Ticagrelor or Prasugrel in Patients With Acute Coronary Syndrome Undergoing Complex Percutaneous Coronary Intervention
| العنوان: | Ticagrelor or Prasugrel in Patients With Acute Coronary Syndrome Undergoing Complex Percutaneous Coronary Intervention |
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| المؤلفون: | Gert Richardt, Erion Xhepa, Jochen Wöhrle, Adnan Kastrati, Massimiliano Fusaro, John Joseph Coughlan, Gjin Ndrepepa, Isabell Bernlochner, Maurizio Menichelli, Karl-Ludwig Laugwitz, Alp Aytekin, Heribert Schunkert, Hendrik B. Sager, Stefanie Schüpke, Salvatore Cassese, Senta Gewalt, Katharina Mayer, Bernhard Witzenbichler, Michael Joner, Franz-Josef Neumann, Sebastian Kufner, Tareq Ibrahim |
| المصدر: | Circulation. Cardiovascular interventions. 14(7) |
| سنة النشر: | 2021 |
| مصطلحات موضوعية: | medicine.medical_specialty, Acute coronary syndrome, Ticagrelor, Randomization, Prasugrel, business.industry, medicine.medical_treatment, Hazard ratio, Percutaneous coronary intervention, medicine.disease, Percutaneous Coronary Intervention, Treatment Outcome, Internal medicine, Conventional PCI, Cardiology, Medicine, Humans, Myocardial infarction, Acute Coronary Syndrome, Cardiology and Cardiovascular Medicine, business, Prasugrel Hydrochloride, Platelet Aggregation Inhibitors, medicine.drug |
| الوصف: | Background: The comparative efficacy and safety of ticagrelor and prasugrel in patients with acute coronary syndrome undergoing complex percutaneous coronary intervention (PCI) has not been defined. Methods: This post hoc analysis included all patients with acute coronary syndrome treated with PCI and randomized to either ticagrelor or prasugrel in the ISAR-REACT 5 trial (Intracoronary Stenting and Antithrombotic Regimen: Rapid Early Action for Coronary Treatment). Complex PCI was defined as at least one of the following: multivessel PCI, ≥3 stents implanted, ≥3 lesions treated, and total stented length >60 mm. The primary efficacy end point was the composite of all-cause death, myocardial infarction, or stroke; the safety end point was Bleeding Academic Research Consortium types 3 to 5 bleeding. Outcomes were assessed out to 12 months after randomization. Results: Among the 3377 patients treated with PCI in the ISAR-REACT 5 trial, 1429 underwent complex PCI (ticagrelor, N=696 and prasugrel, N=733) and 1948 underwent noncomplex PCI (ticagrelor, N=980 and prasugrel, N=968). There was no interaction between PCI complexity, assignment to either ticagrelor or prasugrel, and the primary efficacy or safety end points ( P for interaction: ≥0.13). In the complex PCI group, the primary efficacy end point (11.0% versus 9.2%, hazard ratio: 1.19 [0.85–1.66], P =0.303) and the safety end point (5.2% versus 6.1%, hazard ratio: 0.83 [0.53–1.31], P =0.419) were not statistically different in patients receiving either ticagrelor or prasugrel. In the noncomplex PCI group, the primary efficacy end point occurred more frequently in patients assigned to ticagrelor as compared to prasugrel (8.9% versus 5.5%, hazard ratio: 1.66 [1.18–2.34], P =0.004) without significant difference in terms of the safety end point (5.4% versus 4.1%, hazard ratio: 1.41 [0.92–2.17], P =0.110). Conclusions: In patients with acute coronary syndrome, PCI complexity does not influence the comparative efficacy and safety of ticagrelor and prasugrel. The observed comparable performance of ticagrelor and prasugrel in patients with acute coronary syndrome undergoing complex PCI requires further confirmation. Registration: URL: https://www.clinicaltrials.govTest ; Unique identifier: NCT01944800. |
| تدمد: | 1941-7632 0194-4800 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b0ae28cab546cd2a89a97d42c69d8a6Test https://pubmed.ncbi.nlm.nih.gov/34130479Test |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....9b0ae28cab546cd2a89a97d42c69d8a6 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 19417632 01944800 |
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