Taurine Clinical Trial
Official title:
Evaluation of Serum Taurine as a Prognostic Marker for Graft Function in Adult Egyptian Patients Undergoing Living Donor Liver Transplant : A Prospective Study
Although the hepatoprotective properties of taurine are well established, however the correlation of the perioperative serum level of this amino acid in the recipients of living donor liver transplantation ( LDLT ) and graft function has not been investigated so far. In the present study, we proposed to examine the serum taurine as a prognostic marker for graft function in adult Egyptian patients undergoing LDLT
- All selected adult patients undergoing LDLT will be admitted to the ICU post LDLT
- Preoperative assessment and preparation will be done according to the standard protocol
of the hospital. After full clinical examinations using MELD score corrected for serum
sodium level ), imaging techniques (Abdominal U.S; abdominal triphasic CAT Scan, liver
biopsy, CT volumetry, upper and lower GIT endoscopy, CT chest, bone scan in HCC
patients, renal scan in patients with urinary creatinine clearance < 60 ml/min),
pulmonary function test, carotid duplex and dobutamine ECHO will be done for all
recipients .
- Serum level of AST, ALT, bilirubin, albumin, ALP, GGT, prothrombin, INR, partial
thrombin time, factor V, fasting blood glucose, CBC, CRP, Procalcitonin, urea,
creatinine, urinary creatinine clearance, serum electrolytes, urine and stool analysis
will be done for all patients.
- Analysis of serum levels of specific liver tumor markers including AFP, beside taurine
as a possible new marker will be done for all patients .
- HCV and HBV will be detected for all patients by PCR technique.
- CMV IgM , EBV IgM ,HSV IgM will be done for all patients.
- After 12 hours fasting, 10 ml of venous blood will be collected, in plain tube and
allowed to clot for 1/2 an hour. Then, it will be centrifuged at 3,000 rpm for 10 min.
The serum will be separated and stored at -20 Cº to avoid loss of biological activity
until the batch analysis for serum taurine which will be measured four times for the
recipient ( preoperative before induction of anesthesia , 7, 14 days and 30 days post
transplant ) by high performance liquid chromatography (HPLC) .
Recipient patients will be divided into 3 groups according to preoperative serum taurine .
- Group 1 ( > 30 μmol/L) (20 cases)
- Group 2 (30-20 μmol/L) (20 cases)
- Group 3 (< 20 μmol/L ) (20 cases)
Intraoperatively, both standard anesthetic and piggyback techniques for hepatic
transplantation will be performed by the same anesthesia and surgical team who will be
blinded to study medication. Intraoperative blood loss, graft weight, graft weight to
recipient weight ratio (GWRWR), blood products transfused, and intraoperative adverse events
will be recorded. At the end of surgery, patients will be transferred to the ICU and will be
monitored and receive the standard protocol for postoperative management after liver
transplantation .
All patients will be assessed for primary graft function (PGF) on a daily basis during the
first week post-transplant. Primary graft dysfunction includes one or more of the following
variables: (1) bilirubin ≥10 mg/dL on postoperative day 7; (2) INR ≥1.6 on postoperative day
7; and (3) ALT or AST >2000 IU/L within 7 postoperative days.
The primary outcome include correlation between serum taurine levels ( μmol/L) of recipients
and graft function which will be detected by liver profile. Secondary outcomes include 30
days mortality (days), the duration of ICU and hospital stays (days) and any recorded post
operative complications.
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