Wolfe, Adam;
Phillips, Angela;
Tierney, David M;
Melamed, Roman;
Qadri, Ghazi;
Lillyblad, Matthew;
Smith, Claire;
St. Hill, Catherine;
Stenzel, Ashley E;
Beddow, David;
Kirven, Justin;
Kethireddy, Rajesh;
Patel, Love
Retrospective Analysis of Direct-Acting Oral Anticoagulants (DOACs) Initiation Timing and Outcomes After Thrombolysis in High- and Intermediate-Risk Pulmonary Embolism
You can manage bookmarks using lists, please log in to your user account for this.
Media type:
E-Article
Title:
Retrospective Analysis of Direct-Acting Oral Anticoagulants (DOACs) Initiation Timing and Outcomes After Thrombolysis in High- and Intermediate-Risk Pulmonary Embolism
Contributor:
Wolfe, Adam;
Phillips, Angela;
Tierney, David M;
Melamed, Roman;
Qadri, Ghazi;
Lillyblad, Matthew;
Smith, Claire;
St. Hill, Catherine;
Stenzel, Ashley E;
Beddow, David;
Kirven, Justin;
Kethireddy, Rajesh;
Patel, Love
imprint:
SAGE Publications, 2023
Published in:Clinical and Applied Thrombosis/Hemostasis
Description:
<jats:p> Direct-acting oral anticoagulants (DOACs) are prescribed in the treatment of venous thromboembolism, including pulmonary embolism (PE). Evidence is limited regarding the outcomes and optimal timing of DOACs in patients with intermediate- or high-risk PE treated with thrombolysis. We conducted a retrospective analysis of outcomes among patients with intermediate- and high-risk PE who received thrombolysis, by choice of long-term anticoagulant agent. Outcomes of interest included hospital length of stay (LOS), intensive care unit LOS, bleeding, stroke, readmission, and mortality. Descriptive statistics were used to examine characteristics and outcomes among patients, by anticoagulation group. Patients receiving a DOAC (n = 53) had shorter hospital LOS compared to those in warfarin (n = 39) and enoxaparin (n = 10) groups (mean LOS 3.6, 6.3 and 4.5 days, respectively; P < .0001). This single institution retrospective study suggests DOAC initiation <48 h from thrombolysis may result in shorter hospital LOS compared to DOAC initiation ≥48 h ( P < .0001). Further larger studies with more robust research methodology are needed to address this important clinical question. </jats:p>