Resistance on the Latest Oral and Intravenous P2Y12 ADP Receptor Blockers in Patients with Acute Coronary Syndromes: Fact or Myth?
Peter BlaškoMatej SamošTomáš BolekLucia StančiakováIngrid ŠkorňováMartin Jozef PéčJakub JuricaJan StaskoMarián MokáňPublished in: Journal of clinical medicine (2022)
Novel P2Y12 ADP receptor blockers (ADPRB) should be preferred in dual-antiplatelet therapy in patients with acute coronary syndrome. Nevertheless, there are still patients who do not respond optimally to novel ADP receptor blocker therapy, and this nonoptimal response (so-called "high on-treatment platelet reactivity" or "resistance") could be connected with increased risk of adverse ischemic events, such as myocardial re-infarction, target lesion failure and stent thrombosis. In addition, several risk factors have been proposed as factors associated with the phenomenon of inadequate response on novel ADPRB. These include obesity, multivessel coronary artery disease, high pre-treatment platelet reactivity and impaired metabolic status for prasugrel, as well as elderly, concomitant therapy with beta-blockers, morphine and platelet count for ticagrelor. There is no literature report describing nonoptimal therapeutic response on cangrelor, and cangrelor therapy seems to be a possible approach for overcoming HTPR on prasugrel and ticagrelor. However, the optimal therapeutic management of "resistance" on novel ADPRB is not clear and this issue requires further research. This narrative review article discusses the phenomenon of high on-treatment platelet reactivity on novel ADPRB, its importance in clinical practice and approaches for its therapeutic overcoming.
Keyphrases
- percutaneous coronary intervention
- antiplatelet therapy
- acute coronary syndrome
- coronary artery disease
- st segment elevation myocardial infarction
- st elevation myocardial infarction
- risk factors
- coronary artery bypass grafting
- angiotensin converting enzyme
- clinical practice
- emergency department
- systematic review
- type diabetes
- metabolic syndrome
- adipose tissue
- stem cells
- low dose
- combination therapy
- bone marrow
- cell therapy
- mesenchymal stem cells
- cardiovascular events
- replacement therapy
- blood brain barrier
- binding protein
- body mass index
- electronic health record
- ejection fraction
- adverse drug
- high fat diet induced