| Literature DB >> 24169016 |
Eric Durand1, Didier Blanchard2, Stephan Chassaing3, Martine Gilard4, Marc Laskar5, Bogdan Borz6, Antoine Lafont7, Christophe Barbey3, Matthieu Godin6, Christophe Tron6, Rachid Zegdi7, Didier Chatel3, Olivier Le Page3, Pierre-Yves Litzler6, Jean-Paul Bessou6, Nicolas Danchin7, Alain Cribier6, Hélène Eltchaninoff6.
Abstract
Dual antiplatelet therapy is commonly used in patients undergoing transcatheter aortic valve implantation (TAVI), but the optimal antiplatelet regimen is uncertain and remains to be determined. The objective of this study was to compare 2 strategies of antiplatelet therapy in patients undergoing TAVI. A strategy using monoantiplatelet therapy (group A, n = 164) was prospectively compared with a strategy using dual antiplatelet therapy (group B, n = 128) in 292 consecutive patients undergoing TAVI. The primary end point was a combination of mortality, major stroke, life-threatening bleeding (LTB), myocardial infarction, and major vascular complications at 30 days. All adverse events were adjudicated according to the Valve Academic Research Consortium. The primary end point occurred in 22 patients (13.4%) in the group A and in 30 patients (23.4%) in the group B (hazard ratio 0.51, 95% confidence interval 0.28 to 0.94, p = 0.026). LTB (3.7% vs 12.5%, p = 0.005) and major bleedings (2.4% vs 13.3%, p <0.0001) occurred less frequently in the group A, whereas the incidence of stroke (1.2% vs 4.7%, p = 0.14) and myocardial infarction (1.2% vs 0.8%, p = 1.0) was not significantly different between the 2 groups. The benefit of a strategy using mono versus dual antiplatelet therapy persisted after multivariate adjustment and propensity score analysis (hazard ratio 0.53, 95% confidence interval 0.28 to 0.95, p = 0.033). In conclusion, a strategy using mono versus dual antiplatelet therapy in patients undergoing TAVI reduces LTB and major bleedings without increasing the risk of stroke and myocardial infarction. The results of our study question the justification of dual antiplatelet therapy and require confirmation in a randomized trial.Entities:
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Year: 2013 PMID: 24169016 DOI: 10.1016/j.amjcard.2013.09.033
Source DB: PubMed Journal: Am J Cardiol ISSN: 0002-9149 Impact factor: 2.778