This document discusses pulmonary embolism (PE), including risk factors, symptoms, diagnosis, and treatment. There are inherited and acquired risk factors for PE, such as genetic mutations or advanced age/smoking. Symptoms include dyspnea, tachycardia, and pleuritic pain. Diagnosis involves blood tests, imaging like CT scans, and potentially pulmonary angiography. Treatment involves anticoagulation with drugs like heparin or warfarin, or procedures like fibrinolysis, embolectomy, or IVC filter placement. Prevention focuses on anti-coagulation and mechanical methods like compression stockings.
3. Inherited Factor
• Factor V Leiden mutation
• Prothrombin gene mutation
• Deficiency of antithrombin III, protein C
or protein S
4. Acquired Factor
• Age
• Smoking
• Obesity
• Atherosclerosis disease
• Recent trauma or surgery
• Long-haul air travel
• Oral contraceptives
• Pregnancy
5. Acquired Factor
• Postmenopausal hormone replacement
• Acute infection
• Personal or family history of VTE
• Cancer
• Antiphospholipid antibody syndrome
• Systemic hypertension
• COPD
• Pacemaker or ICD
30. Regimens for VTE prophylaxis
Thoracic suregery:
Heparin 5000units sc TID and
Graduated compression stockings/intermittent
Pneumatic compression
31. Regimens for VTE prophylaxis
Medical patients:
Heparin 5000units sc TID or
Enoxaparin 40mg sc QD or
Dalteparin 5000units sc QD or
Fondaparinux 2.5mg sc QD or
Graduated compression stockings/intermittent
pneumatic compression for patients with
contraindications to anticoagulation
Consider combination pharmacological and
mechanical prophylaxis for very high risk patients
Consider surveillance lower extremity ultrasonography for
ICU patients