Norepinephrine Weaning Guided by the Hypotension Prediction Index in Vasoplegic Shock After Cardiac Surgery (NORAHPI)
Vasoplegia, Shock, Norepinephrine
About this trial
This is an interventional other trial for Vasoplegia focused on measuring vasoplegia, shock, hypotension prediction index, Acumen, CABG, norepinephrine, surgery
Eligibility Criteria
Inclusion Criteria: Age > 18 years The patient was hospitalized in the cardiothoracic-vascular and respiratory intensive care unit of Amiens-Picardy University Hospital. Patient scheduled for on-pomp cardiac surgery [coronary artery bypass grafting, valve replacement, ascending aorta replacement, or combined surgery (valve and bypass grafting)]. Introduction of norepinephrine post-surgery for the treatment of vasoplegic syndrome. On-pomp cardiac surgery in less than 48 hours. Hemodynamically stable patient with MAP > 65 mmHg for more than 4 hours on noradrenaline Monitoring of MAP with a radial or femoral arterial catheter Social security beneficiary Signature of the consent to participate in the study by the patient, preoperatively Exclusion Criteria: Permanent arrhythmia (atrial fibrillation, flutter, or frequent atrial extrasystoles). Treatment with dobutamine, epinephrine, or vasopressin analog Patients with preoperative chronic end-stage renal failure require postoperative extra-renal purification. Pregnant woman The patient is dependent on an internal or external pacemaker. Hypothermia < 36°. Patient under mechanical circulatory assistance after cardiac surgery. Hemorrhagic shock Patient under guardianship or curators
Sites / Locations
- CHU Amiens Picardie
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Standard care arm
Experimental arm (HPI-guided)
MAP-based (MAP > 65 mmHg) norepinephrine weaning protocol
MAP-based (MAP > 65 mmHg) norepinephrine weaning protocol and guided by the HPI (HPI<80) delivered by the Acumen IQ medical device.