Bivalirudin versus heparin monotherapy in non-ST-segment elevation myocardial infarction

Author:

Erlinge David1,Koul Sasha1,Omerovic Elmir2,Fröbert Ole3,Linder Rikard4,Danielewicz Mikael5,Hamid Mehmet6,Venetsanos Dimitrios7,Henareh Loghman7,Pettersson Björn8,Wagner Henrik9,Grimfjärd Per10,Jensen Jens11,Hofmann Robin12,Ulvenstam Anders13,Völz Sebastian2,Petursson Petur2,Östlund Ollie14,Sarno Giovanna14,Wallentin Lars14,Scherstén Fredrik1,Eriksson Peter8,James Stefan14

Affiliation:

1. Department of Cardiology, Lund University, Sweden

2. Department of Cardiology, Sahlgrenska University Hospital, Sweden

3. Department of Cardiology, Örebro University, Sweden

4. Department of Cardiology, Danderyd Hospital, Sweden

5. PCI-Unit, Karlstad Hospital, Sweden

6. Department of Cardiology, Mälarsjukhuset, Sweden

7. Department of Cardiology, Karolinska University Hospital, Sweden

8. Department of Cardiology, Umeå University, Sweden

9. Department of Cardiology, Helsingborg Lasarett, Sweden

10. Department of Internal Medicine, Västmanlands Sjukhus, Sweden

11. Department of Cardiology, Capio S:t Görans Hospital AB, Sweden

12. Department of Clinical Science and Education, Södersjukhuset, Sweden

13. Department of Cardiology, Östersund Hospital, Sweden

14. Department of Medical Sciences, Uppsala University, Sweden

Abstract

Background: The optimal anti-coagulation strategy for patients with non-ST-elevation myocardial infarction treated with percutaneous coronary intervention is unclear in contemporary clinical practice of radial access and potent P2Y12-inhibitors. The aim of this study was to investigate whether bivalirudin was superior to heparin monotherapy in patients with non-ST-elevation myocardial infarction without routine glycoprotein IIb/IIIa inhibitor use. Methods: In a large pre-specified subgroup of the multicentre, prospective, randomised, registry-based, open-label clinical VALIDATE-SWEDEHEART trial we randomised patients with non-ST-elevation myocardial infarction undergoing percutaneous coronary intervention, treated with ticagrelor or prasugrel, to bivalirudin or heparin monotherapy with no planned use of glycoprotein IIb/IIIa inhibitors during percutaneous coronary intervention. The primary endpoint was the rate of a composite of all-cause death, myocardial infarction or major bleeding within 180 days. Results: A total of 3001 patients with non-ST-elevation myocardial infarction, were enrolled. The primary endpoint occurred in 12.1% (182 of 1503) and 12.5% (187 of 1498) of patients in the bivalirudin and heparin groups, respectively (hazard ratio of bivalirudin compared to heparin treatment 0.96, 95% confidence interval 0.78–1.18, p=0.69). The results were consistent in all major subgroups. All-cause death occurred in 2.0% versus 1.7% (hazard ratio 1.15, 0.68–1.94, p=0.61), myocardial infarction in 2.3% versus 2.5% (hazard ratio 0.91, 0.58–1.45, p=0.70), major bleeding in 8.9% versus 9.1% (hazard ratio 0.97, 0.77–1.24, p=0.82) and definite stent thrombosis in 0.3% versus 0.2% (hazard ratio 1.33, 0.30–5.93, p=0.82). Conclusion: Bivalirudin as compared to heparin during percutaneous coronary intervention for non-ST-elevation myocardial infarction did not reduce the composite of all-cause death, myocardial infarction or major bleeding in non-ST-elevation myocardial infarction patients receiving current recommended treatments with modern P2Y12-inhibitors and predominantly radial access.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Critical Care and Intensive Care Medicine,General Medicine

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