The purpose of the project is to elucidate whether it is possible to identify which patients are at risk of forming blood clots that can cause stroke based on analysis of the electrocardiogram. In connection with the operation, the small pouch known as the auricle of the heart is closed, which can be completely removed after closing. This procedure is common in patients with atrial fibrillation to protect the brain from stroke. In the project, all patients will have this auricle closed if they agree to participate in the project. After closure, the auricle is usually discarded. We will analyze the blood and the auricle tissue taken (if available) in connection with the operation itself, together with the analysis of the electrocardiogram recorded before the planned heart operation.
Patients scheduled for elective heart surgery are invited to participate. After informed consent is signed, an ECG and blood samples are gathered the day before surgery or the same day of the surgery is planned. During surgery, the patients undergo closure of the left atrial appendage (LAA). The choice of the device is at the discretion of the surgeon. If possible, the entire LAA is removed and processed for further analysis. The right atrial appendage is likewise removed and follows the same procedure as the LAA. The analyses include measurement of up-/down-regulated thrombosis factors and inflammatory markers. The right and left atrial appendage tissue collected are immediately processed for micro-patch-clamp studies, and the remaining tissue is divided into a part that is frozen for later analyses and a part that is fixed and embedded in paraffin for further histological analyses.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
1,000
systematic closure of the left atrial appendage in addition to the planned heart surgery
Rigshospitalet
Copenhagen, Denmark
RECRUITINGstroke
number of patients with clinical stroke
Time frame: six years
perioperative atrial fibrillation
number of patients with incident atrial fibrillation the days after surgery, prior to discharge
Time frame: 30 days
silent brain infarctions
number of patients in whom asymptomatic ischemic infarctions are identified in brain scans (CTC or MRI)
Time frame: six years
occurrence of atrial fibrillation during follow-up
Time frame: ten years
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