Liver Failure Clinical Trial
Official title:
Metabolic Preconditioning Using Intravenous Dextrose: a Novel Strategy to Improve Hepatic Function After Liver Resection
The goal of the study is to determine whether intravenous glucose administration before liver
resection preserves hepatic glycogen resulting in improved hepatic metabolic function after
the operation.
We further investigate whether the benefit of avoiding preoperative fasting is more
pronounced in patients undergoing more extensive liver resection.
Background. With a reported incidence of up to 70%, liver failure is the most frequent
complication necessitating intensive care and prolonging hospital stay. Animal studies
suggest that the glycogen content of the liver is a key regulator of liver function and that
glycogen depletion, a mandatory consequence of preoperative fasting, is associated with poor
clinical outcome.
The results of a pilot study demonstrate that metabolic preconditioning, i.e. the avoidance
of preoperative fasting by intravenous administration of dextrose preserves hepatic glycogen
and prevents hepatic dysfunction after liver resection. Liver function in this protocol was
assessed by a score originally proposed by Schindl including serum concentrations of total
bilirubin and lactate, prothrombin time and degree of encephalopathy. Due to alterations
induced by anesthesia and surgery, e.g. blood loss necessitating transfusion, hypothermia,
inflammatory responses and use of drugs with impact on hepatobiliary metabolism, liver
function scores do not necessarily reflect functional integrity and metabolic capacity of the
liver. In contrast, measuring the production of proteins that are exclusively synthetized by
hepatocytes such as albumin allows a more specific and quantitative assessment of hepatic
performance under perioperative conditions.
Hypothesis. We propose a randomized double-blinded study to test the hypothesis that, in
patients scheduled for resection of liver cancer, metabolic preconditioning with intravenous
dextrose preserves hepatic glycogen resulting in improved hepatic metabolic function
postoperatively. We further hypothesize that the benefit of avoiding preoperative fasting is
more pronounced in patients undergoing more extensive liver resection. Hepatic synthetic
capacity will be assessed by measuring albumin synthesis using a stable isotope tracer
technique.
Research plan. In order to test the validity of our assumptions, we will perform studies in
patients scheduled for minor (study I; one or two liver segments, n=30) or major (study II;
three or more liver segments, n=20) liver resection. In a double blinded fashion patients
will be randomly assigned to receive either intravenous dextrose at 2 mg/kg/min or saline
from 15:00 on the day before the operation until surgical skin incision. Metabolic processes
at the organ level (liver, muscle), i.e. fractional synthesis rates of albumin, hepatic acute
phase proteins (transthyretin (=prealbumin), fibrinogen, total plasma proteins) and muscle
protein will be determined one day before and one day after the operation using
primed-continuous infusions of L-[2H5]phenylalanine. Stable isotopes (L-[1-13C]leucine,
[6,6-2H2]glucose) will be applied to assess dynamic changes in whole body protein and glucose
metabolism before and after surgery, i.e. protein breakdown, amino acid oxidation, protein
synthesis, glucose production and glucose uptake.
Significance. The demonstration that the preconditioning with dextrose preserves metabolic
performance of the liver would have important implications for the clinical management of
surgical patients with liver cancer. If preoperative dextrose administration attenuates
hepatic dysfunction after liver resection, it will provide these patients with a readily
available, safe and inexpensive therapy.
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