# Analysis of 6-week mortality and influencing factors in patients with liver cirrhosis and portal vein thrombosis complicated by acute gastrointestinal bleeding

**Authors:** Junli Zhang, Ling Feng

PMC · DOI: 10.1371/journal.pone.0345079 · 2026-03-20

## TL;DR

The study identifies elevated ALP levels and treatment failure within five days as risk factors for 6-week mortality in cirrhosis patients with portal vein thrombosis and gastrointestinal bleeding.

## Contribution

The study identifies new independent risk factors for 6-week mortality in a specific patient population with cirrhosis and portal vein thrombosis.

## Key findings

- Elevated ALP levels are positively associated with 6-week mortality in patients with cirrhosis and portal vein thrombosis.
- A 5-day treatment failure is strongly linked to increased 6-week mortality in these patients.

## Abstract

To explore the 6-week mortality of acute gastrointestinal bleeding in patients with liver cirrhosis and portal vein thrombosis and to analyze its influencing factors.

This was a retrospective study. We retrospectively screened 232 patients with liver cirrhosis and portal vein thrombosis complicated by acute gastrointestinal bleeding who were admitted to West China Hospital of Sichuan University from January 1，2020 to November30，2022. Of the 232 patients, 75 had their first bleeding. Additionally, the patients were divided into a mortality group (n = 34) and a non-mortality group (n = 198) based on whether they died within 6 weeks of the onset of gastrointestinal bleeding. Baseline general information, laboratory indicators, and other clinical data of the two groups were compared, and the independent risk factors for 6-week mortality in patients with liver cirrhosis and portal vein thrombosis complicated by acute gastrointestinal bleeding were analyzed.

There were significant differences between the two groups in terms of the etiology of liver cirrhosis, HCC, 5-day treatment failure rate (8.62%), TBiL, ALT, BUN, Na, eGFR, DBiL, AST, GGT, ALP, CR, WBC, PLT, and PT(p < 0.05). Multivariate logistic regression analysis revealed that elevated ALP levels showed a positive association with 6-week mortality [OR=1.01, 95% CI (1.01, 1.01), p < 0.01] and 5-day treatment failure showed a positive association with 6-week mortality [OR=11.27, 95% CI (3.45, 36.81),p < 0.01].

Elevated ALP and 5-day treatment failure were found to be independent risk factors for 6-week mortality in patients with cirrhosis and portal vein thrombosis complicated by acute gastrointestinal bleeding.

## Linked entities

- **Diseases:** portal vein thrombosis (MONDO:0001339), HCC (MONDO:0007256)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, ATHS (atherosclerosis susceptibility (lipoprotein associated)) [NCBI Gene 470] {aka ALP}, GGTLC5P (gamma-glutamyltransferase light chain 5 pseudogene) [NCBI Gene 653590] {aka GGT}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PLAT (plasminogen activator, tissue type) [NCBI Gene 5327] {aka T-PA, TPA}
- **Diseases:** hepatic ischemia (MESH:D007511), cirrhotic (MESH:D000094724), cardiovascular or pulmonary diseases (MESH:D002318), portal cavernoma (MESH:D006975), HCC (MESH:D006528), Acute gastrointestinal bleeding (MESH:D006471), death (MESH:D003643), PVT (MESH:D012170), esophageal and gastric varicose vein rupture (MESH:D014648), bleeding (MESH:D006470), Liver Cirrhosis (MESH:D008103), ACLF (MESH:D065290), thrombotic (MESH:D013927), multiorgan failure (MESH:D051437), hepatic encephalopathy (MESH:D006501), hypercoagulability (MESH:D019851), hepatic impairment (MESH:D008107), varicose (MESH:D014647), liver dysfunction (MESH:D017093), necrosis (MESH:D009336), Cholestasis (MESH:D002779), sepsis (MESH:D018805), hypoxia (MESH:D000860), Cirrhosis (MESH:D005355), ascites (MESH:D001201), esophageal and gastric varices (MESH:D004932), rupture (MESH:D012421), peptic ulcers (MESH:D010437), viral hepatitis (MESH:D014777), hypovolemic shock (MESH:D012769), coagulopathy (MESH:D001778), portal venous outflow obstruction (MESH:D006502), liver damage (MESH:D056486)
- **Chemicals:** GLU (MESH:D005947), bilirubin (MESH:D001663), Na (MESH:D012964), CR (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13004350/full.md

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Source: https://tomesphere.com/paper/PMC13004350