MBBS OSCE · General Medicine
OSCE — Inherited Thrombophilia (Factor V Leiden & Protein C/S Deficiency)
Eight-minute OSCE station on Inherited Thrombophilia (Factor V Leiden & Protein C/S Deficiency): focused history, examination priorities, investigations, emergency and definitive management.
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Brief (to candidate)
You will assess a patient with a presentation consistent with Inherited Thrombophilia (Factor V Leiden & Protein C/S Deficiency).
You have 8 minutes to take a focused history, outline examination, investigations, and management including red flags.
Clinical context
Inherited thrombophilias are genetic disorders increasing the risk of venous thromboembolism (VTE). The commonest are factor V Leiden (activated protein C resistance; the single commonest inherited thrombophilia in Europeans, autosomal dominant, carrier rate 3 to 8 percent) and the prothrombin G20210A mutation (raised prothrombin; 2 percent of Europeans). Less common but higher-risk are deficiencies of the natural anticoagulants — antithrombin, protein C, protein S — which cause more severe, younger-onset, unusual-site thrombosis and warfarin-induced skin necrosis (protein C/S). Hyperhomocysteinaemia (MTHFR mutations) raises both venous and arterial thrombosis risk. Indications to test: VTE
Candidate tasks
- Clarify onset, severity, associated features, and red-flag symptoms.
- State focused examination priorities.
- List first-line investigations and any named score/criteria.
- Give immediate resuscitation steps.
- Outline definitive management with doses/routes where standard.
- Name complications and disposition (ward / HDU / theatre / discharge safety-net).
- Mention one special-population modifier (pregnancy, child, elderly, CKD).
Examiner checklist
| Domain | Pass behaviours |
|---|---|
| Definition | Correct working diagnosis language |
| Assessment | Focused, prioritised, red flags sought |
| Investigations | Appropriate first-line + interpretation |
| Emergency care | ABC / time-critical actions first |
| Definitive care | Specific drugs/procedures, not generic phrases |
| Safety | Unprovoked VTE under 50 years or in unusual sites (cerebral, mesenteric, portal) |
| Safety | Warfarin-induced skin necrosis early in treatment — protein C or S deficiency; s |
| Safety | Recurrent VTE despite anticoagulation or strong family history — antithrombin de |
| Communication | Clear plan and safety-netting |
Model outline
Lead with the working diagnosis and life threats. Resuscitate before definitive tests when unstable. Use guideline-standard therapy with named agents and doses. Document escalation criteria and follow-up. A safe candidate is specific, structured, and never delays critical care for non-urgent imaging.