Transradial approach (TRA) for cardiac catheterization and percutaneous coronary interventions (PCI) is increasingly being used worldwide. At the present is unknown the cocktail of agents necessary to minimize local access site complications. The investigators planned a prospective randomized clinical trial to test the superiority of verapamil vs. heparin in the reduction of access site related complications.
Transradial approach (TRA) for cardiac catheterization and percutaneous coronary interventions (PCI) is increasingly being used worldwide in both elective and emergency procedures because it reduces net adverse clinical events, through a reduction in major bleeding and all-cause mortality, when compared to transfemoral approach. However, radial artery occlusion (RAO) after the procedure (the incidence of which varies from 1% to 10%) remains one of the major limitations of TRA. The aim of the study is to assess the superiority of verapamil versus heparin in the access success during transradial percutaneous coronary interventions (PCI). METHODS Patients referred to the cath-lab of the Cardiovascular Institute of the University Hospital of Ferrara, Italy, for coronary angiography were randomized in 2 groups with a computer-generated random sequence. The study is double-blind. In the first group, patients received intravenous heparin (5000 UI) immediately after a 6 F sheath insertion. In the second group, patients received Verapamil (5 mg) immediately after a 6 F sheath insertion. If after the start of the procedure a radial artery spasm (RAS) occurs, the operators can choose to use bail-out a local vasodilator therapy. After sheath removal, hemostasis was obtained using a TR band (Terumo corporation, Tokyo, Japan) with a plethysmography-guided patent hemostasis technique. Radial artery patency was evaluated at 24 hours (early RAO) and 30 days after the procedure (late RAO) by ultrasound. The aim of the study is to demonstrate that verapamil administration is superior to heparin administration in the reduction of the combined endpoint (occurrence of radial artery occlusion (early RAO), access site complication, radial artery spasm (RAS) requiring local bailout use of vasodilatator) RAO will be assessed by ultrasonography by independent expert reviewer blinded to randomization The investigators defined access site complication the following items: * local haematoma superficial \<5 cm from access site; * haematoma with moderate muscle infiltration \<10 cm; * forearm haematoma and muscular infiltration below the elbow; * haematoma and muscular infiltration above the elbow; * ischemic threat (compartmental syndrome); * radial artery dissection during the procedure; The investigators defined radial artery spasm any spasm occurring during the procedure requiring the administration of local vasodilatators to allow the procedure
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
418
University Hospital of Ferrara
Cona, Ferrara, Italy
number of participants with radial artery-related complications
occurrence of early radial artery occlusion, access site complication, radial artery spasm (RAS) that requires the bailout use of vasodilatator
Time frame: 24 hours
number of participants with each radial artery-related complication
occurrence of each singular component of primary endpoint
Time frame: 24 hours
late radial artery occlusion
occurrence of radial artery occlusion (late RAO)
Time frame: 30 days
reopening early RAO
reopening of the closed radial at 24 hours.
Time frame: 30 days
patient's satisfaction
assessment with questionnaires of the pain and satisfaction of patients
Time frame: 24 hours
long term patient's satisfaction
assessment with questionnaires of the pain and satisfaction of patients
Time frame: 30 days
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