Table 3.
In patients with a worsening clinical status, especially in those without anticoagulant treatment, a diagnosis of VTE must always be suspected |
In patients with suspected VTE, the diagnostic and therapeutic workup must integrate clinical data, laboratory findings, and imaging test results |
Measurement of D-dimer for diagnosing VTE must be performed only if a clinical suspect exists |
Vascular/cardiac ultrasound imaging for diagnosing VTE should precede radiological imaging |
Patients undergoing a CT scan for worsening respiratory status should receive angio-CT sequences to exclude PE |
The use of LMWH for treating a VTE episode is preferred. UFH should be limited to patients with CrCl < 30 mL/min |
An invasive “catheter”-based therapy for PE is indicated in selected cases with contraindication to anticoagulant drugs, recurrent events despite adequate anticoagulation, or when systemic fibrinolysis cannot be performed |
For the risk stratification of patients with VTE, monitoring of the following parameters is useful: troponin, BNP, D-dimer, blood cell count, fibrinogen, prothrombin time, activated partial thromboplastin time, and degradation products of fibrin |
After the initial approach, DOACs may represent an option for in-hospital treatment of a VTE episode in patients with clinical stability and decreasing inflammation |
After a VTE episode, DOACs should represent the therapy of choice at discharge |
BNP brain natriuretic peptide, COVID-19 coronavirus disease 2019, CrCl creatinine clearance, CT computed tomography, DOAC direct oral anticoagulant, LMWH low-molecular weight heparin, PE pulmonary embolism, UFH unfractionated heparin, VTE venous thromboembolism