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Dual vs triple antithrombotic therapy in atrial fibrillation and acute coronary syndrome: An updated meta-analysis of randomized controlled trials.
Sainbayar, Enkhtsogt; Pham, Hoang Nhat; Olson, April; Ibrahim, Ramzi; Grewal, Harneet; Salih, Mohammed; Mamas, Mamas A; Lee, Kwan.
Afiliación
  • Sainbayar E; Department of Medicine, UA College of Medicine, University of Arizona Tucson, Tucson, AZ, USA.
  • Pham HN; Department of Medicine, UA College of Medicine, University of Arizona Tucson, Tucson, AZ, USA.
  • Olson A; Department of Medicine, UA College of Medicine, University of Arizona Tucson, Tucson, AZ, USA.
  • Ibrahim R; Department of Medicine, UA College of Medicine, University of Arizona Tucson, Tucson, AZ, USA.
  • Grewal H; Department of Medicine, Abrazo Health Network, Glendale, AZ, USA.
  • Salih M; Heart Hospital-Baylor University Medical Center, Plano, TX, USA.
  • Mamas MA; Keele Cardiovascular Research Group, Keele University, Keele, UK.
  • Lee K; Department of Cardiovascular Medicine, Mayo Clinic, Phoenix, AZ, USA.
J Investig Med ; : 10815589241270640, 2024 Aug 28.
Article en En | MEDLINE | ID: mdl-39092852
ABSTRACT
Antithrombotic treatment in patients with atrial fibrillation (AF) and acute coronary syndrome (ACS) poses a dilemma. We compared outcomes of dual antithrombotic therapy (DAT) (direct oral anticoagulants (DOACs)/warfarin + antiplatelets) vs triple antithrombotic therapy (TAT) (DOACs/warfarin, aspirin, and P2Y12 inhibitor) in this population. Multiple databases were searched from inception to December 17, 2023 to identify randomized controlled trials (RCTs) comparing DAT vs TAT in patients with AF and ACS. Outcomes included major adverse cardiac events (MACE), bleeding events, stroke, stent thrombosis, and myocardial infarction (MI). Relative risk and 95% confidence intervals were estimated with a random-effects model using the inverse-variance technique. We assigned I2 > 50% as an indicator of statistical heterogeneity. p-Value <0.05 was considered significant. Ten RCTs comprising 6186 patients on TAT (female 26%, mean age 71 ± 9 years) and 6800 patients on DAT (female 27%, mean age 71 ± 9 years) were included. Patients receiving DAT experienced lower rates of bleeding events compared to those receiving TAT, with relative risks of 0.69 [0.55-0.87] (p < 0.001), 0.65 [0.40-1.06] (p = 0.09), and 0.62 [0.46-0.84] (p < 0.001) for TAT durations of 3, 6, and 12 months, respectively. No difference was seen in the occurrence of MACE, MI, stroke, or stent thrombosis between DAT and TAT across all three durations of TAT. This is the largest pooled analysis comparing TAT to DAT stratified by the duration of antithrombotic therapy. Our results revealed that DAT was associated with reduced bleeding risk despite no difference in other outcomes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Investig Med Asunto de la revista: MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Investig Med Asunto de la revista: MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido