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Zaključak

          Venska tromboembolijska bolest je jedan od vodećih uzroka morbiditeta i mortaliteta.
          Pravovremena dijagnostika i liječenje značajno poboljšavaju ishod bolesti. Osnova liječenja je
          primjena antikoagulantne terapije. Decenijama su antagonisti vitamin K bili jedini izbor oralnih
          antikoagulanasa, ali zbog mnogobrojnih nedostataka novi, odnosno direktni oralni antikoagulansi,
          su dobili primat u liječenju zbog svojih farmakoloških karakteristika. DOAC su lijekovi prvog izbora

          ukoliko nisu kontraindikovani. Efikasnost i bezbjednost DOAC potvrđena je nizom multicentričnih
          randomizovanih studija i meta-analiza. Mogu se propisati i kod bolesnika sa malignom bolešću,
          a zbog svog brzog dejstva olakšavaju vanbolničko liječenje VTE ili mogu da skrate vrijeme
          hospitalizacije.






          Abstract

          Venous thromboembolic disease, which includes pulmonary thromboembolism and deep vein thrombosis, is one of the
          most common causes of morbidity and mortality. Management of patients with acute pulmonary thromboembolism is
          challenging, due to the wide spectrum of clinical presentation and possible outcomes. Certainly, anticoagulant therapy
          is the basis of treatment for these patients. Until recently, parenteral anticoagulants and oral vitamin K antagonists were
          used to achieve an anticoagulant effect. These drugs still have their place in the treatment of venous thromboembolic
          disease, but new, i.e. direct oral anticoagulants have replaced oral vitamin K antagonists due to their more favorable
          pharmacological characteristics.  In this paper, based on available literature, clinical trials and good clinical practice
          guidelines, we highlight critical errors and discuss potential advantages and disadvantages of oral anticoagulants.

          Keywords: pulmonary thromboembolism, venous thromboembolic disease, oral anticoagulants, direct oral anticoagulants
          (DOAC)






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          64     DOI: 10.5937/Galmed2305062O
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