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Clinical Trials/NCT05386953
NCT05386953
Unknown
Not Applicable

Intraoperative Normal Saline Administration and Acute Kidney Injury in Patients Undergoing Liver Transplantation: a Retrospective Cohort Study

Seoul National University Hospital1 site in 1 country1,440 target enrollmentStarted: April 1, 2022Last updated:

Overview

Phase
Not Applicable
Enrollment
1,440
Locations
1
Primary Endpoint
Acute kidney injury

Overview

Brief Summary

The investigators attempted to investigate the association of the type of crystalloid administered during liver transplantation with postoperative clinical outcomes. The investigators hypothesized that the greater amount of normal saline or half-saline administered during liver transplantation might be associated with the increased risk of acute kidney injury compared to the balanced crystalloids.

Detailed Description

Liver transplantation requires a long operation time and is often associated with a significant amount of surgical bleeding. It is common for the anesthesiologist to infuse large amounts of fluid or blood products due to bleeding, hemodynamic instability, or ascites drainage. Therefore, in the anesthesia for liver transplantation, optimal management of fluid administration is necessary and the choice of the type of crystalloid may affect the prognosis or the incidence of postoperative complications of patients.

The investigators attempted to investigate the association of the type of crystalloid administered during liver transplantation with postoperative clinical outcomes. The investigators hypothesized that the greater amount of normal saline or half-saline administered during liver transplantation might be associated with the increased risk of acute kidney injury compared to the balanced crystalloids.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
20 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Consecutive patients who underwent living or deceased donor liver transplantation at our tertiary care university hospital between 2004 and 2018

Exclusion Criteria

  • patients with baseline renal dysfunction of hepatorenal syndrome or chronic kidney disease
  • missing preoperative serum creatinine value
  • missing other baseline or outcome variables
  • patients who received retransplantation

Arms & Interventions

Balanced group

Patients who received balanced crystalloids of lactated Ringer's solution or plasma solution during liver transplantation surgery

Intervention: Balanced crystalloid solution (Drug)

Saline group

Patients who received only normal saline during liver transplantation surgery

Intervention: Normal saline (Drug)

Outcomes

Primary Outcomes

Acute kidney injury

Time Frame: the first 7 postoperative days

The investigators defined acute kidney injury by the KDIGO (Kidney Disease Improving Global Outcomes) criteria, which was determined according to the greatest change in serum creatinine level during the postoperative seven days (Stage 1: more than 1.5-fold; stage 2: more than 2-fold; stage 3: more than 3-fold increase of baseline or increase in SCr to ≥ 4.0 mg/dL or the initiation of renal replacement therapy). The most recent SCr level measured before surgery was collected as a baseline value.

Secondary Outcomes

  • In-hospital mortality(the first month after admission)
  • One-year mortality(one year after transplantation)
  • Length of intensive care unit stay(the first month after admission)
  • Length of hospital stay(the first month after admission)
  • Incidence of postoperative hemodialysis(the first month after admission)
  • Early allograft dysfunction(the first 7 postoperative days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Won Ho Kim, MD

Professor

Seoul National University Hospital

Study Sites (1)

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