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One- versus three-month dual antiplatelet therapy in high bleeding risk patients undergoing percutaneous coronary intervention for non-ST-segment elevation acute coronary syndromes.

Publication ,  Journal Article
Cao, D; Vranckx, P; Valgimigli, M; Sartori, S; Angiolillo, DJ; Bangalore, S; Bhatt, DL; Feng, Y; Ge, J; Hermiller, J; Makkar, RR; Neumann, F-J ...
Published in: EuroIntervention
May 20, 2024

BACKGROUND: A short dual antiplatelet therapy (DAPT) duration has been proposed for patients at high bleeding risk (HBR) undergoing drug-eluting coronary stent (DES) implantation. Whether this strategy is safe and effective after a non-ST-segment elevation acute coronary syndrome (NSTE-ACS) remains uncertain. AIMS: We aimed to compare the impact of 1-month versus 3-month DAPT on clinical outcomes after DES implantation among HBR patients with or without NSTE-ACS. METHODS: This is a prespecified analysis from the XIENCE Short DAPT programme involving three prospective, international, single-arm studies evaluating the safety and efficacy of 1-month (XIENCE 28 USA and Global) or 3-month (XIENCE 90) DAPT among HBR patients after implantation of a cobalt-chromium everolimus-eluting stent. Ischaemic and bleeding outcomes associated with 1- versus 3-month DAPT were assessed according to clinical presentation using propensity score stratification. RESULTS: Of 3,364 HBR patients (1,392 on 1-month DAPT and 1,972 on 3-month DAPT), 1,164 (34.6%) underwent DES implantation for NSTE-ACS. At 12 months, the risk of the primary endpoint of death or myocardial infarction was similar between 1- and 3-month DAPT in patients with (hazard ratio [HR] 1.09, 95% confidence interval [CI]: 0.71-1.65) and without NSTE-ACS (HR 0.88, 95% CI: 0.63-1.23; p-interaction=0.34). The key secondary endpoint of Bleeding Academic Research Consortium (BARC) Type 2-5 bleeding was consistently reduced in both NSTE-ACS (HR 0.57, 95% CI: 0.37-0.88) and stable patients (HR 0.84, 95% CI: 0.61-1.15; p-interaction=0.15) with 1-month DAPT. CONCLUSIONS: Among HBR patients undergoing implantation of an everolimus-eluting stent, 1-month, compared to 3-month DAPT, was associated with similar ischaemic risk and reduced bleeding at 1 year, irrespective of clinical presentation.

Duke Scholars

Published In

EuroIntervention

DOI

EISSN

1969-6213

Publication Date

May 20, 2024

Volume

20

Issue

10

Start / End Page

e630 / e642

Location

France

Related Subject Headings

  • Treatment Outcome
  • Time Factors
  • Risk Factors
  • Prospective Studies
  • Platelet Aggregation Inhibitors
  • Percutaneous Coronary Intervention
  • Non-ST Elevated Myocardial Infarction
  • Middle Aged
  • Male
  • Humans
 

Citation

APA
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ICMJE
MLA
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Cao, D., Vranckx, P., Valgimigli, M., Sartori, S., Angiolillo, D. J., Bangalore, S., … Mehran, R. (2024). One- versus three-month dual antiplatelet therapy in high bleeding risk patients undergoing percutaneous coronary intervention for non-ST-segment elevation acute coronary syndromes. EuroIntervention, 20(10), e630–e642. https://doi.org/10.4244/EIJ-D-23-00658
Cao, Davide, Pascal Vranckx, Marco Valgimigli, Samantha Sartori, Dominick J. Angiolillo, Sripal Bangalore, Deepak L. Bhatt, et al. “One- versus three-month dual antiplatelet therapy in high bleeding risk patients undergoing percutaneous coronary intervention for non-ST-segment elevation acute coronary syndromes.EuroIntervention 20, no. 10 (May 20, 2024): e630–42. https://doi.org/10.4244/EIJ-D-23-00658.
Cao D, Vranckx P, Valgimigli M, Sartori S, Angiolillo DJ, Bangalore S, et al. One- versus three-month dual antiplatelet therapy in high bleeding risk patients undergoing percutaneous coronary intervention for non-ST-segment elevation acute coronary syndromes. EuroIntervention. 2024 May 20;20(10):e630–42.
Cao, Davide, et al. “One- versus three-month dual antiplatelet therapy in high bleeding risk patients undergoing percutaneous coronary intervention for non-ST-segment elevation acute coronary syndromes.EuroIntervention, vol. 20, no. 10, May 2024, pp. e630–42. Pubmed, doi:10.4244/EIJ-D-23-00658.
Cao D, Vranckx P, Valgimigli M, Sartori S, Angiolillo DJ, Bangalore S, Bhatt DL, Feng Y, Ge J, Hermiller J, Makkar RR, Neumann F-J, Saito S, Picon H, Toelg R, Maksoud A, Chehab BM, Choi JW, Campo G, De la Torre Hernandez JM, Krucoff MW, Kunadian V, Sardella G, Spirito A, Thiele H, Varenne O, Vogel B, Zhou Y, Windecker S, Mehran R. One- versus three-month dual antiplatelet therapy in high bleeding risk patients undergoing percutaneous coronary intervention for non-ST-segment elevation acute coronary syndromes. EuroIntervention. 2024 May 20;20(10):e630–e642.

Published In

EuroIntervention

DOI

EISSN

1969-6213

Publication Date

May 20, 2024

Volume

20

Issue

10

Start / End Page

e630 / e642

Location

France

Related Subject Headings

  • Treatment Outcome
  • Time Factors
  • Risk Factors
  • Prospective Studies
  • Platelet Aggregation Inhibitors
  • Percutaneous Coronary Intervention
  • Non-ST Elevated Myocardial Infarction
  • Middle Aged
  • Male
  • Humans