ArticleTransplantation direct2026
Prolonged Cold Ischemic Time Before Normothermic Machine Perfusion Accentuates Postreperfusion Hepatocellular Injury.
Article in Transplantation direct, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Pathophysiological mechanisms of cell death affecting graft survival in liver transplantation.World journal of transplantation · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Prolonged cold ischemic time (CIT) before liver transplantation with static cold storage preservation is associated with higher rates of ischemia-related complications. With the introduction of normothermic machine perfusion (NMP), the overall incidence of early allograft dysfunction and biliary complications is lower. NMP can be used as a device-to-donor approach (with short CIT) or back-to-base model which is typically associated with longer CIT. It is unknown if NMP can rehabilitate organs that have suffered from prolonged CIT. Methods: Livers from a Yorkshire cross-bred pig donation after circulatory death model were recovered using conventional in situ flush with University of Wisconsin solution after systemic heparinization, followed by static cold storage in University of Wisconsin solution at 4 °C for short (2 h), long (24 h), or extended (48 h) periods of CIT before ex situ NMP. Visual appearance of the liver, perfusion hemodynamics including pressure and flow, as well as perfusate concentration of lactate, aspartate aminotransferase, and alanine aminotransferase, bile production, and histological evaluation of liver biopsies stained with hematoxylin and eosin and caspase-3 were compared between groups during NMP. Results: In addition to gross visual differences in the heterogeneity of livers with long or extended CIT compared with short CIT, the NMP perfusate from livers with extended CIT demonstrated an elevation in lactate that did not decrease with time. Although livers with long CIT showed a temporal reduction in NMP perfusate lactate concentration similar to those with short CIT, there was associated hepatocellular injury in the long CIT group manifested in the form of higher aspartate aminotransferase and alanine aminotransferase in perfusate, and increased frequency of caspase-3 positive cells indicating increased apoptosis. Conclusions: While NMP offers improved clinical outcomes post-liver transplantation, the application of NMP in back-to-base format with prolonged CIT before NMP requires further evaluation to understand the impact of ischemia-reperfusion injury.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.