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The goal of this clinical trial is to compare two different hemodynamic monitoring techniques during orthotopic liver transplantation.
The main question it aims to answer is: if using a different hemodynamic monitoring might help reducing the intraoperative hypotension time. Participants will be randomized to one of two arms of hemodynamic monitoring:
Intraoperative hypotension is an independent risk factor for the development of complications and postoperative mortality. In non-cardiac surgery, in particular, the time spent under a mean arterial pressure (MAP) of 55 correlates with an increase in myocardial ischemic damage, acute renal failure, and 30-day mortality.
Orthotopic liver transplantation (OLT) is a complex and risky procedure both from a surgical and an anesthesiological standpoint. Difficulties in hemodynamic management arise from the pathophysiological alterations in cirrhotic patients, high-impact surgical procedures (e.g., caval and portal clamping), high bleeding risk, and post-reperfusion syndrome (PRS).
In liver transplantation, the pulmonary artery catheter (PAC) remains the "gold standard" for hemodynamic instability monitoring and is placed in over 90% of patients in the USA.
Transesophageal echocardiography (TEE) is a semi-invasive ultrasound monitoring procedure. As recognized in a recent position paper by the Society for the Advancement of Transplant Anesthesia (SATA), there has been a considerable increase in the use of TEE during OLT in recent years, despite the lack of randomized controlled trials (RCTs) confirming its effectiveness. According to the SATA task force, the increased intraoperative use of TEE is imputable to the chance for a more thorough understanding of hemodynamic pathophysiology and the possibility of identifying new findings, otherwise not identifiable with PAC (cardiac tamponade, gas embolism, intracardiac thrombus, papillary muscle/chordae rupture, left ventricular outflow tract obstruction, etc.). The overall complication rate of TEE in the articles analyzed by SATA was found to be 0.47% compared to 5-10% for PAC complications, thus supporting the safety of the procedure.
Currently, there is a lack of published RCTs comparing these monitoring methods to determine if there is an optimal intraoperative monitoring system during OLT.
The research hypothesis of this study is that TEE monitoring allows for better hemodynamic management during OLT, reducing the duration of hypotension and providing better guidance fo fluid-pharmacological therapy compared to standard monitoring (PAC).
The primary outcome is to compare the impact of two different hemodynamic monitoring systems (TEE and PAC) on intraoperative hemodynamic optimization during OLT.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| PAC hemodynamic monitoring | No Intervention | Patients undergoing Liver Transplantation are monitored using the pulmonary artery catheter. | |
| TEE hemodynamic monitoring | Experimental | Patients undergoing Liver Transplantation are monitored using Transesophageal echocardiography and blinded to the pulmonary artery catheter data (insertion of PAC for patient safety is still mandatory, unblinding is allowed if needed for management by the OR anesthesiologist in charge) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| TEE hemodynamic monitoring | Other | Transesophageal echocardiography monitoring to guide administration of fluids, vasopressor and inotropes during liver transplantation in order to avoid hypotension. |
| Measure | Description | Time Frame |
|---|---|---|
| Number of minutes with mean blood pressure (MAP) less than 65mmHg throughout surgery | Cumulative time (in minutes) spent under mean arterial pressure of 65 mmHg. | From incision to end of procedure (for the entire surgical procedure in a period ranging from 0 to 24 hours). |
| Measure | Description | Time Frame |
|---|---|---|
| New Onset Renal Failure | New onset Renal Failure according to KDIGO( Kidney Disease Improving Global Outcomes) Criteria for Acute Renal Failure | From the end of the surgical procedure until discharge from hospital (whole duration of Hospital admission, considered within 3 months) |
| New Onset Neurological disturbances |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Amedeo Bianchini, MD | Contact | 051 2143101 | +39 | amedeo.bianchini@aosp.bo.it |
| Matteo Bianchin, MD | Contact | matteo.bianchin@gmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Amedeo Bianchini, MD | IRCCS Azienda Ospedaliero-Universitaria di Bologna | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| IRCSS AOU di Bologna | Recruiting | Bologna | Emilia-Romagna | 40138 | Italy |
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Cumulative assessement of new-onset delirium, focal neurological disturbances or alteration of Glasgow Coma Scale GCS (from worst value GCS=3 to best value GCS=15 ) compared to the pre-operative status |
| From the end of surgery for the first 24 hours after withdrawal of sedation in the ICU. |
| New Onset Cardiological events | Cumulative outcome of : new onset acute coronary syndromes, ischemic alterations on post-operative EKG, new onset tricuspid insufficiency. | From the end of the surgical procedure until discharge from hospital (whole duration of Hospital admission, considered within 3 months) |
| Cumulative Incidence of Early Graft Dysfunction / Primary Non Function | Cumulative Incidence of Early Graft Dysfunction / Primary Non Function as markers of graft failure. | According to definition (up to 7 days after procedure). |
| Duration of Post-Reperfusion Syndrome | Duration of Post-Reperfusion Syndrome defined as hypotension (MAP< 65mmHg) lasting more than 1 minute in the first 5 minutes after portal graft anastomosis. | First 5 minutes after portal graft anastomosis. |
| Total amount of fluids administered during surgery | Total amount of crystalloids (in milliliters) administered during surgery | From incision to end of procedure (for the entire surgical procedure in a period ranging from 0 to 24 hours) |
| Cumulative dosage of vasoactive amines administered during surgery | Total amount of norepinephrine and epinephrine (in mcg and in maximum dosage - mcg/kg/h - ) administered during surgery. | From incision to end of procedure (for the entire surgical procedure in a period ranging from 0 to 24 hours) |
| Cumulative incidence of adverse events attributable to the hemodynamic monitoring used | Cumulative incidence of adverse events attributable to the hemodynamic monitoring used | From the end of the surgical procedure until discharge from hospital (whole duration of Hospital admission, considered within 3 months) |
| Duration of ICU admission | Duration of ICU admission in days | From a minimum of 2 days to a maximum of 3 months |
| Mortality at 30 and 90 days | Mortality at 30 and 90 days | 1 month and 3 months after surgical procedure. |