TY - JOUR
T1 - Current Status and Future Direction of Antithrombotic Therapy for Patients with STEMI Undergoing Primary PCI
AU - Vogel, Rosanne F.
AU - Delewi, Ronak
AU - Badimon, Lina
AU - Angiolillo, Dominick J.
AU - Vlachojannis, Georgios J.
N1 - Funding Information: RFV and RD have nothing to disclose. LB declares to have acted as SAB member of Sanofi, to have a Research Grant of AstraZeneca, to have received speaker fees of Sanofi and Bayer and to have founded the Spinoffs Glycardial Diagnostics SL and Ivastatin Therapeutics S (all unrelated to this work). DJA declares that he has received consulting fees or honoraria from Abbott, Amgen, AstraZeneca, Bayer, Biosensors, Boehringer In-gelheim, Bristol-Myers Squibb, Chiesi, Daiichi-Sankyo, Eli Lilly, Haemonetics, Janssen, Merck, PhaseBio, PLx Pharma, Pfizer, and Sanofi. DJA also declares that his institution has received research grants from Amgen, As-traZeneca, Bayer, Biosensors, CeloNova, CSL Behring, Daiichi-Sankyo, Eisai, Eli Lilly, Gilead, Janssen, Matsutani Chemical Industry Co., Merck, Novartis, Osprey Medical, Renal Guard Solutions and Scott R. MacKenzie Foundation. GJV declares that he has received consulting fees or honoraria from AstraZeneca. GJV also declares that his institution has received research grants from Daiichi-Sankyo, MicroPort and Ferrer. Lina Badimon is serving as one of the Editorial Board members of this journal. We declare that Lina Badimon had no involvement in the peer review of this article and has no access to information regarding its peer review. Full responsibility for the editorial process for this article was delegated to Antonio Mangieri, George Dangas and Christian Hengstenberg. Publisher Copyright: © 2022 The Author(s). Published by IMR Press.
PY - 2022/9/1
Y1 - 2022/9/1
N2 - Since the introduction of the first pharmacological therapy for the treatment of patients with acute myocardial infarction in the early 20th century, treatment of myocardial infarction has evolved extensively throughout the years. Mechanical revascularization therapies such as the percutaneous transluminal coronary angioplasty, combined with the ongoing development of pharmacological therapies have successfully improved the survival of patients with acute myocardial infarction. To date, antiplatelet therapy (consisting of aspirin and an oral P2Y12 inhibitor) and anticoagulation therapy represent the main stay of pharmacological treatment in patients with ST-segment elevation myocardial infarction (STEMI) undergoing percutaneous coronary intervention (PCI). The routine use of clopidogrel as antiplatelet agent has been largely replaced by the use of the more potent P2Y12 inhibitors ticagrelor and prasugrel. Unfractionated heparin remains the preferred anticoagulant therapy, despite the development of other anticoagulants, including enoxaparin and bivalirudin. To date, limited evidence exists supporting a pre-hospital initiation of antiplatelet and anticoagulant therapy in STEMI patients. The use of potent intravenous antiplatelet agents, including the glycoprotein IIb/IIIa inhibitors and the intravenous P2Y12 inhibitor cangrelor, is currently restricted to specific clinical settings. While several potent antithrombotic agents already exist, the search for novel potent antithrombotic agents continues, with a focus on balancing antithrombotic properties with an improved safety profile to reduce excess bleeding. This review provides an overview of currently available pharmacological therapies for the treatment of STEMI patients undergoing primary PCI, and an outlook for the ongoing development of novel agents in this field.
AB - Since the introduction of the first pharmacological therapy for the treatment of patients with acute myocardial infarction in the early 20th century, treatment of myocardial infarction has evolved extensively throughout the years. Mechanical revascularization therapies such as the percutaneous transluminal coronary angioplasty, combined with the ongoing development of pharmacological therapies have successfully improved the survival of patients with acute myocardial infarction. To date, antiplatelet therapy (consisting of aspirin and an oral P2Y12 inhibitor) and anticoagulation therapy represent the main stay of pharmacological treatment in patients with ST-segment elevation myocardial infarction (STEMI) undergoing percutaneous coronary intervention (PCI). The routine use of clopidogrel as antiplatelet agent has been largely replaced by the use of the more potent P2Y12 inhibitors ticagrelor and prasugrel. Unfractionated heparin remains the preferred anticoagulant therapy, despite the development of other anticoagulants, including enoxaparin and bivalirudin. To date, limited evidence exists supporting a pre-hospital initiation of antiplatelet and anticoagulant therapy in STEMI patients. The use of potent intravenous antiplatelet agents, including the glycoprotein IIb/IIIa inhibitors and the intravenous P2Y12 inhibitor cangrelor, is currently restricted to specific clinical settings. While several potent antithrombotic agents already exist, the search for novel potent antithrombotic agents continues, with a focus on balancing antithrombotic properties with an improved safety profile to reduce excess bleeding. This review provides an overview of currently available pharmacological therapies for the treatment of STEMI patients undergoing primary PCI, and an outlook for the ongoing development of novel agents in this field.
KW - ST-segment elevation myocardial infarction
KW - STEMI
KW - anticoagulation
KW - antiplatelet therapy
KW - antithrombotic therapy
KW - primary percutaneous coronary intervention
UR - http://www.scopus.com/inward/record.url?scp=85138951950&partnerID=8YFLogxK
U2 - https://doi.org/10.31083/j.rcm2309297
DO - https://doi.org/10.31083/j.rcm2309297
M3 - Review article
VL - 23
JO - Reviews in Cardiovascular Medicine
JF - Reviews in Cardiovascular Medicine
SN - 1530-6550
IS - 9
M1 - 297
ER -