MedPath

Intraoperative Dialysis in Liver Transplantation

Not Applicable
Terminated
Conditions
Multi-organ Failure
Liver Failure
Acute Kidney Disease
Interventions
Device: Continuous renal replacement therapy (CRRT)
Procedure: Standard intraoperative support
Registration Number
NCT01575015
Lead Sponsor
University of Alberta
Brief Summary

Patient with liver failure waiting for liver transplantation are often hospitalized and commonly supported in an intensive care unit prior to surgery. These patients are sick, and in addition to the complications of a failing liver, other organs such as the kidneys often fail as well. As a consequence, these patients are at an increased risk for complications related to their kidney failure during their liver transplantation procedure. One potential method to diminish the risk of these complications is to provide dialysis support to these patients during their liver transplantation in the operating theater in the form of continuous renal replacement therapy (CRRT). While this is increasingly being performed and is theoretically appealing, there is very little information to support this practice. In addition, the use of CRRT during surgery is not entirely without risk. The investigators have performed two preliminary studies on the use of CRRT during liver transplantation and our data would strongly support the need to conduct further higher-quality studies to better evaluate its feasibility, safety and usefulness. Our proposed study is for a randomized trial comparing the use of CRRT during surgery with standard supportive care in sick patients with liver failure scheduled to receive a liver transplantation.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • Consent
  • Adult (age > 18 years on the day of assessment of eligibility)
  • Planned cadaveric orthotopic liver transplantation
  • Pre-operative unadjusted (natural) Modification of End-Stage Liver Disease (MELD) score > 25.
  • Pre-operative AKI, defined by a minimum RIFLE-RISK, AND/OR pre-operative estimated glomerular filtration rate (eGFR) <60 mL/min/1.73m2, calculated by the Modification of Diet in Renal Disease (MDRD) equation.
Exclusion Criteria
  • Planned living-related donor liver transplantation
  • Pre-operative potassium [K] > 4.5 mmol/L AND urine output < 100 mL in the 6 hrs preceding assessment of eligibility
  • Pre-operative pH < 7.3

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intraoperative renal support (CRRT)Continuous renal replacement therapy (CRRT)-
Standard intraoperative support (no CRRT)Standard intraoperative support-
Primary Outcome Measures
NameTimeMethod
Number of patients adhering to the prescribed protocolIntra-operative (From the induction of anesthesia to trasnfer from the OR to the ICU, average 6-8 hours)

Will be defined as the proportion of patients adhering to the prescribed protocol.

Number of patients with adverse eventsIntra-operative (From the induction of anesthesia to trasnfer from the OR to the ICU, average 6-8 hours)

This will be defined by the proportion of patients experiencing intra-operative adverse events, serious adverse events and complications related to the study intervention.

Secondary Outcome Measures
NameTimeMethod
Fluid balanceIn-hospital (patients will be followed for duration of post-operative hospital stay, anticipated average 4 weeks post-operatively)

Will be defined as the changes in fluid accumulation intra- and post-operatively.

Number of patients with post-operative graft dysfunctionIn-hospital (patients will be followed for duration of post-operative hospital stay, anticipated average 4 weeks post-operatively)

Graft dysfunction will include post-operative ultrasonographic-evidence of vascular ischemia/occlusion or venous occlusion; biliary stricture, obstruction or anastomosis leak; primary non-function; biopsy-proven rejection; or need for surgical re-exploration for any reason.

Number of patients with post-operative kidney dysfunctionFrom the date of liver transplant until the date of first documented outcome of interest, assessed until 90-days

Will be defined as post-operative acute kidney injury, defined by RIFLE criteria; along with encompassing receipt of renal replacement therapy (RRT).

Length of stayFrom the date of liver transplant until the date of discharge from ICU/hospital

Will include ICU and hospital lengths of stay

MortalityFrom the date of liver transplant until the date of first documented outcome of interest, assessed until 90-days

Mortality through 90-days.

Number of patients readmitted to hospital within 90-daysFrom the date of liver transplant after hospital discharge, until the date of first documented re-admission to hospital, assessed until 90-days

Will be defined as hospital re-admission within 90-days of liver transplant for any cause.

Trial Locations

Locations (1)

Division of Critical Care Medicine, University of Alberta Hospital

🇨🇦

Edmonton, Alberta, Canada

© Copyright 2025. All Rights Reserved by MedPath