…A bolus of eptifibatide was given for treatment, and the patient was discharged on ticagrelor, 90 mg twice daily, and aspirin, 75 mg daily. 19 Platelet function testing was absent. Olechowski et al reported 3 cases of ticagrelor resistance in patients with ACS receiving DAPT following percutaneous coronary intervention.…”
Section: Discussionmentioning
confidence: 99%
“…For example, in a sub-analysis of the randomized GRAVITAS (Gauging Responsiveness with a Verify Now P2Y12 assay: Impact on Thrombosis and Safety) study [ 24 ], HPR (defined as >208 P2Y12 reaction units when examined with a point-of-care Verify Now ® assay at 12 to 24 h after PCI) was connected with a higher risk of adverse ischemia at 60 days and at 6 months (at 60 days: hazard ratio [HR]: 0.18; 95% confidence interval [CI]: 0.04–0.79; p = 0.02; at 6 months: HR: 0.43; 95% CI: 0.23–0.82; p = 0.01). Additionally, HPR remains independently associated with adverse vascular events (including stent thrombosis) also in individuals treated with novel P2Y12 ADP receptor blockers with stronger platelet inhibition, such as prasugrel and ticagrelor [ 28 , 29 , 30 ]. Summarizing the data, HPR despite oral antiplatelet agents has been consistently connected with the risk of adverse ischemia; thus identifying individuals with insufficient antiplatelet therapy response might help in preventing these possibly fatal events.…”
Section: Viscoelastic Hemostatic Assays and Platelet Function Testmentioning
confidence: 99%