Neuromonitoring in Patients During Aortic Valve Replacement (IMLPBIAVR)
Brain Injury
About this trial
This is an interventional prevention trial for Brain Injury focused on measuring Aortic valve surgery
Eligibility Criteria
Inclusion Criteria:
- Isolated aortic valve stenosis as well as asymptomatic patients with depressed systolic function
- Symptomatic patients with normal or depressed left ventricular function
- Patients with American Society of Anesthesiologist (ASA) physical status classification 2 or 3
Exclusion Criteria:
- History of brain stroke
- EF less than 20%
- History of alcohol abuse
- Epilepsy of history of psychiatric illness and antipsychotic drugs
- Patients with stenosis on carotid arteries
- Patients with preformed surgery or already stented carotid arteries
- Patients with poor or absent acoustic temporal window
- Diagnosed dementia
Sites / Locations
- University Clinical center
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
AVR preformed with full sternotomy
AVR preformed with minimal invasive sternotomy
30 patients, 7 days before and after surgery mini mental test and measurement of visual evoked cerebral blood flow response (VEFR) will be done. Transcranial doppler measurements 1. beginning of the surgery, 2.after sternotomy, 3.during aortic cannulation,4.during CPB,5. during de-airing, 6. opening of the clamp on the aorta, 7. after CPB removal before chest closure. Prolonged de airing if needed
30 patients, 7 days before and after surgery mini mental test and measurement of visual evoked cerebral blood flow response (VEFR) will be done. Transcranial doppler measurements 1. beginning of the surgery, 2.after sternotomy, 3.during aortic cannulation,4.during CPB,5. during de-airing, 6. opening of the clamp on the aorta, 7. after CPB removal before chest closure. Prolonged de airing if needed