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New Oral Anticoagulants in Acute Coronary Syndrome: Is There Any Advantage Over Existing Treatments?


avatar Andrea Messori 1 , * , avatar Valeria Fadda 1 , avatar Roberta Gatto 1 , avatar Dario Maratea 1 , avatar Sabrina Trippoli 1

1 HTA Unit, ESTAV Toscana Centro, Regional Health Service, 50100 Firenze, Italy

How to Cite: Messori A, Fadda V , Gatto R , Maratea D , Trippoli S . New Oral Anticoagulants in Acute Coronary Syndrome: Is There Any Advantage Over Existing Treatments?. Int Cardio Res J. 2017;8(3):e11104.


International Cardiovascular Research Journal: 8 (3); e11104
Published Online: September 30, 2014
Article Type: Brief Report
Received: February 21, 2017
Accepted: March 01, 2014


Background: After an acute coronary syndrome, dual antiplatelet therapy with clopidogrel plus aspirin is still a standard of care, but several new approaches have been investigated.
Objectives: The present study re-examined the studies published thus far on this topic to evaluate the effectiveness of dual antiplatelet therapy in comparison to some of these new approaches (mainly, ticagrelor + aspirin and dual therapy plus a new oral anticoagulant [NOAC]; i.e., “triple therapy”).
Materials and Methods: The clinical material was directly derived from that reported in recent meta-analyses. Our re-analysis relied on standard equivalence methods in which interpretation is based on Relative Risks (RRs) along with their 95% Confidence Intervals (CI). The equivalence margins employed in our statistical testing were directly derived from those reported in randomized studies.
Results: The equivalence margins were initially set at RR ranging from 0.775 to 1.29. According to these margins, triple therapy based on any NOAC proved to be superior to dual therapy alone, but at the same time demonstrated its equivalence with dual therapy. The results for apixaban-based triple therapy were inconclusive (not superior, not not-inferior, not equivalent and, of course, not inferior to the controls). Those for rivaroxaban-based triple therapy showed that this combination treatment was superior to dual therapy alone and failed to meet the criterion of equivalence. In the comparison between rivaroxaban-based triple therapy and ticagrelor + aspirin, the RR was 1 and its 95% CI remained within a post-hoc margin of ± 15%.
Conclusions: Even if one considers the most effective NOAC in combination with clopidogrel + ticagrelor, this triple therapy is not more effective than ticagrelor + aspirin. On the other hand, the increased risk of bleeding with triple regimens is well demonstrated. We therefore conclude that these triple regimens did not play any important roles in the patients experiencing an acute coronary syndrome.


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