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Left Atrial Appendage Thrombus Formation Despite Continuous Non-Vitamin K Antagonist Oral Anticoagulant Therapy in Atrial Fibrillation Patients Undergoing Electrical Cardioversion or Catheter Ablation: A Comparison of Dabigatran and Rivaroxaban

Left atrial appendage thrombus (LAAT) may be detected by transesophageal echocardiography (TOE) in patients with atrial fibrillation (AF) despite continuous anticoagulation therapy. We examined the factors predisposing to LAAT in patients treated with the anticoagulants dabigatran and rivaroxaban. W...

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Detalles Bibliográficos
Autores principales: Gorczyca, Iwona, Chrapek, Magdalena, Jelonek, Olga, Michalska, Anna, Kapłon-Cieślicka, Agnieszka, Uziębło-Życzkowska, Beata, Budnik, Monika, Gawałko, Monika, Krzesiński, Paweł, Jurek, Agnieszka, Scisło, Piotr, Kochanowski, Janusz, Kiliszek, Marek, Gielerak, Grzegorz, Filipiak, Krzysztof J., Opolski, Grzegorz, Wożakowska-Kapłon, Beata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519465/
https://www.ncbi.nlm.nih.gov/pubmed/33014453
http://dx.doi.org/10.1155/2020/1206402
Descripción
Sumario:Left atrial appendage thrombus (LAAT) may be detected by transesophageal echocardiography (TOE) in patients with atrial fibrillation (AF) despite continuous anticoagulation therapy. We examined the factors predisposing to LAAT in patients treated with the anticoagulants dabigatran and rivaroxaban. We retrospectively evaluated 1,256 AF patients from three centres who underwent TOE before electrical cardioversion (n = 611, 51.4%) or catheter ablation (n = 645, 48.6%) from January 2013 to December 2019 and had been on at least three weeks of continuous dabigatran (n = 603, 48%) or rivaroxaban (n = 653, 52%) therapy. Preprocedural TOE diagnosed LAAT in 51 patients (4.1%), including 30 patients (5%) treated with dabigatran and 21 patients (3.2%) treated with rivaroxaban (p=0.1145). In multivariate logistic regression, predictors of LAAT in patients treated with dabigatran were non-paroxysmal AF (vs. paroxysmal AF) (OR = 6.2, p=0.015), heart failure (OR = 3.22, p=0.003), and a eGFR <60 ml/min/1.73 m(2) (OR = 2.65, p=0.012); the predictors in patients treated with rivaroxaban were non-paroxysmal AF (vs. paroxysmal AF) (OR = 5.73, p=0.0221) and heart failure (OR = 3.19, p=0.116). In ROC analysis of the dabigatran group, the area under the curve (AUC) for the CHA(2)DS(2)-VASc-RAF score was significantly higher (0.78) than those for the CHADS(2), CHA(2)DS(2)-VASc, and R(2)CHADS(2) scores (0.67, 0.70, and 0.72, respectively). In the rivaroxaban group, the CHA(2)DS(2)-VASc-RAF score also performed significantly better (AUC of 0.77) than the CHADS(2), CHA(2)DS(2)-VASc, and R(2)CHADS(2) scores (AUC of 0.66, 0.64, and 0.67, respectively). The risk of LAAT was the same for patients in both treatment groups. In all patients, non-paroxysmal AF or heart failure, and in patients treated with dabigatran an eGFR <60 ml/min/1.73 m(2), were independent predictors of LAAT. The new CHA(2)DS(2)-VASc-RAF scale had the highest predictive value for LAAT in the entire study population.