Venous Thromboembolism Prophylaxis
VTE prophylaxis encompasses pharmacological and mechanical measures to prevent DVT and PE in surgical and medical patients, guided by individual risk assessment.
Key Facts
VTE is responsible for approximately 25,000 preventable deaths per year in the UK NICE NG89 mandates VTE risk assessment for all patients admitted to hospital within 14 hours LMWH (e.g., enoxaparin 40mg SC OD) is the standard pharmacological prophylaxis for surgical patients Mechanical prophylaxis (anti-embolism stockings, intermittent pneumatic compression) should be used when pharmacological prophylaxis is contraindicated Extended prophylaxis (28 days post-discharge) is recommended after major orthopaedic surgery and abdominal/pelvic cancer surgery The Department of Health VTE risk assessment tool assesses both thrombotic and bleeding risk DOACs (rivaroxaban 10mg OD) are licensed for post-orthopaedic surgery VTE prophylaxis Fondaparinux 2.5mg SC OD is an alternative in patients with heparin-induced thrombocytopenia
Overview
Key Facts
Venous thromboembolism encompasses deep vein thrombosis and pulmonary embolism. Hospital-associated thrombosis accounts for a significant proportion of preventable hospital deaths. Systematic risk assessment and appropriate prophylaxis are fundamental to safe surgical care.
Epidemiology
VTE affects approximately 1-2 per 1,000 of the UK population annually. Without prophylaxis, DVT rates reach 40-60% after major orthopaedic surgery and 15-30% after general surgery. PE is the direct cause of death in approximately 1-2% of all hospital inpatients.
Aetiology
Virchow's triad underpins VTE pathogenesis:
- Stasis: Immobility, bed rest, long-haul travel, venous obstruction
- Endothelial injury: Surgery, trauma, central venous catheters
- Hypercoagulability: Malignancy, inherited thrombophilia (Factor V Leiden, prothrombin gene mutation), OCP/HRT, pregnancy, antiphospholipid syndrome
Additional surgical risk factors: operative duration >90 minutes, pelvic/abdominal surgery, malignancy, obesity (BMI >30), age >60 years.
Pathophysiology
Venous thrombi typically originate in valve sinuses of deep leg veins where blood flow is slowest. The clot consists of a fibrin-rich red thrombus with entrapped red cells. Proximal propagation increases the risk of embolisation to the pulmonary vasculature. Thrombus formation is initiated by tissue factor exposure and propagated via the coagulation cascade, with inadequate natural anticoagulant regulation (protein C, protein S, antithrombin).
Clinical Presentation
DVT
- Unilateral leg swelling, warmth, and erythema
- Calf tenderness, distended superficial veins
- Homan's sign (unreliable — calf pain on dorsiflexion)
- May be asymptomatic (especially post-operative)
Pulmonary Embolism
- Sudden-onset dyspnoea, pleuritic chest pain, haemoptysis
- Tachycardia, tachypnoea, hypoxia
- Massive PE: cardiovascular collapse, raised JVP, right heart strain
Post-Thrombotic Syndrome
- Chronic leg swelling, pain, skin changes (lipodermatosclerosis)
- Venous ulceration (typically above medial malleolus)
Red Flags
- Bilateral leg swelling with back pain — consider IVC obstruction (malignancy)
- Post-operative sudden cardiovascular collapse — consider massive PE
- Persistent unexplained tachycardia post-surgery — investigate for PE
- Phlegmasia cerulea dolens — massive iliofemoral DVT with limb ischaemia
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Deep vein thrombosis | Unilateral leg swelling, warmth, Wells score ≥2 | D-dimer, compression USS |
| Cellulitis | Erythema, warmth, fever, skin breach | Clinical, blood cultures, CRP |
| Ruptured Baker's cyst | Sudden calf swelling, knee arthropathy | USS knee/calf |
| Muscle tear/haematoma | Trauma history, localised tenderness | USS soft tissue |
| Lymphoedema | Chronic bilateral/unilateral swelling, non-pitting | Clinical assessment, lymphoscintigraphy |
