Device-related thrombus (DRT) is a known complication occurring in up to 7% of patients undergoing percutaneous left atrial appendage closure (LAAC). Since the target population of LAAC is generally ineligible for oral anticoagulant therapies, DRT raises important concerns. The aim of this review will be to summarize available evidence on DRT after LAAC focusing on its possible impact on outcomes. Recent findings showed a tighter association between DRT and neurological ischemic events. Antithrombotic regimen adopted after LAAC may have a protective effect against DRT. Many patient-related and procedural factors have been identified as possible predictors of DRT. A tailored approach, which takes into account DRT, is needed in the patient selection for LAAC and in the postprocedural follow-up.

Impact and predictors of device-related thrombus after percutaneous left atrial appendage closure / Branca, Luca; Tomasoni, Daniela; Cimino, Giuliana; Cersosimo, Angelica; Lombardi, Carlo Mario; Chizzola, Giuliano; Metra, Marco; Adamo, Marianna. - In: JOURNAL OF CARDIOVASCULAR MEDICINE. - ISSN 1558-2027. - Publish Ahead of Print:(2022). [10.2459/JCM.0000000000001394]

Impact and predictors of device-related thrombus after percutaneous left atrial appendage closure

Metra, Marco;
2022-01-01

Abstract

Device-related thrombus (DRT) is a known complication occurring in up to 7% of patients undergoing percutaneous left atrial appendage closure (LAAC). Since the target population of LAAC is generally ineligible for oral anticoagulant therapies, DRT raises important concerns. The aim of this review will be to summarize available evidence on DRT after LAAC focusing on its possible impact on outcomes. Recent findings showed a tighter association between DRT and neurological ischemic events. Antithrombotic regimen adopted after LAAC may have a protective effect against DRT. Many patient-related and procedural factors have been identified as possible predictors of DRT. A tailored approach, which takes into account DRT, is needed in the patient selection for LAAC and in the postprocedural follow-up.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/193801
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