Routine administration of venous thromboembolism (VTE) prophylaxis to medically ill patients at high risk for thrombosis significantly increases the risk of bleeding and has no clear clinical benefit, reveals a recent study, noting that the current practice must be reassessed.
This retrospective cohort study was carried out in a tertiary hospital in Israel to assess the benefit and safety of VTE prophylaxis in acutely ill medical patients hospitalized in medical departments with an admission lasting >48 hours during 2014–2017.
Thirty-day mortality was the primary outcome. Secondary outcomes included 90-day incidence of pulmonary embolism, symptomatic deep vein thrombosis, and major bleeding. The authors performed propensity-weighted logistic multivariate analysis.
Of the 18,890 patient-unique episodes analysed, 3,206 (17.0 percent) received prophylaxis. A total of 1,309 patients (6.9 percent) died, of whom 540/3,206 (16.8 percent) received VTE prophylaxis and 769/15,864 did not. Prophylaxis did not reduce mortality (multivariable-adjusted, propensity-weighted odds ratio (OR), 0.99, 95 percent confidence interval [CI], 0.84–1.14).
VTE occurred in 142 patients (0.7 percent), of whom 44/3,206 (1.4 percent) received prophylaxis and 98/15,864 (0.6 percent) did not. Prophylaxis did not correlate with a reduction in VTE in the whole cohort (multivariable-adjusted, propensity-weighted OR, 1.09, 95 percent CI, 0.52–2.29).
Notably, prophylaxis resulted in an increase in major bleeding (multivariable-adjusted, propensity-weighted OR, 1.24, 95 percent CI, 1.04–1.48).
“Current guidelines recommend pharmacologic prophylaxis for medical patients at high risk for VTE,” according to the authors.