| Superficial thrombophlebitis | Painful, palpable cord along vein | USS to exclude DVT extension |
Diagnosis / Investigation
Bedside
- VTE risk assessment: Department of Health tool — within 14 hours of admission
- Wells score for DVT: Score ≥2 = DVT likely → USS; <2 = unlikely → D-dimer
- Wells score for PE: Score >4 = PE likely → CTPA; ≤4 → D-dimer
Bloods
- D-dimer: High sensitivity, low specificity; age-adjusted cut-off (age × 10 µg/L if >50 years)
- FBC, coagulation screen: Baseline before anticoagulation
- Renal function: Adjust LMWH dose in renal impairment (eGFR <30)
- Thrombophilia screen: Only after acute event treated; not routinely recommended (NICE)
Imaging
- Compression USS: First-line for suspected DVT; sensitivity >95% for proximal DVT
- CTPA: Gold standard for PE diagnosis
- V/Q scan: Alternative if CTPA contraindicated (contrast allergy, renal impairment)
- Echocardiography: Assess right heart strain in massive PE
Special Tests
- Anti-Xa levels: Monitor LMWH in extremes of body weight, renal impairment, pregnancy
- HIT screen: Platelet count monitoring; PF4 antibodies if HIT suspected
Management
Non-pharmacological
- Early mobilisation: The single most important non-pharmacological measure
- Anti-embolism stockings (AES): Thigh-length preferred; contraindicated in peripheral arterial disease (ABPI <0.8)
- Intermittent pneumatic compression (IPC): Recommended for all surgical patients where possible (NICE NG89)
- Adequate hydration: Avoid dehydration perioperatively
Pharmacological
- Standard prophylaxis: Enoxaparin 40mg SC OD (or dalteparin 5,000 units SC OD), started 6-12 hours post-operatively
- Renal impairment (eGFR <30): Unfractionated heparin 5,000 units SC BD/TDS
- Post-orthopaedic surgery: Rivaroxaban 10mg OD for 14 days (knee) or 35 days (hip) — or LMWH for same duration
- Cancer surgery: Extended prophylaxis 28 days with LMWH (ENOXACAN II trial)
- HIT: Fondaparinux 2.5mg SC OD as alternative
- Aspirin 75mg OD: Adjunct only in orthopaedic surgery (not sole prophylaxis)
Surgical/Interventional
- IVC filter: Consider in patients with confirmed proximal DVT and contraindication to anticoagulation
- Retrievable filters: Should be removed once anticoagulation can be safely started
Referral Criteria
- Confirmed VTE — haematology if recurrent or thrombophilia suspected
- HIT — urgent haematology input for alternative anticoagulation
- Massive PE — critical care and consideration of thrombolysis or embolectomy
Prognosis
- Appropriate VTE prophylaxis reduces DVT incidence by 60-70% and fatal PE by 50-65%
- Post-thrombotic syndrome develops in 20-50% of patients after proximal DVT within 2 years
- Mortality from untreated PE is approximately 30%; with treatment, mortality reduces to 2-8%
- Recurrent VTE occurs in approximately 5-10% within 1 year of completing anticoagulation
- Hospital-associated VTE accounts for approximately 50-60% of all VTE events
Other Relevant Information
VTE Risk Factors (Surgical Patients)
| Patient Factors | Surgical Factors |
|---|---|
| Age >60 years | Duration >90 minutes |
| BMI >30 | Pelvic/abdominal surgery |
| Active malignancy | Orthopaedic lower limb surgery |
| Previous VTE | Immobility >3 days |
| Thrombophilia | Central venous catheter |
| OCP/HRT use | Tourniquet use |
LMWH Dosing by Indication
| Indication | Enoxaparin | Dalteparin |
|---|---|---|
| Standard prophylaxis | 40mg SC OD | 5,000 units SC OD |
| Treatment dose | 1.5mg/kg SC OD | 200 units/kg SC OD |
| Renal impairment (eGFR <30) | Use UFH instead | Use UFH instead |
Key Trials
| Trial | Finding |
|---|---|
| ENOXACAN II | Extended LMWH (28 days) reduces VTE after cancer surgery |
| RECORD 1-4 | Rivaroxaban non-inferior to enoxaparin post-orthopaedic surgery |
| CLOTS 1 & 2 | Thigh-length stockings superior; AES do not reduce DVT in stroke |