scholarly journals Prognostic impact of model for end-stage liver disease (MELD) scores greater than 40 in deceased donor liver transplant recipients

2020 ◽  
Vol 34 (1) ◽  
pp. S156-S156
Author(s):  
Byeong-Gon Na ◽  
Shin Hwang ◽  
Gil-Chun Park ◽  
Gi-Won Song ◽  
Dong-Hwan Jung ◽  
...  
Keyword(s):  
Liver Disease ◽  
Liver Transplant ◽  
Deceased Donor ◽  
Prognostic Impact ◽  
Transplant Recipients ◽  
Donor Liver ◽  
End Stage Liver Disease ◽  
Donor Liver Transplant ◽  
End Stage ◽  
Liver Transplant Recipients

Prognostic impact of MELD scores greater than 40 in deceased donor liver transplant recipients

2021 ◽  
Vol 1 (1) ◽  
pp. 2-9
Author(s):  
Byeong-Gon Na ◽  
Shin Hwang ◽  
Gil-Chun Park ◽  
Gi-Won Song ◽  
Dong-Hwan Jung ◽  
...  
Keyword(s):  
Liver Transplant ◽  
Deceased Donor ◽  
Prognostic Impact ◽  
Transplant Recipients ◽  
Donor Liver ◽  
Donor Liver Transplant ◽  
Liver Transplant Recipients

Prognostic impact of MELD scores greater than 40 in deceased donor liver transplant recipients

2021 ◽  
Vol 1 (1) ◽  
pp. 10-17
Author(s):  
Byeong-Gon Na ◽  
Shin Hwang ◽  
Gil-Chun Park ◽  
Gi-Won Song ◽  
Dong-Hwan Jung ◽  
...  
Keyword(s):  
Liver Transplant ◽  
Deceased Donor ◽  
Prognostic Impact ◽  
Transplant Recipients ◽  
Donor Liver ◽  
Donor Liver Transplant ◽  
Liver Transplant Recipients

scholarly journals Hepatitis C disease severity in living versus deceased donor liver transplant recipients: An extended observation study

Hepatology ◽  
2014 ◽  
Vol 59 (4) ◽  
pp. 1311-1319 ◽  
Author(s):  
Norah A. Terrault ◽  
R. Todd Stravitz ◽  
Anna S.F. Lok ◽  
Greg T. Everson ◽  
Robert S. Brown ◽  
...  
Keyword(s):  
Hepatitis C ◽  
Liver Transplant ◽  
Disease Severity ◽  
Deceased Donor ◽  
Transplant Recipients ◽  
Donor Liver ◽  
Observation Study ◽  
Donor Liver Transplant ◽  
Liver Transplant Recipients

scholarly journals Tacrolimus Pharmacokinetics in Living-Donor and Deceased-Donor Liver Transplant in Saudi Patients

2019 ◽  
pp. 288-294
Author(s):  
Hisham S. Abou-Auda ◽  
Eqbal Qaddour ◽  
Hussein Alsisi ◽  
Azizah Ajlan ◽  
Mohammad Alsebayel
Keyword(s):  
Liver Transplant ◽  
Deceased Donor ◽  
Apparent Volume ◽  
Volume Of Distribution ◽  
Transplant Recipients ◽  
Donor Liver ◽  
Apparent Clearance ◽  
Donor Liver Transplant ◽  
Liver Transplant Recipients ◽  
Apparent Volume Of Distribution

Introduction: Tacrolimus is a macrolide immunosuppressant. It has a narrow therapeutic index and serious side effects which necessitate monitoring of tacrolimus blood concentration. The trough concentration of the drug may also differ based on the type of liver transplant. This study was conducted to investigate differences in pharmacokinetics between transplant types and to determine tacrolimus population pharmacokinetic in liver transplant recipients in Saudi Arabia. Method: Patients on tacrolimus, as the main immunosuppressant, who underwent liver transplant throughout2012-2014 were retrospectively studied. Demographic characteristic, tacrolimus blood trough concentrations, liver, renal, biochemistry, and hematology lab results were all collected. The pharmacokinetic parameters were estimated assuming one compartment model. Results: Tacrolimus pharmacokinetic parameters were found to be as following; elimination rate constant () 0.094 ±  0.0123, apparent volume of distribution () 112.48±63.033 L/hr, elimination half-life () 7.46± 1.01 hr and apparent total body clearance () 10.27± 5.69 L/hr (mean ± SD). Statistically significant difference was found between living-donor and deceased-donor liver transplant with respect to apparent clearance and apparent volume of distribution. Living-donor liver transplant recipients have apparent volume of distribution of 97.39±47.00 L (mean ± SD) and an apparent clearance of 8.89±4.24L/hr (mean± SD). On the other hand, deceased-donor liver transplant has an apparent clearance of 12.97±7.09L/hr (mean ± SD) and an apparent volume of distribution of 142.17± 78.65 L (mean ± SD). Conclusions: Tacrolimus pharmacokinetics parameters were accurately determined in liver transplant recipients in Saudi Arabia. The results of the present study can be clinically used in the therapeutic drug monitoring of tacrolimus in the individualization of drug dosage and taking the appropriate clinical decisions to prevent allograft rejection.

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