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...

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Veröffentlicht in:Circulation (New York, N.Y.) N.Y.), 2018-11, Vol.138 (Suppl_1 Suppl 1), p.A16125-A16125
Hauptverfasser: Chi, Gerald, Gibson, Michael, Hernandez, Adrian F, Hull, Russell D, Cohen, Alexander T, Harrington, Robert A, Liu, Yuyin, Kalayci, Arzu, Walia, Sargun, Sharfaei, Sadaf, Pitliya, Anmol, Kazmi, Hassan A, Datta, Sudarshana, Kahe, Farima, Ghaffarpasand, Eiman, Jafarizde, Mehrian, Yee, Megan K, Travis, Ryan S, AlKhalfan, Fahad, Nafee, Tarek, Kerneis, Mathieu, Goldhaber, Samuel Z
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Sprache:eng
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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