Abstract 16125: Prognostic Value of C-Reactive Protein as Inflammatory Marker for Venous Thromboembolism in Acutely Ill Hospitalized Patients: Analysis From the APEX Trial
BackgroundThe link between inflammation and a long-term risk for venous thromboembolism (VTE) is supported by population-based studies. It remains uncertain whether C-reactive protein (CRP), an inflammatory biomarker, would be associated with short-term VTE among acutely ill hospitalized patients de...
Gespeichert in:
Veröffentlicht in: | Circulation (New York, N.Y.) N.Y.), 2018-11, Vol.138 (Suppl_1 Suppl 1), p.A16125-A16125 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | BackgroundThe link between inflammation and a long-term risk for venous thromboembolism (VTE) is supported by population-based studies. It remains uncertain whether C-reactive protein (CRP), an inflammatory biomarker, would be associated with short-term VTE among acutely ill hospitalized patients despite provision of thromboprophylaxis.MethodsIn the APEX trial, 7513 acutely ill hospitalized patients were randomized to receive either extended-duration betrixaban or shorter-duration enoxaparin and followed for 77 days. CRP levels were measured at baseline from a central laboratory. The relationship between baseline CRP (as a continuous or categorical variable) and VTE was assessed by fitting a univariable and multivariable logistic regression model, with adjustment for thromboprophylaxis, index hospitalization event, D-dimer measurement, and other VTE risk factors (including previous history of VTE, thrombophilia, current lower-limb paralysis, cancer, intensive care unit stay, and age >60 years).ResultsBaseline CRP concentrations were obtained from 7320 subjects (median12.4 mg/L; interquartile range3.8 to 60.6 mg/L). The risk of VTE at 77 days appeared to increase with CRP elevation (P for trend 10 mg/L indicates clinically significant inflammation) |
---|---|
ISSN: | 0009-7322 1524-4539 |