Prevalence and Risk Factors for Portal Cavernoma in Adult Patients with Portal Vein Thrombosis.

contrast-enhanced ultrasound hepatocellular carcinoma portal cavernoma portal vein thrombosis thrombophilia

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
06 Jul 2024
Historique:
received: 17 05 2024
revised: 25 06 2024
accepted: 28 06 2024
medline: 13 7 2024
pubmed: 13 7 2024
entrez: 13 7 2024
Statut: epublish

Résumé

Portal vein thrombosis (PVT) represents a restriction or occlusion of the portal vein by a blood clot, which can appear in liver cirrhosis, inherited or acquired thrombophilia, malignancies, abdominal infection, abdominal inflammation, and injury to the portal vein; it can evolve to local venous extension, recanalization, or portal cavernoma (PC). This research represents an observational study of patients admitted with a diagnosis of PVT between January 2018 and December 2022. We assessed the rate of and risk factors for PC. In total, 189 patients with PVT were included; the rate of PC was 14.8%. In univariate and multivariate analysis, the main risk factors for the presence of PC were etiology (thrombophilia, myeloproliferative disorders, local inflammatory diseases, and idiopathic causes), prior PVT, and complete versus incomplete or single-branch portal obstruction. In patients with superior mesenteric vein (SMV) thrombosis, distal obstruction was more prone to PC than proximal obstruction. The main predictive factors were etiology, prior PVT, complete PVT obstruction, and no prior non-selective beta-blocker (NSBB) use; in patients with SMV thrombosis, the distal extension was more significantly associated with the risk of PC. We propose a composite score for the prediction of PC which includes etiology, prior diagnosis of PVT, prior NSBB use, complete versus incomplete PVT, and distal versus proximal SMV thrombosis, with good accuracy (AUC 0.822) and an estimated sensitivity of 76.92% and specificity of 82.39% at a cut-off value of 4.

Identifiants

pubmed: 39001335
pii: diagnostics14131445
doi: 10.3390/diagnostics14131445
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Sergiu Marian Cazacu (SM)

Research Center of Gastroenterology and Hepatology, Gastroenterology Department, University of Medicine and Pharmacy of Craiova, Petru Rares Street no. 2-4, 200349, Craiova, Romania.

Dragoș Ovidiu Alexandru (DO)

Biostatistics Department, University of Medicine and Pharmacy of Craiova, Petru Rares Street no. 2-4, 200349 Craiova, Romania.

Daniela Dumitrescu (D)

Imaging Department, University of Medicine and Pharmacy of Craiova, Petru Rares Street no. 2-4, 200349 Craiova, Romania.

Alexandru Marian Vieru (AM)

Doctoral School, University of Medicine and Pharmacy of Craiova, Petru Rares Street no. 2-4, 200349 Craiova, Romania.

Marinela Cristiana Urhuț (MC)

Doctoral School, University of Medicine and Pharmacy of Craiova, Petru Rares Street no. 2-4, 200349 Craiova, Romania.

Larisa Daniela Săndulescu (LD)

Research Center of Gastroenterology and Hepatology, Gastroenterology Department, University of Medicine and Pharmacy of Craiova, Petru Rares Street no. 2-4, 200349, Craiova, Romania.

Classifications MeSH