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Risk factors for MACE and bleeding in atrial fibrillation patients undergoing surgery: Insights from the bridge trial.
Shu, Liqi; Jack, Naomi; de Havenon, Adam; Goldstein, Eric D; Khan, Farhan; Nguyen, Thanh N; Henninger, Nils; Siegler, James E; Stretz, Christoph; Perelstein, Elizabeth; Kala, Narendra; Rana, Maheen; Furie, Karen L; Douketis, James D; Yaghi, Shadi.
Afiliação
  • Shu L; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI; Department of Neurology, The Miriam Hospital, Providence, RI, USA. Electronic address: liqi_shu@brown.edu.
  • Jack N; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI. Electronic address: naomi_jack@brown.edu.
  • de Havenon A; Department of Neurology, Center for Brain and Mind Health, Yale School of Medicine, New Haven, CT. Electronic address: adam.dehavenon@yale.edu.
  • Goldstein ED; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI. Electronic address: egoldstein@lifespan.org.
  • Khan F; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI. Electronic address: fkhan@lifespan.org.
  • Nguyen TN; Department of Neurology, Boston University School of Medicine, Boston, MA, USA. Electronic address: thanh.nguyen@bmc.org.
  • Henninger N; Department of Neurology, University of Massachusetts Chan Medical School, Worcester, MA, USA; Department of Psychiatry, University of Massachusetts Chan Medical School, Worcester, MA, USA. Electronic address: nils.henninger@umassmed.edu.
  • Siegler JE; Department of Neurology, University of Chicago, Chicago, IL.
  • Stretz C; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI. Electronic address: christoph_stretz@brown.edu.
  • Perelstein E; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI. Electronic address: eperelstein@lifespan.org.
  • Kala N; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI. Electronic address: nkala@lifespan.org.
  • Rana M; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI. Electronic address: mrana@lifespan.org.
  • Furie KL; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI. Electronic address: kfurie@lifespan.org.
  • Douketis JD; Department of Medicine, McMaster University, Hamilton, ON, Canada. Electronic address: jdouket@mcmaster.ca.
  • Yaghi S; Department of Neurology, The Warren Alpert Medical School of Brown University, Providence, RI.
J Stroke Cerebrovasc Dis ; 33(9): 107839, 2024 Jun 27.
Article em En | MEDLINE | ID: mdl-38944363
ABSTRACT

INTRODUCTION:

Patients with atrial fibrillation (AF) undergoing elective procedures are at risk for Major Adverse Cardiovascular Events (MACE) and symptomatic bleeding. We aimed to identify risk factors to guide perioperative risk stratification.

METHODS:

We conducted a post-hoc analysis of the "Bridging Anticoagulation in Patients who Require Temporary Interruption of Warfarin Therapy for an Elective Invasive Procedure or Surgery" randomized trial. The primary outcomes were MACE and symptomatic bleeding. Our statistical approach encompassed standard univariate analysis, logistic stepwise regression, and Cox regression models. Additional interaction analyses evaluated the interplay between low-molecular-weight heparin bridge therapy and other identified risk factors.

RESULTS:

Among a total of 1,813 participants (mean age 71.6 ± 8.8, 73.3 % male), MACE occurred in 25 (1.4 %) individuals, with pre-procedure clopidogrel use (adjusted hazard ratio [aHR] 7.73, 95 % CI 2.63-22.72, p < 0.001) and CHA2DS2-VASc score ≥ 5 (aHR 2.89, 95 % CI 1.26-6.63, p = 0.012) identified as risk factors. Symptomatic bleeding occurred in 57 (3.1 %) individuals, with bridge therapy (aHR 1.84, 95 % CI 1.07-3.19, p = 0.029), renal disease (aHR 2.50, 95 % CI 1.34-4.67, p = 0.004), post-procedure aspirin use (aHR 2.86, 95 % CI 1.66-4.91, p < 0.001), post-procedure nonsteroidal anti-inflammatory drug use excluding aspirin (aHR 3.40, 95 % CI 1.22-9.43, p = 0.019), and major surgery (aHR 3.94, 95 % CI 2.26-6.85, p < 0.001) identified as risk factors. The interactions between risk factors and bridging therapy on MACE and symptomatic bleeding outcomes were not significant (p > 0.05).

CONCLUSION:

We identified predictors for MACE and symptomatic bleeding in AF patients undergoing elective procedures. These insights may help guide perioperative decisions to reduce the risk of adverse outcomes.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article