CURRENT & FUTURE THERAPEUTIC MANAGEMENT OF VENOUS THROMBOEMBOLISM. Gordon Lowe Professor of Vascular Medicine University of Glasgow

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CURRENT & FUTURE THERAPEUTIC MANAGEMENT OF VENOUS THROMBOEMBOLISM Gordon Lowe Professor of Vascular Medicine University of Glasgow

VENOUS THROMBOEMBOLISM Common cause of death and disability 50% hospital-acquired Largely preventable Largely treatable, if promptly diagnosed

VENOUS THROMBOEMBOLISM (VTE) Deep vein thrombosis (DVT) Pulmonary embolism (PE) Post-thrombotic leg syndrome

VENOUS THROMBOEMBOLISM Trauma / surgery / medical illness Activation of blood clotting Stasis in leg veins Calf vein thrombosis

CALF VEIN THROMBOSIS Only becomes symptomatic if occludes most of 6 deep calf veins, or main venous trunk (popliteal, femoral or iliac) Symptoms / signs due to reduced venous return pain / tenderness, swelling / oedema, increased skin temperature / distended superficial veins

PULMONARY EMBOLISM 50% prevalence at routine lung scanning in patients with symptomatic DVT; often asymptomatic Minor PE may present with pleurisy, fever, haemoptysis (infarction)

PULMONARY EMBOLISM Major PE may present with dyspnoea, faintness, ischaemic chest pain, tachycardia, tachypnoea, bronchospasm In 80% of fatal PE, previous DVT / minor PE not clinically recognised

If I wasn t at death s door, I was at least on his patio. Paul Merton (Comedian and PE survivor)

SIGN GUIDELINES ON VTE 1995, 2002 Prophylaxis 1999 Antithrombotic therapy 2010 Both updated 10/12/10, www.sign.ac.uk

VTE PROPHYLAXIS IN ACUTE MEDICAL PATIENTS Chest infection, heart failure, etc. 25% have asymptomatic DVT; reduced to 8% by low-dose heparin (Belch et al, Scott Med J 1980) Heparin also reduces symptomatic DVT, PE and fatal PE (Mismetti et al, JTH 2006) Only 50% receive in UK and worldwide (ENDORSE, Lancet 2009) UK risk assessment tool

VTE PROPHYLAXIS IN ACUTE MEDICAL PATIENTS Start on admission!

CLINICAL SCORE FOR DVT Cancer 1.0 Immobility 1.0 Recent bedrest / surgery 1.0 Calf tenderness 1.0 Unilateral oedema 1.0 Alternative diagnosis - 2.0 (Wells et al, Lancet 1997)

SUSPECTED DVT Clinical score D-dimer If low clinical score and normal D-dimer, can discharge from A and E Otherwise, daily S/C low molecular weight heparin until ultrasound to exclude / confirm

DIAGNOSIS OF DVT BY COLOUR DOPPLER ULTRASOUND

DIAGNOSIS OF DVT BY COMPRESSION ULTRASONOGRAPHY

DIAGNOSIS OF DVT BY VENOGRAPHY 15. Diagnosis of deep vein thrombosis (venogram) Episodes of deep vein thrombosis are often silent and clinical diagnosis is unreliable, therefore a high level of suspicion is necessary. Venography is considered to be the gold standard for diagnosis. However, investigation using a non-invasive ultrasound technique is often regarded as sufficient.

CLINICAL SCORE FOR PE Clinical DVT 3.0 No alternative Dx 3.0 Heart rate over 100 1.5 Immobilisation / surgery 1.5 Previous DVT/PE 1.5 Haemoptysis 1.0 Cancer 1.0 (Wells et al, Ann Intern Med 1998)

SUSPECTED MINOR PE If low clinical score and normal D-dimer, diagnosis excluded Otherwise, daily S/C low molecular weight heparin until lung scan or CT pulmonary angiography (CTPA)

DIAGNOSIS OF PE BY VENTILATION / PERFUSION LUNG SCANNING 11. Diagnosis of pulmonary embolism (perfusion and ventilation scans) In another patient with pulmonary embolism, a perfusion scan shows that an embolus has stopped the blood flow to part of one lung. The ventilation scan shows that this area is ventilated normally.

DIAGNOSIS OF PE BY CT PULMONARY ANGIOGRAPHY 13. Diagnosis of pulmonary embolism (spiral CT scan) Spiral CT is one of the more recently introduced methods for the diagnosis of pulmonary embolism. The entire circulation of both lungs can be visualised in less than half a minute. Here, a large embolus can be seen in the major vessels of both the right and the left lung.

WARFARIN AND VENOUS THROMBOEMBOLISM Start when diagnosis confirmed Continue heparin until INR > 2.0 for 2 days Target INR 2.0 3.0 Duration 3-6 months (longer if PE, idiopathic, continuing risk factors e.g. active cancer, elevated D-dimer at end of course)

CONTINUED S/C HEPARIN INSTEAD OF WARFARIN Pregnancy (warfarin crosses placenta and teratogenic) Active cancer

OTHER MANAGEMENT Massive DVT (venous gangrene) Thrombolysis/PCI? Massive PE Resuscitation (O 2, IV fluids, heparin) ECHO (CCU) / CTPA thrombolysis / PCF / embolectomy?

OTHER MANAGEMENT IVC filter (anticoagulants contraindicated or failed) Compression stockings (symptomatic DVT)

FUTURE MANAGEMENT OF VTE New oral anticoagulants Direct thrombin inhibitors (e.g. dabigatran) Factor Xa inhibitors (e.g. rivaroxaban)

NEW ORAL ANTICOAGULANTS Licenced in UK for prophylaxis in major orthopaedic surgery Probable licence in 2011-12 for prophylaxis in atrial fibrillation (RE-LY, dabigatran, NEJM 2009) Prophylaxis in medical patients Treatment of VTE (e.g. EINSTEIN DVT, rivaroxaban, in preparation)

FUTURE MANAGEMENT OF VTE Improved management of warfarin Education and follow-up (thrombosis nurses) Computerised dosing (Poller et al, J Thromb Haemost 2007; Jowett et al, J Thromb Haemost 2009)

FUTURE MANAGEMENT OF VTE?general practice, after diagnosis Patients will still bleed Thrombosis service and nurses still needed