The purpose of this study is to determine the incidence of major vascular events (ischemic or haemorrhagics) at the third month after initiation of the antithrombotic treatment (oral anticoagulation or dual antiplatelet therapy) in both arms followed TAVI.
Transcatheter aortic valve implantation (TAVI) procedure using any of their vascular access is an option with proven benefit definitively for treatment of severe symptomatic aortic stenosis in patients considered unsuitable for conventional open heart surgery. By avoiding the hemodynamic effects, cardiovascular and cerebral microembolic load of cardiopulmonary bypass circulation, it is assumed that the TAVI procedure is beneficial despite the risk of neurological complications. Currently antithrombotic therapy after the procedure is not standardized. International treatment guidelines recommends that post-operative patients with a conventional surgical aortic bioprosthesis maintain oral anticoagulation for 3 months after the procedure, unless otherwise noted for its continuation. Whereas some studies have postulated that in patients with aortic bioprostheses, dual antiplatelet therapy is as effective to prevent major cardiac and cerebrovascular events as oral anticoagulation, with a lower incidence of bleeding complications at 3 months of treatment, the investigators formulated the following hypothesis: • There is a lower incidence of major cardiac and cerebrovascular events in patients with dual antiplatelet therapy compared to patients with oral anticoagulation for 3 months after implantation of an aortic bioprosthesis TAVI procedure.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
124
100 mg aspirin ;75 mg clopidogrel 3º months
Policlínica de Guipuzcoa.SA
San Sebastián, Guipúzcoa, Spain
Hospital Universitario Álvaro Cunqueiro
Vigo, Pontevedra, Spain
Hospital clinico Universitario Bellvitge
Barcelona, Spain
Hospital Clinico Universitario de Malaga
Málaga, Spain
Evaluate the effectiveness of dual antiplatelet therapy versus oral anticoagulation for prevention of cerebral thromboembolism by the detection of new areas of cerebral infarction by Magnetic Resonance Imaging (MRI) 3 months after TAVI.
Time frame: 3 months
Determine the incidence of new areas of cerebral infarction by MRI between the different routes of vascular access and the various valve devices.
Time frame: 1 hour before TAVI, 1 hour and 24 hours after TAVI
Identify the development of cognitive impairment after TAVI
By the application of: 1)Mini-Mental State Examination (MMSE); 2)SF 36 (spanish version); 3)The NIHSS (National Institute of Health Stroke Scale). The evaluation of the neurological tests will be performed by a certificated neurologist.
Time frame: Pre-TAVI, and at 1º 3º and 6º month after TAVI
Evaluate the Quality of life after TAVI.
By the application of Euroquol EQ5.
Time frame: Pre-TAVI, and at 1º; 3º and 6º month after TAVI.
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