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Deep Vein Thrombosis
• Formation of a semisolid coagulum in deep veins, usually
in lower extremities
Incidence
• DVT-PE causes~50,000 to 200,000 deaths per annum in west.
• DVT occurs in every 100/100,000 population in US.
• Incidence increases with increase in age.
• Only 40% of DVT patients have clinical symptoms
Etiology
• 3 factors described by RUDOLF VIRCHOW
1. Contact of blood with abnormal surface—ENDOTHELIAL
DAMAGE
2. Abnormal flow – STASIS
3. Abnormal blood- HYPERCOAGULABLE STATE
ENDOTHELIAL DAMAGE
• Surgical procedures
• Trauma
• Invasive procedures
• Central line insertion
• eg: Hip,knee surgeries> urological procedures> abdominal
surgeries>neurosurgeries> gynaecological surgeries.
STASIS
• Prolonged bed rest (>3days)
• Paralysis of lower limbs,
• Spinal injuries
• Long travel
Stasis in lower limb – causes initiation of dvt formation in soleal sinuses( MC
SITE)
HYPERCOAGULABLE STATES
• Factor V leiden mutation, prothrombin gene mutation
• Factor C,S, antithrombin 3 deficiency,
• Pregnancy, perperium, high dose ocp/ estrogen therapy.
• Malignacy( higher in mucin producing adeno Ca, pancreas,GIT, lung Ca.)
• nephrotic syndrome, homocystenimea
Pathology
• Virchows triad-> platelet aggregates->+ fibrin forms initial clots->
• Rbcs get trapped-> thrombus formation -> dislodges->emboli
Clinical features
• Pain / tenderness of lower limbs
• Swelling with pitting pedal edema
• Warmth/ redness of limb
• Superficial venous dilation
• Only 40% have symptoms
• Look for tachycardia, tachypnoea, breathlessness.-PE
Rare findings
• Phlegmasia alba dolens
• Due to total occlusion of deep
ileofemoral vessels.
• Painful white swollen limb
• Blenching +, no cyanosis
• Phlegmasia cerula dolens
• Massive edema causes
compromised arterial flow
• Painful blue leg
• Venous gangrene
• If blood flow is not retained
Homans sign
• Resistance( pain) of calf muscle to
forcible dorxiflexion
Moses test
• Gentle squeezing of calf muscle- pain
• not following now
MODIFIED WELLS CRITERIA
• Helps in early risk stratification and diagnosis of DVT
Diagnosis
• Blood investigations:- D-DIMER – NON SPECIFIC
• A FIBRIN DEGRADATION PRODUCT
• 90-95% SENSITIVITY
• 99% NEGATIVE PREDICTIVE VALUE
• ALSO positive in recent surgeries, pregnancies, DIC, ACUTE MI,
collagen vascular diseases, etc
IMAGING STUDIES
1. VENOGRAPHY
• Most accurate method to confirm position of DVT.
• Torniquet is applied to block superficial veins->
dye is injected to venous system
• Invasive technique
Nuclear scanning
• I125 labelled fibrinogen is injected
• Helps to identify old and new thrombus
Impedence plethysmography
• Measures change in venous capacitance and rate of emptying of venous
volume on temporary occlusion and release
2. Duplex scan
• Current test of choice for diagnosis
• Inexpensive , non invasive
• Also helps to distinguish from other causes- tumour, popliteal cyst, abscess,
aneurysum, hematoma, etc.
• Unable to detect pelvic and small vessel thrombosis.
• Operator dependent results
MR venous imaging
• Best for pelvic and ivc thrombosis.
• costly
Management
• GENERAL MEASURES.
• Bed rest
• Encourage to do gentle foot/leg exercise every hourly.
• Avoid deep calf massage
Specific measures
• ANTICOAGULANT THERAPY.
• Traditionally inj. HEPARIN 5000 IU/80IU/Kg bolus within 24 hours of
diagnosis then 18U/Kg/hr to maintain APTT between 60-80sec. for
atleast 5 days
• Followed by WARFARIN to obtain an INR of 2.5-3.0( in an overlap-
start within 72 hours) for minimum 3 months.
