Inclusion criteria |
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Age > 18 years |
Able to give informed consent |
One of the following criteria: Patients naive for P2Y12 inhibition undergoing ad-hoc PCI Patients with STEMI/NSTEMI loaded with oral P2Y12 inhibitors though platelet inhibition still insufficient (< 2 h after oral loading dose) according to operator Patients with STEMI/NSTEMI who vomited after P2Y12 loading dose Patients with OHCA, based on VF/VT due to acute ischemia as the underlying cause, with Return of Spontaneous Circulation (ROSC) who have successfully been defibrillated and/or resuscitated with stable hemodynamics STEMI/NSTEMI patients loaded with oral P2Y12 inhibitors with large thrombus burden (TBG 4 or 5) on initial coronary angiography and undergoing (primary) PCI with expected insufficient P2Y12 inhibition |
Exclusion criteria |
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Patients on current/chronic treatment with P2Y12 inhibitors |
Patients (pre)treated with GPIs |
Patients with recent major bleeding complications or contraindication to DAPT: Hypersensitivity or allergy to and known contraindication to aspirin, clopidogrel, ticagrelor, prasugrel, or cangrelor History of major clinical bleeding or known coagulopathy Active bleeding History of intracerebral mass, aneurysm, arteriovenous malformation, or hemorrhagic stroke Known severe liver dysfunction |
Patients that have received any organ transplant or await any organ transplant |
Patients undergoing dialysis |
Pregnant or lactating female |
Patients currently participating in another investigational drug or drug-coated device study |