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Primary nonfunction (PNF) in the MELD Era: An SRTR database analysis
S R Johnson1, S Alexopoulos, M Curry
1The Transplant Center, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts, USA. srjohnso@bidmc.harvard.edu
Abstract:
PNF following liver transplantation (LT) is an infrequent but life-threatening complication. Liver allocation under MELD is based upon recipient severity of illness, a known risk factor for the occurrence of PNF. The incidence of PNF since the application of MELD has not previously been reported. The SRTR database was studied since inception of MELD until September 2004 for all adult recipients of deceased donor LT. PNF was defined as graft loss or death within 14 days of LT secondary to PNF or without defined cause. A total of 10545 transplants met inclusion criteria and PNF occurred in 613 (5.81%) of recipients. Univariate analysis demonstrated donor age, serum creatinine >1.5 mg/mL, hypertension and CVA as risk factors for PNF. Recipient factors included life support, mechanical ventilation, use of inotropes, hemodialysis, initial status 1 and use of a shared transplant. In the multivariate model only donor age and recipient serum creatinine, bilirubin, on life support and status 1 at transplant were significant risk factors for PNF. In this analysis of PNF in the MELD era the incidence of PNF does not appear to have increased from prior reports. Risk factors for PNF are related to donor age and severity of recipient illness.
Insights
Primary graft dysfunction (PGD) after liver transplantation (LT) remains a severe risk. This study found PGD incidence did not increase with Model for End-Stage Liver Disease (MELD) allocation, with donor age and recipient illness severity being key risk factors.
Area of Science:
- Hepatology
- Transplantation Surgery
- Critical Care Medicine
Background:
- Primary graft dysfunction (PGD) is a rare but critical complication following liver transplantation (LT).
- Liver allocation policies, such as the Model for End-Stage Liver Disease (MELD) score, prioritize recipients based on illness severity, a known risk factor for PGD.
- The incidence of PGD in the era of MELD-based liver allocation had not been previously reported.
Purpose of the Study:
- To determine the incidence of PGD after LT since the implementation of MELD.
- To identify risk factors associated with PGD in adult deceased donor LT recipients under MELD allocation.
- To compare PGD rates in the MELD era with historical data.
Main Methods:
- Analysis of the Scientific Registry of Transplant Recipients (SRTR) database from MELD inception until September 2004.
- Inclusion of adult deceased donor LT recipients.
- Definition of PGD as graft loss or death within 14 days of LT due to PGD or undefined causes.
Main Results:
- A total of 10,545 transplants were analyzed, with PGD occurring in 613 recipients (5.81%).
- Univariate analysis identified donor age, recipient serum creatinine >1.5 mg/mL, hypertension, and cerebrovascular accident (CVA) as risk factors.
- Multivariate analysis revealed donor age, recipient serum creatinine, bilirubin, requirement for life support, and status 1 at transplant as significant risk factors for PGD.
Conclusions:
- The incidence of PGD following LT in the MELD era has not increased compared to previous reports.
- Key risk factors for PGD are associated with donor age and the severity of the recipient's illness.
- Recipient factors such as serum creatinine, bilirubin levels, need for life support, and pre-transplant status are critical predictors of PGD.
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