• Now LMWH is widely used
LMWH
• Selectively inhibits factor XA
• Good bioavailability and efficacy
• No monitoring needed
• Subcutaneous OD/BD doses
• No thrombocytopenia.
• Eg.( Enoxaparin(clexane), daltiparin, tinzaparin)
• .(Enoxaparin 1 mg/kg SC q12hr, OR 1.5 mg/kg SC qDay (administer at same time
each day)
Thrombolytic therapy
Advantages
• Sudden reversal of symptoms
• Restore venous circulation
• Prevent pulmonary embolism
• Preserve venous nalvular function
Disadvantages
• clot propagation and embolism, rethrombosis,
Surgery for DVT
• Major procedure is clot removal and partial interruption of ivc to prevent
pulmonary embolism
• Indicated when anticoagulant therapy is
unsafe
Endovascular reconstruction
• Using percutaneous catheters
• -recanalization by balloon
dilation or stent placement
• first line therapy in ilial occlusions
Vena cava filters
• INDICATIONS
• Recurrent dvt despite of anticoagulants
• DVT with anticoagulant use is contraindicated
• c/c pulmonary embolism
• Propagation ileofemoral venous thrombous in anticoagulation
• Complications of anticoagulants
Retrivable filters used in trauma, short term uses, contraindicated anticoagulants
Prophylaxis
MECHANICAL
1. Advise to start walking within 24-48 hours of surgery
2. Leg excercises
3. Graded compression stalkings
4. Intermittent pneumatic compression devices
Medical prophylaxis
• Low dose unfractionated Heparin 5000 U s/c Q12H-Q8H( traditional)
• LMWH – Subcutaneous dose- OD ( Anti factor Xa& IIa)
• Enoxaparin(CLEXANE) 4000IU/40 mg/ 0.4ml s/c OD in abdominal
surgeries
Thanks…..
skm25®

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Deep vein thrombosis

  • 2. • Formation of a semisolid coagulum in deep veins, usually in lower extremities
  • 3. Incidence • DVT-PE causes~50,000 to 200,000 deaths per annum in west. • DVT occurs in every 100/100,000 population in US. • Incidence increases with increase in age. • Only 40% of DVT patients have clinical symptoms
  • 4. Etiology • 3 factors described by RUDOLF VIRCHOW 1. Contact of blood with abnormal surface—ENDOTHELIAL DAMAGE 2. Abnormal flow – STASIS 3. Abnormal blood- HYPERCOAGULABLE STATE
  • 5. ENDOTHELIAL DAMAGE • Surgical procedures • Trauma • Invasive procedures • Central line insertion • eg: Hip,knee surgeries> urological procedures> abdominal surgeries>neurosurgeries> gynaecological surgeries.
  • 6. STASIS • Prolonged bed rest (>3days) • Paralysis of lower limbs, • Spinal injuries • Long travel Stasis in lower limb – causes initiation of dvt formation in soleal sinuses( MC SITE)
  • 7. HYPERCOAGULABLE STATES • Factor V leiden mutation, prothrombin gene mutation • Factor C,S, antithrombin 3 deficiency, • Pregnancy, perperium, high dose ocp/ estrogen therapy. • Malignacy( higher in mucin producing adeno Ca, pancreas,GIT, lung Ca.) • nephrotic syndrome, homocystenimea
  • 8. Pathology • Virchows triad-> platelet aggregates->+ fibrin forms initial clots-> • Rbcs get trapped-> thrombus formation -> dislodges->emboli
  • 9.
