Evidence map›Paper›PMID 35563662›Full record

ArticleInternational journal of molecular sciences2022

The Benefits of Fibrinolysis Combined with Venous Systemic Oxygen Persufflation (VSOP) in a Rat Model of Donation after Circulatory Death and Orthotopic Liver Transplantation.

Nadja Kröger, Zoltan Czigany, Jipin Jiang, Mamdouh Afify, Pascal Paschenda, Kazuyuki Nagai, Shintaro Yagi, René H Tolba

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Molecular Frontiers in Transplantation-Induced Ischemia-Reperfusion Injury.International journal of molecular sciences · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Nadja KrögerInstitute for Laboratory Animal Science and Experimental Surgery, Faculty of Medicine, RWTH-Aachen University, Pauwelsstraße 30, 52074 Aachen, Germany.
Zoltan CziganyInstitute for Laboratory Animal Science and Experimental Surgery, Faculty of Medicine, RWTH-Aachen University, Pauwelsstraße 30, 52074 Aachen, Germany.ORCID 0000-0003-0373-3210
Jipin JiangInstitute for Laboratory Animal Science and Experimental Surgery, Faculty of Medicine, RWTH-Aachen University, Pauwelsstraße 30, 52074 Aachen, Germany.
Mamdouh AfifyInstitute for Laboratory Animal Science and Experimental Surgery, Faculty of Medicine, RWTH-Aachen University, Pauwelsstraße 30, 52074 Aachen, Germany.
Pascal PaschendaInstitute for Laboratory Animal Science and Experimental Surgery, Faculty of Medicine, RWTH-Aachen University, Pauwelsstraße 30, 52074 Aachen, Germany.
Kazuyuki NagaiInstitute for Laboratory Animal Science and Experimental Surgery, Faculty of Medicine, RWTH-Aachen University, Pauwelsstraße 30, 52074 Aachen, Germany.
Shintaro YagiInstitute for Laboratory Animal Science and Experimental Surgery, Faculty of Medicine, RWTH-Aachen University, Pauwelsstraße 30, 52074 Aachen, Germany.ORCID 0000-0001-7465-5761
René H TolbaInstitute for Laboratory Animal Science and Experimental Surgery, Faculty of Medicine, RWTH-Aachen University, Pauwelsstraße 30, 52074 Aachen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organ shortage has led to the increasing utilization of livers retrieved from donors after circulatory death (DCD). These pre-damaged organs are susceptible to further warm ischemia and exhibit minimal tolerance for cold storage. The aim was thus to examine the effects of fibrinolysis combined with Venous Systemic Oxygen Persufflation (VSOP) on the preservation of DCD livers in vivo. Livers of male Lewis rats were explanted after 45 min of warm ischemia, cold-stored for 18 h, and transplanted into a recipient animal. Livers were left untreated or underwent either VSOP or fibrinolysis via Streptokinase (SK) or received combined SK and VSOP. Combined treatment exhibited improved microvascular flow at 168 h (p = 0.0009) and elevated microperfusion velocity at 24 h post-transplantation (p = 0.0007). Combination treatment demonstrated increased portal venous flow (PVF) at 3 and 24 h post-transplantation (p = 0.0004, p < 0.0001), although SK and VSOP analogously achieved increases at 24 h (p = 0.0036, p = 0.0051). Enzyme release was decreased for combination treatment (p = 0.0002, p = 0.0223) and lactate dehydrogenase (LDH) measurements were lower at 24 h post-transplantation (p = 0.0287). Further supporting findings have been obtained in terms of serum cytokine levels and in the alterations of endothelial injury markers. The combination treatment of SK + VSOP might provide improved organ integrity and viability and may therefore warrant further investigation as a potential therapeutic approach in the clinical setting of DCD.

Indexed as

Liver TransplantationAnimalsFibrinolysisLiverMaleOrgan PreservationOxygenPerfusionRatsRats, Inbred LewOxygencold storageDCDdonors after circulatory deathfibrinolysisischemia-reperfusion injurymicrosurgeryorgan preservationorthotopic liver transplantationoxygenstreptokinaseVSOPwarm ischemia

Identifiers

PMID35563662
PMCPMC9099893

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Registered trials

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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.