Non-Vitamin K Antagonist Oral Anticoagulants in Patients with β-Thalassemia.
Michele MalagùFilomena LongoFederico MarchiniPaolo SirugoAndrea CapanniStefano ClóElisa MariMartina CulcasiMatteo BertiniPublished in: Biology (2023)
Background . Patients with β-thalassemia have a high incidence of atrial fibrillation (AF) and other supraventricular arrhythmias. The use of non-vitamin K antagonist oral anticoagulants (NOACs) for thromboembolic prophylaxis in patients with β-thalassemia has not been systematically evaluated. Methods. We enrolled patients with transfusion-dependent β-thalassemia, who were on treatment with NOACs for thromboembolic prophylaxis of supraventricular arrhythmias. Data on thromboembolic and bleeding events were collected. Results. Eighteen patients were enrolled. The patients had a history of AF (sixteen), typical atrial flutter (five), and atypical atrial flutter (four). The patients were treated with dabigatran (seven), apixaban (five), rivaroxaban (four) or edoxaban (two). The mean follow-up duration was 22 ± 15 months. No thromboembolic events were reported. No major bleedings were observed. Three patients had non-major bleeding events. Two patients reported dyspepsia during treatment with dabigatran and were shifted to a different NOAC. Conclusions. Our study suggests the efficacy and safety of NOACs in patients affected by transfusion-dependent β-thalassemia.
Keyphrases
- atrial fibrillation
- oral anticoagulants
- end stage renal disease
- catheter ablation
- ejection fraction
- newly diagnosed
- chronic kidney disease
- left atrial
- peritoneal dialysis
- helicobacter pylori
- deep learning
- patient reported
- data analysis
- left atrial appendage
- acute coronary syndrome
- percutaneous coronary intervention
- mitral valve
- helicobacter pylori infection