Evidence map›Paper›PMID 42209166›Full record

ReviewZhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology2026

[Pathophysiological mechanisms of coagulation dysfunction associated with liver disease].

H Wang, X Chen, Y Y Lu

Abstract readReviewEnglish Abstract
In one paragraph

Review in Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

H WangDepartment of Transfusion Medicine, the Fifth Medical Centre of Chinese PLA General Hospital, Beijing 100039, China.
X ChenDepartment of Hepatology Medicine, the Fifth Medical Centre of Chinese PLA General Hospital, Beijing 100039, China.
Y Y LuDepartment of Hepatology Medicine, the Fifth Medical Centre of Chinese PLA General Hospital, Beijing 100039, China.

Funding

Prevention and Control of Emerging and Major Infectious Diseases-National Science and Technology Major Project 2025ZD01906300, 2025ZD01906302
6 · The paper itself

Abstract

Coagulation abnormalities associated with liver diseases easily lead to spontaneous and secondary bleeding, which is associated with hemodynamic changes, reduced synthesis of coagulation factors, liver disease-related thrombocytopenia, and pharmacological interventions. On the other hand, patients with liver disease also have a hypercoagulable state, making them prone to portal vein thrombosis, which is associated with hemodynamic changes, reduced synthesis of anticoagulants, abnormal vascular intima structure, inflammation, and pharmacological treatment. Additionally, patients with liver disease are at an intertwined risk of bleeding and thrombosis and are in a fragile state of hemostasis rebalancing for an extended period. Genetic factors and diagnostic and therapeutic procedures further challenge the management of coagulation function in patients with liver disease. This article discusses the mechanisms of coagulation abnormalities from the perspectives of both bleeding and thrombosis, providing assistance for dynamically managing and rebalancing the hemostasis in patients with liver disease.

Indexed as

Blood Coagulation DisordersLiver DiseasesBlood CoagulationHumans

Identifiers

PMID42209166
PMCPMC13223772

What OpenQuestion holds

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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.