  • 10. Clinical features • Pain / tenderness of lower limbs • Swelling with pitting pedal edema • Warmth/ redness of limb • Superficial venous dilation • Only 40% have symptoms • Look for tachycardia, tachypnoea, breathlessness.-PE
  • 11. Rare findings • Phlegmasia alba dolens • Due to total occlusion of deep ileofemoral vessels. • Painful white swollen limb • Blenching +, no cyanosis
  • 12. • Phlegmasia cerula dolens • Massive edema causes compromised arterial flow • Painful blue leg
  • 13. • Venous gangrene • If blood flow is not retained
  • 14. Homans sign • Resistance( pain) of calf muscle to forcible dorxiflexion
  • 15. Moses test • Gentle squeezing of calf muscle- pain • not following now
  • 16. MODIFIED WELLS CRITERIA • Helps in early risk stratification and diagnosis of DVT
  • 17.
  • 18. Diagnosis • Blood investigations:- D-DIMER – NON SPECIFIC • A FIBRIN DEGRADATION PRODUCT • 90-95% SENSITIVITY • 99% NEGATIVE PREDICTIVE VALUE • ALSO positive in recent surgeries, pregnancies, DIC, ACUTE MI, collagen vascular diseases, etc
  • 19. IMAGING STUDIES 1. VENOGRAPHY • Most accurate method to confirm position of DVT. • Torniquet is applied to block superficial veins-> dye is injected to venous system • Invasive technique
  • 20. Nuclear scanning • I125 labelled fibrinogen is injected • Helps to identify old and new thrombus
  • 21. Impedence plethysmography • Measures change in venous capacitance and rate of emptying of venous volume on temporary occlusion and release
  • 22. 2. Duplex scan • Current test of choice for diagnosis • Inexpensive , non invasive • Also helps to distinguish from other causes- tumour, popliteal cyst, abscess, aneurysum, hematoma, etc. • Unable to detect pelvic and small vessel thrombosis. • Operator dependent results
  • 23. MR venous imaging • Best for pelvic and ivc thrombosis. • costly
  • 24. Management • GENERAL MEASURES. • Bed rest • Encourage to do gentle foot/leg exercise every hourly. • Avoid deep calf massage
  • 25. Specific measures • ANTICOAGULANT THERAPY. • Traditionally inj. HEPARIN 5000 IU/80IU/Kg bolus within 24 hours of diagnosis then 18U/Kg/hr to maintain APTT between 60-80sec. for atleast 5 days • Followed by WARFARIN to obtain an INR of 2.5-3.0( in an overlap- start within 72 hours) for minimum 3 months. • Now LMWH is widely used
  • 26. LMWH • Selectively inhibits factor XA • Good bioavailability and efficacy • No monitoring needed • Subcutaneous OD/BD doses • No thrombocytopenia. • Eg.( Enoxaparin(clexane), daltiparin, tinzaparin) • .(Enoxaparin 1 mg/kg SC q12hr, OR 1.5 mg/kg SC qDay (administer at same time each day)
  • 27. Thrombolytic therapy Advantages • Sudden reversal of symptoms • Restore venous circulation • Prevent pulmonary embolism • Preserve venous nalvular function Disadvantages • clot propagation and embolism, rethrombosis,
  • 28. Surgery for DVT • Major procedure is clot removal and partial interruption of ivc to prevent pulmonary embolism • Indicated when anticoagulant therapy is unsafe
  • 29. Endovascular reconstruction • Using percutaneous catheters • -recanalization by balloon dilation or stent placement • first line therapy in ilial occlusions
  • 30. Vena cava filters • INDICATIONS • Recurrent dvt despite of anticoagulants • DVT with anticoagulant use is contraindicated • c/c pulmonary embolism • Propagation ileofemoral venous thrombous in anticoagulation • Complications of anticoagulants Retrivable filters used in trauma, short term uses, contraindicated anticoagulants
  • 31.
  • 32. Prophylaxis MECHANICAL 1. Advise to start walking within 24-48 hours of surgery 2. Leg excercises 3. Graded compression stalkings 4. Intermittent pneumatic compression devices
  • 33.
  • 34.
  • 35. Medical prophylaxis • Low dose unfractionated Heparin 5000 U s/c Q12H-Q8H( traditional) • LMWH – Subcutaneous dose- OD ( Anti factor Xa& IIa) • Enoxaparin(CLEXANE) 4000IU/40 mg/ 0.4ml s/c OD in abdominal surgeries