Splanchnic vein thrombosis associated with SARS-CoV-2 infection: A VALDIG case-control study.

Portal vein thrombosis SARS-CoV-2 infection Splanchnic vein thrombosis

Journal

JHEP reports : innovation in hepatology
ISSN: 2589-5559
Titre abrégé: JHEP Rep
Pays: Netherlands
ID NLM: 101761237

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 02 06 2023
revised: 28 07 2023
accepted: 14 08 2023
medline: 16 10 2023
pubmed: 16 10 2023
entrez: 16 10 2023
Statut: epublish

Résumé

Whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is a risk factor for splanchnic vein thrombosis (SVT) is unknown. This study aims to assess the impact of SARS-CoV-2 infection on the presentation and prognosis of recent SVT and to identify specific characteristics of SARS-CoV-2-associated SVT. This is a retrospective study collecting health-related data of 27 patients presenting with recent SVT in the context of SARS-CoV-2 infection in 12 Vascular Liver Disease Group (VALDIG) centres and in comparison with 494 patients with recent SVT before the SARS-CoV-2 pandemic. Twenty-one patients with SARS-CoV-2 had portal vein thrombosis with or without thrombosis of another splanchnic vein, two had superior mesenteric vein thrombosis, one had splenic vein thrombosis, and three had hepatic vein thrombosis. Diagnosis of SVT was made 10 days (95% CI 0-24 days) after the diagnosis of SARS-CoV-2 infection. Fever (52 SARS-CoV-2 infection can be associated with recent SVT. Intestinal infarction leading to intestinal resection might be more frequent in patients with SARS-CoV-2. SARS-CoV-2 infection can be associated with recent SVT. SVT occurring during SARS-CoV-2 infection is characterised by a higher frequency of respiratory symptoms and a lower lymphocyte count. Intestinal infarction leading to intestinal resection appears to occur more frequently in patients with SARS-CoV-2.

Sections du résumé

Background & Aims UNASSIGNED
Whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is a risk factor for splanchnic vein thrombosis (SVT) is unknown. This study aims to assess the impact of SARS-CoV-2 infection on the presentation and prognosis of recent SVT and to identify specific characteristics of SARS-CoV-2-associated SVT.
Methods UNASSIGNED
This is a retrospective study collecting health-related data of 27 patients presenting with recent SVT in the context of SARS-CoV-2 infection in 12 Vascular Liver Disease Group (VALDIG) centres and in comparison with 494 patients with recent SVT before the SARS-CoV-2 pandemic.
Results UNASSIGNED
Twenty-one patients with SARS-CoV-2 had portal vein thrombosis with or without thrombosis of another splanchnic vein, two had superior mesenteric vein thrombosis, one had splenic vein thrombosis, and three had hepatic vein thrombosis. Diagnosis of SVT was made 10 days (95% CI 0-24 days) after the diagnosis of SARS-CoV-2 infection. Fever (52
Conclusions UNASSIGNED
SARS-CoV-2 infection can be associated with recent SVT. Intestinal infarction leading to intestinal resection might be more frequent in patients with SARS-CoV-2.
Impact and implications UNASSIGNED
SARS-CoV-2 infection can be associated with recent SVT. SVT occurring during SARS-CoV-2 infection is characterised by a higher frequency of respiratory symptoms and a lower lymphocyte count. Intestinal infarction leading to intestinal resection appears to occur more frequently in patients with SARS-CoV-2.

Identifiants

pubmed: 37841638
doi: 10.1016/j.jhepr.2023.100894
pii: S2589-5559(23)00225-2
pmc: PMC10570588
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100894

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

The authors have no competing interests to declare. Please refer to the accompanying ICMJE disclosure forms for further details.

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Auteurs

Pierre Deltenre (P)

CUB Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
Clinique St Luc, Bouge, Belgium.
CHU UCL Namur, Université Catholique de Louvain, Yvoir, Belgium.

Audrey Payancé (A)

Université de Paris, AP-HP, Hôpital Beaujon, Service d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, VALDIG Group, Centre de recherche sur l'inflammation, Inserm, UMR 1149, Paris, France.

Laure Elkrief (L)

Hôpital Trousseau, CHU de Tours, FILFOIE, ERN RARE-LIVER, VALDIG Group, Tours, France.

Vincenzo La Mura (V)

IRCCS Fondazione Ca' Granda - Ospedale Maggiore Policlinico, ERN RARE-LIVER, VALDIG Group, Milan, Italy.

Florent Artru (F)

Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Anna Baiges (A)

Barcelona Hepatic Hemodynamic Lab, Clinic Barcelona Hospital, CIBEREHD, IDIBAPS, Universitat de Barcelona, ERN RARE-LIVER, VALDIG Group, Barcelona, Spain.

Jean-Paul Cervoni (JP)

CHU, Besançon, France.

Louise China (L)

Royal Free Hospital, London, UK.

Isabelle Colle (I)

Algemeen Stedelijk Ziekenhuis ASZ, Aalst, Belgium.

Elise Lemaitre (E)

CHU, Lille, France.

Bogdan Procopet (B)

Regional Institute of Gastroenterology and Hepatology, Cluj-Napoca, Romania.

Dietmar Schiller (D)

Ordensklinikum Linz Barmherzige Schwestern, Linz, Austria.

Christophe Bureau (C)

Hôpital Universitaire Rangueil Toulouse, FILFOIE, ERN RARE-LIVER, VALDIG Group, Toulouse, France.

Odile Goria (O)

Hôpital Universitaire Charles Nicolle de Rouen, Rouen, France.

Isabelle Ollivier (I)

Hôpital Universitaire Côte de la Nacre, FILFOIE, ERN RARE-LIVER, VALDIG Group, Caen, France.

Alexandre Nuzzo (A)

Paris Cité University, AP-HP, Beaujon Hospital, Intestinal Stroke Center, Gastroenterology, IBD, Intestinal Failure Department, Inserm, UMR 1148, Paris, France.

Pierre-Emmanuel Rautou (PE)

Université de Paris, AP-HP, Hôpital Beaujon, Service d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, VALDIG Group, Centre de recherche sur l'inflammation, Inserm, UMR 1149, Paris, France.

Aurélie Plessier (A)

Université de Paris, AP-HP, Hôpital Beaujon, Service d'Hépatologie, DMU DIGEST, Centre de Référence des Maladies Vasculaires du Foie, FILFOIE, ERN RARE-LIVER, VALDIG Group, Centre de recherche sur l'inflammation, Inserm, UMR 1149, Paris, France.

Classifications MeSH