Evidence map›Paper›PMID 42087180›Full record

ArticlePerioperative medicine (London, England)2026

Phase-specific dynamics of coagulation factors V, VIII, and XIII during liver transplantation: insights from a prospective study.

Sarah Thaler, Anna Zorn, Isabell Aster, Dionysios Koliogiannis, Markus Guba, Bernhard W Renz, Philipp Groene

Abstract read
In one paragraph

Article in Perioperative medicine (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Sarah ThalerDepartment of Anaesthesiology, LMU University Hospital, LMU Munich, Marchioninistr. 15, Munich, 81377, Germany. sarah.thaler@med.uni-muenchen.de.ORCID http://orcid.org/0000-0002-7957-9822
Anna ZornDepartment of Anaesthesiology, LMU University Hospital, LMU Munich, Marchioninistr. 15, Munich, 81377, Germany.
Isabell AsterDepartment of Anaesthesiology, LMU University Hospital, LMU Munich, Marchioninistr. 15, Munich, 81377, Germany.
Dionysios KoliogiannisDepartment of General, Visceral and Transplantation Surgery, LMU University Hospital, LMU Munich, Munich, Germany.
Markus GubaDepartment of General, Visceral and Transplantation Surgery, LMU University Hospital, LMU Munich, Munich, Germany.
Bernhard W RenzDepartment of General, Visceral and Transplantation Surgery, LMU University Hospital, LMU Munich, Munich, Germany.
Philipp GroeneDepartment of Anaesthesiology, LMU University Hospital, LMU Munich, Marchioninistr. 15, Munich, 81377, Germany.ORCID http://orcid.org/0000-0001-8357-5552

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLiver dysfunction is associated with a rebalanced but fragile hemostatic system, in which alterations in coagulation factor synthesis and activity contribute to both bleeding and thrombotic risks. During liver transplantation, this fragile equilibrium is further challenged by major physiological stress. This study aimed to characterize the phase-specific intraoperative dynamics of coagulation factors V, VIII, and XIII (FV, FVIII, and FXIII) to better understand hemostatic modulation and its clinical implications during liver transplantation.

methodsA subset of 17 liver transplant recipients receiving transfusion support without administration of recombinant FVIII or FXIII was analyzed. Measurements were obtained at three defined intraoperative time points: T1 anesthesia induction, T2 end of anhepatic phase, T3 end of surgery. Activities of FV, FVIII, and FXIII were quantified and analyzed for temporal trends.

resultsAll three coagulation factors declined during surgery. FV was already markedly reduced at T1 (37% (22/55)) and further decreased to 26% at T3 ((19/34); p = 0.0309). FVIII showed supranormal levels at T1 (193% (160/254) and declined to near-normal levels at T3 (109% ((67/143); p < 0.0001). FXIII remained close to the lower limit of normal (T1: 68% (50/85)); T3: (63% (55/78)) without significant change.

conclusionThis prospective analysis reveals distinct, phase-specific trajectories of FV, FVIII, and FXIII during liver transplantation. Understanding these differential patterns may help identify critical periods of hemostatic vulnerability and guide individualized factor-specific therapeutic interventions to optimize perioperative coagulation management in liver transplant recipients.

trial registrationGerman Clinical Trials Register (DRKS00032827).

Indexed as

Coagulation managementFactor V (FV)Factor VIII (FVIII)Factor XIII (FXIII)FibrinolysisHemostasisLiver transplantationPerioperative monitoring

Identifiers

PMID42087180
PMCPMC13147594

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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.