Abstract |
In patients with an acute coronary syndrome undergoing percutaneous coronary intervention, novel P2Y12 receptor inhibitors, prasugrel and ticagrelor, are proposed as "first-line" antiplatelet agents in the absence of contraindications and up to a year from the index event. However, de-escalation of treatment to clopidogrel occurs with a variable frequency in real-life practice, most commonly due to an increased bleeding potential, more frequent side effects, and a higher cost for the novel agents. Pharmacodynamic studies provide most of the data on guidance for de-escalation. Despite positive messages from recent trials and registries, lack of definitive efficacy or safety results of such a strategy remains an obstacle to suggest de-escalation in a routine basis. Carefully designed studies are likely to improve our understanding of the impact of de-escalation and help to better define its position in current pharmacotherapy.
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Authors | Dimitrios Alexopoulos, Ioannis Lianos, Panagiotis Vlachakis, Danai Sfantou, Vassiliki-Maria Dragona, Charalambos Varlamos |
Journal | Journal of cardiovascular pharmacology and therapeutics
(J Cardiovasc Pharmacol Ther)
Vol. 24
Issue 4
Pg. 304-314
(07 2019)
ISSN: 1940-4034 [Electronic] United States |
PMID | 30722685
(Publication Type: Journal Article, Review)
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Chemical References |
- Platelet Aggregation Inhibitors
- Purinergic P2Y Receptor Antagonists
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Topics |
- Acute Coronary Syndrome
(diagnosis, therapy)
- Administration, Oral
- Animals
- Clinical Decision-Making
- Coronary Thrombosis
(etiology, prevention & control)
- Drug Administration Schedule
- Drug Substitution
- Hemorrhage
(chemically induced)
- Humans
- Percutaneous Coronary Intervention
(adverse effects)
- Platelet Aggregation Inhibitors
(administration & dosage, adverse effects)
- Purinergic P2Y Receptor Antagonists
(administration & dosage, adverse effects)
- Risk Factors
- Treatment Outcome
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