Predicting the Risk of Venous Thromboembolism in Patients Hospitalized with Heart Failure.

Link to article at PubMed

Predicting the Risk of Venous Thromboembolism in Patients Hospitalized with Heart Failure.

Circulation. 2014 Jun 26;

Authors: Mebazaa A, Spiro TE, Büller HR, Haskell L, Hu D, Hull R, Merli G, Schellong S, Spyropoulos AC, Tapson VF, De Sanctis Y, Cohen AT

BACKGROUND: -Whether heart failure (HF) increases the risk of venous thromboembolism (VTE) is not well established. In the phase III MAGELLAN trial, extended-duration rivaroxaban was compared with standard-duration enoxaparin followed by placebo for VTE prevention in 8101 hospitalized acutely ill patients with or without HF. The aim of this analysis was to evaluate the relationship between HF severity and the risk of VTE in MAGELLAN patients.
METHODS AND RESULTS: -Hospitalized patients diagnosed with HF were included according to New York Heart Association class III or IV at admission (n=2593). HF severity was determined by N-terminal pro-brain natriuretic peptide (NT-proBNP) plasma concentrations (median 1904 pg/mL). Baseline plasma D-dimer concentrations ranged from 0.6 to 1.7 µg/L for the less and more severe HF subgroups. Patients with more severe HF had a greater incidence of VTE versus patients with less severe HF, with a significant trend up to Day 10 (4.3% vs 2.2%; P=0.0108) and Day 35 (7.2% vs 4.1%; P=0.0150). Multivariable analysis confirmed that NT-proBNP concentration was associated with VTE risk up to Day 10 (P=0.017) and D-dimer concentration with VTE risk up to Day 35 (P=0.005). The association between VTE risk and HF severity that was observed in the enoxaparin/placebo group was not seen in the extended-duration rivaroxaban group.
CONCLUSIONS: -Patients with more severe HF, as defined by high NT-proBNP plasma concentration, were at increased risk of VTE. NT-proBNP may be useful to identify high short-term risk, whereas elevated D-dimer may be suggestive of high mid-term risk. Clinical Trial Registration Identifier: NCT00571649.

PMID: 24970782 [PubMed - as supplied by publisher]

Leave a Reply

Your email address will not be published. Required fields are marked *