The main objectives are: * To establish the prevalence of major bleeding in patients treated with higher than recommended thromboprophylaxis doses. * To identify variables associated to higher risk of bleeding.
Study Type
OBSERVATIONAL
Enrollment
2,430
Manuel Monreal
Badalona, Barcelona, Spain
Bleeding events and complications
Study endpoints are clinically recognized (and objectively confirmed) major and minor bleeding complications, and death.
Time frame: 30 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.