How Venous Thrombosis Occurs
Causes of VTE
Virchow's triad
- Blood flow — abnormalities of haemorheology and turbulence at vessel bifurcations and stenotic regions
- Vessel walls — abnormalities in the endothelium, such as atherosclerosis and associated vascular inflammation
- Blood components — abnormalities in coagulation and fibrinolytic pathways
Advances in laboratory techniques now enable clinicians to quantify some of these thrombosis-related factors that, when abnormal, confer a “prothrombotic” or “hypercoagulable” state.28 This state is associated with an increased risk of VTE and other cardiovascular diseases, including atrial fibrillation, coronary heart disease, and heart failure.
Who is at risk?
Major orthopaedic surgery is an example of an exposing risk factor. These surgical procedures are associated with about twice the rate of VTE as general surgery. Consistent with Virchow’s triad, the increased risk of VTE in major orthopaedic surgery may be linked to3, 26:
- Venous stasis, from postoperative immobility
- Damage to the vessel wall during the procedure
- Increased procoagulant activity, such as increased thrombin generation
The need for primary prevention
Important predisposing risk factors for VTE include:
- Hip and knee arthroplasty
- Hip and other lower extremity fracture
- Multiple trauma
- Major surgery for malignancy
- Arthroscopic repair of cruciate ligament and meniscectomy
- Other surgical procedures, duration >30 minutes
- Plaster cast immobilisation of lower limb
Nonsurgical conditions and factors3
- Stroke with paralysis
- Acute decompensated COPD
- Acute heart failure, NYHA III or IV
- Sepsis
- Acute infection with immobilisation
- Acute inflammatory disease with immobilisation
- Central venous catheter
Important predisposing risk factors for VTE include29, 30, 31:
- Thrombophilia
- History of VTE
- Active malignancy
- Pregnancy
- Age >60 years
- Obesity (BMI >30)
- Oestrogen therapy
- Chronic heart failure
- Varicose veins
Imbalances in the coagulation system and thrombosis
- 25 - Turpie AG, Chin BS, Lip GY. Venous thromboembolism: pathophysiology, clinical features, and prevention. BMJ. 2002;325(7369):887-890.
- 26 - Merli GJ. Pathophysiology of venous thrombosis, thrombophilia, and the diagnosis of deep vein thrombosis-pulmonary embolism in the elderly. Clin Geriatr Med. 2006;22(1):75-92, viii-ix.
- 27 - Jerjes-Sanchez C. Venous and arterial thrombosis: a continuous spectrum of the same disease? Eur Heart J. 2005; 26(1):3-4.
- 28 - Lip GY, Blann AD. Thrombogenesis and fibrinolysis in acute coronary syndromes. Important facets of a prothrombotic or hypercoagulable state? J Am Coll Cardiol. 2000;36(7):2044-2046.
- 3 - Geerts WH, Bergqvist D, Pineo GF, Heit JA, Samama CM, Lassen MR, and Colwell CW. Prevention of Venous Thromboembolism: American College of Chest Physicians (ACCP) Evidence-Based Clinical Practice Guidelines (8th Edition). Chest. Jun 2008: 381S–453S.
- 29 - Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften. Guidelines for VTE prevention (German AWMF), 2003. Available at http://www.uni-duesseldorf.de/awmf/ll/003-001.htm. Accessed April 14, 2008.
- 30 - Alikhan R, Cohen AT, Combe S, et al; MEDENOX Study. Risk factors for venous thromboembolism in hospitalized patients with acute medical illness: analysis of the MEDENOX Study. Arch Intern Med. 2004;164(9):963-968.
- 31 - Kucher N, Koo S, Quiroz R, et al. Electronic alerts to prevent venous thromboembolism among hospitalized patients. N Engl J Med. 2005;352(10):969-977.
- 32 - Seligsohn U, Lubetsky A. Genetic susceptibility to venous thrombosis. N Engl J Med. 2001;344(16):1222-1231.
- Venous thromboembolism
- A condition in which a blood clot (thrombus) forms in a vein, which in some cases then breaks free and enters the circulation as an embolus, finally lodging in and completely obstructing a blood vessel, e.g., in lungs causing a PE. The term encompasses both DVT and PE.
- Procoagulant
- A substance that promotes the coagulation of blood.
- Thrombin
- Also called Factor IIa, thrombin performs two functions in the coagulation cascade: activating platelets, and catalysing the conversion of soluble fibrinogen into insoluble fibrin. It is formed from prothrombin by a reaction that is catalysed by Factor Xa.
- American College of Chest Physicians
- Multidisciplinary international medical society based in Northbrook, Illinois, USA, that focuses on the treatment and prevention of all diseases of the chest. It has over 16,000 active members with physicians representing all chest medicine disciplines. Publishes the journal Chest.
- Thromboprophylaxis
- The use of medication or medical devices to prevent the formation of blood clots.
- Venous catheter
- A tube inserted into a vein to deliver medication (such as chemotherapy) to a patient.
- Antithrombin
- Antithrombin, also known as antithrombin III, is the most important member of a larger family of antithrombins. It is a small protein molecule (a glycoprotein) produced in the liver that binds to a specific pentasaccharide sequence on heparin. This binding to heparin leads to an anticoagulant effect through two different mechanisms: It causes a conformational change in antithrombin that allows antithrombin to bind to and thereby inhibit Factor Xa, which leads to a subsequent decrease in thrombin levels It causes a direct increase of thrombin inhibition as a result of antithrombin binding to the heparin pentasaccharide sequence and thrombin binding to an adjacent segment of heparin at the same time.
- Hypercoagulability
- A potentially dangerous state of an increased tendency for blood to coagulate, even within blood vessels. Hypercoagulability can be an inherited condition (e.g., Factor V Leiden mutation) or acquired through circumstance (e.g., cancer).


