Perfusion Pressure Cerebral Infarction Trial (PPCI) (PPCI)
Embolic Stroke, Postoperative Cognitive Dysfunction
About this trial
This is an interventional prevention trial for Embolic Stroke focused on measuring Ischemic stroke, Embolic stroke, Postoperative Cognitive Dysfunction, Cardiac Bypass Surgery, Cardiac Anaesthesia
Eligibility Criteria
Inclusion Criteria:
- ≥ 18 years of age.
- scheduled elective or subacute cardiac surgery with the use of CPB.
- type of surgery either coronary artery bypass grafting (CABG) and/or heart valve surgery (provided that the valve prosthesis used is MRI compatible).
Exclusion Criteria:
- a history of stroke.
- a history of reversible ischemic deficits (duration of symptoms 24-72 hours)
- a history of transitory ischemic attacks (duration of symptoms < 24 hours)
- diagnosis of neurodegenerative disorders such as Alzheimers, Multiple Sclerosis etc.
Sites / Locations
- Department of Cardiothoracic Surgery 2152 and Department of Cardiothoracic Anesthesiology 4142, Rigshospitalet / Copenhagen University Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Increased bloodpressure during CPB
Regular bloodpressure during CPB
The cardiopulmonary bypass (CPB) procedure is conducted according to department guidelines with the modification that MAP is kept between 70 and 80 mm Hg. This is achieved by refract intravenous doses of phenylephrine to a total maximum of 2.0 mg, and after that continuous intravenous infusion of norepinephrine up to 0.4 μg/kg/min if necessary.
The cardiopulmonary bypass (CPB) procedure is conducted in accordance with departmental guidelines, where MAP is sought to be ≥ 45 mm Hg. This is achieved by refract intravenous doses of phenylephrine to a total maximum of 2.0 mg, and after that continuous intravenous infusion of norepinephrine up to 0.4 μg/kg/min if necessary.