Thrombotic Long-Term Consequences of SARS-CoV-2 Infection in Patients with Compensated Cirrhosis: A Propensity Score-Matched Analysis of a U.S. Database.

Thrombotic Long-Term Consequences of SARS-CoV-2 Infection in Patients with Compensated Cirrhosis: A Propensity Score-Matched Analysis of a U.S. Database.

Publication date: Jul 17, 2024

Cirrhosis causes an imbalance in the coagulation pathway and leads to a tendency for both bleeding and clotting. SARS-CoV-2 has been reported to be associated with a hypercoagulable state. This study examines SARS-CoV-2’s impact on hemostasis in compensated patients with cirrhosis. We analyzed the US Collaborative Network, which comprises 63 HCOs in the U. S.A. Compensated cirrhosis patients were split into two groups: SARS-CoV-2-positive and -negative. Patients’ baseline characteristics were used in a 1:1 propensity score-matched module to create comparable cohorts. We compared the risk of portal vein thrombosis (PVT), deep venous thrombosis (DVT), and pulmonary embolism (PE) at 6 months, and 1 and 3 years. Of 330,521 patients, 27% tested positive and 73% remained negative. After PSM, both cohorts included 74,738 patients. Patients with SARS-CoV-2 had a higher rate of PVT compared to those without at 6 months (0. 63% vs 0. 5%, p < 0. 05), 1 year (0. 8% vs 0. 6%, p < 0. 05), and 3 years (1% vs. 0. 7%, p < 0. 05), a higher rate of DVT at 6 months (0. 8% vs. 0. 4%, p < 0. 05), 1 year (1% vs. 0. 5%, p < 0. 05), and 3 years (1. 4% vs. 0. 8%, p < 0. 05), and a higher rate of PE at 6 months (0. 6% vs. 0. 3%, p < 0. 05), 1 year (0. 7% vs. 0. 4%, p < 0. 05), and 3 years (1% vs. 0. 6%, p < 0. 05). The presence of SARS-CoV-2 infection in patients with compensated cirrhosis was associated with a higher rate of PVT, DVT, and PE at 6 months, and 1 and 3 years.

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Concepts Keywords
Database cirrhosis
Hemostasis coagulation
Months COVID
DVT
PE
PVT
SARS-CoV-2
thrombosis

Semantics

Type Source Name
disease MESH SARS-CoV-2 Infection
pathway REACTOME SARS-CoV-2 Infection
disease MESH Cirrhosis
disease MESH causes
disease MESH bleeding
disease MESH thrombosis
disease MESH deep venous thrombosis
disease MESH pulmonary embolism
disease VO USA
disease MESH complications
disease MESH venous thromboembolism
drug DRUGBANK Coenzyme M
disease VO population
disease MESH emergency
disease VO effective
disease IDO production
drug DRUGBANK Phylloquinone
disease VO time
disease IDO history
disease MESH esophageal varices
disease MESH hepatic encephalopathy
disease MESH peritonitis
disease MESH jaundice
disease MESH ascites
disease MESH hepatorenal syndrome
drug DRUGBANK Methionine
disease MESH hypertension
disease MESH COPD
disease MESH stroke
drug DRUGBANK Ticlopidine
drug DRUGBANK Ticagrelor
drug DRUGBANK Acetylsalicylic acid
drug DRUGBANK Vorapaxar
drug DRUGBANK Cangrelor
drug DRUGBANK Clopidogrel
drug DRUGBANK Dipyridamole
drug DRUGBANK Prasugrel
drug DRUGBANK Dabigatran
drug DRUGBANK Rivaroxaban
drug DRUGBANK Warfarin
drug DRUGBANK Desirudin
drug DRUGBANK Defibrotide
drug DRUGBANK Apixaban
drug DRUGBANK Argatroban
drug DRUGBANK Edoxaban
drug DRUGBANK Heparin
drug DRUGBANK Fondaparinux
drug DRUGBANK Bivalirudin
drug DRUGBANK Enoxaparin
drug DRUGBANK Dalteparin
drug DRUGBANK Tirofiban
drug DRUGBANK Eptifibatide

Original Article

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