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

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.

Related Concept Videos

Other Nuclides: 31P, 19F, 15N NMR01:16

Other Nuclides: 31P, 19F, 15N NMR

Many organic, inorganic, and biological molecules contain spin-half nuclei such as nitrogen-15, fluorine-19, and phosphorus-31. As a result, NMR studies of these nuclei have found extensive applications in chemical and biological research.
While fluorine-19 and phosphorous-31 have high natural abundances (100%) and positive gyromagnetic ratios, nitrogen-15 has a low natural abundance and a negative gyromagnetic ratio. However, nitrogen-15 is still preferred over nitrogen-14 (which has a high...
Methods of Documentation II: POMR01:26

Methods of Documentation II: POMR

The Problem-Oriented Medical Record (POMR) revolutionized medical record-keeping by introducing a systematic approach focusing on the patient's problems rather than merely listing symptoms. Dr. Lawrence Weed's introduction of this method in the 1960s marked a significant advancement in medical documentation. The POMR framework consists of four key components: the database, problem list, plan of care, and progress notes.
¹H NMR: Pople Notation01:09

¹H NMR: Pople Notation

The Pople nomenclature system classifies spin systems based on the difference between their chemical shifts. Coupled spins are denoted by capital letters with subscripts indicating the number of equivalent nuclei. When the coupled nuclei have well-separated chemical shifts, they are assigned letters that are far apart in the alphabet, such as A and X. When the difference in chemical shifts is small, coupled nuclei are named using adjacent letters of the alphabet (AB, MN, or XY).
A proton...
¹H NMR: Complex Splitting01:13

¹H NMR: Complex Splitting

A proton M that is coupled to a proton X results in doublet signals for M. However, NMR-active nuclei can be simultaneously coupled to more than one nonequivalent nucleus. When M is coupled to a second proton A, such as in styrene oxide, each peak in the doublet is split into another doublet.
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied first.
Insensitive Nuclei Enhanced by Polarization Transfer (INEPT)01:15

Insensitive Nuclei Enhanced by Polarization Transfer (INEPT)

Insensitive Nuclei Enhanced by Polarization Transfer (INEPT) is an advanced Nuclear Magnetic Resonance (NMR) technique specifically designed to detect and enhance the signals of low-abundance nuclei, such as carbon-13 and nitrogen-15, in small molecules. The fundamental principle behind INEPT is the transfer of polarization from a more abundant and highly polarizable nucleus, typically hydrogen-1, to the low-abundance nucleus of interest. This process effectively boosts the NMR signal of the...
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)01:20

¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)

When proton-coupled carbon-13 spectra are simplified by a broadband proton decoupling technique, structural information about the coupled protons is lost. Distortionless enhancement by polarization transfer (DEPT) is a technique that provides information on the number of hydrogens attached to each carbon in a molecule. While the DEPT experiment utilizes complex pulse sequences, the pulse delay and flip angle are specifically manipulated. The resulting signals have different phases depending on...