Literature DB >> 29385429

Antithrombotic therapy use and clinical outcomes following thrombo-embolic events in patients with atrial fibrillation: insights from ARISTOTLE.

Shinya Goto1, Peter Merrill2, Lars Wallentin3, Daniel M Wojdyla2, Michael Hanna4, Alvaro Avezum5, J Donald Easton6, Veli-Pekka Harjola7, Kurt Huber8, Basil S Lewis9, Alexander Parkhomenko10, Jun Zhu11, Christopher B Granger12, Renato D Lopes13, John H Alexander12.   

Abstract

Aims: We investigated baseline characteristics, antithrombotic use, and clinical outcomes of patients with atrial fibrillation (AF) and a thrombo-embolic event in the Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation (ARISTOTLE) study to better inform the care of these high-risk patients. Method and results: Thrombo-embolic events were defined as stroke (ischaemic or unknown cause) or systemic embolism (SE). Clinical outcomes were estimated using the Kaplan-Meier method. All-cause mortality and International Society on Thrombosis and Haemostasis (ISTH) major bleeding after events were analysed using a Cox proportional hazards model with time-dependent covariates. Of 18 201 patients in ARISTOTLE, 365 experienced a thrombo-embolic event [337 strokes (ischaemic or unknown cause), 28 SE]; 46 (12.6%) of which were fatal. In the 30 days before and after a thrombo-embolic event, 11% and 37% of patients, respectively, were not taking an oral anticoagulant. During follow-up (median 1.8 years), 22 patients (7.1%/year) had a recurrent stroke, 97 (30.1%/year) died, and 10 (6.7%/year) had major bleeding. Compared with patients without a thrombo-embolic event, the short- and long-term adjusted hazards of death in patients with a thrombo-embolic event were high [≤30 days: hazard ratio (HR) 54.3%, 95% confidence interval (95% CI) 41.4-71.3; >30 days: HR 3.5, 95% CI 2.5-4.8; both P < 0.001]. The adjusted hazards of major bleeding were also high short-term (HR 10.37, 95% CI 3.87-27.78; P < 0.001) but not long-term (HR 1.7, 95% CI: 0.77-3.88; P = 0.18). Conclusions: Thrombo-embolic events were rare but associated with high short- and long-term morbidity and mortality. Substantial numbers of patients are not receiving oral anticoagulattherapy before and, despite this risk, after a first thrombo-embolic event. Clinical Trial Registration: ClinicalTrials.gov (NCT00412984).

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Year:  2018        PMID: 29385429     DOI: 10.1093/ehjcvp/pvy002

Source DB:  PubMed          Journal:  Eur Heart J Cardiovasc Pharmacother


  1 in total

1.  The personalized antithrombotic management of atrial fibrillation with intermediate thromboembolic risk: a case report.

Authors:  Andreas Hammer; Sebastian Schnaubelt; Alexander Niessner; Patrick Sulzgruber
Journal:  Eur Heart J Case Rep       Date:  2020-09-09
  1 in total

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