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Long-term outcomes and periprocedural safety and efficacy of percutaneous left atrial appendage closure in a United Kingdom tertiary center: An 11-year experience.
Briosa E Gala, Andre; Pope, Michael T B; Monteiro, Cristiana; Leo, Milena; Dawkins, Sam; Newton, James D; Betts, Timothy R.
Afiliação
  • Briosa E Gala A; Department of Cardiology, Oxford University Hospitals NHS Trust, Oxford, United Kingdom.
  • Pope MTB; Department of Cardiology, Oxford University Hospitals NHS Trust, Oxford, United Kingdom; Department of Cardiology, University of Southampton, Southampton, United Kingdom.
  • Monteiro C; Department of Cardiology, Oxford University Hospitals NHS Trust, Oxford, United Kingdom; Biomedical Research Centre, University of Oxford, Oxford, United Kingdom.
  • Leo M; Department of Cardiology, Oxford University Hospitals NHS Trust, Oxford, United Kingdom.
  • Dawkins S; Department of Cardiology, Oxford University Hospitals NHS Trust, Oxford, United Kingdom.
  • Newton JD; Department of Cardiology, Oxford University Hospitals NHS Trust, Oxford, United Kingdom.
  • Betts TR; Department of Cardiology, Oxford University Hospitals NHS Trust, Oxford, United Kingdom; Biomedical Research Centre, University of Oxford, Oxford, United Kingdom. Electronic address: tim.betts@ouh.nhs.uk.
Heart Rhythm ; 18(10): 1724-1732, 2021 10.
Article em En | MEDLINE | ID: mdl-34126270
BACKGROUND: Left atrial appendage occlusion (LAAO) has been widely adopted as a strategy for stroke prevention in patients with atrial fibrillation ineligible for oral anticoagulation. OBJECTIVE: The purpose of this study was to explore longer-term "real-world" safety and efficacy outcomes in patients undergoing LAAO given varied practices in antithrombotic regimens and adoption of same-day discharge. METHODS: Analysis of acute procedural and long-term outcome data was performed for all patients undergoing LAAO implant in a United Kingdom tertiary center over an 11-year period. Rates of adverse events were calculated and compared to predicted rates in historical cohorts according to CHA2DS2-VASc and HAS-BLED scores. RESULTS: Device implantation was attempted in 229 patients, with an acute procedural success rate of 98.2% and low rate of major procedural complications of 2.6% at 30 days, including 1.3% procedure-related mortality. In the last year of enrollment, 75% of patients were discharged on the same day of the procedure. A strategy of early cessation of antithrombotic therapy was adopted, with a low rate of device-related thrombus. Over total follow-up of 889 patient-years, there were low rates of thromboembolic events (2.2/100 patient-years) and of significant bleeding events (intracranial bleed 0.6/100 patient-years; nonprocedural major bleeding 2.3/100 patient-years). CONCLUSION: LAAO with a same-day discharge strategy and early cessation of antiplatelet therapy seems to be safe and effective in reducing the risk of stroke and major bleeding over mean follow-up approaching 4 years. Although these data are reassuring, results from randomized trials with strict shorter periods of postprocedural antithrombotic therapy are eagerly awaited.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Tromboembolia / Sistema de Registros / Medição de Risco / Apêndice Atrial / Previsões / Procedimentos Cirúrgicos Cardíacos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Tromboembolia / Sistema de Registros / Medição de Risco / Apêndice Atrial / Previsões / Procedimentos Cirúrgicos Cardíacos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article